{"meta":{"query_hash":"dd054e9cb202","filters":{"topic":"Genetic Syndromes and Imprinting"},"cohort_total":808,"direct_labels_cover":1,"predictions_cover":808,"exported":808,"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/dd054e9cb202","api":"https://metacan.xera.ac/api/v1/cohort?topic=Genetic+Syndromes+and+Imprinting"},"results":[{"id":"W1481125586","doi":"10.1002/stem.1405","title":"Zac1 Regulates Astroglial Differentiation of Neural Stem Cells Through <i>Socs3</i>","year":2013,"lang":"en","type":"article","venue":"Stem Cells","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"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 Science Council; University of Toronto; Deutsche Forschungsgemeinschaft; University of Cambridge","keywords":"Biology; Neural stem cell; Cell biology; SOCS3; Embryonic stem cell; Cellular differentiation; Gene knockdown; STAT3; Stem cell; Signal transduction; Apoptosis; Gene; Genetics","score_opus":0.009138094209769049,"score_gpt":0.20363846561396384,"score_spread":0.1945003714041948,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1481125586","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975826,0.00035080392,0.00058538554,0.000041141844,0.00054574665,0.0002915393,0.000015012819,0.000012517279,0.00057522074],"genre_scores_gemma":[0.996251,0.000060189006,0.0006549376,0.000058335205,0.00015316288,0.000014535372,0.000017063661,0.000027102966,0.002763669],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988277,0.000056526398,0.00033693365,0.00032528857,0.0001551954,0.00029838414],"domain_scores_gemma":[0.99926424,0.000012020215,0.00019465233,0.00036906288,0.000098289725,0.00006171816],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006426062,0.00018237217,0.00020758223,0.000020308098,0.000051325045,0.00003749945,0.00020154807,0.00013949965,0.00008822464],"category_scores_gemma":[0.0000014043609,0.00016467704,0.00013868594,0.000059230002,0.00005368654,0.0000081204,0.00014522822,0.000064241714,0.000054633965],"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":[0.000004295742,0.000036243393,0.0016509927,0.00004613383,0.000034223438,2.3186384e-7,0.000075313845,0.00012130693,0.99101305,0.000010084332,0.001048946,0.0059591704],"study_design_scores_gemma":[0.0003854555,0.00021219124,0.004235707,0.000016770116,0.0000209786,0.0000047398075,0.00022110576,0.00031886154,0.9924699,0.000026128015,0.0019208202,0.000167309],"about_ca_topic_score_codex":0.00005243518,"about_ca_topic_score_gemma":0.0000027123624,"teacher_disagreement_score":0.0057918616,"about_ca_system_score_codex":0.000007650053,"about_ca_system_score_gemma":0.000019533398,"threshold_uncertainty_score":0.67153347},"labels":[],"label_agreement":null},{"id":"W1483213138","doi":"10.1016/s1937-6448(09)76005-8","title":"Chapter 5 Imprinting and Extraembryonic Tissues—Mom Takes Control","year":2009,"lang":"en","type":"review","venue":"International review of cell and molecular biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto","funders":"","keywords":"Biology; Neuroectoderm; Genomic imprinting; Endoderm; Imprinting (psychology); Yolk sac; Gastrulation; Placentation; Epigenetics; Genetics; Cell biology; Embryonic stem cell; Body plan; Zebrafish; Mesoderm; Embryo; Gene; Placenta; DNA methylation; Gene expression; Fetus","score_opus":0.011299033730312774,"score_gpt":0.3085661714741187,"score_spread":0.2972671377438059,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1483213138","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00032919904,0.99484605,0.0013527601,0.00009327695,0.00015646304,0.0004216124,0.00003192881,0.000004929995,0.0027637917],"genre_scores_gemma":[0.0024788573,0.99555844,0.0009719069,0.00048548012,0.000108247375,0.000025870457,0.00015956102,0.000028183347,0.00018344486],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9983986,0.000106576954,0.0006556068,0.0005258277,0.00009814202,0.00021524828],"domain_scores_gemma":[0.99903214,0.000027524919,0.00047549655,0.00027421035,0.00011096637,0.00007963935],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00029376088,0.00033891285,0.0009689712,0.00008092455,0.00002738881,0.000016043094,0.00028717978,0.0002606011,0.000041486048],"category_scores_gemma":[0.000117565614,0.00027682667,0.00031235325,0.000036961253,0.00011104249,0.0000023959299,0.0001477771,0.00014255758,0.000005095687],"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":[0.0000016146471,0.000019790932,0.000014483263,0.009596455,0.00016886585,0.000004020588,0.0000022807558,6.1667954e-8,0.013065607,0.00095304893,0.000025757756,0.976148],"study_design_scores_gemma":[0.0002471456,0.00020049552,0.00001740268,0.009103057,0.00028466727,0.00022850723,0.0000024197873,0.0000028081236,0.00086549803,0.00007988926,0.9886949,0.00027322394],"about_ca_topic_score_codex":0.000004676416,"about_ca_topic_score_gemma":5.0661e-7,"teacher_disagreement_score":0.98866916,"about_ca_system_score_codex":0.0000063590082,"about_ca_system_score_gemma":0.00005277569,"threshold_uncertainty_score":0.9999684},"labels":[],"label_agreement":null},{"id":"W1488234983","doi":"10.1080/15592294.2015.1057383","title":"Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi","year":2015,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pediatric Oncology Group","funders":"","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Methylation; DNA methylation; Biology; Chorionic villi; Imprinting (psychology); Differentially methylated regions; Genetics; Fetus; Internal medicine; Andrology; Prenatal diagnosis; Pregnancy; Gene; Medicine; Gene expression","score_opus":0.014964852298395202,"score_gpt":0.2582650396297488,"score_spread":0.24330018733135358,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1488234983","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9888351,0.005526493,0.00444097,0.0001334721,0.00017298997,0.00020774174,0.000028739318,0.000013425962,0.00064107816],"genre_scores_gemma":[0.99624294,0.0007048224,0.0018627034,0.00006928722,0.000066184395,0.000060542498,0.00032380575,0.000030452682,0.00063928706],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983985,0.000100342724,0.0003878492,0.000488871,0.0002542173,0.0003702072],"domain_scores_gemma":[0.99911237,0.000018896997,0.00012553649,0.00046483014,0.000092871174,0.00018548191],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003850292,0.00021037398,0.00027962629,0.00016415722,0.000047662343,0.00004203737,0.0002526742,0.0002077303,0.00006761935],"category_scores_gemma":[0.0001640882,0.00021755061,0.00014723167,0.0005576502,0.000049399703,0.000005020162,0.00022516023,0.0001003317,0.000035105917],"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":[0.000020768945,0.0003757289,0.9236492,0.000043259763,0.000941495,0.00001837374,0.00045789246,0.020650892,0.034749467,0.000025017092,0.0033824095,0.015685493],"study_design_scores_gemma":[0.0026733517,0.0016911612,0.6628118,0.000056929544,0.0007104088,0.000077973826,0.00060042494,0.0039533745,0.27057356,0.00058681646,0.05474566,0.0015185281],"about_ca_topic_score_codex":0.00014746899,"about_ca_topic_score_gemma":0.00021461016,"teacher_disagreement_score":0.2608374,"about_ca_system_score_codex":0.000041004623,"about_ca_system_score_gemma":0.0000714347,"threshold_uncertainty_score":0.88714564},"labels":[],"label_agreement":null},{"id":"W1491300853","doi":"10.1111/j.1758-8111.2012.00032.x","title":"Autonomic nervous system dysfunction in obesity and Prader–Willi syndrome: current evidence and implications for future obesity therapies","year":2011,"lang":"en","type":"article","venue":"Clinical Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"","keywords":"Medicine; Obesity; Autonomic nervous system; Childhood obesity; Bioinformatics; Endocrinology; Internal medicine; Heart rate; Blood pressure; Biology","score_opus":0.06107436963152304,"score_gpt":0.3204256370358156,"score_spread":0.2593512674042926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1491300853","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99051416,0.006144559,0.0019845904,0.00021271742,0.0004926764,0.00058714097,0.000015579439,0.000024728368,0.000023872828],"genre_scores_gemma":[0.9957252,0.0024505786,0.0014478074,0.000058399426,0.00020257948,0.00005374447,0.000014388733,0.000015449932,0.000031809122],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99843395,0.00014428665,0.0004859084,0.0006214117,0.000055164004,0.00025930846],"domain_scores_gemma":[0.99909335,0.00009685625,0.00018414593,0.0004047436,0.000077809746,0.00014308524],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00077473524,0.00018750703,0.00032337147,0.000034789868,0.00016946238,0.000030701944,0.00017072569,0.00025132953,0.000003964804],"category_scores_gemma":[0.00017781236,0.00017241259,0.00011100285,0.000066555185,0.00014604887,0.000014758937,0.00020421873,0.00017506597,0.000003604707],"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":[0.000008751895,0.00022768973,0.9815671,0.00014462355,0.00003079855,3.2161702e-7,0.000087200846,9.4395836e-7,0.000706443,0.00029344167,0.00007024059,0.016862467],"study_design_scores_gemma":[0.0005009918,0.0004068465,0.9969146,0.00009642858,0.000045996578,0.000065607754,0.00016797244,0.00010329411,0.00014817026,0.00027945958,0.0010715066,0.00019909938],"about_ca_topic_score_codex":0.000051171122,"about_ca_topic_score_gemma":0.00007094879,"teacher_disagreement_score":0.016663367,"about_ca_system_score_codex":0.000027076367,"about_ca_system_score_gemma":0.000068840134,"threshold_uncertainty_score":0.70307815},"labels":[],"label_agreement":null},{"id":"W1493379081","doi":"10.1111/cge.12143","title":"Beckwith–Wiedemann and Silver–Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth","year":2013,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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":"Canadian Institutes of Health Research; Canada Research Chairs","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Phenotype; Embryonic stem cell; Genetics; Function (biology); Gene; Loss function; Endocrinology; DNA methylation; Gene expression","score_opus":0.04321345216059616,"score_gpt":0.3246826767803114,"score_spread":0.28146922461971524,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1493379081","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3906268,0.6085366,0.000023116341,0.0000055983232,0.00022312006,0.0004773886,0.000014378895,0.00000599577,0.00008704515],"genre_scores_gemma":[0.039174158,0.95837075,0.0017674504,0.000028789727,0.0001122202,0.00003657688,0.00011855318,0.000061758634,0.0003297756],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9970888,0.0001997308,0.0013001589,0.0008609698,0.00016913125,0.00038123457],"domain_scores_gemma":[0.99874747,0.00010003651,0.0005389694,0.0003313429,0.000074066425,0.00020811164],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00044881072,0.0004804374,0.0012963153,0.00011838274,0.000051501735,0.000041088173,0.00026697645,0.0007523557,0.000021130554],"category_scores_gemma":[0.00014862276,0.00041850473,0.0002676521,0.00016270066,0.0003201022,0.000005175666,0.0005829736,0.00031159678,0.0000130110175],"study_design_candidate":"design_other","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":[0.000033580316,0.00034780594,0.058443893,0.008575195,0.00081719435,0.000006826289,0.00004530012,0.0000016727312,0.0017622003,0.000023692946,0.00037592757,0.9295667],"study_design_scores_gemma":[0.006071073,0.0063317376,0.28126904,0.013881728,0.0025453104,0.001689828,0.0006830165,0.00020992476,0.0019896892,0.00029205525,0.68092763,0.004108954],"about_ca_topic_score_codex":0.000013979649,"about_ca_topic_score_gemma":0.000014799497,"teacher_disagreement_score":0.9254578,"about_ca_system_score_codex":0.0000251976,"about_ca_system_score_gemma":0.00022410681,"threshold_uncertainty_score":0.99982667},"labels":[],"label_agreement":null},{"id":"W1494956959","doi":"10.1186/1471-2156-2-22","title":"A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues","year":2001,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Alberta","funders":"Medical Research Council; Canadian Institutes of Health Research; RIKEN; Alberta Heritage Foundation for Medical Research; Fondation pour la Recherche Médicale; University of Alberta; Eunice Kennedy Shriver National Institute of Child Health and Human Development; University of Miami; March of Dimes Foundation","keywords":"Genomic imprinting; Angelman syndrome; Genetics; Biology; Imprinting (psychology); Gene; Chromosome 15; Synteny; Allele; UBE3A; Gene cluster; Uniparental disomy; Chromosome 7 (human); Chromosome; Autism; Human genome; Neurodevelopmental disorder; Genome; Gene expression; DNA methylation; Karyotype; Medicine","score_opus":0.025309143560509898,"score_gpt":0.25171348208316513,"score_spread":0.22640433852265524,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1494956959","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969796,0.0019151767,0.00049155304,0.0001091729,0.00006822994,0.0003154175,0.0000031523116,0.0000066489724,0.00011106634],"genre_scores_gemma":[0.99662185,0.0006987041,0.0022027576,0.00011697627,0.00006868649,0.0000148998715,0.000007797238,0.000018371898,0.0002499806],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99864775,0.00017635197,0.00034872914,0.00041187755,0.00014072757,0.00027455215],"domain_scores_gemma":[0.9990107,0.0000218779,0.00016555793,0.0007094988,0.000041899573,0.000050511284],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003717926,0.00017911494,0.00017756592,0.00003640412,0.00016118793,0.000035617497,0.0003173858,0.00015217355,0.0000054224656],"category_scores_gemma":[0.00006799004,0.00012251077,0.00006874386,0.00012123414,0.00025202855,0.0000032980076,0.0005033157,0.00012512942,4.744631e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000002092722,0.000032671112,0.41648823,0.00003089605,0.000005643211,0.0000014174017,0.00032802884,0.000022331476,0.5824915,0.000010179279,0.000054032447,0.0005329569],"study_design_scores_gemma":[0.0005151776,0.00013744165,0.8951276,0.000033803917,0.000014738598,0.00022720695,0.00064893806,0.00007879719,0.10065362,0.00016722531,0.002217394,0.00017806939],"about_ca_topic_score_codex":0.000038940845,"about_ca_topic_score_gemma":0.00016985698,"teacher_disagreement_score":0.4818379,"about_ca_system_score_codex":0.0000058550804,"about_ca_system_score_gemma":0.00003406714,"threshold_uncertainty_score":0.49958444},"labels":[],"label_agreement":null},{"id":"W1508174106","doi":"10.1111/j.1399-0004.2005.00420.x","title":"Inherited microdeletions that give rise to Beckwith–Wiedemann syndrome","year":2005,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Spinal Cord Injury BC; Pacific Centre for Reproductive Medicine","funders":"","keywords":"Citation; Associate editor; Medicine; Library science; Computer science","score_opus":0.046803420956331145,"score_gpt":0.3402945591288867,"score_spread":0.2934911381725555,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1508174106","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.991508,0.0015251959,0.0038037985,0.0013245326,0.00041809492,0.00036731028,0.000026637868,0.000032566903,0.0009938687],"genre_scores_gemma":[0.95810497,0.0007952152,0.035694525,0.0020015892,0.0004810292,0.000031037023,0.000049541377,0.00005937949,0.0027827276],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9978139,0.000113194765,0.00065695733,0.00071643287,0.00019420702,0.0005053427],"domain_scores_gemma":[0.99847335,0.000040855623,0.00013774175,0.0008032401,0.00013814867,0.00040665639],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00039742028,0.00026764037,0.0003375041,0.000060978422,0.00012522169,0.00005314158,0.00045335002,0.00034741338,0.00011011367],"category_scores_gemma":[0.00023321444,0.00026968773,0.00026404567,0.000166057,0.00014317041,0.000002971046,0.0004345033,0.00020491626,0.00044295526],"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":[0.00021066843,0.0026354822,0.3152566,0.000118272284,0.0009811568,0.000057183042,0.00054449023,0.011820228,0.34817523,0.00010183339,0.07771373,0.24238515],"study_design_scores_gemma":[0.0011952344,0.0019253489,0.24710457,0.000045899156,0.000092366194,0.00023469047,0.00013474684,0.0007933998,0.019541763,0.00004972588,0.728138,0.0007442536],"about_ca_topic_score_codex":0.000007988101,"about_ca_topic_score_gemma":0.000041474756,"teacher_disagreement_score":0.6504243,"about_ca_system_score_codex":0.000015787004,"about_ca_system_score_gemma":0.00008123249,"threshold_uncertainty_score":0.9999755},"labels":[],"label_agreement":null},{"id":"W1508259436","doi":"10.1111/j.1399-0004.2006.00595b.x","title":"The beat goes on: ciliary proteins are defective in Meckel syndrome.","year":2006,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Pacific Centre for Reproductive Medicine","funders":"","keywords":"Citation; Library science; Medicine; Computer science","score_opus":0.02120420260376018,"score_gpt":0.3003213630940957,"score_spread":0.2791171604903355,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1508259436","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99480426,0.0019527616,0.00020136016,0.00035559278,0.0003832319,0.00043574226,0.000009802622,0.000012349752,0.0018449217],"genre_scores_gemma":[0.996235,0.00068037945,0.0011820542,0.0002709396,0.00028353222,0.000055137698,0.000017677978,0.000033451186,0.0012418098],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99807936,0.0001881509,0.0006089301,0.0005273276,0.00018234234,0.0004139187],"domain_scores_gemma":[0.9988882,0.000141008,0.00016880424,0.000637185,0.00007676874,0.00008803582],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005553566,0.00021003463,0.0002446267,0.000028888355,0.00014356678,0.000045631296,0.0003594526,0.0002759141,0.000008407019],"category_scores_gemma":[0.00035138088,0.00015773716,0.00020114054,0.00012477809,0.00022220965,0.0000013490555,0.00022824794,0.0002553969,0.000048080266],"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":[0.00010305131,0.0010917564,0.934618,0.000044891083,0.00014640395,0.000068189576,0.000028317265,0.0017692598,0.019565683,0.0003041837,0.0052983253,0.03696197],"study_design_scores_gemma":[0.00085214106,0.0011256405,0.95106566,0.000046361918,0.000019885136,0.000050197807,0.00009989002,0.00018147998,0.009534878,0.0010494924,0.03567506,0.00029931258],"about_ca_topic_score_codex":0.000026754045,"about_ca_topic_score_gemma":0.00027271782,"teacher_disagreement_score":0.036662657,"about_ca_system_score_codex":0.000015632988,"about_ca_system_score_gemma":0.00006944898,"threshold_uncertainty_score":0.6432335},"labels":[],"label_agreement":null},{"id":"W1509596159","doi":"10.1002/0471719188.ch11","title":"Genomic Imprinting: An Epigenetic Modification","year":2005,"lang":"en","type":"other","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Waterloo","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Epigenetics; Computational biology; Genetics; Biology; DNA methylation; Gene; Gene expression","score_opus":0.014443267439466466,"score_gpt":0.26154370902221824,"score_spread":0.24710044158275177,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1509596159","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.06822219,0.002956746,0.007968316,0.00006955963,0.00038726185,0.00050595077,0.000017601236,0.00013359718,0.91973877],"genre_scores_gemma":[0.09990321,0.00079376757,0.01279119,0.00019318073,0.0014678352,0.000028976114,0.00030041323,0.00056299457,0.88395846],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9987679,0.000033928216,0.00022024376,0.00058597815,0.00010005562,0.00029185857],"domain_scores_gemma":[0.9989177,0.0000015524639,0.00015665803,0.00078789005,0.000024625324,0.00011158819],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00009535238,0.00026333064,0.00018301819,0.00009012362,0.000034735545,0.000035060068,0.00032726413,0.00039785934,0.0024216957],"category_scores_gemma":[0.000013033334,0.00026394977,0.00009382617,0.000039710943,0.000039025515,7.3276055e-7,0.00013526628,0.00008123709,0.00027167433],"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":[0.00000290945,0.00012069085,0.0016321978,0.00005288184,0.00013490199,6.697246e-7,0.000023594543,0.000086969885,0.76691204,0.00013321418,0.08362757,0.14727233],"study_design_scores_gemma":[0.00022927472,0.0001189703,0.008052944,0.000013194825,0.000026697899,0.00001962373,0.00002607343,0.00015880313,0.01377089,0.00000832849,0.977145,0.00043017522],"about_ca_topic_score_codex":0.00012368642,"about_ca_topic_score_gemma":0.00011723843,"teacher_disagreement_score":0.89351743,"about_ca_system_score_codex":0.000010466236,"about_ca_system_score_gemma":0.000057099693,"threshold_uncertainty_score":0.9999813},"labels":[],"label_agreement":null},{"id":"W1511421526","doi":"10.25011/cim.v31i4.4814","title":"INVESTIGATING THE MOLECULAR AND DEVELOPMENTAL EFFECTS OF VARIOUS CULTURE REGIMES IN A MOUSE MODEL SYSTEM","year":2008,"lang":"en","type":"article","venue":"Clinical and investigative medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Epigenetics; DNA methylation; Biology; Embryonic stem cell; Genetics; Methylation; Blastocyst; Embryo; Embryogenesis; Gene; Gene expression","score_opus":0.04804502277395591,"score_gpt":0.28375778637825905,"score_spread":0.23571276360430313,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1511421526","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996344,0.0020842948,0.0003769441,0.00060811226,0.00004651272,0.00021871041,0.0000013232456,0.0000057857937,0.0003143546],"genre_scores_gemma":[0.9942383,0.00040920937,0.004267373,0.00069984247,0.00005618808,0.000014493842,0.0000066758635,0.000010686456,0.00029720707],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99888253,0.00013455689,0.0004306244,0.0002943819,0.000112711794,0.00014519981],"domain_scores_gemma":[0.9994898,0.000057859008,0.00013087475,0.00013291836,0.000051114966,0.00013744984],"candidate_categories":["sts"],"consensus_categories":[],"category_scores_codex":[0.00034472835,0.00014463246,0.00029832523,0.000024075396,0.00007787304,0.000003380764,0.00010118779,0.00011692941,4.301245e-7],"category_scores_gemma":[0.0013191961,0.00008800019,0.00003125494,0.000082265455,0.0037036168,0.0000039633596,0.00015242326,0.00016595624,3.393467e-7],"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":[0.000006776251,0.000041359526,0.17070255,0.00034232822,0.00008897157,0.000011326253,0.0038498736,0.000051441497,0.8206483,0.002583804,0.00048111903,0.0011921626],"study_design_scores_gemma":[0.008177242,0.0031184817,0.25487128,0.002128876,0.00015305445,0.00062027393,0.006914006,0.011068397,0.7037284,0.0073630186,0.0009841927,0.0008727865],"about_ca_topic_score_codex":0.000041002666,"about_ca_topic_score_gemma":0.000005454001,"teacher_disagreement_score":0.11691992,"about_ca_system_score_codex":0.0000048756633,"about_ca_system_score_gemma":0.00007233111,"threshold_uncertainty_score":0.99900776},"labels":[],"label_agreement":null},{"id":"W1523114210","doi":"10.14740/jmc.v6i6.2108","title":"13q Deletion in a Girl Contributing to Antenatal Stroke, Insulin Resistance and Lymphedema Praecox: Expanding the Clinical Spectrum","year":2015,"lang":"en","type":"article","venue":"Journal of Medical Cases","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Lymphedema; Phenotype; Pediatrics; Internal medicine; Genetics; Biology; Gene; Cancer","score_opus":0.034914787226028234,"score_gpt":0.34096686581080904,"score_spread":0.3060520785847808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1523114210","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.988869,0.003460561,0.0018354417,0.005375311,0.00028906134,0.000080668186,0.0000037193906,0.0000017102338,0.00008451005],"genre_scores_gemma":[0.997582,0.0005866999,0.00062665483,0.00051350566,0.0006322359,0.0000016056905,0.0000017131363,0.000007523813,0.000048051075],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983973,0.00017130873,0.00059459865,0.00015036644,0.0004268229,0.00025961138],"domain_scores_gemma":[0.99909484,0.00016217785,0.0002267591,0.00011163708,0.00009825927,0.0003063298],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0036547615,0.00008833789,0.00021964603,0.00004518845,0.000055572647,0.000033549084,0.00019235177,0.00013390597,0.000009615117],"category_scores_gemma":[0.00805572,0.000058425205,0.00006822017,0.000079717756,0.00008287964,0.0000054409948,0.000186857,0.00015203547,0.0000011889953],"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":[0.0015369543,0.0005149255,0.8514206,0.0000971141,0.00025732044,0.0028691685,0.00075215905,0.00007241199,0.014325818,0.00016883954,0.013181313,0.1148034],"study_design_scores_gemma":[0.02420128,0.008273452,0.7715743,0.0021059886,0.00017907919,0.026821684,0.012603182,0.0010405317,0.02717626,0.0006880136,0.12423093,0.0011053035],"about_ca_topic_score_codex":0.000021335829,"about_ca_topic_score_gemma":0.00014562465,"teacher_disagreement_score":0.113698095,"about_ca_system_score_codex":0.000022872191,"about_ca_system_score_gemma":0.00022953731,"threshold_uncertainty_score":0.96440303},"labels":[],"label_agreement":null},{"id":"W1524830710","doi":"10.1111/j.1365-2052.2007.01576.x","title":"<i>IGF2</i> gene characterization and association with rib eye area in beef cattle","year":2007,"lang":"en","type":"article","venue":"Animal Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Saskatchewan","funders":"Natural Sciences and Engineering Research Council of Canada; University of Saskatchewan","keywords":"Biology; Exon; SNP; Intron; Genetics; Single-nucleotide polymorphism; Allele; Insulin-like growth factor 2; Gene; Beef cattle; Pseudogene; Molecular biology; Genotype; Gene expression; Genome","score_opus":0.007008328429296687,"score_gpt":0.22174429415542435,"score_spread":0.21473596572612766,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1524830710","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963992,0.00030139743,0.0027551635,0.000072076495,0.00005232105,0.00013097882,0.000009259573,0.000006954707,0.00027260493],"genre_scores_gemma":[0.9968964,0.0003588845,0.0019371486,0.00016803233,0.00010885485,0.0000046511295,0.000107260086,0.000021723808,0.00039707837],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9991199,0.000018206381,0.00019143726,0.00026450527,0.00012807481,0.00027792229],"domain_scores_gemma":[0.99961495,0.0000080810405,0.00010273153,0.00014141596,0.00006911474,0.00006371733],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002384662,0.00012247323,0.000109325425,0.00004122598,0.000043948112,0.000027279802,0.00006975101,0.00014282878,0.000005854969],"category_scores_gemma":[0.000028535202,0.00012136191,0.000020535017,0.00010333602,0.000023914494,0.0000031371933,0.00006666596,0.00006615262,0.0000034780478],"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":[0.000013906765,0.000022165668,0.39671957,0.000004635,0.000010327018,0.000001137253,0.000039623537,0.00001024348,0.6008837,0.000002625774,0.000011202506,0.0022808334],"study_design_scores_gemma":[0.00032688538,0.0003406137,0.7065491,0.000006646241,0.000010440668,0.000011704555,0.000035722234,0.000059816964,0.2886789,0.0000026019013,0.0038506584,0.0001268916],"about_ca_topic_score_codex":0.000015926877,"about_ca_topic_score_gemma":0.00009796411,"teacher_disagreement_score":0.3122048,"about_ca_system_score_codex":0.00002235243,"about_ca_system_score_gemma":0.000030196003,"threshold_uncertainty_score":0.4948995},"labels":[],"label_agreement":null},{"id":"W1527923796","doi":"10.1002/ajmg.c.31363","title":"Molecular Findings in Beckwith–Wiedemann Syndrome","year":2013,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":218,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Phenotype; Biology; Gene; Genetics; Imprinting (psychology); Chromosome; Chromosomal region; Gene cluster; Computational biology; Gene expression; DNA methylation","score_opus":0.017444303452404154,"score_gpt":0.32568973281826974,"score_spread":0.3082454293658656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1527923796","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.18388352,0.81391925,0.00034502178,0.00030994506,0.00089177553,0.00053070753,0.000010501576,0.000006542253,0.00010275146],"genre_scores_gemma":[0.006657907,0.9882662,0.0035225914,0.0005908992,0.0005265266,0.00007383519,0.000061541585,0.00020391165,0.00009654975],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.988775,0.00097405177,0.0038803918,0.0010520648,0.0039175083,0.0014009528],"domain_scores_gemma":[0.9951686,0.00032361964,0.00150708,0.0010205598,0.00023068917,0.0017494421],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":["research_integrity"],"category_scores_codex":[0.0038086146,0.0010451428,0.0035319014,0.00076212385,0.000056301447,0.000077976205,0.0032272977,0.001772099,0.0004918047],"category_scores_gemma":[0.0025112075,0.00090564595,0.0009174897,0.0011834512,0.0012457167,0.0000067579585,0.001157169,0.0024771572,0.000047909518],"study_design_candidate":"design_other","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":[0.000008504956,0.00036593154,0.0010244652,0.0011092442,0.0002825337,0.0016644131,0.000080847145,0.000064825246,0.000046608464,0.0000053002505,0.0013996824,0.9939476],"study_design_scores_gemma":[0.0013543608,0.0031736712,0.00031850568,0.024412487,0.00041559138,0.01150446,0.00033764428,0.00025067877,0.00011448887,0.000043020354,0.95682895,0.0012461343],"about_ca_topic_score_codex":0.000031266667,"about_ca_topic_score_gemma":0.000027270404,"teacher_disagreement_score":0.99270153,"about_ca_system_score_codex":0.00014707197,"about_ca_system_score_gemma":0.0026929323,"threshold_uncertainty_score":0.99982417},"labels":[],"label_agreement":null},{"id":"W1530079397","doi":"10.1159/000106818","title":"Possible Non-Mendelian Mechanisms of Thyroid Dysgenesis","year":2007,"lang":"en","type":"review","venue":"Endocrine development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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; Université de Montréal","funders":"Endocrine Fellows Foundation","keywords":"Thyroid; Dysgenesis; Mendelian inheritance; Agenesis; Hypoplasia; Ectopic thyroid; PAX8; Medicine; Biology; Bioinformatics; Pathology; Genetics; Internal medicine; Gene; Transcription factor","score_opus":0.02826277671095831,"score_gpt":0.31069866190791323,"score_spread":0.28243588519695495,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1530079397","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0006768785,0.99016845,0.006394373,0.0000052545793,0.0004040029,0.0005503763,0.000016131391,0.000014315648,0.0017701962],"genre_scores_gemma":[0.0004855468,0.9612248,0.03387292,0.00003214514,0.00012719801,0.00008448859,0.00035476696,0.00009026432,0.0037278929],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9976301,0.00003883614,0.00092905643,0.0005968567,0.00027320476,0.0005318996],"domain_scores_gemma":[0.9988253,0.000014165991,0.00038481853,0.0005450024,0.00009610038,0.00013460335],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00028384518,0.00048770194,0.0009576107,0.0002153357,0.00007227751,0.000017961424,0.00046169505,0.00020545618,0.00008100963],"category_scores_gemma":[0.000033012584,0.0004266614,0.00033497394,0.00023238707,0.000030762054,0.0000016263591,0.00047393097,0.00013352142,0.00006479568],"study_design_candidate":"design_other","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":[0.0000019126783,0.000059294252,0.000012966578,0.0029385956,0.00028975087,0.000010787557,0.000020082727,0.0000013229371,0.0030884868,0.000023025686,0.00044182787,0.99311197],"study_design_scores_gemma":[0.0002211541,0.00012780861,0.00008320267,0.0011450879,0.00010273736,0.00016352237,0.00002522687,5.232083e-7,0.048286583,0.000012281714,0.94936734,0.0004645489],"about_ca_topic_score_codex":0.000010737999,"about_ca_topic_score_gemma":0.000006448178,"teacher_disagreement_score":0.9926474,"about_ca_system_score_codex":0.00004626714,"about_ca_system_score_gemma":0.00055891037,"threshold_uncertainty_score":0.9998185},"labels":[],"label_agreement":null},{"id":"W1530807287","doi":"10.1155/2015/474097","title":"PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication","year":2015,"lang":"en","type":"article","venue":"Case Reports in Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Shared Health; Winnipeg Regional Health Authority","funders":"","keywords":"Multiplex ligation-dependent probe amplification; Angelman syndrome; Genetics; Gene duplication; Genomic imprinting; Copy-number variation; Imprinting (psychology); Chromosome 15; Uniparental disomy; Biology; Medicine; Gene; Chromosome; DNA methylation; Genome; Karyotype","score_opus":0.023169774058054888,"score_gpt":0.2889852929844233,"score_spread":0.26581551892636845,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1530807287","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957726,0.0015299607,0.00046682122,0.000026272177,0.00034659388,0.00020022389,0.000004643136,0.000007366097,0.0016455106],"genre_scores_gemma":[0.99587876,0.00017374152,0.0030596324,0.000042651634,0.0001388171,0.000013416108,0.0000308111,0.000026249252,0.0006359109],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986453,0.00003399283,0.00055267784,0.00037748428,0.00015642495,0.0002340962],"domain_scores_gemma":[0.998765,0.000005252915,0.00027822543,0.00063403556,0.00018609875,0.00013139729],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035681392,0.00015050647,0.00018207807,0.0000597778,0.000022127242,0.000017455848,0.00008505049,0.00015057914,0.000021372434],"category_scores_gemma":[0.00011947368,0.00015356946,0.00005994351,0.00009807586,0.000076842865,0.0000019796348,0.00012682595,0.000068391535,0.0000076008705],"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":[0.000018452763,0.00013560841,0.25679436,0.0000663873,0.00004995158,0.0033491428,0.00020639112,0.0010526358,0.72708595,0.000036559464,0.0007204118,0.010484158],"study_design_scores_gemma":[0.0005748335,0.00038860028,0.021710824,0.0000365628,0.00003174433,0.079680264,0.00024323969,0.00021320133,0.83962435,0.0002960136,0.056870118,0.0003302757],"about_ca_topic_score_codex":0.00026482443,"about_ca_topic_score_gemma":0.00003650606,"teacher_disagreement_score":0.23508354,"about_ca_system_score_codex":0.000021563921,"about_ca_system_score_gemma":0.00017864333,"threshold_uncertainty_score":0.62623805},"labels":[],"label_agreement":null},{"id":"W1533681919","doi":"10.1023/a:1009489624045","title":"Toward a More Meaningful In Vitro Fertilization Success Rate","year":2000,"lang":"en","type":"article","venue":"Journal of Assisted Reproduction and Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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":"Reproductive medicine; In vitro fertilisation; Human fertilization; Biology; Andrology; Medicine; Gynecology; Pregnancy; Genetics","score_opus":0.018220350293160843,"score_gpt":0.2636646057124651,"score_spread":0.24544425541930423,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1533681919","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996231,0.0023358578,0.00035627442,0.000634805,0.00022795485,0.00006732248,0.0000012194702,0.0000030109761,0.00014256395],"genre_scores_gemma":[0.99498713,0.0021084063,0.0020114086,0.00007917969,0.0002828644,0.0000012089661,0.000007151898,0.000013154574,0.0005094669],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99902284,0.000073684154,0.00039456208,0.00024183217,0.00011769599,0.00014937515],"domain_scores_gemma":[0.999416,0.000004066899,0.00017611079,0.00019228907,0.00014651255,0.00006503879],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004307452,0.000102079466,0.00015359145,0.000059317943,0.00004560138,0.00003447687,0.000084599444,0.00009065695,0.000024940424],"category_scores_gemma":[0.0000948656,0.000092218404,0.000058860238,0.00013959048,0.00004370084,0.0000062097406,0.000027838963,0.000102404214,0.0000011603476],"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":[0.00016946266,0.00009897518,0.0073834145,0.0000280332,0.000042932566,0.0000064483297,0.00036780752,0.0021779842,0.7961617,6.1498304e-7,0.00014394247,0.1934187],"study_design_scores_gemma":[0.0015907564,0.0005006554,0.46333376,0.000048524533,0.00004372423,0.0014446442,0.0006709518,0.0006103824,0.5053109,0.000037401194,0.026154207,0.00025410732],"about_ca_topic_score_codex":0.0000052481914,"about_ca_topic_score_gemma":0.0000031101802,"teacher_disagreement_score":0.45595032,"about_ca_system_score_codex":0.000011112238,"about_ca_system_score_gemma":0.00003652414,"threshold_uncertainty_score":0.37605575},"labels":[],"label_agreement":null},{"id":"W1541412888","doi":"10.1038/npg.els.0001451","title":"Chromosomal Genetic Disease: Numerical Aberrations","year":2001,"lang":"en","type":"other","venue":"Encyclopedia of Life Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Meiosis; Biology; Mitosis; Genetics; Disease; Gene; Medicine; Pathology","score_opus":0.010357884867660077,"score_gpt":0.2539945433579645,"score_spread":0.24363665849030444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1541412888","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.031087568,0.018213222,0.002226779,0.00022772278,0.001107398,0.00035377708,0.00006586493,0.00004189984,0.9466758],"genre_scores_gemma":[0.08530525,0.018853001,0.021072667,0.00031256996,0.0034581022,0.000068908914,0.00012394527,0.00031187144,0.8704937],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99862444,0.000044163462,0.00026837995,0.0004824714,0.0002964461,0.0002840699],"domain_scores_gemma":[0.9992145,0.000009790079,0.00021459344,0.00033548276,0.000025450436,0.00020024071],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00008854208,0.00020389375,0.00022273237,0.00009929809,0.00007784837,0.000015223771,0.0004429262,0.00014977477,0.0016484279],"category_scores_gemma":[0.00017283071,0.00018160856,0.00010888474,0.00021455176,0.0003218573,0.0000019549145,0.00014492503,0.00006287475,0.000046354347],"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":[0.0000042111524,0.00018704409,0.15026768,0.00012486753,0.000108758766,0.0000069149673,0.00004783253,0.00028610104,0.0021608872,0.00008292015,0.83765113,0.009071672],"study_design_scores_gemma":[0.00014093085,0.00016216989,0.028876863,0.000052890588,0.000029807343,0.000008383813,0.00004494068,0.000057244128,0.00006388661,0.00002906769,0.970245,0.00028879492],"about_ca_topic_score_codex":0.0001291979,"about_ca_topic_score_gemma":0.00003014272,"teacher_disagreement_score":0.13259391,"about_ca_system_score_codex":0.0000034591808,"about_ca_system_score_gemma":0.0003828141,"threshold_uncertainty_score":0.9992642},"labels":[],"label_agreement":null},{"id":"W1542745269","doi":"10.1002/mrd.22220","title":"Epigenetic regulation of genomic imprinting from germ line to preimplantation","year":2013,"lang":"en","type":"review","venue":"Molecular Reproduction and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"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":"Natural Sciences and Engineering Research Council of Canada; Children's Health Research Institute","keywords":"Biology; Epigenetics; Genomic imprinting; Reprogramming; DNA methylation; Genetics; Imprinting (psychology); Epigenome; Gene; Gene expression","score_opus":0.029224737161846006,"score_gpt":0.28547310980945634,"score_spread":0.25624837264761036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1542745269","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.12449198,0.8613782,0.01276176,0.000017304745,0.00028194557,0.0009843317,0.0000065545732,0.000014121323,0.00006383518],"genre_scores_gemma":[0.009503469,0.9473801,0.041350648,0.000034241446,0.0002561168,0.00017870385,0.0007450967,0.00008110562,0.00047050236],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9979913,0.00007894196,0.0007090094,0.0008655751,0.00015394451,0.00020121591],"domain_scores_gemma":[0.99886715,0.0000065955087,0.00038690597,0.0005354035,0.000109455905,0.000094490715],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00023916615,0.0002928848,0.00052729016,0.00013390946,0.000064931926,0.000035159723,0.00012835792,0.0002037228,0.000034750847],"category_scores_gemma":[0.000073098774,0.00028219362,0.000101504804,0.00009687403,0.000024313897,0.000002965494,0.00025111518,0.00008376069,0.00004596214],"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":[0.0000019127506,0.00001560727,0.000017068507,0.00069877104,0.000110132234,3.5066728e-7,0.000066681256,0.000040476825,0.13358894,0.0000027049757,0.00003114561,0.8654262],"study_design_scores_gemma":[0.00016067731,0.00008883197,0.0029482024,0.0007007035,0.00012265301,0.00007013657,0.00002619114,0.0000054574302,0.120235875,0.000018176663,0.8751856,0.00043746823],"about_ca_topic_score_codex":0.000030573934,"about_ca_topic_score_gemma":0.0000023481775,"teacher_disagreement_score":0.8751545,"about_ca_system_score_codex":0.00003126597,"about_ca_system_score_gemma":0.00017045943,"threshold_uncertainty_score":0.99996305},"labels":[],"label_agreement":null},{"id":"W1547804365","doi":"10.1071/rdv16n1ab26","title":"26 ABERRANT REPROGRAMMING OF IMPRINTED GENE EXPRESSION IN ENLARGED PLACENTAS OF MICE CLONED FROM ES CELLS TREATED WITH TSA OR 5AZAC","year":2004,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Cegep de Saint Hyacinthe; Université de Montréal; University of Guelph","funders":"International Council for Canadian Studies; Natural Sciences and Engineering Research Council of Canada; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu; Ontario Ministry of Agriculture, Food and Rural Affairs","keywords":"Genomic imprinting; Biology; DNA methylation; Reprogramming; Epigenetics; Molecular biology; XIST; Gene; Gene expression; Somatic cell nuclear transfer; Histone; Housekeeping gene; Andrology; Genetics; X-inactivation; Blastocyst; X chromosome; Embryogenesis","score_opus":0.01444423078156517,"score_gpt":0.23031228009727714,"score_spread":0.21586804931571196,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1547804365","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971353,0.00052274857,0.0019550393,0.000031284122,0.000055098142,0.00027652833,0.0000046171413,0.000012505025,0.0000069104303],"genre_scores_gemma":[0.9644708,0.00010385583,0.03529401,0.000005993205,0.000013956309,0.000016815886,0.0000423449,0.000012426744,0.000039781073],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99858606,0.000048034843,0.00044969795,0.0006149706,0.00013220526,0.000169047],"domain_scores_gemma":[0.99930054,0.000007921983,0.00017281994,0.00037194416,0.0000961496,0.00005062205],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031845004,0.00014403713,0.0002285473,0.00004986359,0.00004804836,0.000007689197,0.00006789319,0.00009428612,0.000012062058],"category_scores_gemma":[0.00007208543,0.000112007394,0.00002827355,0.00011857505,0.00006373739,0.0000060001007,0.00008670965,0.000060178783,7.2195684e-7],"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":[0.0007765665,0.00022194025,0.028111665,0.000061848565,0.000044289467,0.0000013654184,0.0005405984,0.00012873912,0.9631313,2.1476546e-7,0.0000016514771,0.006979791],"study_design_scores_gemma":[0.0010183463,0.00013596498,0.27119362,0.000078586505,0.000007927431,0.0000073789106,0.0003280635,0.0000037261202,0.72687346,0.000005147432,0.0002489552,0.00009878859],"about_ca_topic_score_codex":0.00033166722,"about_ca_topic_score_gemma":0.00010012959,"teacher_disagreement_score":0.24308197,"about_ca_system_score_codex":0.000026194619,"about_ca_system_score_gemma":0.00011721123,"threshold_uncertainty_score":0.4567529},"labels":[],"label_agreement":null},{"id":"W1569183880","doi":"10.1034/j.1399-0004.2000.570505.x","title":"Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15","year":2000,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":105,"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 Health Research Institute; BC Research (Canada); University of British Columbia; Children's & Women's Health Centre of British Columbia","funders":"Medical Research Council","keywords":"Uniparental disomy; Biology; Genetics; Meiosis II; Meiosis; Chromosome; Trisomy; Chromosome 21; Nondisjunction; Aneuploidy; Angelman syndrome; Chromosome 15; Karyotype; Gene","score_opus":0.03454083384588958,"score_gpt":0.3398858196890891,"score_spread":0.3053449858431995,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1569183880","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914955,0.00023950261,0.006095914,0.00053196505,0.00033914673,0.0010994538,0.00014230786,0.000009767006,0.000046474725],"genre_scores_gemma":[0.9922351,0.00020585093,0.004868206,0.0004351363,0.00043524324,0.00009956862,0.000073228555,0.000041376876,0.0016062729],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9978233,0.00012056191,0.0009071947,0.0004925044,0.00020323397,0.00045323677],"domain_scores_gemma":[0.9987342,0.00013214775,0.0001895402,0.00056670356,0.00013291063,0.0002445254],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055355165,0.00023096493,0.00040342766,0.000034313893,0.000116124276,0.000037978447,0.0004926106,0.00018938529,0.00009429609],"category_scores_gemma":[0.00047732834,0.0001673005,0.00023499808,0.00016361219,0.00012176348,0.0000036750587,0.00018900771,0.00009943012,0.000055705794],"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":[0.0014948447,0.0014467655,0.12478314,0.0004954326,0.00073775824,0.000015858346,0.0013441017,0.015289028,0.5689222,0.000052373372,0.005311413,0.28010708],"study_design_scores_gemma":[0.0117438715,0.024296252,0.19967037,0.00097002106,0.00060422136,0.00028707564,0.0008717131,0.014738739,0.56371814,0.000687458,0.18016236,0.0022497694],"about_ca_topic_score_codex":0.0000084833455,"about_ca_topic_score_gemma":0.000053459913,"teacher_disagreement_score":0.2778573,"about_ca_system_score_codex":0.000018104756,"about_ca_system_score_gemma":0.00010852469,"threshold_uncertainty_score":0.68223166},"labels":[],"label_agreement":null},{"id":"W1580157617","doi":"10.1046/j.1432-1327.2000.01438.x","title":"<i>H19</i> sense and antisense transgenes modify insulin‐like growth factor‐II mRNA levels","year":2000,"lang":"en","type":"article","venue":"European Journal of Biochemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University; Jewish General Hospital; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Sense (electronics); Transgene; Messenger RNA; Insulin-like growth factor; Antisense RNA; Biology; Cell biology; Growth factor; Molecular biology; Genetics; Chemistry; Gene; Receptor","score_opus":0.012952441494805346,"score_gpt":0.216362423715647,"score_spread":0.20340998222084167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1580157617","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9935821,0.003240423,0.00023250577,0.00016550343,0.00012927364,0.000050236304,0.000034877106,0.000008658703,0.0025563857],"genre_scores_gemma":[0.9947099,0.0019114877,0.0014825246,0.00025801623,0.0004612962,2.919797e-7,0.0000093405915,0.00004841544,0.001118706],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985363,0.00013217151,0.00052101444,0.00031607147,0.00019854105,0.00029589745],"domain_scores_gemma":[0.9991152,0.000010710266,0.00021975292,0.00027738523,0.00013363198,0.00024329314],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034749703,0.00025674686,0.00024846953,0.000036384135,0.00013260187,0.000050623024,0.000188402,0.000090249996,0.00011311869],"category_scores_gemma":[0.0000552606,0.0002355181,0.00017644523,0.00007763052,0.00012281653,0.000007592035,0.000090669,0.00020785943,0.0000093584895],"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":[0.00004372581,0.000058225134,0.0005633992,0.000040321876,0.00008333878,0.0001401656,0.0001553765,0.000017169274,0.9767953,4.619222e-7,0.0005676156,0.02153486],"study_design_scores_gemma":[0.001482206,0.00049400056,0.015121409,0.00008437557,0.000045175435,0.004191363,0.000099211284,0.000014888675,0.961825,0.000008568864,0.016266359,0.00036742626],"about_ca_topic_score_codex":0.000002198558,"about_ca_topic_score_gemma":2.0316489e-7,"teacher_disagreement_score":0.021167433,"about_ca_system_score_codex":0.000008638591,"about_ca_system_score_gemma":0.000059940416,"threshold_uncertainty_score":0.96041495},"labels":[],"label_agreement":null},{"id":"W1580837527","doi":"10.1108/978-1-60752-633-9","title":"A Recipe for Success","year":2007,"lang":"en","type":"book","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"","keywords":"Recipe; Computer science; History; Ancient history","score_opus":0.0152232298869932,"score_gpt":0.27150528701785326,"score_spread":0.25628205713086005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1580837527","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0019006734,0.0011589961,0.015861042,0.000043576063,0.00047312758,0.00047279647,0.000030315927,0.000016263768,0.98004323],"genre_scores_gemma":[0.0016004659,0.00013803657,0.005270606,0.00034444415,0.00085768406,0.00002395406,0.0004770763,0.00006116741,0.99122655],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990152,0.0000052853743,0.00022078112,0.0003932635,0.000092162816,0.00027329568],"domain_scores_gemma":[0.99935645,0.000014025913,0.0000959238,0.0003585291,0.00010507654,0.000070017886],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017829215,0.00020274981,0.00018807569,0.00006944616,0.00004260126,0.000022173455,0.00021980552,0.00047078615,0.00011740943],"category_scores_gemma":[0.00003984062,0.00019078613,0.00019261685,0.000022824126,0.000037176087,4.014471e-7,0.000117903066,0.00007588316,0.000025650077],"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":[0.0000433489,0.000052094078,0.00031616172,0.00035715892,0.00036616725,0.0000033595538,0.000018752056,0.000008761119,0.037009086,0.004056873,0.86624163,0.09152661],"study_design_scores_gemma":[0.00026650992,0.00021428322,0.00010560722,0.000027380836,0.000026627202,0.000021093661,0.000004484489,0.000006219779,0.010317039,0.00054801966,0.98818874,0.00027397613],"about_ca_topic_score_codex":0.0000036226604,"about_ca_topic_score_gemma":0.000017954351,"teacher_disagreement_score":0.12194713,"about_ca_system_score_codex":0.0000147853625,"about_ca_system_score_gemma":0.00016526616,"threshold_uncertainty_score":0.7780033},"labels":[],"label_agreement":null},{"id":"W1581926946","doi":"10.1038/npg.els.0002013","title":"Autosomal Recessive Traits and Diseases","year":2006,"lang":"en","type":"other","venue":"Encyclopedia of Life Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Loss of heterozygosity; Consanguinity; Genetics; Biology; Phenotype; Mutant; Gene; Evolutionary biology; Allele","score_opus":0.007398009793705506,"score_gpt":0.24103135174946375,"score_spread":0.23363334195575824,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1581926946","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.09363033,0.020586414,0.00005960709,0.000072392126,0.00032085017,0.00018214944,0.00009193038,0.000022117685,0.8850342],"genre_scores_gemma":[0.16789629,0.016619354,0.009035113,0.00022599404,0.0025691031,0.000037143192,0.0000940683,0.00027268502,0.80325025],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990208,0.000029932853,0.00018153018,0.00039167248,0.00018130307,0.00019476825],"domain_scores_gemma":[0.9995756,0.000011870296,0.00020532795,0.00010237741,0.000016459087,0.00008835509],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000074164236,0.00016243468,0.00020620221,0.00008346328,0.000050952942,0.000013670439,0.00023684405,0.0001440569,0.000081112616],"category_scores_gemma":[0.00011625125,0.00013560122,0.00005367716,0.00009696309,0.00040366733,0.0000019914542,0.000118032,0.00003982906,0.0000030058295],"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":[0.00000457441,0.0000994578,0.06687187,0.00023739696,0.00007981379,0.0000026199025,0.00005524959,0.00001890484,0.0046449024,0.00011621396,0.9001131,0.027755896],"study_design_scores_gemma":[0.00026935202,0.00026772116,0.08178629,0.00010006926,0.000037431335,0.000009578026,0.00007817211,0.000009520544,0.00027646215,0.000079095415,0.9167323,0.0003540103],"about_ca_topic_score_codex":0.00008478276,"about_ca_topic_score_gemma":0.000048133414,"teacher_disagreement_score":0.08178395,"about_ca_system_score_codex":0.0000013478041,"about_ca_system_score_gemma":0.00016784084,"threshold_uncertainty_score":0.55296576},"labels":[],"label_agreement":null},{"id":"W1589590998","doi":"10.1038/ejhg.2009.106","title":"Beckwith–Wiedemann syndrome","year":2009,"lang":"en","type":"review","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":690,"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; SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Beckwith–Wiedemann syndrome; Epigenetics; Genomic imprinting; Imprinting (psychology); Monozygotic twin; Epigenesis; Genetics; Biology; Genetic disorder; Carcinogenesis; Medicine; DNA methylation; Cancer; Gene","score_opus":0.03914682175189165,"score_gpt":0.3037019688950376,"score_spread":0.26455514714314593,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1589590998","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.004222236,0.99076366,0.00017319275,0.000008016014,0.00041920762,0.00020641122,0.000008024937,0.000007417343,0.004191848],"genre_scores_gemma":[0.0019527113,0.9929088,0.0018777986,0.000058722388,0.0011036433,0.000001021019,0.000047564714,0.00016804684,0.0018817299],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9966633,0.00062002765,0.0015425335,0.00041458406,0.0003357976,0.00042376932],"domain_scores_gemma":[0.9972966,0.000012145656,0.0015392323,0.00071146665,0.00019037927,0.0002502063],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0009566522,0.00055140286,0.0012693973,0.00022953318,0.00012918812,0.00010058067,0.001135251,0.00017308386,0.000068524976],"category_scores_gemma":[0.000059762187,0.0004628596,0.0009959018,0.00013374926,0.00008909009,0.000002872973,0.00029414185,0.00047981515,0.00011534556],"study_design_candidate":"design_other","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":[0.0000021173532,0.00011837322,0.00001071384,0.0012780139,0.00046292643,0.0004902469,0.000035564128,0.000011885149,0.00052479387,0.0000060423035,0.0054485635,0.99161077],"study_design_scores_gemma":[0.00033047318,0.002711429,0.00029143825,0.0029576875,0.0006257927,0.0073222225,0.000015727712,2.6107423e-7,0.00003997283,0.000012533327,0.985206,0.00048647614],"about_ca_topic_score_codex":2.3318864e-7,"about_ca_topic_score_gemma":4.874499e-7,"teacher_disagreement_score":0.9911243,"about_ca_system_score_codex":0.00002635196,"about_ca_system_score_gemma":0.00018290158,"threshold_uncertainty_score":0.9997823},"labels":[],"label_agreement":null},{"id":"W1611812925","doi":"","title":"Fetal-placental calcium metabolism in mice partly or fully deficient in parathyroid hormone","year":2010,"lang":"en","type":"dissertation","venue":"Memorial University Research Repository (Memorial University)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Canadian Institutes of Health Research; American Society for Bone and Mineral Research","keywords":"Internal medicine; Endocrinology; Parathyroid hormone; Fetus; Calcium metabolism; Placenta; Homeostasis; Calcium; Biology; Medicine; Pregnancy","score_opus":0.020281668304955307,"score_gpt":0.26809375791952195,"score_spread":0.24781208961456663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1611812925","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9727066,0.0003490452,0.000015893647,0.000028524371,0.005665484,0.00091174204,0.00004958521,0.000024965124,0.020248136],"genre_scores_gemma":[0.918122,0.0005679025,0.00019376534,0.000005769426,0.0029894577,0.0000021215765,0.0006431625,0.0000666667,0.07740914],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9952535,0.0008893947,0.00045461315,0.0013794582,0.0008965881,0.0011264359],"domain_scores_gemma":[0.99806315,0.00009598257,0.00027148752,0.0007008663,0.0004846453,0.00038388107],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.0009080549,0.00052505115,0.0006872155,0.0014100828,0.00057857716,0.00013198795,0.0013941922,0.001364908,0.00003697682],"category_scores_gemma":[0.00025130197,0.0006163937,0.00031507853,0.001433123,0.0002764616,0.00004971254,0.00063700264,0.0017211583,0.00002955036],"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":[0.007332069,0.00043643833,0.00039673896,0.00007732241,0.000117964264,0.001737778,0.00059179054,0.00011421068,0.9863766,0.00016435664,0.002167141,0.0004876008],"study_design_scores_gemma":[0.020908011,0.00225589,0.023302104,0.00026724394,0.0003471267,0.000181201,0.03843221,0.00022942151,0.43189442,0.00003406186,0.4795105,0.0026377998],"about_ca_topic_score_codex":0.00370523,"about_ca_topic_score_gemma":0.010171701,"teacher_disagreement_score":0.55448216,"about_ca_system_score_codex":0.0005138157,"about_ca_system_score_gemma":0.0018423628,"threshold_uncertainty_score":0.9999315},"labels":[],"label_agreement":null},{"id":"W1633153776","doi":"10.1523/jneurosci.0777-15.2015","title":"<i>Zac1</i>Regulates the Differentiation and Migration of Neocortical Neurons via<i>Pac1</i>","year":2015,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Alberta Children's Hospital; University of Calgary","funders":"Alberta Children's Hospital Research Institute; Agence Nationale de la Recherche; Canadian Institutes of Health Research; March of Dimes Foundation","keywords":"Biology; Gene knockdown; Transcription factor; Neuropeptide; Cell biology; Gene; Genetics; Receptor","score_opus":0.017933263176699594,"score_gpt":0.24574910639225991,"score_spread":0.2278158432155603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1633153776","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952783,0.00017393571,0.0035479597,0.0006788684,0.00024991133,0.000042939948,6.166262e-7,9.513526e-7,0.000026528256],"genre_scores_gemma":[0.9993348,0.000093604016,0.00022603486,0.00023658278,0.00007009794,4.5134624e-7,3.093868e-7,0.0000039741344,0.000034146527],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99935895,0.000050140938,0.00021694954,0.000097466014,0.00018225532,0.00009422584],"domain_scores_gemma":[0.9994882,0.000013613013,0.00020402053,0.000112228256,0.00011007236,0.00007188667],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002113586,0.00005643972,0.000080438585,0.000025227635,0.00004027269,0.000026693917,0.0001442458,0.00002543742,5.1140387e-7],"category_scores_gemma":[0.00024291249,0.00003627237,0.000040196755,0.00007908538,0.0001226881,0.000008752714,0.00006838633,0.00005798804,1.6862887e-7],"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":[0.0000067826545,0.000022356617,0.0127820065,0.0000026579855,0.0000016047145,6.6767115e-7,0.00004611098,0.00012992685,0.98526925,0.000009652896,0.00013761134,0.0015913501],"study_design_scores_gemma":[0.00038594473,0.0010476221,0.68787885,0.000011439099,0.000025073141,0.00062345114,0.00007917504,0.003142007,0.30315965,0.0002153789,0.0033526067,0.00007881755],"about_ca_topic_score_codex":0.00000434729,"about_ca_topic_score_gemma":0.000003094388,"teacher_disagreement_score":0.6821096,"about_ca_system_score_codex":0.0000023690357,"about_ca_system_score_gemma":0.00004233108,"threshold_uncertainty_score":0.14791442},"labels":[],"label_agreement":null},{"id":"W16865929","doi":"10.1007/978-0-387-70765-5_15","title":"Respiratory control abnormalities in necdinnull mice: implications for the pathogenesis of Prader-Willi syndrome","year":2007,"lang":"en","type":"book-chapter","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Pathogenesis; Respiratory system; Medicine; Pediatrics; Pathology; Internal medicine","score_opus":0.03275829016341943,"score_gpt":0.2724878892491701,"score_spread":0.23972959908575067,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W16865929","genre_codex":"other","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.24818347,0.098769404,0.06988097,0.0045234268,0.00194311,0.014977948,0.004127422,0.00013566203,0.5574586],"genre_scores_gemma":[0.8601789,0.001213889,0.0016885836,0.0014698391,0.00031480376,0.00025721124,0.000167241,0.00015627878,0.13455325],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9985811,0.000018175693,0.00059906836,0.00039103453,0.00010941371,0.00030118623],"domain_scores_gemma":[0.9987378,0.00013157983,0.0002938746,0.00060796866,0.00017451022,0.000054281758],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046319692,0.000276139,0.00036058968,0.00010800974,0.00007746977,0.000015357995,0.00034396615,0.00043603423,0.000058687776],"category_scores_gemma":[0.000059121106,0.00021903167,0.00026459392,0.000029319011,0.00014053682,0.000002079751,0.000097462806,0.00011381318,0.000004159359],"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":[0.00009936155,0.0003926241,0.059285067,0.0018914831,0.0034113957,0.000008469361,0.00039078805,0.00066028035,0.5964177,0.20218192,0.012673801,0.12258707],"study_design_scores_gemma":[0.0019821327,0.0008848135,0.22225256,0.00015251867,0.00031887082,0.00019785145,0.00020617024,0.00003448647,0.003657456,0.0020851702,0.7672797,0.0009482783],"about_ca_topic_score_codex":0.000025769796,"about_ca_topic_score_gemma":0.00009838864,"teacher_disagreement_score":0.7546059,"about_ca_system_score_codex":0.000017868793,"about_ca_system_score_gemma":0.00012869823,"threshold_uncertainty_score":0.89318526},"labels":[],"label_agreement":null},{"id":"W1710646799","doi":"10.1002/047001153x.g103106","title":"Imprinting and epigenetic inheritance in human disease","year":2005,"lang":"en","type":"other","venue":"Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Epigenetics; Genetics; Biology; Phenotype; Inheritance (genetic algorithm); Gene silencing; Gene; Disease; DNA methylation; Gene expression; Medicine","score_opus":0.005710718871114667,"score_gpt":0.22088864432457747,"score_spread":0.21517792545346281,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1710646799","genre_codex":"empirical","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.91871125,0.025570914,0.001346111,0.00009386187,0.00034215304,0.0019448732,0.0002046324,0.000032266402,0.051753953],"genre_scores_gemma":[0.1637598,0.31423062,0.41271523,0.00044124617,0.0025438713,0.00020773329,0.0005662209,0.0015088127,0.10402647],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99784565,0.00003514453,0.00095117174,0.00051728304,0.00016596705,0.0004847798],"domain_scores_gemma":[0.9984473,0.00000919796,0.0006439908,0.0006063581,0.000050353996,0.00024280034],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00027982277,0.00049899606,0.00055196555,0.0002528932,0.00006756602,0.00005253858,0.0003252637,0.00043124703,0.000042980126],"category_scores_gemma":[0.00006718806,0.0005421504,0.00009552155,0.00008079307,0.00027749452,0.0000055959663,0.000607747,0.00022217204,0.0000046068058],"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":[0.00014988292,0.00082390715,0.25435302,0.011100148,0.0009774237,0.000022521932,0.003810909,0.00096115255,0.18177655,0.00038898838,0.019292105,0.5263434],"study_design_scores_gemma":[0.004341036,0.0010165648,0.09827338,0.0012717027,0.00028740917,0.000066144145,0.0008744969,0.0044500143,0.01538667,0.00057933596,0.86970705,0.003746214],"about_ca_topic_score_codex":0.0000749667,"about_ca_topic_score_gemma":0.00020102141,"teacher_disagreement_score":0.85041493,"about_ca_system_score_codex":0.000025844432,"about_ca_system_score_gemma":0.00015740062,"threshold_uncertainty_score":0.999703},"labels":[],"label_agreement":null},{"id":"W1721320528","doi":"10.1071/rdv16n1ab35","title":"35 ANALYSIS OF EPIGENETIC MODIFICATIONS AND GENOMIC IMPRINTING IN NUCLEAR TRANSFER DERIVED BOS GAURUS × B. TAURUS CONCEPTI","year":2004,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Guelph","funders":"International Council for Canadian Studies; Natural Sciences and Engineering Research Council of Canada; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu; Ontario Ministry of Agriculture, Food and Rural Affairs","keywords":"XIST; Genomic imprinting; Biology; Imprinting (psychology); Epigenetics; Somatic cell nuclear transfer; X-inactivation; Genetics; Locus (genetics); Reprogramming; DNA methylation; X chromosome; Molecular biology; Embryo; Gene; Blastocyst; Embryogenesis; Gene expression","score_opus":0.018384983305854505,"score_gpt":0.23603074126735674,"score_spread":0.21764575796150223,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1721320528","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99521226,0.0008382505,0.0036047173,0.000074437936,0.00003480549,0.00017643879,0.0000021719686,0.000007001046,0.000049939026],"genre_scores_gemma":[0.99540675,0.00025151463,0.0042559067,0.000019219644,0.0000103762095,0.000012320094,0.000016785716,0.000008240924,0.000018872452],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99886143,0.000030322559,0.00036354113,0.00051896024,0.000073416515,0.00015232326],"domain_scores_gemma":[0.9995659,0.0000038548033,0.00004908052,0.00027746384,0.000050257957,0.000053439522],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002695092,0.00010809674,0.00018952585,0.00010706176,0.00008923753,0.000014696543,0.000054790948,0.00007216664,0.0000131392335],"category_scores_gemma":[0.00004494474,0.00011420237,0.00004018387,0.00017763505,0.00009012613,0.0000044358,0.00006180995,0.00005180372,0.000001044144],"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":[0.000029906634,0.000086570355,0.033738703,0.00003807076,0.00018697834,2.4655264e-7,0.0015536943,0.0020712337,0.93997616,0.000021480648,3.6791764e-7,0.022296593],"study_design_scores_gemma":[0.0003280577,0.000032364944,0.8302135,0.000008127016,0.000043886746,0.0000042951233,0.0003971197,0.000074114105,0.16845705,0.000022786202,0.00031237202,0.00010635063],"about_ca_topic_score_codex":0.00010622048,"about_ca_topic_score_gemma":0.00006999569,"teacher_disagreement_score":0.79647475,"about_ca_system_score_codex":0.000024664583,"about_ca_system_score_gemma":0.00006727877,"threshold_uncertainty_score":0.46570373},"labels":[],"label_agreement":null},{"id":"W1724866995","doi":"10.1007/978-0-387-77576-0_6","title":"Genomic Imprinting and Human Psychology: Cognition, Behavior and Pathology","year":2008,"lang":"en","type":"article","venue":"Advances in experimental medicine and biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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; University of Toronto","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Cognition; Psychology; Neuropathology; Angelman syndrome; Autism; Neuroscience; Developmental psychology; Biology; Genetics; Gene; Disease; DNA methylation; Medicine","score_opus":0.027430392531922598,"score_gpt":0.3617527594039637,"score_spread":0.3343223668720411,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1724866995","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96501774,0.033927437,0.000043537962,0.000101564096,0.00011948958,0.0001348943,0.000001706757,0.000005865188,0.0006477547],"genre_scores_gemma":[0.990105,0.008475994,0.00065677066,0.0005436321,0.00012364473,0.000038697628,0.000028866049,0.000009755513,0.000017671186],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9991119,0.000046182915,0.00021611877,0.0003986644,0.000022200185,0.0002049468],"domain_scores_gemma":[0.9997453,0.000013332538,0.00006198094,0.00010634775,0.000013890757,0.000059128215],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009822086,0.00013568324,0.00019829335,0.000059634443,0.00011109403,0.000002207329,0.000053209154,0.00011941429,0.000014235123],"category_scores_gemma":[0.000024237186,0.00011513062,0.000012519862,0.00003290447,0.000776926,0.0000055079063,0.0001443664,0.00007743165,5.4631874e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0000066575276,0.000026485384,0.25132442,0.0000047026297,0.00000418457,0.000007304059,0.00013848986,5.2106127e-8,0.7418843,0.00008536395,0.000008057949,0.0065100086],"study_design_scores_gemma":[0.0039813546,0.0036141195,0.8784125,0.00003978938,0.000025885465,0.0042327824,0.0017182699,0.0000055889377,0.09457026,0.0005518348,0.012443265,0.00040438335],"about_ca_topic_score_codex":0.000020303385,"about_ca_topic_score_gemma":0.000011972097,"teacher_disagreement_score":0.647314,"about_ca_system_score_codex":0.0000033026781,"about_ca_system_score_gemma":0.0000051057873,"threshold_uncertainty_score":0.46948904},"labels":[],"label_agreement":null},{"id":"W1725933063","doi":"10.1002/ajmg.a.35249","title":"Energy homeostasis in Prader–Willi Syndrome: How clinical research informs studies of animal models of genetic obesity","year":2012,"lang":"en","type":"letter","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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":"Medical genetics; Gerontology; Library science; Medicine; Genetics; Biology; Gene","score_opus":0.09859789480529922,"score_gpt":0.3847313034169727,"score_spread":0.28613340861167347,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1725933063","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9423451,0.027900357,0.00069180795,0.028246224,0.0005607674,0.0001857698,0.000028841663,0.0000025509034,0.000038590282],"genre_scores_gemma":[0.92629725,0.062271602,0.0032813423,0.0062855664,0.0016685099,0.000012035966,0.000025571188,0.000075498545,0.00008261213],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99230504,0.0010579258,0.0024731115,0.0004999384,0.0027040585,0.0009599235],"domain_scores_gemma":[0.9952125,0.0003965417,0.002148965,0.00076209835,0.0010437685,0.0004361354],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.004166266,0.0004457851,0.0019170381,0.0004958145,0.00005155097,0.0000222973,0.0014042354,0.0010275937,0.00003136178],"category_scores_gemma":[0.0011657324,0.0003674675,0.0005754166,0.0005640929,0.0022267003,0.000010650915,0.0008744078,0.0020365822,0.0000013974601],"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":[0.00017855775,0.0017665899,0.15595074,0.0017526149,0.0053806924,0.00061509927,0.0013999877,0.00027002222,0.0033811007,0.000021110203,0.47000656,0.35927692],"study_design_scores_gemma":[0.0065459083,0.051095452,0.18953405,0.0046752305,0.0011937808,0.0067110728,0.007997754,0.0013115952,0.0056556235,0.0008006676,0.7217,0.002778834],"about_ca_topic_score_codex":0.0000688257,"about_ca_topic_score_gemma":0.00001798044,"teacher_disagreement_score":0.3564981,"about_ca_system_score_codex":0.000048581573,"about_ca_system_score_gemma":0.0010928033,"threshold_uncertainty_score":0.99987775},"labels":[],"label_agreement":null},{"id":"W1774553629","doi":"10.1385/1-59259-983-4:273","title":"Phenotypic Analysis of the Mouse Placenta","year":2005,"lang":"en","type":"article","venue":"Humana Press eBooks","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"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":"Phenotype; Placenta; Biology; Mutant; Identification (biology); Computational biology; Genetics; Gene; Bioinformatics; Pregnancy; Fetus","score_opus":0.02372172660308965,"score_gpt":0.25178871776819794,"score_spread":0.22806699116510828,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1774553629","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98045367,0.00090219406,0.00013246936,0.000013353384,0.000035225086,0.000097678356,0.000007993757,0.0000055796017,0.018351847],"genre_scores_gemma":[0.9912645,0.00003493866,0.00022493493,0.00010370668,0.00007114263,0.000006783798,0.000009863067,0.000009990535,0.008274094],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994034,0.000031334457,0.0001590139,0.00017316356,0.000095035386,0.00013804021],"domain_scores_gemma":[0.9993861,0.000003570805,0.00008335106,0.00046872813,0.000030342837,0.000027911045],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006741401,0.00008205273,0.00011566748,0.000030385927,0.000055749064,0.000011624068,0.00025393837,0.000052876734,0.000027704786],"category_scores_gemma":[0.000011771055,0.00006196739,0.00015210819,0.000023621138,0.000055243014,7.32131e-7,0.00018239518,0.000041299827,0.0000016508517],"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":[0.000032489148,0.00015629883,0.00731341,0.000057913283,0.0031148319,4.2212247e-7,0.0009967829,0.007944124,0.8863813,0.0032336318,0.0034163294,0.08735244],"study_design_scores_gemma":[0.00045942687,0.00005433506,0.038222335,0.0000069040384,0.00059010735,0.0000023179853,0.000053058648,0.0011818801,0.7872859,0.000014481227,0.17192225,0.0002070056],"about_ca_topic_score_codex":0.0000784865,"about_ca_topic_score_gemma":0.00016951762,"teacher_disagreement_score":0.16850592,"about_ca_system_score_codex":0.0000046519185,"about_ca_system_score_gemma":0.000011131725,"threshold_uncertainty_score":0.25269565},"labels":[],"label_agreement":null},{"id":"W1792639881","doi":"10.1186/1471-2164-16-s1-s12","title":"Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome","year":2015,"lang":"en","type":"article","venue":"BMC Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Toronto; Trillium Health Centre; Credit Valley Hospital; Hospital for Sick Children","funders":"Hospital for Sick Children; University of Toronto; Government of Ontario; Genome Canada; Ontario Genomics; Ontario Genomics Institute","keywords":"Frameshift mutation; Biology; Exome sequencing; Autopsy; Exome; Genetics; Mutation; Computational biology; Evolutionary biology; Pathology; Medicine; Gene","score_opus":0.022054261627680583,"score_gpt":0.2584966924874054,"score_spread":0.23644243085972483,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1792639881","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99696743,0.0005614941,0.0020041692,0.000029015318,0.000040660205,0.00022679695,0.00005703289,0.0000036724962,0.00010973002],"genre_scores_gemma":[0.98921555,0.000030285873,0.010461163,0.000024323232,0.000011876732,0.00003086911,0.00012702013,0.000017229704,0.00008169038],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99888074,0.00006168404,0.0004371832,0.00028570878,0.00014644714,0.0001882226],"domain_scores_gemma":[0.99912935,0.000026350013,0.0002684299,0.0003622942,0.00013014508,0.000083396415],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002735047,0.0001381646,0.00039967787,0.00018241923,0.000013196677,0.00001103667,0.00015034234,0.00012156214,0.000009981916],"category_scores_gemma":[0.00012080023,0.00013186848,0.00011116157,0.00036860837,0.00007556722,0.0000034038565,0.000090688976,0.00004886839,0.0000023901912],"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":[0.00006128452,0.00023227012,0.8273186,0.00012621537,0.00074556674,0.000016217104,0.0008508452,0.019214923,0.14998478,0.000051558567,0.000046529487,0.001351179],"study_design_scores_gemma":[0.0015122722,0.0012149884,0.9363091,0.000058343576,0.0006625474,0.00010512809,0.0012627229,0.0014991013,0.056113556,0.00009176436,0.00083579443,0.0003346851],"about_ca_topic_score_codex":0.00018278342,"about_ca_topic_score_gemma":0.00043307422,"teacher_disagreement_score":0.10899047,"about_ca_system_score_codex":0.00002930159,"about_ca_system_score_gemma":0.00015365958,"threshold_uncertainty_score":0.53774405},"labels":[],"label_agreement":null},{"id":"W1803951751","doi":"10.3109/10409238.2015.1064350","title":"Epigenetic events regulating monoallelic gene expression","year":2015,"lang":"en","type":"review","venue":"Critical Reviews in Biochemistry and Molecular Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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","funders":"","keywords":"Biology; Epigenetics; Genomic imprinting; DNA methylation; Genetics; Epigenetics of physical exercise; Chromatin; Gene; Histone; Regulation of gene expression; Gene expression","score_opus":0.04445219793211987,"score_gpt":0.38385586590428317,"score_spread":0.3394036679721633,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1803951751","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0015943433,0.99547297,0.0016521866,0.000031995973,0.0001934929,0.0006829686,0.00003038456,0.000011578834,0.00033006762],"genre_scores_gemma":[0.0013175579,0.9898566,0.0074184034,0.000119073826,0.00025340205,0.00027006277,0.0005442408,0.00007680364,0.00014382594],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9960323,0.00058557076,0.0012032544,0.0013429045,0.00013295213,0.00070300896],"domain_scores_gemma":[0.9982789,0.00006212221,0.00027720458,0.000941684,0.00008857998,0.00035151426],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0008933898,0.00072376564,0.0018030792,0.00009174893,0.00007484217,0.000027297145,0.0005053458,0.0012045208,0.000019850508],"category_scores_gemma":[0.0018676626,0.00062139385,0.00044785708,0.00019091621,0.00026714607,0.0000029457942,0.0007498864,0.00042586878,0.00001917442],"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":[0.000005301604,0.00009115952,0.000051755826,0.0089715915,0.00005234008,0.000014884254,0.000008331604,5.356733e-7,0.15517561,0.00007192317,0.00023311541,0.83532345],"study_design_scores_gemma":[0.0003060215,0.00016757191,0.0000031486009,0.005972267,0.00019675509,0.0003227447,0.000009063108,0.0000033089998,0.023390217,0.0005422059,0.9682899,0.00079677353],"about_ca_topic_score_codex":0.0000033409867,"about_ca_topic_score_gemma":5.4741037e-7,"teacher_disagreement_score":0.9680568,"about_ca_system_score_codex":0.000047573016,"about_ca_system_score_gemma":0.00022236389,"threshold_uncertainty_score":0.9996237},"labels":[],"label_agreement":null},{"id":"W1833365966","doi":"10.1210/jc.2015-2503","title":"Macronutrient Regulation of Ghrelin and Peptide YY in Pediatric Obesity and Prader-Willi Syndrome","year":2015,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Institute of Nutrition, Metabolism and Diabetes; National Institute of Diabetes and Digestive and Kidney Diseases; American Diabetes Association; Canadian Institutes of Health Research; Children's Hospital Foundation; Children's Miracle Network Hospitals; Children's Health Research Institute; Women and Children's Health Research Institute; Foundation for Prader-Willi Research; National Institutes of Health; Stollery Children’s Hospital Foundation; National Center for Research Resources","keywords":"Ghrelin; Internal medicine; Endocrinology; Peptide YY; Postprandial; Medicine; Insulin; Body mass index; Obesity; Crossover study; Hormone; Neuropeptide; Neuropeptide Y receptor; Receptor","score_opus":0.03420403284976331,"score_gpt":0.3181829048476714,"score_spread":0.2839788719979081,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1833365966","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9859043,0.012724166,0.00017006525,0.000742972,0.0002983613,0.00010340674,0.0000013969754,0.0000016070228,0.000053750184],"genre_scores_gemma":[0.98639345,0.012024939,0.0011149879,0.000102477425,0.00029118775,9.557547e-7,0.0000011131239,0.000009040341,0.000061850005],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9980832,0.00041560322,0.000974439,0.00015962211,0.00015441715,0.00021274522],"domain_scores_gemma":[0.99875325,0.00014226953,0.0006187815,0.00020627948,0.00015392211,0.00012548342],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016518497,0.0001158636,0.00046983533,0.000082918086,0.000027870065,0.0000063376438,0.00018307973,0.00013256675,0.0000037593552],"category_scores_gemma":[0.00086366106,0.00008050645,0.000087357694,0.00008493577,0.0002200792,0.000007833592,0.00019505314,0.00028582662,0.0000010633676],"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":[0.00010122745,0.00027202928,0.98123276,0.000041200943,0.0001304252,0.0000096248605,0.00026254635,0.00019291282,0.0064249677,0.0002964151,0.0004454352,0.010590479],"study_design_scores_gemma":[0.0020654537,0.00049640983,0.98986477,0.00001093954,0.00013110443,0.0012435752,0.00013267272,0.00003422075,0.00095926155,0.0009698567,0.0040124943,0.00007925301],"about_ca_topic_score_codex":0.000022024864,"about_ca_topic_score_gemma":0.000008318935,"teacher_disagreement_score":0.010511225,"about_ca_system_score_codex":0.0000034914262,"about_ca_system_score_gemma":0.0000960805,"threshold_uncertainty_score":0.32829577},"labels":[],"label_agreement":null},{"id":"W1838511334","doi":"10.1684/j.1950-6945.2005.tb00126.x","title":"Atypical absences and recurrent absence status in an adult with Angelman syndrome due to the UBE3A mutation","year":2005,"lang":"en","type":"article","venue":"Epileptic Disorders","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Toronto Western Hospital; University of Toronto","funders":"","keywords":"Angelman syndrome; UBE3A; Epilepsy; Pediatrics; Status epilepticus; Mentally retarded; Medicine; Psychomotor retardation; Chromosome 15; Psychology; Psychiatry; Genetics; Chromosome; Biology; Developmental psychology; Pathology","score_opus":0.005778018916728868,"score_gpt":0.23643874636807274,"score_spread":0.2306607274513439,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1838511334","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99717075,0.0002942331,0.00061687006,0.0013829328,0.000059446855,0.00026701516,0.0000041016774,0.000007467042,0.00019721148],"genre_scores_gemma":[0.99758524,0.00012651671,0.0018415792,0.00027866146,0.000043043303,0.000040385647,0.00002266454,0.000013051764,0.000048845217],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9990606,0.00004839814,0.00015857721,0.00032842526,0.000119103126,0.00028494332],"domain_scores_gemma":[0.9995926,0.00001307534,0.000041612508,0.0002161463,0.000032148473,0.000104412284],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011294527,0.0001248455,0.00010542462,0.000036799134,0.00006850716,0.000039270355,0.00012834407,0.000051887233,0.000020440992],"category_scores_gemma":[0.000053294807,0.00008975034,0.00002018399,0.00011250927,0.00007865595,0.000008581772,0.00005638167,0.00007363151,0.000013227153],"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":[0.00019045426,0.00035919918,0.23958354,0.000054774446,0.000055566303,0.000023902849,0.0031222622,0.0046524084,0.0046658777,0.00033282384,0.00039459486,0.74656457],"study_design_scores_gemma":[0.0005221076,0.0011845025,0.99062246,0.000040160452,0.000008708291,0.00012283912,0.0015942882,0.0012544477,0.00021729941,0.00009221747,0.004116328,0.00022463368],"about_ca_topic_score_codex":0.0000946144,"about_ca_topic_score_gemma":0.0064939447,"teacher_disagreement_score":0.7510389,"about_ca_system_score_codex":0.000009661672,"about_ca_system_score_gemma":0.000029545616,"threshold_uncertainty_score":0.36599126},"labels":[],"label_agreement":null},{"id":"W1844199574","doi":"10.1038/ejhg.2015.224","title":"Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling","year":2015,"lang":"en","type":"review","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"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","funders":"Ministero della Salute; Institut National de la Santé et de la Recherche Médicale; Instituto de Salud Carlos III; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research","keywords":"Beckwith–Wiedemann syndrome; Genetic counseling; Genetic testing; Genetics; Prenatal diagnosis; Molecular genetics; Medicine; Biology; Computational biology; Pregnancy; Gene; Fetus","score_opus":0.050556555618824904,"score_gpt":0.30741652546420895,"score_spread":0.25685996984538406,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1844199574","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.08235083,0.90183425,0.014681799,0.000009349711,0.00012065898,0.0008357736,0.00007175761,0.000008170054,0.000087403554],"genre_scores_gemma":[0.026496204,0.9170595,0.05529474,0.000047665588,0.0005281075,0.000031563868,0.00013983747,0.00031426066,0.00008815019],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99659175,0.00035868026,0.0014358236,0.00075452693,0.00032161758,0.00053762837],"domain_scores_gemma":[0.9969364,0.000087195775,0.0013964926,0.0005432592,0.0006642625,0.00037243648],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0012805146,0.00067503523,0.0016176502,0.000401123,0.00017850685,0.00017279694,0.0005685864,0.00021606548,0.000002290813],"category_scores_gemma":[0.00028229208,0.00061908824,0.00077635073,0.00023957055,0.00013694815,0.000006288852,0.00030871638,0.0002623333,0.0000010832548],"study_design_candidate":"design_other","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":[0.00002986464,0.0001997673,0.000103634804,0.016400512,0.007657333,0.00038439015,0.0003872079,0.00070467324,0.009524207,0.000020929785,0.00023133581,0.9643561],"study_design_scores_gemma":[0.0066752825,0.021997,0.00038501003,0.012434288,0.047412153,0.008593984,0.00049379724,0.0011699224,0.0023752942,0.00046023878,0.8935434,0.0044596153],"about_ca_topic_score_codex":0.0000011670838,"about_ca_topic_score_gemma":0.0000019082663,"teacher_disagreement_score":0.9598965,"about_ca_system_score_codex":0.000028103132,"about_ca_system_score_gemma":0.0002071605,"threshold_uncertainty_score":0.99962604},"labels":[],"label_agreement":null},{"id":"W1849159271","doi":"10.1139/o11-033","title":"CTCF function is modulated by neighboring DNA binding factors","year":2011,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"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":"CTCF; Enhancer; Biology; DNA; DNA methylation; Genetics; Repressor; Molecular biology; Gene; Transcription factor; Gene expression","score_opus":0.021969894719404845,"score_gpt":0.25034473504490296,"score_spread":0.2283748403254981,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1849159271","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.123063795,0.87446004,0.000048301496,0.0000021877781,0.00031953404,0.00019317519,0.00015946719,0.000022401518,0.001731074],"genre_scores_gemma":[0.03145032,0.96279997,0.00004878029,0.000030453097,0.00023167794,0.000028557753,0.0022028955,0.000063788,0.0031435469],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9979003,0.00006697017,0.00048685065,0.0009978209,0.00005387161,0.00049420405],"domain_scores_gemma":[0.9989165,0.00001761155,0.00035421978,0.0004996776,0.00003918535,0.0001728113],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.000118473836,0.00059983117,0.0007772563,0.000054519372,0.00013832268,0.00003194203,0.00029446118,0.0013487071,0.00013847406],"category_scores_gemma":[0.000025378864,0.0005150085,0.00031776907,0.000115012306,0.00012401323,0.000002629877,0.0002984295,0.0002476569,0.000021793277],"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":[0.0000064333626,0.00006164301,0.00029808807,0.003206086,0.000279612,7.817229e-7,0.000019483701,3.3520212e-8,0.67890173,0.0000042092884,0.001487656,0.31573427],"study_design_scores_gemma":[0.00016006305,0.00015722589,0.000008998999,0.00028034332,0.00024049064,0.000024455827,0.00002846682,9.649355e-7,0.1690238,0.0000062334957,0.8295496,0.0005193671],"about_ca_topic_score_codex":0.000015507152,"about_ca_topic_score_gemma":2.449841e-7,"teacher_disagreement_score":0.82806194,"about_ca_system_score_codex":0.000021011778,"about_ca_system_score_gemma":0.000090385984,"threshold_uncertainty_score":0.9999477},"labels":[],"label_agreement":null},{"id":"W1857882766","doi":"10.1111/biom.12380","title":"Optimum Study Design for Detecting Imprinting and Maternal Effects Based on Partial Likelihood","year":2015,"lang":"en","type":"article","venue":"Biometrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Natural Sciences and Engineering Research Council of Canada; National Science Foundation","keywords":"Imprinting (psychology); Statistics; Econometrics; Computer science; Mathematics; Biology; Genetics","score_opus":0.033288574217492164,"score_gpt":0.2804025703448232,"score_spread":0.24711399612733104,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1857882766","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.84054565,0.00015738994,0.15840459,0.00001279386,0.00029022474,0.00053937617,0.0000021810304,0.000014741749,0.0000330353],"genre_scores_gemma":[0.9723721,0.000004032905,0.027264906,0.000058305937,0.00019393286,0.000053992626,0.000003958514,0.000028278278,0.000020477983],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99887395,0.000072533636,0.00019081219,0.00036696647,0.00017093343,0.0003248101],"domain_scores_gemma":[0.999325,0.000100394915,0.00009458748,0.00022348741,0.00010034647,0.00015621555],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008824722,0.00015640938,0.00014750102,0.00026603654,0.00008960331,0.00008160075,0.00012781506,0.000097632896,8.6024585e-7],"category_scores_gemma":[0.0011039639,0.00014546438,0.000049891394,0.00038549688,0.00001815515,0.0000024750789,0.00011859279,0.00005196198,0.0000029464875],"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":[0.0002201796,0.0005711753,0.21934123,0.00016262812,0.00014527862,0.000010495133,0.0001555685,0.001410497,0.5308626,0.0000041296503,0.00020557875,0.2469106],"study_design_scores_gemma":[0.006821854,0.012323016,0.09724372,0.000043045908,0.000104809114,0.000030420406,0.00036865904,0.04710907,0.83370554,0.00004220798,0.0015706165,0.00063704123],"about_ca_topic_score_codex":0.00001344648,"about_ca_topic_score_gemma":5.957182e-7,"teacher_disagreement_score":0.3028429,"about_ca_system_score_codex":0.00001623516,"about_ca_system_score_gemma":0.000050232935,"threshold_uncertainty_score":0.5931865},"labels":[],"label_agreement":null},{"id":"W1909009273","doi":"10.1034/j.1399-0004.2001.590303.x","title":"The role of genomic imprinting in human developmental disorders: lessons from Prader–Willi syndrome","year":2001,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"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":"Genomic imprinting; Angelman syndrome; Biology; Imprinting (psychology); Genetics; Gene; Human genome; Allele; Chromosome 15; Chromatin; Gene expression; DNA methylation; Chromosome; Genome","score_opus":0.059810896672741545,"score_gpt":0.3811113413316443,"score_spread":0.3213004446589028,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1909009273","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.15209518,0.8464732,0.00003862707,0.00001588453,0.00027385657,0.0005343954,0.000034354995,0.000007461385,0.00052703626],"genre_scores_gemma":[0.022881396,0.9742891,0.0020518173,0.000015760023,0.000210796,0.00005250481,0.00019569637,0.00009935603,0.00020352569],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9959557,0.00033593437,0.0020919696,0.0008546645,0.00019689846,0.0005648254],"domain_scores_gemma":[0.9979421,0.00025724276,0.0008159605,0.00080295186,0.00004467271,0.00013706881],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0007207275,0.0004805312,0.0012528088,0.00006813098,0.00016044812,0.000053399803,0.0010432372,0.0007681579,0.00003012605],"category_scores_gemma":[0.0002322818,0.00038803412,0.0006781235,0.00017892696,0.00030563347,0.0000017986611,0.0010063048,0.00053860404,0.000036657664],"study_design_candidate":"design_other","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":[6.0834697e-7,0.00013663515,0.00999683,0.000235845,0.00023158356,0.0000012567639,0.000016483425,0.0000055015653,0.0003672228,0.000013762061,0.000019770478,0.9889745],"study_design_scores_gemma":[0.00035566743,0.00023953033,0.018579211,0.0009058898,0.00020215267,0.00005320374,0.00016334186,0.000015362919,0.000043012285,0.00033930247,0.9786053,0.00049803895],"about_ca_topic_score_codex":0.000059302158,"about_ca_topic_score_gemma":0.00019375255,"teacher_disagreement_score":0.98847646,"about_ca_system_score_codex":0.00003849828,"about_ca_system_score_gemma":0.00037600598,"threshold_uncertainty_score":0.9998571},"labels":[],"label_agreement":null},{"id":"W1910203405","doi":"10.1002/047001153x.g103207","title":"Imprinting and epigenetics in mouse models and embryogenesis: understanding the requirement for both parental genomes","year":2005,"lang":"en","type":"other","venue":"Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Epigenetics; Genetics; Embryogenesis; Genome; Embryo; Gene; Embryonic stem cell; Parthenogenesis; X-inactivation; Cell fate determination; DNA methylation; X chromosome; Gene expression","score_opus":0.020167740544627073,"score_gpt":0.23715973019542183,"score_spread":0.21699198965079475,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1910203405","genre_codex":"empirical","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.839311,0.07991156,0.054929968,0.00030413753,0.00062707154,0.0070752404,0.0008033062,0.000046835154,0.016990893],"genre_scores_gemma":[0.10268887,0.5118601,0.35176793,0.00032366673,0.0012220991,0.00026827326,0.0002916988,0.0008474922,0.030729871],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99788266,0.000035471843,0.0009247071,0.00048552832,0.00016271787,0.00050890667],"domain_scores_gemma":[0.99866897,0.000029366734,0.00065118796,0.00046853736,0.000042885295,0.00013904394],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005094249,0.0004905735,0.00052909274,0.00019586588,0.00013417965,0.000091774426,0.0002908861,0.00041884344,0.0000068167565],"category_scores_gemma":[0.00003450295,0.0004372135,0.00009600452,0.00005605111,0.0003180212,0.000009117501,0.000620593,0.00015549352,5.028388e-7],"study_design_candidate":"design_other","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":[0.00044482562,0.00092650217,0.08586234,0.017807504,0.0040203794,0.0000064170295,0.02290502,0.010525319,0.19427232,0.004434341,0.013484544,0.64531046],"study_design_scores_gemma":[0.021488601,0.0058640325,0.010893296,0.0023442348,0.0018065211,0.00038935308,0.042740475,0.2396589,0.07220825,0.008220527,0.5824189,0.0119668655],"about_ca_topic_score_codex":0.00005001991,"about_ca_topic_score_gemma":0.00026060877,"teacher_disagreement_score":0.7366221,"about_ca_system_score_codex":0.000055239856,"about_ca_system_score_gemma":0.00014037493,"threshold_uncertainty_score":0.99980795},"labels":[],"label_agreement":null},{"id":"W1918246687","doi":"10.1002/ajmg.c.31362","title":"Molecular Mechanisms of Childhood Overgrowth","year":2013,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research","keywords":"PI3K/AKT/mTOR pathway; PTEN; Gene; Biology; Somatic cell; Cell biology; Genetics; Signal transduction","score_opus":0.004497885081645766,"score_gpt":0.24888345646908588,"score_spread":0.24438557138744013,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1918246687","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9777008,0.005856038,0.014159616,0.0012221752,0.0005612191,0.0002237068,0.0000046740256,0.000005054054,0.00026668035],"genre_scores_gemma":[0.96945626,0.014662125,0.0141038075,0.0013344863,0.00032976578,0.000012957272,0.000010922553,0.00006416762,0.00002552813],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99389696,0.0003283531,0.0016856784,0.0004453418,0.002945837,0.0006978126],"domain_scores_gemma":[0.9969744,0.00012030743,0.0008449109,0.00058757904,0.00035593266,0.0011168862],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0017123729,0.0003687762,0.0008132639,0.00021314749,0.000038908653,0.000026463895,0.001503934,0.00047018868,0.0006538586],"category_scores_gemma":[0.0016188492,0.00033113314,0.00030965114,0.00047695497,0.0008515649,0.000005543559,0.0005450702,0.0006755767,0.000012006879],"study_design_candidate":"design_other","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":[0.00006285692,0.002136692,0.029146554,0.000121182195,0.000575277,0.00030761564,0.00053159625,0.0010139203,0.13219856,0.00026538307,0.0040617,0.82957864],"study_design_scores_gemma":[0.014603316,0.04278948,0.15339921,0.0054073543,0.0006327231,0.009608253,0.0076159234,0.010920458,0.6935266,0.009366614,0.048176434,0.003953618],"about_ca_topic_score_codex":0.000031078962,"about_ca_topic_score_gemma":0.000007302159,"teacher_disagreement_score":0.82562506,"about_ca_system_score_codex":0.0000259418,"about_ca_system_score_gemma":0.00082201476,"threshold_uncertainty_score":0.99991405},"labels":[],"label_agreement":null},{"id":"W1944638690","doi":"10.1002/ajmg.a.37286","title":"Autism spectrum disorder in Prader–Willi syndrome: A systematic review","year":2015,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Glenrose Rehabilitation Hospital; University of Alberta; Alberta Health Services","funders":"","keywords":"Autism spectrum disorder; CINAHL; Neurodevelopmental disorder; Autism; Uniparental disomy; Medicine; Angelman syndrome; Clinical psychology; MEDLINE; Meta-analysis; Psychology; Psychiatry; Genetics; Psychological intervention; Chromosome; Pathology; Biology","score_opus":0.02094389307874395,"score_gpt":0.32905415314357767,"score_spread":0.3081102600648337,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1944638690","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004385704,0.9971922,0.00025065645,0.00069847517,0.00047505405,0.00088246155,0.000010174314,0.0000044850367,0.000047907808],"genre_scores_gemma":[0.0003207729,0.9982856,0.00047991288,0.0003754371,0.00020197572,0.000060570434,0.000032434993,0.00009145727,0.00015186016],"study_design_codex":"systematic_review","study_design_gemma":"not_applicable","domain_scores_codex":[0.99386936,0.0009181123,0.0026592675,0.0004733218,0.001487517,0.00059239246],"domain_scores_gemma":[0.99605775,0.000085062726,0.0023335053,0.0007513039,0.00009118964,0.00068121677],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0030184155,0.0005700113,0.004215818,0.00022392311,0.000032131622,0.000035861583,0.0013404285,0.00038564627,0.000080141515],"category_scores_gemma":[0.0010063981,0.00041836442,0.00079514645,0.00059718924,0.00031739834,0.0000033105996,0.00037677115,0.00079196424,0.00003621894],"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":[0.0000016472092,0.00033560934,0.00013371995,0.52219594,0.0011994033,0.00025787583,0.000057448306,0.0000071435843,0.0000010065851,0.000014794485,0.0042141997,0.47158125],"study_design_scores_gemma":[0.000310384,0.0010966696,0.00002450935,0.3125844,0.0012397924,0.0092980815,0.00006026186,0.0000064832757,2.0288516e-7,0.000013178342,0.67496186,0.00040417656],"about_ca_topic_score_codex":0.000013217658,"about_ca_topic_score_gemma":0.000011502413,"teacher_disagreement_score":0.67074764,"about_ca_system_score_codex":0.00007338943,"about_ca_system_score_gemma":0.001702769,"threshold_uncertainty_score":0.9998268},"labels":[],"label_agreement":null},{"id":"W1945471693","doi":"10.1152/ajpregu.2000.279.6.r2287","title":"Intestinal transport of monosaccharides and amino acids during postnatal development of mink","year":2000,"lang":"en","type":"article","venue":"American Journal of Physiology-Regulatory, Integrative and Comparative Physiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"","keywords":"Amino acid; Mink; Biology; Methionine; Biochemistry; Phenylalanine; Leucine; Brush border; Internal medicine; Endocrinology; Chemistry; Vesicle","score_opus":0.01195266600690161,"score_gpt":0.24814148793251675,"score_spread":0.23618882192561513,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1945471693","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99888176,0.0007625907,0.000119175296,0.00001515933,0.000039950017,0.000095820295,0.000011241107,0.000002431655,0.00007189725],"genre_scores_gemma":[0.99525714,0.00018774498,0.004392132,0.000027564249,0.00006577401,0.0000053960925,0.00001378396,0.000010441527,0.000040044313],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99846286,0.00015874516,0.0007038949,0.00032792246,0.0001083334,0.00023826279],"domain_scores_gemma":[0.9987125,0.00005059158,0.0006795056,0.00017600562,0.00028105942,0.00010036192],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001333204,0.00028199033,0.00087071594,0.00010001038,0.00007929069,0.000003301147,0.00021159781,0.00007152022,0.000050221628],"category_scores_gemma":[0.000016647055,0.0002147623,0.00013698112,0.00011405251,0.001432229,0.000015148999,0.00006380095,0.00018258838,8.073634e-7],"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":[0.00048456702,0.00010857606,0.007089761,0.000038716884,0.00030894094,8.255282e-7,0.0018967795,0.00007745494,0.98507166,0.000051790917,0.000008936772,0.00486197],"study_design_scores_gemma":[0.00040660676,0.0015825849,0.55925167,0.00006974862,0.00002514721,0.00009272931,0.0021566974,0.00001977665,0.43614945,0.00005545882,0.000063876294,0.00012628592],"about_ca_topic_score_codex":0.000022942455,"about_ca_topic_score_gemma":0.000008788641,"teacher_disagreement_score":0.5521619,"about_ca_system_score_codex":0.000011030311,"about_ca_system_score_gemma":0.00012365366,"threshold_uncertainty_score":0.8757753},"labels":[],"label_agreement":null},{"id":"W1951209160","doi":"10.1139/bcb-2015-0032","title":"A role for chromatin topology in imprinted domain regulation","year":2015,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"","keywords":"Chromatin; Scaffold/matrix attachment region; ChIA-PET; Topology (electrical circuits); Genomic imprinting; Biology; Nucleoporin; Regulation of gene expression; Computational biology; Chromosome conformation capture; Lamin; Genetics; Chromatin remodeling; Gene; Cell biology; Cell nucleus; Gene expression; DNA methylation; Nuclear transport","score_opus":0.01535157294503909,"score_gpt":0.2854822223928596,"score_spread":0.2701306494478205,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1951209160","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.023485309,0.974039,0.00014377164,0.000013669173,0.00012453692,0.00056116434,0.00007575861,0.000010656079,0.0015461443],"genre_scores_gemma":[0.007073859,0.987045,0.0019421064,0.000030119561,0.0004038208,0.00027985647,0.001992617,0.00005140888,0.0011812461],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9982039,0.00010756713,0.0005211271,0.0007312812,0.000040950952,0.0003951992],"domain_scores_gemma":[0.9991297,0.000032091644,0.00027812863,0.00039578756,0.00005699189,0.00010727389],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00036014523,0.00037439342,0.00081411755,0.00006425699,0.000046239922,0.0000148873,0.00023822587,0.0011110944,0.000019459474],"category_scores_gemma":[0.000073835334,0.00034045885,0.0001973576,0.0000898027,0.00013627579,0.0000012942776,0.00023097599,0.0001509011,0.0000051345273],"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":[0.000019146835,0.00007485639,0.00004629763,0.0045151906,0.00007433371,9.323473e-7,0.000027465314,5.3531096e-7,0.32056716,0.000047498736,0.0003372746,0.6742893],"study_design_scores_gemma":[0.0005868421,0.00024070655,0.00001235904,0.00028809358,0.00006871493,0.00008307498,0.0000675171,0.000007721518,0.019843034,0.00043776532,0.97796637,0.00039777783],"about_ca_topic_score_codex":0.000012849841,"about_ca_topic_score_gemma":0.0000053801523,"teacher_disagreement_score":0.9776291,"about_ca_system_score_codex":0.00003551094,"about_ca_system_score_gemma":0.00023409587,"threshold_uncertainty_score":0.99990475},"labels":[],"label_agreement":null},{"id":"W1953305292","doi":"10.1111/j.1468-3148.2011.00625.x","title":"Assessing Joint Attention Responding and Initiation in Children with Angelman Syndrome","year":2011,"lang":"en","type":"article","venue":"Journal of Applied Research in Intellectual Disabilities","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; Hamilton Health Sciences; Deer Lodge Centre; McMaster Children's Hospital","funders":"","keywords":"Joint attention; Angelman syndrome; Psychology; Autism; Remedial education; Cognition; Autism spectrum disorder; Mental age; Developmental psychology; Neurodevelopmental disorder; Cognitive psychology; Psychiatry","score_opus":0.10162146939252144,"score_gpt":0.33365181758738954,"score_spread":0.23203034819486812,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1953305292","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996927,0.00015659063,0.00016369767,0.000030193236,0.00002721312,0.00019141436,7.5838017e-7,0.0000017973889,0.0025012956],"genre_scores_gemma":[0.99875945,0.000120554556,0.0010096376,0.000008072337,0.000043699987,0.000011884629,0.0000033646522,0.00001516613,0.00002818477],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99868006,0.00015743179,0.00039765,0.00020081218,0.00027702877,0.00028704733],"domain_scores_gemma":[0.9994133,0.00018964188,0.00009558983,0.00012865094,0.00010849629,0.000064320855],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018067919,0.00010193541,0.00018189239,0.0005368272,0.00006323157,0.00006963496,0.00012678042,0.000086959284,0.00004069317],"category_scores_gemma":[0.0008958286,0.00008273233,0.000034087174,0.0003203209,0.0002660176,0.000023101173,0.0001206892,0.00034664327,0.000001786289],"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":[0.0009556684,0.0006700599,0.6419742,0.00022587557,0.0002069111,0.000025510833,0.027038936,0.00014557353,0.31251276,0.0011811991,0.00013883646,0.014924449],"study_design_scores_gemma":[0.00093407085,0.0013703656,0.92445606,0.0002611164,0.000007754622,0.00064522226,0.04974225,0.000034054083,0.02024449,0.002104073,0.000026671056,0.00017384233],"about_ca_topic_score_codex":0.00003373219,"about_ca_topic_score_gemma":0.00002425868,"teacher_disagreement_score":0.29226828,"about_ca_system_score_codex":0.000059476446,"about_ca_system_score_gemma":0.000090874266,"threshold_uncertainty_score":0.33737266},"labels":[],"label_agreement":null},{"id":"W1964340841","doi":"10.1086/302817","title":"Identification of Novel Imprinted Transcripts in the Prader-Willi Syndrome and Angelman Syndrome Deletion Region: Further Evidence for Regional Imprinting Control","year":2000,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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":"Genomic imprinting; Angelman syndrome; Imprinting (psychology); Biology; Genetics; UBE3A; Gene; Locus (genetics); Allele; Phenotype; Gene expression; DNA methylation","score_opus":0.03826544508161572,"score_gpt":0.2959085618659046,"score_spread":0.25764311678428886,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964340841","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98841184,0.0015427618,0.00853891,0.0011110803,0.00003985156,0.000344414,0.000003786374,0.0000021635772,0.0000051834736],"genre_scores_gemma":[0.9983843,0.000664996,0.00058387325,0.00021332732,0.00008330584,0.0000141073415,0.0000023023374,0.00002190819,0.000031906366],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9984683,0.00016928518,0.00069582346,0.00021113548,0.00022913213,0.00022634087],"domain_scores_gemma":[0.9986089,0.00009057183,0.0007354787,0.00035345907,0.00016457262,0.00004701664],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009705466,0.00015613815,0.0002900823,0.00007391386,0.000111788875,0.000037055543,0.0004681893,0.00004939936,0.000004767668],"category_scores_gemma":[0.000057345434,0.000108720255,0.00015318593,0.00015045295,0.00036548977,0.000010272477,0.000023854218,0.00014826574,3.3250168e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000068314366,0.00018379546,0.012883303,0.000057048193,0.00016370253,0.000003973309,0.0014375934,0.00078891637,0.9613714,0.000035146702,0.00004315906,0.022963636],"study_design_scores_gemma":[0.002201797,0.0045319046,0.97542554,0.00024294932,0.00021653781,0.007034112,0.002167587,0.0010492305,0.006064637,0.00021105964,0.0005580689,0.00029655197],"about_ca_topic_score_codex":0.000020715635,"about_ca_topic_score_gemma":0.0000091752645,"teacher_disagreement_score":0.96254224,"about_ca_system_score_codex":0.00001349519,"about_ca_system_score_gemma":0.00004470039,"threshold_uncertainty_score":0.44334832},"labels":[],"label_agreement":null},{"id":"W1964384703","doi":"10.4161/epi.23063","title":"Tissue-specific relationship of S-adenosylhomocysteine with allele-specific<i>H19/Igf2</i>methylation and imprinting in mice with hyperhomocysteinemia","year":2012,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"Child and Family Research Institute; University of British Columbia; Canadian Institutes of Health Research; Sick Kids Foundation; Heart and Stroke Foundation of Canada; American Heart Association","keywords":"Methylation; Genomic imprinting; Imprinting (psychology); Biology; Hyperhomocysteinemia; DNA methylation; Cystathionine beta synthase; Homocysteine; Allele; Methyltransferase; Molecular biology; Gene expression; Endocrinology; Gene; Genetics; Methionine","score_opus":0.016643573123072696,"score_gpt":0.23330077874052926,"score_spread":0.21665720561745658,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964384703","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9819085,0.0088048205,0.0077665257,0.0000564112,0.000069455855,0.00032797866,0.0000048672914,0.000011176308,0.0010502468],"genre_scores_gemma":[0.9765067,0.00062862295,0.02233594,0.000016925398,0.00019520737,0.000017028553,0.000044015665,0.000051981293,0.00020355775],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9984288,0.00008749482,0.00044514387,0.00038325688,0.00022033059,0.000434952],"domain_scores_gemma":[0.99908423,0.000052192303,0.00023136457,0.0003872914,0.00011617582,0.00012872698],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038291863,0.00024923513,0.0002730923,0.00010735648,0.00007763984,0.000024922829,0.00014834758,0.0001780752,0.00001539816],"category_scores_gemma":[0.000042800537,0.00021825911,0.000031680833,0.00024853688,0.00012825613,0.000012276976,0.00014561997,0.00015685511,0.0000051888765],"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":[0.00005309017,0.000076294775,0.38957876,0.000063117026,0.00002839774,0.000002113384,0.0004727481,0.00044801776,0.5979248,0.00019195882,0.000027451386,0.011133216],"study_design_scores_gemma":[0.0013871084,0.0006424484,0.52114,0.00008056612,0.000026675021,0.000113435344,0.00048113073,0.000039354596,0.46550682,0.000031660136,0.010156076,0.00039475723],"about_ca_topic_score_codex":0.000026002706,"about_ca_topic_score_gemma":0.000043117765,"teacher_disagreement_score":0.132418,"about_ca_system_score_codex":0.000020665166,"about_ca_system_score_gemma":0.000035123187,"threshold_uncertainty_score":0.8900348},"labels":[],"label_agreement":null},{"id":"W1965277298","doi":"10.1111/j.1601-183x.2011.00678.x","title":"Imprinted<i>Rasgrf1</i>expression in neonatal mice affects olfactory learning and memory","year":2011,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; National Institutes of Health","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Allele; Offspring; Phenotype; Weaning; Olfactory bulb; Endocrinology; Internal medicine; Genetics; Gene expression; Gene; Pregnancy; Central nervous system; Medicine","score_opus":0.01717042876871631,"score_gpt":0.2434507548125402,"score_spread":0.2262803260438239,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965277298","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966752,0.0023666013,0.00022296408,0.000015645668,0.00017583667,0.00023327259,0.000003379549,0.000020389152,0.0002867356],"genre_scores_gemma":[0.99714404,0.00018462833,0.0016056979,0.000076027936,0.00007704242,0.000051304112,0.000026347618,0.000037122354,0.0007978116],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988159,0.000093799485,0.00018605807,0.00046057798,0.00010300037,0.0003406674],"domain_scores_gemma":[0.99954474,0.000021557116,0.00007506201,0.00022027596,0.000027299364,0.00011104379],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020934334,0.00019996034,0.0001611646,0.0000723476,0.00007819108,0.000019055244,0.00015589723,0.00018347689,0.000084952364],"category_scores_gemma":[0.000079830585,0.00020109117,0.00006559627,0.00006416973,0.00007002169,0.0000064840124,0.00030157727,0.00016252823,0.000010439614],"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":[0.000010581106,0.000032444525,0.07276525,0.000012950806,0.0000051839643,0.000012738699,0.00040837628,0.000002153653,0.8713062,9.582012e-7,0.000039663224,0.055403505],"study_design_scores_gemma":[0.0005041376,0.00019465656,0.25528914,0.000027275084,0.000013418844,0.00008848926,0.0005481446,0.0000108486065,0.73786145,0.0000019679012,0.005219892,0.00024058626],"about_ca_topic_score_codex":0.00006703739,"about_ca_topic_score_gemma":0.000048301983,"teacher_disagreement_score":0.18252388,"about_ca_system_score_codex":0.000010635989,"about_ca_system_score_gemma":0.00003277711,"threshold_uncertainty_score":0.82002604},"labels":[],"label_agreement":null},{"id":"W1965313969","doi":"10.1006/geno.2002.6695","title":"Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome","year":2002,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Memorial University of Newfoundland; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Biology; Haploinsufficiency; Genetics; Fluorescence in situ hybridization; Chromosomal inversion; Chromosome 7 (human); Chromosomal rearrangement; Chromosome; Gene mapping; Gene duplication; Gene; Karyotype; Phenotype","score_opus":0.020667762265171828,"score_gpt":0.25141422851481726,"score_spread":0.23074646624964543,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965313969","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9915035,0.0075895153,0.000041553518,0.00003753795,0.000097610166,0.00015985899,0.0000052098353,0.000005706648,0.0005595048],"genre_scores_gemma":[0.9973122,0.0010141418,0.0012691751,0.000079803816,0.000041924974,0.000012655967,0.000008381901,0.00003061561,0.00023113581],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988951,0.00003572275,0.00036025405,0.00032251482,0.000097493066,0.000288891],"domain_scores_gemma":[0.9993856,0.0000060350035,0.00010559078,0.0004056322,0.000045421,0.00005172194],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010132631,0.00016534726,0.00025831515,0.00007428576,0.00004013399,0.000009187541,0.00022411652,0.00011085138,0.000049478815],"category_scores_gemma":[0.000028599536,0.00017593965,0.000095356394,0.00010492867,0.00009578884,0.000001818268,0.00018449343,0.00006959551,0.000022211187],"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":[0.0000013053593,0.000059702994,0.0062417444,0.000048736845,0.000077402634,0.0000232161,0.00020228552,0.0007130679,0.9914706,0.000033544096,0.00008495443,0.0010434608],"study_design_scores_gemma":[0.0023879863,0.0016219221,0.13448128,0.00011884231,0.00009944057,0.00063780375,0.00089630793,0.0006881028,0.85095173,0.0007387824,0.0062811924,0.0010966182],"about_ca_topic_score_codex":0.000013890981,"about_ca_topic_score_gemma":0.000010696256,"teacher_disagreement_score":0.14051886,"about_ca_system_score_codex":0.000025459263,"about_ca_system_score_gemma":0.000014039549,"threshold_uncertainty_score":0.7174611},"labels":[],"label_agreement":null},{"id":"W1968650685","doi":"10.1016/j.psychres.2006.11.010","title":"Parent-of-origin effect and genomic imprinting of the HTR2A receptor gene T102C polymorphism in psychosis","year":2007,"lang":"en","type":"article","venue":"Psychiatry Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Centre for Addiction and Mental Health; University of Toronto","funders":"","keywords":"Allele; Genomic imprinting; Imprinting (psychology); Psychosis; Locus (genetics); Genetics; Bipolar disorder; Gene; Biology; Gene expression; Psychology; Endocrinology; Psychiatry","score_opus":0.024107403603671754,"score_gpt":0.3393161368432285,"score_spread":0.3152087332395567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968650685","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99567896,0.0026914226,0.000067131485,0.00024648142,0.0004511484,0.00032859892,0.000005028439,0.0000026398855,0.00052859576],"genre_scores_gemma":[0.99759096,0.00027651704,0.0018062235,0.000019393185,0.00017232276,0.000012185251,0.0000040908935,0.000021428184,0.000096868236],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983761,0.00018095638,0.00038018645,0.000346844,0.00026343096,0.00045249003],"domain_scores_gemma":[0.99920267,0.00005801739,0.000110633766,0.00047712435,0.00007482197,0.0000767579],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021974065,0.00012461301,0.00018198705,0.00014001093,0.000082151215,0.00001237069,0.0003552577,0.00013611674,0.000025077303],"category_scores_gemma":[0.00012104037,0.000097965065,0.000095612326,0.00032792348,0.00017509644,0.0000022764953,0.00031923509,0.00023278836,0.000003539411],"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":[0.000024374593,0.00003112449,0.52287143,0.00004645845,0.000016865617,7.526053e-8,0.000032042823,0.0000016885188,0.4705901,0.00001833281,0.000082192084,0.0062852665],"study_design_scores_gemma":[0.00063194643,0.0003038939,0.8815149,0.00006397559,0.0000065598065,0.00001136941,0.00013475378,0.000015471047,0.11621259,0.000067843604,0.0009333159,0.00010335114],"about_ca_topic_score_codex":0.00028108642,"about_ca_topic_score_gemma":0.00010323664,"teacher_disagreement_score":0.35864347,"about_ca_system_score_codex":0.000014675625,"about_ca_system_score_gemma":0.00007741603,"threshold_uncertainty_score":0.39948994},"labels":[],"label_agreement":null},{"id":"W1968720872","doi":"10.1002/ajmg.a.36790","title":"Prader–Willi syndrome and Tay–Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq","year":2014,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hamilton Health Sciences; St. Joseph’s Healthcare Hamilton; Hamilton Regional Laboratory Medicine Program; McMaster University","funders":"","keywords":"Girl; Isochromosome; Association (psychology); Medicine; Genetics; Tay-Sachs disease; Pediatrics; Psychology; Disease; Biology; Internal medicine; Karyotype; Chromosome; Gene","score_opus":0.004336278804184094,"score_gpt":0.2275572275702251,"score_spread":0.22322094876604098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968720872","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967022,0.0013839947,0.00045922145,0.0011987264,0.00010962544,0.00011852607,0.0000070700285,0.0000025743664,0.00001809273],"genre_scores_gemma":[0.9970978,0.0016663681,0.0007482646,0.0002901639,0.000117838594,0.000008071163,0.00000833546,0.000025472616,0.00003771954],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9978506,0.0002588843,0.0005682328,0.00031428802,0.0006222579,0.00038576964],"domain_scores_gemma":[0.9987865,0.000052854917,0.00043985114,0.00017196761,0.00006228663,0.00048653278],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00074583146,0.00021229533,0.00045543446,0.00011713766,0.00003981818,0.000051243274,0.00022586403,0.00011653255,0.00001933501],"category_scores_gemma":[0.0002365811,0.00017930738,0.0000581126,0.00014952922,0.00027887634,0.00000959141,0.0001546604,0.00027639992,0.000001279329],"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":[0.000027065835,0.00010571921,0.98486626,0.000030699637,0.00006797523,0.000035160392,0.00014278182,0.00008051535,0.0015227922,0.0000036959043,0.00008738355,0.013029978],"study_design_scores_gemma":[0.0020969375,0.0017221366,0.9900927,0.0002885925,0.00004482404,0.00062664365,0.00026308093,0.0010159704,0.00044680331,0.00003513114,0.0031200647,0.0002471337],"about_ca_topic_score_codex":0.00006907464,"about_ca_topic_score_gemma":0.00009871694,"teacher_disagreement_score":0.012782844,"about_ca_system_score_codex":0.0000354801,"about_ca_system_score_gemma":0.00013188171,"threshold_uncertainty_score":0.73119426},"labels":[],"label_agreement":null},{"id":"W1969373798","doi":"10.1159/000083333","title":"Genetic Diversity among the Arabs","year":2005,"lang":"en","type":"review","venue":"Public Health Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":88,"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":"","keywords":"Consanguinity; Founder effect; Population; Genetics; Genetic heterogeneity; Medicine; Demography; Biology; Allele; Environmental health; Haplotype; Gene; Phenotype","score_opus":0.06483115023011855,"score_gpt":0.3099430890941076,"score_spread":0.24511193886398908,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969373798","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0019083825,0.9952476,0.00042974373,0.00053991907,0.00047175557,0.0008630281,0.000046515906,0.000017221593,0.00047581122],"genre_scores_gemma":[0.0004996989,0.99585253,0.00083978893,0.0008306267,0.0010764141,0.00005376923,0.00016101444,0.00007073807,0.00061544566],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9973498,0.00030334867,0.00068518665,0.00063582446,0.00018734291,0.00083847146],"domain_scores_gemma":[0.9980007,0.000028676975,0.0005547494,0.0009843647,0.00006379014,0.00036775618],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0009108195,0.00040569954,0.00078513206,0.00008513091,0.0006214416,0.00010620495,0.0010377576,0.0003781731,0.000046407666],"category_scores_gemma":[0.000089782174,0.0003060378,0.00044114704,0.0001742004,0.00012900673,0.0000028326895,0.001569163,0.00035813512,0.00008710925],"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":[2.0986964e-7,0.00002160963,0.00022636256,0.00084350776,0.00009584581,5.020652e-7,0.00006705973,0.0000043939453,4.2708857e-7,0.000009418402,0.0020592588,0.9966714],"study_design_scores_gemma":[0.00009444328,0.00006258186,0.0017674783,0.00013613161,0.000057935013,0.00007992505,0.000036312806,0.000012213896,1.8131858e-7,0.000004148813,0.99745464,0.00029401606],"about_ca_topic_score_codex":0.000107426415,"about_ca_topic_score_gemma":0.00007518267,"teacher_disagreement_score":0.9963774,"about_ca_system_score_codex":0.00018218669,"about_ca_system_score_gemma":0.0014016501,"threshold_uncertainty_score":0.99993914},"labels":[],"label_agreement":null},{"id":"W1969676656","doi":"10.2350/13-02-1300-cr.1","title":"Nested Stromal Epithelial Tumor of the Liver in Beckwith-Wiedemann Syndrome","year":2013,"lang":"en","type":"article","venue":"Pediatric and Developmental Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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; Hospital for Sick Children; London Health Sciences Centre; University of Toronto","funders":"","keywords":"Hepatoblastoma; Pathology; Medicine; Beckwith–Wiedemann syndrome; Wilms' tumor; CD117; Stromal tumor; Abdominal mass; Malignancy; Liver tumor; Stromal cell; Hepatocellular carcinoma; Internal medicine; Biology","score_opus":0.005840488438307744,"score_gpt":0.18793312557421915,"score_spread":0.1820926371359114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969676656","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986447,0.0006227904,0.000033213175,0.000042938664,0.00012937175,0.00022326378,0.0000054735915,0.0000037551786,0.00029449593],"genre_scores_gemma":[0.99765813,0.0001529821,0.0017796898,0.00012641467,0.00004943378,0.000027224107,0.000007109827,0.000010835016,0.00018816412],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991296,0.000054324093,0.00025856594,0.00024968118,0.00007873569,0.0002290798],"domain_scores_gemma":[0.9997029,0.000014245003,0.000089194255,0.00011868628,0.000028498429,0.000046481953],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011253818,0.00012218612,0.00015711931,0.00005231197,0.000048408136,0.000008187975,0.00014400677,0.000092318594,0.000047895483],"category_scores_gemma":[0.00005681284,0.00009191288,0.00003974377,0.00011523008,0.00008579419,0.0000043257965,0.00028783458,0.00007429603,0.000019411124],"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":[0.000005367123,0.000052298838,0.9317161,0.000035009878,0.000009215818,0.00002066695,0.00016647979,0.0000037619468,0.06584504,0.000014513463,0.00013479602,0.0019967488],"study_design_scores_gemma":[0.0004419462,0.00011454528,0.9945961,0.000004392434,0.000009407002,0.0010543005,0.00020201095,0.000013169478,0.0032815095,0.00004474739,0.00011688999,0.00012093061],"about_ca_topic_score_codex":0.00007049933,"about_ca_topic_score_gemma":0.000019511706,"teacher_disagreement_score":0.062880054,"about_ca_system_score_codex":0.000008037934,"about_ca_system_score_gemma":0.000071405084,"threshold_uncertainty_score":0.37480983},"labels":[],"label_agreement":null},{"id":"W1969702194","doi":"10.1016/j.ando.2015.03.028","title":"Pseudohypoparathyroidism type Ib in 2015","year":2015,"lang":"fr","type":"review","venue":"Annales d Endocrinologie","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"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":"Ministry of Health, British Columbia; Ministero della Salute","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Brachydactyly; Short stature; Osteodystrophy; Endocrinology; Parathyroid hormone; Internal medicine; Medicine; Genetics; Biology; Gene","score_opus":0.1011404986461075,"score_gpt":0.36225239294170747,"score_spread":0.2611118942956,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969702194","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.023686294,0.96728575,0.000019077728,0.0004365545,0.001904723,0.0005908299,0.000046522513,0.000029389006,0.006000848],"genre_scores_gemma":[0.015500124,0.97336847,0.00086541125,0.00015679089,0.0006001884,0.0000744044,0.00044676778,0.00009616091,0.008891693],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9958226,0.00038740804,0.0009921347,0.0011576894,0.0002683757,0.0013717585],"domain_scores_gemma":[0.9979097,0.000049939743,0.00036358513,0.0011058553,0.0002912914,0.00027960623],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00037807523,0.00083336816,0.0014227228,0.00020183642,0.00007846745,0.000071211085,0.00095382286,0.0007825509,0.00012085413],"category_scores_gemma":[0.00052594487,0.0007925195,0.0004383032,0.00043541376,0.0002897357,0.000008928365,0.00096108305,0.0006756017,0.0019176665],"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":[0.000019870593,0.00029122375,0.0022920945,0.001880678,0.00032335095,0.00022431726,0.000055545584,0.00009125676,0.0009939161,0.0002561175,0.08124751,0.91232413],"study_design_scores_gemma":[0.0005348108,0.00069114973,0.0009016354,0.00073555496,0.00015280923,0.000865095,0.000105752966,0.000014017896,0.0003694317,0.00016997596,0.9946271,0.0008326292],"about_ca_topic_score_codex":0.00010050932,"about_ca_topic_score_gemma":0.0000759144,"teacher_disagreement_score":0.9133796,"about_ca_system_score_codex":0.00014352915,"about_ca_system_score_gemma":0.0009839243,"threshold_uncertainty_score":0.9994526},"labels":[],"label_agreement":null},{"id":"W1969874642","doi":"10.1002/ajmg.c.10013","title":"Mental deficiency, alterations in performance, and CNS abnormalities in Overgrowth syndromes","year":2003,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Dalhousie University","funders":"","keywords":"Macrocephaly; Proteus syndrome; Costello syndrome; Sotos syndrome; Medicine; Genetic syndromes; Hypoglycemia; Autism; Epilepsy; Neurofibromatosis; Pediatrics; Internal medicine; Endocrinology; Pathology; Diabetes mellitus; Psychiatry; Cancer","score_opus":0.018004094589624917,"score_gpt":0.31456919267068306,"score_spread":0.29656509808105813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969874642","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.32227123,0.67663854,0.00005196631,0.00009420146,0.0004905912,0.0002451681,0.0000112789285,0.0000020831094,0.0001949158],"genre_scores_gemma":[0.031309392,0.96648735,0.0014952625,0.00025661523,0.00022907609,0.000030440955,0.00004074291,0.00006885179,0.00008225021],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9933817,0.0006834548,0.0025267259,0.0006199617,0.0019199416,0.00086821965],"domain_scores_gemma":[0.99772936,0.0002064535,0.00080720533,0.00043013346,0.00008381313,0.00074303267],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.002900176,0.0005977113,0.0018559499,0.0006133787,0.00006140085,0.000050345105,0.0010470692,0.00074969506,0.00013018493],"category_scores_gemma":[0.00072212244,0.00053064723,0.00027195897,0.00078574364,0.001039534,0.000008357766,0.00048087921,0.0013375456,0.0000035117982],"study_design_candidate":"design_other","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":[0.000014173075,0.00035097022,0.012888819,0.0010611326,0.00007282237,0.00023273722,0.00030811457,0.00005466797,0.0000067632413,0.000009805737,0.0004987844,0.9845012],"study_design_scores_gemma":[0.0021435847,0.004345421,0.0031463045,0.022630077,0.00022674077,0.010106514,0.0013975832,0.0007831615,0.000040885803,0.00003262618,0.9539095,0.0012376131],"about_ca_topic_score_codex":0.000023946077,"about_ca_topic_score_gemma":0.00008689554,"teacher_disagreement_score":0.9832636,"about_ca_system_score_codex":0.0001086891,"about_ca_system_score_gemma":0.0018087114,"threshold_uncertainty_score":0.9997145},"labels":[],"label_agreement":null},{"id":"W1970011619","doi":"10.4161/epi.3.6.7109","title":"Novel imprinted transcripts from the<i>Dlk1-Gtl2</i>intergenic region,<i>Mico1</i>and<i>Mico1os</i>, show circadian oscillations","year":2008,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Douglas Mental Health University Institute; McGill University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Intergenic region; Genetics; Transcription (linguistics); Gene; Circadian rhythm; Imprinting (psychology); Chromosome; Genome; Gene expression; DNA methylation; Neuroscience","score_opus":0.02562780136574606,"score_gpt":0.2236606763590861,"score_spread":0.19803287499334005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970011619","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96536297,0.0036223382,0.028183945,0.0010462827,0.0005687556,0.00031860467,0.00006444438,0.000034372762,0.000798297],"genre_scores_gemma":[0.990748,0.003170591,0.0035100104,0.0011296252,0.00039953177,0.000023035182,0.00011407141,0.000065957865,0.00083917734],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99812096,0.00007649981,0.00044865932,0.0006472517,0.00020742531,0.00049920665],"domain_scores_gemma":[0.9986688,0.000048315967,0.00012939383,0.0008090983,0.00012788034,0.00021655085],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00013874419,0.000327767,0.0002578195,0.000045838202,0.000401615,0.000050386294,0.00045608624,0.00023863329,0.000051209485],"category_scores_gemma":[0.00011712018,0.00029183071,0.00020574468,0.00016128669,0.00024300705,0.000005492622,0.00025769515,0.00020586261,0.000025386598],"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":[0.0000116229385,0.00007366464,0.032674372,0.000007761736,0.00014317781,0.000004692876,0.00073263317,0.0000908924,0.9595944,0.000060155533,0.0023254585,0.004281113],"study_design_scores_gemma":[0.0021427032,0.00040143772,0.5447138,0.000057017947,0.00016292564,0.0007719393,0.00041254034,0.0006802115,0.2361887,0.00030227148,0.21309228,0.0010741483],"about_ca_topic_score_codex":0.00029893903,"about_ca_topic_score_gemma":0.00030353424,"teacher_disagreement_score":0.7234058,"about_ca_system_score_codex":0.000017523194,"about_ca_system_score_gemma":0.0001173117,"threshold_uncertainty_score":0.9999534},"labels":[],"label_agreement":null},{"id":"W1970069693","doi":"10.1371/journal.pone.0101012","title":"Clinically Important Age-Related Differences in Sleep Related Disordered Breathing in Infants and Children with Prader-Willi Syndrome","year":2014,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto; Hospital for Sick Children","funders":"","keywords":"Polysomnogram; Medicine; Pediatrics; Obstructive sleep apnea; Apnea; Polysomnography; Central sleep apnea; Sleep apnea; Population; Internal medicine","score_opus":0.012072076897587571,"score_gpt":0.20838486092879188,"score_spread":0.1963127840312043,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970069693","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99876297,0.0004809703,0.000016912756,0.00016349592,0.000018146295,0.00033147735,0.0000034783243,0.000016180544,0.00020639194],"genre_scores_gemma":[0.99802804,0.00043293575,0.0012866786,0.000048726037,0.00001261436,0.000019165056,0.000051560208,0.000028432194,0.00009186953],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9982545,0.00010490322,0.00065108464,0.0004942127,0.00016603015,0.00032926325],"domain_scores_gemma":[0.999362,0.000032917073,0.00019829684,0.00029581055,0.000023346425,0.00008765846],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038961985,0.0001994222,0.00038419457,0.00008285782,0.000043794913,0.00003328904,0.00016155108,0.00023748267,0.000013101948],"category_scores_gemma":[0.0002522005,0.00016898432,0.00003265694,0.0001642478,0.00010582131,0.000006718221,0.00013277124,0.0002452134,0.000002848756],"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":[0.0000050627586,0.000364031,0.984514,0.000021215566,0.00016725705,0.000004762913,0.00018957333,0.000008575452,0.013609523,0.000008843962,6.8611905e-7,0.0011064612],"study_design_scores_gemma":[0.0017301271,0.00074015337,0.9953069,0.00026015556,0.000044351567,0.00009180875,0.00004257248,0.00089107675,0.000450993,0.00017968043,0.0000025046986,0.0002596583],"about_ca_topic_score_codex":0.00013236281,"about_ca_topic_score_gemma":0.00012413504,"teacher_disagreement_score":0.01315853,"about_ca_system_score_codex":0.0000071497534,"about_ca_system_score_gemma":0.000023483688,"threshold_uncertainty_score":0.68909806},"labels":[],"label_agreement":null},{"id":"W1970925597","doi":"10.1002/ijc.20280","title":"Allelic loss but absence of mutations in the polyspecific transporter gene <i>BWR1A</i> on 11p15.5 in hepatoblastoma","year":2004,"lang":"en","type":"article","venue":"International Journal of Cancer","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University; Jewish General Hospital","funders":"","keywords":"Hepatoblastoma; Biology; Molecular biology; Allele; Loss of heterozygosity; Exon; Locus (genetics); Gene; Hepatocellular carcinoma; Tumor suppressor gene; Southern blot; Cancer research; Genetics; Carcinogenesis; Internal medicine; Medicine","score_opus":0.010240876873024702,"score_gpt":0.27786967359744685,"score_spread":0.26762879672442214,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970925597","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971144,0.0006708979,0.00054579077,0.0011962502,0.00026722052,0.000049173603,0.000013298588,5.4445326e-7,0.00014239734],"genre_scores_gemma":[0.9985157,0.00064114475,0.00025978094,0.00036458677,0.00018222116,0.0000048370234,0.000004319769,0.000006547006,0.000020815925],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99917346,0.000020176425,0.00035099697,0.00009412967,0.00026581416,0.000095419295],"domain_scores_gemma":[0.99957544,0.0000113900705,0.00017552917,0.000085631684,0.00013066325,0.000021357046],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014958877,0.00006947593,0.00009578335,0.000095203795,0.000009752038,0.000010914902,0.00030875526,0.000040979892,0.000024246381],"category_scores_gemma":[0.000016122929,0.000052996806,0.00008100849,0.00006747862,0.000042133834,0.0000056585236,0.000012846668,0.000101027814,0.0000012285601],"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":[0.000248446,0.0004411627,0.15935992,0.0000128658385,0.00021809181,0.00018329738,0.0017533116,0.041009586,0.7838361,0.00048526982,0.00008729754,0.012364634],"study_design_scores_gemma":[0.002505467,0.00033129606,0.7923201,0.00019341797,0.000012689908,0.000329861,0.0004934666,0.000027246531,0.20046288,0.0007508636,0.0024362325,0.00013652137],"about_ca_topic_score_codex":0.00018647489,"about_ca_topic_score_gemma":0.00044408411,"teacher_disagreement_score":0.63296014,"about_ca_system_score_codex":0.000038131122,"about_ca_system_score_gemma":0.000112457936,"threshold_uncertainty_score":0.2161147},"labels":[],"label_agreement":null},{"id":"W1971653306","doi":"10.1016/s0002-9440(10)64652-4","title":"p57KIP2 Is Not Mutated in Hepatoblastoma but Shows Increased Transcriptional Activity in a Comparative Analysis of the Three Imprinted Genes p57KIP2, IGF2, and H19","year":2000,"lang":"en","type":"article","venue":"American Journal Of Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"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; Jewish General Hospital; Montreal Children's Hospital","funders":"Deutsche Forschungsgemeinschaft","keywords":"Loss of heterozygosity; Hepatoblastoma; Biology; Locus (genetics); Allele; Gene; Molecular biology; Tumor suppressor gene; Cancer research; Genetics; Carcinogenesis; Internal medicine","score_opus":0.012686565279806895,"score_gpt":0.2579052578158719,"score_spread":0.24521869253606504,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971653306","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99905556,0.00020980317,0.00037083265,0.00015482257,0.000027949087,0.00009133489,0.00003642963,0.0000013188052,0.00005196831],"genre_scores_gemma":[0.99903566,0.00014175868,0.000591211,0.00018371882,0.00001901473,0.0000039014394,0.000003430395,0.0000073109973,0.000014019988],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986379,0.00031406977,0.00046583638,0.00023373461,0.00013609524,0.00021236138],"domain_scores_gemma":[0.99925166,0.000040772025,0.00035644462,0.00019266525,0.00009567176,0.000062762636],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003254646,0.00015006414,0.0005639855,0.00022676383,0.00002927873,0.000007157614,0.00020354058,0.00007581272,0.000075959484],"category_scores_gemma":[0.000029590936,0.00011741591,0.0001968543,0.0005387038,0.00040239864,0.0000063394637,0.000046647547,0.00018818471,5.025003e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021932194,0.00011105642,0.26823348,0.0000034039301,0.00021754042,0.000019039406,0.0004299286,0.0003661348,0.71342564,0.0000026802786,0.000001773841,0.01696998],"study_design_scores_gemma":[0.00087173877,0.0006210019,0.90235966,0.00001479283,0.00013158833,0.0003193563,0.00038271843,0.0017720115,0.09335063,0.000016274991,0.00004990596,0.000110309484],"about_ca_topic_score_codex":0.00054568006,"about_ca_topic_score_gemma":0.0012238073,"teacher_disagreement_score":0.6341262,"about_ca_system_score_codex":0.000019045227,"about_ca_system_score_gemma":0.00009125465,"threshold_uncertainty_score":0.4788082},"labels":[],"label_agreement":null},{"id":"W1972060342","doi":"10.1097/mph.0b013e3181dccd1e","title":"Simultaneous Occurrence of Pancreatoblastoma and Neuroblastoma in a Newborn With Beckwith-Wiedemann Syndrome","year":2010,"lang":"en","type":"article","venue":"Journal of Pediatric Hematology/Oncology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pediatric Oncology Group","funders":"","keywords":"Beckwith–Wiedemann syndrome; Medicine; Neuroblastoma; Pediatrics; Genetics","score_opus":0.005851744240814266,"score_gpt":0.24857802119655317,"score_spread":0.2427262769557389,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1972060342","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99804974,0.0008051865,0.00030309922,0.0002159775,0.00029855157,0.00015192879,0.0000073748233,0.0000044022327,0.0001637587],"genre_scores_gemma":[0.9920611,0.00043616377,0.007231973,0.00007189632,0.00015642247,0.0000050857507,0.0000019696104,0.000018329732,0.000017094886],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99819505,0.00012944026,0.00081807707,0.00030830147,0.0001720314,0.00037708797],"domain_scores_gemma":[0.9982067,0.00025408284,0.0008631963,0.00024626649,0.00024141399,0.00018836057],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004846841,0.0002245635,0.0007123907,0.00028894335,0.000038526865,0.000009589319,0.0002971552,0.0003948467,0.00001738651],"category_scores_gemma":[0.0005764956,0.00018158948,0.00009205462,0.0002606015,0.00022170234,0.000010064785,0.0001475502,0.0005155156,0.000002643419],"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":[0.0007998825,0.0011123475,0.78085154,0.00038425636,0.00027029167,0.0035140852,0.0006599306,0.00055146596,0.18501917,0.00012331973,0.0008964077,0.025817322],"study_design_scores_gemma":[0.018316982,0.049981643,0.42992717,0.0002029553,0.0010545535,0.41541657,0.0020372358,0.0010280211,0.03732335,0.00037297278,0.042438693,0.0018998471],"about_ca_topic_score_codex":0.000013287531,"about_ca_topic_score_gemma":0.0001303572,"teacher_disagreement_score":0.4119025,"about_ca_system_score_codex":0.000014418875,"about_ca_system_score_gemma":0.0004978019,"threshold_uncertainty_score":0.74050045},"labels":[],"label_agreement":null},{"id":"W1972213660","doi":"10.4161/epi.4.2.7954","title":"Temporal stability and age-related prevalence of loss of imprinting of the insulin-like growth factor-2 gene","year":2009,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Saskatchewan","funders":"National Center for Research Resources; National Cancer Institute; National Institutes of Health","keywords":"Imprinting (psychology); Genomic imprinting; Epigenetics; Insulin-like growth factor 2; Biology; Allele; Colorectal cancer; Internal medicine; Genetics; Gene; Cancer; DNA methylation; Gene expression; Medicine","score_opus":0.011882103867257406,"score_gpt":0.23128833388590742,"score_spread":0.21940623001865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1972213660","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974733,0.0017245866,0.00029348434,0.00003539327,0.00009627021,0.00019793666,0.00003044386,0.0000033302922,0.0001452686],"genre_scores_gemma":[0.99698937,0.00062860956,0.0022808353,0.000016556967,0.000018577806,0.0000011241472,0.000004572769,0.000010854227,0.000049523336],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987689,0.000084194646,0.00053589797,0.00026014957,0.00016727851,0.00018353242],"domain_scores_gemma":[0.99893004,0.000019514477,0.00035916892,0.00047176288,0.00017130033,0.00004824512],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024005977,0.00013969232,0.00023147918,0.000024572531,0.000035381247,0.0000046662303,0.00027468195,0.00013640251,0.000013127355],"category_scores_gemma":[0.00016899788,0.00011360513,0.00010903951,0.00011927914,0.00028267398,0.0000021328995,0.00027193935,0.00008254802,1.7826841e-7],"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":[0.0000054467,0.000056454646,0.31041017,0.00013347606,0.000023168222,2.1320798e-7,0.00016759757,0.000020373891,0.68655926,0.000021515585,0.0000016221176,0.0026006806],"study_design_scores_gemma":[0.00018384923,0.00018249775,0.48552364,0.000021013217,0.00001537143,0.0000041739268,0.000021105818,0.00002619302,0.51373374,0.00020743269,0.000017618086,0.00006339083],"about_ca_topic_score_codex":0.000035638648,"about_ca_topic_score_gemma":0.0000046089494,"teacher_disagreement_score":0.17511345,"about_ca_system_score_codex":0.0000051507836,"about_ca_system_score_gemma":0.00005917084,"threshold_uncertainty_score":0.46326828},"labels":[],"label_agreement":null},{"id":"W1973288730","doi":"10.1002/ajmg.1356","title":"Aggressive behavior and Brunner Syndrome: No evidence for the C936T mutation in a population sample","year":2001,"lang":"en","type":"letter","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université de Montréal; McGill University","funders":"Medical Research Council; Pan American Health Organization","keywords":"Population; Library science; Psychology; Sociology; Demography; Computer science","score_opus":0.02442307126887433,"score_gpt":0.32129385469764515,"score_spread":0.2968707834287708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973288730","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92840964,0.0086398665,0.005527326,0.056387898,0.000602088,0.0004102192,0.00001801282,0.000002267323,0.0000026714347],"genre_scores_gemma":[0.88790387,0.023569783,0.010987094,0.071955234,0.0050423243,0.00008935989,0.00016680863,0.00011519658,0.00017031141],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.997967,0.00014001598,0.0006341818,0.00027181,0.00068040943,0.0003065952],"domain_scores_gemma":[0.99793774,0.00044273704,0.0010339757,0.00024569192,0.00022371594,0.00011614904],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00062177575,0.00021289231,0.00038201507,0.00009491314,0.00006013164,0.000043332384,0.0004396332,0.00036015816,0.00003289274],"category_scores_gemma":[0.0019505518,0.00015527185,0.0001779884,0.00012798118,0.0002573216,0.000003946672,0.000114280556,0.0006346236,9.982326e-7],"study_design_candidate":"design_other","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":[0.00012062476,0.00014505965,0.056423664,0.00022422001,0.00046299282,0.0013489514,0.00025015205,0.00025828727,0.0010094946,0.00000165556,0.08617407,0.85358083],"study_design_scores_gemma":[0.00396342,0.015186174,0.37055218,0.0030998325,0.0014946435,0.035398077,0.0006588955,0.0023341002,0.00026042853,0.00019734849,0.565318,0.0015368898],"about_ca_topic_score_codex":0.00024282963,"about_ca_topic_score_gemma":0.000033566947,"teacher_disagreement_score":0.8520439,"about_ca_system_score_codex":0.000026605367,"about_ca_system_score_gemma":0.00021460651,"threshold_uncertainty_score":0.63318026},"labels":[],"label_agreement":null},{"id":"W1973753171","doi":"10.1016/j.jval.2011.08.525","title":"PND59 A Common Road Map for Rational Clinical and Policy Decisionmaking: Application of the MCDA-Based Evidem Framework to Growth Hormone Use in Patients with Prader-Willi Syndrome","year":2011,"lang":"en","type":"article","venue":"Value in Health","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal","funders":"","keywords":"Multiple-criteria decision analysis; Context (archaeology); Stakeholder; Population; Medicine; Scientific evidence; Psychology; Operations research; Political science; Geography; Public relations; Environmental health; Engineering","score_opus":0.05530843422811118,"score_gpt":0.33005054087963487,"score_spread":0.2747421066515237,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973753171","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98422384,0.00012875453,0.013789418,0.00077556324,0.00003947058,0.0010219269,0.000015628819,0.0000025254997,0.0000028820914],"genre_scores_gemma":[0.97091275,0.000020918556,0.02827607,0.00066426303,0.000026152971,0.000065843284,0.000016392089,0.000014727332,0.000002874335],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987132,0.00015319856,0.00050609716,0.00029127553,0.00013463062,0.00020160213],"domain_scores_gemma":[0.99923456,0.000103185695,0.00020649016,0.00030398753,0.00006960132,0.0000821503],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000571351,0.00010118041,0.00020095613,0.0000735196,0.000047369762,0.00000847289,0.00014472511,0.00012196492,5.8943533e-7],"category_scores_gemma":[0.000505313,0.00007676831,0.00003977893,0.00018461797,0.000055218083,0.000004724599,0.00007567196,0.00010036962,4.7529556e-7],"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":[0.00003778174,0.00017806466,0.99516284,0.000046848025,0.0000070340193,3.9004114e-8,0.00009062638,0.00037388358,0.00006164485,0.0004342713,0.000023009332,0.0035839623],"study_design_scores_gemma":[0.00089695776,0.0010456424,0.99575883,0.00013611818,0.000003331944,0.0000018705209,0.000014525272,0.0010006692,0.00007739183,0.00080641086,0.00017586617,0.00008238941],"about_ca_topic_score_codex":0.0012183074,"about_ca_topic_score_gemma":0.000088366054,"teacher_disagreement_score":0.01448665,"about_ca_system_score_codex":0.000024254425,"about_ca_system_score_gemma":0.00019404065,"threshold_uncertainty_score":0.3130521},"labels":[],"label_agreement":null},{"id":"W1974350437","doi":"10.1158/0008-5472.can-06-0037","title":"The c-Myc Oncogene Directly Induces the H19 Noncoding RNA by Allele-Specific Binding to Potentiate Tumorigenesis","year":2006,"lang":"en","type":"article","venue":"Cancer Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":457,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Gene knockdown; Genomic imprinting; Chromatin immunoprecipitation; Cancer research; Carcinogenesis; Long non-coding RNA; Oncogene; Transcription factor; Gene; Gene expression; Molecular biology; RNA; Genetics; Promoter; DNA methylation; Cell cycle","score_opus":0.039916658065585,"score_gpt":0.336401392140191,"score_spread":0.29648473407460596,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974350437","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9836903,0.011548966,0.00014184583,0.0019488283,0.0003028748,0.0003651761,0.000021348991,0.0000113004735,0.0019693498],"genre_scores_gemma":[0.98847675,0.0038917721,0.000098285804,0.000079132085,0.0007532465,0.0001933757,0.000024855433,0.00004263782,0.006439935],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99775857,0.00020342699,0.00025719794,0.0004881234,0.00049617526,0.00079651724],"domain_scores_gemma":[0.9989998,0.00007719899,0.000063208754,0.0005344382,0.00021065543,0.00011474437],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012717313,0.00016563966,0.0001320813,0.000063858955,0.0010547332,0.0002533161,0.0007471304,0.000092375514,0.00004572659],"category_scores_gemma":[0.00007125505,0.00010607151,0.00009232616,0.0004165074,0.00015066628,0.000004212656,0.00041926856,0.00023053602,0.000053305885],"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":[0.000015431811,0.00001558181,0.0005382147,0.000005730317,0.000031123862,0.0000017489788,0.000038761467,0.00008229085,0.94234943,0.000026755257,0.03275912,0.024135796],"study_design_scores_gemma":[0.00014450555,0.000074178584,0.0019409228,0.000015501766,0.000004230154,0.0000058224123,0.00024317863,0.0000066363673,0.65459985,0.000024587755,0.34281316,0.00012744578],"about_ca_topic_score_codex":0.0008483597,"about_ca_topic_score_gemma":0.00022797794,"teacher_disagreement_score":0.31005406,"about_ca_system_score_codex":0.00008402618,"about_ca_system_score_gemma":0.00013802425,"threshold_uncertainty_score":0.8112261},"labels":[],"label_agreement":null},{"id":"W1974744326","doi":"10.1002/ajmg.a.33065","title":"Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell–Silver syndrome","year":2009,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":110,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"North York General Hospital; University of Toronto; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Fundação para a Ciência e a Tecnologia; Genome Canada; Howard Hughes Medical Institute","keywords":"Epigenetics; DNA methylation; Genomic imprinting; Methylation; Biology; Imprinting (psychology); Genetics; Uniparental disomy; Epigenomics; Chromosome; Chromosome 7 (human); DNA; Gene; Karyotype; Gene expression","score_opus":0.015151807453028519,"score_gpt":0.2758209344289794,"score_spread":0.2606691269759509,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974744326","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9923219,0.0011009522,0.0056014843,0.00070340565,0.000086777305,0.00016397946,0.0000043542464,0.0000011263652,0.00001600272],"genre_scores_gemma":[0.9989084,0.0005512003,0.00036950316,0.00005683534,0.00006151608,0.0000025880697,0.0000036570223,0.000010386467,0.000035905345],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9980542,0.00023291347,0.0007703173,0.00014601841,0.0006139768,0.00018257456],"domain_scores_gemma":[0.9985623,0.00009919888,0.00085366395,0.00022811792,0.00017024955,0.00008648166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008543847,0.00012019844,0.0003075291,0.00007740107,0.000050164766,0.0000061594656,0.0002941791,0.00008302135,0.000021081514],"category_scores_gemma":[0.00037106732,0.000065474596,0.00014888366,0.00029854532,0.0003541096,0.0000029576356,0.00007930624,0.00016246241,3.7329227e-7],"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":[0.00014829841,0.00020100757,0.0017583367,0.00003679228,0.0001272791,0.000018504958,0.0007436776,0.005972236,0.8579743,0.000005483403,0.000033249762,0.13298081],"study_design_scores_gemma":[0.0015208509,0.006322256,0.19188567,0.00045274117,0.00018358706,0.002271053,0.001357877,0.0046522003,0.7894291,0.000038216738,0.0016406247,0.0002458343],"about_ca_topic_score_codex":0.000014751842,"about_ca_topic_score_gemma":0.000021367669,"teacher_disagreement_score":0.19012733,"about_ca_system_score_codex":0.000014374253,"about_ca_system_score_gemma":0.00011936527,"threshold_uncertainty_score":0.26699767},"labels":[],"label_agreement":null},{"id":"W1974960512","doi":"10.1016/j.fertnstert.2011.06.055","title":"Embryonic imprinting perturbations do not originate from superovulation-induced defects in DNA methylation acquisition","year":2011,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":116,"is_retracted":false,"has_abstract":false,"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; Canadian Institutes of Health Research; Western University","keywords":"Imprinting (psychology); Oocyte; DNA methylation; Genomic imprinting; Biology; Andrology; Human fertilization; Blastocyst; Embryo; Methylation; Embryogenesis; Genetics; Gene; Medicine; Gene expression","score_opus":0.02988302671186601,"score_gpt":0.2533522563495421,"score_spread":0.2234692296376761,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974960512","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981321,0.0001282657,0.00096436625,0.000038018105,0.00012847174,0.00020411155,0.000016080787,0.000014815383,0.00037377334],"genre_scores_gemma":[0.99911106,0.000013020387,0.00065489725,0.00005579837,0.000033280598,0.000017343009,0.00007852489,0.000009522814,0.000026543627],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9988196,0.00013964802,0.00027680895,0.0004615759,0.00009184644,0.00021053778],"domain_scores_gemma":[0.9994301,0.000025528849,0.000069944326,0.00034204518,0.00006635566,0.000066012755],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003775464,0.00014312007,0.00015776497,0.00003983706,0.00010711412,0.000036933983,0.00008835042,0.00015665982,0.00007656902],"category_scores_gemma":[0.000119681994,0.00014556288,0.000060955528,0.000081590486,0.00004042521,0.000018855466,0.00011621742,0.00009094446,0.0000050302187],"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":[0.00034517163,0.000070376766,0.20677267,0.000024720333,0.000017454626,4.4673763e-7,0.00061130273,0.000003735083,0.78162163,0.00001181314,9.970465e-7,0.010519664],"study_design_scores_gemma":[0.00034864392,0.00007573641,0.86279553,0.000012084612,0.00001059577,0.0000010388585,0.00010798015,0.0004868561,0.13542718,0.000555296,0.000051321404,0.00012774306],"about_ca_topic_score_codex":0.0004594072,"about_ca_topic_score_gemma":0.00022737443,"teacher_disagreement_score":0.65602285,"about_ca_system_score_codex":0.00002206261,"about_ca_system_score_gemma":0.000032614244,"threshold_uncertainty_score":0.59358823},"labels":[],"label_agreement":null},{"id":"W1975168528","doi":"10.1002/jbmr.408","title":"Exclusion of the <i>GNAS</i> locus in PHP-Ib patients with broad <i>GNAS</i> methylation changes: Evidence for an autosomal recessive form of PHP-Ib?","year":2011,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"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":"National Institute of Diabetes and Digestive and Kidney Diseases; Instituto de Salud Carlos III; National Institutes of Health","keywords":"GNAS complex locus; Locus (genetics); Genetics; Pseudohypoparathyroidism; Allele; Biology; Uniparental disomy; Genomic imprinting; Epigenetics; Copy-number variation; DNA methylation; Internal medicine; Medicine; Gene; Chromosome; Karyotype; Parathyroid hormone","score_opus":0.08765229711357614,"score_gpt":0.3486915315984225,"score_spread":0.26103923448484634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975168528","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9979882,0.0012485567,0.00015824444,0.000118336015,0.000053994114,0.00030092,0.0000066101175,5.70945e-7,0.00012455793],"genre_scores_gemma":[0.9979704,0.00058073446,0.0011722149,0.000028591125,0.0000737165,0.000007670195,0.0000040864825,0.00001172099,0.00015083814],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99868566,0.0001279246,0.00039160592,0.00016264655,0.00039533593,0.00023684284],"domain_scores_gemma":[0.9985593,0.000056955363,0.00037326725,0.00019024669,0.0007437778,0.0000764272],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001144128,0.00009619882,0.00023002579,0.00012996538,0.00006364748,0.000011123186,0.0001779835,0.00009531952,0.000005071292],"category_scores_gemma":[0.00036865025,0.000059952567,0.00006733938,0.00018351967,0.00012010324,0.000026676844,0.00016137719,0.00015757034,7.9291944e-8],"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":[0.0006852772,0.00020956824,0.043646257,0.00012449315,0.00003184434,0.0000012295546,0.00097029895,0.000008595627,0.9292273,0.000008244053,0.00018936305,0.024897551],"study_design_scores_gemma":[0.0034199224,0.009060919,0.30280656,0.00087137235,0.0000424668,0.000039036007,0.0007260075,0.00012802046,0.68136054,0.00034358454,0.0010268335,0.00017474659],"about_ca_topic_score_codex":0.00018595689,"about_ca_topic_score_gemma":0.0002914638,"teacher_disagreement_score":0.2591603,"about_ca_system_score_codex":0.000014714164,"about_ca_system_score_gemma":0.0001295954,"threshold_uncertainty_score":0.24447946},"labels":[],"label_agreement":null},{"id":"W1975445070","doi":"10.1007/s00431-008-0683-4","title":"Clinical and radiological findings in Schinzel–Giedion syndrome","year":2008,"lang":"en","type":"article","venue":"European Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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":"Hospital for Sick Children","keywords":"Medicine; Radiological weapon; Radiology","score_opus":0.02433723706154628,"score_gpt":0.26046366487720896,"score_spread":0.23612642781566268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975445070","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967348,0.0018015483,0.00065084576,0.00007043351,0.0003102022,0.000037381014,8.982858e-7,0.000002527832,0.00039134873],"genre_scores_gemma":[0.9902543,0.005294606,0.0036405919,0.00009067756,0.00062896713,1.2102542e-7,0.0000016402336,0.000015118568,0.00007401922],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986699,0.00028607686,0.0005787268,0.00017012877,0.00012318802,0.00017192886],"domain_scores_gemma":[0.99949324,0.000030690884,0.00018007464,0.000113643284,0.000054859767,0.0001274968],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013838684,0.000101258775,0.00020713713,0.0000929304,0.00004656111,0.000012013586,0.000183102,0.00006101349,0.0000071462846],"category_scores_gemma":[0.0004972518,0.00008372674,0.00010062537,0.00009731699,0.00009770347,0.000004878877,0.00013059199,0.00026271117,0.000007865416],"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":[0.000022432141,0.000063117295,0.99072623,0.0000112129155,0.000010310984,0.00069864397,0.00006549703,0.000030946358,0.0032845961,0.000005216375,0.0013415733,0.0037402047],"study_design_scores_gemma":[0.0009989702,0.0010419273,0.98754907,0.000009296344,0.000013825311,0.006267194,0.000035660185,0.000007189923,0.00007167244,0.000009407544,0.0038836559,0.00011212814],"about_ca_topic_score_codex":5.6011345e-7,"about_ca_topic_score_gemma":1.8346996e-7,"teacher_disagreement_score":0.006480556,"about_ca_system_score_codex":0.000004474696,"about_ca_system_score_gemma":0.000045142715,"threshold_uncertainty_score":0.34142774},"labels":[],"label_agreement":null},{"id":"W1975501413","doi":"10.1159/000090847","title":"New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome","year":2006,"lang":"en","type":"article","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Monozygotic twin; Genomic imprinting; Biology; Genetics; DNA methylation; Uniparental disomy; Methylation; Karyotype; Phenotype; Twin study; Chromosome; Gene; Heritability","score_opus":0.023737361495145076,"score_gpt":0.2839545408517143,"score_spread":0.2602171793565692,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975501413","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.987491,0.00863635,0.00086424913,0.00015343254,0.00004661976,0.00052849663,0.000008689155,0.000011393009,0.0022597797],"genre_scores_gemma":[0.98618406,0.0005437663,0.002153708,0.000026467975,0.00019883591,0.000046293633,0.00005615595,0.000056821176,0.0107339],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9973495,0.00013994308,0.00036853508,0.0008019973,0.00043092069,0.0009091084],"domain_scores_gemma":[0.99897593,0.000031149324,0.00006213935,0.00056226255,0.00012372922,0.0002447755],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00060185464,0.00026970328,0.00030877907,0.00027188117,0.00020421515,0.0001266356,0.00036482158,0.00019762405,0.0001690388],"category_scores_gemma":[0.000032729382,0.0002444472,0.000061817744,0.0004515688,0.00022385447,0.0000075117036,0.00034478883,0.00023471564,0.00008367403],"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":[0.00007602072,0.00016189605,0.146232,0.00015695996,0.00010167367,0.00020355034,0.00019299475,0.0010186188,0.8467225,0.00015823575,0.00032380628,0.004651762],"study_design_scores_gemma":[0.001743014,0.0012122084,0.9543992,0.00007804945,0.000027053376,0.001199868,0.00031398775,0.00006333743,0.03144334,0.00067946163,0.008259131,0.0005813417],"about_ca_topic_score_codex":0.00094218575,"about_ca_topic_score_gemma":0.00065695605,"teacher_disagreement_score":0.8152791,"about_ca_system_score_codex":0.00004065401,"about_ca_system_score_gemma":0.00027357918,"threshold_uncertainty_score":0.9968268},"labels":[],"label_agreement":null},{"id":"W1975838349","doi":"10.1002/ajmg.a.33204","title":"Methylation profiling in individuals with Russell–Silver syndrome","year":2010,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"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; Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Methylation; CpG site; RSS; DNA methylation; Genomic imprinting; Biology; Differentially methylated regions; Epigenetics; Imprinting (psychology); Genetics; Bioinformatics; Gene; Gene expression; Computer science","score_opus":0.008323810880665215,"score_gpt":0.2683808778984834,"score_spread":0.2600570670178182,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975838349","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99742246,0.00031202918,0.0013534431,0.00044309036,0.00025215093,0.000093476745,0.0000018706033,0.0000026688786,0.00011878715],"genre_scores_gemma":[0.9849064,0.00029301128,0.014306792,0.0002160565,0.0002148629,0.0000044357957,0.00000628426,0.000023457123,0.000028713295],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9981698,0.000094140414,0.00051491114,0.00020826093,0.0007215659,0.00029134087],"domain_scores_gemma":[0.9989629,0.00003738669,0.00038082988,0.00022877246,0.00011323768,0.00027689207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011593985,0.0001480502,0.0002986768,0.000113654794,0.000031234795,0.000024558643,0.00037687938,0.00013304333,0.00007773782],"category_scores_gemma":[0.00025598102,0.00011502826,0.000075753494,0.00023004216,0.00026236364,0.000003961471,0.00009171169,0.00045570682,0.000004321729],"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":[0.000039141014,0.0002483598,0.6405935,0.000023783265,0.00022549495,0.000096770964,0.00029143115,0.00042120522,0.23257218,0.000046148303,0.00019838651,0.12524359],"study_design_scores_gemma":[0.0057818377,0.009908525,0.75903916,0.00039817652,0.00019990999,0.010475414,0.0019065457,0.0011842486,0.13850479,0.00025065787,0.07115797,0.0011927926],"about_ca_topic_score_codex":0.000011686622,"about_ca_topic_score_gemma":0.000025767473,"teacher_disagreement_score":0.1240508,"about_ca_system_score_codex":0.000006616076,"about_ca_system_score_gemma":0.00030243426,"threshold_uncertainty_score":0.46907163},"labels":[],"label_agreement":null},{"id":"W1976122890","doi":"10.1071/rdv27n1ab80","title":"80 DNA METHYLATION OF INSULIN-LIKE GROWTH FACTOR 2 (IGF2) GENE IN DAY 14 IN VITRO-PRODUCED BOVINE EMBRYOS OF DIFFERENT SIZES","year":2014,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Biology; Embryo; Genomic imprinting; Andrology; Methylation; DNA methylation; Embryo culture; Pronucleus; Reprogramming; Bisulfite sequencing; Genetics; Embryogenesis; Gene; Molecular biology; Zygote; Gene expression","score_opus":0.014876506521756063,"score_gpt":0.23113201408733625,"score_spread":0.21625550756558018,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976122890","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982759,0.00045564407,0.0007354722,0.000086158674,0.00018061162,0.00022920252,0.000002535544,0.000005374243,0.000029119383],"genre_scores_gemma":[0.99798894,0.00009104642,0.0017571138,0.000012266931,0.000031751028,0.000014969063,0.000046342306,0.00000888226,0.000048706504],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99844724,0.00013091169,0.0005608463,0.0005557627,0.00014532887,0.0001598929],"domain_scores_gemma":[0.9993327,0.000015489892,0.00015794428,0.00034090359,0.00011227075,0.000040670806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00068888057,0.00014093955,0.00026846002,0.00009852666,0.000028467044,0.0000060700113,0.00007350852,0.000095293595,0.0000069511657],"category_scores_gemma":[0.0004837616,0.00012947184,0.000032793992,0.000119348675,0.000045976518,0.0000064982955,0.00010660536,0.00006634181,6.1461213e-7],"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":[0.00013290126,0.00014876924,0.04607151,0.00009782968,0.000017750555,7.1248984e-8,0.00039652165,0.000015606947,0.92016685,0.000002466939,0.0000020783295,0.032947633],"study_design_scores_gemma":[0.0003064582,0.000055069973,0.4835609,0.000009898674,0.000002117124,9.3003473e-7,0.00002653771,0.000020103545,0.515767,0.00003507064,0.00014887901,0.00006705243],"about_ca_topic_score_codex":0.000042808777,"about_ca_topic_score_gemma":0.000022179363,"teacher_disagreement_score":0.43748936,"about_ca_system_score_codex":0.000025886471,"about_ca_system_score_gemma":0.00005207764,"threshold_uncertainty_score":0.5279708},"labels":[],"label_agreement":null},{"id":"W1976371489","doi":"10.1177/0883073812443591","title":"Angelman Syndrome Due to a Termination Codon Mutation of the <i>UBE3A</i> Gene","year":2012,"lang":"en","type":"article","venue":"Journal of Child Neurology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Mount Sinai Hospital; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"UBE3A; Angelman syndrome; Microcephaly; Genetics; Uniparental disomy; Imprinting (psychology); Biology; Phenotype; Intellectual disability; Speech delay; Ubiquitin ligase; Neurodevelopmental disorder; Gene; Mutation; Global developmental delay; Chromosome; Ubiquitin; Karyotype","score_opus":0.005556435576545026,"score_gpt":0.21905262722758612,"score_spread":0.21349619165104108,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976371489","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99315435,0.0002705899,0.00032329778,0.005370434,0.000568826,0.000096572265,0.0000026382388,0.0000012403308,0.00021203372],"genre_scores_gemma":[0.99599373,0.000019269475,0.00015185005,0.003551952,0.00023747086,0.0000014759378,0.0000018721638,0.000011572888,0.000030785628],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992161,0.000105501225,0.0003004874,0.00008829951,0.00012297719,0.00016666733],"domain_scores_gemma":[0.9993426,0.000013746838,0.00031972298,0.00016962436,0.00008588178,0.00006838359],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026070053,0.00007997475,0.00015229208,0.000060951385,0.00004089544,0.0000049059277,0.000186914,0.0000866255,0.000009174182],"category_scores_gemma":[0.00012452368,0.00005896654,0.000104451,0.00008336854,0.00003315003,0.0000057024636,0.000087813256,0.000113817405,0.0000021287121],"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":[0.00010272773,0.00024035218,0.05416472,0.000030896106,0.00009394829,0.000039641578,0.00025314075,0.00051006285,0.92938304,0.000050675873,0.002155322,0.012975458],"study_design_scores_gemma":[0.0003737906,0.0009880576,0.7304015,0.000010818029,0.000030152163,0.018059077,0.0000066174402,0.000009624901,0.2358092,0.000024228957,0.014220428,0.00006647239],"about_ca_topic_score_codex":0.000002198137,"about_ca_topic_score_gemma":0.000002044354,"teacher_disagreement_score":0.69357383,"about_ca_system_score_codex":0.0000036181773,"about_ca_system_score_gemma":0.000020888741,"threshold_uncertainty_score":0.24045858},"labels":[],"label_agreement":null},{"id":"W1977286970","doi":"10.1016/j.ydbio.2011.01.008","title":"Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction","year":2011,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"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 British Columbia","funders":"Canadian Institutes of Health Research; University of British Columbia","keywords":"Biology; Trophoblast; Genetics; Genomic imprinting; Placentation; Allele; Placenta; Phenotype; Embryonic stem cell; Population; Cell biology; Gene; Fetus; Gene expression; Pregnancy; DNA methylation","score_opus":0.015555433931360569,"score_gpt":0.21395170461981253,"score_spread":0.19839627068845195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977286970","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989216,0.00013093007,0.00020223856,0.00003324302,0.00028564007,0.00011993989,0.000010049494,0.0000039381225,0.0002924222],"genre_scores_gemma":[0.9984741,0.00045740604,0.00091876084,0.0000653649,0.000028360415,0.000006325306,0.0000327637,0.0000068864,0.000010015675],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999463,0.000036510977,0.0001494316,0.00017866513,0.000039560768,0.000132784],"domain_scores_gemma":[0.999738,0.000006374819,0.00010424174,0.000098751836,0.000026246546,0.000026395343],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000075317585,0.000093903385,0.000107306136,0.000023453877,0.000033699733,0.0000021686587,0.000093082876,0.0001275814,0.000018245302],"category_scores_gemma":[0.000026759548,0.00006847608,0.00003253554,0.000051162548,0.00011903389,0.0000020321274,0.00017710832,0.000048044036,8.973983e-7],"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":[0.000056607278,0.000025957692,0.33356053,0.000023064755,0.00006795619,3.1198127e-7,0.000076554665,3.346906e-7,0.664642,0.0004086169,0.00009827059,0.0010398538],"study_design_scores_gemma":[0.00026925662,0.00022349079,0.5268211,0.000008970131,0.000013696189,0.00003362086,0.000060339575,0.0000018877587,0.4714904,0.00021467195,0.0007959387,0.00006664362],"about_ca_topic_score_codex":0.00008704575,"about_ca_topic_score_gemma":0.00007033169,"teacher_disagreement_score":0.19326057,"about_ca_system_score_codex":0.0000068588834,"about_ca_system_score_gemma":0.000028537688,"threshold_uncertainty_score":0.27923736},"labels":[],"label_agreement":null},{"id":"W1977311839","doi":"10.1111/cge.12001","title":"<i>PIK3CA</i>, a hotspot for postzygotic mutations in nonhereditary overgrowth syndromes","year":2012,"lang":"en","type":"letter","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Citation; Library science; Genealogy; Columbia university; Genetics; History; Biology; Sociology; Computer science; Media studies","score_opus":0.05307838364426483,"score_gpt":0.3379449713470265,"score_spread":0.2848665877027617,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977311839","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.89134425,0.014209034,0.0023629724,0.07886565,0.008093662,0.0029138653,0.00076109165,0.000068185924,0.0013812726],"genre_scores_gemma":[0.52985305,0.0046809083,0.029025387,0.3872228,0.032287557,0.00058657874,0.008123943,0.00071095105,0.007508846],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99633986,0.00020450927,0.0012713587,0.0009583111,0.00027608272,0.0009498813],"domain_scores_gemma":[0.99799544,0.00032948275,0.00037044936,0.0009471026,0.00017047934,0.00018706618],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.0005825898,0.0005208224,0.0007244703,0.00012632692,0.000082471546,0.000050132272,0.0006264522,0.0019684094,0.00005600737],"category_scores_gemma":[0.0005499321,0.0005427373,0.0006026597,0.00015302873,0.00023601837,0.0000037675034,0.0003258217,0.0010052964,0.00006418637],"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":[0.00004221046,0.00045880035,0.044119526,0.0005091865,0.00043583513,0.00006902623,0.000054902783,0.000105087034,0.002036925,0.000007836442,0.9420434,0.010117267],"study_design_scores_gemma":[0.0015670608,0.0016318293,0.04810821,0.00012216192,0.000284454,0.00016439524,0.000034198125,0.00015492352,0.00049807207,0.0003431563,0.9461241,0.00096744776],"about_ca_topic_score_codex":0.000013169556,"about_ca_topic_score_gemma":0.000019237108,"teacher_disagreement_score":0.36149123,"about_ca_system_score_codex":0.000027721975,"about_ca_system_score_gemma":0.00027789167,"threshold_uncertainty_score":0.9997024},"labels":[],"label_agreement":null},{"id":"W1977459685","doi":"10.1016/j.cub.2008.09.044","title":"Global Survey of Genomic Imprinting by Transcriptome Sequencing","year":2008,"lang":"en","type":"article","venue":"Current Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":166,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada Research Chairs","funders":"","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Locus (genetics); Gene; Transcriptome; Genome; Allele; Computational biology; Gene expression; DNA methylation","score_opus":0.040187519973288406,"score_gpt":0.2898789089047664,"score_spread":0.24969138893147802,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977459685","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98973066,0.0056182295,0.0037142283,0.000009786286,0.00048199695,0.00009880749,0.00012662499,0.00000950865,0.00021019082],"genre_scores_gemma":[0.9985869,0.0007029228,0.00029154634,0.000025044195,0.000065842636,0.0000051645065,0.00028456896,0.000011261076,0.000026755632],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99883986,0.000112780996,0.00032429345,0.00035103038,0.000051418905,0.0003206153],"domain_scores_gemma":[0.9994552,0.000011115848,0.00012712793,0.0002491116,0.00008971234,0.00006771333],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023560812,0.00015097014,0.0002189485,0.000024070032,0.00006428543,0.000003680455,0.00023507293,0.00012961976,0.000022527223],"category_scores_gemma":[0.000082583174,0.00014646947,0.00008977977,0.00009458946,0.00015651487,0.0000016040609,0.00011462947,0.00006583525,0.000008542045],"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":[0.000004394439,0.00001853952,0.37631038,0.000011354542,0.000020068237,1.5073451e-7,0.000016441172,0.0000064488054,0.61739796,0.000011829502,0.0002770034,0.0059254323],"study_design_scores_gemma":[0.00060967176,0.00026966576,0.92727524,0.000011446188,0.000012262167,0.000099225166,0.000023896608,0.000073096824,0.06127035,0.00003419507,0.010035891,0.00028504492],"about_ca_topic_score_codex":0.00031949347,"about_ca_topic_score_gemma":0.000030866526,"teacher_disagreement_score":0.5561276,"about_ca_system_score_codex":0.000024396046,"about_ca_system_score_gemma":0.00011445983,"threshold_uncertainty_score":0.59728515},"labels":[],"label_agreement":null},{"id":"W1977520107","doi":"10.1371/journal.pgen.1003752","title":"Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences","year":2013,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Canadian Institutes of Health Research; Institut National de la Santé et de la Recherche Médicale; Agence Nationale de la Recherche","keywords":"Allele; Genomic imprinting; Biology; Imprinting (psychology); Genetics; Context (archaeology); Epigenetics; Allelic exclusion; Gene silencing; Gene; Gene expression; DNA methylation","score_opus":0.02239412840058208,"score_gpt":0.20857546569764904,"score_spread":0.18618133729706696,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977520107","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966391,0.00046479993,0.0023742805,0.0001262003,0.000022210277,0.00030815814,0.0000167483,0.0000043445475,0.0000442071],"genre_scores_gemma":[0.99816877,0.00007202271,0.0014906452,0.00003631124,0.000013563515,0.000035187295,0.000007719165,0.00002255616,0.00015322228],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988765,0.0000421225,0.00034138802,0.00029399345,0.00021153918,0.00023442521],"domain_scores_gemma":[0.99923724,0.00002131118,0.00018679447,0.00033774076,0.00015931949,0.000057605866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000081657556,0.00016980647,0.00021807458,0.000051145307,0.000059835304,0.000018963352,0.0001976942,0.000118456395,0.000016998878],"category_scores_gemma":[0.00005818877,0.00012648282,0.000048974234,0.000095045485,0.00046552837,0.0000044626972,0.00017871047,0.000110169945,0.0000010818304],"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":[0.0000027677538,0.00012981707,0.029531833,0.00008030514,0.00007930516,2.2189856e-7,0.0001959099,0.03060399,0.93923724,0.00002446019,0.000012472568,0.00010168293],"study_design_scores_gemma":[0.0016831696,0.0012171511,0.14013308,0.00021241333,0.00010871031,0.00018636636,0.000802351,0.07216072,0.7824183,0.0005342801,0.000017090037,0.00052633253],"about_ca_topic_score_codex":0.000057798796,"about_ca_topic_score_gemma":0.00010794905,"teacher_disagreement_score":0.1568189,"about_ca_system_score_codex":0.000010081159,"about_ca_system_score_gemma":0.00015750999,"threshold_uncertainty_score":0.51578194},"labels":[],"label_agreement":null},{"id":"W1977614198","doi":"10.1111/j.1432-0436.2008.00281.x","title":"The Prader–Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation","year":2008,"lang":"en","type":"article","venue":"Differentiation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"Myogenesis; MyoD; Myocyte; Biology; Cellular differentiation; Embryonic stem cell; Cell biology; Transactivation; Cytoplasm; Myosin; Myotome; Molecular biology; Gene; Biochemistry; Gene expression","score_opus":0.00711462439299974,"score_gpt":0.1967704049808753,"score_spread":0.18965578058787558,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977614198","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99408597,0.00028863727,0.004090847,0.00051606324,0.00016264609,0.0007998795,0.000008887139,0.000017950193,0.000029139544],"genre_scores_gemma":[0.9988982,0.00013540134,0.00011581911,0.000031042346,0.0000938913,0.00010776801,0.000169687,0.000033747398,0.0004144202],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99848276,0.00015522554,0.00037237367,0.0003807621,0.00032102727,0.00028783098],"domain_scores_gemma":[0.99892265,0.00004648829,0.0004211619,0.00039368734,0.00015384318,0.00006217509],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015038937,0.0002561451,0.00020912364,0.000057943053,0.0004423512,0.00008954469,0.00020288848,0.00012851928,0.00001080157],"category_scores_gemma":[0.00008403735,0.00014998384,0.00008182828,0.00012981452,0.00016414908,0.000021915987,0.00014792036,0.00014139806,0.000002640872],"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":[0.00004323469,0.0002448699,0.095406406,0.00013204804,0.0002750051,8.391933e-7,0.0009745514,0.000024598095,0.8972472,0.00016485938,0.00023200877,0.0052544093],"study_design_scores_gemma":[0.00077208644,0.0005188386,0.86791134,0.00007878182,0.000056526133,0.00007749569,0.00018114748,0.0008439602,0.12898092,0.000054209147,0.00031322803,0.00021149279],"about_ca_topic_score_codex":0.00002408767,"about_ca_topic_score_gemma":0.00007734001,"teacher_disagreement_score":0.7725049,"about_ca_system_score_codex":0.000018711702,"about_ca_system_score_gemma":0.000040348783,"threshold_uncertainty_score":0.6116163},"labels":[],"label_agreement":null},{"id":"W1978634652","doi":"10.1111/j.1399-0004.2009.01171_3.x","title":"<i>ZFP57 </i>mutations cause an autosomal recessive imprinting disorder","year":2009,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Imprinting (psychology); Genetics; Biology; Genomic imprinting; Mutation; DNA methylation; Gene; Gene expression","score_opus":0.03435661318581114,"score_gpt":0.3623240367160443,"score_spread":0.32796742353023317,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1978634652","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9936661,0.0005735286,0.0030101885,0.00027910597,0.00041832752,0.00019666262,0.0000083582345,0.000038627313,0.0018090914],"genre_scores_gemma":[0.98560786,0.00050822017,0.011738113,0.0008727489,0.0006733522,0.00000795728,0.00009464695,0.00003337769,0.00046369885],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9979889,0.00013704224,0.0006819675,0.00061475276,0.00015804652,0.00041932348],"domain_scores_gemma":[0.9986726,0.000038820934,0.00019829196,0.00067244173,0.0001571368,0.00026071593],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032324312,0.0002175436,0.00023882574,0.000033938468,0.00015598872,0.0000652389,0.0003559915,0.00029383463,0.000029582838],"category_scores_gemma":[0.00039308766,0.00021671642,0.00018048541,0.00012352433,0.00013092786,0.0000052205883,0.000148411,0.00021444044,0.0000300163],"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":[0.000031650703,0.0011233801,0.31202564,0.000018408797,0.00015418987,0.000012162864,0.00017194812,0.0016340546,0.15825066,0.00019383842,0.0010982297,0.52528584],"study_design_scores_gemma":[0.0018503605,0.0036796264,0.91511524,0.000028661858,0.00013735812,0.00008273432,0.00029385847,0.0030259094,0.022706449,0.0012466329,0.050972108,0.00086104457],"about_ca_topic_score_codex":0.0000046810082,"about_ca_topic_score_gemma":0.000016695372,"teacher_disagreement_score":0.60308963,"about_ca_system_score_codex":0.000006147025,"about_ca_system_score_gemma":0.00010578783,"threshold_uncertainty_score":0.88374394},"labels":[],"label_agreement":null},{"id":"W1979477332","doi":"10.1016/j.placenta.2011.12.009","title":"TMED2/p24β1 is expressed in all gestational stages of human placentas and in choriocarcinoma cell lines","year":2011,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital; McGill University Health Centre; McGill University","funders":"Canadian Institutes of Health Research","keywords":"Cytotrophoblast; Syncytiotrophoblast; Golgi apparatus; Endoplasmic reticulum; Cell biology; Placenta; Choriocarcinoma; Biology; Fetus; Genetics; Pregnancy","score_opus":0.03274435760820587,"score_gpt":0.26311413368400566,"score_spread":0.23036977607579978,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1979477332","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984201,0.00056470186,0.000009474496,0.000030703406,0.000039606257,0.00012573814,0.000025790474,0.000002336352,0.0007815408],"genre_scores_gemma":[0.9986814,0.00021609051,0.00073856185,0.0000680005,0.000022049899,0.000009105456,0.00005555018,0.000011912796,0.00019727704],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992483,0.000031847616,0.00022118259,0.00024300227,0.000077958946,0.00017765378],"domain_scores_gemma":[0.99970406,0.000010084975,0.000069552436,0.0001521955,0.000020258776,0.000043829117],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010663027,0.00010557898,0.00012209768,0.000061786704,0.000015011706,0.000006667735,0.00010468802,0.00007612573,0.000061672545],"category_scores_gemma":[0.000014604079,0.000108787484,0.000024553421,0.000043325068,0.00004004258,0.000003674452,0.000102879734,0.000055866047,0.0000017040634],"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":[0.000020228108,0.00008465172,0.51589334,0.000036205263,0.0000062401364,0.0000019794998,0.00048330473,0.000003122104,0.4831766,0.0000066030643,0.00015786295,0.00012988204],"study_design_scores_gemma":[0.0008793587,0.00010379164,0.52255696,0.000018702549,0.0000043896425,0.0000035475284,0.00030570818,0.000026984477,0.47552973,0.000024476112,0.00045117774,0.00009513805],"about_ca_topic_score_codex":0.00029354737,"about_ca_topic_score_gemma":0.00021792208,"teacher_disagreement_score":0.0076468345,"about_ca_system_score_codex":0.0000074593663,"about_ca_system_score_gemma":0.000021532764,"threshold_uncertainty_score":0.44362247},"labels":[],"label_agreement":null},{"id":"W1979892065","doi":"10.1016/j.cell.2011.12.035","title":"Base-Resolution Analyses of Sequence and Parent-of-Origin Dependent DNA Methylation in the Mouse Genome","year":2012,"lang":"en","type":"article","venue":"Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":564,"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 Health Network; Hospital for Sick Children","funders":"National Institute of Environmental Health Sciences; National Human Genome Research Institute","keywords":"Biology; Genomic imprinting; DNA methylation; Differentially methylated regions; Imprinting (psychology); Epigenetics; Genetics; Methylation; CpG site; Genome; RNA-Directed DNA Methylation; Illumina Methylation Assay; Gene; Gene expression","score_opus":0.060456148872561954,"score_gpt":0.3116637991607433,"score_spread":0.25120765028818137,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1979892065","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966644,0.002014269,0.0009720009,0.000009180012,0.00001892875,0.0000683071,0.000004705058,8.5330106e-7,0.00024736978],"genre_scores_gemma":[0.99907297,0.00018010767,0.0006355751,0.000012402103,0.000024728613,0.0000031968245,0.00002809339,0.0000035570047,0.000039384373],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995653,0.000054695083,0.00013107437,0.000084632455,0.00006303581,0.00010127541],"domain_scores_gemma":[0.9997436,0.000008461225,0.000072010655,0.00013721889,0.00001935473,0.000019368734],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023992186,0.00004888225,0.000065112894,0.000024108745,0.00001362987,0.0000032984317,0.00006602093,0.000038671806,0.000007604186],"category_scores_gemma":[0.000018118822,0.000037171332,0.000024302817,0.000046351284,0.000026383314,0.0000025957906,0.000033842796,0.000023798184,7.13705e-7],"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":[0.0000018746344,0.000026699936,0.022424918,0.000019180206,0.0000050088934,6.465819e-8,0.00012571154,0.00017586761,0.976809,0.000005179384,0.000004522553,0.00040195463],"study_design_scores_gemma":[0.00013665673,0.000048752587,0.10602372,0.0000023225587,0.0000147121245,0.0000028541426,0.0002194389,0.000119003846,0.8930581,0.000008747828,0.0003184592,0.00004719993],"about_ca_topic_score_codex":0.000066013155,"about_ca_topic_score_gemma":0.000006601759,"teacher_disagreement_score":0.08375089,"about_ca_system_score_codex":0.0000039261354,"about_ca_system_score_gemma":0.000010146679,"threshold_uncertainty_score":0.15158029},"labels":[],"label_agreement":null},{"id":"W1980941373","doi":"10.1086/508500","title":"Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies","year":2006,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":135,"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. Thomas Hospital","funders":"","keywords":"RYR1; Genetics; Epigenetics; Allele; Gene silencing; Biology; Gene","score_opus":0.01334378897392324,"score_gpt":0.2715675876359422,"score_spread":0.25822379866201894,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980941373","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964645,0.002237503,0.00069091085,0.00014417245,0.00008536561,0.00010234359,0.0000031929108,0.0000033073015,0.00026873683],"genre_scores_gemma":[0.9967422,0.0003819253,0.0022241229,0.000114228555,0.00035670216,0.000004217125,0.0000097087,0.000028944627,0.00013796154],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9985714,0.00013789558,0.0005944401,0.0001805044,0.00021362354,0.00030216848],"domain_scores_gemma":[0.9987148,0.000036975027,0.0006999605,0.00030866195,0.00017763636,0.0000619634],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037691716,0.00016937018,0.00027918958,0.0001135351,0.0001435261,0.00003690741,0.00042588433,0.000041778465,0.000016244156],"category_scores_gemma":[0.000052705684,0.00013325551,0.00012666873,0.00021830371,0.00034593468,0.0000033511308,0.000101848396,0.00018082898,0.0000035852615],"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":[0.00001913256,0.00009760945,0.03353625,0.00000995185,0.000052973635,0.000015277497,0.00053421117,0.011456409,0.9424189,0.000037615595,0.00045280336,0.011368878],"study_design_scores_gemma":[0.0016900476,0.006577848,0.70701987,0.00014098862,0.00016798318,0.0008813496,0.008459969,0.0004393504,0.2659217,0.004682559,0.0032457975,0.000772534],"about_ca_topic_score_codex":0.00008689332,"about_ca_topic_score_gemma":0.00009244697,"teacher_disagreement_score":0.67649716,"about_ca_system_score_codex":0.000023950435,"about_ca_system_score_gemma":0.00009884074,"threshold_uncertainty_score":0.54340017},"labels":[],"label_agreement":null},{"id":"W1981005523","doi":"10.4161/epi.21495","title":"A genome-wide approach reveals novel imprinted genes expressed in the human placenta","year":2012,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":94,"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":"Fondation pour la Recherche Médicale","keywords":"Genomic imprinting; Biology; Gene; Genetics; Human genome; Genome; Candidate gene; Single-nucleotide polymorphism; DNA microarray; Imprinting (psychology); Computational biology; Gene expression; DNA methylation; Genotype","score_opus":0.027120757413477622,"score_gpt":0.26441057039743643,"score_spread":0.2372898129839588,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1981005523","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9865651,0.0024596585,0.007361156,0.00007211574,0.00012920983,0.00039802134,0.000013756686,0.000010642686,0.0029903164],"genre_scores_gemma":[0.9926498,0.00023510502,0.0057967287,0.00032862762,0.0003765631,0.00006422001,0.000109781824,0.00004054264,0.00039864721],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9983426,0.00011464408,0.00037053067,0.00035288668,0.00020225087,0.00061714137],"domain_scores_gemma":[0.9989887,0.000027237735,0.00011583338,0.0007127544,0.00004468989,0.00011076772],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006102676,0.0002337502,0.00019122502,0.00005582886,0.00012547961,0.00004405989,0.00054410077,0.00016826246,0.000022780529],"category_scores_gemma":[0.00008492258,0.000190142,0.000104486724,0.00014495866,0.000073731826,0.0000038207036,0.0003483217,0.00014449906,0.0000133468475],"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":[0.0000039098018,0.00022372168,0.12610085,0.00002204086,0.000025822985,3.7278238e-7,0.00042337965,0.00013182215,0.8724541,0.000041419717,0.000099921104,0.0004726209],"study_design_scores_gemma":[0.0009143678,0.0001971205,0.8235614,0.000013588734,0.000032082757,0.000044104516,0.0009617923,0.000065736305,0.13980484,0.00006228412,0.03388311,0.0004596263],"about_ca_topic_score_codex":0.00002591291,"about_ca_topic_score_gemma":0.000008445128,"teacher_disagreement_score":0.73264927,"about_ca_system_score_codex":0.000016266267,"about_ca_system_score_gemma":0.000026397154,"threshold_uncertainty_score":0.7753766},"labels":[],"label_agreement":null},{"id":"W1981086785","doi":"10.1086/303072","title":"Multipoint Genetic Mapping with Uniparental Disomy Data","year":2000,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of British Columbia","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences; National Institutes of Health; March of Dimes Foundation","keywords":"Crossover; Uniparental disomy; Nondisjunction; International HapMap Project; Genetics; Chromosome; Computer science; Genetic algorithm; Set (abstract data type); Computational biology; Data mining; Biology; Algorithm; Artificial intelligence; Machine learning; Single-nucleotide polymorphism; Aneuploidy; Genotype; Gene; Karyotype","score_opus":0.02058943391585121,"score_gpt":0.26395974785119264,"score_spread":0.24337031393534142,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1981086785","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99722016,0.0010303102,0.0011995703,0.00012699292,0.000047514586,0.00010921908,0.000009183496,0.0000039222373,0.00025313455],"genre_scores_gemma":[0.9891218,0.00060462323,0.009447991,0.00018881184,0.00038123853,0.000001676943,0.000017263224,0.000036469864,0.00020010155],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99866754,0.00011270201,0.00042329595,0.00024947076,0.00025288167,0.0002941017],"domain_scores_gemma":[0.99843776,0.000013833209,0.0004183801,0.00092548726,0.00008846761,0.000116059986],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024300796,0.0001856671,0.00025451928,0.00004531975,0.00016021341,0.000049387618,0.0011053362,0.000025956286,0.00008218638],"category_scores_gemma":[0.000011987528,0.00012217037,0.000078164405,0.00013586505,0.00040911124,0.000004386364,0.0002267363,0.00015686358,0.000008525125],"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":[0.00019345597,0.00034023647,0.09548813,0.000024183819,0.000739675,0.00004718208,0.00087603985,0.006072862,0.36821795,0.0000060565862,0.0016552099,0.52633905],"study_design_scores_gemma":[0.0030175813,0.011261459,0.88569224,0.00017761548,0.0003682972,0.005395351,0.0043216147,0.0013986776,0.021836914,0.00014250286,0.06528677,0.0011009475],"about_ca_topic_score_codex":0.000027449922,"about_ca_topic_score_gemma":0.000015873828,"teacher_disagreement_score":0.79020417,"about_ca_system_score_codex":0.000010798304,"about_ca_system_score_gemma":0.00007462756,"threshold_uncertainty_score":0.4981963},"labels":[],"label_agreement":null},{"id":"W1981409564","doi":"10.1007/s10803-006-0225-8","title":"Characterization of an Autism-Associated Segmental Maternal Heterodisomy of the Chromosome 15q11–13 Region","year":2006,"lang":"en","type":"article","venue":"Journal of Autism and Developmental Disorders","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto; York University","funders":"Canadian Institutes of Health Research; Sick Kids Foundation; Genome Canada; Howard Hughes Medical Institute","keywords":"Autism; Angelman syndrome; Genetics; Locus (genetics); Gene duplication; Developmental disorder; Fluorescence in situ hybridization; Psychology; Copy-number variation; Chromosome 15; Linkage disequilibrium; Biology; Heritability of autism; Chromosome; Gene; Autism spectrum disorder; Developmental psychology; Genotype; Single-nucleotide polymorphism; Genome","score_opus":0.004208866993457113,"score_gpt":0.19112138704434414,"score_spread":0.18691252005088704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1981409564","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99916697,0.00010530313,0.00021216404,0.0001510479,0.00017249872,0.000087161345,0.000011896463,0.000001725198,0.00009125703],"genre_scores_gemma":[0.9992774,0.00016106243,0.00035899764,0.00003083911,0.00001634273,0.0000010209117,0.000034981567,0.000010981096,0.000108335465],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99912256,0.000044048364,0.00042769546,0.00011102181,0.00016537218,0.000129325],"domain_scores_gemma":[0.99938315,0.0000032479581,0.00047619583,0.00007407592,0.000026370744,0.00003698548],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000103930004,0.000107528336,0.00016200432,0.000044793895,0.00006224272,0.00001436904,0.00013644902,0.00007664822,0.00000968547],"category_scores_gemma":[0.000008817442,0.00008317523,0.000077566394,0.00006919174,0.000084443636,0.000017097025,0.00008522579,0.000054692257,2.4224266e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000018039584,0.00010784632,0.14486851,0.000020231071,0.000044855624,9.906133e-7,0.00012063868,0.00001019959,0.85181534,0.000016210053,0.000022333732,0.0029548004],"study_design_scores_gemma":[0.0007499337,0.00020285854,0.8725417,0.00006025898,0.000014941783,0.00015402968,0.00011900429,0.000020330928,0.12572616,0.00016437744,0.00015963339,0.00008671812],"about_ca_topic_score_codex":0.000063131025,"about_ca_topic_score_gemma":0.00004031502,"teacher_disagreement_score":0.72767323,"about_ca_system_score_codex":0.00001645223,"about_ca_system_score_gemma":0.000057634705,"threshold_uncertainty_score":0.33917877},"labels":[],"label_agreement":null},{"id":"W1983185429","doi":"10.1002/ajmg.a.36845","title":"A population‐based profile of 160 Australians with Prader‐Willi syndrome: Trends in diagnosis, birth prevalence and birth characteristics","year":2014,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":100,"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":"State Government of Victoria","keywords":"Medicine; Gestational age; Uniparental disomy; Birth weight; Gestation; Population; Pediatrics; Epidemiology; Quarter (Canadian coin); Pregnancy; Obstetrics; Internal medicine; Biology; Genetics","score_opus":0.009621312756666363,"score_gpt":0.26305490539451176,"score_spread":0.2534335926378454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983185429","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99815965,0.00036788508,0.00087561953,0.00039828158,0.000079159065,0.00007947826,0.000018104127,0.0000026079454,0.000019247034],"genre_scores_gemma":[0.9947862,0.0009271325,0.0038924797,0.00016577383,0.000094738236,0.000010094977,0.000015512469,0.000023267165,0.000084786334],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9981518,0.00015746622,0.00062163937,0.00023589238,0.0005614157,0.00027179354],"domain_scores_gemma":[0.9987434,0.000050713883,0.0005990691,0.00023400065,0.00009968343,0.00027311887],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005548367,0.00017383516,0.00043284878,0.00015543622,0.000027993088,0.000015874803,0.0002691448,0.00009878904,0.00012416966],"category_scores_gemma":[0.00022053573,0.00013890503,0.00006935603,0.00027079583,0.00029451452,0.0000040800815,0.00006435705,0.00019026983,6.061834e-7],"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":[0.000011133125,0.00012407772,0.94211745,0.00008937218,0.00004181931,0.000005821376,0.00004745349,0.000072818846,0.0007137106,0.0000038012145,0.00008408053,0.056688465],"study_design_scores_gemma":[0.00085333176,0.0034029742,0.9887497,0.00029148895,0.000041110918,0.00035290333,0.000056755012,0.0005245933,0.0007595259,0.0000039420897,0.004790808,0.0001728648],"about_ca_topic_score_codex":0.00003726748,"about_ca_topic_score_gemma":0.000020213043,"teacher_disagreement_score":0.0565156,"about_ca_system_score_codex":0.000009949543,"about_ca_system_score_gemma":0.00012527974,"threshold_uncertainty_score":0.56643826},"labels":[],"label_agreement":null},{"id":"W1983528383","doi":"10.1002/ajmg.10702","title":"Evidence for imprinting on chromosome 16: The effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies","year":2002,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":114,"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","funders":"Canadian Institutes of Health Research; Killam Trusts","keywords":"Uniparental disomy; Genomic imprinting; Trisomy; Imprinting (psychology); Biology; Genetics; Chromosome 15; Intrauterine growth restriction; Aneuploidy; Chromosome; Fetus; Pregnancy; Karyotype; Gene; Gene expression","score_opus":0.03753954184212826,"score_gpt":0.3112880723604011,"score_spread":0.27374853051827286,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983528383","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99378484,0.0027406483,0.0014359152,0.0014737555,0.00021271422,0.00026338833,0.0000073420474,0.0000017460584,0.00007962996],"genre_scores_gemma":[0.9976009,0.0015792712,0.00025510887,0.00023898961,0.00024583496,0.000011267028,0.0000015508176,0.000020860562,0.0000461785],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9978254,0.00025552773,0.000732694,0.00018156138,0.0007341847,0.0002706627],"domain_scores_gemma":[0.9976667,0.0008548651,0.00084549945,0.0003945958,0.00011113004,0.0001272032],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011584341,0.00018617623,0.00042510018,0.000044852728,0.00007583012,0.000013418038,0.00079884223,0.00008130264,0.000060276612],"category_scores_gemma":[0.0020595137,0.00009726845,0.00033050205,0.00016906692,0.0005880365,0.000002717008,0.00014935482,0.00025140392,0.0000014069025],"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":[0.0003547028,0.00042792832,0.13602977,0.00030023712,0.0006646621,0.0000062738795,0.00051244244,0.0007769996,0.113986135,0.00008574447,0.0032221803,0.7436329],"study_design_scores_gemma":[0.0044887033,0.057313535,0.046040647,0.0027576769,0.0004984889,0.00043323118,0.002351913,0.0018680401,0.86945784,0.000063611,0.014079771,0.00064655225],"about_ca_topic_score_codex":0.000013908639,"about_ca_topic_score_gemma":0.0000023013502,"teacher_disagreement_score":0.7554717,"about_ca_system_score_codex":0.000022541784,"about_ca_system_score_gemma":0.000049680937,"threshold_uncertainty_score":0.3966492},"labels":[],"label_agreement":null},{"id":"W1983611341","doi":"10.1002/ajmg.a.35704","title":"Special section. Syndrome‐specific growth charts","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; Children's Hospital of Eastern Ontario; University of British Columbia","funders":"Barth Syndrome Foundation","keywords":"Geneticist; Terminology; Identification (biology); Normative; Disease; Medical genetics; Psychology; Medicine; Biology; Genetics; Pathology; Political science","score_opus":0.011881965174896172,"score_gpt":0.25256468583822755,"score_spread":0.24068272066333138,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983611341","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98940146,0.0022308344,0.0016829156,0.000598036,0.005042495,0.00006487369,0.0000027187389,0.000004485282,0.00097220705],"genre_scores_gemma":[0.9712261,0.0035848801,0.0017725576,0.00044463493,0.022779845,0.000002953483,0.000005062326,0.000032128588,0.00015187109],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9977861,0.00012716775,0.0005650473,0.00018581626,0.0008480672,0.00048776862],"domain_scores_gemma":[0.9985071,0.00002675936,0.00038746287,0.00023731696,0.00016811483,0.00067329133],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009016265,0.00018227081,0.0003306083,0.00008589792,0.000072528295,0.000026840466,0.0004132313,0.00013338416,0.0004956811],"category_scores_gemma":[0.00019097063,0.00015932665,0.00019668134,0.0001910631,0.00030169915,0.0000058819724,0.0001513733,0.00028592677,0.000032669912],"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":[0.00014806486,0.0012324906,0.22669359,0.000059240134,0.00088609895,0.00016546773,0.0011795149,0.000059463062,0.05025656,0.00023942925,0.3169379,0.4021422],"study_design_scores_gemma":[0.00083323737,0.0019783576,0.101984896,0.00006243444,0.000049829785,0.0068197404,0.00060854363,0.000009436693,0.0058285,0.000019701281,0.88146627,0.00033906053],"about_ca_topic_score_codex":0.000004668002,"about_ca_topic_score_gemma":0.0000012022201,"teacher_disagreement_score":0.56452835,"about_ca_system_score_codex":0.00001886594,"about_ca_system_score_gemma":0.00014793072,"threshold_uncertainty_score":0.6497152},"labels":[],"label_agreement":null},{"id":"W1983877345","doi":"10.4021/jocmr2009.04.1234","title":"Schatzki’s Ring in Angelman Syndrome: A Diagnostic Dilemma in Neurodevelopmentally Disabled Patients","year":2009,"lang":"en","type":"article","venue":"Journal of Clinical Medicine Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"U.S. Department of Defense","keywords":"Angelman syndrome; Medicine; Epilepsy; Cognition; Pediatrics; Psychiatry; Genetics","score_opus":0.085706213401256,"score_gpt":0.44808550450900464,"score_spread":0.36237929110774864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983877345","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99612194,0.00032748468,0.00001923657,0.00202403,0.0002820392,0.00020478416,5.035478e-7,0.0000014090965,0.0010185975],"genre_scores_gemma":[0.9978571,0.0011912662,0.0003705609,0.00022306654,0.00028319855,0.0000032331068,0.0000044435665,0.000012521714,0.000054614724],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9966307,0.00046982488,0.0014759516,0.0002765362,0.0006897088,0.00045722054],"domain_scores_gemma":[0.9983495,0.00065332046,0.00024832823,0.00021942484,0.0002841337,0.0002453146],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.004607569,0.00012415652,0.00048213697,0.00032024563,0.000036559337,0.000016188824,0.0003961356,0.00014787269,0.000034938977],"category_scores_gemma":[0.014134975,0.0000950391,0.00008968185,0.00039398836,0.00014621628,0.000010231592,0.0001495066,0.000817838,0.000005574814],"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":[0.00009880803,0.00050592364,0.9251866,0.000021616052,0.000016778435,0.00021622577,0.000052496904,0.000028730634,0.0029130292,0.000009711443,0.000611666,0.07033841],"study_design_scores_gemma":[0.0037221466,0.0040443004,0.9888403,0.0005454474,0.0000049373293,0.000109374574,0.000083165985,0.00004172112,0.0002874954,0.0002463842,0.0019821425,0.00009257554],"about_ca_topic_score_codex":0.000027927737,"about_ca_topic_score_gemma":0.000036992027,"teacher_disagreement_score":0.07024584,"about_ca_system_score_codex":0.00003419962,"about_ca_system_score_gemma":0.00018912414,"threshold_uncertainty_score":0.99416935},"labels":[],"label_agreement":null},{"id":"W1984422705","doi":"10.1186/1297-9686-39-5-599","title":"NNAT and DIRAS3 genes are paternally expressed in pigs","year":2007,"lang":"en","type":"article","venue":"Genetics Selection Evolution","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Ministry of Agriculture","funders":"National Natural Science Foundation of China","keywords":"Biology; Genomic imprinting; Epigenetics; Gene; Genetics; Imprinting (psychology); Gene expression; DNA methylation","score_opus":0.00777835974045534,"score_gpt":0.22748769520441509,"score_spread":0.21970933546395974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984422705","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9641713,0.0024022644,0.032849096,0.00003432394,0.00020333823,0.00014240918,0.000003437375,0.000015785663,0.00017806121],"genre_scores_gemma":[0.99684584,0.0006022117,0.0019604627,0.00004758501,0.0002127375,0.000008745003,0.000016235477,0.000021419537,0.00028476902],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99892026,0.000038239155,0.0002502537,0.00035017607,0.00012630348,0.00031473915],"domain_scores_gemma":[0.9995759,0.0000067485603,0.0001016711,0.00014811015,0.000092576185,0.000074988675],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027691093,0.00013999395,0.000106516985,0.00011439111,0.000081555496,0.000025323736,0.000079158395,0.00016504107,0.0000082263105],"category_scores_gemma":[0.00003624383,0.00015466302,0.000035970737,0.00015780506,0.00003629843,0.000004007616,0.00007217798,0.000080482474,0.000004488368],"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":[0.000012211522,0.000023596029,0.35960868,0.000010415523,0.000008127942,6.326155e-7,0.000021986114,0.00029085248,0.6345943,0.000009710823,0.000058264734,0.0053612096],"study_design_scores_gemma":[0.0004644308,0.00015357514,0.8400579,0.000015107433,0.000008137635,0.00004688048,0.00009430571,0.00088396325,0.15491167,0.00014838387,0.0030342129,0.0001814536],"about_ca_topic_score_codex":0.00007177908,"about_ca_topic_score_gemma":0.00049160287,"teacher_disagreement_score":0.4804492,"about_ca_system_score_codex":0.00004057021,"about_ca_system_score_gemma":0.000030203146,"threshold_uncertainty_score":0.6306975},"labels":[],"label_agreement":null},{"id":"W1984678352","doi":"10.1016/j.placenta.2006.01.015","title":"Epigenetics and Imprinting of the Trophoblast – A Workshop Report","year":2006,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital","funders":"Biotechnology and Biological Sciences Research Council","keywords":"Genomic imprinting; Imprinting (psychology); Epigenetics; Trophoblast; Placenta; Biology; Genetics; Gene; DNA methylation; Bioinformatics; Gene expression; Pregnancy; Fetus","score_opus":0.005609102866246421,"score_gpt":0.2138508686830016,"score_spread":0.2082417658167552,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984678352","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99722177,0.0005030813,0.0004118799,0.00011218308,0.00013298655,0.000098755714,0.0000025047168,0.0000035049784,0.0015133212],"genre_scores_gemma":[0.99733466,0.00004591958,0.0010990457,0.000027844262,0.000095270254,0.0000031148618,0.000007224108,0.00001184876,0.001375083],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99932826,0.000020851876,0.00021060987,0.00019664038,0.00008775555,0.00015586677],"domain_scores_gemma":[0.9995039,0.000009405777,0.00012333156,0.00030622992,0.00003230662,0.000024810222],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011580737,0.00008469569,0.00008711814,0.000012227338,0.00005558902,0.000013470669,0.00011566776,0.000061631705,0.000008606354],"category_scores_gemma":[0.00006883134,0.00006550754,0.000055154513,0.000056410638,0.00006807656,8.137564e-7,0.00023447661,0.000047529134,7.935607e-7],"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":[0.000003883774,0.000026009997,0.20378588,0.000015799134,0.000014755381,0.000001663644,0.000018563027,0.00009988871,0.79355556,0.000027406171,0.0004582566,0.0019923092],"study_design_scores_gemma":[0.00041810027,0.000046748493,0.48812658,0.0000310389,0.000023923896,0.0003164606,0.00015149624,0.00015472331,0.49202055,0.00007474642,0.018478133,0.00015751107],"about_ca_topic_score_codex":0.000065433356,"about_ca_topic_score_gemma":0.00004233307,"teacher_disagreement_score":0.30153504,"about_ca_system_score_codex":0.0000044843696,"about_ca_system_score_gemma":0.000023804658,"threshold_uncertainty_score":0.267132},"labels":[],"label_agreement":null},{"id":"W1985679507","doi":"10.1007/s10735-011-9367-x","title":"Spatiotemporal expression pattern of Mirg, an imprinted non-coding gene, during mouse embryogenesis","year":2011,"lang":"en","type":"article","venue":"Journal of Molecular Histology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre","funders":"","keywords":"Biology; Embryogenesis; MEG3; Gene silencing; Gene expression; Gene; In situ hybridization; Embryonic stem cell; Genomic imprinting; Embryo; Cell biology; Developmental biology; RNA; Molecular biology; Genetics; Long non-coding RNA","score_opus":0.013257861066157513,"score_gpt":0.22818592376859867,"score_spread":0.21492806270244116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985679507","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9552081,0.00047805966,0.043851726,0.00001335448,0.00024151913,0.000078949735,0.0000030403528,0.0000037903296,0.000121416844],"genre_scores_gemma":[0.9903467,0.00008522938,0.009314473,0.000050294773,0.00006718573,0.0000026326318,0.000007720859,0.000036163507,0.000089542846],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985568,0.00012039037,0.00064587704,0.00025103852,0.00016828759,0.00025762056],"domain_scores_gemma":[0.99854296,0.000004445942,0.00069470564,0.00038100322,0.00023821065,0.00013864964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022506417,0.00018206141,0.0003482027,0.00016804489,0.000052120373,0.0000060352777,0.00036089416,0.00020644286,0.0000411692],"category_scores_gemma":[0.000056616504,0.00017449743,0.00022064947,0.000064145264,0.00007893684,0.000009126562,0.00014716951,0.00013299964,0.0000017550577],"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":[0.00006565851,0.00011942604,0.014637784,0.000036753852,0.00007221412,0.000053910884,0.00018833623,0.000030801555,0.9833451,0.0000016614289,0.000019029072,0.0014293629],"study_design_scores_gemma":[0.00077359116,0.00062532094,0.036476433,0.00002900975,0.000040542167,0.00065577147,0.00010586689,0.000036023095,0.961005,0.0000069455564,0.00007997839,0.00016557239],"about_ca_topic_score_codex":0.00006426417,"about_ca_topic_score_gemma":0.0000104925775,"teacher_disagreement_score":0.035138614,"about_ca_system_score_codex":0.000022264085,"about_ca_system_score_gemma":0.0000784074,"threshold_uncertainty_score":0.71157986},"labels":[],"label_agreement":null},{"id":"W1985876152","doi":"10.1017/s0140525x01273968","title":"Genomic imprinting and culture in mammals","year":2001,"lang":"en","type":"article","venue":"Behavioral and Brain Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Imprinting (psychology); Receptivity; Genomic imprinting; Biology; Genomic information; Evolutionary biology; Gene; Psychology; Genetics; Genome; Gene expression","score_opus":0.02694687285279374,"score_gpt":0.3011778499987616,"score_spread":0.2742309771459679,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985876152","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9983748,0.0008338781,0.0000192495,0.00035417764,0.0000354417,0.00006303275,8.653216e-7,0.000003544607,0.00031500548],"genre_scores_gemma":[0.99795187,0.00021851629,0.0011551793,0.0001280889,0.00003925783,0.0000036579077,0.0000016229907,0.0000031604575,0.00049862626],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993734,0.00001686175,0.00010373626,0.00026400678,0.00005823683,0.00018380814],"domain_scores_gemma":[0.9998518,0.000003831112,0.000028663508,0.00006083574,0.000009579716,0.00004528329],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024520268,0.00007322767,0.00007089997,0.000030449666,0.00010010672,0.000058331403,0.00008697916,0.000051772106,0.000008303514],"category_scores_gemma":[0.000016012173,0.000057707584,0.000015915462,0.00008371518,0.000166922,0.0000048538423,0.00013594895,0.000036797155,9.809224e-7],"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":[9.0085456e-7,0.000009883646,0.49124992,0.0000019112385,5.5877047e-7,0.0000015968078,0.00009748412,0.0000016148916,0.48187694,0.000015404403,0.000031127176,0.026712677],"study_design_scores_gemma":[0.0002697724,0.00027677647,0.98212445,0.000012998806,0.0000037388397,0.00018927443,0.0007258313,0.000055186825,0.008132059,0.00015176961,0.007894817,0.00016333332],"about_ca_topic_score_codex":0.0000869929,"about_ca_topic_score_gemma":0.000071435556,"teacher_disagreement_score":0.49087453,"about_ca_system_score_codex":0.0000020917641,"about_ca_system_score_gemma":0.000014145005,"threshold_uncertainty_score":0.2353247},"labels":[],"label_agreement":null},{"id":"W1986515247","doi":"10.1016/j.jpeds.2008.12.033","title":"Body mass index in children with Prader-Willi Syndrome during human growth hormone therapy: A real world situation","year":2009,"lang":"en","type":"letter","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Medicine; Body mass index; Human growth hormone; Growth hormone; Index (typography); Pediatrics; Endocrinology; Hormone","score_opus":0.007093148032011679,"score_gpt":0.21984410935736265,"score_spread":0.21275096132535096,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1986515247","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.988266,0.0017089559,0.00012694212,0.009428537,0.00007556202,0.00028537173,0.000005952954,0.0000055309165,0.00009712881],"genre_scores_gemma":[0.9839113,0.0069295545,0.00021795915,0.0049104346,0.0035267551,0.000003212663,0.000062504834,0.00006489514,0.00037341387],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9980424,0.00018536908,0.0006101683,0.00024014575,0.00051721383,0.0004047269],"domain_scores_gemma":[0.99846727,0.00002303299,0.00094360136,0.00034661597,0.00015968466,0.000059779133],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00054048776,0.00033191885,0.0003912593,0.00038563195,0.00011469713,0.000055855155,0.00055429916,0.0003987659,0.0000055133246],"category_scores_gemma":[0.00002718768,0.00022773714,0.00013652342,0.00034306027,0.00005028293,0.000010238286,0.00006948483,0.0012734627,0.0000016244685],"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":[0.000044676923,0.00016693657,0.9166445,0.00012370372,0.00030631694,0.00010108452,0.00021373545,0.00039934888,0.033585455,0.000001826392,0.047919948,0.000492435],"study_design_scores_gemma":[0.0014413833,0.0009704876,0.994713,0.00003116969,0.00016458248,0.0012660937,0.000020263495,0.0000018823999,0.00031375574,0.000086146465,0.00066257804,0.00032864552],"about_ca_topic_score_codex":0.00007588216,"about_ca_topic_score_gemma":0.00001557605,"teacher_disagreement_score":0.07806848,"about_ca_system_score_codex":0.00005802995,"about_ca_system_score_gemma":0.00014176819,"threshold_uncertainty_score":0.92868507},"labels":[],"label_agreement":null},{"id":"W1987171500","doi":"10.1002/ajmg.a.35377","title":"Beckwith–Wiedemann syndrome in sibs discordant for IC2 methylation","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto; University of British Columbia; Hospital for Sick Children; Rare Disease Foundation; Child and Family Research Institute","funders":"Division of Materials Research; Canadian Institutes of Health Research","keywords":"DNA methylation; Genomic imprinting; Epigenetics; Biology; Beckwith–Wiedemann syndrome; Methylation; Genetics; Methylated DNA immunoprecipitation; CpG site; Differentially methylated regions; Imprinting (psychology); Molecular biology; Gene; Gene expression","score_opus":0.016458215481712245,"score_gpt":0.3035539655127694,"score_spread":0.2870957500310572,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987171500","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.980784,0.0025997844,0.015230449,0.00068329467,0.00048750264,0.0001380158,0.0000036684785,0.0000022467477,0.000071068236],"genre_scores_gemma":[0.9898666,0.00085931405,0.008383384,0.0002883374,0.00047336242,0.000011975874,0.0000097884085,0.000027018816,0.00008018027],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99815375,0.00010647667,0.0006233299,0.00016761618,0.0005124284,0.00043641296],"domain_scores_gemma":[0.99888045,0.00006052014,0.00039175688,0.00019757805,0.00009281459,0.00037689146],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013707911,0.00015330651,0.00034209795,0.00009150211,0.00003611426,0.00001528682,0.00032000436,0.000084781765,0.00004708268],"category_scores_gemma":[0.00041538928,0.00012796978,0.00016288845,0.0001547167,0.0001694022,0.000005734064,0.000100086574,0.00016655418,0.0000046575738],"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":[0.00025880535,0.0012340926,0.35725492,0.00014024721,0.00068309007,0.00006886135,0.0012837321,0.00062064367,0.16832605,0.00020732879,0.0037813594,0.46614087],"study_design_scores_gemma":[0.006961542,0.013411855,0.58819133,0.00061499863,0.00036755472,0.007249249,0.004251621,0.0014730692,0.059114713,0.0005267356,0.31627348,0.00156386],"about_ca_topic_score_codex":0.000011848903,"about_ca_topic_score_gemma":0.000011366297,"teacher_disagreement_score":0.464577,"about_ca_system_score_codex":0.000017042988,"about_ca_system_score_gemma":0.0001526205,"threshold_uncertainty_score":0.52184564},"labels":[],"label_agreement":null},{"id":"W1987244404","doi":"10.1007/s10508-011-9805-6","title":"New MRI Studies Support the Blanchard Typology of Male-to-Female Transsexualism","year":2011,"lang":"en","type":"letter","venue":"Archives of Sexual Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health","funders":"","keywords":"Typology; Sexual behavior; Psychology; Public health; Adult male; Clinical psychology; Developmental psychology; Medicine; Internal medicine; Pathology; Sociology","score_opus":0.04285654855545794,"score_gpt":0.2998062101823736,"score_spread":0.2569496616269156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987244404","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9705828,0.0022569702,0.000549119,0.02188498,0.001069061,0.0010178533,0.00032244125,0.000014428931,0.0023023877],"genre_scores_gemma":[0.7664441,0.0020420414,0.029404929,0.092510216,0.006880094,0.00047276297,0.0018215805,0.0004731665,0.09995113],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99823254,0.00010012886,0.0005370791,0.000527175,0.00018410197,0.00041898404],"domain_scores_gemma":[0.99871725,0.00006140505,0.00027728258,0.0008092134,0.00005926032,0.00007558405],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000110346264,0.00033506443,0.00055981794,0.00010565463,0.00004865779,0.0000059183676,0.00072784716,0.00032215135,0.00020892714],"category_scores_gemma":[0.00003379296,0.000256872,0.00015175878,0.000059373153,0.00037429837,0.000001875355,0.000355265,0.00035881306,0.000015155857],"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":[0.00007787574,0.00014408286,0.010822415,0.0006095903,0.000818078,0.00006835967,0.0067270687,0.0000054756674,0.57862884,0.00004439375,0.36580953,0.036244288],"study_design_scores_gemma":[0.0018739259,0.008711699,0.07043459,0.00017577255,0.0017263866,0.0007826524,0.004423445,7.386295e-7,0.23790278,0.00018212404,0.67229104,0.0014948512],"about_ca_topic_score_codex":0.00012720325,"about_ca_topic_score_gemma":0.0000249265,"teacher_disagreement_score":0.34072608,"about_ca_system_score_codex":0.0000031242223,"about_ca_system_score_gemma":0.00013065507,"threshold_uncertainty_score":0.9999884},"labels":[],"label_agreement":null},{"id":"W1987825638","doi":"10.2337/db11-1314","title":"Transgenerational Glucose Intolerance With <i>Igf2</i>/<i>H19</i> Epigenetic Alterations in Mouse Islet Induced by Intrauterine Hyperglycemia","year":2012,"lang":"en","type":"article","venue":"Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":310,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Offspring; Impaired glucose tolerance; Gestational diabetes; Genomic imprinting; Endocrinology; Epigenetics; Internal medicine; Biology; Islet; Diabetes mellitus; DNA methylation; Pregnancy; Gestation; Type 2 diabetes; Gene; Medicine; Gene expression; Genetics","score_opus":0.007940225014701258,"score_gpt":0.2156889418735279,"score_spread":0.20774871685882665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987825638","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99696475,0.0014405156,0.00081671,0.00018948413,0.00013201006,0.0001933283,0.000037825666,0.000013375511,0.00021201889],"genre_scores_gemma":[0.9963138,0.00016097806,0.0021071855,0.0006030263,0.00024258049,0.00009888781,0.0002876294,0.00003428781,0.00015161702],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99879247,0.00005418403,0.00025799405,0.00029944294,0.00013237372,0.0004635645],"domain_scores_gemma":[0.9994956,0.0000112642565,0.000058330952,0.00026770847,0.00004657567,0.00012049898],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013333154,0.00020576545,0.00017510579,0.000045460936,0.00007367251,0.00003926953,0.00014869316,0.00011208302,0.00003604509],"category_scores_gemma":[0.00002184011,0.00019139929,0.000044571047,0.00012267368,0.000048199254,0.00001471679,0.000042892276,0.00010693647,0.00001105051],"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":[0.000006754864,0.000121140285,0.028317675,0.000013995066,0.000027052727,1.4823453e-7,0.000104249455,0.0001426523,0.9679331,0.000028191384,0.00024815663,0.0030568363],"study_design_scores_gemma":[0.0007320558,0.00021410864,0.012279528,0.000015117715,0.000009650515,0.00000404061,0.00002836104,0.00021164377,0.9790294,0.000010762569,0.007183463,0.00028182424],"about_ca_topic_score_codex":0.000021144391,"about_ca_topic_score_gemma":0.000025360008,"teacher_disagreement_score":0.016038146,"about_ca_system_score_codex":0.000014131191,"about_ca_system_score_gemma":0.000039821305,"threshold_uncertainty_score":0.7805037},"labels":[],"label_agreement":null},{"id":"W1988289925","doi":"10.1097/01.mop.0000187191.74295.97","title":"Advances in overgrowth syndromes: clinical classification to molecular delineation in Sotos syndrome and Beckwith-Wiedemann syndrome","year":2005,"lang":"en","type":"review","venue":"Current Opinion in Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Institute of Genetics; SickKids Foundation; University of Toronto; Hospital for Sick Children","funders":"","keywords":"Sotos syndrome; Medicine; Bioinformatics; Pediatrics; Biology","score_opus":0.08456372896538565,"score_gpt":0.42098775594155646,"score_spread":0.3364240269761708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988289925","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.032124676,0.9634108,0.0008922963,0.00003553654,0.0019613535,0.0014923896,0.000039781564,0.0000142605595,0.000028921733],"genre_scores_gemma":[0.012824278,0.9850213,0.0006777708,0.000018207267,0.0003920566,0.00034070312,0.0006349228,0.00007608463,0.000014673854],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9953775,0.0003656253,0.0020317906,0.0012985801,0.0003445008,0.00058201415],"domain_scores_gemma":[0.9984777,0.000105372346,0.00055599835,0.00057275506,0.00007403476,0.00021413839],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0010198306,0.000592908,0.0013252624,0.000926897,0.00003743222,0.000057420846,0.00044662334,0.0007207722,0.000006809029],"category_scores_gemma":[0.0005339671,0.00061059423,0.0002640532,0.0010829305,0.000056918816,0.000027398188,0.0003580784,0.000648592,0.000028457274],"study_design_candidate":"design_other","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":[0.000007903558,0.00030445342,0.02171083,0.007197165,0.000013574354,0.000013139352,0.000026702983,0.00012715018,0.0000024584886,0.00004851351,0.00010358502,0.9704445],"study_design_scores_gemma":[0.0011654734,0.00063620595,0.034147155,0.007088439,0.00010869703,0.00058110734,0.0000547117,0.00025208833,4.7396514e-7,0.000045491422,0.9547368,0.0011833427],"about_ca_topic_score_codex":0.000010217293,"about_ca_topic_score_gemma":0.000020659923,"teacher_disagreement_score":0.96926117,"about_ca_system_score_codex":0.00014857732,"about_ca_system_score_gemma":0.00033417638,"threshold_uncertainty_score":0.99963456},"labels":[],"label_agreement":null},{"id":"W1989369027","doi":"10.1093/hmg/ddi059","title":"Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth","year":2005,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":133,"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":"Biology; Cell biology; Genetics; Neuroscience","score_opus":0.009450473847293918,"score_gpt":0.25020741792656936,"score_spread":0.24075694407927545,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989369027","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98376024,0.0031131648,0.011167612,0.00045821647,0.000078967765,0.0010427922,0.000011945697,0.000014581575,0.00035249259],"genre_scores_gemma":[0.99181366,0.00005426529,0.006661579,0.00026732826,0.00026785137,0.00024018071,0.00006496997,0.000070488626,0.00055966125],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9981967,0.00006969942,0.00040791748,0.00053455355,0.00024390532,0.00054723263],"domain_scores_gemma":[0.9990948,0.000012816216,0.000120654666,0.0006001634,0.00007546056,0.00009609371],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00026363498,0.00027799146,0.00020708787,0.00007141714,0.00018147733,0.00007794273,0.0004953365,0.00019992534,0.000041603213],"category_scores_gemma":[0.000049823568,0.00025024396,0.00019262836,0.00011275521,0.000113361726,0.000003664773,0.00023384042,0.00015463859,0.0000154526],"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":[0.00000393147,0.00013116679,0.0019920685,0.000025595806,0.00007614899,0.0000031944137,0.000078360834,0.0023128828,0.9907274,0.0004630956,0.00018741773,0.0039987243],"study_design_scores_gemma":[0.004311893,0.0016754073,0.16827217,0.00009544056,0.00016375113,0.00035911248,0.0004061892,0.0062500476,0.6913687,0.0018147948,0.123769805,0.0015127112],"about_ca_topic_score_codex":0.000019175293,"about_ca_topic_score_gemma":0.000078514255,"teacher_disagreement_score":0.29935873,"about_ca_system_score_codex":0.000023256101,"about_ca_system_score_gemma":0.000076541015,"threshold_uncertainty_score":0.999995},"labels":[],"label_agreement":null},{"id":"W1990582768","doi":"10.1016/j.jpeds.2010.01.018","title":"Non-Immune Goiter and Hypothyroidism in a 19-Week Fetus: A Plea for Conservative Treatment","year":2010,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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","funders":"Canadian Child Health Clinician Scientist Program","keywords":"Medicine; Polyhydramnios; Amniotic fluid; Fetus; Goiter; Psychomotor learning; Obstetrics; Pregnancy; Internal medicine; Endocrinology; Thyroid","score_opus":0.012848678023731453,"score_gpt":0.24863960195418663,"score_spread":0.23579092393045517,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1990582768","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967994,0.0016598268,0.00067993236,0.0004552602,0.0001764121,0.00015920163,0.000006757277,7.785622e-7,0.000062439656],"genre_scores_gemma":[0.9953159,0.0016074801,0.0023725925,0.00009946205,0.0003718822,0.000004290806,0.0000024712665,0.0000110371175,0.00021486747],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99942064,0.000025186899,0.00026498872,0.00007829493,0.00006536184,0.0001455488],"domain_scores_gemma":[0.9994498,0.00007939739,0.00020716984,0.00012666128,0.000080564205,0.000056415178],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043101874,0.00009348912,0.00014085317,0.000048227055,0.000049300124,0.000015440817,0.00011955763,0.000071814495,0.000003134305],"category_scores_gemma":[0.00015730484,0.00005992817,0.00006569135,0.000059085385,0.000042811836,0.0000031625127,0.000045269746,0.00010820361,7.796006e-7],"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":[0.00025055488,0.00029194378,0.078342065,0.000060914994,0.000054449058,0.000007372499,0.0022890063,0.000058173995,0.9101397,0.000036493326,0.0012489647,0.0072203707],"study_design_scores_gemma":[0.018415356,0.013030253,0.781418,0.000037042566,0.00076001586,0.0020343447,0.004350128,0.00043425,0.12914452,0.0020124034,0.047428023,0.0009356517],"about_ca_topic_score_codex":0.00003293973,"about_ca_topic_score_gemma":0.000043289507,"teacher_disagreement_score":0.7809952,"about_ca_system_score_codex":0.0000089031955,"about_ca_system_score_gemma":0.00009694394,"threshold_uncertainty_score":0.24438},"labels":[],"label_agreement":null},{"id":"W1990626904","doi":"10.1371/journal.pgen.1002600","title":"Critical Evaluation of Imprinted Gene Expression by RNA–Seq: A New Perspective","year":2012,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":230,"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":"Canadian Institutes of Health Research","keywords":"Biology; Genomic imprinting; Genetics; Allele; Gene; Computational biology; False positive paradox; Concordance; RNA-Seq; Transcriptome; Pyrosequencing; Gene expression; DNA methylation; Statistics","score_opus":0.03333032953320142,"score_gpt":0.3172731554300056,"score_spread":0.2839428258968042,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1990626904","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98566717,0.008451735,0.0041125235,0.00009085717,0.00019422888,0.00024064699,0.00001639159,0.000009126447,0.0012173157],"genre_scores_gemma":[0.98964864,0.00014859591,0.0096450895,0.000049235627,0.00028758412,0.00001648002,0.00003524381,0.000031787975,0.00013733428],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985587,0.00011478673,0.00026577682,0.00028973495,0.00041734747,0.00035366428],"domain_scores_gemma":[0.9987929,0.00001865456,0.0000938146,0.0003968339,0.0004916865,0.0002061195],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029509605,0.00016551302,0.00016132853,0.000036526875,0.00004939645,0.000014778501,0.00017341023,0.0001638342,0.00013513774],"category_scores_gemma":[0.00054764585,0.00016347077,0.00008644717,0.000077108016,0.00006817909,0.0000049724667,0.00017405702,0.000079032274,0.000014643075],"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":[0.000007806414,0.00020102969,0.0026007863,0.000012383311,0.000043975444,5.8423662e-8,0.00020670299,0.00003030885,0.99457085,0.00003051503,0.0009265471,0.0013690294],"study_design_scores_gemma":[0.0005071855,0.00022009929,0.00168235,0.000019815392,0.000121191035,0.0000109674,0.00030153556,0.0011824896,0.9950321,0.00019366315,0.0005420001,0.00018663137],"about_ca_topic_score_codex":0.000013467549,"about_ca_topic_score_gemma":0.0000014471633,"teacher_disagreement_score":0.008303138,"about_ca_system_score_codex":0.0000341393,"about_ca_system_score_gemma":0.000125856,"threshold_uncertainty_score":0.6666145},"labels":[],"label_agreement":null},{"id":"W1991089031","doi":"10.1002/ajmg.a.32283","title":"Sotos syndrome: Antenatal presentation","year":2008,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Saskatchewan; Izaak Walton Killam Health Centre","funders":"","keywords":"Sotos syndrome; Macrocephaly; Presentation (obstetrics); Medicine; Pregnancy; Polyhydramnios; Pediatrics; Differential diagnosis; Obstetrics; Fetus; Pathology; Biology; Genetics","score_opus":0.013302933233658495,"score_gpt":0.27514576478104585,"score_spread":0.26184283154738736,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1991089031","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9940687,0.0011057801,0.0037152648,0.0005372907,0.00036513704,0.00006646018,0.000002635631,0.0000036390861,0.00013512564],"genre_scores_gemma":[0.9933457,0.0030707773,0.002636626,0.00037790005,0.00036645922,0.0000028237325,0.0000077236855,0.000021390162,0.00017063213],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9981223,0.00009536157,0.00050025753,0.00018271264,0.0008255305,0.00027383486],"domain_scores_gemma":[0.99888825,0.000024791863,0.00035160972,0.00021755115,0.00015899411,0.00035877773],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003929137,0.00013437569,0.00026510624,0.00006522682,0.00006963903,0.000012372998,0.0004124486,0.000087834815,0.00010728407],"category_scores_gemma":[0.00027804865,0.00011480504,0.00014941563,0.00014773737,0.0004171372,0.0000033144179,0.00013120253,0.00019084723,0.00001237911],"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":[0.00027469298,0.0011518485,0.3601902,0.000088607165,0.0013913738,0.0033773808,0.0015869272,0.00083732296,0.18029085,0.000039917843,0.040929116,0.40984178],"study_design_scores_gemma":[0.0060474346,0.015183521,0.54525554,0.00033734966,0.00020681244,0.15173319,0.0026456953,0.0014194674,0.06227595,0.00009546038,0.21348415,0.0013154172],"about_ca_topic_score_codex":0.0000115885405,"about_ca_topic_score_gemma":0.0000022076074,"teacher_disagreement_score":0.40852636,"about_ca_system_score_codex":0.0000082461265,"about_ca_system_score_gemma":0.0002886474,"threshold_uncertainty_score":0.46816137},"labels":[],"label_agreement":null},{"id":"W1992543365","doi":"10.1002/ajmg.1587","title":"Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith Syndrome","year":2001,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto; Toronto Western Hospital; Hospital for Sick Children","funders":"","keywords":"Pedigree chart; Genetics; Beckwith–Wiedemann syndrome; Genetic linkage; Biology; Penetrance; Haplotype; Phenotype; Linkage (software); Gene; Allele","score_opus":0.007550696874891125,"score_gpt":0.26074247557279473,"score_spread":0.2531917786979036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992543365","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975549,0.0010890665,0.00048265426,0.0005940992,0.00007435,0.00014682829,0.0000011037947,0.0000031405768,0.000053838947],"genre_scores_gemma":[0.99524903,0.002365573,0.0018094209,0.00036688507,0.00013619548,0.0000035087971,0.0000014102008,0.000027237877,0.00004073157],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99808055,0.00014155252,0.0005158159,0.0002660733,0.0006737873,0.00032220644],"domain_scores_gemma":[0.9990352,0.00003215958,0.00025224,0.00022727114,0.00010097986,0.0003521472],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005777521,0.00019184023,0.00041729386,0.00011371863,0.00003974779,0.000032238277,0.00034093807,0.00009537975,0.000023517083],"category_scores_gemma":[0.00013380927,0.00014253081,0.000053202435,0.00023269324,0.00035563475,0.000003963606,0.00018809641,0.00027958694,0.000001981461],"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":[0.000112416674,0.00048406224,0.8565603,0.000017368455,0.00015945698,0.0007013007,0.0006025652,0.00007093136,0.004832264,0.0000012442487,0.00003329721,0.1364248],"study_design_scores_gemma":[0.002572776,0.01744288,0.95726055,0.00016213358,0.00006173115,0.012662633,0.006537187,0.00011726879,0.00044865318,0.000006602574,0.0024286837,0.0002989138],"about_ca_topic_score_codex":0.00005028416,"about_ca_topic_score_gemma":0.0000976534,"teacher_disagreement_score":0.13612588,"about_ca_system_score_codex":0.00001050062,"about_ca_system_score_gemma":0.00017221543,"threshold_uncertainty_score":0.5812238},"labels":[],"label_agreement":null},{"id":"W1993696633","doi":"10.1159/000133352","title":"Localization of mouse parathyroid hormone-like peptide gene (Pthlh) to distal chromosome 6 using interspecific backcross mice and in situ hybridization","year":2008,"lang":"en","type":"article","venue":"Cytogenetics and Cell Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Royal Victoria Hospital; Royal Victoria Regional Health Centre","funders":"National Human Genome Research Institute; Kementerian Pendidikan Nasional","keywords":"Biology; Molecular biology; Locus (genetics); Chromosome 17 (human); Genetics; Gene; Chromosome","score_opus":0.015799603880987338,"score_gpt":0.23001029173731763,"score_spread":0.2142106878563303,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1993696633","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97932523,0.00698333,0.013203209,0.0000088179295,0.000067051005,0.00029634722,0.00004095448,0.00000578938,0.00006925357],"genre_scores_gemma":[0.98491186,0.0087325815,0.0059059006,0.00007514641,0.00007331275,0.000005498748,0.00010293208,0.000042325308,0.00015045934],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9984987,0.00004848423,0.00046993306,0.00047531092,0.00016761235,0.00033996778],"domain_scores_gemma":[0.9992082,0.000009425517,0.00014437384,0.0003288279,0.00013184357,0.00017733856],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00010427335,0.00026198465,0.00026066703,0.00010425979,0.00011485847,0.00003730641,0.00015051324,0.00015492615,0.0000027325239],"category_scores_gemma":[0.00001703998,0.00029637676,0.000051854116,0.00019433952,0.00017192929,0.0000049607056,0.00028877918,0.00007001313,0.0000023660855],"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":[0.000029856357,0.000085519154,0.016171714,0.000032244458,0.000014825642,0.000003870135,0.00039007195,0.006653967,0.9762351,0.0000015510966,0.00009787859,0.00028340681],"study_design_scores_gemma":[0.0008620169,0.0005138104,0.01179753,0.000015150965,0.00002636719,0.00011529884,0.00033637867,0.0018099915,0.98223794,0.00000772154,0.0019045905,0.000373182],"about_ca_topic_score_codex":0.000018341809,"about_ca_topic_score_gemma":0.00003079894,"teacher_disagreement_score":0.007297309,"about_ca_system_score_codex":0.000020813504,"about_ca_system_score_gemma":0.00006341043,"threshold_uncertainty_score":0.99994886},"labels":[],"label_agreement":null},{"id":"W1993901957","doi":"10.1111/j.1365-2052.2008.01838.x","title":"<i>TCOF1 T</i>/<i>Ser</i> variant and brachycephaly in dogs","year":2009,"lang":"he","type":"article","venue":"Animal Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"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 Key Research and Development Program of China","keywords":"Biology; Genetics; Polymorphism (computer science); Genotype; Gene","score_opus":0.008933073643971957,"score_gpt":0.2400342641506596,"score_spread":0.23110119050668765,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1993901957","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97241503,0.02152704,0.00022107096,0.0010838568,0.00022523345,0.00034849983,0.000022698052,0.0000130315275,0.0041435626],"genre_scores_gemma":[0.985049,0.009224947,0.003188076,0.0014543633,0.00041727856,0.000005236467,0.00003159967,0.000049059192,0.00058040826],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99723727,0.000119134646,0.00064564595,0.0009218243,0.00023801884,0.0008380905],"domain_scores_gemma":[0.99885726,0.000021017384,0.00017176359,0.00058909634,0.0000900443,0.00027082386],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00033122915,0.00047213933,0.00043061553,0.00009910917,0.00011706719,0.00013887831,0.00035433224,0.00048876,0.00006059759],"category_scores_gemma":[0.000067244386,0.00051421206,0.00013200154,0.0002453716,0.00018354143,0.0000068530385,0.000301138,0.00028434137,0.00004323505],"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":[0.00011371662,0.00052963936,0.051251452,0.000099734716,0.00009602504,0.00012797333,0.00047575287,0.0001476445,0.87209165,0.00048551374,0.0012243128,0.07335656],"study_design_scores_gemma":[0.0037210982,0.008632858,0.82917386,0.00018944863,0.00018278883,0.0010482039,0.00058314914,0.002089446,0.07476877,0.00064655906,0.07714289,0.0018209398],"about_ca_topic_score_codex":0.00011147487,"about_ca_topic_score_gemma":0.00011135559,"teacher_disagreement_score":0.7973229,"about_ca_system_score_codex":0.000022563227,"about_ca_system_score_gemma":0.0001421304,"threshold_uncertainty_score":0.99973094},"labels":[],"label_agreement":null},{"id":"W1994577070","doi":"10.1006/bbrc.1999.1982","title":"Methylation Patterns of Human Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Gene Promoters Are Established Several Weeks Prior to Onset of Their Function","year":2000,"lang":"en","type":"article","venue":"Biochemical and Biophysical Research Communications","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Montreal Children's Hospital; Jewish General Hospital; Royal Victoria Hospital; McGill University","funders":"","keywords":"Methylation; Promoter; CpG site; Parathyroid hormone; DNA methylation; Endocrinology; Biology; Internal medicine; Receptor; Kidney; Demethylation; Parathyroid hormone receptor; Gene; Gene expression; Hormone receptor; Genetics; Medicine; Calcium; Cancer","score_opus":0.03458819274314194,"score_gpt":0.31331456998512397,"score_spread":0.278726377241982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1994577070","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99802667,0.0005454951,0.00009472588,0.00066284876,0.000009492186,0.0003898375,0.000112039976,0.000010334629,0.00014855934],"genre_scores_gemma":[0.99737674,0.00065535714,0.0010148055,0.000026485799,0.000045194574,0.00005296478,0.0004524324,0.000018031331,0.0003580106],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9984168,0.0002549458,0.00040128396,0.00035754233,0.00027162678,0.0002978313],"domain_scores_gemma":[0.9983843,0.00007948331,0.00010789847,0.00094725844,0.00030433762,0.00017670039],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041894993,0.00015477175,0.00024101479,0.00008291811,0.00019486093,0.000028268032,0.00051117246,0.00017184897,0.000037223777],"category_scores_gemma":[0.00015024246,0.00013386941,0.00010770559,0.00033147802,0.00031557586,0.000009800225,0.00039551273,0.00025691712,0.000009034372],"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":[0.0000739781,0.0003178276,0.0005009802,0.000023548784,0.00005525651,8.827027e-8,0.00012651487,0.0000027605151,0.9912428,0.000028970613,0.0005327508,0.007094496],"study_design_scores_gemma":[0.00055742246,0.0010935153,0.09344802,0.00006303546,0.000021696917,0.0000036702982,0.00027217195,0.00021658825,0.9024437,0.00019346533,0.0014906579,0.00019603723],"about_ca_topic_score_codex":0.00016290836,"about_ca_topic_score_gemma":0.000012017676,"teacher_disagreement_score":0.092947036,"about_ca_system_score_codex":0.000019687695,"about_ca_system_score_gemma":0.000047693764,"threshold_uncertainty_score":0.5459036},"labels":[],"label_agreement":null},{"id":"W1996207676","doi":"10.1139/g06-042","title":"Loss of genomic imprinting in<i>Drosophila</i>clones","year":2006,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; Evolutionary biology; Gene; DNA methylation; Gene expression","score_opus":0.006412581397798147,"score_gpt":0.21114850784494216,"score_spread":0.204735926447144,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1996207676","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99631375,0.0008870616,0.00020382562,0.00005144751,0.000082172926,0.00010057412,0.000006112564,0.0000057278016,0.0023493343],"genre_scores_gemma":[0.9981672,0.00006588343,0.001262676,0.000030080884,0.00020035612,0.00000636457,0.000029953877,0.000019963529,0.00021751205],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99909556,0.000018286579,0.00029790486,0.00025683868,0.000071109025,0.00026029657],"domain_scores_gemma":[0.9995535,0.000004396651,0.000098320554,0.00027268694,0.0000427059,0.000028372271],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014571195,0.00011327226,0.00015022793,0.000054474116,0.000027757076,0.000009640672,0.00017119378,0.000083811494,0.000022500928],"category_scores_gemma":[0.000014344056,0.00012005542,0.00006586886,0.00009155747,0.000039678547,0.0000015516351,0.00016065013,0.00005074331,0.000017549015],"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":[0.0000029696841,0.000027396396,0.062163766,0.000019544861,0.000007640576,0.000001476738,0.000016412667,0.00061635615,0.9367577,0.00008038396,0.0000045294846,0.00030181758],"study_design_scores_gemma":[0.00039250893,0.00006935739,0.9112718,0.0000069072557,0.0000054503985,0.000036523525,0.000029378258,0.000019553721,0.08421974,0.00032193787,0.0034668837,0.00015992591],"about_ca_topic_score_codex":0.00015441378,"about_ca_topic_score_gemma":0.000052642037,"teacher_disagreement_score":0.852538,"about_ca_system_score_codex":0.000009842058,"about_ca_system_score_gemma":0.000033390374,"threshold_uncertainty_score":0.48957178},"labels":[],"label_agreement":null},{"id":"W1996868983","doi":"10.1159/000095837","title":"Beckwith-Wiedemann Syndrome Presenting with an Elevated Triple Screen in the Second Trimester of Pregnancy","year":2006,"lang":"en","type":"article","venue":"Fetal Diagnosis and Therapy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Women's Health Research Institute","funders":"","keywords":"Medicine; Beckwith–Wiedemann syndrome; Pregnancy; Obstetrics; Gynecology; Neonatology; Genetics","score_opus":0.013884707242240316,"score_gpt":0.24062652272720758,"score_spread":0.22674181548496727,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1996868983","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994578,0.0041664,0.00001879865,0.00006264244,0.000024440613,0.0003802483,0.000014050462,0.000004499899,0.0007509343],"genre_scores_gemma":[0.9985055,0.00051787426,0.00022888237,0.00008093358,0.00003875478,0.00007706761,0.000045873923,0.00001835136,0.0004868116],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991129,0.000084818515,0.00021948859,0.00026712197,0.00010917084,0.00020646656],"domain_scores_gemma":[0.99956435,0.000020489415,0.00009841962,0.00025768543,0.000031142135,0.000027913698],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015810813,0.00014168992,0.00017364195,0.000038452148,0.00005527129,0.00003813748,0.00015610606,0.00007628263,0.00004234015],"category_scores_gemma":[0.000006658135,0.00009103067,0.000051853356,0.00011083989,0.000062101935,0.000009648412,0.000032323904,0.00005857979,7.0016e-7],"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":[0.000100024845,0.0008922187,0.91890943,0.00006698507,0.00012622109,0.000024290237,0.00026454328,0.000022392682,0.064712755,0.000087272376,0.00028242698,0.014511411],"study_design_scores_gemma":[0.0017415044,0.0015455078,0.94637084,0.0000726006,0.000011004654,0.0000804114,0.00009910985,0.00003495515,0.045139175,0.000121913065,0.0045967386,0.000186248],"about_ca_topic_score_codex":0.00018719175,"about_ca_topic_score_gemma":0.00016679864,"teacher_disagreement_score":0.027461374,"about_ca_system_score_codex":0.0000017778715,"about_ca_system_score_gemma":0.000017353768,"threshold_uncertainty_score":0.3712123},"labels":[],"label_agreement":null},{"id":"W1997094167","doi":"10.1016/j.modgep.2007.09.005","title":"The PcG gene Sfmbt2 is paternally expressed in extraembryonic tissues","year":2007,"lang":"en","type":"article","venue":"Gene Expression Patterns","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"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; University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources","keywords":"Biology; Genomic imprinting; Genetics; Gene; Imprinting (psychology); Trophoblast; Embryo; CpG site; Placenta; DNA methylation; Gene expression; Fetus","score_opus":0.01176749455415954,"score_gpt":0.26196194538071566,"score_spread":0.2501944508265561,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997094167","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98703355,0.0017587233,0.009977069,0.00015510528,0.0004040196,0.00020990371,0.000022859573,0.000016468875,0.00042231716],"genre_scores_gemma":[0.9945705,0.0010092932,0.0014510262,0.0003576513,0.0003546342,0.000028546554,0.000041936753,0.000043372664,0.0021430538],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99805504,0.000071193324,0.000460124,0.0005338123,0.00026910062,0.0006107354],"domain_scores_gemma":[0.9988985,0.000030144527,0.00014749737,0.0007348389,0.000057026937,0.00013198341],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005172054,0.00024051416,0.0001699531,0.000058035574,0.00016818824,0.00007344937,0.0005164698,0.00018342644,0.00012010217],"category_scores_gemma":[0.00003931188,0.00018035495,0.00010969281,0.00007805815,0.000043332286,0.0000059297,0.0003540539,0.00014482277,0.00003169991],"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":[0.000021114418,0.000036660655,0.05248974,0.0000089374635,0.000013967008,0.000013665204,0.00018880914,0.00001578382,0.9334656,9.569249e-7,0.0012553661,0.012489374],"study_design_scores_gemma":[0.0004927528,0.00008183017,0.12854025,0.0000482448,0.000004487693,0.000028636741,0.0001441576,0.000022425525,0.84729207,0.000037366357,0.023094498,0.00021326957],"about_ca_topic_score_codex":0.00008825791,"about_ca_topic_score_gemma":0.00007633309,"teacher_disagreement_score":0.08617354,"about_ca_system_score_codex":0.000016742402,"about_ca_system_score_gemma":0.00003585927,"threshold_uncertainty_score":0.7354661},"labels":[],"label_agreement":null},{"id":"W1997214852","doi":"10.1371/journal.pone.0008638","title":"The Imprinted Retrotransposon-Like Gene PEG11 (RTL1) Is Expressed as a Full-Length Protein in Skeletal Muscle from Callipyge Sheep","year":2010,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"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","funders":"Meat and Livestock Australia; Australian Wool Innovation; Utah State University","keywords":"Retrotransposon; Biology; Genetics; Gene; Genomic imprinting; Skeletal muscle; Gene expression; Phenotype; Regulation of gene expression; Genome; Molecular biology; Transposable element; DNA methylation; Anatomy","score_opus":0.01252471206177212,"score_gpt":0.2105023382397632,"score_spread":0.19797762617799108,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997214852","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99792224,0.00027448495,0.00008729901,0.00056083116,0.00010738548,0.0006028682,0.000043092565,0.00003087168,0.00037092183],"genre_scores_gemma":[0.9936566,0.00020406034,0.004932525,0.00017577402,0.00026087792,0.0001588555,0.0000680745,0.000049365815,0.0004938893],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982419,0.00006522003,0.0003494832,0.00057030376,0.00029390602,0.00047918077],"domain_scores_gemma":[0.99883556,0.000023722716,0.000103346145,0.00080828316,0.00009636895,0.0001327205],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002129526,0.00024063705,0.00023176687,0.000037754628,0.00013212739,0.000061110746,0.00047905993,0.0002661389,0.0001708128],"category_scores_gemma":[0.00015548922,0.00020399646,0.00011710517,0.00011168889,0.000102958635,0.000005374847,0.00017636863,0.0003950364,0.000058534548],"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":[0.000023495033,0.00033470293,0.00121736,0.000019206433,0.00011484235,0.0000042494967,0.00012672774,7.217265e-7,0.9956095,0.000008681986,0.000027836015,0.0025126727],"study_design_scores_gemma":[0.0008639713,0.0002910868,0.022507174,0.000054659264,0.000037222504,0.0000043642995,0.000066429355,0.00054839865,0.97092086,0.0000957056,0.0043120314,0.00029808615],"about_ca_topic_score_codex":0.00041159434,"about_ca_topic_score_gemma":0.000566405,"teacher_disagreement_score":0.024688633,"about_ca_system_score_codex":0.000011565908,"about_ca_system_score_gemma":0.00007387012,"threshold_uncertainty_score":0.8318734},"labels":[],"label_agreement":null},{"id":"W1997905518","doi":"10.1006/bbrc.2001.5500","title":"Evidence against GRB10 as the Gene Responsible for Silver–Russell Syndrome","year":2001,"lang":"en","type":"article","venue":"Biochemical and Biophysical Research Communications","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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":"","keywords":"Imprinting (psychology); Genomic imprinting; Gene; GRB10; Gene isoform; Biology; Genetics; Gene family; Gene expression; Endocrinology; Insulin; Insulin receptor; Insulin resistance","score_opus":0.11080214553273457,"score_gpt":0.3841055938591597,"score_spread":0.27330344832642517,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997905518","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9842658,0.004853404,0.00014451356,0.009605878,0.000021235644,0.00048184837,0.000015235496,0.000013359347,0.0005986927],"genre_scores_gemma":[0.98529226,0.010390144,0.0025188252,0.00031923404,0.00012050801,0.00019043995,0.000068686895,0.000018934827,0.0010809727],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9984377,0.00022558705,0.00021548934,0.0003904812,0.0002837958,0.00044696144],"domain_scores_gemma":[0.9974546,0.00062672247,0.000043468284,0.0013934162,0.00029989853,0.00018191402],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000829351,0.00013992688,0.00013981493,0.00004549948,0.0006043763,0.0000924204,0.0011050816,0.00013773076,0.000009872003],"category_scores_gemma":[0.0011423308,0.00010107002,0.00011387208,0.0003412308,0.0007852383,0.0000073989654,0.0009885927,0.000285961,0.000034936216],"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":[0.000048428246,0.00011712569,0.00017508268,0.000014235529,0.000025964753,8.820876e-7,0.000025027079,6.738137e-7,0.9925492,0.00068578654,0.0014808234,0.0048768087],"study_design_scores_gemma":[0.0005538392,0.0010128805,0.008121116,0.00013935305,0.00003290155,0.00016026526,0.00025890055,0.0011315095,0.84388983,0.003054977,0.14125392,0.00039052323],"about_ca_topic_score_codex":0.000044047414,"about_ca_topic_score_gemma":0.0000061382457,"teacher_disagreement_score":0.14865935,"about_ca_system_score_codex":0.000018256687,"about_ca_system_score_gemma":0.00015627456,"threshold_uncertainty_score":0.46484348},"labels":[],"label_agreement":null},{"id":"W1998116517","doi":"10.1002/1097-0223(200101)21:1<36::aid-pd979>3.0.co;2-1","title":"Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy","year":2001,"lang":"en","type":"article","venue":"Prenatal Diagnosis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of British Columbia; BC Research (Canada)","funders":"","keywords":"Uniparental disomy; Trisomy; Aneuploidy; Chorionic villus sampling; Biology; Chorionic villi; Placenta; Chromosome; Genetics; Andrology; Fetus; Nondisjunction; Karyotype; Pregnancy; Prenatal diagnosis; Medicine; Gene","score_opus":0.023843175649213975,"score_gpt":0.27039333692654727,"score_spread":0.24655016127733329,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1998116517","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980495,0.00046912648,0.00053108827,0.00006093117,0.000087624314,0.00034345972,0.00018807486,0.000011561143,0.00025866317],"genre_scores_gemma":[0.997346,0.00021649439,0.001737341,0.000041100753,0.00011846656,0.00017132387,0.00024265687,0.000029143368,0.00009749588],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990391,0.000018177392,0.00022581688,0.0003018118,0.00013570854,0.00027936156],"domain_scores_gemma":[0.9995002,0.00004148637,0.00011843303,0.00019922832,0.000057546717,0.0000831187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006235455,0.00016747013,0.00019821212,0.000039460756,0.00007580141,0.000023206352,0.00017316242,0.000060757164,0.00007341045],"category_scores_gemma":[0.000051779123,0.00015223183,0.000083495994,0.00006650498,0.0000806775,0.0000070760957,0.00018662061,0.000043103923,0.00000256904],"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":[0.00026482195,0.00043575614,0.75033474,0.00019400405,0.0002864332,0.00002423467,0.00011524082,0.00017783308,0.23885016,0.000105380605,0.00021263718,0.008998739],"study_design_scores_gemma":[0.002534895,0.0010171892,0.059462152,0.00019123948,0.0000676919,0.00034470073,0.00017444738,0.00013769332,0.9341639,0.000026343629,0.0015890733,0.00029061857],"about_ca_topic_score_codex":0.00023721908,"about_ca_topic_score_gemma":0.000111630376,"teacher_disagreement_score":0.6953138,"about_ca_system_score_codex":0.000014078739,"about_ca_system_score_gemma":0.000027646543,"threshold_uncertainty_score":0.6207834},"labels":[],"label_agreement":null},{"id":"W1998591794","doi":"10.1002/(sici)1097-0215(20000601)86:5<690::aid-ijc14>3.0.co;2-k","title":"ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers","year":2000,"lang":"en","type":"article","venue":"International Journal of Cancer","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto","funders":"National Cancer Institute; Ovarian Cancer Research Fund","keywords":"Loss of heterozygosity; Cancer research; Biology; Ovarian cancer; Tumor suppressor gene; Breast cancer; Allele; Cancer; Genetics; Gene; Carcinogenesis","score_opus":0.006103453788862071,"score_gpt":0.2647152003580528,"score_spread":0.2586117465691907,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1998591794","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961038,0.000837874,0.000030341796,0.0022352834,0.00020627955,0.00003283708,0.000019183119,3.3492387e-7,0.00053403137],"genre_scores_gemma":[0.9964912,0.0023622029,0.0000486555,0.0006822686,0.00026685727,0.0000020757225,0.0000022540162,0.000005280353,0.0001391841],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999473,0.00001746086,0.00020067807,0.00007705224,0.00016103422,0.00007080666],"domain_scores_gemma":[0.99968714,0.0000054944644,0.00011864061,0.00005999432,0.00010525806,0.00002348965],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000091470756,0.000054432312,0.000072363095,0.00003680324,0.000011241808,0.0000117167365,0.00014962547,0.000033054577,0.00031159903],"category_scores_gemma":[0.000006429732,0.00003914577,0.00004792317,0.000025895155,0.000032349773,0.0000040472733,0.000019283883,0.000063391475,9.977401e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006656578,0.0001853271,0.14487664,0.000021588485,0.0008397227,0.000017652063,0.00088802987,0.004835453,0.42510793,0.000105877836,0.003310153,0.41914597],"study_design_scores_gemma":[0.0035160475,0.0004185057,0.8185793,0.00039537688,0.00003150975,0.0008266585,0.00015760744,0.00034575965,0.06411252,0.00017320165,0.11124057,0.00020291097],"about_ca_topic_score_codex":0.00019897288,"about_ca_topic_score_gemma":0.00008229939,"teacher_disagreement_score":0.67370266,"about_ca_system_score_codex":0.000034845234,"about_ca_system_score_gemma":0.00006168554,"threshold_uncertainty_score":0.34117907},"labels":[],"label_agreement":null},{"id":"W1999357871","doi":"10.1111/j.1541-0420.2006.00610.x","title":"Quantifying Genomic Imprinting in the Presence of Linkage","year":2006,"lang":"en","type":"article","venue":"Biometrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Genetic linkage; Genetics; Biology; Computational biology; Gene","score_opus":0.029310173032650415,"score_gpt":0.2739906408264836,"score_spread":0.2446804677938332,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999357871","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956955,0.0014888372,0.0016955263,0.000032847536,0.000094991505,0.000107534666,0.0000029107712,0.0000032459545,0.0008786265],"genre_scores_gemma":[0.99724084,0.00009429187,0.0024572096,0.000026625523,0.00009618043,0.0000042264624,0.000010598224,0.00000913638,0.00006091004],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992,0.00004164425,0.00024903627,0.00018517791,0.00012873215,0.0001953978],"domain_scores_gemma":[0.99951977,0.000046006924,0.0001048454,0.00027656346,0.000038822793,0.000014003414],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000520164,0.000079078316,0.000092259776,0.00024786824,0.00003451788,0.000022288617,0.0002946693,0.00007756976,0.000003587842],"category_scores_gemma":[0.00022173382,0.00006256593,0.00005782581,0.0009802782,0.00003945955,0.0000015928608,0.00013014922,0.000057664034,0.0000033843048],"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":[0.0000010330622,0.000030875854,0.19607462,0.000023575512,0.000004051862,8.8671834e-7,0.000026284195,0.00006748496,0.7976496,0.0000939203,0.000068336165,0.005959273],"study_design_scores_gemma":[0.00025146132,0.00007977389,0.88772196,0.00001212588,0.000005891626,0.000017129478,0.00016883001,0.00028333266,0.105855376,0.000038852017,0.005447117,0.00011817764],"about_ca_topic_score_codex":0.00019336988,"about_ca_topic_score_gemma":0.000019245723,"teacher_disagreement_score":0.6917943,"about_ca_system_score_codex":0.0000058919977,"about_ca_system_score_gemma":0.000022204325,"threshold_uncertainty_score":0.25513646},"labels":[],"label_agreement":null},{"id":"W2000287799","doi":"10.1002/jnr.20493","title":"Mice with the deleted neurofilament of low molecular weight (Nefl) gene: 2. Effects on motor functions and spatial orientation","year":2005,"lang":"en","type":"article","venue":"Journal of Neuroscience Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"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; Hôpital Saint-Luc; Montreal General Hospital","funders":"","keywords":"Cerebellum; Brainstem; Morris water navigation task; Ataxia; Neuroscience; Neurofilament; Open field; Water maze; Biology; Psychology; Internal medicine; Endocrinology; Medicine; Hippocampal formation","score_opus":0.015502149338215719,"score_gpt":0.29861235707100503,"score_spread":0.28311020773278933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000287799","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952858,0.00013848228,0.0032088163,0.0010531178,0.00010721288,0.0001586452,0.000001389958,9.4853095e-7,0.000045548357],"genre_scores_gemma":[0.9991009,0.00013915685,0.00030486286,0.00020184444,0.0001345822,0.000004200718,5.4118675e-7,0.000008545309,0.000105350795],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99869984,0.00018197804,0.00016976979,0.00018683332,0.0005482978,0.00021325084],"domain_scores_gemma":[0.9992987,0.00005629391,0.00012633097,0.00016718819,0.00026294996,0.000088552704],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053333474,0.00007433986,0.00008773057,0.00010356188,0.00013614894,0.000040259434,0.00021452953,0.0000319985,0.0000016884684],"category_scores_gemma":[0.00021662096,0.00004614383,0.000040360163,0.00021735475,0.0001677455,0.000007870133,0.00008113686,0.00018879,8.4632813e-7],"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":[0.0000588819,0.000048835922,0.000734016,0.000012160402,0.000005074665,0.0000078539,0.000026918147,0.00037914564,0.9897503,0.0000045196707,0.00008833104,0.008883924],"study_design_scores_gemma":[0.00048565198,0.003557376,0.07952442,0.00002739254,0.000008932014,0.0002103028,0.00004798661,0.00087574165,0.9133211,0.0000035100252,0.0018816035,0.0000559837],"about_ca_topic_score_codex":0.000007373329,"about_ca_topic_score_gemma":0.0000024389071,"teacher_disagreement_score":0.07879041,"about_ca_system_score_codex":0.000011863542,"about_ca_system_score_gemma":0.00010554786,"threshold_uncertainty_score":0.18816908},"labels":[],"label_agreement":null},{"id":"W2000472408","doi":"10.1354/vp.45-5-663","title":"Laboratory Findings, Histopathology, and Immunophenotype of Lymphoma in Domestic Ferrets","year":2008,"lang":"en","type":"article","venue":"Veterinary Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Guelph","funders":"University of Guelph; University of Saskatchewan","keywords":"Lymphoma; Pathology; Immunophenotyping; Medicine; Histopathology; Anaplastic large-cell lymphoma; T-cell lymphoma; Immunology","score_opus":0.01577691926152182,"score_gpt":0.24810112811157575,"score_spread":0.23232420885005395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000472408","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965641,0.002832547,0.00005112562,0.000022777826,0.00019241309,0.00008551034,0.0000093153385,0.0000070322208,0.0002352071],"genre_scores_gemma":[0.99762166,0.0005844093,0.0015554442,0.000077647055,0.00002589867,0.00001270444,0.0000143268735,0.00001726539,0.00009063552],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99906135,0.00010851325,0.0002439352,0.00031087303,0.000047011043,0.00022834609],"domain_scores_gemma":[0.99957216,0.000014871326,0.00006547257,0.00027339443,0.000034550925,0.000039542425],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016541038,0.00013205047,0.00021954894,0.00010198415,0.000047356967,0.0000021815358,0.00012497438,0.00017139535,0.0000107393935],"category_scores_gemma":[0.0000831966,0.00013978839,0.000032836848,0.000100864876,0.0002844757,0.0000030354179,0.00020626945,0.000054888787,0.0000048230095],"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":[0.000040234467,0.00005948476,0.045546018,0.000026227459,0.000004738989,0.0007275133,0.00016848129,0.000004598659,0.9520069,0.00002119632,0.00002746014,0.0013671881],"study_design_scores_gemma":[0.00094817695,0.0016177677,0.9701849,0.000015577982,0.0000063646985,0.014787502,0.00004992445,0.000012507884,0.009376951,0.000035468616,0.0027829835,0.00018183826],"about_ca_topic_score_codex":0.000011917094,"about_ca_topic_score_gemma":0.0000018636501,"teacher_disagreement_score":0.94262993,"about_ca_system_score_codex":0.000010001288,"about_ca_system_score_gemma":0.000055998946,"threshold_uncertainty_score":0.5700405},"labels":[],"label_agreement":null},{"id":"W2001481979","doi":"10.1186/1471-213x-9-9","title":"In vitroculture and somatic cell nuclear transfer affect imprinting of SNRPN gene in pre- and post-implantation stages of development in cattle","year":2009,"lang":"en","type":"article","venue":"BMC Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"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; Cegep de Saint Hyacinthe","funders":"Institute of Human Development, Child and Youth Health; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Conselho Nacional de Desenvolvimento Científico e Tecnológico","keywords":"Genomic imprinting; Biology; Somatic cell nuclear transfer; Imprinting (psychology); Reprogramming; DNA methylation; Epigenetics; Methylation; Genetics; Somatic cell; Embryo; Andrology; Molecular biology; Gene expression; Gene; Blastocyst; Embryogenesis","score_opus":0.005892786256505913,"score_gpt":0.22557095788970113,"score_spread":0.21967817163319522,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001481979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993395,0.0002618643,0.000097661556,0.000012704769,0.000019576502,0.00020545101,0.0000051331563,0.0000017728944,0.000056287776],"genre_scores_gemma":[0.987294,0.00011121898,0.0124853,0.000041718155,0.0000042569177,0.0000059133313,0.000038760536,0.0000063844122,0.000012405032],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9991499,0.000050815055,0.0003511108,0.00022945293,0.000039802657,0.00017888883],"domain_scores_gemma":[0.9998387,0.000012935988,0.00005419012,0.000052950338,0.000016091743,0.000025114256],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018584108,0.000116113006,0.00020184576,0.000105022504,0.000014709065,0.0000041833787,0.00006775554,0.0001262465,0.000006034248],"category_scores_gemma":[0.000022361959,0.000109126784,0.000015378906,0.000080750906,0.000036984726,0.0000071720206,0.00006053645,0.000053963366,4.9012573e-7],"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":[0.000022211365,0.000041657586,0.25772232,0.00007340223,0.0000035277226,5.072297e-7,0.001205447,0.000004264036,0.73836446,0.000009391469,4.2565392e-7,0.002552361],"study_design_scores_gemma":[0.0005774674,0.00010906492,0.58555645,0.0000253076,0.0000014453091,0.00002125517,0.00027755112,0.0000053829103,0.41331694,0.0000122714255,0.000020227058,0.00007667077],"about_ca_topic_score_codex":0.000064930246,"about_ca_topic_score_gemma":0.0002822046,"teacher_disagreement_score":0.3278341,"about_ca_system_score_codex":0.000016545724,"about_ca_system_score_gemma":0.00006304119,"threshold_uncertainty_score":0.4450061},"labels":[],"label_agreement":null},{"id":"W2001973648","doi":"10.1210/jc.2011-2406","title":"Muscle-Bone Characteristics in Children with Prader-Willi Syndrome","year":2011,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université de Montréal; McGill University","funders":"Canadian Institutes of Health Research","keywords":"Endocrinology; Short stature; Internal medicine; Medicine; Bone mineral; Lumbar spine; Bone density; Osteoporosis; Surgery","score_opus":0.03494359590288171,"score_gpt":0.2962059595211334,"score_spread":0.26126236361825167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001973648","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99686295,0.0018037468,0.0002780833,0.00030620376,0.0004024013,0.00015125911,0.0000033875529,0.0000045624697,0.00018738146],"genre_scores_gemma":[0.99407756,0.0031034148,0.0017856024,0.0004677781,0.0004416609,0.0000030634358,0.0000033176666,0.000026421218,0.000091202055],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9975179,0.00042659044,0.0012379811,0.00021729927,0.00017731397,0.00042292778],"domain_scores_gemma":[0.99838847,0.00006989291,0.000840846,0.00043991112,0.00013482884,0.00012607861],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011090079,0.00019793677,0.0006768888,0.00008626575,0.000051699524,0.000008694518,0.0005359175,0.00016579413,0.000053970696],"category_scores_gemma":[0.00039830603,0.00012056794,0.00019280735,0.00010783109,0.000337154,0.000008362389,0.00017138867,0.000603597,0.000011826998],"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":[0.0000684975,0.00046588003,0.9587104,0.00000703795,0.0005739889,0.000034011267,0.00018187975,0.000009597599,0.0041982047,0.00020175622,0.00010741838,0.035441376],"study_design_scores_gemma":[0.0017958122,0.00078603043,0.9847397,0.00001793014,0.00017443062,0.006116957,0.00006634555,0.0000028999707,0.0007662108,0.00013347113,0.005255706,0.00014450835],"about_ca_topic_score_codex":0.000037675905,"about_ca_topic_score_gemma":0.00000851611,"teacher_disagreement_score":0.035296865,"about_ca_system_score_codex":0.000003614497,"about_ca_system_score_gemma":0.00011923278,"threshold_uncertainty_score":0.49166176},"labels":[],"label_agreement":null},{"id":"W2002012888","doi":"10.1111/j.1399-0004.2010.01615.x","title":"19p13.2 microduplication causes a Sotos syndrome‐like phenotype and alters gene expression","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Children's Hospital of Eastern Ontario; University of British Columbia","funders":"Javna Agencija za Raziskovalno Dejavnost RS","keywords":"Sotos syndrome; Gene duplication; Genetics; Haploinsufficiency; Biology; Gene; Copy-number variation; Macrocephaly; Pseudogene; Phenotype; Genome","score_opus":0.02157716342541003,"score_gpt":0.31028473006809004,"score_spread":0.28870756664268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002012888","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968254,0.0008342479,0.0010559647,0.00012642468,0.00077381846,0.00024790398,0.000009659036,0.000018892904,0.00010768783],"genre_scores_gemma":[0.97743267,0.0011020437,0.020177832,0.00043204092,0.00037920912,0.00001933291,0.0000543267,0.00003999893,0.0003625497],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99839526,0.00006348752,0.0004838445,0.0006334813,0.00012262656,0.00030130945],"domain_scores_gemma":[0.9987622,0.00004422613,0.00015649038,0.0007196015,0.0000938481,0.00022364043],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032686326,0.00019877272,0.00021978783,0.00003126137,0.00010856634,0.000045371133,0.00025218521,0.0003326596,0.000030169313],"category_scores_gemma":[0.00021157143,0.00018846417,0.000103451224,0.00006347774,0.0002153738,0.0000027731064,0.00032013038,0.00023925904,0.000030865584],"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":[0.000009206698,0.00008590755,0.06382133,0.000013885066,0.000025532056,0.0000018531949,0.000017978535,0.0000089228,0.92508554,0.000004509644,0.000513556,0.010411742],"study_design_scores_gemma":[0.0011442205,0.0008551039,0.4519526,0.000024344348,0.00007291973,0.00025878625,0.00004763222,0.00021887674,0.47586268,0.00014502177,0.06886472,0.0005530811],"about_ca_topic_score_codex":0.0000060170223,"about_ca_topic_score_gemma":0.000014227712,"teacher_disagreement_score":0.4492229,"about_ca_system_score_codex":0.0000029647072,"about_ca_system_score_gemma":0.000060615184,"threshold_uncertainty_score":0.76853454},"labels":[],"label_agreement":null},{"id":"W2002733724","doi":"10.1002/ajmg.a.37058","title":"Mild Angelman syndrome phenotype due to a mosaic methylation imprinting defect","year":2015,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Library of Parliament; Hospital for Sick Children; University of Toronto","funders":"Bundesministerium für Bildung und Forschung","keywords":"Imprinting (psychology); Angelman syndrome; Genomic imprinting; Phenotype; Genetics; Mosaic; Methylation; DNA methylation; Biology; DNA; Gene; History","score_opus":0.021693031545645825,"score_gpt":0.29237799957478466,"score_spread":0.27068496802913883,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002733724","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98422396,0.0014178444,0.012728415,0.0008195933,0.00049545703,0.000113298716,0.0000030438634,0.000006661595,0.00019174641],"genre_scores_gemma":[0.98733246,0.00017284944,0.011086028,0.00079804857,0.00049855345,0.0000049869377,0.000008099237,0.00003600268,0.00006296815],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99760395,0.00018958765,0.00062081247,0.0002793359,0.00091122603,0.00039505895],"domain_scores_gemma":[0.998054,0.000037651553,0.0003978929,0.00031713865,0.00029038006,0.000902899],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001593156,0.00019552499,0.0004118227,0.000115725416,0.000049052112,0.000035604073,0.0005088017,0.000120421464,0.000041142914],"category_scores_gemma":[0.000910344,0.00017420479,0.00019860314,0.0003075911,0.00014511065,0.000004064345,0.00026532222,0.00024164116,0.000026558708],"study_design_candidate":"design_other","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":[0.00022573787,0.00046649677,0.044129655,0.00006488697,0.0010412806,0.00037544678,0.0018029303,0.0031829004,0.122275874,0.00004515317,0.015413231,0.8109764],"study_design_scores_gemma":[0.008905135,0.0371269,0.18791112,0.0008798108,0.0008334519,0.019093368,0.007107777,0.003495393,0.07315795,0.00073502725,0.6577404,0.0030136665],"about_ca_topic_score_codex":0.000036612288,"about_ca_topic_score_gemma":0.000014474775,"teacher_disagreement_score":0.8079627,"about_ca_system_score_codex":0.000027968457,"about_ca_system_score_gemma":0.00037314423,"threshold_uncertainty_score":0.7103865},"labels":[],"label_agreement":null},{"id":"W2004543571","doi":"10.1359/jbmr.090825","title":"Parathyroid hormone regulates fetal-placental mineral homeostasis","year":2009,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":91,"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; Memorial University of Newfoundland","funders":"Canadian Institutes of Health Research; American Society for Bone and Mineral Research; Canadian Diabetes Association","keywords":"Endocrinology; Internal medicine; Parathyroid hormone; Homeostasis; Fetus; Calcium metabolism; Placenta; Hypoparathyroidism; Calcium; Parathyroid chief cell; Hyperphosphatemia; Biology; Calcium-sensing receptor; Medicine; Pregnancy","score_opus":0.026351582055128553,"score_gpt":0.31806359985978394,"score_spread":0.2917120178046554,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2004543571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98039544,0.01773646,0.000026835913,0.001056532,0.00004333927,0.00007804309,0.0000030490169,0.0000018249654,0.0006584792],"genre_scores_gemma":[0.9919752,0.0036493838,0.0013171191,0.000096230986,0.00041619665,0.0000010304843,0.000008145264,0.000010792656,0.0025259014],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9985876,0.00008900822,0.00037104447,0.00018658522,0.00037665025,0.00038907782],"domain_scores_gemma":[0.99921995,0.000019201398,0.00011826654,0.0001622984,0.0002760232,0.0002042855],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00091718516,0.00012278353,0.00023612121,0.00016788681,0.00010675028,0.000072071285,0.00011616703,0.00010717069,0.000011324687],"category_scores_gemma":[0.00017553488,0.00009777589,0.00012007922,0.00014301318,0.00009640146,0.000011047949,0.00009134452,0.00024478065,0.0000037359493],"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":[0.000117074545,0.00008026574,0.00051060715,0.0000052522482,0.00003290274,0.00003250428,0.00005083239,0.000007807145,0.9539498,0.00001629793,0.021805735,0.023390887],"study_design_scores_gemma":[0.0060605635,0.014286433,0.5771675,0.00011131193,0.00006687087,0.005431879,0.0012581231,0.0002600605,0.28615052,0.00080706715,0.10771866,0.0006809738],"about_ca_topic_score_codex":0.000015608326,"about_ca_topic_score_gemma":0.0000055025585,"teacher_disagreement_score":0.6677993,"about_ca_system_score_codex":0.0000143160005,"about_ca_system_score_gemma":0.0000777772,"threshold_uncertainty_score":0.39871854},"labels":[],"label_agreement":null},{"id":"W2004708536","doi":"10.1074/jbc.m110.170704","title":"Phosphatidylinositol 3-Kinase (PI3K) Signaling via Glycogen Synthase Kinase-3 (Gsk-3) Regulates DNA Methylation of Imprinted Loci","year":2010,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":91,"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 Center for Advancing Translational Sciences; National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; National Cancer Institute; National Institute on Aging","keywords":"GSK-3; Biology; DNA methylation; Glycogen synthase; Signal transduction; Molecular biology; Cell biology; Biochemistry; Phosphorylation; Gene; Gene expression","score_opus":0.011350909381504794,"score_gpt":0.24519431364529648,"score_spread":0.2338434042637917,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2004708536","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969718,0.00082048075,0.0016452165,0.000080188656,0.00017734227,0.00009017742,0.000011921121,0.000008284701,0.00019462922],"genre_scores_gemma":[0.9948387,0.000086595486,0.0044682943,0.000038822567,0.0004517611,0.0000028570462,0.000041073537,0.000017921313,0.00005395814],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99834615,0.000052382566,0.0008004065,0.00029836842,0.0002099378,0.00029272508],"domain_scores_gemma":[0.9982585,0.000065167034,0.00078431796,0.0003220847,0.00037615746,0.0001937914],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055405445,0.00023853937,0.00039556003,0.000033994056,0.00006863335,0.000022962047,0.0003871726,0.00047268218,0.00025569866],"category_scores_gemma":[0.0006722247,0.00018464855,0.0003380934,0.00011932564,0.00017531324,0.000007373252,0.0001563425,0.00036626885,0.0000024180242],"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":[0.00008471343,0.00014139284,0.0038733757,0.00004872295,0.00010040769,0.000011860613,0.00001472342,0.0000359269,0.9896763,0.0000033400925,0.00004311407,0.0059661013],"study_design_scores_gemma":[0.0006269772,0.00036088316,0.0058568786,0.00003912044,0.000049175123,0.00026008885,0.000072503826,0.00009825024,0.9911604,0.00016393622,0.0010945618,0.00021722884],"about_ca_topic_score_codex":0.000005472535,"about_ca_topic_score_gemma":5.6157836e-7,"teacher_disagreement_score":0.0057488726,"about_ca_system_score_codex":0.000014401785,"about_ca_system_score_gemma":0.00007758624,"threshold_uncertainty_score":0.7529749},"labels":[],"label_agreement":null},{"id":"W2005611432","doi":"10.1038/ejhg.2013.132","title":"Clinical utility gene card for: Beckwith–Wiedemann Syndrome","year":2013,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":70,"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":"National Institute of General Medical Sciences; Instituto de Salud Carlos III; Agence Nationale de la Recherche; Assistance publique-Hôpitaux de Paris; Bundesministerium für Bildung und Forschung; Institut National de la Santé et de la Recherche Médicale; Action Medical Research","keywords":"Beckwith–Wiedemann syndrome; Genetics; Gene; Medicine; Biology; Computational biology; Gene expression","score_opus":0.038195041901473,"score_gpt":0.3009586668574965,"score_spread":0.2627636249560235,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2005611432","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99094146,0.0016393993,0.005035706,0.00007707612,0.0005606191,0.0002524717,0.0000075785338,0.0000068451827,0.0014788281],"genre_scores_gemma":[0.98418224,0.000258915,0.013765214,0.00018757295,0.00085852755,0.0000026966793,0.000016876756,0.00006649467,0.0006614376],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9976484,0.00034564236,0.0011065447,0.0003234054,0.0002180651,0.000357953],"domain_scores_gemma":[0.99821985,0.00002237097,0.00054281956,0.00051618135,0.00043827487,0.000260507],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014330007,0.0002209046,0.0003548161,0.00006190467,0.00013954822,0.00007506351,0.00056940696,0.00008283263,0.00006325622],"category_scores_gemma":[0.00013829414,0.00019765242,0.00042854535,0.000050355688,0.00013912785,0.0000056815634,0.00022069392,0.00020059991,0.000047112637],"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":[0.000055306846,0.0006727798,0.1523027,0.00013671031,0.0010514279,0.0001292875,0.00029350715,0.00027531412,0.7004808,0.00003226693,0.041729786,0.10284011],"study_design_scores_gemma":[0.0024609605,0.006916416,0.8967501,0.00005972135,0.00016784205,0.0014335548,0.0001896632,0.00011183741,0.019323343,0.00022851907,0.071815476,0.0005425664],"about_ca_topic_score_codex":0.0000018360078,"about_ca_topic_score_gemma":0.00000155606,"teacher_disagreement_score":0.7444474,"about_ca_system_score_codex":0.000008614865,"about_ca_system_score_gemma":0.00006223225,"threshold_uncertainty_score":0.80600315},"labels":[],"label_agreement":null},{"id":"W2006583840","doi":"10.1007/s00439-007-0440-1","title":"A genome-wide approach to identifying novel-imprinted genes","year":2007,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":70,"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 Institute for Cancer Research; McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Genomic imprinting; Biology; Genetics; Gene; Imprinting (psychology); Genome; Candidate gene; Allele; Genotyping; Human genome; DNA microarray; Computational biology; Gene expression; Genotype; DNA methylation","score_opus":0.03568799286872105,"score_gpt":0.28333428553889034,"score_spread":0.2476462926701693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2006583840","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.76545054,0.0007394642,0.22688428,0.000013418561,0.00014927515,0.00028332873,0.0000033372608,0.000025922876,0.0064504547],"genre_scores_gemma":[0.95338446,0.00005974338,0.044252865,0.00030847668,0.00039441988,0.000017501465,0.000076540404,0.000069521804,0.0014364552],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9980068,0.00002109281,0.0004456492,0.00063609396,0.00024309248,0.000647242],"domain_scores_gemma":[0.998791,0.0000099367835,0.00010596738,0.0006854919,0.00013779373,0.00026983663],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00043570148,0.00027300123,0.00020548192,0.00013765424,0.00020745299,0.00008313907,0.00047956203,0.00017833602,0.000026886899],"category_scores_gemma":[0.00005177869,0.00029744112,0.00013347497,0.00019340162,0.0000629827,0.000002241807,0.00048619378,0.00011256551,0.00004848098],"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":[0.000005386919,0.000120951176,0.013046735,0.000029424918,0.00005204164,0.0000013606912,0.00017519864,0.00029565333,0.98429215,0.00006954135,0.00006683056,0.0018447408],"study_design_scores_gemma":[0.000745753,0.00042554297,0.4215498,0.000017273756,0.000042005402,0.000086178974,0.0004279071,0.00009790986,0.49555317,0.00005136587,0.080307655,0.0006954219],"about_ca_topic_score_codex":0.0000116667425,"about_ca_topic_score_gemma":0.000027789982,"teacher_disagreement_score":0.48873895,"about_ca_system_score_codex":0.000026645152,"about_ca_system_score_gemma":0.000036598587,"threshold_uncertainty_score":0.9999478},"labels":[],"label_agreement":null},{"id":"W2007318061","doi":"10.1002/ajmg.a.33251","title":"Review and hypothesis: Syndromes with severe intrauterine growth restriction and very short stature—Are they related to the epigenetic mechanism(s) of fetal survival involved in the developmental origins of adult health and disease?","year":2010,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"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 & Women's Health Centre of British Columbia","funders":"","keywords":"Epigenetics; Intrauterine growth restriction; Fetus; DNA methylation; Mechanism (biology); Biology; Disease; Epigenesis; Short stature; Genomic imprinting; Genetics; Phenotype; Natural history; Bioinformatics; Physiology; Pregnancy; Medicine; Endocrinology; Gene; Internal medicine; Gene expression","score_opus":0.020407634992451497,"score_gpt":0.28533117824163123,"score_spread":0.2649235432491797,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2007318061","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.23067571,0.76773787,0.00005759756,0.0009301257,0.00008092218,0.0004791305,0.000034168716,0.0000011816455,0.000003303052],"genre_scores_gemma":[0.07870991,0.91975045,0.0010453474,0.00039244446,0.000042707532,0.00001698028,0.000014325134,0.00002652204,0.0000013222507],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9974933,0.00047084384,0.0009569332,0.00029659376,0.00053692877,0.0002453754],"domain_scores_gemma":[0.998272,0.00012789792,0.00079781754,0.00024412877,0.00013718453,0.00042098336],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001040082,0.00029365983,0.0011719926,0.00009923231,0.00005348412,0.000017779332,0.00039352963,0.00013397606,0.0000031585582],"category_scores_gemma":[0.00053410686,0.00016008689,0.0001046716,0.00027525288,0.00031447076,0.000003671689,0.00018800929,0.00046404047,1.445165e-7],"study_design_candidate":"design_other","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":[0.000055760356,0.00013993782,0.0042583984,0.008572762,0.0005741424,0.00003038926,0.00040417069,0.0000015861406,0.00003492219,0.00013072211,0.00017607842,0.98562115],"study_design_scores_gemma":[0.0045318934,0.02323804,0.0790974,0.15995316,0.0073369937,0.019855613,0.0112989005,0.000050128383,0.0001416924,0.0010877594,0.68998957,0.0034188284],"about_ca_topic_score_codex":0.000042864354,"about_ca_topic_score_gemma":0.000109506094,"teacher_disagreement_score":0.9822023,"about_ca_system_score_codex":0.000022735801,"about_ca_system_score_gemma":0.0008868849,"threshold_uncertainty_score":0.6528154},"labels":[],"label_agreement":null},{"id":"W2007808077","doi":"10.1006/dbio.2000.9839","title":"Activation of Fgf4 Gene Expression in the Myotomes Is Regulated by Myogenic bHLH Factors and by Sonic Hedgehog","year":2000,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McMaster University","funders":"National Cancer Institute","keywords":"MYF5; MyoD; Myotome; Biology; Enhancer; Limb bud; Sonic hedgehog; Cell biology; PITX2; Apical ectodermal ridge; Myogenesis; Genetics; Mesoderm; Gene expression; Myocyte; Homeobox; Somite; Gene; Embryonic stem cell; Signal transduction; Embryo; Embryogenesis","score_opus":0.007355290269801694,"score_gpt":0.22264130273161137,"score_spread":0.21528601246180967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2007808077","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988056,0.0007177986,0.00003383694,0.00008568785,0.000024226465,0.00014695786,0.000023875518,0.0000037856316,0.00015822283],"genre_scores_gemma":[0.99814785,0.00049920287,0.00044371677,0.00021511526,0.000009701755,0.000012007406,0.0004043535,0.000009044093,0.00025899918],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991958,0.00006751437,0.00021780284,0.00027087698,0.000054468048,0.0001935394],"domain_scores_gemma":[0.99976104,0.000014991711,0.000063613814,0.00011946586,0.000013106829,0.000027799982],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010673119,0.00013190483,0.00013303546,0.000028672152,0.000053599586,0.0000073746805,0.00014251981,0.00016315092,0.00013187104],"category_scores_gemma":[0.00001423128,0.00009305369,0.000030329758,0.00008401671,0.000078386474,0.0000033990643,0.00006259422,0.00005522822,0.0000030241404],"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":[0.000010088873,0.000026698908,0.06982259,0.0000043655477,0.000016759586,7.999689e-8,0.00025766884,3.8803384e-7,0.92114216,6.1835453e-7,0.0011978694,0.0075206878],"study_design_scores_gemma":[0.00033057938,0.000095049,0.10741974,0.000008307867,0.000002696803,0.000011394316,0.00022862839,0.0000044122494,0.88022155,0.000015084573,0.011551799,0.00011074155],"about_ca_topic_score_codex":0.00004057857,"about_ca_topic_score_gemma":0.0000027957426,"teacher_disagreement_score":0.040920615,"about_ca_system_score_codex":0.000012002913,"about_ca_system_score_gemma":0.000027039514,"threshold_uncertainty_score":0.37946194},"labels":[],"label_agreement":null},{"id":"W2008346671","doi":"10.1006/geno.2001.6502","title":"Maternal and Paternal Chromosomes 7 Show Differential Methylation of Many Genes in Lymphoblast DNA","year":2001,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"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":"Biology; Genomic imprinting; DNA methylation; Methylation; Genetics; Gene; Imprinting (psychology); Lymphoblast; Uniparental disomy; Chromosome; Molecular biology; Gene expression; Karyotype; Cell culture","score_opus":0.008352606942159734,"score_gpt":0.21516008379199053,"score_spread":0.2068074768498308,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2008346671","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99771553,0.0006547164,0.0013390068,0.000015444055,0.000103805985,0.000068820256,0.0000073046062,0.0000024935284,0.00009289876],"genre_scores_gemma":[0.99746233,0.0015546603,0.0006993177,0.000014320115,0.00011486601,0.0000033359545,0.000014211805,0.000012983306,0.00012394456],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993986,0.000020030853,0.0001912067,0.0001801961,0.000056613662,0.00015334971],"domain_scores_gemma":[0.9997468,0.0000030812037,0.00007147778,0.00012437628,0.000018773533,0.000035487676],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006277324,0.00009423227,0.00011781079,0.000041237483,0.000020828435,0.000017264118,0.00008539544,0.000073886964,0.000032795215],"category_scores_gemma":[0.0000051478473,0.00009302027,0.0000352503,0.000028565628,0.000032658816,0.000002284015,0.000113165675,0.000024931107,0.0000017506077],"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":[0.000013481192,0.000012376205,0.23579438,0.000014863135,0.000014586368,0.0000012186212,0.00003212267,0.00006285804,0.7412341,0.0000060501343,0.0000025996217,0.022811329],"study_design_scores_gemma":[0.000503877,0.00008660511,0.58982354,0.000009274374,0.000007479208,0.00006233006,0.000027140948,0.00058899634,0.40769187,0.00004367198,0.0010612317,0.000093952935],"about_ca_topic_score_codex":0.00006822053,"about_ca_topic_score_gemma":0.00003798674,"teacher_disagreement_score":0.35402918,"about_ca_system_score_codex":0.000011042613,"about_ca_system_score_gemma":0.000018569099,"threshold_uncertainty_score":0.37932566},"labels":[],"label_agreement":null},{"id":"W2009408130","doi":"10.1210/jc.2014-3098","title":"Novel Microdeletions Affecting the GNAS Locus in Pseudohypoparathyroidism: Characterization of the Underlying Mechanisms","year":2015,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":58,"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 de Sherbrooke","funders":"Instituto de Salud Carlos III; Agence Nationale de la Recherche; Marmara Üniversitesi; Ministero della Salute; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Institut National de la Santé et de la Recherche Médicale; Università degli Studi di Torino; Università degli Studi di Milano; Université Paris-Sud; Aix-Marseille Université","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Genetics; Locus (genetics); Biology; Haploinsufficiency; Multiplex ligation-dependent probe amplification; Phenotype; Gene; Exon; Medicine; Internal medicine; Parathyroid hormone","score_opus":0.07914498551181033,"score_gpt":0.34857838084654236,"score_spread":0.26943339533473204,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2009408130","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98166716,0.0012543764,0.013024862,0.0027359189,0.0010695765,0.00017032702,0.0000028642914,0.0000023003934,0.0000725878],"genre_scores_gemma":[0.99758166,0.00068376685,0.0007551164,0.00053150166,0.00034411578,0.0000025518104,0.0000015967763,0.000015029006,0.000084635474],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9976518,0.0006915531,0.0010385907,0.00014613148,0.00019869927,0.00027321684],"domain_scores_gemma":[0.99816036,0.00018331522,0.0009559316,0.00041611918,0.00022254114,0.000061743565],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022752418,0.00013620753,0.00038581702,0.000044497327,0.00010517291,0.00001338307,0.0006743303,0.00012412915,0.000003234428],"category_scores_gemma":[0.0010667691,0.00006841307,0.00024425096,0.0001650593,0.00024237287,0.000008186782,0.00027128894,0.0005065164,0.0000021398355],"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":[0.000048938946,0.00009736387,0.0012627495,0.0000027164667,0.00008057583,9.5217666e-7,0.00020352576,0.00038138698,0.99445194,0.00060656475,0.00005438688,0.0028088784],"study_design_scores_gemma":[0.0059805745,0.00074421224,0.60406846,0.00007821207,0.0005089194,0.0027587716,0.0022065006,0.00033806375,0.3651377,0.0038413412,0.013987411,0.0003498163],"about_ca_topic_score_codex":0.000033300726,"about_ca_topic_score_gemma":0.00002223436,"teacher_disagreement_score":0.62931424,"about_ca_system_score_codex":0.0000070180113,"about_ca_system_score_gemma":0.0001822684,"threshold_uncertainty_score":0.2789804},"labels":[],"label_agreement":null},{"id":"W2010123584","doi":"10.1016/j.diff.2011.01.007","title":"Developmental regulation of somatic imprints","year":2011,"lang":"en","type":"review","venue":"Differentiation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":71,"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":"Biology; Genomic imprinting; Epigenetics; DNA methylation; Genetics; Differentially methylated regions; Germline; Somatic cell; Allele; Methylation; Imprinting (psychology); Gene; Gene expression","score_opus":0.033754861202277074,"score_gpt":0.2729172209514721,"score_spread":0.239162359749195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2010123584","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.018192207,0.9788556,0.0016171184,6.1171085e-7,0.00018759294,0.00040108495,0.0000113334645,0.000008562044,0.000725857],"genre_scores_gemma":[0.021129597,0.97667825,0.0010586141,0.000002407923,0.000066837274,0.000032335072,0.0006560093,0.00003293268,0.00034301254],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990435,0.000056122546,0.00044583753,0.00024314408,0.00008469785,0.00012668045],"domain_scores_gemma":[0.9993387,0.0000054751717,0.00040774606,0.0001750116,0.00004278822,0.000030300267],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007669415,0.00019050183,0.00041579103,0.00007624448,0.000027717118,0.000009432243,0.0001431386,0.00032640944,0.00010207399],"category_scores_gemma":[0.00003386519,0.00016866435,0.00020226522,0.00006287674,0.000017198401,0.0000018077649,0.000113348055,0.000072341114,0.000028996008],"study_design_candidate":"design_other","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":[7.3245616e-7,0.00003667372,0.00019091854,0.003103112,0.00012962322,3.3939873e-8,0.00003164811,1.3707009e-7,0.004195451,0.000045060555,0.00003568661,0.99223095],"study_design_scores_gemma":[0.00058833405,0.00019974043,0.061282907,0.0057415096,0.0009606844,0.00008078391,0.00004186598,0.00003535808,0.011232825,0.00024858926,0.9185663,0.0010210873],"about_ca_topic_score_codex":0.000004664834,"about_ca_topic_score_gemma":0.0000021643862,"teacher_disagreement_score":0.99120986,"about_ca_system_score_codex":0.000018140918,"about_ca_system_score_gemma":0.0000773618,"threshold_uncertainty_score":0.68779325},"labels":[],"label_agreement":null},{"id":"W2011000812","doi":"10.2217/epi.10.61","title":"Genetic and Epigenetic Dysregulation of Imprinted Genes In The Brain","year":2010,"lang":"en","type":"review","venue":"Epigenomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"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; Lawson Health Research Institute; Western University","funders":"Canadian Institutes of Health Research; International Rett Syndrome Foundation","keywords":"Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Gene; Genetics; Function (biology); Allele; Regulation of gene expression; Loss function; Phenotype; Epigenesis; DNA methylation; Gene expression; Neuroscience","score_opus":0.018345341647778287,"score_gpt":0.2819315596565236,"score_spread":0.2635862180087453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011000812","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.083020024,0.915657,0.00042593476,0.000025855421,0.00015145217,0.00061385334,0.000017679053,0.0000030238723,0.000085170446],"genre_scores_gemma":[0.0046434905,0.99255425,0.0022964561,0.000038480594,0.0002031266,0.00004532913,0.00007826566,0.000053170384,0.00008742864],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9983266,0.00018763244,0.00065607077,0.00044905965,0.00010674626,0.00027386186],"domain_scores_gemma":[0.9988251,0.000071337396,0.0003472101,0.000669832,0.00003824755,0.000048326987],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046121492,0.00031260532,0.00063163624,0.0001109343,0.000049397946,0.00003003842,0.00043951542,0.00045020433,0.00000860015],"category_scores_gemma":[0.000095233016,0.00024058204,0.00020820339,0.00013956867,0.00012122019,0.0000012855055,0.00020635065,0.00023565057,0.000004641428],"study_design_candidate":"design_other","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":[0.0000013678565,0.000023437304,0.00034989047,0.0009766733,0.00003732205,0.000001150073,0.00006756082,0.000009592805,0.004458686,0.000021384762,0.000015189125,0.99403775],"study_design_scores_gemma":[0.00017537283,0.00011208786,0.008652742,0.00032429755,0.0001241564,0.00013105808,0.000034780784,0.000027596641,0.00031780146,0.00006630548,0.98972005,0.00031376546],"about_ca_topic_score_codex":0.000032292603,"about_ca_topic_score_gemma":0.00007664487,"teacher_disagreement_score":0.993724,"about_ca_system_score_codex":0.000011927429,"about_ca_system_score_gemma":0.00015411468,"threshold_uncertainty_score":0.9810651},"labels":[],"label_agreement":null},{"id":"W2011113753","doi":"10.1007/s00018-014-1714-0","title":"What does genetics tell us about imprinting and the placenta connection?","year":2014,"lang":"en","type":"review","venue":"Cellular and Molecular Life Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Placentation; Biology; Epigenetics; Genetics; Placenta; Gene; Evolutionary biology; DNA methylation; Fetus; Gene expression; Pregnancy","score_opus":0.014176130280955672,"score_gpt":0.27660229299133227,"score_spread":0.2624261627103766,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011113753","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.046876956,0.9504368,0.0009856144,0.00007125054,0.0007624431,0.0005501882,0.0000034536342,0.0000105345525,0.0003027808],"genre_scores_gemma":[0.013201807,0.9855005,0.00038407976,0.00033968702,0.00026502428,0.00003721507,0.000024697865,0.000038433882,0.00020854083],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9975391,0.00033665364,0.00050687214,0.00091334374,0.00025777673,0.00044627005],"domain_scores_gemma":[0.9988577,0.000080198195,0.00033521352,0.00048369105,0.000053878997,0.00018932295],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0012158786,0.00043450095,0.00077818776,0.00008357264,0.00046344387,0.0005038858,0.0004923791,0.00029281512,0.000009651061],"category_scores_gemma":[0.00022063711,0.00025037155,0.0002964356,0.00016636835,0.001121198,0.000009457442,0.00064538606,0.0002052595,0.0000055525948],"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":[0.000013400889,0.00006045276,0.00054051244,0.0071465005,0.0006406405,0.000013172142,0.0002614387,0.00005311752,0.01325962,0.0013805768,0.00023101535,0.97639954],"study_design_scores_gemma":[0.0005318184,0.00012593654,0.000021430305,0.0010855088,0.00039304252,0.00013780272,0.00029252018,0.00024170695,0.003431706,0.000077822835,0.99313676,0.0005239426],"about_ca_topic_score_codex":0.000020420903,"about_ca_topic_score_gemma":0.0000061968103,"teacher_disagreement_score":0.99290574,"about_ca_system_score_codex":0.0000060102902,"about_ca_system_score_gemma":0.00016496406,"threshold_uncertainty_score":0.9999949},"labels":[],"label_agreement":null},{"id":"W2011643481","doi":"10.1177/08830738060210042201","title":"Diagnosing Sotos Syndrome in the Setting of Global Developmental Delay and Macrocephaly","year":2006,"lang":"en","type":"article","venue":"Journal of Child Neurology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University Health Centre; Montreal Children's Hospital","funders":"","keywords":"Sotos syndrome; Macrocephaly; Bone age; Pediatrics; Medicine; Gigantism; Internal medicine","score_opus":0.0034159345315114206,"score_gpt":0.20904925262427945,"score_spread":0.20563331809276802,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011643481","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99502456,0.0007284602,0.00005720424,0.003550323,0.00008653538,0.000061579376,0.0000020053512,7.63281e-7,0.00048854],"genre_scores_gemma":[0.997992,0.00006967716,0.000271921,0.0015775696,0.000077794786,9.635842e-7,0.0000013260213,0.0000060017387,0.000002790175],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991686,0.000084056985,0.0003720043,0.00011430744,0.00009821783,0.00016282724],"domain_scores_gemma":[0.9996146,0.000030557614,0.00023500645,0.00006622156,0.000030975476,0.000022634931],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027196438,0.00008649099,0.00016185961,0.000031736672,0.00003946358,0.0000111154595,0.00015513305,0.00007883395,0.00000410757],"category_scores_gemma":[0.00005691647,0.00006524835,0.000054246113,0.00007850163,0.000050947583,0.0000036808087,0.00007018599,0.00013108095,3.6821407e-7],"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":[0.000033959383,0.0000838053,0.98132753,0.000015362708,0.000026461672,0.00014578922,0.000044647273,0.00015952461,0.0147422515,0.000055294728,0.00046991906,0.0028954514],"study_design_scores_gemma":[0.0005722496,0.00043940893,0.9611825,0.000014892141,0.000012121173,0.03217617,0.000018943518,0.000014579773,0.0028212406,0.00010267321,0.0025829442,0.00006232513],"about_ca_topic_score_codex":0.000018796356,"about_ca_topic_score_gemma":0.000040606654,"teacher_disagreement_score":0.03203038,"about_ca_system_score_codex":0.00000440603,"about_ca_system_score_gemma":0.000033068907,"threshold_uncertainty_score":0.26607504},"labels":[],"label_agreement":null},{"id":"W2011958888","doi":"10.1007/s00335-004-2434-9","title":"Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors","year":2005,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University; McGill University and Génome Québec Innovation Centre; Royal Victoria Hospital; McGill University Health Centre; Royal Victoria Regional Health Centre","funders":"Canadian Institutes of Health Research; Genome Canada; Burroughs Wellcome Fund","keywords":"Genomic imprinting; Biology; Epigenetics; Imprinting (psychology); Human genetics; Genetics; Epigenesis; DNA methylation; Computational biology; Gene; Gene expression","score_opus":0.008027411001838255,"score_gpt":0.21961980099758147,"score_spread":0.2115923899957432,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011958888","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99781597,0.00043218536,0.0011775662,0.00011187185,0.000031001244,0.00026705768,0.000036535715,0.0000042306765,0.0001235646],"genre_scores_gemma":[0.9945154,0.000029604906,0.0050579985,0.00015509663,0.000072965435,0.000008020442,0.000010010892,0.000030844076,0.00012003334],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99850434,0.00005646886,0.000534141,0.00042246806,0.00012176136,0.00036083168],"domain_scores_gemma":[0.9993035,0.000028808754,0.0001630978,0.00030219523,0.00005175115,0.00015062015],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000190262,0.00020690054,0.00033480788,0.00015629851,0.000032303116,0.000012338182,0.00023418518,0.00012750896,0.000075673466],"category_scores_gemma":[0.000101192185,0.00021938667,0.000080052276,0.00013082537,0.00007337501,0.0000022353427,0.00028419646,0.00007132762,0.0000073982433],"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":[0.000012067616,0.000037982536,0.10449469,0.000060349386,0.000023392291,0.000001445166,0.00040772173,0.00062511105,0.8900084,0.000003797345,0.0000071301465,0.0043179127],"study_design_scores_gemma":[0.0003959163,0.00021174329,0.76660126,0.00001510314,0.000011615213,0.000017248914,0.00012299226,0.00014948139,0.23118512,0.000010098513,0.0010987947,0.00018061798],"about_ca_topic_score_codex":0.00029676044,"about_ca_topic_score_gemma":0.00014905854,"teacher_disagreement_score":0.6621066,"about_ca_system_score_codex":0.000020810327,"about_ca_system_score_gemma":0.000056597484,"threshold_uncertainty_score":0.8946329},"labels":[],"label_agreement":null},{"id":"W2012362930","doi":"10.1007/s00335-013-9454-2","title":"Recommendations for the investigation of animal models of Prader–Willi syndrome","year":2013,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Foundation for Prader-Willi Research","keywords":"Human genetics; Biology; Computational biology; Genetics; Evolutionary biology; Bioinformatics; Gene","score_opus":0.03346389664720976,"score_gpt":0.2451336213330381,"score_spread":0.21166972468582834,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2012362930","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914823,0.000348735,0.0058832183,0.0015522796,0.00006117951,0.00047718393,0.00003371932,0.0000035447365,0.0001578227],"genre_scores_gemma":[0.99257493,0.00004313769,0.006607539,0.000088654364,0.000038216687,0.000082555795,0.00007018576,0.000015339796,0.00047942973],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993289,0.00002461103,0.00026908456,0.00016018574,0.00006780936,0.00014942301],"domain_scores_gemma":[0.9993961,0.000019965933,0.00015476407,0.00027196005,0.000117291354,0.000039930965],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014853352,0.00008565673,0.00011395161,0.000030203757,0.000055320368,0.000011661921,0.00018275288,0.00006617596,0.000064573454],"category_scores_gemma":[0.000025590247,0.000068878144,0.0000786268,0.0000698838,0.0000749821,0.0000058401242,0.00007058246,0.000031632466,0.0000041906414],"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":[0.0000021967064,0.000021175034,0.003149668,0.00007394324,0.0000773879,3.1681704e-8,0.00022906736,0.00042660185,0.99275154,0.0003828456,0.00072838523,0.0021571533],"study_design_scores_gemma":[0.0014841965,0.0027148428,0.7640919,0.00006498223,0.00015528029,0.00011196211,0.0017539624,0.007534957,0.18930453,0.0061585936,0.025993355,0.0006314533],"about_ca_topic_score_codex":0.000060523365,"about_ca_topic_score_gemma":0.0000031011084,"teacher_disagreement_score":0.803447,"about_ca_system_score_codex":0.0000048841657,"about_ca_system_score_gemma":0.000033221706,"threshold_uncertainty_score":0.2808769},"labels":[],"label_agreement":null},{"id":"W2012768593","doi":"10.1159/000354038","title":"Interstitial Deletions at 6q14.1q15 Associated with Developmental Delay and a Marfanoid Phenotype","year":2013,"lang":"en","type":"article","venue":"Molecular Syndromology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; Alberta Health; Alberta Health Services; Alberta Children's Hospital","funders":"","keywords":"Haploinsufficiency; Phenotype; Arachnodactyly; Scoliosis; Marfan syndrome; Genetics; Pectus excavatum; Comparative genomic hybridization; Microdeletion syndrome; Cataracts; Short stature; Biology; Chromosome; Developmental disorder; Medicine; Gene; Autism; Pediatrics; Internal medicine","score_opus":0.005318222675318374,"score_gpt":0.1928868455536051,"score_spread":0.18756862287828674,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2012768593","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99195904,0.0002754824,0.005348395,0.00016082119,0.00009566291,0.00028964216,0.0000073658125,0.00002188816,0.0018417203],"genre_scores_gemma":[0.9945881,0.00001844254,0.0036972319,0.00046481862,0.000021384136,0.00007628899,0.00014130496,0.000043323977,0.0009491361],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986284,0.00009810396,0.00022601687,0.0004884362,0.00012152688,0.00043755956],"domain_scores_gemma":[0.99943686,0.000012956799,0.00008726051,0.00022298782,0.00009619556,0.0001437192],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009423965,0.00023836848,0.0002182205,0.00006128499,0.00014091884,0.000035752455,0.00016695616,0.00021638811,0.00027399138],"category_scores_gemma":[0.000090110836,0.00022247247,0.000057435373,0.0000949691,0.00019419225,0.000005238465,0.00036146026,0.00010520167,0.00008639571],"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":[0.00005098341,0.00019609794,0.016311368,0.000030797055,0.0007568929,0.0013372726,0.00019347756,0.00007028723,0.9736713,0.0002834242,0.001645943,0.0054521095],"study_design_scores_gemma":[0.0144836325,0.011694398,0.4585431,0.00037868303,0.00071964867,0.2524978,0.0007940875,0.0021848595,0.22210433,0.0012780166,0.029355763,0.0059656757],"about_ca_topic_score_codex":0.00009937053,"about_ca_topic_score_gemma":0.00011819281,"teacher_disagreement_score":0.751567,"about_ca_system_score_codex":0.00004826998,"about_ca_system_score_gemma":0.00006780569,"threshold_uncertainty_score":0.90721637},"labels":[],"label_agreement":null},{"id":"W2013013633","doi":"10.1007/s10048-007-0086-0","title":"Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes","year":2007,"lang":"en","type":"article","venue":"Neurogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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","funders":"","keywords":"Autism; Angelman syndrome; UBE3A; Autism Diagnostic Observation Schedule; Neurodevelopmental disorder; Intellectual disability; Autism spectrum disorder; Psychology; Genetics; Uniparental disomy; Heritability of autism; Psychiatry; Clinical psychology; Biology; Gene; Chromosome; Ubiquitin ligase","score_opus":0.023731863856325527,"score_gpt":0.2810377759084099,"score_spread":0.25730591205208436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013013633","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99612796,0.0015696138,0.00059741957,0.00014880518,0.00013419535,0.00043503413,0.000008926719,0.0000096467475,0.00096837315],"genre_scores_gemma":[0.99749374,0.000062715284,0.0020327885,0.000206548,0.000034013952,0.000014733198,0.000014163429,0.000037737038,0.0001035729],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9980567,0.00012808162,0.00044982077,0.00042828222,0.0005353032,0.00040178662],"domain_scores_gemma":[0.99925005,0.000017670965,0.0001105797,0.00038397443,0.00009683625,0.00014087213],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012537569,0.00018339072,0.00019375475,0.00016742552,0.000037099435,0.000012993257,0.000257211,0.0001689274,0.000017871827],"category_scores_gemma":[0.00014459396,0.0002056654,0.00007952395,0.00031498802,0.000042806358,0.0000019320041,0.00016034005,0.000084006424,0.0000074466543],"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":[0.000010955743,0.00009317371,0.009602551,0.000020231308,0.000031003012,0.000012168857,0.00013331926,0.0026248412,0.88357705,0.000064452826,0.0001079882,0.10372224],"study_design_scores_gemma":[0.0007509372,0.00052439887,0.7546257,0.000029193852,0.00006195608,0.00017660308,0.000063600164,0.00047281076,0.23078276,0.00008182286,0.0122014955,0.00022875049],"about_ca_topic_score_codex":0.000019451301,"about_ca_topic_score_gemma":0.00012319392,"teacher_disagreement_score":0.74502313,"about_ca_system_score_codex":0.000023774843,"about_ca_system_score_gemma":0.00010012099,"threshold_uncertainty_score":0.8386792},"labels":[],"label_agreement":null},{"id":"W2013044331","doi":"10.1080/01677060600685840","title":"THE INHERITANCE OF COGNITIVE SKILLS: DOES GENOMIC IMPRINTING PLAY A ROLE?","year":2006,"lang":"en","type":"article","venue":"Journal of Neurogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University; SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Cognition; Neuroscience; Psychology; Population; Genetics; Developmental psychology; Evolutionary biology; Gene; DNA methylation; Gene expression; Medicine","score_opus":0.004083189693964786,"score_gpt":0.22040159442597507,"score_spread":0.21631840473201028,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013044331","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957615,0.0031212727,0.00027748497,0.000058880243,0.0003296535,0.00008771162,0.00000620483,0.0000018539693,0.0003554395],"genre_scores_gemma":[0.99735856,0.00092773495,0.0010895467,0.000051059513,0.00045157966,0.0000015328599,0.0000015494828,0.00002494932,0.00009348293],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99877185,0.000069694746,0.000592202,0.00014617853,0.00018813944,0.00023192243],"domain_scores_gemma":[0.99879813,0.00007986489,0.00062195695,0.0001890084,0.00025931993,0.000051741456],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025577587,0.0001353347,0.00017973494,0.000036635178,0.00009132173,0.000034218505,0.0002883872,0.000074304284,0.00000289994],"category_scores_gemma":[0.00020898155,0.00008909805,0.00017168473,0.000074675954,0.00010945175,0.0000021836615,0.00012904781,0.00012855884,0.0000011830023],"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":[0.000017156492,0.0000673014,0.05506622,0.000008208871,0.000061840045,0.000004880082,0.00004521075,0.00023670106,0.93769884,0.000015813266,0.00004666747,0.006731153],"study_design_scores_gemma":[0.00070062553,0.00049831293,0.30958283,0.00005702496,0.00006377721,0.00040605033,0.00032256503,0.000060080933,0.6812447,0.00034402852,0.0065628104,0.00015720939],"about_ca_topic_score_codex":0.000005554397,"about_ca_topic_score_gemma":0.000012904615,"teacher_disagreement_score":0.25645417,"about_ca_system_score_codex":0.000006569285,"about_ca_system_score_gemma":0.000078541525,"threshold_uncertainty_score":0.36333132},"labels":[],"label_agreement":null},{"id":"W2013787654","doi":"10.1534/genetics.103.026211","title":"Intralocus Sexual Conflict Can Drive the Evolution of Genomic Imprinting","year":2004,"lang":"en","type":"article","venue":"Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":225,"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; Queen's University","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Epigenetics; Evolutionary biology; Sexual dimorphism; Genetics; Allele; DNA methylation; Gene; Zoology; Gene expression","score_opus":0.00867627261508725,"score_gpt":0.2246560516171975,"score_spread":0.21597977900211027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013787654","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99292046,0.0011256561,0.005165826,0.00016159652,0.00015233507,0.00017693065,0.000009871623,0.000007584416,0.0002797686],"genre_scores_gemma":[0.99672854,0.00010017117,0.0027628613,0.00006716077,0.00020455793,0.000007344454,0.000012912444,0.000022126727,0.000094331204],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990467,0.00002993305,0.00026498054,0.0002560951,0.000118778225,0.0002835251],"domain_scores_gemma":[0.99928963,0.0000068286945,0.00013066398,0.000426724,0.00008910107,0.00005702169],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014818355,0.00013658249,0.000121554185,0.000028963743,0.000091805145,0.000017189004,0.00027515407,0.000107223925,0.000008733799],"category_scores_gemma":[0.00003660471,0.00011373858,0.00006406153,0.00007217555,0.00012912996,8.991237e-7,0.00020419245,0.00008663711,0.000008019524],"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":[0.0000025631982,0.000022126687,0.008337458,0.000011821764,0.00004234512,4.075225e-7,0.00024755424,0.0039729606,0.9827934,0.00017815859,0.000033216656,0.004358002],"study_design_scores_gemma":[0.0010914485,0.00072628574,0.21679904,0.00001652472,0.000067498535,0.000121123216,0.002087947,0.0002345876,0.77155155,0.00044333568,0.006490183,0.00037047823],"about_ca_topic_score_codex":0.00024294609,"about_ca_topic_score_gemma":0.00017815207,"teacher_disagreement_score":0.21124184,"about_ca_system_score_codex":0.000044210905,"about_ca_system_score_gemma":0.00017659296,"threshold_uncertainty_score":0.46381247},"labels":[],"label_agreement":null},{"id":"W2014049913","doi":"10.1210/en.2010-0709","title":"Impaired Hypothalamic Regulation of Endocrine Function and Delayed Counterregulatory Response to Hypoglycemia in Magel2-Null Mice","year":2011,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"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":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research","keywords":"Endocrinology; Internal medicine; Ghrelin; Corticosterone; Hypoglycemia; Endocrine system; Medicine; Basal (medicine); Hypothalamus; Circadian rhythm; Null allele; Insulin; Hormone; Biology; Phenotype; Gene","score_opus":0.013549559793782178,"score_gpt":0.22500294999875048,"score_spread":0.2114533902049683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2014049913","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99816537,0.0003632876,0.00065866165,0.00008214421,0.00018190697,0.00021624437,0.000006035104,0.000012860303,0.00031349572],"genre_scores_gemma":[0.99789995,0.00004167975,0.0015279391,0.00009101612,0.000039249175,0.00002290367,0.000014969271,0.00002112602,0.00034116898],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9987754,0.00012910321,0.0003212154,0.00036860324,0.00007258368,0.00033309672],"domain_scores_gemma":[0.99944746,0.000025999543,0.000099510034,0.0003094721,0.000055171975,0.00006241087],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014686355,0.00015195324,0.00019390201,0.00016939123,0.000028224396,0.000004396364,0.0001201093,0.00009310959,0.00004929326],"category_scores_gemma":[0.0001143297,0.00016395249,0.000044166733,0.00010335575,0.000085989945,0.000005415756,0.00016342585,0.00007504175,0.000009163339],"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":[0.0011703687,0.00003775846,0.031102093,0.0000125576125,0.000031388725,0.0000052359296,0.00016786279,0.000021016924,0.962348,0.00008333537,0.0000620443,0.0049583726],"study_design_scores_gemma":[0.0010914463,0.00094945275,0.76992154,0.000010475593,0.000015396063,0.00022184069,0.00015707243,0.00005766287,0.22596562,0.00019961734,0.0012690953,0.00014076458],"about_ca_topic_score_codex":0.00013854064,"about_ca_topic_score_gemma":0.00006736243,"teacher_disagreement_score":0.7388195,"about_ca_system_score_codex":0.000019380486,"about_ca_system_score_gemma":0.00003896655,"threshold_uncertainty_score":0.66857886},"labels":[],"label_agreement":null},{"id":"W2016293553","doi":"10.1006/geno.2001.6549","title":"Imprinting Status of 11p15 Genes in Beckwith–Wiedemann Syndrome Patients with CDKN1C Mutations","year":2001,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"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 Institute for Cancer Research; University of Toronto; Hospital for Sick Children","funders":"National Cancer Institute","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Genomic imprinting; Biology; Genetics; Pedigree chart; Proband; Gene; Phenotype; Germline mutation; Mutation; Gene expression; DNA methylation","score_opus":0.006807924696443324,"score_gpt":0.21335701509634938,"score_spread":0.20654909039990607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016293553","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982798,0.00033712527,0.0005631295,0.000013730702,0.00006774111,0.00021012453,0.000015078551,0.0000060204675,0.000507256],"genre_scores_gemma":[0.99479413,0.00023444286,0.0046735946,0.0000312226,0.000026221573,0.000012016826,0.00009953614,0.000028541477,0.00010029808],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989068,0.00002228446,0.00029797072,0.0002813883,0.00010128385,0.00039029008],"domain_scores_gemma":[0.9994013,0.000008338204,0.00014202793,0.00027933484,0.000089871595,0.00007915411],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000092310125,0.00014031708,0.00017083185,0.00007609212,0.00004766277,0.000015070473,0.00013789251,0.00008333971,0.000016294116],"category_scores_gemma":[0.000034232977,0.00013486935,0.000049097118,0.00013494719,0.000052560208,0.0000041496323,0.0001160856,0.00005987333,0.0000059101444],"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":[0.000019317413,0.00010461345,0.931198,0.000024164401,0.00005019838,0.000004498406,0.00016986774,0.0030091526,0.053782165,0.000013278384,0.0000058749984,0.011618894],"study_design_scores_gemma":[0.0011217571,0.00033761605,0.98511696,0.00002184441,0.00002017059,0.000049581817,0.00032331777,0.00017860837,0.008447846,0.000030084318,0.0041174786,0.00023470915],"about_ca_topic_score_codex":0.00011197228,"about_ca_topic_score_gemma":0.000115130075,"teacher_disagreement_score":0.05391901,"about_ca_system_score_codex":0.000028093013,"about_ca_system_score_gemma":0.00008996448,"threshold_uncertainty_score":0.54998124},"labels":[],"label_agreement":null},{"id":"W2016355843","doi":"10.1016/j.metabol.2008.07.012","title":"Impact of genetic and epigenetic factors from early life to later disease","year":2008,"lang":"en","type":"review","venue":"Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":43,"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 de l’Université de Montréal","funders":"","keywords":"Epigenetics; Epigenomics; Adaptation (eye); Biology; Disease; Genomic imprinting; Genetics; Genome; Epigenesis; DNA methylation; Evolutionary biology; Gene; Medicine; Neuroscience; Internal medicine; Gene expression","score_opus":0.02338435163053608,"score_gpt":0.29266239695386287,"score_spread":0.2692780453233268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016355843","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.44969317,0.54968315,0.000028322529,0.0000016090398,0.000108488835,0.00027325458,0.00019444145,0.0000041771523,0.00001337374],"genre_scores_gemma":[0.04968388,0.9489356,0.00060166063,0.00002035203,0.0003101395,0.000033012922,0.00015672247,0.0000863519,0.00017224654],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9980755,0.00012831925,0.0005834718,0.0006635604,0.0001758535,0.00037331606],"domain_scores_gemma":[0.99839777,0.000023609702,0.00024481432,0.0007076947,0.00005926493,0.0005668732],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000043043532,0.00051843596,0.0012351946,0.00012409031,0.000050652696,0.00003211398,0.00032722583,0.0002721487,0.00006038204],"category_scores_gemma":[0.00014053476,0.00039001644,0.0007069008,0.00012220241,0.00007112513,0.0000013239239,0.00032805713,0.00012092127,0.000023135668],"study_design_candidate":"design_other","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":[0.000018308061,0.00013035972,0.032961898,0.001288079,0.0014836336,0.000012731272,0.00022901727,0.000031227424,0.002052218,0.0000018028152,0.00056011014,0.96123064],"study_design_scores_gemma":[0.00016346764,0.000096944714,0.54694664,0.00030279483,0.00046680417,0.00000819639,0.0000022849893,8.366083e-7,0.000047645677,0.0000073604174,0.4515578,0.00039922836],"about_ca_topic_score_codex":0.00027922748,"about_ca_topic_score_gemma":0.0000037701209,"teacher_disagreement_score":0.9608314,"about_ca_system_score_codex":0.000009011213,"about_ca_system_score_gemma":0.0002692206,"threshold_uncertainty_score":0.99985516},"labels":[],"label_agreement":null},{"id":"W2016686236","doi":"10.1002/jbmr.461","title":"Parathyroid hormone signaling via Gαs is selectively inhibited by an NH2-terminally truncated Gαs: Implications for pseudohypoparathyroidism","year":2011,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Royal Victoria Regional Health Centre; Royal Victoria Hospital; Victoria Hospital; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research","keywords":"Pseudohypoparathyroidism; Internal medicine; Endocrinology; Parathyroid hormone; Parathyroid hormone receptor; Gs alpha subunit; GNAS complex locus; Receptor; Chemistry; Calcitonin; G protein; Biology; Hormone receptor; Medicine; Calcium; Biochemistry","score_opus":0.06707259939033473,"score_gpt":0.34368085917957547,"score_spread":0.27660825978924075,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016686236","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99078125,0.00517907,0.003301433,0.00031711673,0.000019753788,0.00024407303,0.000025370731,0.0000034481843,0.00012848547],"genre_scores_gemma":[0.9938398,0.0007580397,0.00428394,0.00011733156,0.00019033416,0.000024731922,0.000031838834,0.0000274404,0.00072654855],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.998425,0.00011184739,0.00050795433,0.00030044816,0.00021557536,0.00043914627],"domain_scores_gemma":[0.99840695,0.00003436563,0.00022169662,0.00019996963,0.00087712577,0.00025987273],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011046694,0.00015718819,0.00026291548,0.0001762196,0.00021211363,0.000061160885,0.0001751983,0.00015322966,0.000006749271],"category_scores_gemma":[0.00015140393,0.00013591621,0.00011882717,0.00020530134,0.00010516561,0.00002335416,0.00008645629,0.00024795695,0.0000016534253],"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":[0.00018663412,0.0001750138,0.0007122766,0.000008627999,0.0000647372,0.0000033341976,0.00032576508,0.0000014609251,0.9816594,0.00001327219,0.013874567,0.0029749074],"study_design_scores_gemma":[0.0028443255,0.009223566,0.07187975,0.000029145069,0.000075192205,0.0010583876,0.0005040758,0.0002943462,0.9044038,0.0014494003,0.007824727,0.00041326153],"about_ca_topic_score_codex":0.00005891805,"about_ca_topic_score_gemma":0.000008583606,"teacher_disagreement_score":0.077255584,"about_ca_system_score_codex":0.000018560719,"about_ca_system_score_gemma":0.00015518258,"threshold_uncertainty_score":0.55425024},"labels":[],"label_agreement":null},{"id":"W2016725540","doi":"10.1002/acn3.126","title":"Unusual Stüve‐Wiedemann syndrome with complete maternal chromosome 5 isodisomy","year":2014,"lang":"en","type":"article","venue":"Annals of Clinical and Translational Neurology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"National Institutes of Health; National Heart, Lung, and Blood Institute; Helse Vest","keywords":"Medicine; Beckwith–Wiedemann syndrome; Chromosome; Genetics; Gene; Biology","score_opus":0.05766965772263427,"score_gpt":0.3323834499655032,"score_spread":0.2747137922428689,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016725540","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99433935,0.00016762537,0.0012762657,0.0032181586,0.00009859813,0.00009217826,0.000025207231,0.0000064983974,0.0007761198],"genre_scores_gemma":[0.996588,0.00013434417,0.0005232178,0.0024918448,0.00014970211,0.00000457809,0.000040226438,0.0000149344705,0.00005316477],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99860495,0.00015001874,0.00052013237,0.00036665803,0.00014027096,0.0002179784],"domain_scores_gemma":[0.9993636,0.00011684244,0.0001478388,0.00017212468,0.0000870615,0.00011255022],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003588066,0.00013916343,0.00033304704,0.000033113658,0.000050665578,0.000009146301,0.00013088339,0.0001572016,0.000026825079],"category_scores_gemma":[0.000045854496,0.00011327546,0.00011096137,0.000043249223,0.00033549106,0.0000049722626,0.00004413091,0.0001296426,0.0000063678335],"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":[0.00040890227,0.00017137804,0.97932786,0.000059953964,0.0001980288,0.000012545636,0.000013125058,0.00024852031,0.0033652093,0.0026108504,0.0001223413,0.0134612685],"study_design_scores_gemma":[0.0010734262,0.0021428468,0.9761218,0.000009527722,0.000017560893,0.0002895898,0.0000013404596,0.0004011274,0.0007273458,0.0014953533,0.017587598,0.00013252917],"about_ca_topic_score_codex":0.000009017017,"about_ca_topic_score_gemma":0.000009258631,"teacher_disagreement_score":0.017465256,"about_ca_system_score_codex":3.8764448e-8,"about_ca_system_score_gemma":0.000027812306,"threshold_uncertainty_score":0.46192396},"labels":[],"label_agreement":null},{"id":"W2017331347","doi":"10.1016/s1567-133x(03)00113-3","title":"Prader–Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain","year":2003,"lang":"en","type":"article","venue":"Gene Expression Patterns","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":81,"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":"Biology; Forebrain; Phenotype; Gene; Genetics; Candidate gene; Genomic imprinting; Hindbrain; Gene expression; Endocrinology; Central nervous system; DNA methylation","score_opus":0.018783811972188397,"score_gpt":0.23437029238686372,"score_spread":0.21558648041467532,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017331347","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9774455,0.00017812796,0.021213127,0.0005517922,0.00017459985,0.00031063517,0.000034007695,0.0000095555,0.000082700964],"genre_scores_gemma":[0.9962519,0.00007485181,0.0027597419,0.00037307735,0.000025820946,0.000046936413,0.000014508948,0.000034721474,0.0004184623],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.998309,0.00024171539,0.00042583348,0.00045535897,0.00021588735,0.0003522139],"domain_scores_gemma":[0.99899566,0.000024126637,0.00020702093,0.0006428926,0.000052969735,0.00007734475],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020516424,0.0002092541,0.00023316575,0.000054464614,0.00009093522,0.000018596114,0.00038697684,0.00017121725,0.000031818105],"category_scores_gemma":[0.00016986097,0.00016060089,0.00012939367,0.00013069005,0.000055595425,0.00000555998,0.00012350926,0.00013738831,0.0000021774617],"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":[0.000002434849,0.000063043924,0.06913438,0.00004234261,0.000013471705,0.0000018776035,0.00016428727,0.00014773039,0.92987984,0.00002904734,0.0003858312,0.00013570054],"study_design_scores_gemma":[0.000568986,0.000050077062,0.19460087,0.00018762013,0.0000053909544,0.00003106662,0.00029681885,0.0000068876175,0.80114174,0.00006904142,0.0028390083,0.00020248271],"about_ca_topic_score_codex":0.000021731119,"about_ca_topic_score_gemma":0.00002384166,"teacher_disagreement_score":0.1287381,"about_ca_system_score_codex":0.000016025806,"about_ca_system_score_gemma":0.00009261657,"threshold_uncertainty_score":0.65491146},"labels":[],"label_agreement":null},{"id":"W2017472084","doi":"10.1002/gene.20027","title":"Loss‐of‐imprinting of <i>Peg1</i> in mouse interspecies hybrids is correlated with altered growth","year":2004,"lang":"en","type":"article","venue":"genesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"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":"Biology; Hybrid; Allele; Genomic imprinting; Imprinting (psychology); Loss of heterozygosity; Genetics; Gene; Molecular biology; Gene expression; DNA methylation; Botany","score_opus":0.006878149184088171,"score_gpt":0.20624724860276855,"score_spread":0.1993690994186804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017472084","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997399,0.00037704903,0.0015991632,0.00006955175,0.00006348098,0.00011220201,0.000010788214,0.0000065082345,0.00036227776],"genre_scores_gemma":[0.99640846,0.00020615822,0.003072718,0.00006617843,0.000033392513,0.0000058738938,0.000010338705,0.000024049898,0.00017283893],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99903125,0.00002041463,0.00032850468,0.00027825634,0.00011796627,0.00022361573],"domain_scores_gemma":[0.9993818,0.0000067373594,0.00015989513,0.00029137012,0.00011742439,0.00004281779],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010641751,0.00014484876,0.0002198976,0.000080210135,0.000021478761,0.000007800774,0.00018923193,0.00008336834,0.000020288175],"category_scores_gemma":[0.000038744125,0.00013260025,0.00007980681,0.00016603556,0.00009875798,0.0000034731872,0.00013329099,0.00005505441,0.0000030136916],"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":[0.000034111737,0.00007876358,0.10261207,0.000062352236,0.00006316099,0.0000023319799,0.00033907947,0.00043048206,0.8952974,0.00003173019,0.000036024725,0.0010124684],"study_design_scores_gemma":[0.0010323222,0.0002755332,0.049773972,0.0000644639,0.000016674005,0.000038818667,0.00037737077,0.000018878483,0.9480997,0.000028827068,0.00011616374,0.00015727528],"about_ca_topic_score_codex":0.00037861377,"about_ca_topic_score_gemma":0.00003658112,"teacher_disagreement_score":0.052838102,"about_ca_system_score_codex":0.000013843236,"about_ca_system_score_gemma":0.00006118951,"threshold_uncertainty_score":0.54072815},"labels":[],"label_agreement":null},{"id":"W2017994263","doi":"10.1067/mpd.2003.81","title":"Myeloid leukemia in Prader-Willi syndrome","year":2003,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Medicine; Myeloid leukemia; Leukemia; Epidemiology; Population; Cancer; Oncology; Internal medicine; Myeloid; Surveillance, Epidemiology, and End Results; Cancer registry; Environmental health","score_opus":0.008989734299718565,"score_gpt":0.22613640058675352,"score_spread":0.21714666628703497,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017994263","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99502826,0.003179624,0.00073695456,0.000096731375,0.00028730193,0.000057764668,8.3833146e-7,0.0000013067474,0.0006112354],"genre_scores_gemma":[0.9961364,0.0023232137,0.0009792515,0.000100258876,0.00019494457,5.464732e-7,7.3488206e-7,0.000013552471,0.00025104577],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99907976,0.0001231646,0.00034073574,0.000081147955,0.00017145327,0.00020373426],"domain_scores_gemma":[0.99940985,0.000034855468,0.0002366909,0.00018460305,0.00007281515,0.00006118769],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00090315746,0.000096398515,0.0001344861,0.00007303218,0.000041185252,0.000013424114,0.00023974279,0.00008743588,0.000015625583],"category_scores_gemma":[0.0003111267,0.00006744436,0.00007220847,0.00017533073,0.000029234965,0.0000036621116,0.000044924087,0.0001910884,0.0000066965786],"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":[0.000028880713,0.00030264244,0.7313778,0.00030115413,0.00010473744,0.00007548903,0.00137667,0.015767915,0.22657363,0.00040376387,0.01511564,0.008571691],"study_design_scores_gemma":[0.004615395,0.0028632132,0.87586784,0.00005874599,0.0003720129,0.016002692,0.0023934778,0.00006410066,0.025201034,0.0015700527,0.07001757,0.0009738782],"about_ca_topic_score_codex":0.000007130874,"about_ca_topic_score_gemma":0.000004173731,"teacher_disagreement_score":0.20137261,"about_ca_system_score_codex":0.000039668717,"about_ca_system_score_gemma":0.00025351878,"threshold_uncertainty_score":0.2750301},"labels":[],"label_agreement":null},{"id":"W2019161989","doi":"10.1172/jci68035","title":"Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi–like features","year":2013,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":147,"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 Diabetes and Digestive and Kidney Diseases; Société Francophone du Diabète","keywords":"Haploinsufficiency; Obesity; Loss function; Internal medicine; Endocrinology; Biology; Gene; Genetics; Medicine; Phenotype","score_opus":0.03152585440061885,"score_gpt":0.32689034302281816,"score_spread":0.29536448862219933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019161989","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963778,0.00021284288,0.001593251,0.0013987839,0.0002449143,0.0001397781,0.0000016159544,0.0000013250856,0.000029684345],"genre_scores_gemma":[0.9952012,0.000094038514,0.003896669,0.00054594263,0.00017824712,0.0000027483422,0.000008004578,0.0000054425964,0.00006776621],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99884963,0.00010894431,0.00070960924,0.000119558514,0.000117735835,0.00009455085],"domain_scores_gemma":[0.9990003,0.000089726855,0.00041147333,0.00009284032,0.00026489198,0.00014074685],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00066099135,0.00006750887,0.00020049333,0.000054864937,0.00002412781,0.000020431771,0.000068490015,0.00013427586,0.000008298929],"category_scores_gemma":[0.0014771598,0.000057452206,0.000071961214,0.000087036206,0.00008553407,0.000013523996,0.000037610072,0.00014317661,0.000002640757],"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":[0.000010864191,0.00007275836,0.90758014,0.000021706663,0.00004807253,5.276008e-7,0.00008213997,0.0004417305,0.08203797,0.0000668801,0.001539009,0.008098215],"study_design_scores_gemma":[0.00060755434,0.0006051218,0.98964614,0.000048425467,0.000022362026,0.000023866196,0.00006842572,0.00010353072,0.0058741705,0.0019067555,0.0010314299,0.00006224408],"about_ca_topic_score_codex":0.000029723229,"about_ca_topic_score_gemma":0.000018680828,"teacher_disagreement_score":0.082065985,"about_ca_system_score_codex":0.0000054052707,"about_ca_system_score_gemma":0.00007621509,"threshold_uncertainty_score":0.2342833},"labels":[],"label_agreement":null},{"id":"W2019946659","doi":"10.1111/j.1399-0004.2010.01554.x","title":"Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Macrocephaly; X-inactivation; Genetics; Skewed X-inactivation; X chromosome; Biology; Macroglossia; Mutation; Gene; Medicine; Pathology; Tongue","score_opus":0.044260759650186464,"score_gpt":0.391640784283223,"score_spread":0.3473800246330366,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019946659","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99828386,0.0006287712,0.00017849826,0.00007257288,0.00040783145,0.00031375475,0.000019628977,0.000008642805,0.000086437976],"genre_scores_gemma":[0.98692226,0.0011210755,0.011504105,0.000097688826,0.00020686189,0.000015777661,0.000035238994,0.00002928242,0.000067714325],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99782336,0.00016297452,0.0010237565,0.00053780887,0.00018401415,0.00026809238],"domain_scores_gemma":[0.99856925,0.00032214966,0.0003300691,0.00044075228,0.00020738904,0.0001304024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00088409486,0.00020561709,0.00048774495,0.000066031454,0.00006477161,0.000020506364,0.00020590154,0.00024942943,0.000010143952],"category_scores_gemma":[0.0011421954,0.00017956283,0.00010284659,0.00017051098,0.00068674254,0.000006698311,0.00025166036,0.00036429445,0.0000041578724],"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":[0.000024852008,0.0003324324,0.9653095,0.000036833815,0.00016967104,0.0000039154775,0.00012330053,0.00008835148,0.019982278,0.000030217792,0.000028105853,0.0138705345],"study_design_scores_gemma":[0.0022951548,0.0017057124,0.98715794,0.000049548613,0.00009873494,0.000051172632,0.00065746164,0.0002016975,0.0065617524,0.0002075672,0.0007405296,0.00027274553],"about_ca_topic_score_codex":0.00001718551,"about_ca_topic_score_gemma":0.0002285724,"teacher_disagreement_score":0.021848416,"about_ca_system_score_codex":0.000005745941,"about_ca_system_score_gemma":0.0001393929,"threshold_uncertainty_score":0.73223597},"labels":[],"label_agreement":null},{"id":"W2020816946","doi":"10.3389/fgene.2015.00058","title":"Epigenetic consequences of artificial reproductive technologies to the bovine imprinted genes SNRPN, H19/IGF2, and IGF2R","year":2015,"lang":"en","type":"article","venue":"Frontiers in Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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":"Genomic imprinting; Epigenetics; Biology; Genetics; Reproductive technology; Somatic cell; Offspring; Imprinting (psychology); DNA methylation; Gene; Computational biology; Gene expression; Pregnancy; Embryogenesis","score_opus":0.018855963081406184,"score_gpt":0.2514591098466592,"score_spread":0.232603146765253,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2020816946","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96788627,0.015605796,0.014022852,0.0012167509,0.00069617457,0.00043297774,0.000014438131,0.000017711529,0.000107057225],"genre_scores_gemma":[0.95697296,0.0012826058,0.04137913,0.000058747926,0.000120562356,0.00003431789,0.000008418274,0.000021947293,0.00012129265],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99848974,0.00008085483,0.00039521948,0.0005319618,0.00017683917,0.0003253948],"domain_scores_gemma":[0.99894065,0.000010268522,0.00013119342,0.00066436175,0.00017588759,0.000077669814],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043477383,0.00019597218,0.00025750336,0.00012097818,0.00005460959,0.00002569604,0.00039456598,0.0001638504,0.0000016103788],"category_scores_gemma":[0.00047929652,0.00015968307,0.000047928537,0.00027250437,0.00047727732,0.0000026495686,0.0004106523,0.00010494507,0.0000023744706],"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":[0.00010726342,0.00010227057,0.15514061,0.000040397226,0.00011927366,0.0000043989726,0.00084031007,0.001665965,0.6483482,0.00006160094,0.003928295,0.18964143],"study_design_scores_gemma":[0.0003788613,0.0010790977,0.017056486,0.00002810551,0.00003717623,0.000046839185,0.005954928,0.0005642042,0.95272654,0.0023039042,0.019476498,0.0003473732],"about_ca_topic_score_codex":0.000051008123,"about_ca_topic_score_gemma":0.000059958227,"teacher_disagreement_score":0.30437833,"about_ca_system_score_codex":0.000019002962,"about_ca_system_score_gemma":0.000121377154,"threshold_uncertainty_score":0.65116864},"labels":[],"label_agreement":null},{"id":"W2021120315","doi":"10.1210/en.2005-1487","title":"Coding<i>GNAS</i>Mutations Leading to Hormone Resistance Impair<i>in Vitro</i>Agonist- and Cholera Toxin-Induced Adenosine Cyclic 3′,5′-Monophosphate Formation Mediated by Human XLαs","year":2006,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":56,"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; Royal Victoria Hospital; Royal Victoria Regional Health Centre","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; U.S. Public Health Service","keywords":"GNAS complex locus; Gs alpha subunit; Cholera toxin; G protein-coupled receptor; Endocrinology; Internal medicine; Biology; Receptor; Pseudohypoparathyroidism; Signal transduction; Wild type; G protein; Cell biology; Mutant; Parathyroid hormone; Biochemistry; Medicine; Calcium; Gene","score_opus":0.008624274444104416,"score_gpt":0.2448305225797903,"score_spread":0.2362062481356859,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021120315","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9947593,0.0021502469,0.00054185075,0.0011870315,0.00009940359,0.00031533197,0.000034436565,0.000035060548,0.0008773064],"genre_scores_gemma":[0.9971222,0.00015897867,0.0008702361,0.00040800028,0.000076946395,0.00007696408,0.00044707622,0.000031510866,0.0008080333],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9983334,0.000059455782,0.00044503136,0.00046654715,0.00010558304,0.00058998074],"domain_scores_gemma":[0.9994223,0.000023862165,0.00013574307,0.0002697584,0.000052063733,0.00009623317],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00009867195,0.00022777618,0.00026358938,0.00012812327,0.00019010587,0.000045985234,0.0001709121,0.00013024936,0.0000073436313],"category_scores_gemma":[0.00006126024,0.0002542553,0.000049086208,0.00018738623,0.000066035136,0.000014569094,0.00012908144,0.00014554475,0.00002082423],"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":[0.000028920886,0.0000481444,0.0006844676,0.000015231325,0.00001355296,0.000007698534,0.00010352476,0.000021710115,0.99667454,0.000090836955,0.0016916103,0.0006197494],"study_design_scores_gemma":[0.0015232915,0.00025874274,0.035635076,0.000016051748,0.000018395795,0.00006965165,0.0001011649,0.000045216402,0.9434608,0.00009521157,0.018447068,0.00032931828],"about_ca_topic_score_codex":0.000202328,"about_ca_topic_score_gemma":0.00019554625,"teacher_disagreement_score":0.05321374,"about_ca_system_score_codex":0.000043959986,"about_ca_system_score_gemma":0.000021776692,"threshold_uncertainty_score":0.99999094},"labels":[],"label_agreement":null},{"id":"W2021178751","doi":"10.1016/j.mehy.2004.05.010","title":"Just how happy is the happy puppet? An emotion signaling and kinship theory perspective on the behavioral phenotype of children with Angelman syndrome","year":2004,"lang":"en","type":"article","venue":"Medical Hypotheses","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":62,"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 Cancer Institute; National Institute of General Medical Sciences; Natural Sciences and Engineering Research Council of Canada; National Institute on Aging; National Institutes of Health","keywords":"Genomic imprinting; Angelman syndrome; Genetics; Phenotype; Biology; Kinship; UBE3A; Gene; Imprinting (psychology); Developmental psychology; Psychology; Gene expression; DNA methylation","score_opus":0.026931989710451867,"score_gpt":0.2631787664788764,"score_spread":0.23624677676842454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021178751","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99574965,0.0003940755,0.0004833296,0.002871324,0.00003758579,0.00024281317,0.0000118047055,0.000009575819,0.00019984739],"genre_scores_gemma":[0.9989861,0.00004920111,0.0002099142,0.00054944406,0.000107653665,0.000012797076,0.0000067910937,0.000024394905,0.000053689917],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9988653,0.00013919153,0.00012331031,0.00031512138,0.0003370446,0.00022002708],"domain_scores_gemma":[0.9993422,0.000067308145,0.00008625032,0.00034072893,0.00006256032,0.00010094098],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045780258,0.0001646498,0.00015185923,0.000026614902,0.00019974622,0.000051851723,0.00028413234,0.00012272186,0.00007807567],"category_scores_gemma":[0.0002879041,0.00008590244,0.00005822596,0.00008056661,0.0005578279,0.0000056456406,0.00008069113,0.00017605149,0.0000022027286],"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":[0.0011994336,0.005487155,0.21981156,0.00026976728,0.0029776793,0.00014785456,0.039816666,0.0004112267,0.51341224,0.091106966,0.00097606593,0.12438338],"study_design_scores_gemma":[0.0020383757,0.007882823,0.7848678,0.00062196166,0.00035560562,0.0010943128,0.024561435,0.00005339138,0.17142847,0.005823722,0.00045258182,0.00081948086],"about_ca_topic_score_codex":0.00013949178,"about_ca_topic_score_gemma":0.000039135404,"teacher_disagreement_score":0.56505626,"about_ca_system_score_codex":0.000013821842,"about_ca_system_score_gemma":0.0000793012,"threshold_uncertainty_score":0.35029995},"labels":[],"label_agreement":null},{"id":"W2021548102","doi":"10.1016/j.jpeds.2008.07.058","title":"Retrospective Study of the Potential Benefits and Adverse Events during Growth Hormone Treatment in Children with Prader-Willi Syndrome","year":2008,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"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; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Body mass index; Growth hormone; Internal medicine; Pediatrics; Adverse effect; Endocrinology; Obstructive sleep apnea; Hormone; Gastroenterology","score_opus":0.005606803000168144,"score_gpt":0.1931648111970808,"score_spread":0.18755800819691265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021548102","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984523,0.0011998018,0.000008811793,0.000031532585,0.00004078381,0.0002577505,0.000003990546,8.5522646e-7,0.0000041535964],"genre_scores_gemma":[0.9965815,0.0032174604,0.00006265961,0.000003868539,0.0001003708,0.0000014114783,5.2282115e-7,0.0000109111925,0.000021305124],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992182,0.000076579134,0.00024928903,0.00010242641,0.00022068311,0.00013277587],"domain_scores_gemma":[0.9994022,0.0000047478597,0.00031492554,0.0001589196,0.00008114962,0.000038058854],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015352301,0.00010983259,0.00016387796,0.00005374642,0.00009963218,0.0000021833955,0.00016358579,0.000042949214,6.8837033e-7],"category_scores_gemma":[0.000027608889,0.000058379042,0.00004949788,0.00014750312,0.00003954858,0.000005384306,0.00009596252,0.00010397981,1.3875785e-7],"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":[0.000015101108,0.00023564609,0.9956785,0.0000037696257,0.000057444107,0.0000027023184,0.00044416692,0.00070321804,0.002811971,3.018504e-7,0.0000026613984,0.00004453747],"study_design_scores_gemma":[0.002237621,0.0022247795,0.9920202,0.000005853302,0.00015382205,0.0023643828,0.00041838625,0.0000020349644,0.0005008701,0.000004812315,3.4031538e-7,0.00006688133],"about_ca_topic_score_codex":0.00007064885,"about_ca_topic_score_gemma":0.000015462982,"teacher_disagreement_score":0.0036582642,"about_ca_system_score_codex":0.000026178404,"about_ca_system_score_gemma":0.000052156392,"threshold_uncertainty_score":0.23806283},"labels":[],"label_agreement":null},{"id":"W2022030369","doi":"10.1155/2012/585024","title":"Epigenetic Mechanisms of Genomic Imprinting: Common Themes in the Regulation of Imprinted Regions in Mammals, Plants, and Insects","year":2012,"lang":"en","type":"article","venue":"Genetics Research International","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":87,"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; Dalhousie University; Western University","funders":"Natural Sciences and Engineering Research Council of Canada; Mount Allison University; Dalhousie University; Nova Scotia Health Research Foundation","keywords":"Genomic imprinting; Epigenetics; Imprinting (psychology); Biology; DNA methylation; Genetics; Gene; Locus (genetics); Regulation of gene expression; Gene expression","score_opus":0.05222290356522752,"score_gpt":0.34007468910862443,"score_spread":0.2878517855433969,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022030369","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99690676,0.0009972552,0.0008375844,0.0001817861,0.000098129225,0.00026602155,0.000011070479,0.000001509762,0.0006998975],"genre_scores_gemma":[0.99771315,0.00076268316,0.0013191208,0.000019129075,0.000067954425,0.000022039952,0.00003319616,0.000013368666,0.000049338065],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99850285,0.0002257446,0.0003885703,0.00020168218,0.0003615883,0.00031956373],"domain_scores_gemma":[0.9993331,0.00008111365,0.00011704275,0.00030022033,0.00012059006,0.000047943606],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013147733,0.00009880258,0.00013399367,0.0002543021,0.000034231296,0.00001548876,0.00041323417,0.00010263192,0.000020454114],"category_scores_gemma":[0.00013939268,0.0000857715,0.000040251107,0.0001299614,0.00014326423,0.000004914624,0.00036884198,0.00016272892,0.0000016962587],"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":[0.000022209844,0.000111588255,0.11570064,0.000023927898,0.000023502695,4.1976446e-7,0.0006259805,0.00020601325,0.87743896,0.0021950847,0.00001955928,0.0036321252],"study_design_scores_gemma":[0.0003979735,0.00012632346,0.75964534,0.00003142321,0.0000021167302,0.00002743656,0.00072032074,0.00084026676,0.23500353,0.002751131,0.0003789173,0.000075229116],"about_ca_topic_score_codex":0.00015602868,"about_ca_topic_score_gemma":0.000113170725,"teacher_disagreement_score":0.6439447,"about_ca_system_score_codex":0.000021848191,"about_ca_system_score_gemma":0.0000529323,"threshold_uncertainty_score":0.34976602},"labels":[],"label_agreement":null},{"id":"W2022051629","doi":"10.1038/ng1487","title":"Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":252,"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","funders":"Division of Materials Research; National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Biology; Genomic imprinting; Genetics; Exon; Imprinting (psychology); Epigenetics; Allele; Gene; Internal medicine; DNA methylation; Parathyroid hormone; Gene expression; Medicine","score_opus":0.007878920898433147,"score_gpt":0.24176156477481606,"score_spread":0.2338826438763829,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022051629","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9948743,0.0041184463,0.00038948638,0.0000725883,0.0003386179,0.00014893846,0.000006061758,0.00000413196,0.00004741668],"genre_scores_gemma":[0.99747276,0.0011835187,0.0011140716,0.000046300906,0.00007713283,0.0000017469534,0.0000092890905,0.000019029003,0.00007617707],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999149,0.000040792776,0.00025125413,0.00023340546,0.00016227645,0.00016322223],"domain_scores_gemma":[0.9992358,0.0000050145195,0.00018723893,0.00034886628,0.00017940476,0.000043667747],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007337613,0.00014283755,0.00016011468,0.000030891348,0.000043816064,0.000010920417,0.00021145403,0.0003297154,0.0000025552454],"category_scores_gemma":[0.000052984695,0.00010779307,0.00007352945,0.00010900487,0.0001132681,0.0000017173769,0.00019991797,0.00015959043,6.6015366e-7],"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":[0.000023620358,0.000038679205,0.042241916,0.00003413056,0.000053828477,0.0000010590667,0.00005168346,0.00023663399,0.9561484,0.00007060062,0.000028415527,0.0010710253],"study_design_scores_gemma":[0.00042820448,0.00017699134,0.32621098,0.000022933533,0.000036813824,0.00007068312,0.000012475447,0.0000127320955,0.67224306,0.0004388775,0.00026003126,0.000086213025],"about_ca_topic_score_codex":0.000021801448,"about_ca_topic_score_gemma":0.000018746823,"teacher_disagreement_score":0.28396904,"about_ca_system_score_codex":0.000007851533,"about_ca_system_score_gemma":0.00006635815,"threshold_uncertainty_score":0.4395674},"labels":[],"label_agreement":null},{"id":"W2022617739","doi":"10.1159/000133150","title":"Mapping of the gene coding for the muscle protein nebulin (Neb) to the proximal region of mouse Chromosome 2","year":2008,"lang":"en","type":"article","venue":"Cytogenetics and Cell Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University Health Centre; Montreal General Hospital","funders":"","keywords":"Biology; Molecular biology; Genetics; Gene; Chromosome","score_opus":0.023713547358050008,"score_gpt":0.21810274760076617,"score_spread":0.19438920024271616,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022617739","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.987368,0.0035951817,0.0071540526,0.00033513125,0.000128277,0.001334832,0.000028644634,0.000003841015,0.000052053874],"genre_scores_gemma":[0.992713,0.0016664799,0.004423744,0.0001424375,0.0001954998,0.00009062001,0.000006592005,0.000039726652,0.00072194275],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986559,0.00005943586,0.00042094867,0.00033617392,0.00020594287,0.00032156077],"domain_scores_gemma":[0.99867433,0.000034839075,0.0002454088,0.00078733277,0.00018474222,0.00007335143],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022568255,0.00020556634,0.00019704772,0.0000305939,0.0003313861,0.000018309089,0.0005576281,0.0001246639,0.0000027128785],"category_scores_gemma":[0.00006453729,0.00012458277,0.00015944957,0.00017094327,0.00024990164,0.0000014099992,0.00043518812,0.000087059554,7.637351e-7],"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":[0.000010313696,0.00004781133,0.0037618638,0.00007014968,0.00003513049,3.6484448e-7,0.00041813366,0.0010035564,0.9919013,0.000017880982,0.00018636325,0.0025471542],"study_design_scores_gemma":[0.00045147192,0.00041409754,0.011277533,0.000025188237,0.000036117603,0.000041442316,0.00036022026,0.0007212499,0.97025096,0.000023820103,0.016222533,0.00017537527],"about_ca_topic_score_codex":0.000014913921,"about_ca_topic_score_gemma":0.000010845177,"teacher_disagreement_score":0.021650327,"about_ca_system_score_codex":0.0000072905223,"about_ca_system_score_gemma":0.000101397614,"threshold_uncertainty_score":0.5080338},"labels":[],"label_agreement":null},{"id":"W2022971808","doi":"10.1016/j.jpeds.2012.07.042","title":"Longitudinal Evaluation of Sleep-Disordered Breathing in Children with Prader-Willi Syndrome during 2 Years of Growth Hormone Therapy","year":2012,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"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 Health Network; Toronto Western Hospital; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Polysomnography; Pediatrics; Context (archaeology); Obstructive sleep apnea; Sleep disordered breathing; Sleep apnea; Body mass index; Apnea; Growth hormone; Internal medicine; Hormone","score_opus":0.013658074120025595,"score_gpt":0.24225123566068635,"score_spread":0.22859316154066076,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022971808","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9894621,0.010119628,0.00018919837,0.000024257894,0.000045709236,0.00014162934,0.000002271567,8.9624456e-7,0.000014305866],"genre_scores_gemma":[0.99661106,0.0027234794,0.0004909634,0.0000039011666,0.00015021366,0.0000010516129,0.000002312775,0.000013797406,0.000003203439],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99888855,0.00012534036,0.00035460765,0.000068698915,0.00039020195,0.00017262812],"domain_scores_gemma":[0.99907196,0.00002030619,0.00051087444,0.00014943401,0.00020667538,0.000040757157],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013975794,0.0000895091,0.00017410897,0.00010493582,0.000025101896,0.0000048586544,0.00018209881,0.000063755106,0.000004139175],"category_scores_gemma":[0.00010146071,0.000064148946,0.00005909685,0.00018595351,0.00003775337,0.000012820614,0.000048176305,0.000118920965,2.7779168e-7],"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":[0.000016096945,0.000116162526,0.9660338,0.000019727886,0.000054539196,2.2729944e-7,0.0004232622,0.00082357356,0.030977022,0.0000014308428,0.0000073214696,0.0015268201],"study_design_scores_gemma":[0.0014520425,0.00045549354,0.99278957,0.000011091918,0.00014205337,0.0006462221,0.00015774748,0.000013914492,0.0042381063,0.000017701379,0.0000014347705,0.00007462443],"about_ca_topic_score_codex":0.00003592821,"about_ca_topic_score_gemma":0.0000017730448,"teacher_disagreement_score":0.026755752,"about_ca_system_score_codex":0.00001452356,"about_ca_system_score_gemma":0.00006715124,"threshold_uncertainty_score":0.2615918},"labels":[],"label_agreement":null},{"id":"W2023174704","doi":"10.1371/journal.pone.0004291","title":"Loss of Magel2, a Candidate Gene for Features of Prader-Willi Syndrome, Impairs Reproductive Function in Mice","year":2009,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; University of California, San Diego; University of Alberta; Canadian Diabetes Association","keywords":"Loss function; Gene; Function (biology); Genetics; Candidate gene; Biology; Medicine; Internal medicine; Endocrinology; Phenotype","score_opus":0.013706530261128185,"score_gpt":0.22517955467328649,"score_spread":0.2114730244121583,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023174704","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9979562,0.0009549862,0.00026449875,0.00024776938,0.000032051186,0.0003915497,0.000029508128,0.0000046958426,0.00011874578],"genre_scores_gemma":[0.99419445,0.00013757953,0.0051659048,0.00004473854,0.00006932424,0.000018857714,0.000057840112,0.000012922924,0.00029838635],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99909,0.00002618735,0.00025911388,0.00032408367,0.000114543465,0.00018603602],"domain_scores_gemma":[0.99938834,0.000008905249,0.00016017361,0.00028925805,0.00012103541,0.0000322926],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017268458,0.000109534296,0.00023599034,0.000061789906,0.000019957926,0.0000045000957,0.00010313486,0.00009788589,0.0000051719553],"category_scores_gemma":[0.00014009923,0.00010917737,0.000066813045,0.000109343426,0.000039272578,0.000003714177,0.000035292695,0.00005513035,5.4126497e-7],"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":[0.000033406683,0.00041204118,0.010552627,0.00011497678,0.0001275555,5.0918595e-7,0.0000725871,0.000026617941,0.987507,0.000010941301,0.00006381818,0.0010779186],"study_design_scores_gemma":[0.0005340922,0.0011223261,0.32141906,0.00006034046,0.000058288806,0.00001841996,0.000057863275,0.0000140167585,0.67644167,0.00013109365,0.000047120193,0.00009571751],"about_ca_topic_score_codex":0.000055460932,"about_ca_topic_score_gemma":0.000014549755,"teacher_disagreement_score":0.31106535,"about_ca_system_score_codex":0.0000094975485,"about_ca_system_score_gemma":0.000036622623,"threshold_uncertainty_score":0.4452124},"labels":[],"label_agreement":null},{"id":"W2023332321","doi":"10.1002/ajmg.a.31274","title":"Overgrowth with severe developmental delay following IVF/ICSI: A newly recognized syndrome?","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; SickKids Foundation; Mount Sinai Hospital","funders":"","keywords":"Intracytoplasmic sperm injection; In vitro fertilisation; Medicine; Global developmental delay; Pathogenesis; Genomic imprinting; Pregnancy; Pediatrics; Biology; Internal medicine; Genetics; Phenotype","score_opus":0.005980403779854638,"score_gpt":0.2294149075923145,"score_spread":0.22343450381245986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023332321","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99317825,0.00090650696,0.0044006086,0.00036253425,0.00029119104,0.00010237211,0.0000036034464,0.0000068204945,0.0007480996],"genre_scores_gemma":[0.97074085,0.0003524935,0.027907357,0.00042407287,0.0003164744,0.000005022633,0.000016406322,0.000046622434,0.00019066974],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.99735546,0.00011268957,0.0007020553,0.0003160744,0.0010399886,0.0004737455],"domain_scores_gemma":[0.99875915,0.000039969073,0.0004654717,0.00020474219,0.00014029599,0.0003903569],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000624479,0.00026175205,0.00046624697,0.0000874801,0.000092678536,0.000045906898,0.0004784318,0.00013698004,0.00009225879],"category_scores_gemma":[0.00013884345,0.00021088506,0.00022461114,0.00026259746,0.00022652873,0.0000058477804,0.00016156417,0.00027180664,0.000010073723],"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":[0.0007312115,0.0011677801,0.49562818,0.00009374724,0.0029910514,0.0038558957,0.0005212953,0.0013334458,0.06201014,0.000038399496,0.01648791,0.41514096],"study_design_scores_gemma":[0.027317885,0.030936934,0.2689431,0.0020252045,0.0012175603,0.23462382,0.0050841235,0.0007764778,0.026579946,0.0004577757,0.39746344,0.0045737335],"about_ca_topic_score_codex":0.000055105913,"about_ca_topic_score_gemma":0.000040849878,"teacher_disagreement_score":0.41056722,"about_ca_system_score_codex":0.000033321176,"about_ca_system_score_gemma":0.0006642438,"threshold_uncertainty_score":0.8599643},"labels":[],"label_agreement":null},{"id":"W2023847394","doi":"10.1016/j.placenta.2009.07.007","title":"Unearthing the Roles of Imprinted Genes in the Placenta","year":2009,"lang":"en","type":"review","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":92,"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":"Genomic imprinting; Epigenetics; Biology; Placentation; Placenta; Conceptus; Imprinting (psychology); Genetics; Gene; Phenotype; Epigenesis; Embryo; DNA methylation; Fetus; Gene expression; Pregnancy","score_opus":0.026513536937667708,"score_gpt":0.3024756736617026,"score_spread":0.27596213672403486,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023847394","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0046664076,0.9938447,0.000027864118,0.00008846213,0.00013099593,0.00057709776,0.000017763585,0.0000045701513,0.00064213504],"genre_scores_gemma":[0.002712123,0.9965797,0.00010627005,0.00010958714,0.00015172901,0.00002782592,0.00011513808,0.000027222532,0.0001704038],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99833024,0.0003051246,0.000512873,0.00035319093,0.00019040513,0.0003081723],"domain_scores_gemma":[0.9988633,0.000074660726,0.00029325244,0.00071101537,0.000026613994,0.000031181902],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059551076,0.00029728873,0.00054619304,0.000054497163,0.000071008995,0.000042100208,0.0008551161,0.00022992311,0.000016672177],"category_scores_gemma":[0.00007990841,0.00016342431,0.00032627294,0.00017531158,0.00006819942,0.0000016599173,0.00023403417,0.00027125626,0.000010697383],"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":[0.0000044980698,0.00006405978,0.00015442546,0.00087432977,0.000094565796,0.0000024940298,0.00015989908,0.000010279864,0.00059642136,0.00002968345,0.00052204705,0.9974873],"study_design_scores_gemma":[0.00018657296,0.000074380005,0.00018653371,0.001107613,0.00013423756,0.0001269213,0.00032990603,0.000014133741,0.0004452119,0.000007576263,0.99718827,0.0001986526],"about_ca_topic_score_codex":0.000035047862,"about_ca_topic_score_gemma":0.000112153946,"teacher_disagreement_score":0.99728864,"about_ca_system_score_codex":0.000014555491,"about_ca_system_score_gemma":0.00011348946,"threshold_uncertainty_score":0.666425},"labels":[],"label_agreement":null},{"id":"W2024054703","doi":"10.1016/s0893-133x(00)00127-5","title":"The Genes for Major Psychosis Aberrant Sequence or Regulation?","year":2000,"lang":"en","type":"review","venue":"Neuropsychopharmacology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":81,"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 Addiction and Mental Health; University of Toronto","funders":"National Alliance for Research on Schizophrenia and Depression","keywords":"Epigenetics; Genetics; Genomic imprinting; Biology; DNA methylation; Psychosis; Bipolar disorder; Allele; Genetic association; Gene; Genotype; Psychology; Neuroscience; Psychiatry; Single-nucleotide polymorphism; Gene expression","score_opus":0.0546937931192884,"score_gpt":0.380805176764032,"score_spread":0.3261113836447436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024054703","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00049878197,0.99419725,0.00009200017,0.00020757526,0.0025991043,0.0017576308,0.00008930783,0.00002747371,0.00053088344],"genre_scores_gemma":[0.000046676614,0.98775125,0.00047998704,0.00051920617,0.001151745,0.0010452016,0.00013193034,0.0001331387,0.008740842],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.997302,0.00029962315,0.0007339244,0.00091627357,0.00013438072,0.0006137948],"domain_scores_gemma":[0.99849397,0.00018822309,0.00037179203,0.0007296731,0.00008853386,0.00012781688],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00025465805,0.0005069687,0.00072209525,0.00007371057,0.00039534047,0.0000672693,0.000834835,0.0004154028,0.00025466035],"category_scores_gemma":[0.00005658663,0.00032533996,0.00055294775,0.00021307435,0.00017108035,0.0000025537124,0.00010794973,0.00023907058,0.00008017568],"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":[0.00008118276,0.00003659866,0.0000019753195,0.00074017496,0.00021153943,0.0000031147738,0.0000036801657,0.0000042604033,0.0034583511,0.0000075656653,0.021674834,0.9737767],"study_design_scores_gemma":[0.00065362046,0.0003865441,0.000022129043,0.00018175448,0.00045987088,0.00035645528,0.0000024018384,0.000014946643,0.00009448731,0.000022678729,0.9974391,0.00036600407],"about_ca_topic_score_codex":0.0000032008866,"about_ca_topic_score_gemma":0.000007890638,"teacher_disagreement_score":0.9757643,"about_ca_system_score_codex":0.00001850968,"about_ca_system_score_gemma":0.00020890057,"threshold_uncertainty_score":0.9999199},"labels":[],"label_agreement":null},{"id":"W2024184784","doi":"10.1007/s11695-011-0503-1","title":"Reply to the Letter of Scheimann et al.","year":2011,"lang":"en","type":"letter","venue":"Obesity Surgery","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"","keywords":"Medicine; General surgery","score_opus":0.02141018257372177,"score_gpt":0.2324022489736346,"score_spread":0.21099206639991283,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024184784","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.1725413,0.00059069024,0.00028748994,0.823544,0.0010561098,0.00026296236,0.00003891812,0.000013480161,0.0016650389],"genre_scores_gemma":[0.014086037,0.00015035146,0.00037018448,0.9807587,0.0010993703,0.000021649417,0.00021402002,0.00005290028,0.0032467735],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99841917,0.0001551408,0.0003472221,0.0004961591,0.00022029216,0.0003620243],"domain_scores_gemma":[0.9985138,0.00006575488,0.00021205815,0.0010614801,0.000101333535,0.000045532564],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006447983,0.00025028203,0.00035195064,0.00007561339,0.00005576075,0.000024553463,0.00037856706,0.00030992847,0.00008767247],"category_scores_gemma":[0.00018897023,0.00019451645,0.0003433528,0.0000856414,0.00006107,0.0000018050945,0.0003467601,0.0004441575,0.00009697416],"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":[0.0000029933626,0.000017023653,0.005368224,0.000038646114,0.000078182224,0.000011591222,0.000021483298,0.0000010397277,0.0046852143,8.1629173e-7,0.98916274,0.00061206793],"study_design_scores_gemma":[0.00003448833,0.0000341852,0.010631675,0.000051775038,0.000023594232,0.000031484877,0.000004153873,4.271686e-7,0.013818517,0.0000066268376,0.97512877,0.00023430718],"about_ca_topic_score_codex":0.00018094096,"about_ca_topic_score_gemma":0.0000074542895,"teacher_disagreement_score":0.15845527,"about_ca_system_score_codex":0.0000059806634,"about_ca_system_score_gemma":0.00009325537,"threshold_uncertainty_score":0.7932151},"labels":[],"label_agreement":null},{"id":"W2024495278","doi":"10.1139/o03-052","title":"The many roles of the transcriptional regulator CTCF","year":2003,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":67,"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 Manitoba","funders":"","keywords":"CTCF; Regulator; Imprinting (psychology); Transcriptional regulation; Biology; Genetics; Psychological repression; Gene; Insulator (electricity); Regulation of gene expression; YY1; Transcription factor; Mechanism (biology); Function (biology); Repressor; Computational biology; Cell biology; Gene expression; Promoter; Enhancer","score_opus":0.01213321326155398,"score_gpt":0.24364173381532198,"score_spread":0.231508520553768,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024495278","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.008312516,0.9894078,0.000013023114,0.00002215054,0.0002514814,0.00020078765,0.00006143978,0.0000030301817,0.0017278162],"genre_scores_gemma":[0.006419721,0.98893976,0.000058245685,0.00003202317,0.000165434,0.000033618802,0.00009358355,0.000022668219,0.004234947],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9986795,0.00013514636,0.00041789375,0.0004287084,0.00006939182,0.0002693202],"domain_scores_gemma":[0.9990009,0.000032470238,0.00029348437,0.0005743367,0.000042284493,0.000056522298],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020991573,0.00029594405,0.00044089908,0.000011286068,0.0001808079,0.000016325921,0.00045125585,0.0005851517,0.00001620776],"category_scores_gemma":[0.000035304747,0.00016374676,0.0003937617,0.000070467264,0.00041202074,6.1264626e-7,0.0001641884,0.00017511904,0.0000020374562],"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":[0.000011442976,0.0000734806,0.00011705486,0.0045957086,0.00030991188,4.5247506e-7,0.000013335663,4.6435335e-7,0.3272378,0.0005601409,0.0010285169,0.6660517],"study_design_scores_gemma":[0.00011863342,0.000044766748,0.000020136313,0.00021945825,0.00013157669,0.00006851892,0.000024707719,4.7156684e-7,0.047061108,0.00003807985,0.9520865,0.000186008],"about_ca_topic_score_codex":0.000001367352,"about_ca_topic_score_gemma":8.928205e-7,"teacher_disagreement_score":0.95105803,"about_ca_system_score_codex":0.000008045166,"about_ca_system_score_gemma":0.00018366058,"threshold_uncertainty_score":0.6677399},"labels":[],"label_agreement":null},{"id":"W2024628398","doi":"10.1139/o11-043","title":"Setting up and maintaining differential insulators and boundaries for genomic imprinting","year":2011,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"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":"Cancer Research UK","keywords":"CTCF; Chromatin; Genomic imprinting; Biology; Insulator (electricity); Epigenetics; Gene; Genetics; Genome; Locus (genetics); Imprinting (psychology); Genomic organization; Somatic cell; Regulation of gene expression; Transcription factor; Computational biology; DNA methylation; Gene expression; Enhancer","score_opus":0.015561035741652915,"score_gpt":0.2599823396318963,"score_spread":0.2444213038902434,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024628398","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.26924908,0.72985274,0.00018619007,0.0000039536503,0.00020183934,0.00026899923,0.000058488105,0.000010284,0.0001684502],"genre_scores_gemma":[0.13441585,0.86353636,0.00085508043,0.000021735133,0.00036293012,0.00006200942,0.0003409456,0.000053777494,0.00035132378],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99812615,0.000057813544,0.00045553385,0.00087371725,0.000028271743,0.00045851202],"domain_scores_gemma":[0.999176,0.000047500376,0.00032593793,0.00027283025,0.000035110053,0.00014259253],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00022323224,0.00047429654,0.00074097805,0.000045019886,0.00032879008,0.000110172,0.00016324357,0.00077536056,0.000009647046],"category_scores_gemma":[0.00008375146,0.00042777965,0.00015942799,0.00003247334,0.00042774004,0.0000023333087,0.0006264183,0.00019605391,7.0275786e-7],"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":[0.000014082129,0.000017522027,0.00056778546,0.007253464,0.00020868368,6.8612485e-7,0.000088151995,2.1807736e-8,0.13547456,0.00015351915,0.000031109998,0.8561904],"study_design_scores_gemma":[0.0005864644,0.00023580997,0.0001034577,0.0005191919,0.00038132526,0.00021810993,0.00017175898,0.000009966446,0.016764458,0.00012155956,0.9801441,0.00074381777],"about_ca_topic_score_codex":0.000012308265,"about_ca_topic_score_gemma":9.328542e-7,"teacher_disagreement_score":0.98011297,"about_ca_system_score_codex":0.000011060374,"about_ca_system_score_gemma":0.0001497823,"threshold_uncertainty_score":0.9998174},"labels":[],"label_agreement":null},{"id":"W2024673645","doi":"10.1016/s0002-9440(10)62964-1","title":"Developmental Abnormalities of Neuronal Structure and Function in Prenatal Mice Lacking the Prader-Willi Syndrome Gene Necdin","year":2005,"lang":"en","type":"article","venue":"American Journal Of Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":98,"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","funders":"Canadian Institutes of Health Research; Fondation pour la Recherche Médicale","keywords":"Gene; Biology; Genetics; Medicine; Endocrinology; Internal medicine; Pathology","score_opus":0.005945838220352216,"score_gpt":0.2127885638113434,"score_spread":0.20684272559099118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024673645","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99867237,0.0006096624,0.00035596755,0.00021143169,0.000072253,0.000045638095,0.000006710962,0.0000010307488,0.000024967385],"genre_scores_gemma":[0.9950883,0.00012609837,0.0044573066,0.00020977274,0.000087550434,9.611246e-7,0.000003832802,0.0000095333635,0.000016643251],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9991784,0.000112830065,0.00032797456,0.00012596254,0.00009180783,0.00016301397],"domain_scores_gemma":[0.9995056,0.000022621256,0.0003243742,0.000064767235,0.00004718854,0.00003547237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002027833,0.00009759836,0.00018946601,0.000064592496,0.000033701148,0.000007996544,0.00012646495,0.000045639812,0.000012194494],"category_scores_gemma":[0.000043354063,0.00007342788,0.00004254047,0.00007314241,0.00023574915,0.000007855476,0.00008293206,0.00013922754,3.1278537e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000030645086,0.0000445754,0.16909395,0.000019711099,0.00008451552,0.000026034219,0.0010388963,0.0006988503,0.7585443,0.000025643001,0.000029047134,0.07036379],"study_design_scores_gemma":[0.00056901044,0.0013101131,0.94035244,0.000020698602,0.00002262749,0.02030927,0.0018231312,0.00003381241,0.03441424,0.00003926411,0.0009807195,0.00012465882],"about_ca_topic_score_codex":0.000011453127,"about_ca_topic_score_gemma":0.000016056703,"teacher_disagreement_score":0.77125853,"about_ca_system_score_codex":0.000010657068,"about_ca_system_score_gemma":0.000064250264,"threshold_uncertainty_score":0.29943022},"labels":[],"label_agreement":null},{"id":"W2024727939","doi":"10.1016/j.fertnstert.2015.03.020","title":"Deoxyribonucleic acid methylation profiling of single human blastocysts by methylated CpG-island amplification coupled with CpG-island microarray","year":2015,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre","funders":"Society for Reproduction and Fertility; Medical Research Council; Newlife the Charity for Disabled Children","keywords":"DNA methylation; Differentially methylated regions; CpG site; Biology; Methylation; Blastocyst; Microarray; Methylated DNA immunoprecipitation; Molecular biology; Genetics; DNA microarray; Embryo; DNA; Gene; Embryogenesis; Gene expression","score_opus":0.023678935345627126,"score_gpt":0.2528869824133242,"score_spread":0.22920804706769707,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024727939","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9761095,0.00048671974,0.022705628,0.000032229524,0.000049013302,0.00036458968,0.00006678827,0.000015754,0.00016975697],"genre_scores_gemma":[0.9983585,0.0000047053186,0.0011605468,0.000018469089,0.000020526462,0.000030118012,0.00032160705,0.000017143188,0.0000683892],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99850845,0.00015578879,0.0004116888,0.0005069533,0.00017564946,0.0002414642],"domain_scores_gemma":[0.9989649,0.000013800241,0.00020327907,0.00044041398,0.00024409013,0.00013349176],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00062508875,0.00020356754,0.0002895065,0.000033384465,0.00010403766,0.0000421437,0.00012195833,0.00017977014,0.000016618189],"category_scores_gemma":[0.00011139586,0.00017696794,0.00005033984,0.00010716056,0.00016870015,0.000013732151,0.000087025175,0.00008827838,0.000001217588],"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":[0.0009822391,0.00012094629,0.02493031,0.000081289065,0.000047418,1.9522588e-7,0.00017309266,0.000015665159,0.97283,0.0000012800612,0.000026487314,0.0007910905],"study_design_scores_gemma":[0.0010111763,0.0006925311,0.33656126,0.000020349718,0.000036747544,0.0000062911395,0.00016057001,0.00047822803,0.66044074,0.00013706391,0.0002632174,0.00019181475],"about_ca_topic_score_codex":0.00014747815,"about_ca_topic_score_gemma":0.0002842425,"teacher_disagreement_score":0.31238925,"about_ca_system_score_codex":0.000023128876,"about_ca_system_score_gemma":0.000051046707,"threshold_uncertainty_score":0.7216543},"labels":[],"label_agreement":null},{"id":"W2024941354","doi":"10.1007/s00439-007-0442-z","title":"Parental transmission of HLA-DRB1*15 in multiple sclerosis","year":2007,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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":"Multiple Sclerosis Society","keywords":"Biology; Human genetics; Multiple sclerosis; Human leukocyte antigen; Metabolic disease; Transmission (telecommunications); Genetics; Molecular medicine; Evolutionary biology; Immunology; Antigen; Gene","score_opus":0.03670862111484145,"score_gpt":0.2617135730244857,"score_spread":0.22500495190964426,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024941354","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953195,0.0012325753,0.002487104,0.000008234244,0.00007304957,0.00014251994,0.000004717605,0.000005881253,0.00072645536],"genre_scores_gemma":[0.99570954,0.00020682313,0.0037671656,0.00003085366,0.000075902164,0.0000033104016,0.000038875478,0.000024256417,0.00014327365],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99890465,0.00002354599,0.0003709256,0.0002667219,0.00013936592,0.00029481374],"domain_scores_gemma":[0.9995106,0.00000916235,0.00008353539,0.00027114013,0.0000418151,0.000083758394],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022168063,0.000136082,0.00014879687,0.0000719035,0.00005420476,0.000008853071,0.00018187269,0.00013664916,0.00004402423],"category_scores_gemma":[0.000015601696,0.00014203656,0.00008540863,0.00009261837,0.00007251732,0.0000012529641,0.00008521562,0.00006911301,0.000003887367],"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":[0.000009677349,0.00010065746,0.14633678,0.000021194941,0.000009526006,9.804679e-7,0.00011489832,0.00011048166,0.8369931,0.0000069331663,0.00006343139,0.016232362],"study_design_scores_gemma":[0.00068411813,0.00024295069,0.4608729,0.000032988522,0.0000070653487,0.000005502208,0.00013883732,0.00008782097,0.5348697,0.000025616404,0.0028963895,0.00013613845],"about_ca_topic_score_codex":0.00003499887,"about_ca_topic_score_gemma":0.00013358546,"teacher_disagreement_score":0.31453612,"about_ca_system_score_codex":0.00001001598,"about_ca_system_score_gemma":0.000021536516,"threshold_uncertainty_score":0.57920825},"labels":[],"label_agreement":null},{"id":"W2026012701","doi":"10.1159/000056887","title":"Analysis of DEXI/&lt;i&gt;Dexi&lt;/i&gt; refines the organization of the mouse 7C and human 15q11→q13 imprinting clusters","year":2001,"lang":"en","type":"article","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Biology; Angelman syndrome; Genetics; Gene; Imprinting (psychology); Chromosome; Genomic imprinting; Gene expression","score_opus":0.026756667633003474,"score_gpt":0.296731008099264,"score_spread":0.2699743404662605,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026012701","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963668,0.0024212014,0.00032442113,0.00021224495,0.000019150557,0.00027350674,0.0000121738785,0.0000038831013,0.00036661225],"genre_scores_gemma":[0.99668133,0.0018649991,0.00016975756,0.00003569775,0.00006296657,0.000009248255,0.000029750183,0.00002688325,0.00111934],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99824107,0.00022730533,0.0003879366,0.0004100805,0.0003468235,0.00038677332],"domain_scores_gemma":[0.9986852,0.00005387478,0.00015385723,0.00064908684,0.00036835193,0.00008966172],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00093053485,0.00015957333,0.00026282493,0.00018743816,0.00039130327,0.000048456994,0.0004137171,0.0001359664,0.00004070701],"category_scores_gemma":[0.0001908719,0.00010984488,0.00010242539,0.000983475,0.0004962126,0.0000036910915,0.00077093777,0.000120150835,0.0000012668094],"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":[0.000005447411,0.00002769353,0.11407435,0.000039796498,0.00023178718,4.014958e-7,0.0002174043,0.00028785696,0.8832563,0.0000857611,0.000023678454,0.0017495188],"study_design_scores_gemma":[0.00043702795,0.00021444436,0.86313105,0.000017489016,0.00022397721,0.000029596731,0.00033461506,0.00034087923,0.13001741,0.000046145455,0.0050190934,0.00018829295],"about_ca_topic_score_codex":0.00008998109,"about_ca_topic_score_gemma":0.00014214842,"teacher_disagreement_score":0.7532389,"about_ca_system_score_codex":0.000012960058,"about_ca_system_score_gemma":0.00006882337,"threshold_uncertainty_score":0.44793442},"labels":[],"label_agreement":null},{"id":"W2026126802","doi":"10.1016/s0925-4773(02)00018-7","title":"Cloning of the mouse Sef gene and comparative analysis of its expression with Fgf8 and Spry2 during embryogenesis","year":2002,"lang":"en","type":"article","venue":"Mechanisms of Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"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":"Centre National de la Recherche Scientifique; Institut national de la recherche scientifique","keywords":"FGF8; Biology; Forebrain; Cloning (programming); Hindbrain; Embryo; Embryogenesis; Limb bud; Neuroepithelial cell; Gene; EMX2; Morphogen; Genetics; Fibroblast growth factor; Embryonic stem cell; Cell biology; Gene expression; Anatomy; Homeobox; Neuroscience; Central nervous system","score_opus":0.016155251214197145,"score_gpt":0.2104422705748611,"score_spread":0.19428701936066395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026126802","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974999,0.0005477009,0.0017704007,0.000008297811,0.000010036529,0.00010586427,0.000005704092,0.0000015602956,0.000050528528],"genre_scores_gemma":[0.9816357,0.00010005237,0.018020513,0.000005923782,0.0000025854522,0.0000057867187,0.0000046593505,0.000005120737,0.00021968731],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993371,0.000025382627,0.00022409824,0.00018322973,0.00012795912,0.00010225723],"domain_scores_gemma":[0.99956197,0.0000054504535,0.0001832664,0.0001500433,0.000068133646,0.000031142474],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008374287,0.000098763405,0.00022302628,0.00006123815,0.000056919096,0.000004088392,0.0000837744,0.000044460365,0.00001186546],"category_scores_gemma":[0.000008140294,0.00006934116,0.000034997207,0.00013126197,0.000032858192,0.0000022285774,0.00017557594,0.000022215934,7.86767e-8],"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":[0.000008161329,0.000025489488,0.0052519073,0.000045711196,0.00025900756,1.613765e-7,0.00040597635,0.00023638214,0.99351364,0.000018027347,0.0000013771896,0.00023417153],"study_design_scores_gemma":[0.00026429485,0.00006516642,0.07752444,0.000034335757,0.00008279838,0.0000048816846,0.00030927645,0.00019139223,0.92142355,0.0000017862762,0.000018870158,0.00007920148],"about_ca_topic_score_codex":0.000005209527,"about_ca_topic_score_gemma":0.000009496299,"teacher_disagreement_score":0.07227253,"about_ca_system_score_codex":0.000004116603,"about_ca_system_score_gemma":0.000014131073,"threshold_uncertainty_score":0.28276503},"labels":[],"label_agreement":null},{"id":"W2026274018","doi":"10.1016/j.ydbio.2008.04.025","title":"Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae","year":2008,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":163,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; Hospital for Sick Children; University of Toronto","funders":"Fundação para a Ciência e a Tecnologia; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Epigenetics; Imprinting (psychology); Placenta; DNA methylation; Methylation; Fetus; Cord blood; Gene; Gene expression; Genetics; Molecular biology; Andrology; Pregnancy","score_opus":0.032253366362057924,"score_gpt":0.2585050768203609,"score_spread":0.22625171045830297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026274018","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982971,0.00009159178,0.0011739985,0.00003953416,0.000088596615,0.00025438532,0.00000983221,0.0000030407894,0.000041927393],"genre_scores_gemma":[0.991087,0.000049677106,0.008417459,0.000051679293,0.0000319824,0.00003035824,0.00023519114,0.000008542066,0.0000880837],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993255,0.000049407623,0.00022347592,0.00022862898,0.000030531,0.00014247204],"domain_scores_gemma":[0.99974066,0.000015438965,0.00010010778,0.000091286296,0.000028384111,0.000024102092],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008801738,0.00009315221,0.00011260508,0.00003837478,0.00008730686,0.0000026345565,0.000098493554,0.000106071086,0.0000040994555],"category_scores_gemma":[0.000039039445,0.00007439482,0.000034711476,0.000046197012,0.00010065089,0.0000019977954,0.00014131068,0.00003655222,2.9577163e-7],"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":[0.000009025825,0.000018655865,0.16235475,0.000008813955,0.000007877359,4.4556816e-7,0.0001225208,0.0000029112705,0.8370094,0.000032113137,0.000024573766,0.00040896537],"study_design_scores_gemma":[0.00060793065,0.000059663824,0.36661297,0.000010496075,0.0000018050696,0.000072876035,0.000043459295,0.000009936162,0.63193744,0.000094484974,0.00047892588,0.000070015216],"about_ca_topic_score_codex":0.00003371515,"about_ca_topic_score_gemma":0.00007240051,"teacher_disagreement_score":0.20507191,"about_ca_system_score_codex":0.000017408047,"about_ca_system_score_gemma":0.00004152171,"threshold_uncertainty_score":0.30337328},"labels":[],"label_agreement":null},{"id":"W2027258743","doi":"10.1007/s10735-011-9337-3","title":"Imprinting and expression analysis of a non-coding RNA gene in the mouse Dlk1-Dio3 domain","year":2011,"lang":"en","type":"article","venue":"Journal of Molecular Histology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Princess Margaret Cancer Centre","funders":"RIKEN; National Natural Science Foundation of China; Heilongjiang Youth Development Foundation","keywords":"Genomic imprinting; Imprinting (psychology); Gene; Gene expression; RNA; Developmental biology; Biology; Genetics; Coding (social sciences); Computational biology; Molecular biology; Mathematics; DNA methylation; Statistics","score_opus":0.011018480282029624,"score_gpt":0.23399685307248191,"score_spread":0.2229783727904523,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027258743","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97547454,0.001119668,0.02293154,0.000040591553,0.00005528281,0.00006132838,7.6478557e-7,8.604646e-7,0.00031541724],"genre_scores_gemma":[0.9880967,0.00014911089,0.011598224,0.000103299564,0.0000267977,0.0000021504454,0.000002503853,0.00001063812,0.000010576937],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988529,0.00015698941,0.00049886556,0.00017211979,0.00013164367,0.00018748014],"domain_scores_gemma":[0.9991268,0.000016242037,0.0004686388,0.00025465118,0.000086024935,0.00004763023],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00065494963,0.00011542486,0.00033868806,0.0002685781,0.000036986832,0.0000064339406,0.0002723482,0.0001232488,0.000008733577],"category_scores_gemma":[0.000095391486,0.00008759767,0.00019814396,0.00019740961,0.00008692909,0.000003770008,0.00011384012,0.00014430191,1.9495238e-7],"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":[0.000025058516,0.000051511648,0.0101034995,0.000011033913,0.000190133,0.000041770953,0.00085736765,0.000072979616,0.98757666,0.000022343615,0.0000164033,0.0010312579],"study_design_scores_gemma":[0.00071448094,0.0003775974,0.05988882,0.000019230574,0.00026665576,0.00039482868,0.00071094395,0.0001360524,0.9369844,0.00007513074,0.00029660683,0.00013524802],"about_ca_topic_score_codex":0.000026941121,"about_ca_topic_score_gemma":0.000009549831,"teacher_disagreement_score":0.050592236,"about_ca_system_score_codex":0.000011200414,"about_ca_system_score_gemma":0.000034842098,"threshold_uncertainty_score":0.35721293},"labels":[],"label_agreement":null},{"id":"W2027302112","doi":"10.1053/plac.2002.0892","title":"‘Imprinting and Growth Congress’ 2002, London, UK","year":2002,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Calgary","funders":"","keywords":"Imprinting (psychology); Biology; Genetics","score_opus":0.011164740113076346,"score_gpt":0.21433378095238323,"score_spread":0.20316904083930687,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027302112","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99033237,0.002239782,0.00016483435,0.00019692328,0.00020687768,0.00009968812,0.000004045444,0.000011907582,0.0067435587],"genre_scores_gemma":[0.9944786,0.00076231884,0.0007737242,0.00022485753,0.00012278263,0.000005376481,0.000007954123,0.000016822885,0.003607571],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992124,0.000021630283,0.00014258006,0.00028681775,0.000081137216,0.0002554638],"domain_scores_gemma":[0.9996196,0.0000096491885,0.00005329713,0.00019265752,0.00003703761,0.00008774269],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000089102396,0.00012101807,0.000101441365,0.000023930214,0.000077981254,0.000040031806,0.00010998596,0.00007856404,0.0004013979],"category_scores_gemma":[0.00008365533,0.00011951791,0.000037576443,0.00004399559,0.00004969219,0.0000021285975,0.00017636854,0.0000635066,0.000057139758],"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":[0.0000101266,0.00008523468,0.48318553,0.000066656445,0.00009654076,0.0000080000655,0.00012745729,0.000008529103,0.46375123,0.00017130321,0.034036625,0.018452784],"study_design_scores_gemma":[0.0045875306,0.0006061113,0.28545228,0.00011245826,0.000093518865,0.00082894816,0.0004170802,0.0031984176,0.49145535,0.00014124262,0.21169643,0.0014106483],"about_ca_topic_score_codex":0.00002561112,"about_ca_topic_score_gemma":0.0000067803176,"teacher_disagreement_score":0.19773325,"about_ca_system_score_codex":0.0000045322313,"about_ca_system_score_gemma":0.0000049976825,"threshold_uncertainty_score":0.48737988},"labels":[],"label_agreement":null},{"id":"W2027976282","doi":"10.1016/j.ygeno.2011.10.007","title":"Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression","year":2011,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Kingston General Hospital; Queen's University; Hospital for Sick Children; BC Cancer Agency","funders":"National Institute of General Medical Sciences","keywords":"Biology; Genomic imprinting; DNA methylation; Chromosomal translocation; Genetics; Epigenetics; Chromosome; Gene; Gene expression","score_opus":0.033697568164484826,"score_gpt":0.24765140357620719,"score_spread":0.21395383541172236,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027976282","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985324,0.00016091946,0.0009959876,0.000018255263,0.000015628564,0.00013878911,0.000018027124,0.0000017056487,0.000118296804],"genre_scores_gemma":[0.9929163,0.00026481986,0.006703139,0.0000042245697,0.0000127294215,0.0000031313189,0.000051682044,0.000008824851,0.00003516646],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99922544,0.000041223284,0.0004040491,0.00016599958,0.000075723445,0.00008758763],"domain_scores_gemma":[0.999542,0.000010130408,0.00018829598,0.00016954003,0.00005550984,0.00003453528],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015669718,0.000077073455,0.00013991162,0.00008617132,0.000026620295,0.0000017239637,0.000082936065,0.000100084755,0.00001825885],"category_scores_gemma":[0.0000145768345,0.00006932619,0.00004203211,0.0000724934,0.00008211026,0.0000050815033,0.000028289383,0.000032685228,1.6530858e-7],"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":[0.00010527043,0.000055575263,0.003923646,0.00006632103,0.000008576205,1.4114103e-7,0.00088465924,0.00012378355,0.9918979,0.00002420536,0.000004748837,0.002905193],"study_design_scores_gemma":[0.0006955847,0.00022509835,0.2760101,0.000074823925,0.000012466929,0.0000058240807,0.0001423456,0.00018892981,0.72238785,0.00012437657,0.000074600146,0.000057987672],"about_ca_topic_score_codex":0.00009096949,"about_ca_topic_score_gemma":0.000021546468,"teacher_disagreement_score":0.27208647,"about_ca_system_score_codex":0.000006937933,"about_ca_system_score_gemma":0.000044188386,"threshold_uncertainty_score":0.282704},"labels":[],"label_agreement":null},{"id":"W2028231466","doi":"10.1016/j.jpeds.2006.08.077","title":"Normal minipuberty of infancy in boys with Prader-Willi syndrome","year":2006,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université de Montréal","funders":"","keywords":"Medicine; Endocrinology; Testosterone (patch); Internal medicine; Degeneration (medical); Hormone; Gonadotropin; Pathology","score_opus":0.004796305795310028,"score_gpt":0.20431633553648984,"score_spread":0.1995200297411798,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028231466","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971522,0.0016661225,0.00047430702,0.00013272214,0.0000890884,0.00006236754,0.0000024893695,9.575427e-7,0.0004197368],"genre_scores_gemma":[0.9979195,0.00041711415,0.0012415906,0.000027757056,0.0002343465,5.432289e-7,0.0000021898504,0.000011570023,0.00014536656],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991028,0.000053125368,0.00040162375,0.00006998943,0.00019786954,0.00017464864],"domain_scores_gemma":[0.99927413,0.000028902794,0.00039131386,0.00016378712,0.00010709455,0.000034789235],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004359155,0.00009426247,0.00016238842,0.00007937289,0.00002484789,0.0000074497652,0.00022213583,0.000070674185,0.000007068485],"category_scores_gemma":[0.000051431278,0.0000585021,0.000057551035,0.00018108675,0.000043617274,0.0000053621543,0.00005762836,0.00013088615,9.3403764e-7],"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":[0.00001561895,0.00014049147,0.97976387,0.00008310471,0.00001630826,0.0000079343545,0.00012079363,0.0024874231,0.015595687,0.000013081084,0.0011265778,0.0006291118],"study_design_scores_gemma":[0.00092572405,0.000850256,0.9912271,0.000017596665,0.000081741775,0.0013233506,0.00017556026,0.000015178102,0.0041845953,0.000058201862,0.0010140174,0.0001266668],"about_ca_topic_score_codex":0.000054948698,"about_ca_topic_score_gemma":0.00003217365,"teacher_disagreement_score":0.0114632435,"about_ca_system_score_codex":0.0000048146276,"about_ca_system_score_gemma":0.00010502226,"threshold_uncertainty_score":0.23856464},"labels":[],"label_agreement":null},{"id":"W2028337288","doi":"10.1002/1096-8628(20001113)95:2<182::aid-ajmg18>3.0.co;2-8","title":"Sacrococcygeal teratoma in two cases of Sotos syndrome","year":2000,"lang":"en","type":"letter","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Glenrose Rehabilitation Hospital; University of Alberta; Alberta Hospital Edmonton; University of Alberta Hospital","funders":"","keywords":"Sotos syndrome; Medicine; Pediatrics","score_opus":0.008802131237567724,"score_gpt":0.28080934008242137,"score_spread":0.27200720884485363,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028337288","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97246164,0.0029771249,0.0001432934,0.023827769,0.00032547908,0.00013559758,0.000026514772,0.0000026208495,0.000099969235],"genre_scores_gemma":[0.9418681,0.0048908773,0.0022914922,0.048588827,0.0020867526,0.0000057994157,0.000047241672,0.00008685208,0.00013402403],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9963602,0.0002656213,0.001302253,0.00034991573,0.0011978179,0.00052418356],"domain_scores_gemma":[0.9980963,0.000100295016,0.0009641296,0.00043889423,0.00015321215,0.00024718238],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005140575,0.0003572306,0.00096533645,0.0002495997,0.000024847433,0.000023001056,0.0009775151,0.0004411742,0.00025852502],"category_scores_gemma":[0.00021462856,0.00031777678,0.00034000803,0.00024756923,0.00056886877,0.0000023646942,0.00018634598,0.0012843647,0.0000056387585],"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":[0.00019476765,0.00072377606,0.031372648,0.0005281758,0.0013490883,0.018980136,0.0004049496,0.00049453444,0.015334688,0.0000020027483,0.29592082,0.6346944],"study_design_scores_gemma":[0.0033766867,0.009635628,0.01214837,0.0013310052,0.000270089,0.051726732,0.0003725373,0.000119713186,0.007550747,0.0000506019,0.912277,0.0011408781],"about_ca_topic_score_codex":0.00010395838,"about_ca_topic_score_gemma":0.000021805481,"teacher_disagreement_score":0.63355356,"about_ca_system_score_codex":0.000024530593,"about_ca_system_score_gemma":0.000717038,"threshold_uncertainty_score":0.9999274},"labels":[],"label_agreement":null},{"id":"W2028882980","doi":"10.1007/s10024001-0110-6","title":"Association of Alveolar Rhabdomyosarcoma with the Beckwith-Wiedemann Syndrome","year":2001,"lang":"en","type":"article","venue":"Pediatric and Developmental Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"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; Canada Research Chairs; University of Toronto","funders":"","keywords":"Beckwith–Wiedemann syndrome; Alveolar rhabdomyosarcoma; Hepatoblastoma; Medicine; Rhabdomyosarcoma; Pathology; Wilms' tumor; Neuroblastoma; PAX3; Embryonal rhabdomyosarcoma; Sarcoma; Internal medicine; Biology","score_opus":0.004815583387863834,"score_gpt":0.1945053870438261,"score_spread":0.18968980365596227,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028882980","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971726,0.00083219627,0.0005284837,0.0003337899,0.00005619952,0.00011963316,0.0000034045895,0.0000061492383,0.0009475471],"genre_scores_gemma":[0.9957892,0.00068294886,0.0021203898,0.00017664589,0.00006568645,0.000014170426,0.000017447122,0.000011603874,0.0011219522],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99921954,0.000048344296,0.00017422988,0.00022474903,0.0001163927,0.00021672592],"domain_scores_gemma":[0.999644,0.000028482162,0.00013307473,0.00010517452,0.000047207544,0.000042101856],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025372146,0.00011515869,0.00014224464,0.000038780443,0.00009706963,0.000009539675,0.00010455794,0.00010909832,0.000021205227],"category_scores_gemma":[0.000045306526,0.00007966896,0.00003084356,0.00011975586,0.000052793945,0.0000033767408,0.00012314427,0.000066366134,0.0000080758955],"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":[0.000014460738,0.000030455558,0.9897621,0.000013854702,0.00004380224,0.00002023976,0.00013344447,0.0000030530828,0.0076373806,0.0000117173595,0.0007865238,0.0015429676],"study_design_scores_gemma":[0.00062621024,0.0003205762,0.9886243,0.0000027979052,0.000053050942,0.0021065972,0.00038049972,0.000003785027,0.0011275985,0.000030690826,0.0065616816,0.0001622609],"about_ca_topic_score_codex":0.000009010989,"about_ca_topic_score_gemma":0.000017628197,"teacher_disagreement_score":0.0065097823,"about_ca_system_score_codex":0.000011927102,"about_ca_system_score_gemma":0.00005356028,"threshold_uncertainty_score":0.3248806},"labels":[],"label_agreement":null},{"id":"W2029294068","doi":"10.1007/s00438-002-0731-0","title":"Genomic imprinting in Drosophila is maintained by the products of Suppressor of variegation and trithorax group, but not Polycomb group, genes","year":2002,"lang":"en","type":"article","venue":"Molecular Genetics and Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Biology; Polycomb-group proteins; Genetics; Gene; Suppressor; Genomic imprinting; Variegation (histology); Gene expression; DNA methylation; Repressor","score_opus":0.008347261510660066,"score_gpt":0.2033848917433187,"score_spread":0.19503763023265863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2029294068","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9860611,0.011945242,0.0011010485,0.00033620844,0.000057864974,0.0003964093,0.000046852994,0.0000030846443,0.000052184474],"genre_scores_gemma":[0.9923091,0.0032112852,0.0041255206,0.00017720183,0.00004716574,0.000013775325,0.000030598516,0.000040049214,0.000045303874],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985043,0.00008184344,0.00050074095,0.0004775022,0.0001361539,0.00029948927],"domain_scores_gemma":[0.9991511,0.000017867473,0.00023722815,0.0004538326,0.00007322508,0.00006676201],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032370095,0.0002268482,0.0002778627,0.00006862029,0.00007450327,0.000036354853,0.00022888636,0.00015866649,0.0000057434518],"category_scores_gemma":[0.00004177134,0.0002118502,0.00006806126,0.00011635036,0.0001901083,0.0000036619097,0.00034324793,0.000100052835,4.6259441e-7],"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":[0.000017812847,0.00006106312,0.004321569,0.00006954919,0.000051147043,0.0000011744107,0.00020624988,0.00009799412,0.98494726,0.00010952953,0.000021498507,0.010095167],"study_design_scores_gemma":[0.00096837414,0.00035269855,0.034122184,0.000015291076,0.000052369956,0.000051085306,0.00015818705,0.0041515925,0.9581366,0.0002663782,0.0014523471,0.00027284765],"about_ca_topic_score_codex":0.000089318375,"about_ca_topic_score_gemma":0.000008987443,"teacher_disagreement_score":0.029800616,"about_ca_system_score_codex":0.000011270501,"about_ca_system_score_gemma":0.00001821042,"threshold_uncertainty_score":0.8639},"labels":[],"label_agreement":null},{"id":"W2029736005","doi":"10.1007/s00335-001-2095-x","title":"Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at different stages of development","year":2002,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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; Royal Victoria Hospital","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Allele; Genetics; Offspring; Imprinting (psychology); Mendelian inheritance; Genome; Embryo; Non-Mendelian inheritance; Gene; Meiotic drive; Pregnancy","score_opus":0.014799566627643063,"score_gpt":0.20804145210537517,"score_spread":0.1932418854777321,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2029736005","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99898005,0.00048548257,0.00016678887,0.000048749953,0.000030315048,0.00016532054,0.000040776686,0.0000022914123,0.00008025144],"genre_scores_gemma":[0.99680907,0.00019324009,0.00038391125,0.000015367334,0.000014790292,0.000010691601,0.000015737862,0.000017371896,0.0025398007],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99896026,0.000041880645,0.00044265416,0.00020835044,0.00013673806,0.00021011982],"domain_scores_gemma":[0.9992878,0.0000038808207,0.00023258945,0.00038903838,0.000047569138,0.000039145805],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006841503,0.00013592717,0.00021440351,0.00004497629,0.00002644488,0.000003932146,0.00032420817,0.00007185336,0.00013403317],"category_scores_gemma":[0.000011212196,0.0001063993,0.00008577879,0.0000588417,0.0000613437,0.0000015144226,0.00033668548,0.000050253897,0.0000019000025],"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":[0.0000053315443,0.000054504726,0.2866072,0.00008097094,0.000029117607,5.902293e-7,0.0002889993,0.00004661076,0.7125907,0.0000064040787,0.0000033284132,0.00028623195],"study_design_scores_gemma":[0.00021398051,0.000048878395,0.5784791,0.000016068401,0.000003726524,0.0000054527254,0.000064800246,0.000004694076,0.4200644,0.0000025903212,0.0010263639,0.00006993488],"about_ca_topic_score_codex":0.000049682196,"about_ca_topic_score_gemma":0.00019086448,"teacher_disagreement_score":0.2925263,"about_ca_system_score_codex":0.000026274314,"about_ca_system_score_gemma":0.0000121241865,"threshold_uncertainty_score":0.43388373},"labels":[],"label_agreement":null},{"id":"W2031586320","doi":"10.1006/geno.2002.6732","title":"Methylation Dynamics of Imprinted Genes in Mouse Germ Cells","year":2002,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":417,"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; Royal Victoria Hospital; Montreal Children's Hospital","funders":"","keywords":"Biology; Genomic imprinting; Methylation; DNA methylation; Genetics; Differentially methylated regions; Bisulfite sequencing; Gene; Gene expression","score_opus":0.01045759288624632,"score_gpt":0.21502962807787065,"score_spread":0.20457203519162434,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2031586320","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99506414,0.0004974632,0.0035954278,0.000030324603,0.000092611095,0.000103768914,0.0000142937615,0.000004233088,0.00059775665],"genre_scores_gemma":[0.9952704,0.000738947,0.0032333666,0.000028028362,0.0000406294,0.0000036670478,0.000029395946,0.000018006309,0.0006376121],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99933577,0.000022114144,0.00023709852,0.00018960802,0.000051360275,0.00016402581],"domain_scores_gemma":[0.99958396,0.0000054825123,0.00009296146,0.00024865606,0.00003631172,0.000032650725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001028272,0.00009209915,0.000117012685,0.000051099214,0.000017137565,0.000007640392,0.00012727261,0.00010334894,0.000036838104],"category_scores_gemma":[0.000015888072,0.000101226964,0.000056497625,0.000062220905,0.000026959979,0.0000014842431,0.00009283465,0.00004682693,0.000010174659],"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":[0.0000024750966,0.0000316009,0.0032428515,0.000011868958,0.000012844559,3.2522837e-7,0.00006259348,0.0010910431,0.9772299,0.00002643841,0.0000160979,0.018271964],"study_design_scores_gemma":[0.00035568612,0.0000834925,0.004256262,0.000003496544,0.0000066717053,0.0000066360576,0.00010028246,0.02712983,0.96565384,0.00004182886,0.0022107968,0.0001511861],"about_ca_topic_score_codex":0.00003677175,"about_ca_topic_score_gemma":0.000068135676,"teacher_disagreement_score":0.026038788,"about_ca_system_score_codex":0.000025720647,"about_ca_system_score_gemma":0.000013159629,"threshold_uncertainty_score":0.41279158},"labels":[],"label_agreement":null},{"id":"W2031791275","doi":"10.1006/geno.2000.6155","title":"Alterations of H19 Imprinting and IGF2 Replication Timing Are Infrequent in Beckwith–Wiedemann Syndrome","year":2000,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"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; Ontario Institute for Cancer Research","funders":"National Cancer Institute","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Beckwith–Wiedemann syndrome; DNA methylation; Replication timing; Genetics; Methylation; Insulin-like growth factor 2; Gene; DNA replication; Gene expression","score_opus":0.013001737606654226,"score_gpt":0.24067449648459494,"score_spread":0.2276727588779407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2031791275","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984162,0.00036565156,0.00031434468,0.00008342243,0.000025857395,0.00015266967,0.000005682375,0.000004676194,0.0006314924],"genre_scores_gemma":[0.995676,0.0003187233,0.0036574183,0.00006704485,0.000031469022,0.0000132399855,0.000027268774,0.00001394404,0.00019488513],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992122,0.00001940724,0.00027874854,0.00028778854,0.00004678952,0.00015505202],"domain_scores_gemma":[0.999476,0.000006171611,0.000103535844,0.00034905173,0.000027907787,0.000037314687],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018372262,0.00008993707,0.000123077,0.00004140813,0.00004782201,0.000017954146,0.00009184021,0.00007509552,0.000023330907],"category_scores_gemma":[0.000036267975,0.000099756355,0.000033316115,0.0000580794,0.000030606232,0.0000036355352,0.000066407374,0.00005111542,0.000004435973],"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":[0.0000074357986,0.000047338115,0.06859632,0.000056452947,0.000031840835,0.0000022828656,0.00035244186,0.002372656,0.88710153,0.00006853218,0.000025348498,0.041337825],"study_design_scores_gemma":[0.0008431442,0.00023642894,0.8534142,0.00009466425,0.000028872837,0.00035778966,0.00045461862,0.0029899548,0.13400672,0.0002698522,0.0068927654,0.000411021],"about_ca_topic_score_codex":0.000047280508,"about_ca_topic_score_gemma":0.000032249995,"teacher_disagreement_score":0.7848179,"about_ca_system_score_codex":0.000015264619,"about_ca_system_score_gemma":0.000027624732,"threshold_uncertainty_score":0.4067946},"labels":[],"label_agreement":null},{"id":"W2032030931","doi":"10.1002/ajmg.a.32669","title":"A patient with the Simpson–Golabi–Behmel syndrome displays a loss‐of‐function point mutation in <i>GPC3</i> that inhibits the attachment of this proteoglycan to the cell surface","year":2009,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Health Sciences Centre; University of Toronto; Sunnybrook Health Science Centre","funders":"","keywords":"Medicine; Chemistry","score_opus":0.005504491112100869,"score_gpt":0.23195294459630225,"score_spread":0.2264484534842014,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032030931","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9873892,0.00092038675,0.0043814033,0.006722687,0.00009296748,0.00043635842,0.0000046323325,0.0000014047936,0.00005098147],"genre_scores_gemma":[0.9977776,0.00041466948,0.00063022156,0.0010723384,0.000054867098,0.0000098506125,0.0000030035314,0.000014034745,0.000023417531],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99780864,0.0002478062,0.0005655818,0.00019332301,0.00091760186,0.00026702948],"domain_scores_gemma":[0.99857,0.00006691679,0.00069361966,0.00035328668,0.00016606023,0.00015009088],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010016819,0.000171798,0.00029273127,0.000039530652,0.0000669315,0.000018476368,0.00043029655,0.00006478717,0.000017277374],"category_scores_gemma":[0.00007692596,0.00008282432,0.0001141595,0.0003098767,0.00029066886,0.0000042005317,0.00009034164,0.0002703085,0.000001398855],"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":[0.0023506985,0.002988687,0.09120511,0.00022633087,0.0009708128,0.0002765083,0.023769643,0.09608302,0.32339564,0.000061869774,0.010063878,0.44860777],"study_design_scores_gemma":[0.0068584275,0.08678553,0.34318203,0.0015512632,0.0006888616,0.006846852,0.023389883,0.0032499735,0.46884188,0.0001437285,0.05712567,0.0013359124],"about_ca_topic_score_codex":0.00005278627,"about_ca_topic_score_gemma":0.000046352012,"teacher_disagreement_score":0.44727188,"about_ca_system_score_codex":0.000018344715,"about_ca_system_score_gemma":0.00020036,"threshold_uncertainty_score":0.33774778},"labels":[],"label_agreement":null},{"id":"W2032393199","doi":"10.1091/mbc.e06-10-0920","title":"Bsr, a Nuclear-retained RNA with Monoallelic Expression","year":2007,"lang":"en","type":"article","venue":"Molecular Biology of the Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université de Sherbrooke","funders":"European Commission","keywords":"Biology; Non-coding RNA; Intron; RNA; Transcription (linguistics); Small nucleolar RNA; Gene; Gene expression; Molecular biology; Genetics; RNA splicing; Mature messenger RNA; Cell biology","score_opus":0.004162566628859801,"score_gpt":0.21397114972129436,"score_spread":0.20980858309243455,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032393199","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9851661,0.0005858062,0.010180645,0.00012874416,0.00009196043,0.00016484463,0.0000021823125,0.000007961217,0.0036717686],"genre_scores_gemma":[0.99451625,0.000022133196,0.0047045685,0.00027175597,0.000034593708,0.0000023256318,0.000010153187,0.00002593837,0.0004122572],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990806,0.000064939006,0.00019929776,0.00028818275,0.0000815432,0.00028542874],"domain_scores_gemma":[0.9991939,0.000007929646,0.00014471372,0.0005400774,0.00005585268,0.00005750662],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022094705,0.00014886132,0.00014597217,0.00003115284,0.000070038375,0.00000543104,0.00037937902,0.00017342139,0.000018669354],"category_scores_gemma":[0.00003033681,0.000097083284,0.00012118707,0.000084204185,0.0001633036,9.877268e-7,0.00027010436,0.00009222179,0.0000051676],"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":[0.0000323065,0.000038781338,0.001935901,0.00001155774,0.000024935585,0.0000018421127,0.000034592867,0.000041092408,0.9964751,0.000051797746,0.00009779585,0.0012543023],"study_design_scores_gemma":[0.00051563006,0.00032828376,0.0038893435,0.000014957646,0.000017609342,0.000022647462,0.000078707795,0.00001573674,0.9893543,0.00009001377,0.0055380156,0.00013471715],"about_ca_topic_score_codex":0.000015176791,"about_ca_topic_score_gemma":0.0000043562836,"teacher_disagreement_score":0.009350186,"about_ca_system_score_codex":0.000005744514,"about_ca_system_score_gemma":0.000026551059,"threshold_uncertainty_score":0.39589414},"labels":[],"label_agreement":null},{"id":"W2032664909","doi":"10.1016/j.placenta.2008.02.013","title":"Morphological and Electrical Properties of Human Trophoblast Choriocarcinoma, BeWo Cells","year":2008,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"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":"PKD Foundation","keywords":"Syncytium; Syncytiotrophoblast; Cytotrophoblast; Cell biology; Cell fusion; Intracellular; Biology; Trophoblast; Cell type; Multinucleate; Cell culture; Cell; Chemistry; Placenta; Biochemistry","score_opus":0.020723166809227398,"score_gpt":0.21537077266496624,"score_spread":0.19464760585573884,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032664909","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99842554,0.0010788966,0.000027641234,0.000019087202,0.000039599454,0.00009881904,0.0000025201346,0.000005387051,0.0003025086],"genre_scores_gemma":[0.99892133,0.00024296464,0.00029313646,0.00004408997,0.00006151073,0.000005201018,0.0000070762258,0.000010148893,0.00041453133],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99931705,0.000028158342,0.00015570073,0.0002268572,0.000085085645,0.00018714595],"domain_scores_gemma":[0.99970853,0.0000032362486,0.000046582332,0.00015453728,0.000026183148,0.00006092851],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000049429476,0.00010062746,0.00013514522,0.000022178021,0.00007836273,0.0000058014293,0.00009767498,0.00008414431,0.000019719766],"category_scores_gemma":[0.000018909803,0.00008173221,0.000044757326,0.0000411586,0.00012424099,0.0000013079522,0.000110321205,0.00006128878,0.000004179436],"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":[0.000014673248,0.000052992502,0.04100493,0.0000098177425,0.000012623245,0.000004054183,0.00003969054,0.0000015794326,0.9582001,0.0000058524247,0.00044007145,0.00021360259],"study_design_scores_gemma":[0.0004429961,0.00050202274,0.09091158,0.000006952076,0.000008309059,0.00020405755,0.000035169767,0.00003841149,0.9067461,0.0000035050675,0.000990759,0.00011011786],"about_ca_topic_score_codex":0.00003170956,"about_ca_topic_score_gemma":0.000002132019,"teacher_disagreement_score":0.051453996,"about_ca_system_score_codex":0.0000051290126,"about_ca_system_score_gemma":0.000019258725,"threshold_uncertainty_score":0.33329427},"labels":[],"label_agreement":null},{"id":"W2033993581","doi":"10.1002/ajmg.1549","title":"Evidence for linkage disequilibrium between the alpha 7‐nicotinic receptor gene (CHRNA7) locus and schizophrenia in Azorean families*","year":2001,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":85,"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; Centre for Addiction and Mental Health","funders":"Medical Research Council; Medical Research Council Canada; National Institute of Mental Health; National Alliance for Research on Schizophrenia and Depression","keywords":"Biology; Genetics; Linkage disequilibrium; Transmission disequilibrium test; Exon; Locus (genetics); Genetic association; Candidate gene; Allele; Haplotype; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.027603197175483804,"score_gpt":0.3084062842291854,"score_spread":0.2808030870537016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033993581","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9835102,0.009154008,0.00404071,0.0028738186,0.00021895996,0.00017583999,0.0000070446354,0.0000030417757,0.00001635967],"genre_scores_gemma":[0.96978337,0.024244439,0.0044472525,0.00038573588,0.0010651513,0.000006376415,0.0000065683366,0.000030044152,0.00003106662],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9979462,0.00016238984,0.00070027966,0.00028032786,0.00051935157,0.00039144108],"domain_scores_gemma":[0.99854475,0.0002647784,0.00040714146,0.0003150641,0.0001258216,0.00034242013],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011768673,0.00019271902,0.00036907382,0.00007314872,0.00006470381,0.000037814905,0.00066377234,0.00013358249,0.000024446212],"category_scores_gemma":[0.0010688218,0.0001383442,0.00014373881,0.00021184537,0.0005174388,0.000005733715,0.00024424875,0.00029884372,0.000002059496],"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":[0.00020155268,0.0000848543,0.24833536,0.000033297412,0.00016028095,0.000014144502,0.00019695482,0.00005814542,0.051849496,0.0000060731586,0.0006895314,0.6983703],"study_design_scores_gemma":[0.008426997,0.014117733,0.8379306,0.0012699775,0.00043564237,0.0016132487,0.0020804368,0.001560742,0.04603878,0.00035386518,0.084815115,0.001356814],"about_ca_topic_score_codex":0.000027724733,"about_ca_topic_score_gemma":0.000017622328,"teacher_disagreement_score":0.6970135,"about_ca_system_score_codex":0.000015969983,"about_ca_system_score_gemma":0.00027505142,"threshold_uncertainty_score":0.5641513},"labels":[],"label_agreement":null},{"id":"W2034236394","doi":"10.1182/blood-2010-12-325431","title":"May-Hegglin anomaly","year":2012,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"London Health Sciences Centre","funders":"","keywords":"Medicine; Anomaly (physics); Dermatology; Gynecology","score_opus":0.009888508255464501,"score_gpt":0.23192826110470452,"score_spread":0.22203975284924002,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2034236394","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9904024,0.0015287981,0.00013959267,0.000038904625,0.00015625008,0.000051108866,0.000002063551,0.00000904752,0.007671807],"genre_scores_gemma":[0.9961387,0.00004113511,0.002076704,0.00012327381,0.00044985765,0.000006300779,0.000013287101,0.000013835085,0.0011368867],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99945956,0.000015503552,0.00009138185,0.00012629652,0.000054500077,0.00025275673],"domain_scores_gemma":[0.99965775,0.000002510756,0.000027882446,0.00021528015,0.000016605865,0.00007997863],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009818529,0.00007585568,0.00006110753,0.000013601378,0.00003423747,0.000009808113,0.00009194072,0.00006845077,0.00005453878],"category_scores_gemma":[0.000028705508,0.00007185317,0.000050101047,0.000033076485,0.000017654746,0.0000014215932,0.00008499212,0.000031906307,0.00007302552],"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":[0.0000012356433,0.00017695538,0.36644888,0.0000073933493,0.00004082598,4.983828e-7,0.000029506467,9.644327e-7,0.63023293,0.000064835906,0.00054981216,0.0024461558],"study_design_scores_gemma":[0.00070251507,0.00012618654,0.3611489,0.000004852529,0.00003701173,0.00012722211,0.000054200525,0.0000023660689,0.5436796,0.000012765894,0.093914844,0.00018957064],"about_ca_topic_score_codex":0.0000082179595,"about_ca_topic_score_gemma":0.0000015709461,"teacher_disagreement_score":0.093365036,"about_ca_system_score_codex":0.0000012423512,"about_ca_system_score_gemma":0.00001276365,"threshold_uncertainty_score":0.2930087},"labels":[],"label_agreement":null},{"id":"W203558109","doi":"10.69645/gwdb6005","title":"Imprinting disorders associated with molecular changes on chromosome 11p15","year":2014,"lang":"en","type":"article","venue":"˜The œbiomedical & life sciences collection.","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Chromosome; Biology; Genetics; Gene; DNA methylation","score_opus":0.00827545662295314,"score_gpt":0.23322259708629792,"score_spread":0.22494714046334477,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W203558109","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9834481,0.00016705423,0.007212128,0.0032500422,0.0005901839,0.00027592547,0.0000032254147,0.00004333709,0.0050099953],"genre_scores_gemma":[0.99730533,0.000045201876,0.00031882254,0.0012932335,0.00027322522,0.000041927986,0.000013980653,0.000018293662,0.0006899812],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9981322,0.00015264447,0.00019594718,0.0005169859,0.0005352527,0.0004669468],"domain_scores_gemma":[0.9992673,0.00007734147,0.0001372981,0.00027403922,0.000059965983,0.00018407147],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008796663,0.00018604792,0.00016394065,0.000100622754,0.00069769187,0.000070652255,0.00044006118,0.00013113441,0.000036147863],"category_scores_gemma":[0.0004937123,0.000121468525,0.00007108377,0.00088618527,0.0007029097,0.0000032871812,0.000154384,0.00014985539,0.000012513069],"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":[0.00011650167,0.0013536533,0.03584326,0.000090176356,0.00079938775,0.0000075175262,0.00070686237,0.003282054,0.8107292,0.0010866801,0.031188121,0.11479656],"study_design_scores_gemma":[0.008197148,0.027327092,0.19070224,0.0004961476,0.00027865267,0.00022838125,0.0024563377,0.051233474,0.06471224,0.0016936442,0.6493161,0.0033585688],"about_ca_topic_score_codex":0.000058139303,"about_ca_topic_score_gemma":0.00024430026,"teacher_disagreement_score":0.746017,"about_ca_system_score_codex":0.00002273196,"about_ca_system_score_gemma":0.00016216036,"threshold_uncertainty_score":0.5366152},"labels":[],"label_agreement":null},{"id":"W2035693514","doi":"10.1067/mpd.2003.82","title":"Hypercalciuria in Beckwith-Wiedemann syndrome","year":2003,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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":"Nephrocalcinosis; Medicine; Hypercalciuria; Beckwith–Wiedemann syndrome; Gastroenterology; Hyperuricosuria; Internal medicine; Urology; Incidence (geometry); Metabolic disorder; Endocrinology; Urine; Kidney","score_opus":0.009807503404749344,"score_gpt":0.23377623133643285,"score_spread":0.22396872793168351,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2035693514","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99513745,0.003081307,0.000582926,0.000115751325,0.00028955584,0.00005438799,7.9517395e-7,0.000001181794,0.00073665334],"genre_scores_gemma":[0.9972441,0.0012374807,0.0009975887,0.0001022588,0.0001810257,5.228479e-7,6.001832e-7,0.000012782027,0.00022360588],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991209,0.00012171691,0.00032934904,0.00007727111,0.00016058132,0.00019019116],"domain_scores_gemma":[0.9994626,0.000032341755,0.00018961943,0.00017957871,0.00007641585,0.000059444556],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009875664,0.00009115458,0.00013745898,0.00007201608,0.000039234652,0.000012109426,0.00023102615,0.00007882963,0.000017836048],"category_scores_gemma":[0.00030591004,0.00006193057,0.00007395881,0.00016120421,0.000027237975,0.0000031728189,0.00004395723,0.0001539268,0.0000080539585],"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":[0.00013912239,0.0007119519,0.6879053,0.0002594223,0.00011197095,0.0002204666,0.0013377914,0.0057652197,0.28318828,0.0006844328,0.01321416,0.006461842],"study_design_scores_gemma":[0.00677384,0.0042903833,0.85333383,0.000081091246,0.00062249985,0.025889434,0.0032941776,0.000052889045,0.039395005,0.0029166488,0.06202151,0.0013286857],"about_ca_topic_score_codex":0.000004993264,"about_ca_topic_score_gemma":0.0000046150844,"teacher_disagreement_score":0.24379328,"about_ca_system_score_codex":0.000011426706,"about_ca_system_score_gemma":0.000095263866,"threshold_uncertainty_score":0.25254554},"labels":[],"label_agreement":null},{"id":"W2036611166","doi":"10.1002/ajmg.a.30020","title":"<i>CDKN1C</i> mutation in Wiedemann–Beckwith syndrome patients reduces RNA splicing efficiency and identifies a splicing enhancer","year":2004,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"RNA splicing; Beckwith–Wiedemann syndrome; Genetics; Enhancer; Exonic splicing enhancer; Mutation; Biology; RNA; Computational biology; Gene; Gene expression; DNA methylation","score_opus":0.005352674133553476,"score_gpt":0.2548464087881549,"score_spread":0.24949373465460142,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036611166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9955939,0.001181482,0.0024326255,0.00035694745,0.00026850935,0.00011152873,0.0000013656598,0.0000032587288,0.0000503693],"genre_scores_gemma":[0.9965731,0.0016621416,0.0013385692,0.00024282272,0.00013334089,0.0000043705827,0.000004297784,0.000022310189,0.00001902759],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99798733,0.00007207015,0.00066481886,0.00028352643,0.0006588743,0.00033338423],"domain_scores_gemma":[0.9989891,0.000027034836,0.00044735614,0.00016001787,0.00012791634,0.00024859275],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005722374,0.00017773427,0.00033969054,0.00012501371,0.0000660994,0.00004183391,0.00027594907,0.000094024275,0.0000120010955],"category_scores_gemma":[0.00027011373,0.00015577985,0.000078066245,0.00023268805,0.00029609742,0.000008540775,0.00013785237,0.00021290744,0.000002487054],"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":[0.00019849159,0.001330336,0.08250072,0.00020726245,0.00046922412,0.00045064656,0.0057718637,0.013900319,0.4346794,0.000033853503,0.000303522,0.46015435],"study_design_scores_gemma":[0.01450608,0.01862651,0.5192755,0.003893946,0.0003539721,0.0069819796,0.009032996,0.0012938653,0.4199761,0.0006474982,0.003247826,0.0021637506],"about_ca_topic_score_codex":0.00006587651,"about_ca_topic_score_gemma":0.00003528901,"teacher_disagreement_score":0.45799062,"about_ca_system_score_codex":0.00002809141,"about_ca_system_score_gemma":0.00020018105,"threshold_uncertainty_score":0.6352518},"labels":[],"label_agreement":null},{"id":"W2036775365","doi":"10.1159/000268822","title":"No Effect of Parental Age on Risk of Multiple Sclerosis: A Population-Based Study","year":2009,"lang":"en","type":"article","venue":"Neuroepidemiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine; Multiple sclerosis; Population; Pediatrics; Demography; Environmental health; Psychiatry","score_opus":0.0224120161089832,"score_gpt":0.27600682344375904,"score_spread":0.25359480733477585,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036775365","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99920017,0.000067240006,0.00007468483,0.00002103783,0.0001574076,0.00035065762,0.000018387986,0.000007388093,0.00010302571],"genre_scores_gemma":[0.999335,0.000020075662,0.00028959627,0.00020319915,0.000058431517,0.000012885267,0.000052624073,0.000012348105,0.000015823674],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99819,0.0007194237,0.00044370344,0.00035211528,0.00008378032,0.00021099987],"domain_scores_gemma":[0.9989017,0.0002926013,0.0003083919,0.00040945737,0.00003845234,0.000049388993],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004824167,0.00016280198,0.00042301984,0.000053270374,0.00003709777,0.0000020087236,0.00016166593,0.000103258615,0.000008379518],"category_scores_gemma":[0.0023155191,0.00013448767,0.00016154909,0.00006324695,0.000032778727,0.0000010356359,0.000038942053,0.00010142334,0.0000044583935],"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":[0.00011933418,0.00017669122,0.81643826,0.000011311317,0.000024453582,0.000001048157,0.0000062702397,0.001655588,0.17886633,0.0000020066816,0.00006851367,0.0026301774],"study_design_scores_gemma":[0.0012775956,0.009157643,0.9602197,0.000017640801,0.00003698794,0.000001855844,0.0000061078326,0.0004681059,0.028627835,0.000010164855,0.00008492132,0.00009146126],"about_ca_topic_score_codex":0.00016880796,"about_ca_topic_score_gemma":0.000019169398,"teacher_disagreement_score":0.1502385,"about_ca_system_score_codex":0.0000049859145,"about_ca_system_score_gemma":0.000011357828,"threshold_uncertainty_score":0.5484248},"labels":[],"label_agreement":null},{"id":"W2038744986","doi":"10.1002/mc.20126","title":"DNA methylation in the CTCF‐binding site I and the expression pattern of the <i>H19</i> gene: Does positive expression predict poor prognosis in early stage head and neck carcinomas?","year":2005,"lang":"en","type":"article","venue":"Molecular Carcinogenesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Princess Margaret Cancer Centre; University of Toronto; Ontario Institute for Cancer Research","funders":"Fundação para o Desenvolvimento da UNESP; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Division of Materials Research; Fundação de Amparo à Pesquisa do Estado de São Paulo","keywords":"CTCF; Biology; Methylation; Gene silencing; DNA methylation; Genomic imprinting; Imprinting (psychology); Cancer research; Gene; Molecular biology; Chromatin; Gene expression; Genetics; Enhancer","score_opus":0.00651171642146533,"score_gpt":0.2160510322379391,"score_spread":0.20953931581647375,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2038744986","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99592173,0.0024840198,0.00028183332,0.00043890942,0.0000398896,0.00075214717,0.000041269974,0.0000032155647,0.000036980866],"genre_scores_gemma":[0.9990187,0.0001960604,0.0003892661,0.0001944131,0.000046728397,0.00008443169,0.000022634707,0.000025193887,0.000022533333],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.998068,0.0006047453,0.00034895897,0.0004323419,0.0002678186,0.0002781614],"domain_scores_gemma":[0.9993157,0.000054350425,0.00016955838,0.00036970284,0.00004690914,0.000043824464],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005975946,0.00021695983,0.00022147005,0.00006768886,0.0001450234,0.000047987432,0.00025801547,0.00014203489,0.0000018038048],"category_scores_gemma":[0.00006421926,0.00011315328,0.000110214314,0.00017033363,0.00014578918,0.000012533271,0.00032552428,0.00014188026,3.863267e-7],"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":[0.000029183679,0.00002434415,0.3209528,0.000018661754,0.000010436827,0.0000023781824,0.001022164,0.000051428455,0.67584956,0.0000012923174,0.0000028747863,0.002034861],"study_design_scores_gemma":[0.0008267824,0.000054190907,0.4304654,0.000061108556,0.000022667744,0.000009950713,0.00025786436,0.00013191598,0.56803614,0.000003712208,0.000041542167,0.000088709],"about_ca_topic_score_codex":0.0003672151,"about_ca_topic_score_gemma":0.00017895589,"teacher_disagreement_score":0.109512605,"about_ca_system_score_codex":0.000015451576,"about_ca_system_score_gemma":0.000027108827,"threshold_uncertainty_score":0.46142566},"labels":[],"label_agreement":null},{"id":"W2039283181","doi":"10.1203/pdr.0b013e3180457660","title":"Growth Regulation, Imprinted Genes, and Chromosome 11p15.5","year":2007,"lang":"en","type":"review","venue":"Pediatric Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":116,"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","funders":"","keywords":"Genomic imprinting; Biology; Epigenetics; Genetics; Imprinting (psychology); Gene; DNA methylation; Beckwith–Wiedemann syndrome; Gene duplication; Gene expression","score_opus":0.08896719396499418,"score_gpt":0.40192033114789316,"score_spread":0.31295313718289897,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2039283181","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0022936198,0.9955963,0.00017604438,0.000015079351,0.00016563293,0.00067245413,0.00001609474,0.0000147311775,0.0010500428],"genre_scores_gemma":[0.00045202463,0.9945832,0.00059841655,0.000007760627,0.0020786533,0.00007036564,0.0002116224,0.00008507664,0.0019129046],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9969152,0.00030548507,0.00060065126,0.00086933404,0.00053992757,0.0007693947],"domain_scores_gemma":[0.99837786,0.00012779637,0.00017242346,0.00065318466,0.00041732407,0.00025141684],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0019244866,0.00034731193,0.00065264036,0.0005214073,0.00020293098,0.00009732278,0.00048366401,0.0006160916,0.000065640765],"category_scores_gemma":[0.00045492745,0.00030453064,0.00022398145,0.0008009218,0.00012923572,0.0000032901917,0.00082746183,0.00052260526,0.00009205135],"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":[0.0000030695517,0.000043074564,0.00088345597,0.0075373994,0.0000883265,0.000008452338,0.000011239643,1.6285453e-7,0.00028249764,0.00006742249,0.002430061,0.98864484],"study_design_scores_gemma":[0.0001772212,0.00015919041,0.00074630365,0.00018997487,0.000115736984,0.00017290373,0.000008268009,0.0000035344,0.00010631599,0.000055427972,0.99791235,0.0003527985],"about_ca_topic_score_codex":0.00004814169,"about_ca_topic_score_gemma":0.000004193493,"teacher_disagreement_score":0.99548227,"about_ca_system_score_codex":0.00004704444,"about_ca_system_score_gemma":0.00045883562,"threshold_uncertainty_score":0.9999407},"labels":[],"label_agreement":null},{"id":"W2040096570","doi":"10.1038/oby.2005.224","title":"Evaluation of Prader‐Willi Syndrome Gene <i>MAGEL2</i> in Severe Childhood‐Onset Obesity","year":2005,"lang":"en","type":"article","venue":"Obesity Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"University of Alberta; Wellcome Trust","keywords":"Obesity; Medicine; Gene; Genomic imprinting; Neurodevelopmental disorder; Internal medicine; Allele; Endocrinology; Genetics; Bioinformatics; Biology; Gene expression","score_opus":0.04253667839914183,"score_gpt":0.3377563221438153,"score_spread":0.29521964374467347,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040096570","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99632746,0.0010934953,0.000033521424,0.00032275214,0.0000443536,0.00054550817,0.000018362542,0.000006879486,0.0016076431],"genre_scores_gemma":[0.99791205,0.00024857253,0.001124511,0.00004128303,0.00010681535,0.000032461732,0.000060876573,0.000021326194,0.00045208426],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9967855,0.00070500677,0.00032789065,0.0004907075,0.0011633888,0.0005275074],"domain_scores_gemma":[0.9986389,0.000033739776,0.00007405247,0.0005959628,0.0005428531,0.000114456976],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0052305534,0.00014949044,0.00021572268,0.0001622518,0.00012311958,0.000028593377,0.00038014268,0.00020653185,0.00017296898],"category_scores_gemma":[0.0005744741,0.00015591807,0.00008630339,0.00035608144,0.00012467161,0.000009712876,0.0003760232,0.00029030748,0.00007050011],"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":[0.000008626666,0.0013198003,0.6963819,0.00010227756,0.00012690455,0.00000495814,0.00052286073,0.0015417738,0.26325807,0.000016869404,0.0016388306,0.035077114],"study_design_scores_gemma":[0.0009686297,0.00027006023,0.9322932,0.000039481976,0.000020427895,0.00017233586,0.000121711986,0.0005320989,0.063903585,0.00016386878,0.0013329269,0.0001816669],"about_ca_topic_score_codex":0.00015793672,"about_ca_topic_score_gemma":0.00022917964,"teacher_disagreement_score":0.2359113,"about_ca_system_score_codex":0.000084297986,"about_ca_system_score_gemma":0.0003790214,"threshold_uncertainty_score":0.63581544},"labels":[],"label_agreement":null},{"id":"W2040114279","doi":"10.1139/g01-013","title":"Imprinting and deviation from Mendelian transmission ratios","year":2001,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Royal Victoria Hospital","funders":"McGill University","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Allele; Mendelian inheritance; Gene; Gene expression","score_opus":0.009623054575879447,"score_gpt":0.22403843145084426,"score_spread":0.2144153768749648,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040114279","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97554684,0.0010437213,0.022150796,0.00015177242,0.00004435858,0.000083688275,0.0000026647444,0.000008971577,0.00096720736],"genre_scores_gemma":[0.99411446,0.0004209904,0.0048309783,0.000110266825,0.00015067031,0.0000047971353,0.00006277857,0.000011959231,0.00029310165],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994246,0.000017640177,0.0001302872,0.00022633561,0.00005677332,0.00014439554],"domain_scores_gemma":[0.99973917,0.0000035620014,0.00003878006,0.00013634117,0.000022112865,0.000060024155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000080568665,0.000082053884,0.00006976405,0.000020205316,0.00007230582,0.000025728365,0.000061218656,0.00006694754,0.00006690858],"category_scores_gemma":[0.000011718091,0.00007952226,0.000028239916,0.000038736493,0.000012781815,0.000002449762,0.00004729089,0.000034564473,0.000010373731],"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":[0.000002784864,0.0000062842632,0.0066789766,0.000003224028,0.000012006816,6.068798e-7,0.00006658158,0.000021059635,0.95249695,0.0000063203547,0.0000053830267,0.040699843],"study_design_scores_gemma":[0.0010422688,0.00021439907,0.69938016,0.000019798166,0.000033999157,0.00006904512,0.00030138163,0.0006975173,0.1297409,0.00046908052,0.16759625,0.00043523507],"about_ca_topic_score_codex":0.000037807542,"about_ca_topic_score_gemma":0.000006423074,"teacher_disagreement_score":0.82275605,"about_ca_system_score_codex":0.0000045185875,"about_ca_system_score_gemma":0.000013878834,"threshold_uncertainty_score":0.32428235},"labels":[],"label_agreement":null},{"id":"W2040929679","doi":"10.1074/jbc.m110.162347","title":"Epigenetic Silencing of β-Spectrin, a TGF-β Signaling/Scaffolding Protein in a Human Cancer Stem Cell Disorder","year":2010,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute","keywords":"Biology; Epigenetics; Cancer research; Gene silencing; Cancer; Genetics; Cell biology; Gene","score_opus":0.01288980656884443,"score_gpt":0.2508291214340931,"score_spread":0.23793931486524866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040929679","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99799323,0.0014228291,0.00010999854,0.0000361993,0.000067824876,0.00010961342,0.000003984776,0.0000031467152,0.0002531499],"genre_scores_gemma":[0.9985976,0.00013124158,0.000863531,0.000015282374,0.00024808268,0.0000094377565,0.0000027445979,0.000013984761,0.000118086886],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.998619,0.000036121193,0.0006556759,0.00024679024,0.00015134423,0.00029102285],"domain_scores_gemma":[0.9990287,0.000018421111,0.00052026234,0.0001954547,0.00012957225,0.00010762622],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003961936,0.00017715029,0.00032747752,0.000037536436,0.000041710442,0.0000144868645,0.00033283676,0.0002934051,0.00014382071],"category_scores_gemma":[0.000071719565,0.0001381516,0.0001856575,0.00011257916,0.00011133937,0.0000032909954,0.00011972793,0.00035139528,4.8172154e-7],"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":[0.000018390054,0.00011714898,0.036218125,0.000072176575,0.000019983305,0.000006010255,0.000035506688,0.000104043684,0.96179205,0.0000023832642,0.0000072783673,0.0016069085],"study_design_scores_gemma":[0.00061491906,0.00027727778,0.009884425,0.00008973296,0.000011175156,0.000048457594,0.0002497456,0.000017521636,0.9882792,0.000060688224,0.00029872468,0.00016813703],"about_ca_topic_score_codex":0.00002095988,"about_ca_topic_score_gemma":0.00000810381,"teacher_disagreement_score":0.02648715,"about_ca_system_score_codex":0.00001738632,"about_ca_system_score_gemma":0.00009061387,"threshold_uncertainty_score":0.5633659},"labels":[],"label_agreement":null},{"id":"W2041081418","doi":"10.1159/000350525","title":"Update on Body Composition and Bone Density in Children with Prader-Willi Syndrome","year":2013,"lang":"en","type":"article","venue":"Hormone Research in Paediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"","keywords":"Lean body mass; Medicine; Internal medicine; Endocrinology; Bone mineral; Obesity; Fat mass; Bone density; Body fat percentage; Body weight; Osteoporosis","score_opus":0.014919690099754681,"score_gpt":0.26866408874493014,"score_spread":0.25374439864517545,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041081418","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99687076,0.0019451461,0.00004983933,0.0004144388,0.000014549359,0.00057150464,0.0000045376332,0.0000062541976,0.00012298556],"genre_scores_gemma":[0.99628997,0.0027904694,0.00063908927,0.000051645737,0.00006279196,0.000053490527,0.00006391423,0.000021104877,0.000027519498],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983672,0.00016071441,0.00020859893,0.00041567604,0.0003421495,0.0005056543],"domain_scores_gemma":[0.9994194,0.000031526375,0.000043896005,0.00028195578,0.000089764966,0.00013346992],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000636639,0.00013809277,0.00016352463,0.0002876521,0.000078183046,0.000064810534,0.00013298506,0.00014804037,0.0000042870183],"category_scores_gemma":[0.000052138792,0.00012231071,0.000022746604,0.00042585877,0.000101065954,0.000009622911,0.00020986362,0.00034241975,0.00003207659],"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":[0.000009722335,0.00023871931,0.9500504,0.000017794368,0.000023865825,0.000011120392,0.000028517094,0.000055680408,0.045462646,0.00004190773,0.0009653871,0.00309425],"study_design_scores_gemma":[0.00092383183,0.0007942477,0.99596566,0.000011789461,0.000003888107,0.00022526288,0.00003790675,0.0001599326,0.0014912308,0.00011662844,0.000107671985,0.0001619332],"about_ca_topic_score_codex":0.00027623805,"about_ca_topic_score_gemma":0.00001892557,"teacher_disagreement_score":0.045915287,"about_ca_system_score_codex":0.00003494174,"about_ca_system_score_gemma":0.000053712443,"threshold_uncertainty_score":0.4987686},"labels":[],"label_agreement":null},{"id":"W2041342968","doi":"10.1515/jpem.2000.13.s1.845","title":"Gonadotropin-dependent Sexual Precocity in a Boy Affected by Pseudohypoparathyroidism","year":2000,"lang":"en","type":"article","venue":"Journal of Pediatric Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"University of Toronto","keywords":"Pseudohypoparathyroidism; Hyperphosphatemia; Internal medicine; Medicine; Endocrinology; Precocious puberty; Basal (medicine); Vitamin D and neurology; Gynecomastia; Testosterone (patch); Thyroid; Hormone; Parathyroid hormone; Calcium","score_opus":0.006460576607177535,"score_gpt":0.23201299209491064,"score_spread":0.2255524154877331,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041342968","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9662653,0.032884233,0.00007904214,0.00017713004,0.00027974223,0.00009568222,0.000009139498,0.000004091042,0.00020563845],"genre_scores_gemma":[0.98189956,0.015791794,0.00054678664,0.00012804045,0.00073853915,0.000005001554,0.0000049947685,0.0000140888105,0.00087118486],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986441,0.00014865349,0.00045440122,0.00024692848,0.00012621381,0.00037968045],"domain_scores_gemma":[0.9994592,0.000015485688,0.0001978185,0.00015126241,0.000056880086,0.00011934417],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019467813,0.00017225914,0.00032525568,0.00012196464,0.000051597766,0.000016497966,0.00018347631,0.00014779526,0.00005317524],"category_scores_gemma":[0.00007791215,0.00015265238,0.00007279956,0.00010821401,0.000042524287,0.0000100675215,0.0000520791,0.0002852127,0.000006439697],"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":[0.00033268018,0.001154654,0.15524517,0.00008053926,0.00043380258,0.00021127862,0.0005183434,0.0002304088,0.67265385,0.00014391076,0.026233293,0.1427621],"study_design_scores_gemma":[0.0060079074,0.0009116625,0.9266842,0.000004898309,0.0002613917,0.0028848867,0.00024974596,0.000018143754,0.016363196,0.00020518331,0.04591071,0.0004980698],"about_ca_topic_score_codex":0.00003532829,"about_ca_topic_score_gemma":0.000011633247,"teacher_disagreement_score":0.771439,"about_ca_system_score_codex":0.000007920614,"about_ca_system_score_gemma":0.00007224308,"threshold_uncertainty_score":0.6224984},"labels":[],"label_agreement":null},{"id":"W2041665669","doi":"10.1038/ejhg.2015.38","title":"Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1","year":2015,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Graduate School, University of Maryland","keywords":"Brachydactyly; Biology; Frameshift mutation; Genetics; Noggin; Phenotype; Anatomy; Bone morphogenetic protein; Gene; Endocrinology","score_opus":0.043439506672161135,"score_gpt":0.2688178148046308,"score_spread":0.22537830813246967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041665669","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965453,0.0009320649,0.00091213814,0.000044984958,0.00020549148,0.00007175368,0.0000046790356,0.000004554263,0.0012790408],"genre_scores_gemma":[0.9973628,0.00003648045,0.001832151,0.0001207061,0.00032789577,2.2783244e-7,0.000013967196,0.00005953288,0.0002462502],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99856657,0.00022179564,0.00045780092,0.0002115674,0.00026637487,0.00027592265],"domain_scores_gemma":[0.99859565,0.0000086844175,0.0004947661,0.00026397826,0.00036647727,0.00027041597],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007709483,0.00017954136,0.00020756102,0.0000927858,0.000059012444,0.00006468021,0.0002541277,0.000032454816,0.000010130574],"category_scores_gemma":[0.00025420194,0.00015789425,0.000062936204,0.00013910462,0.000059867943,0.0000063571006,0.00013628296,0.00018394287,0.000006016251],"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":[0.0002396583,0.00089201354,0.4398525,0.000035514586,0.00031263873,0.0011021943,0.0006952397,0.014973502,0.53815544,0.00002138663,0.0015416117,0.0021782788],"study_design_scores_gemma":[0.004715365,0.0021250816,0.9862688,0.00029044776,0.00010265814,0.0003666663,0.0003886135,0.00020279802,0.0033289124,0.000034362343,0.0017586534,0.00041762934],"about_ca_topic_score_codex":0.0000021707433,"about_ca_topic_score_gemma":0.000020964299,"teacher_disagreement_score":0.5464163,"about_ca_system_score_codex":0.000030304645,"about_ca_system_score_gemma":0.00014836875,"threshold_uncertainty_score":0.64387405},"labels":[],"label_agreement":null},{"id":"W2043170079","doi":"10.1016/j.ydbio.2003.10.017","title":"Murine numb regulates granule cell maturation in the cerebellum","year":2003,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":44,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Direction de l’hospitalisation et de l’offre de Soins; McGill University; U.S. Department of Energy","keywords":"NUMB; Biology; Granule cell; Cerebellum; Cell biology; Neurogenesis; Progenitor cell; Notch signaling pathway; Centrosome; Granule (geology); Neuroscience; Stem cell; Cell; Signal transduction; Central nervous system; Cell cycle; Genetics; Dentate gyrus","score_opus":0.00725058020780578,"score_gpt":0.2146110699844447,"score_spread":0.20736048977663893,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043170079","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.990107,0.00027819403,0.00009793907,0.00010238811,0.00014868804,0.00014471958,0.00000244959,0.0000048569373,0.009113784],"genre_scores_gemma":[0.995419,0.000068785,0.0034871586,0.00033625806,0.000032106473,0.000013815799,0.00012685801,0.00000858067,0.0005074319],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992103,0.000101174825,0.00018087447,0.00023724147,0.0000427152,0.00022767446],"domain_scores_gemma":[0.99977326,0.000010318474,0.00004428746,0.00013383219,0.000015619948,0.000022672806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000214645,0.000111575806,0.000087444256,0.000029914701,0.00006590637,0.000013221258,0.00014794935,0.0001104551,0.00006467664],"category_scores_gemma":[0.000031910582,0.00008265237,0.000032315,0.000089204266,0.000047963855,0.0000017850356,0.00004985185,0.00006234196,0.0000378965],"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":[0.000009810125,0.00005539436,0.039682955,0.000008682374,0.000010102202,0.0000016217336,0.00020222194,0.0000039723036,0.95706415,0.00025224156,0.00066084374,0.0020480268],"study_design_scores_gemma":[0.0006750999,0.00013461294,0.1365247,0.000005431947,0.000003917113,0.00018387483,0.00081920763,0.00000670015,0.7440948,0.00049195014,0.116819955,0.0002397403],"about_ca_topic_score_codex":0.000019962697,"about_ca_topic_score_gemma":0.000039002723,"teacher_disagreement_score":0.21296933,"about_ca_system_score_codex":0.000011525333,"about_ca_system_score_gemma":0.000039609866,"threshold_uncertainty_score":0.33704656},"labels":[],"label_agreement":null},{"id":"W2046155010","doi":"10.1126/science.1228633","title":"An Exon Splice Enhancer Primes IGF2:IGF2R Binding Site Structure and Function Evolution","year":2012,"lang":"en","type":"article","venue":"Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Canada's Michael Smith Genome Sciences Centre","funders":"Cancer Research UK; Wellcome Trust","keywords":"Enhancer; Exon; splice; Function (biology); Genetics; Computational biology; Biology; Gene; Transcription factor","score_opus":0.006335964942303857,"score_gpt":0.24666241209349718,"score_spread":0.24032644715119333,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046155010","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99571437,0.0011084435,0.0025309057,0.0000106866,0.0003479228,0.00007100604,0.0000036185813,0.000008658632,0.00020440936],"genre_scores_gemma":[0.99812037,0.000036252128,0.0014661168,0.000036396257,0.00020857166,0.0000022259437,0.000009616524,0.000006020286,0.000114449685],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992109,0.000015552576,0.00007841508,0.00027543702,0.00013345452,0.00028623934],"domain_scores_gemma":[0.9995907,0.00000231839,0.000046642894,0.00020439719,0.00004613823,0.00010982477],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025940363,0.00007952154,0.000051268657,0.00004543426,0.00019815397,0.000035946083,0.00010859772,0.00005751509,0.000018735927],"category_scores_gemma":[0.00003409856,0.000070728565,0.000014188971,0.00015757735,0.00014016278,0.00003055077,0.00008807606,0.000043155862,0.000008941418],"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":[0.00000217196,0.000008191857,0.05162484,0.000004311916,0.0000017359149,2.1159353e-8,0.00007381451,0.000010260909,0.94175124,0.000021582871,0.0000122852725,0.0064895693],"study_design_scores_gemma":[0.00007940847,0.000113896465,0.50681764,0.0000055348423,0.000006458494,0.000020330877,0.00011030856,0.00013799833,0.49019846,0.000023864472,0.0023842617,0.00010179576],"about_ca_topic_score_codex":0.00001650317,"about_ca_topic_score_gemma":0.0000063642638,"teacher_disagreement_score":0.45519283,"about_ca_system_score_codex":0.00001713921,"about_ca_system_score_gemma":0.000046295423,"threshold_uncertainty_score":0.2884227},"labels":[],"label_agreement":null},{"id":"W2046258358","doi":"10.1016/j.jpag.2008.01.026","title":"Incipient/Premature Ovarian Failure in a Teenage Girl with the Van Wyk Grumbach Syndrome","year":2008,"lang":"en","type":"article","venue":"Journal of Pediatric and Adolescent Gynecology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Medicine; Premature ovarian failure; Ovarian hyperstimulation syndrome; Girl; Controlled ovarian hyperstimulation; Pediatrics; Gynecology; Population; Pregnancy; Infertility","score_opus":0.006194630991661926,"score_gpt":0.20220537655381443,"score_spread":0.1960107455621525,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046258358","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99621516,0.0018696398,0.0003256984,0.0011767346,0.00015252634,0.00015012738,0.0000019802887,0.000002627367,0.000105497726],"genre_scores_gemma":[0.9966452,0.0016846558,0.00064144016,0.00039155048,0.00039017975,0.0000027435683,0.000002703197,0.000016326341,0.00022519744],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99888146,0.00010138045,0.000345674,0.00020748995,0.00015717142,0.00030680766],"domain_scores_gemma":[0.9992777,0.000036745205,0.00031156887,0.00017513303,0.00008938478,0.00010944057],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029591567,0.00016679389,0.00027008142,0.00011884077,0.000115134295,0.000014802648,0.00022956131,0.00018968739,0.000020930767],"category_scores_gemma":[0.000089048146,0.00010394071,0.00008113623,0.00018350754,0.000094681374,0.0000075406533,0.00012098802,0.00037234786,0.0000027503877],"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":[0.000101628444,0.00037271163,0.97818464,0.00010730262,0.00010714439,0.0005666747,0.00034551986,0.0002627675,0.005594241,0.000025377109,0.012832395,0.0014995972],"study_design_scores_gemma":[0.0018033384,0.0010233609,0.97708744,0.000020577256,0.000075399425,0.0070420653,0.00034208674,0.000013081102,0.00012768872,0.000023447239,0.012253919,0.00018762272],"about_ca_topic_score_codex":0.0000027150347,"about_ca_topic_score_gemma":0.000031995758,"teacher_disagreement_score":0.0064753904,"about_ca_system_score_codex":0.000017749291,"about_ca_system_score_gemma":0.00014429311,"threshold_uncertainty_score":0.4238579},"labels":[],"label_agreement":null},{"id":"W2046632949","doi":"10.1002/ajmg.a.20458","title":"Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature","year":2003,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":76,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Kingston General Hospital; Queen's University; McMaster University; Hamilton Health Sciences; Hamilton Regional Laboratory Medicine Program","funders":"","keywords":"Karyotype; Genetic counseling; Genetics; Chromosome analysis; Chromosome; Phenotype; Biology; Gene","score_opus":0.01306908285347114,"score_gpt":0.29288358884756444,"score_spread":0.2798145059940933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046632949","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.009752559,0.98902494,0.00009030078,0.00052085036,0.00020255966,0.00035748066,0.000020938083,0.000001647338,0.000028720542],"genre_scores_gemma":[0.0009874009,0.9957015,0.0021927087,0.00070079457,0.0001990158,0.0000060946927,0.000012924456,0.000054457953,0.00014512156],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99705243,0.0004487632,0.001065975,0.0003997037,0.00070143834,0.00033166792],"domain_scores_gemma":[0.99717873,0.00006176334,0.001445449,0.00055777613,0.00018821715,0.00056805124],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00083871046,0.00044300227,0.0016204903,0.00007795029,0.000070507915,0.000039636623,0.0004915466,0.00030073838,0.000040744737],"category_scores_gemma":[0.00042993366,0.00025433273,0.00034007308,0.00044401636,0.0005293397,0.0000036659847,0.00028262593,0.0006658766,7.6614657e-7],"study_design_candidate":"design_other","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":[0.0000032358219,0.00005786078,0.00027398864,0.013287332,0.0006048969,0.00033348225,0.000074151336,5.04105e-7,0.000008260549,0.000004247818,0.0049385307,0.9804135],"study_design_scores_gemma":[0.00034852017,0.0014915861,0.00010192879,0.055017814,0.0009440906,0.13748346,0.00007046998,0.0000010638963,0.0000051250036,0.000005000768,0.80425286,0.00027806134],"about_ca_topic_score_codex":0.000014017745,"about_ca_topic_score_gemma":0.000006451586,"teacher_disagreement_score":0.98013544,"about_ca_system_score_codex":0.000012805386,"about_ca_system_score_gemma":0.001350356,"threshold_uncertainty_score":0.9999909},"labels":[],"label_agreement":null},{"id":"W2047164593","doi":"10.1159/000213487","title":"Increased Nuchal Translucency and Other Ultrasound Findings in a Case of Simpson-Golabi-Behmel Syndrome","year":2008,"lang":"en","type":"article","venue":"Fetal Diagnosis and Therapy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McMaster University Medical Centre","funders":"","keywords":"Medicine; Macroglossia; Polyhydramnios; Nuchal Translucency Measurement; Proband; Prenatal diagnosis; Fetal echocardiography; Fetus; Craniosynostosis; Obstetrics; Gestation; Nuchal translucency; Pregnancy; Anatomy; Pathology; Tongue; Genetics; Mutation","score_opus":0.015762748595486802,"score_gpt":0.243726719434031,"score_spread":0.2279639708385442,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047164593","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9929169,0.0066677392,0.000018678384,0.000033813365,0.000035349018,0.00019863174,0.000032598316,0.0000044418584,0.0000918938],"genre_scores_gemma":[0.9886578,0.010865565,0.00022914643,0.00014072872,0.000021923543,0.0000350126,0.0000066953166,0.000020673539,0.000022455546],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99920535,0.000036314494,0.00021240198,0.0002822221,0.00006524743,0.00019847814],"domain_scores_gemma":[0.9996683,0.000042166437,0.000046659003,0.00014710093,0.000018574156,0.00007718542],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011576089,0.00015565849,0.00021575822,0.00005373508,0.00006780047,0.0000121124785,0.000062730134,0.00011312917,0.000048183996],"category_scores_gemma":[0.000026200321,0.00013946438,0.000063301224,0.000081428574,0.00012374441,0.000005179791,0.000023370712,0.000060489052,8.0987814e-7],"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":[0.000046510326,0.00031942868,0.862115,0.000036158493,0.000072064744,0.00020234258,0.0005964354,0.0000028796642,0.12572412,0.000027177774,0.00004675115,0.01081109],"study_design_scores_gemma":[0.0029846164,0.001366363,0.92984194,0.00006386826,0.000015679845,0.008863504,0.00023192992,0.00003703605,0.05255621,0.00006852837,0.0035958951,0.00037444476],"about_ca_topic_score_codex":0.00066202413,"about_ca_topic_score_gemma":0.00006756874,"teacher_disagreement_score":0.07316792,"about_ca_system_score_codex":0.0000031368459,"about_ca_system_score_gemma":0.000018253706,"threshold_uncertainty_score":0.56871927},"labels":[],"label_agreement":null},{"id":"W2047811624","doi":"10.1016/s0304-3835(00)00347-5","title":"Loss of IGF-II imprinting in endometrial tumors: overexpression in carcinosarcoma","year":2000,"lang":"en","type":"article","venue":"Cancer Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto; St. Michael's Hospital","funders":"Medical Research Council","keywords":"Carcinosarcoma; Endometrium; Biology; Endometrial cancer; Cancer research; Imprinting (psychology); Endocrinology; Gene; Internal medicine; Cancer; Carcinoma; Medicine; Genetics","score_opus":0.009034487653785363,"score_gpt":0.24710054909120052,"score_spread":0.23806606143741516,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047811624","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988679,0.0003725454,0.000018495333,0.00021499641,0.00007363202,0.00013080268,0.0000053332637,0.0000031198397,0.00031315372],"genre_scores_gemma":[0.99913126,0.00009088179,0.00020890348,0.0002958124,0.00016301603,0.000020691932,0.0000070846236,0.000014072464,0.00006824864],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990235,0.000040211475,0.0002918807,0.00027339676,0.00010054756,0.0002704837],"domain_scores_gemma":[0.99966115,0.000011405856,0.00007146953,0.00020821941,0.000012381711,0.000035398396],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013348158,0.00011271208,0.00017510809,0.0000964386,0.00002302158,0.0000068756917,0.00016278648,0.00006684373,0.00013848215],"category_scores_gemma":[0.000039939438,0.000113562346,0.00006297849,0.0001795707,0.000045503886,0.000003757284,0.00009676672,0.00009596852,0.0000020336931],"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":[0.000029478886,0.000022121412,0.19454506,0.000022481336,0.0000055254964,0.0000038731396,0.00009542876,0.0006232627,0.7952598,0.0000012609905,0.00009797272,0.009293787],"study_design_scores_gemma":[0.0023901167,0.000104958635,0.37131247,0.0003193703,0.0000036819315,0.000012212436,0.0000414653,0.00009590688,0.62304157,0.000009366006,0.0024536662,0.00021523217],"about_ca_topic_score_codex":0.0006143932,"about_ca_topic_score_gemma":0.00004364901,"teacher_disagreement_score":0.17676741,"about_ca_system_score_codex":0.000029871318,"about_ca_system_score_gemma":0.00004073403,"threshold_uncertainty_score":0.46309382},"labels":[],"label_agreement":null},{"id":"W2047876270","doi":"10.1007/s00467-013-2461-4","title":"Bone metabolism in the fetus and neonate","year":2013,"lang":"en","type":"review","venue":"Pediatric Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre","funders":"","keywords":"Internal medicine; Fetus; Endocrinology; Medicine; Calcitriol; Calcium metabolism; Fetal circulation; Parathyroid hormone; Bone remodeling; Calcium; Calcitonin; Placenta; Pregnancy; Biology","score_opus":0.017632468209040082,"score_gpt":0.2702975116756923,"score_spread":0.25266504346665225,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047876270","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.012275317,0.986617,0.000015469644,0.00008102257,0.00021454024,0.00057499454,0.000008213109,0.000005510661,0.00020790187],"genre_scores_gemma":[0.00047021807,0.99727094,0.00031671536,0.00041908422,0.0010327261,0.00019589957,0.000060836246,0.00003582743,0.00019776344],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99821323,0.00031504425,0.0004570701,0.0005001116,0.0000961091,0.00041841876],"domain_scores_gemma":[0.9991676,0.00007289228,0.00022769166,0.0004474553,0.00002526117,0.000059077043],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003887818,0.00032856298,0.000796423,0.00015473527,0.000051973642,0.000034150005,0.0003576891,0.00047926596,0.000037452355],"category_scores_gemma":[0.00007552832,0.00021722712,0.00018939828,0.0002216674,0.000064668595,0.0000018744897,0.00029031158,0.00030380543,0.00005333444],"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":[0.0000014592249,0.000029966697,0.000103665174,0.001131028,0.000060313807,0.000011044941,0.000038484235,4.5323978e-7,0.000038336526,0.000058415066,0.002958097,0.99556875],"study_design_scores_gemma":[0.00018899297,0.0000660001,0.00083282666,0.000017031189,0.00037493955,0.0005052516,0.000010676921,0.0000011997608,7.843856e-7,0.00006022328,0.99772084,0.00022120762],"about_ca_topic_score_codex":0.00005246791,"about_ca_topic_score_gemma":0.000010912155,"teacher_disagreement_score":0.9953475,"about_ca_system_score_codex":0.000005021401,"about_ca_system_score_gemma":0.000098900324,"threshold_uncertainty_score":0.8858265},"labels":[],"label_agreement":null},{"id":"W2047900106","doi":"10.1007/s00427-008-0267-3","title":"Genomic Imprinting in Drosophila has properties of both mammalian and insect imprinting","year":2008,"lang":"en","type":"article","venue":"Development Genes and Evolution","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"National Research Council Canada; Dalhousie University; Mount Allison University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Genetics; Drosophila melanogaster; Gene silencing; Gene; Somatic cell; DNA methylation; Gene expression","score_opus":0.026688093591510816,"score_gpt":0.2013895589304301,"score_spread":0.17470146533891928,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047900106","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99615175,0.0032565654,0.00030342134,0.000032705248,0.00005525984,0.00013155166,5.2368415e-7,0.0000058701157,0.000062358944],"genre_scores_gemma":[0.9958606,0.0005943019,0.0033758557,0.000014828565,0.000044369943,0.000011413865,0.000005463451,0.0000134984675,0.00007970083],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990977,0.000023477496,0.00029999836,0.00028026602,0.00007596797,0.00022257165],"domain_scores_gemma":[0.99971884,0.0000024336578,0.00009282223,0.00010748419,0.00003351249,0.000044893583],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020379697,0.00012953779,0.00014505046,0.00007537055,0.00016240246,0.000015949206,0.00006327418,0.0000835072,0.0000015718705],"category_scores_gemma":[0.00002126219,0.00012464178,0.000023875478,0.0000631727,0.00009586212,0.0000058992828,0.00020814972,0.00004771375,9.024298e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000005033967,0.000010426894,0.38956124,0.00003868216,0.000008985309,5.163613e-7,0.00028316915,0.000017944318,0.60458964,0.0000082477445,0.0000020399439,0.005474086],"study_design_scores_gemma":[0.0003251206,0.00004378366,0.8421507,0.000035685523,0.000003371211,0.000084882246,0.00015321537,0.0001884519,0.15613617,0.0000110837045,0.00071897084,0.00014860202],"about_ca_topic_score_codex":0.00016504967,"about_ca_topic_score_gemma":0.000055886183,"teacher_disagreement_score":0.45258942,"about_ca_system_score_codex":0.000020236233,"about_ca_system_score_gemma":0.00010459815,"threshold_uncertainty_score":0.50827444},"labels":[],"label_agreement":null},{"id":"W2048726057","doi":"10.1136/bcr-2013-202729","title":"Prolonged spontaneous normocalcaemia in pseudohypoparathyroidism from resorption of soft tissue calcium deposits: a cautionary tale","year":2014,"lang":"en","type":"article","venue":"BMJ Case Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"","keywords":"Medicine; Pseudohypoparathyroidism; Hypocalcaemia; Calcium; Calcitriol; Parathyroid hormone; Hyperphosphatemia; Internal medicine; Osteodystrophy; Soft tissue; Calcinosis; Calcification; Endocrinology; Surgery","score_opus":0.010873681568878631,"score_gpt":0.2665576406642031,"score_spread":0.2556839590953245,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2048726057","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99619496,0.00067153084,0.0021522501,0.000045352677,0.00016271051,0.00039674895,0.0000060515986,0.000012115019,0.00035825203],"genre_scores_gemma":[0.9979036,0.000012258412,0.0014531427,0.0000432875,0.0001730839,0.00004982634,0.0001283029,0.000021952319,0.00021455862],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.99850106,0.000094299394,0.00057450583,0.0004378271,0.00015790347,0.00023442598],"domain_scores_gemma":[0.99902725,0.000021550215,0.0002869489,0.00051136024,0.000070684786,0.000082213875],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035366943,0.00015915213,0.00023029516,0.000051546438,0.00004807712,0.000011793079,0.00005326208,0.00020253786,0.000011683238],"category_scores_gemma":[0.00024939363,0.00016126601,0.00007040536,0.00008290139,0.00005111576,0.0000040225164,0.00010858739,0.00008943271,0.000005614434],"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":[0.00004438492,0.000095430594,0.013397975,0.00002581168,0.000025378373,0.06011983,0.00008795953,0.0003632872,0.9205212,0.00000466229,0.00027216313,0.00504193],"study_design_scores_gemma":[0.0005140169,0.00040206124,0.057576258,0.00004948432,0.000043178974,0.65615326,0.00008504103,0.00076010963,0.28096086,0.00014343127,0.0029666459,0.00034562696],"about_ca_topic_score_codex":0.00077410846,"about_ca_topic_score_gemma":0.0004778553,"teacher_disagreement_score":0.63956034,"about_ca_system_score_codex":0.000022100161,"about_ca_system_score_gemma":0.00008226341,"threshold_uncertainty_score":0.6576237},"labels":[],"label_agreement":null},{"id":"W2050173466","doi":"10.3109/17518423.2012.676101","title":"Neurodevelopmental outcomes in children with Angelman syndrome after 1 year of behavioural intervention","year":2012,"lang":"en","type":"article","venue":"Developmental Neurorehabilitation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; Hamilton Health Sciences; McMaster Children's Hospital","funders":"Hamilton Health Sciences","keywords":"Angelman syndrome; Intervention (counseling); Cognition; Psychology; Randomized controlled trial; Clinical psychology; Pediatrics; Medicine; Physical therapy; Psychiatry","score_opus":0.00925460367021961,"score_gpt":0.22461933935163925,"score_spread":0.21536473568141964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050173466","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994487,0.00004239395,0.00003353387,0.000016061203,0.00008832452,0.00030635466,0.000009075695,0.000007362593,0.00004816145],"genre_scores_gemma":[0.9939191,0.0000033861318,0.0058163977,0.000033928318,0.000007553457,0.000058998423,0.00009132177,0.000022208005,0.000047131198],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990403,0.000054721226,0.00029926564,0.00022428032,0.00015069709,0.00023075416],"domain_scores_gemma":[0.9997157,0.000008116081,0.00008182392,0.000113159986,0.000027298747,0.00005388933],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014867289,0.00014332047,0.00013757402,0.0000964376,0.000021978834,0.000008381939,0.00008662986,0.000052426534,0.000029266841],"category_scores_gemma":[0.00003372174,0.00013033528,0.000056300265,0.00011272626,0.000056639772,0.000020202373,0.000092548435,0.00005844662,0.000008066637],"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":[0.000019253916,0.0001928337,0.98840535,0.000012121912,0.000021302189,5.142141e-7,0.00024544942,0.0000022747333,0.009502978,0.000003148761,0.0000043001196,0.0015904903],"study_design_scores_gemma":[0.00068959553,0.00030822094,0.993178,0.00002365719,0.000007920522,0.000108132685,0.0002740768,9.564463e-7,0.005238967,0.000002686962,0.000013886995,0.00015388886],"about_ca_topic_score_codex":0.000034353892,"about_ca_topic_score_gemma":0.000024562567,"teacher_disagreement_score":0.0057828636,"about_ca_system_score_codex":0.000027771686,"about_ca_system_score_gemma":0.00002173678,"threshold_uncertainty_score":0.5314919},"labels":[],"label_agreement":null},{"id":"W2050466071","doi":"10.1101/gr.077115.108","title":"Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, <i>TFPI2</i>/<i>Tfpi2</i>, which requires EHMT2 and EED for allelic-silencing","year":2008,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"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","funders":"Medical Research Council; Sickkids Research Institute; Medical Research Council Canada; Agence Nationale de la Recherche; Hospital for Sick Children; Wellcome Trust; Genome Canada; Wellbeing of Women; March of Dimes Foundation","keywords":"Biology; Genomic imprinting; Histone; Genetics; DNA methylation; Imprinting (psychology); Molecular biology; Histone methylation; Gene; Gene expression","score_opus":0.07297829103464612,"score_gpt":0.3466313032178899,"score_spread":0.2736530121832438,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050466071","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994373,0.003554845,0.00037774543,0.00006968756,0.000025817792,0.0010920926,0.00016060374,0.000016090009,0.00033007833],"genre_scores_gemma":[0.994319,0.0020139792,0.0021711264,0.000022976526,0.00015790288,0.00014663098,0.0003741614,0.000042866333,0.0007513093],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99674916,0.0002420542,0.0006565418,0.0010042506,0.0004914913,0.0008564727],"domain_scores_gemma":[0.9980606,0.000088870045,0.0002061613,0.00067821017,0.0006838657,0.00028229976],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0011003849,0.00032533854,0.00077492016,0.00049717247,0.0005696013,0.000071141534,0.00038958693,0.00022874994,0.000060678758],"category_scores_gemma":[0.00009282102,0.00032276183,0.00017563706,0.0008845302,0.00062619615,0.0000171869,0.00064810563,0.00025841853,0.0000032585356],"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":[0.00007634789,0.00011765574,0.0070959544,0.00011795955,0.0006519198,0.0000045118713,0.0011061729,0.00005716157,0.99042815,0.000046893147,0.00018237521,0.00011491379],"study_design_scores_gemma":[0.002504235,0.0020682765,0.14622271,0.000050004783,0.00018175611,0.0001494316,0.0013751969,0.0008046733,0.84356874,0.000054293163,0.0023376888,0.0006829635],"about_ca_topic_score_codex":0.00010327941,"about_ca_topic_score_gemma":0.00008819497,"teacher_disagreement_score":0.14685936,"about_ca_system_score_codex":0.000059722523,"about_ca_system_score_gemma":0.00013413835,"threshold_uncertainty_score":0.99992245},"labels":[],"label_agreement":null},{"id":"W2050592293","doi":"10.1093/humrep/dem268","title":"A survey of assisted reproductive technology births and imprinting disorders","year":2007,"lang":"en","type":"article","venue":"Human Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":165,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Hospital for Sick Children","keywords":"Genomic imprinting; Imprinting (psychology); Angelman syndrome; Assisted reproductive technology; Allele; Epigenetics; Medicine; Cohort; Uniparental disomy; Genetics; Pregnancy; Gene; Biology; Internal medicine; DNA methylation; Infertility; Chromosome","score_opus":0.017189344132017354,"score_gpt":0.2766048440626119,"score_spread":0.25941549993059454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050592293","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974506,0.00075939094,0.00092386536,0.00008157951,0.00016539237,0.00016566199,0.0000013035277,0.00002237091,0.0004298241],"genre_scores_gemma":[0.9984729,0.00006172054,0.0009727142,0.0000046711602,0.00013515384,0.0000044505027,0.00002209863,0.000017891118,0.00030840051],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9987077,0.000041115953,0.00028882027,0.0006856025,0.00008062233,0.00019615257],"domain_scores_gemma":[0.9989825,0.000006709032,0.00018727644,0.0006229372,0.00017177191,0.00002879363],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001349654,0.00010815952,0.00013886628,0.00013365452,0.00010336991,0.000008335039,0.00008314565,0.0001150391,0.0000045101465],"category_scores_gemma":[0.00064844504,0.00011362231,0.00003176261,0.00025121597,0.00016638143,0.0000027737751,0.00013996394,0.00008376757,9.383342e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000009118029,0.000037107042,0.2355902,0.000016935352,0.000026195677,1.4881036e-7,0.00004106672,0.0000041456965,0.6879829,0.00004522417,0.000015194094,0.07623172],"study_design_scores_gemma":[0.00016700935,0.0001646133,0.75322896,0.0000068844,0.0000072618823,0.000038299968,0.00016235324,0.0000022458976,0.24524312,0.00013380677,0.0007484615,0.00009700241],"about_ca_topic_score_codex":0.00025150014,"about_ca_topic_score_gemma":0.00031925715,"teacher_disagreement_score":0.51763874,"about_ca_system_score_codex":0.000008181332,"about_ca_system_score_gemma":0.000014879294,"threshold_uncertainty_score":0.46333832},"labels":[],"label_agreement":null},{"id":"W2050939151","doi":"10.1007/s10549-008-0042-1","title":"Mutations of the MYH gene do not substantially contribute to the risk of breast cancer","year":2008,"lang":"en","type":"article","venue":"Breast Cancer Research and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Women's College Hospital; University of Toronto","funders":"","keywords":"Breast cancer; Gene; Medicine; Oncology; Cancer; Genetics; Mutation; Biology; Internal medicine; Cancer research","score_opus":0.02861996030288757,"score_gpt":0.31702780802881747,"score_spread":0.2884078477259299,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050939151","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9931235,0.0020895435,0.000041999647,0.0021947282,0.00005505944,0.0004299477,0.0019853786,0.0000018071378,0.00007806401],"genre_scores_gemma":[0.99416655,0.004957976,0.000073266376,0.000028040651,0.000110764275,0.00015270927,0.000008714238,0.000011337301,0.0004906484],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99893796,0.00010473474,0.0001713838,0.00023570914,0.00026762192,0.00028260026],"domain_scores_gemma":[0.9991099,0.000026974103,0.000078424375,0.0003485349,0.0003394613,0.00009670093],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001787533,0.000108342494,0.00014420919,0.000032694203,0.00026636705,0.000012710174,0.00017875864,0.000044215212,0.00006154032],"category_scores_gemma":[0.000017635813,0.000058537455,0.00008212632,0.00018637777,0.00024056778,0.0000022612905,0.00013186055,0.000062203835,0.0000013548027],"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":[0.0006003537,0.00044194033,0.5534496,0.00003328662,0.0010832279,0.000006066586,0.0009022627,0.00084202434,0.36524612,0.000092629954,0.0011663751,0.07613614],"study_design_scores_gemma":[0.0008441469,0.0002302423,0.86309445,0.000027179663,0.00003870111,0.00012987497,0.00009508318,0.00001970988,0.13382798,0.000016827596,0.0016119335,0.00006385768],"about_ca_topic_score_codex":0.007168092,"about_ca_topic_score_gemma":0.0017516294,"teacher_disagreement_score":0.30964488,"about_ca_system_score_codex":0.00004363282,"about_ca_system_score_gemma":0.0003275221,"threshold_uncertainty_score":0.99944323},"labels":[],"label_agreement":null},{"id":"W2051494278","doi":"10.1002/ajmg.a.32144","title":"Paternal deletion 6q24.3: A new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance","year":2008,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; McMaster University","funders":"","keywords":"Biology; Frontal Bossing; Genetics; Brachycephaly; Phenotype; Genomic imprinting; Short stature; Breakpoint; Anatomy; Chromosome; Gene; Gene expression; Skull","score_opus":0.008252025591810189,"score_gpt":0.20964208383381613,"score_spread":0.20139005824200595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051494278","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994891,0.0003751536,0.0042670416,0.00022235898,0.00012449836,0.00009243611,0.000008405962,0.0000059598647,0.0000131771485],"genre_scores_gemma":[0.995006,0.0015365039,0.0029256167,0.00021050873,0.00023715515,0.0000033850336,0.000013480195,0.00003075268,0.000036593126],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9980375,0.00009087555,0.00054493913,0.0002710511,0.0006812386,0.000374397],"domain_scores_gemma":[0.99873817,0.000017053484,0.00043600457,0.00010415902,0.000170433,0.00053415954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028068328,0.00023350275,0.00039902,0.000071484596,0.00009444915,0.00003639232,0.0002863021,0.00012123844,0.00003609764],"category_scores_gemma":[0.00017591947,0.00019684627,0.0000790843,0.00015066392,0.00045330814,0.000009428213,0.00012341782,0.00025439242,0.000004232129],"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":[0.000348325,0.0003083654,0.9074441,0.000027573718,0.0011596796,0.0016339663,0.0007775493,0.000014939574,0.030497437,0.000007235905,0.00040586336,0.057374924],"study_design_scores_gemma":[0.0019351931,0.004419323,0.96677005,0.00014896819,0.00006463384,0.02262009,0.00009716267,0.00006893616,0.0016341355,0.000009507713,0.001885299,0.0003467087],"about_ca_topic_score_codex":0.00008846813,"about_ca_topic_score_gemma":0.00004449538,"teacher_disagreement_score":0.059325904,"about_ca_system_score_codex":0.000023614146,"about_ca_system_score_gemma":0.00043496978,"threshold_uncertainty_score":0.8027158},"labels":[],"label_agreement":null},{"id":"W2051574088","doi":"10.1002/ajmg.a.31323","title":"Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":83,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Ontario Institute for Cancer Research; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Epigenetics; Wilms' tumor; Methylation; DNA methylation; Uniparental disomy; Cancer research; Beckwith–Wiedemann syndrome; Biology; Tumor progression; Cancer; Internal medicine; Chromosome; Karyotype; Oncology; Gene; Genetics; Medicine","score_opus":0.006484700487838024,"score_gpt":0.24059588803180695,"score_spread":0.23411118754396892,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051574088","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99524266,0.001119512,0.002596264,0.0006881803,0.00008242638,0.0001985064,0.00004155433,0.000010483422,0.000020420712],"genre_scores_gemma":[0.9919031,0.00021057136,0.0075963526,0.00011884083,0.00009720197,0.00001576528,0.000027984834,0.000017011602,0.000013165768],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99819005,0.000081241975,0.00049597333,0.0003696672,0.00052925973,0.00033382807],"domain_scores_gemma":[0.9988054,0.00008207389,0.0006220099,0.00019648089,0.00018419558,0.00010983531],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00068917096,0.00020375024,0.00045238208,0.0000865664,0.000086757515,0.000030564726,0.0002342269,0.00013046834,0.000006275898],"category_scores_gemma":[0.0006193868,0.0001523903,0.00007896925,0.00030470605,0.0010304822,0.0000061464298,0.00008202945,0.00026996448,2.8184581e-7],"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":[0.00020642667,0.00040861245,0.95473474,0.000019459538,0.0010448797,0.0001359551,0.00014925514,0.00041234036,0.016547477,0.000053215186,0.00086891337,0.025418729],"study_design_scores_gemma":[0.020518318,0.022518283,0.8390473,0.0017901519,0.0011733301,0.0073549137,0.005283209,0.00076066656,0.07311957,0.0007216095,0.025761122,0.0019514997],"about_ca_topic_score_codex":0.000038725866,"about_ca_topic_score_gemma":0.000032555035,"teacher_disagreement_score":0.115687415,"about_ca_system_score_codex":0.00002758786,"about_ca_system_score_gemma":0.00032985938,"threshold_uncertainty_score":0.6214296},"labels":[],"label_agreement":null},{"id":"W2051640192","doi":"10.4161/rdis.24421","title":"Leptin signaling defects in a mouse model of Prader-Willi syndrome","year":2013,"lang":"en","type":"article","venue":"Rare Diseases","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Alberta Heritage Foundation for Medical Research; University of Alberta; Canadian Institutes of Health Research; Women and Children's Health Research Institute; Children's Health Research Institute","keywords":"Leptin; Cell biology; Internal medicine; Chemistry; Endocrinology; Neuroscience; Biology; Medicine; Obesity","score_opus":0.011602234532805683,"score_gpt":0.2238802197965938,"score_spread":0.21227798526378813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051640192","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998371,0.0008166873,0.00041656793,0.000026370699,0.000021083693,0.00021589367,0.000034372824,0.000009875482,0.000088141365],"genre_scores_gemma":[0.9985709,0.000035873207,0.000820962,0.00007147362,0.000019001509,0.00004600007,0.000044818626,0.00002109293,0.0003698811],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99918854,0.00003051804,0.00020714985,0.00024582696,0.00010185598,0.00022611787],"domain_scores_gemma":[0.9995333,0.000011220327,0.00007076954,0.00024389247,0.000048680253,0.00009211351],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000036946214,0.00012363496,0.0001567574,0.00004947968,0.000024619207,0.000017244158,0.00013973452,0.000071648166,0.000052174226],"category_scores_gemma":[0.00009056898,0.00011970019,0.00009688459,0.000061845865,0.00003611366,0.0000054620205,0.00009536489,0.000040376137,0.00001202221],"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":[0.0000014632673,0.00012790824,0.10944181,0.00009371787,0.000024534393,0.0000010172744,0.000048607508,0.0062893,0.8828688,0.0000133573585,0.00014198465,0.0009474858],"study_design_scores_gemma":[0.0021598972,0.0006405938,0.4511913,0.00025204074,0.000084862826,0.00006979705,0.00087432103,0.017484356,0.5252294,0.00082066306,0.00017621873,0.0010165271],"about_ca_topic_score_codex":0.00004704835,"about_ca_topic_score_gemma":0.0000046612604,"teacher_disagreement_score":0.3576394,"about_ca_system_score_codex":0.000006881228,"about_ca_system_score_gemma":0.00005812946,"threshold_uncertainty_score":0.4881232},"labels":[],"label_agreement":null},{"id":"W2052272439","doi":"10.1007/s10024-005-1154-9","title":"Beckwith-Wiedemann Syndrome: Historical, Clinicopathological, and Etiopathogenetic Perspectives","year":2005,"lang":"en","type":"review","venue":"Pediatric and Developmental Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":197,"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":"","keywords":"Beckwith–Wiedemann syndrome; Macroglossia; Medicine; Omphalocele; Hemihypertrophy; Wilms' tumor; Rhabdomyosarcoma; Haploinsufficiency; Hydronephrosis; Costello syndrome; Pediatrics; Hepatoblastoma; Pathology; Anatomy; Internal medicine; Pregnancy; Cancer; Tongue; Fetus; Genetics; Sarcoma; Biology","score_opus":0.030959401645255777,"score_gpt":0.29186141433675933,"score_spread":0.26090201269150354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052272439","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.048192553,0.9504778,0.000085118525,0.000027386857,0.00026433088,0.00047692202,0.000025328407,0.000029217526,0.00042137108],"genre_scores_gemma":[0.0025594519,0.98767394,0.007423399,0.00007878713,0.00049905013,0.00012891307,0.000094989766,0.00007517747,0.0014663063],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9968393,0.00024121597,0.00084767735,0.001356953,0.00015993252,0.00055494],"domain_scores_gemma":[0.99895483,0.000074476535,0.00037163237,0.00029843912,0.000052537303,0.00024805553],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004418194,0.00065720244,0.001357182,0.00022623391,0.00022753232,0.000049486254,0.00026427442,0.0008504293,0.00005811381],"category_scores_gemma":[0.000225477,0.0005647652,0.00023542957,0.00020105965,0.00020189134,0.000005498661,0.00075283716,0.00035800107,0.00006976692],"study_design_candidate":"design_other","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":[0.0000073305628,0.00020319087,0.0046593104,0.0021642419,0.000076009135,0.00025828174,0.000255501,2.1632997e-7,0.000047263133,0.000017655933,0.001588724,0.9907223],"study_design_scores_gemma":[0.00043035648,0.0006277679,0.00739375,0.00016802584,0.0005369693,0.017541222,0.00025904356,4.981514e-7,0.0000010050561,0.000021081056,0.9720758,0.0009444361],"about_ca_topic_score_codex":0.0000033168585,"about_ca_topic_score_gemma":0.0000027500766,"teacher_disagreement_score":0.98977786,"about_ca_system_score_codex":0.000113333444,"about_ca_system_score_gemma":0.00027403267,"threshold_uncertainty_score":0.9996804},"labels":[],"label_agreement":null},{"id":"W2052515804","doi":"10.4161/epi.25812","title":"Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome","year":2013,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Pediatric Oncology Group","funders":"","keywords":"Beckwith–Wiedemann syndrome; DNA methylation; Methylation; Biology; Epigenetics; Reproductive technology; Macroglossia; Genetics; Internal medicine; Endocrinology; Pathology; Pregnancy; Medicine; Gene","score_opus":0.013296094425825944,"score_gpt":0.2591895653496462,"score_spread":0.24589347092382027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052515804","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97616935,0.0014380779,0.020165196,0.00015840125,0.00019188863,0.00043309078,0.0000107221995,0.000017462646,0.0014158097],"genre_scores_gemma":[0.9850607,0.00018330023,0.013398482,0.00009033124,0.000048992755,0.00006224941,0.00017608344,0.000036261168,0.0009435886],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9982589,0.00011840465,0.0005070285,0.00051117997,0.00019205357,0.00041247084],"domain_scores_gemma":[0.9989597,0.000051800736,0.0001875667,0.00050299213,0.00017968431,0.00011822979],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025616374,0.0002404272,0.00031593267,0.0002666663,0.00011210259,0.000060748505,0.00023714361,0.00021727357,0.00017711113],"category_scores_gemma":[0.00019740901,0.00024446673,0.00017324566,0.0007244955,0.0000807584,0.000010615865,0.00018070088,0.00012967161,0.00017057953],"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":[0.000018277728,0.00025458212,0.18551862,0.000042814823,0.0011490771,0.0000057254374,0.000880412,0.020344473,0.7716556,0.0007702837,0.00028859806,0.019071542],"study_design_scores_gemma":[0.00034908456,0.00046879877,0.9775531,0.000010719169,0.00021150307,0.000006460591,0.00038699442,0.0069821556,0.011713828,0.0012223939,0.0006943294,0.00040058084],"about_ca_topic_score_codex":0.00034383818,"about_ca_topic_score_gemma":0.0004420677,"teacher_disagreement_score":0.7920345,"about_ca_system_score_codex":0.000027774753,"about_ca_system_score_gemma":0.00006997615,"threshold_uncertainty_score":0.99690646},"labels":[],"label_agreement":null},{"id":"W2053330159","doi":"10.1002/ajmg.a.32030","title":"Severe presentation of Beckwith–Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15","year":2007,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University Medical Centre; Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Beckwith–Wiedemann syndrome; Macroglossia; Hepatoblastoma; Uniparental disomy; Medicine; Gigantism; Genetics; Biology; Internal medicine; Karyotype; Chromosome; Pathology; DNA methylation; Gene","score_opus":0.015576308560413263,"score_gpt":0.2805095904989016,"score_spread":0.26493328193848836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053330159","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97618014,0.00028776226,0.022947446,0.00011995481,0.00018748829,0.00015021091,0.000089584166,0.0000019838458,0.00003543145],"genre_scores_gemma":[0.9959574,0.00010477669,0.0036331073,0.000061237915,0.00014153888,0.0000032522855,0.000046632158,0.000016410875,0.000035685807],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99782336,0.00006785351,0.0007939261,0.00018109543,0.00084915786,0.0002846209],"domain_scores_gemma":[0.998099,0.0001004653,0.0009993673,0.00014856044,0.00040672632,0.00024582617],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00080602,0.00015791418,0.00043137427,0.00008074467,0.00004182315,0.000008032246,0.0003127301,0.00011254237,0.000056478224],"category_scores_gemma":[0.00029014243,0.00012776158,0.00014838575,0.00015732399,0.0010179195,0.0000055408577,0.00007739934,0.00012883013,3.6136885e-7],"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":[0.0010993892,0.0020263246,0.61948353,0.00030018445,0.0038209232,0.00016143963,0.00071802264,0.003336115,0.3044865,0.0006730018,0.00073943724,0.06315512],"study_design_scores_gemma":[0.006830174,0.014558163,0.8577155,0.00088077044,0.000366863,0.002990048,0.0014013557,0.0002442092,0.112721,0.00018123434,0.001559649,0.0005510476],"about_ca_topic_score_codex":0.000020330443,"about_ca_topic_score_gemma":0.000018139715,"teacher_disagreement_score":0.23823196,"about_ca_system_score_codex":0.00002157108,"about_ca_system_score_gemma":0.0004285204,"threshold_uncertainty_score":0.52099663},"labels":[],"label_agreement":null},{"id":"W2053631009","doi":"10.1111/j.1528-1167.2006.00969.x","title":"Lamotrigine Therapy of Epilepsy with Angelman's Syndrome","year":2007,"lang":"en","type":"article","venue":"Epilepsia","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":29,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; Hôpital Notre-Dame","funders":"","keywords":"Lamotrigine; Carbamazepine; Medicine; Valproic Acid; Phenytoin; Clonazepam; Levetiracetam; Epilepsy; Topiramate; Tolerability; Pediatrics; Angelman syndrome; Generalized epilepsy; Anesthesia; Oxcarbazepine; Adverse effect; Internal medicine; Psychiatry","score_opus":0.00889768180664113,"score_gpt":0.2369867826109439,"score_spread":0.22808910080430278,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053631009","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99181205,0.0010136422,0.003846374,0.000050920007,0.00009441085,0.00016134593,0.0000037001325,0.000012773231,0.0030047772],"genre_scores_gemma":[0.99511766,0.00022852352,0.0038115089,0.00011359953,0.000089088506,0.0000051075913,0.00002269463,0.00002817189,0.00058364245],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990335,0.000019614667,0.00023324447,0.00026810274,0.00014832053,0.00029722022],"domain_scores_gemma":[0.9993475,0.000013513531,0.00011191334,0.00037578313,0.00007064766,0.00008063107],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029878152,0.00014936949,0.00018287635,0.000056160126,0.000037893496,0.000007883899,0.00017791444,0.000099269,0.00006691103],"category_scores_gemma":[0.00001791983,0.00011954021,0.00007313928,0.0001377326,0.0000818514,0.0000024745607,0.00004988073,0.00006735882,0.000011098059],"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":[0.00014502254,0.00019145336,0.3391993,0.000039139082,0.00018051869,0.000040418083,0.000089032495,0.000046804264,0.6328186,0.0002990088,0.00084659003,0.026104135],"study_design_scores_gemma":[0.0010602865,0.0013635014,0.75346,0.000031099353,0.000008728269,0.00033215107,0.00006986811,0.000010055798,0.20749712,0.00003137489,0.035907585,0.00022826111],"about_ca_topic_score_codex":0.000023795817,"about_ca_topic_score_gemma":0.000010402581,"teacher_disagreement_score":0.42532146,"about_ca_system_score_codex":0.0000054405577,"about_ca_system_score_gemma":0.00003328322,"threshold_uncertainty_score":0.48747084},"labels":[],"label_agreement":null},{"id":"W2054408230","doi":"10.1016/j.celrep.2015.02.011","title":"Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features","year":2015,"lang":"en","type":"article","venue":"Cell Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; McGill University and Génome Québec Innovation Centre; McGill Genome Centre","funders":"Ministry of Education, Culture, Sports, Science and Technology; Hamad Medical Corporation; Qatar Foundation","keywords":"Sotos syndrome; Intellectual disability; Frameshift mutation; Haploinsufficiency; Gene knockdown; Loss function; Mutation; Biology; Kabuki syndrome; Exon; Exome sequencing; Gene; Genetics; Bioinformatics; Phenotype","score_opus":0.013061462145936016,"score_gpt":0.24165785369586984,"score_spread":0.22859639154993383,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054408230","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963043,0.0007363082,0.00026072795,0.000014319373,0.0003481761,0.00013324608,6.5688425e-7,0.0000067850447,0.0021955234],"genre_scores_gemma":[0.9985045,0.000020817808,0.0003282148,0.000027044598,0.000041156694,0.000010611464,0.00004510741,0.000013520339,0.0010090319],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99921536,0.000022780465,0.00026215133,0.00023747116,0.00012256867,0.00013967355],"domain_scores_gemma":[0.9994402,0.0000040640293,0.00016505895,0.00025506417,0.000075696844,0.000059903814],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019994176,0.00009034983,0.00011479953,0.000049130114,0.000014956831,0.000010356512,0.000043818305,0.00010635137,0.000008455491],"category_scores_gemma":[0.00010320925,0.00008805048,0.000044302207,0.000077013014,0.000028071205,0.000003226878,0.000050146402,0.00004875839,0.000003439633],"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":[0.000029149236,0.00018615303,0.38038358,0.00011540199,0.00004003565,0.0007542841,0.000290973,0.0018956332,0.6117202,0.000012045254,0.0017259031,0.002846617],"study_design_scores_gemma":[0.00060222717,0.00064305327,0.4726686,0.000040446328,0.000031291136,0.0043613776,0.00038176298,0.000025939204,0.5123241,0.00056055555,0.008070593,0.00029006248],"about_ca_topic_score_codex":0.000086238455,"about_ca_topic_score_gemma":0.000023255563,"teacher_disagreement_score":0.099396095,"about_ca_system_score_codex":0.00001098476,"about_ca_system_score_gemma":0.00008331157,"threshold_uncertainty_score":0.35905945},"labels":[],"label_agreement":null},{"id":"W2054749794","doi":"10.1002/ajmg.a.31800","title":"Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5","year":2007,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Fetus; Intrauterine growth restriction; Placenta; Uniparental disomy; Biology; Dysplasia; Fetal growth; Beckwith–Wiedemann syndrome; Gene duplication; Andrology; Medicine; Pregnancy; Genetics; Gene; Karyotype; Chromosome","score_opus":0.004601525110106319,"score_gpt":0.2339378782255773,"score_spread":0.229336353115471,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054749794","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977441,0.00048346186,0.001388191,0.000115891635,0.0001429198,0.000062779225,0.000008391434,0.0000010912933,0.000053196713],"genre_scores_gemma":[0.99858916,0.00034864002,0.00084940833,0.00007579391,0.00009658103,4.5532846e-7,0.000004417001,0.000013810161,0.000021748869],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99829143,0.00008945043,0.0005184311,0.00012924413,0.0007483047,0.00022312388],"domain_scores_gemma":[0.99876875,0.00004254962,0.00071611867,0.00013755304,0.00015109312,0.00018390937],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007796647,0.00012249468,0.00028150427,0.000040704,0.000033710367,0.0000071213685,0.00026577423,0.00009139915,0.000022010183],"category_scores_gemma":[0.00018859038,0.000081300095,0.00009353217,0.00013952341,0.00060176314,0.000002442389,0.00012117144,0.0001667156,1.8852477e-7],"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":[0.00024722627,0.00016322387,0.8594576,0.000023883165,0.0003468407,0.000015688413,0.00014474994,0.00008386068,0.11953531,0.000015366028,0.00019625883,0.019769995],"study_design_scores_gemma":[0.0018289448,0.0042023836,0.8272361,0.00027541164,0.00011997237,0.0011118653,0.00053005526,0.00028196318,0.16337247,0.000015328855,0.00085388817,0.00017159879],"about_ca_topic_score_codex":0.000027317612,"about_ca_topic_score_gemma":0.000033140477,"teacher_disagreement_score":0.043837152,"about_ca_system_score_codex":0.000012013739,"about_ca_system_score_gemma":0.0001560246,"threshold_uncertainty_score":0.33153215},"labels":[],"label_agreement":null},{"id":"W205517805","doi":"10.1007/978-3-642-17426-1_8","title":"The Strategies of the Genes: Genomic Conflicts, Attachment Theory, and Development of the Social Brain","year":2011,"lang":"en","type":"book-chapter","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"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","funders":"","keywords":"Psychology; Maladaptation; Offspring; Schizophrenia (object-oriented programming); Developmental psychology; Genomic imprinting; Epigenetics; Autism; Attachment theory; Psychosis; Psychiatry; Genetics; Biology; Gene; DNA methylation","score_opus":0.020445739118320597,"score_gpt":0.24979530169838704,"score_spread":0.22934956258006645,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W205517805","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5314507,0.009057948,0.00095890905,0.0005478892,0.0006406794,0.0013306914,0.000045303692,0.000009454797,0.45595846],"genre_scores_gemma":[0.823897,0.0006796735,0.0002954188,0.0001800155,0.00012638612,0.000014306917,0.00001047915,0.000048253947,0.17474845],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990697,0.000054711585,0.0003607316,0.00021795876,0.00013985371,0.00015705691],"domain_scores_gemma":[0.9991552,0.000029619412,0.00033146548,0.00039640302,0.0000663251,0.000020971484],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039784343,0.0002031973,0.00018445462,0.0000105166255,0.00025583067,0.000020174513,0.0004630656,0.00019829563,0.000051200288],"category_scores_gemma":[0.000012279099,0.00009717323,0.0001378726,0.000008464183,0.00041460534,8.251192e-7,0.0006182828,0.000095166215,0.0000014670541],"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":[0.000049971033,0.000040844578,0.0010312594,0.00022342552,0.001373514,2.5450896e-7,0.0037034515,0.00000606829,0.4379518,0.46049207,0.0011612015,0.09396611],"study_design_scores_gemma":[0.00046091052,0.00011298768,0.033384543,0.00008059859,0.00009890035,0.000019962732,0.0019585053,0.0000011298,0.13633871,0.0067168702,0.8204417,0.00038513474],"about_ca_topic_score_codex":0.000010641891,"about_ca_topic_score_gemma":0.000057832975,"teacher_disagreement_score":0.81928056,"about_ca_system_score_codex":0.000009324792,"about_ca_system_score_gemma":0.00027173394,"threshold_uncertainty_score":0.39626092},"labels":[],"label_agreement":null},{"id":"W2055529397","doi":"10.1016/j.mce.2014.03.003","title":"Modulation of imprinted gene expression following superovulation","year":2014,"lang":"en","type":"article","venue":"Molecular and Cellular Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital; McGill University Health Centre","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Embryo; Placenta; Ovulation; Andrology; Gene expression; Gestation; Gene; Endocrinology; Fetus; Spontaneous conception; Internal medicine; Genetics; Pregnancy; DNA methylation; Medicine; In vitro fertilisation","score_opus":0.005959176298004178,"score_gpt":0.21483477426686473,"score_spread":0.20887559796886054,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055529397","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8285362,0.0004557628,0.17041276,0.00002838391,0.00011367969,0.00009696556,8.9888846e-7,0.000009925735,0.00034538505],"genre_scores_gemma":[0.99537665,0.000025580623,0.004341405,0.00004856082,0.000043577056,0.000008685652,0.00007414945,0.000021272495,0.000060139984],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989849,0.00009831247,0.00023835312,0.00033298426,0.000099788245,0.00024568578],"domain_scores_gemma":[0.9995046,0.000008008294,0.00007914943,0.00031043874,0.000043041997,0.000054712986],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010831085,0.00013864161,0.00017689228,0.000062562074,0.000053955086,0.000009496615,0.00009973562,0.00011237608,0.000009160995],"category_scores_gemma":[0.00006411012,0.00014092597,0.00010797904,0.000052317082,0.000046244135,0.0000035083428,0.00014864556,0.000059106285,0.0000022602044],"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":[0.000006186248,0.000018763223,0.009130193,0.000013658096,0.000028027123,0.0000024011524,0.000020517964,0.0002026113,0.98536825,0.00028832466,0.0000036128627,0.00491744],"study_design_scores_gemma":[0.0005718326,0.00018835404,0.011080359,0.000009067434,0.000021170617,0.000031430915,0.000021934115,0.0011670436,0.9857166,0.00024420666,0.00080710236,0.00014090593],"about_ca_topic_score_codex":0.000018153209,"about_ca_topic_score_gemma":0.0000013316002,"teacher_disagreement_score":0.16684039,"about_ca_system_score_codex":0.0000039578704,"about_ca_system_score_gemma":0.00001090205,"threshold_uncertainty_score":0.5746794},"labels":[],"label_agreement":null},{"id":"W2055538355","doi":"10.1016/j.ydbio.2009.09.023","title":"An imprinted GFP insertion reveals long-range epigenetic regulation in embryonic lineages","year":2009,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of British Columbia","funders":"Canadian Institutes of Health Research; Agence Nationale pour la Gestion des Déchets Radioactifs; Canada Research Chairs; Michael Smith Health Research BC","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Epigenetics; Genetics; Allele; DNA methylation; Gene; Gene silencing; Gene expression","score_opus":0.010725525482593498,"score_gpt":0.2654735012324604,"score_spread":0.2547479757498669,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055538355","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963992,0.00038147703,0.0023309265,0.00016811241,0.00013436838,0.00022979984,0.00000390678,0.000020363357,0.00033181385],"genre_scores_gemma":[0.9947426,0.00015145012,0.0039955494,0.0003915797,0.00008721861,0.00001593948,0.00039329077,0.000014028231,0.00020838693],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99868923,0.00010808761,0.00033806943,0.0004593905,0.00006132723,0.00034388274],"domain_scores_gemma":[0.99955547,0.0000069528505,0.00009228146,0.00022277079,0.000045660843,0.00007685873],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024758856,0.00018168955,0.00018060692,0.00010818569,0.000060304643,0.000016751206,0.00019282558,0.00024276941,0.00004768773],"category_scores_gemma":[0.00005156189,0.00018086337,0.000046530968,0.00014821795,0.000045395846,0.0000062010067,0.00006140985,0.00008601039,0.00002880681],"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":[0.000020131713,0.000060082522,0.16701034,0.000004681847,0.0000094892885,0.000001394519,0.00004662933,0.000016074137,0.8099377,0.000023550096,0.00002390967,0.022846034],"study_design_scores_gemma":[0.00047376746,0.00048700004,0.84217495,0.000015069488,0.000003593538,0.00004688281,0.000043613312,0.00007790993,0.15559618,0.0002007493,0.0006683363,0.00021194937],"about_ca_topic_score_codex":0.000023404307,"about_ca_topic_score_gemma":0.00009185531,"teacher_disagreement_score":0.67516464,"about_ca_system_score_codex":0.000044490786,"about_ca_system_score_gemma":0.00006238876,"threshold_uncertainty_score":0.7375394},"labels":[],"label_agreement":null},{"id":"W2058376960","doi":"10.1002/ajmg.c.30064","title":"Risk of tumorigenesis in overgrowth syndromes: A comprehensive review","year":2005,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":277,"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":"","keywords":"Sotos syndrome; Head circumference; Wilms' tumor; Medicine; Pediatrics; Gigantism; Internal medicine; Oncology; Biology; Genetics; Birth weight","score_opus":0.02377447417847817,"score_gpt":0.3496704162534198,"score_spread":0.32589594207494166,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2058376960","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.02979819,0.9684353,0.0001663492,0.0002130229,0.00069064205,0.0005893763,0.000046050252,0.000004527848,0.000056569817],"genre_scores_gemma":[0.0011084276,0.9935627,0.0036986033,0.00057265395,0.00078834454,0.000037988942,0.000057542904,0.0001438056,0.000029911102],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9877128,0.0017037555,0.0049852952,0.0008820825,0.0037074762,0.0010085774],"domain_scores_gemma":[0.9930763,0.0006304288,0.0036231093,0.0010655405,0.00037955752,0.00122503],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.004113422,0.00093787117,0.0048074545,0.00058595237,0.000043430824,0.000019724348,0.0026834959,0.0010826946,0.00036156262],"category_scores_gemma":[0.003578407,0.0007958341,0.0011805183,0.0013694525,0.001288115,0.000004946127,0.0008828958,0.0020074293,0.000011933156],"study_design_candidate":"design_other","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":[0.000016796761,0.00043379824,0.0014494552,0.0063114013,0.00038936108,0.00031596585,0.000050973485,0.00004344967,0.000008240626,0.0000013334993,0.0015376293,0.9894416],"study_design_scores_gemma":[0.0009644265,0.002598896,0.00051821984,0.087039284,0.00092036027,0.0035029063,0.00016833779,0.000085246465,0.000027207174,0.000011003495,0.90342575,0.00073834794],"about_ca_topic_score_codex":0.000035305806,"about_ca_topic_score_gemma":0.00003768591,"teacher_disagreement_score":0.98870325,"about_ca_system_score_codex":0.0001250427,"about_ca_system_score_gemma":0.0031375533,"threshold_uncertainty_score":0.99944925},"labels":[],"label_agreement":null},{"id":"W2059877822","doi":"10.1074/jbc.m111.242479","title":"Latent Transforming Growth Factor β-Binding Proteins-2 and -3 Inhibit the Proprotein Convertase 5/6A","year":2011,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"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","funders":"Canadian Institutes of Health Research","keywords":"Endoplasmic reticulum; Furin; Proprotein Convertases; Zymogen; Secretory pathway; Proprotein convertase; Cell biology; Biochemistry; Biology; Protein precursor; Golgi apparatus; Chemistry; LDL receptor; Enzyme","score_opus":0.0304132524043616,"score_gpt":0.224037293452257,"score_spread":0.1936240410478954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059877822","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984271,0.0006045428,0.0002918298,0.00011175766,0.00004221817,0.00016677048,0.000005894146,0.000004151348,0.00034573636],"genre_scores_gemma":[0.99862117,0.0002537898,0.00080941856,0.000058945956,0.00015104642,0.000007655933,0.0000036879567,0.000009378719,0.000084895044],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99909383,0.00003313413,0.00035549712,0.0001821758,0.00011368321,0.00022166458],"domain_scores_gemma":[0.99942684,0.000010983188,0.00022975742,0.00012069429,0.00009751649,0.00011419883],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027106993,0.00015321573,0.00018353113,0.000012247343,0.00008442254,0.000021660473,0.00021068059,0.00018926761,0.000089431436],"category_scores_gemma":[0.00015569819,0.00008420193,0.00012668062,0.000037576043,0.00013893998,0.0000051539378,0.00008848758,0.00022410917,0.0000014797257],"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":[0.00004136326,0.00004280661,0.015257719,0.000035651894,0.000043825316,0.00000955477,0.00009622586,1.484147e-7,0.98165745,0.000004275739,0.000014170627,0.0027967943],"study_design_scores_gemma":[0.0004297504,0.00039278588,0.011694712,0.00004124377,0.000014138561,0.0005199857,0.00014024145,0.0000032995665,0.9859326,0.000087165936,0.0006089248,0.00013517703],"about_ca_topic_score_codex":0.0000059165945,"about_ca_topic_score_gemma":3.6159187e-7,"teacher_disagreement_score":0.004275111,"about_ca_system_score_codex":0.000009542368,"about_ca_system_score_gemma":0.000039645143,"threshold_uncertainty_score":0.34336552},"labels":[],"label_agreement":null},{"id":"W2060000733","doi":"10.1159/000090828","title":"Lessons from comparative analysis of species-specific imprinted genes","year":2006,"lang":"en","type":"review","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Gene; Genetics; Evolutionary biology; Evolution of mammals; DNA methylation; Gene expression","score_opus":0.23716001289428498,"score_gpt":0.4401018496342546,"score_spread":0.2029418367399696,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2060000733","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.024262045,0.97240645,0.00045931697,0.0000091720885,0.00005623758,0.0005685343,0.0005967387,0.0000058387645,0.0016356527],"genre_scores_gemma":[0.0144095095,0.9812918,0.000662291,0.0000027945234,0.00026611105,0.00006614153,0.0018215183,0.000044029068,0.0014358605],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9964629,0.00050731,0.0008218327,0.0011002596,0.00046626353,0.0006414392],"domain_scores_gemma":[0.9980291,0.0001572943,0.00028253224,0.0010175443,0.0003241996,0.00018931145],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006365146,0.0004573124,0.0018961146,0.000750988,0.00017793097,0.0000816573,0.0006454406,0.00045267382,0.00018930208],"category_scores_gemma":[0.000026407686,0.00040016422,0.0006809668,0.001289346,0.00052034116,0.0000017086122,0.00079442,0.00034494116,0.000026946049],"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":[0.000022930695,0.0002811158,0.0011382987,0.002696102,0.0097089,0.000013347448,0.0002097902,0.000113585374,0.07410876,0.00017406655,0.00051149965,0.9110216],"study_design_scores_gemma":[0.00018249564,0.00017339193,0.010218235,0.00026619693,0.0011705586,0.000009537296,0.00012116705,0.000015574236,0.0010436772,0.000018509741,0.9863768,0.00040384155],"about_ca_topic_score_codex":0.00017292227,"about_ca_topic_score_gemma":0.00007520923,"teacher_disagreement_score":0.9858653,"about_ca_system_score_codex":0.00004317785,"about_ca_system_score_gemma":0.00025340103,"threshold_uncertainty_score":0.999845},"labels":[],"label_agreement":null},{"id":"W2061999591","doi":"10.1016/j.jpeds.2013.03.058","title":"Thyroid Function from Birth to Adolescence in Prader-Willi Syndrome","year":2013,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"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; BC Children's Hospital; University of British Columbia","funders":"","keywords":"Medicine; Internal medicine; Endocrinology; Triiodothyronine; Thyroid function; Hormone; Thyroid-stimulating hormone; Thyroid; Congenital hypothyroidism; Free thyroxine; Reference range","score_opus":0.006844456755075083,"score_gpt":0.20790392653583603,"score_spread":0.20105946978076095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2061999591","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9938201,0.0016429962,0.0035473865,0.00048748206,0.0003254455,0.00012119326,0.00000248744,0.0000021157014,0.000050807113],"genre_scores_gemma":[0.99735844,0.0007442077,0.000976597,0.0003185004,0.00046179988,0.0000017831252,0.0000017249371,0.000012697798,0.00012427154],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991498,0.000070861635,0.00031159143,0.00010323786,0.00017975245,0.00018474675],"domain_scores_gemma":[0.9993806,0.000028797449,0.00019375938,0.00019711691,0.00010867455,0.0000910651],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033175948,0.00009686914,0.00012420487,0.0000788994,0.0000365923,0.000025409054,0.0002753052,0.000073307885,0.000034847377],"category_scores_gemma":[0.00013956099,0.00006729664,0.000054211014,0.00018130067,0.000017093163,0.0000074449467,0.000098187054,0.00016037594,0.00004693216],"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":[0.000022005346,0.00016742831,0.55648464,0.000053041498,0.000028703187,0.0000048629845,0.00048083614,0.0022603362,0.4177455,0.0000065888003,0.01102022,0.011725838],"study_design_scores_gemma":[0.00039464724,0.00076535763,0.99509615,0.000015295782,0.000037783186,0.00015148839,0.0003628196,0.000021319593,0.0014224456,0.00017733866,0.0014283515,0.0001270248],"about_ca_topic_score_codex":0.00008227808,"about_ca_topic_score_gemma":0.0000119673505,"teacher_disagreement_score":0.4386115,"about_ca_system_score_codex":0.000013547249,"about_ca_system_score_gemma":0.000057074692,"threshold_uncertainty_score":0.27442774},"labels":[],"label_agreement":null},{"id":"W2062755230","doi":"10.1371/journal.pgen.1004265","title":"Parent-of-Origin Effects Implicate Epigenetic Regulation of Experimental Autoimmune Encephalomyelitis and Identify Imprinted Dlk1 as a Novel Risk Gene","year":2014,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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; Vetenskapsrådet; Multiple Sclerosis Society; Multiple Sclerosis Society of Canada; Wellcome Trust","keywords":"Biology; Epigenetics; Genetics; Genomic imprinting; Imprinting (psychology); Allele; Experimental autoimmune encephalomyelitis; Locus (genetics); Disease; Immunology; Gene; Immune system; DNA methylation; Gene expression; Medicine","score_opus":0.012785828114457524,"score_gpt":0.26633892611671917,"score_spread":0.25355309800226167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2062755230","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98854095,0.0030402888,0.0077266153,0.0000099498,0.00014912104,0.00038148867,0.000021472624,0.000012726563,0.00011736562],"genre_scores_gemma":[0.9927563,0.00058832,0.006372114,0.000017125345,0.00009270576,0.000036056652,0.00005210904,0.000042509855,0.000042737513],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9983597,0.000095000236,0.000526529,0.0004816589,0.00022572208,0.0003114049],"domain_scores_gemma":[0.9987276,0.00003992128,0.00037774362,0.0006031136,0.00013974815,0.00011186548],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00018017377,0.00024789083,0.00033438206,0.00007396212,0.00007191241,0.000021134483,0.00024077829,0.00017400982,0.000021444723],"category_scores_gemma":[0.0001399687,0.00026002855,0.00011415101,0.00011017996,0.00016655779,0.0000037978639,0.00029369423,0.000081126745,0.0000052184578],"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":[0.000014209009,0.00016216512,0.026622752,0.00008568664,0.00010568852,1.6221006e-7,0.00013141679,0.00008433759,0.96571535,0.000035581732,0.000003798725,0.0070388564],"study_design_scores_gemma":[0.0006667732,0.0006395212,0.3273187,0.00003928132,0.00006415943,0.000017456172,0.00003234963,0.0018303883,0.668951,0.0001009806,0.00016579861,0.00017359795],"about_ca_topic_score_codex":0.000043502292,"about_ca_topic_score_gemma":0.0000031377008,"teacher_disagreement_score":0.30069596,"about_ca_system_score_codex":0.000012100774,"about_ca_system_score_gemma":0.000044057466,"threshold_uncertainty_score":0.9999852},"labels":[],"label_agreement":null},{"id":"W2063012163","doi":"10.1007/s00335-002-2244-x","title":"Alternative splicing and imprinting control of the Meg3/Gtl2-Dlk1 locus in mouse embryos","year":2003,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Royal Victoria Hospital","funders":"National Center for Research Resources; National Cancer Institute; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; MEG3; Locus (genetics); Imprinting (psychology); Genetics; Gene; Exon; Uniparental disomy; Allele; RNA splicing; Gene expression; Molecular biology; Chromosome; RNA; DNA methylation; Long non-coding RNA","score_opus":0.006323893910373239,"score_gpt":0.2093807934480102,"score_spread":0.20305689953763695,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063012163","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966139,0.00049279834,0.0013746882,0.00005315142,0.00007844094,0.00022917795,0.000007471643,0.0000030936542,0.0011472799],"genre_scores_gemma":[0.9984831,0.000030632073,0.00037131298,0.00011413536,0.000043227083,0.000009615927,0.0000016157891,0.00001927689,0.00092706754],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99901205,0.000089370864,0.00026101153,0.0002772572,0.00009317468,0.0002671265],"domain_scores_gemma":[0.99946517,0.000010915896,0.00012746263,0.0003063141,0.000039952512,0.00005017922],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030049143,0.00013464417,0.00016825263,0.00003995985,0.000053734213,0.000018249631,0.00017590045,0.00007463649,0.000016571626],"category_scores_gemma":[0.00010134301,0.00011005864,0.0000649258,0.000082948405,0.00006912483,0.0000025282516,0.00011663478,0.00009007675,0.000002387873],"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":[0.000004694684,0.000018974028,0.0468659,0.000022516397,0.000026122425,0.0000012634624,0.0001620722,0.00040574948,0.95139945,0.00018907136,0.000001904401,0.00090230315],"study_design_scores_gemma":[0.0022084753,0.00017823931,0.13814744,0.000032706037,0.000024944484,0.00007746752,0.0005577402,0.00033716272,0.85366005,0.00023662219,0.0041864216,0.0003526972],"about_ca_topic_score_codex":0.00012797434,"about_ca_topic_score_gemma":0.000041994623,"teacher_disagreement_score":0.097739354,"about_ca_system_score_codex":0.00001348531,"about_ca_system_score_gemma":0.000030236872,"threshold_uncertainty_score":0.4488061},"labels":[],"label_agreement":null},{"id":"W2063715238","doi":"10.1210/endo.143.4.8746","title":"Localization and Regulation of a Functional GHRH Receptor in the Rat Renal Medulla","year":2002,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Hôpital Notre-Dame","funders":"","keywords":"Endocrinology; Internal medicine; Internalization; Receptor; Growth hormone–releasing hormone; Biology; In situ hybridization; Riboprobe; Angiotensin II; Messenger RNA; Hormone; Chemistry; Growth hormone; Biochemistry; Medicine","score_opus":0.015360612477738622,"score_gpt":0.21797610340465154,"score_spread":0.20261549092691292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063715238","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9938601,0.0008978883,0.0032471407,0.000471278,0.000116498086,0.00009014791,0.000001139422,0.0000029228731,0.0013128634],"genre_scores_gemma":[0.99893963,0.00021966196,0.0001861466,0.000127685,0.00006909203,0.000009138616,0.000026031672,0.000004447194,0.00041814506],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99949193,0.00006651649,0.00013269791,0.00013689214,0.000054992648,0.000116971525],"domain_scores_gemma":[0.999784,0.0000130735425,0.000046302124,0.000120274155,0.000024694984,0.000011673427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006146358,0.000053842894,0.00006452797,0.00003422591,0.000030103556,0.000004281132,0.000053228156,0.00004896449,0.00015084061],"category_scores_gemma":[0.000050704217,0.00004281654,0.000019035178,0.00005985761,0.00006722396,0.0000015862241,0.000035662637,0.00003905365,0.0000044438407],"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":[0.00003223416,0.0001114738,0.053580444,0.000027373642,0.000038007976,0.0000014663777,0.00033567255,0.00093136035,0.88953865,0.0031807232,0.011637664,0.040584937],"study_design_scores_gemma":[0.0032229046,0.0010962228,0.33355275,0.000037230137,0.000036746333,0.0008451802,0.00078863616,0.0042287135,0.29937807,0.0011479071,0.35523647,0.00042916648],"about_ca_topic_score_codex":0.000012426664,"about_ca_topic_score_gemma":0.000020077674,"teacher_disagreement_score":0.59016055,"about_ca_system_score_codex":0.0000038427183,"about_ca_system_score_gemma":0.0000060060006,"threshold_uncertainty_score":0.17460078},"labels":[],"label_agreement":null},{"id":"W2064431299","doi":"10.1016/j.ygeno.2004.03.008","title":"The KCNQ1OT1 promoter, a key regulator of genomic imprinting in human chromosome 11p15.5","year":2004,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genomic imprinting; Regulator; Imprinting (psychology); Genetics; Key (lock); Chromosome; Gene; Computational biology; DNA methylation; Gene expression","score_opus":0.0076892163561273486,"score_gpt":0.2260845621412258,"score_spread":0.21839534578509845,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2064431299","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982747,0.00063148607,0.00020651896,0.00010100075,0.00012273628,0.0002524423,0.0000041802723,0.0000066139687,0.00040034766],"genre_scores_gemma":[0.99759233,0.00014968643,0.0018885734,0.00003758612,0.00014174616,0.000013483218,0.000012343213,0.00003204154,0.00013220825],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99882835,0.000027085363,0.00040499694,0.00030426952,0.00008327568,0.00035199148],"domain_scores_gemma":[0.99922985,0.0000065325667,0.00016901139,0.00050021295,0.00004120044,0.000053165586],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003303233,0.0001497818,0.00016696773,0.000039617637,0.00013029647,0.000031060645,0.00035394233,0.00011438068,0.000005781378],"category_scores_gemma":[0.000034447356,0.00013085017,0.00009880211,0.00006763122,0.00009797674,0.000002336472,0.00029090888,0.00010012601,0.000007872829],"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":[0.000004867004,0.000031235362,0.0026151626,0.000017105418,0.000023641804,0.0000010473002,0.0001863924,0.00058973534,0.99365556,0.00031157213,0.0000067474357,0.0025569443],"study_design_scores_gemma":[0.0016367492,0.00033580753,0.12527737,0.00003888865,0.00001676725,0.00007943443,0.00030455066,0.00007723486,0.86068845,0.0016810718,0.009506341,0.0003573143],"about_ca_topic_score_codex":0.000081978214,"about_ca_topic_score_gemma":0.00009211879,"teacher_disagreement_score":0.13296707,"about_ca_system_score_codex":0.000057906193,"about_ca_system_score_gemma":0.0001210595,"threshold_uncertainty_score":0.5335915},"labels":[],"label_agreement":null},{"id":"W2066684435","doi":"10.1371/journal.pone.0097535","title":"Epigenetic Characterization of the Growth Hormone Gene Identifies SmcHD1 as a Regulator of Autosomal Gene Clusters","year":2014,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Simon Fraser University","funders":"University of California, San Diego","keywords":"Biology; DNA methylation; Epigenetics; Promoter; Gene; Genomic imprinting; Gene cluster; Genetics; Regulation of gene expression; Gene expression; Methylation; Enhancer; Locus control region; Molecular biology","score_opus":0.010552217995584241,"score_gpt":0.1889003701747626,"score_spread":0.17834815217917838,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2066684435","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99844235,0.00019170565,0.0007732916,0.00012775186,0.00006834346,0.00022917251,0.000014160746,0.0000069215657,0.0001462843],"genre_scores_gemma":[0.99785626,0.0001913266,0.0011581446,0.00007396282,0.000119266166,0.000013532021,0.000049783644,0.000025063404,0.00051266217],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988965,0.00007783609,0.0003435569,0.0002486007,0.00024914785,0.00018439641],"domain_scores_gemma":[0.99903303,0.000008557471,0.0002695035,0.00047717412,0.00016321173,0.000048495953],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015540751,0.00013031607,0.00022343773,0.000037858783,0.000054443466,0.000012110795,0.00026839992,0.00011091702,0.0000134088505],"category_scores_gemma":[0.0001484293,0.00011054658,0.00009938249,0.00011802355,0.0001044202,0.0000036268932,0.00021102728,0.000046547484,0.000004892956],"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":[0.000012802808,0.00017586385,0.006276711,0.000075549484,0.00012894787,8.080259e-8,0.00006207503,0.000006505221,0.9929022,0.000021365891,0.0000063219422,0.00033155293],"study_design_scores_gemma":[0.00027688732,0.00019741626,0.24110508,0.000036884983,0.00007066778,0.000004499095,0.000009341367,0.00020683641,0.7579242,0.000052566764,0.000023944665,0.00009166682],"about_ca_topic_score_codex":0.000019527046,"about_ca_topic_score_gemma":0.0000020888056,"teacher_disagreement_score":0.23497802,"about_ca_system_score_codex":0.0000060272846,"about_ca_system_score_gemma":0.00003852633,"threshold_uncertainty_score":0.45079586},"labels":[],"label_agreement":null},{"id":"W2068519968","doi":"10.1016/s1499-2671(11)52031-3","title":"Unique metabolic profile in children with Prader-Willi Syndrome: Heightened insulin sensitivity relative to body mass index","year":2011,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Medicine; Adiponectin; Body mass index; Internal medicine; Endocrinology; Obesity; Lean body mass; Insulin sensitivity; Insulin; Fat mass; Insulin resistance; Body weight","score_opus":0.007171056441082646,"score_gpt":0.1898451893152519,"score_spread":0.18267413287416925,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068519968","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99830127,0.0006937578,0.00025204,0.00012055384,0.000064527485,0.00024286124,0.00002303697,0.0000022652555,0.00029968412],"genre_scores_gemma":[0.9961886,0.000013969021,0.0034730088,0.00016924657,0.00005137876,0.0000075107873,0.000010171134,0.000027729233,0.0000583956],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988345,0.00013263315,0.0002887655,0.0002167219,0.00010262667,0.0004247485],"domain_scores_gemma":[0.99897045,0.000010241518,0.00017566262,0.00020272093,0.000151914,0.00048898906],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029886267,0.00017578351,0.00028560686,0.0002487301,0.000057749476,0.000024217057,0.00016791381,0.00013289641,0.000034522072],"category_scores_gemma":[0.00013036244,0.00015040899,0.00006787835,0.00023458773,0.00007218674,0.000015523705,0.000025599495,0.00020749979,0.00000516142],"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":[7.647631e-7,0.000018165056,0.9875786,0.000004360303,0.0001722673,0.000006622032,0.00014320968,0.000035935453,0.011047603,0.00002900867,0.000041545143,0.0009219547],"study_design_scores_gemma":[0.0004749123,0.0005491019,0.9774201,0.00006205778,0.000030395719,0.00012692134,0.00007345082,0.00001796846,0.020588847,0.00009066513,0.00036135898,0.00020424063],"about_ca_topic_score_codex":0.0008175495,"about_ca_topic_score_gemma":0.0031497008,"teacher_disagreement_score":0.010158484,"about_ca_system_score_codex":0.000030381374,"about_ca_system_score_gemma":0.00059145154,"threshold_uncertainty_score":0.6133501},"labels":[],"label_agreement":null},{"id":"W2068741665","doi":"10.1002/dvdy.21615","title":"Loss of the Prader‐Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons","year":2008,"lang":"en","type":"article","venue":"Developmental Dynamics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"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":"Fondation pour la Recherche Médicale","keywords":"Biology; Superior cervical ganglion; Endocrinology; Sympathetic nervous system; Internal medicine; Embryonic stem cell; Nervous system; Neuroscience; Medicine","score_opus":0.008480482013126636,"score_gpt":0.2012182157645916,"score_spread":0.19273773375146497,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068741665","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99892104,0.000103440914,0.0003292641,0.00008954821,0.00009378389,0.00029526989,0.000038586015,0.0000046646906,0.00012440169],"genre_scores_gemma":[0.9985507,0.000085151216,0.0009920743,0.0000141608025,0.000008067177,0.000016732805,0.000035056095,0.000018761039,0.0002793024],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99908626,0.00006120404,0.00025877487,0.00024300012,0.00017037957,0.00018039794],"domain_scores_gemma":[0.9995585,0.0000125886545,0.00015020826,0.00016413842,0.00007128377,0.000043276155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009178874,0.00015124166,0.00017558037,0.000034561468,0.00010859912,0.0000060134857,0.00016010497,0.000088360124,0.0000045511656],"category_scores_gemma":[0.000060314305,0.00012545881,0.000073438394,0.00012117028,0.00025451984,0.000004562917,0.00021084606,0.00007486575,0.0000011522042],"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":[0.000004372264,0.00012243657,0.8357551,0.000091369344,0.000121965786,0.0000048509887,0.00046215052,0.00007181554,0.1626666,0.00029870897,0.00001623113,0.0003843969],"study_design_scores_gemma":[0.0003802526,0.00017924228,0.9660719,0.00004674614,0.000017493545,0.0012123227,0.00035548085,0.00028532746,0.031105215,0.000062148734,0.00009739357,0.00018644992],"about_ca_topic_score_codex":0.000040857656,"about_ca_topic_score_gemma":0.00016238425,"teacher_disagreement_score":0.13156138,"about_ca_system_score_codex":0.0000274701,"about_ca_system_score_gemma":0.0001740924,"threshold_uncertainty_score":0.51160616},"labels":[],"label_agreement":null},{"id":"W2069432272","doi":"10.1002/dvg.20658","title":"Loss of Necdin impairs myosin activation and delays cell polarization","year":2010,"lang":"en","type":"article","venue":"genesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"National Institute of General Medical Sciences; RIKEN; Canadian Institutes of Health Research; Heritage Medical Research Institute","keywords":"Cell polarity; Myosin; Cell biology; Biology; Null cell; PAX3; Neuroscience; Cell; Genetics; Cell culture; Gene; Transcription factor","score_opus":0.0046401020041517615,"score_gpt":0.20715645552047163,"score_spread":0.20251635351631986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069432272","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99561733,0.000104751576,0.0038235374,0.000052392184,0.00007965656,0.00007039151,0.000003906244,0.0000043678588,0.00024368425],"genre_scores_gemma":[0.9963223,0.00004963939,0.0033050822,0.00003887159,0.000065014814,0.0000032751277,0.000026841855,0.000011855503,0.00017716608],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995507,0.000013893923,0.000116892545,0.00015789033,0.000055569675,0.00010507221],"domain_scores_gemma":[0.9996748,0.0000052112155,0.00006827039,0.00016347223,0.000050415892,0.000037814494],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000085421954,0.000070493836,0.00006792581,0.000029238769,0.000039291554,0.000009804835,0.000060426235,0.00010465841,0.000017462615],"category_scores_gemma":[0.000030620155,0.00007066176,0.000029544366,0.000054162345,0.000031142878,0.0000026112532,0.00005602787,0.00003412466,0.0000017237355],"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":[0.0000033116507,0.000012239515,0.074654974,0.00001447588,0.0000065174936,6.5631525e-8,0.000032024152,0.000010346277,0.9204316,0.000013496399,0.00003790528,0.0047830557],"study_design_scores_gemma":[0.00016717668,0.000061909755,0.19755946,0.0000024643134,0.000008520392,0.000007196289,0.00004523518,0.00008680657,0.8009318,0.000018416018,0.0010409661,0.000070028575],"about_ca_topic_score_codex":0.000068419075,"about_ca_topic_score_gemma":0.000010374146,"teacher_disagreement_score":0.122904494,"about_ca_system_score_codex":0.0000017426964,"about_ca_system_score_gemma":0.0000231432,"threshold_uncertainty_score":0.2881503},"labels":[],"label_agreement":null},{"id":"W2069564940","doi":"10.1053/plac.2001.0695","title":"The Human Achaete Scute Homolog 2 Gene Contains Two Promotors, Generating Overlapping Transcripts and Encoding Two Proteins with Different Nuclear Localization","year":2001,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"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":"Institute of Genetics; University of Cambridge","keywords":"Biology; Gene; Molecular biology; Gene expression; Homology (biology); Transcription (linguistics); Coding region; Messenger RNA; Fusion protein; Nucleolus; Nuclear protein; Genetics; Transcription factor; Nucleus; Cell biology; Recombinant DNA","score_opus":0.011833631285774544,"score_gpt":0.23662429757765885,"score_spread":0.2247906662918843,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069564940","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9915779,0.00041811622,0.0070185806,0.00011852189,0.00007792199,0.0005433208,0.000004541752,0.000021841557,0.00021926098],"genre_scores_gemma":[0.99848247,0.00023266082,0.0006868067,0.00012429051,0.00017332753,0.000036864658,0.00004886314,0.000037051374,0.00017765598],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99882126,0.000081944716,0.00021916284,0.00037705022,0.00014294514,0.00035766652],"domain_scores_gemma":[0.9994987,0.000008244052,0.00010479903,0.0002554615,0.000044117012,0.00008866699],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016705095,0.00020225089,0.0001499188,0.000025011226,0.00067103765,0.00012838353,0.00015094927,0.0000605917,0.000008202463],"category_scores_gemma":[0.000018323248,0.00014448407,0.000043632524,0.000059734215,0.000095104755,0.000007426313,0.00010434214,0.00010117665,8.7652853e-7],"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":[0.000021949398,0.000034095046,0.03211304,0.00001578125,0.00006577251,0.0000057173215,0.00024367028,0.00019594717,0.96487594,0.00013186639,0.000020736652,0.0022754895],"study_design_scores_gemma":[0.015236912,0.0037057188,0.07704709,0.0005299558,0.00035308005,0.0020383599,0.0027766214,0.055824332,0.79989165,0.00016985074,0.039966743,0.0024596883],"about_ca_topic_score_codex":0.00010081935,"about_ca_topic_score_gemma":0.0002735392,"teacher_disagreement_score":0.16498429,"about_ca_system_score_codex":0.00002524284,"about_ca_system_score_gemma":0.000020214722,"threshold_uncertainty_score":0.58918893},"labels":[],"label_agreement":null},{"id":"W2069928748","doi":"10.1210/jc.2004-0553","title":"The<i>Insulin-Like Growth Factor-II Receptor</i>Gene Is Associated with Type 1 Diabetes: Evidence of a Maternal Effect","year":2004,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Montreal Children's Hospital","funders":"","keywords":"Insulin-like growth factor 2 receptor; Single-nucleotide polymorphism; Biology; Genomic imprinting; Linkage disequilibrium; Allele; Genetics; SNP; Imprinting (psychology); Haplotype; Gene; Genotype; Receptor; DNA methylation; Insulin-like growth factor 1 receptor; Gene expression; Growth factor","score_opus":0.025050048350509002,"score_gpt":0.31311042205817785,"score_spread":0.28806037370766885,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069928748","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98432815,0.013290733,0.00006833975,0.0009888228,0.0011446544,0.00014489693,0.000005021082,0.000005007615,0.000024380326],"genre_scores_gemma":[0.98507196,0.01344338,0.00035216837,0.00054954697,0.00044630168,0.0000025011284,0.0000014695729,0.000024830882,0.00010785718],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9971228,0.00073280494,0.0011327487,0.00021506766,0.00033297474,0.00046357498],"domain_scores_gemma":[0.9970216,0.0006662933,0.0012134655,0.00042946247,0.0005476147,0.00012156382],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017756803,0.00022705006,0.00069571054,0.00004075219,0.0001832577,0.000017486838,0.0007952226,0.00017648382,0.000020513282],"category_scores_gemma":[0.0024929345,0.00011457618,0.00031374468,0.00015471378,0.00048165204,0.000010885034,0.00025070756,0.00051097275,0.0000066999432],"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":[0.0030987272,0.0005716266,0.16074176,0.00006731113,0.00503887,0.00003654924,0.00049826916,0.0002651399,0.7945258,0.00013984025,0.0012955108,0.033720594],"study_design_scores_gemma":[0.0048930477,0.007471562,0.39517507,0.000283272,0.0006166487,0.00041998943,0.00004737074,0.000007670587,0.58013624,0.00038059428,0.010277852,0.00029067433],"about_ca_topic_score_codex":0.000021692958,"about_ca_topic_score_gemma":0.000007166787,"teacher_disagreement_score":0.23443332,"about_ca_system_score_codex":0.000010789211,"about_ca_system_score_gemma":0.00022464793,"threshold_uncertainty_score":0.46722808},"labels":[],"label_agreement":null},{"id":"W2070045006","doi":"10.1002/jcb.20365","title":"Chromatin modification of the human imprinted <i>NDN</i> (necdin) gene detected by in vivo footprinting","year":2005,"lang":"en","type":"article","venue":"Journal of Cellular Biochemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Sherbrooke; University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"Genomic imprinting; Chromatin; Epigenetics; Biology; Gene; Allele; Footprinting; Genetics; Imprinting (psychology); DNA methylation; Transcription (linguistics); Chromosome conformation capture; Molecular biology; Transcription factor; Gene expression; Enhancer","score_opus":0.006626311671510045,"score_gpt":0.22549247214543974,"score_spread":0.2188661604739297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2070045006","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969873,0.000954074,0.00148597,0.00013809605,0.00007980694,0.00009192041,0.0000038730395,0.0000031595548,0.0002558029],"genre_scores_gemma":[0.99776375,0.00004041003,0.0016052808,0.000028924123,0.00020494466,0.0000026288078,0.00000671257,0.000021810305,0.00032554142],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985363,0.00005204798,0.0007451956,0.00020760097,0.00023647393,0.00022237236],"domain_scores_gemma":[0.9986003,0.000009400017,0.0007433486,0.00040440797,0.00017305244,0.00006951052],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003944222,0.00016446199,0.00021657944,0.000041687177,0.00006037479,0.000018832841,0.00047175787,0.00018644496,0.000020551124],"category_scores_gemma":[0.00013189792,0.00013772871,0.00020193268,0.00014162279,0.00007873603,0.000004740366,0.00014821863,0.00020488077,5.97737e-7],"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":[0.0000063437633,0.00009016461,0.003927158,0.000039180042,0.000034622106,7.052465e-7,0.00002734509,0.00009121483,0.99470395,0.0000016247184,0.00019129584,0.0008864092],"study_design_scores_gemma":[0.0006572121,0.000066185385,0.002856452,0.00006847771,0.000021141024,0.00007717613,0.000059969923,0.00011785792,0.9951704,0.000012702774,0.00075273775,0.00013964492],"about_ca_topic_score_codex":0.000010639077,"about_ca_topic_score_gemma":0.000002124887,"teacher_disagreement_score":0.001070706,"about_ca_system_score_codex":0.000039762475,"about_ca_system_score_gemma":0.0000846866,"threshold_uncertainty_score":0.5616414},"labels":[],"label_agreement":null},{"id":"W2070502226","doi":"10.1371/journal.pgen.0030065","title":"Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution","year":2007,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":114,"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":"Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics; Wellcome Trust; National Center for Research Resources; Ontario Genomics Institute; Howard Hughes Medical Institute","keywords":"Biology; Genomic imprinting; Genetics; Epigenomics; DNA methylation; Epigenetics; CpG site; Human genome; Chromatin immunoprecipitation; Gene; Gene expression; Genome; Promoter","score_opus":0.03302141642389157,"score_gpt":0.26380843551479244,"score_spread":0.23078701909090088,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2070502226","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9801267,0.00062409096,0.018501427,0.000027357952,0.0002540086,0.00026634784,0.000009428031,0.000013642505,0.0001770241],"genre_scores_gemma":[0.9992896,0.00011852918,0.0002060206,0.00001733702,0.00012619494,0.0000048908146,0.000024622224,0.000026012618,0.00018681015],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987426,0.00004748237,0.00047237318,0.00028228541,0.00021147064,0.00024381919],"domain_scores_gemma":[0.9990753,0.000010553192,0.00021787398,0.00045849764,0.00019008257,0.00004766952],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018253658,0.00013962774,0.00011294458,0.00005373384,0.0001371649,0.000026824631,0.00026780245,0.00015120706,0.00002126211],"category_scores_gemma":[0.000038822636,0.00012319138,0.00010728705,0.00018517314,0.000073850744,0.0000035001524,0.00007620577,0.00008947678,0.000005959483],"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":[0.0000059946206,0.00007656774,0.008269666,0.000026039037,0.000034522443,9.091952e-8,0.000079000645,0.000084609936,0.99045855,0.00007670806,0.000022307911,0.0008659294],"study_design_scores_gemma":[0.0002788273,0.00009481151,0.14353968,0.000018853589,0.00001902217,0.0000047218955,0.00011526242,0.00027187294,0.8551083,0.000077777986,0.00035211138,0.0001187178],"about_ca_topic_score_codex":0.0000037389473,"about_ca_topic_score_gemma":0.00004190635,"teacher_disagreement_score":0.13535023,"about_ca_system_score_codex":0.000036559955,"about_ca_system_score_gemma":0.00004406433,"threshold_uncertainty_score":0.50235987},"labels":[],"label_agreement":null},{"id":"W2070677464","doi":"10.1182/blood-2009-03-212746","title":"An upstream insulator regulates DLK1 imprinting in AML","year":2010,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Genomic imprinting; Biology; Methylation; Imprinting (psychology); Molecular biology; Allele; Epigenetics; DNA methylation; Myeloid leukemia; Uniparental disomy; Cancer research; Genetics; Gene; Gene expression; Chromosome","score_opus":0.004282711526569268,"score_gpt":0.22481929011371826,"score_spread":0.220536578587149,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2070677464","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99880666,0.00007434774,0.000022586033,0.00002766899,0.00014146596,0.0000923763,0.0000022748966,0.000016021586,0.0008165838],"genre_scores_gemma":[0.99647593,0.000013438087,0.0030979624,0.000045007375,0.00022556957,0.0000090263675,0.00001920372,0.000023467037,0.000090373156],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991356,0.000021002972,0.00018785766,0.00031937298,0.00007030061,0.00026583488],"domain_scores_gemma":[0.9993773,0.000004835603,0.000056091405,0.00044740338,0.000032296713,0.00008203304],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017382641,0.00012236547,0.00010797985,0.000042479296,0.000044120403,0.00003358184,0.00020611162,0.00015422494,0.000031088384],"category_scores_gemma":[0.000071243296,0.00012064735,0.000048773498,0.0000727445,0.00003589835,0.0000034566103,0.000098883516,0.00013249778,0.000010005715],"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":[0.0000012989068,0.00013474183,0.21191977,0.0000049262276,0.000009986864,0.0000014151784,0.000029461175,0.0000061852797,0.78369,0.00003611965,0.000004468526,0.00416162],"study_design_scores_gemma":[0.0006552672,0.00011035576,0.35388115,0.0000062007957,0.000008443325,0.00005186846,0.000049185743,0.00005790522,0.64395493,0.00007859335,0.0010033477,0.00014277475],"about_ca_topic_score_codex":0.000056381636,"about_ca_topic_score_gemma":0.000097419615,"teacher_disagreement_score":0.14196137,"about_ca_system_score_codex":0.0000016232875,"about_ca_system_score_gemma":0.000032508153,"threshold_uncertainty_score":0.49198565},"labels":[],"label_agreement":null},{"id":"W2071121505","doi":"10.1097/00019605-200404000-00008","title":"Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell???Silver syndrome?","year":2004,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; University of Manitoba","funders":"","keywords":"Medicine; Failure to thrive; Uniparental disomy; Karyotype; Forehead; Dermatology; Anatomy; Pediatrics; Genetics; Chromosome; Biology","score_opus":0.015443451725337043,"score_gpt":0.2720193214719298,"score_spread":0.25657586974659274,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071121505","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99781543,0.00037013847,0.00045600408,0.00020928978,0.00028113194,0.00032009327,0.000023218558,0.000013905607,0.0005108035],"genre_scores_gemma":[0.9930573,0.00016262832,0.0058277007,0.00047804145,0.000053283242,0.000035315672,0.00006593155,0.000046444886,0.00027333337],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99738497,0.00014841725,0.000950651,0.0007933562,0.00017589125,0.000546731],"domain_scores_gemma":[0.9986248,0.00006854694,0.00029509718,0.0007506166,0.00008785789,0.00017307047],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00051204464,0.0002971625,0.00070804625,0.000105495084,0.000040290695,0.000012470429,0.00039475568,0.0005119404,0.00012462569],"category_scores_gemma":[0.00024787727,0.00024557643,0.0002140011,0.00029433548,0.00040512162,0.000006344405,0.00028679534,0.0003726049,0.000047244142],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010558248,0.004143576,0.7960052,0.00039661396,0.0011472057,0.0089445915,0.0005263631,0.0069322386,0.1714952,0.0007417938,0.001011766,0.007599617],"study_design_scores_gemma":[0.009139316,0.0069335606,0.9406074,0.00022348748,0.00012251301,0.0305368,0.0002293104,0.00003764767,0.0066762217,0.000703781,0.0038882026,0.0009017067],"about_ca_topic_score_codex":0.00015512214,"about_ca_topic_score_gemma":0.000065125554,"teacher_disagreement_score":0.16481899,"about_ca_system_score_codex":0.000023604174,"about_ca_system_score_gemma":0.00023883904,"threshold_uncertainty_score":0.99999964},"labels":[],"label_agreement":null},{"id":"W2071975392","doi":"10.1210/jcem.86.10.7940","title":"Gαs Transcripts Are Biallelically Expressed in the Human Kidney Cortex: Implications for Pseudohypoparathyroidism Type 1b","year":2001,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University","funders":"","keywords":"Pseudohypoparathyroidism; GNAS complex locus; Internal medicine; Endocrinology; Biology; Genomic imprinting; Locus (genetics); Exon; Imprinting (psychology); Allele; Genetics; Parathyroid hormone; Gene expression; Medicine; Gene","score_opus":0.07749785752955718,"score_gpt":0.38442556502469705,"score_spread":0.30692770749513987,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071975392","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9762114,0.0030245844,0.0011208749,0.018499639,0.0005388424,0.00030264643,0.0000115546945,0.0000047165495,0.00028573285],"genre_scores_gemma":[0.9876424,0.005380262,0.0005026812,0.0050984183,0.0011429122,0.000018157381,0.000010032541,0.00002098706,0.00018414542],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99748385,0.0005448526,0.0011981252,0.00023016606,0.00013582152,0.0004071922],"domain_scores_gemma":[0.9981588,0.000264101,0.0006094317,0.0005609172,0.00027528158,0.00013146157],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001400524,0.00017706068,0.00049892947,0.00005763221,0.00016942533,0.000021356733,0.00097639946,0.0001712256,0.000011855481],"category_scores_gemma":[0.0011749978,0.00010466571,0.00034983485,0.00014061911,0.0002855278,0.0000071806803,0.000074157455,0.0004585676,0.000004291882],"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":[0.00047899387,0.000962914,0.02529698,0.000012869074,0.00039587973,0.00001660208,0.00037021152,0.0000814755,0.9282762,0.0031147832,0.03179435,0.009198744],"study_design_scores_gemma":[0.0031266415,0.00051235943,0.6081323,0.000011483948,0.00019297669,0.00065916963,0.00023874846,0.000007195776,0.002012101,0.0025939092,0.38236925,0.00014387247],"about_ca_topic_score_codex":0.000013917402,"about_ca_topic_score_gemma":0.000022580225,"teacher_disagreement_score":0.9262641,"about_ca_system_score_codex":0.0000036568379,"about_ca_system_score_gemma":0.00013971726,"threshold_uncertainty_score":0.4268144},"labels":[],"label_agreement":null},{"id":"W2072627772","doi":"10.1186/1471-213x-10-50","title":"Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome","year":2010,"lang":"en","type":"article","venue":"BMC Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Cancer Institute; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Placentation; Biology; Genomic imprinting; Genetics; Epigenetics; Gene; Phenotype; Imprinting (psychology); Gene silencing; Allele; X-inactivation; Genetic screen; Placenta; X chromosome; DNA methylation; Gene expression; Fetus","score_opus":0.014895957353840273,"score_gpt":0.24016786050549213,"score_spread":0.22527190315165185,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2072627772","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964648,0.00007305347,0.0023505508,0.000007767985,0.00017637845,0.00017235464,0.000027893724,0.000004719533,0.0007224943],"genre_scores_gemma":[0.95718706,0.000015397201,0.042541053,0.000027042366,0.000013309965,0.000014678213,0.00007535189,0.000015507349,0.00011057587],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989181,0.000033108823,0.0004046932,0.00031161195,0.000075377226,0.00025707434],"domain_scores_gemma":[0.9995961,0.000014473144,0.00011048559,0.00018688041,0.000040886156,0.000051139745],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022998304,0.00015020325,0.00025630477,0.00008665986,0.000023817525,0.000002914206,0.000252229,0.00021898978,0.00004622837],"category_scores_gemma":[0.00010626427,0.0001428292,0.0000604104,0.000098915436,0.00012673298,0.000003384412,0.00026577103,0.00010128562,0.0000071333875],"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":[0.000025847188,0.00007045558,0.074062526,0.00003223652,0.00002091178,5.92734e-7,0.000060321716,0.000071352835,0.92418915,0.0010142911,0.0000067065816,0.0004456083],"study_design_scores_gemma":[0.0020027885,0.00057730946,0.1850772,0.000056407378,0.00002060717,0.00024352927,0.00040647993,0.002367224,0.8066287,0.0018367796,0.0002498239,0.00053312746],"about_ca_topic_score_codex":0.00005929917,"about_ca_topic_score_gemma":0.00048264224,"teacher_disagreement_score":0.11756043,"about_ca_system_score_codex":0.000011829682,"about_ca_system_score_gemma":0.00020040054,"threshold_uncertainty_score":0.58244056},"labels":[],"label_agreement":null},{"id":"W2073875831","doi":"10.1002/ajmg.a.33172","title":"Pseudohypoparathyroidism type 1a and the <i>GNAS</i> p.R231H mutation: Somatic mosaicism in a mother with two affected sons","year":2010,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"BC Children's Hospital; Child and Family Research Institute; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Mutation; Genetics; Somatic cell; Germline mutation; Biology; Endocrinology; Germline mosaicism; Internal medicine; Medicine; Parathyroid hormone; Gene","score_opus":0.004315960447831264,"score_gpt":0.25215557719935416,"score_spread":0.2478396167515229,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073875831","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99537694,0.0011816175,0.0009417686,0.0020689995,0.00018611396,0.00012705736,0.0000010398168,0.0000027251858,0.00011372055],"genre_scores_gemma":[0.9949504,0.0006136643,0.0034693833,0.0006352159,0.00024791586,0.0000062803992,0.0000024010646,0.00002246364,0.00005228454],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99858946,0.00015920617,0.0003841482,0.00017488783,0.00045114686,0.00024117812],"domain_scores_gemma":[0.9990883,0.000062974985,0.00029545912,0.00023510639,0.00010632647,0.00021184547],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007748755,0.00014919053,0.0002996255,0.000047434765,0.000050421895,0.000033431785,0.0002951209,0.000076177836,0.000028379303],"category_scores_gemma":[0.00025785196,0.00009144968,0.00005827234,0.00019941233,0.0006031499,0.000002932807,0.00008338551,0.00036985677,0.0000026877701],"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":[0.0012945199,0.00096896157,0.059727326,0.000079342986,0.001124113,0.00038004553,0.004981498,0.0014034066,0.67426986,0.00057477725,0.0061298246,0.24906631],"study_design_scores_gemma":[0.11365962,0.040533416,0.4592528,0.0015212937,0.0017835028,0.06705485,0.019832106,0.041153416,0.11210117,0.0046414263,0.13333282,0.0051335846],"about_ca_topic_score_codex":0.000031428845,"about_ca_topic_score_gemma":0.00010722015,"teacher_disagreement_score":0.5621687,"about_ca_system_score_codex":0.00000401781,"about_ca_system_score_gemma":0.0002171851,"threshold_uncertainty_score":0.37292096},"labels":[],"label_agreement":null},{"id":"W2073877274","doi":"10.1159/000078197","title":"Genetic and genomic approaches to study placental development","year":2004,"lang":"en","type":"review","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"","keywords":"Biology; Computational biology; Profiling (computer programming); Context (archaeology); Identification (biology); Genetic engineering; Gene expression profiling; Evolutionary biology; Genetics; Bioinformatics; Gene; Gene expression; Computer science","score_opus":0.25139101583879053,"score_gpt":0.373508512475132,"score_spread":0.12211749663634147,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073877274","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.25248405,0.7451879,0.000085501066,0.00000806168,0.00004016758,0.00206877,0.000011949439,0.0000069070124,0.00010667969],"genre_scores_gemma":[0.039951254,0.954141,0.0045144074,0.00001070346,0.00021391056,0.0004623412,0.000058013346,0.00012125364,0.00052710105],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99633884,0.00034606512,0.00062239805,0.0013921255,0.00041335993,0.0008871936],"domain_scores_gemma":[0.99864084,0.00003436249,0.00009494646,0.0006616095,0.00006084494,0.00050738046],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0009319825,0.0005454573,0.0008694137,0.00035117555,0.00041278222,0.00016332352,0.00051208225,0.00033432525,0.000024611165],"category_scores_gemma":[0.00004499282,0.0004891336,0.0001160961,0.00029669734,0.00019085845,0.0000016356521,0.001899112,0.00035128157,0.00008330635],"study_design_candidate":"design_other","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":[0.000008689673,0.00020927016,0.0007187218,0.0032974004,0.0004409285,0.00001773935,0.00058286695,0.000013570318,0.00065888016,0.0000051966326,0.000007784713,0.99403894],"study_design_scores_gemma":[0.0009732766,0.0015616581,0.026697854,0.00096323335,0.00026082125,0.0006221584,0.0008267469,0.0000015847977,0.00011949846,0.000026067242,0.966841,0.0011061111],"about_ca_topic_score_codex":0.000018400151,"about_ca_topic_score_gemma":0.000015610807,"teacher_disagreement_score":0.99293286,"about_ca_system_score_codex":0.00009826281,"about_ca_system_score_gemma":0.00068233727,"threshold_uncertainty_score":0.99975604},"labels":[],"label_agreement":null},{"id":"W2074305055","doi":"10.1016/j.mce.2007.04.002","title":"Regulation of growth hormone expression by Delta-like protein 1 (Dlk1)","year":2007,"lang":"en","type":"article","venue":"Molecular and Cellular Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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 Institute of General Medical Sciences; National Institutes of Health; Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; University of Missouri","keywords":"Transcription factor; Biology; Psychological repression; Transfection; Promoter; Reporter gene; Regulation of gene expression; Epidermal growth factor; Gene; Gene expression; Molecular biology; Cell biology; Cell culture; Genetics","score_opus":0.004979355010618277,"score_gpt":0.20639719844591228,"score_spread":0.201417843435294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2074305055","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9289041,0.0047902344,0.06533387,0.000061332714,0.000056673354,0.00022149805,0.000005296357,0.0000117849795,0.0006152076],"genre_scores_gemma":[0.99698615,0.00009326239,0.0023221986,0.00007406955,0.000033735232,0.000012431675,0.00011922059,0.000026456244,0.00033249578],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987117,0.000060767816,0.0003088395,0.00038772944,0.00013423827,0.00039674927],"domain_scores_gemma":[0.99939764,0.0000065730883,0.00012441441,0.000301047,0.00008183299,0.00008851312],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015734792,0.00017690622,0.00019124994,0.00006802567,0.000060463986,0.000008851767,0.00013816392,0.00016423475,0.000014472405],"category_scores_gemma":[0.000038592156,0.00017631946,0.00007953546,0.0000783314,0.0001173691,0.0000035069907,0.00017660382,0.00008965654,0.0000025801655],"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":[0.00003230915,0.000045992,0.0008267424,0.000022799619,0.000028953786,0.000010112722,0.00001892941,0.0000032631451,0.9958593,0.00041720495,0.00025085357,0.0024835179],"study_design_scores_gemma":[0.0006850529,0.0003600401,0.003998436,0.000010171774,0.00001764016,0.00006742985,0.000052725754,0.000014589259,0.98918116,0.00023499617,0.005196167,0.00018158763],"about_ca_topic_score_codex":0.00004650301,"about_ca_topic_score_gemma":0.0000024323797,"teacher_disagreement_score":0.068082035,"about_ca_system_score_codex":0.000005997999,"about_ca_system_score_gemma":0.000016591635,"threshold_uncertainty_score":0.7190099},"labels":[],"label_agreement":null},{"id":"W2077085008","doi":"10.1210/jcem.86.3.7364","title":"Analysis of the P3 Promoter of the Human Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Gene in Pseudohypoparathyroidism Type 1b1","year":2001,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Royal Victoria Hospital","funders":"Novo Nordisk","keywords":"Promoter; Pseudohypoparathyroidism; Gene; Parathyroid hormone; DNA methylation; Methylation; Biology; Molecular biology; Coding region; Receptor; Internal medicine; Endocrinology; Genetics; Gene expression; Medicine; Calcium","score_opus":0.0295266382144212,"score_gpt":0.32701195916770187,"score_spread":0.2974853209532807,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077085008","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98853636,0.009338326,0.000030301802,0.0011832941,0.00048355013,0.00020221173,0.0000058067076,0.0000024091262,0.00021772257],"genre_scores_gemma":[0.99299586,0.0056898897,0.00021993858,0.00024635665,0.00025154377,0.0000024102312,0.000003536334,0.00001952513,0.00057095225],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9958351,0.0011526968,0.002070516,0.00024726737,0.00030487264,0.00038950873],"domain_scores_gemma":[0.99687624,0.0001474103,0.0016902079,0.0008965561,0.00031212292,0.00007745872],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001669422,0.00021992758,0.00095640606,0.00012628645,0.000102801576,0.00000790705,0.0011854427,0.00023892742,0.000038247483],"category_scores_gemma":[0.0007363124,0.00011205849,0.0008439821,0.00073437573,0.00057717075,0.000007834339,0.00040823937,0.0007036928,0.0000040237924],"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":[0.00019028748,0.0002963731,0.052807197,0.0000028567986,0.0015426629,0.000003860786,0.00020096019,0.0007914528,0.94208604,0.0000971705,0.0006846883,0.0012964766],"study_design_scores_gemma":[0.0019017712,0.00046800642,0.92205584,0.000013207265,0.0014100991,0.00022797199,0.00012310361,0.000064735395,0.06578394,0.00028337396,0.0075247767,0.00014315116],"about_ca_topic_score_codex":0.000063140484,"about_ca_topic_score_gemma":0.000043479977,"teacher_disagreement_score":0.87630206,"about_ca_system_score_codex":0.000008091202,"about_ca_system_score_gemma":0.00014019023,"threshold_uncertainty_score":0.45696127},"labels":[],"label_agreement":null},{"id":"W2077235837","doi":"10.1016/j.artres.2008.08.309","title":"P1.01 TREATMENT WITH DEXAMETHASONE REVERSES IMPARED ELASTOGENESIS AND COLLAGENOGENESIS IN CULTURES OF FIBROBLASTS FROM PATIENTS WITH LOEYS-DIETZ SYNDROME (LDS)","year":2008,"lang":"en","type":"article","venue":"Artery Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Medicine; Dexamethasone; Internal medicine","score_opus":0.027110418449368647,"score_gpt":0.2762683297107883,"score_spread":0.24915791126141965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077235837","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985752,0.0007951268,0.00002808089,0.00003204936,0.000013931484,0.0004140261,0.000050096343,0.0000050778663,0.00008641527],"genre_scores_gemma":[0.9971866,0.0006231318,0.0017258707,0.000012008651,0.000020258594,0.000053773954,0.00006883166,0.000029692168,0.0002798043],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983436,0.0001633613,0.00022626402,0.00049898954,0.0003488832,0.00041890287],"domain_scores_gemma":[0.9991911,0.000061977335,0.00006939336,0.00038802807,0.00016178904,0.00012772485],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014502107,0.00019834042,0.00029053952,0.00012342089,0.00012612095,0.000018764626,0.0001452441,0.000107893626,0.000033111326],"category_scores_gemma":[0.000030514411,0.00014266194,0.00004089532,0.00027738736,0.00025970166,0.0000084649555,0.00012376437,0.0000629766,0.000004615063],"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":[0.00033275533,0.00028210663,0.8376716,0.000027916187,0.00019244023,0.00004150943,0.00047422652,0.000061795065,0.158862,3.553706e-7,0.000123041,0.0019302751],"study_design_scores_gemma":[0.0023627104,0.0042945924,0.9053004,0.00008232517,0.000020772051,0.000098597884,0.0004618953,0.000013951807,0.08670952,0.0000042872794,0.00045413748,0.00019684764],"about_ca_topic_score_codex":0.0008013573,"about_ca_topic_score_gemma":0.000700484,"teacher_disagreement_score":0.07215247,"about_ca_system_score_codex":0.00004058839,"about_ca_system_score_gemma":0.00013147449,"threshold_uncertainty_score":0.58175856},"labels":[],"label_agreement":null},{"id":"W2077822383","doi":"10.1073/pnas.0805291105","title":"A <i>Drosophila</i> model for Angelman syndrome","year":2008,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; Howard Hughes Medical Institute","keywords":"UBE3A; Angelman syndrome; Mushroom bodies; Ubiquitin ligase; Biology; Ubiquitin; Genetics; Loss function; Ataxia; Neurodevelopmental disorder; Missense mutation; Null allele; Drosophila melanogaster; Drosophila (subgenus); Mutation; Mutant; Cell biology; Neuroscience; Gene; Phenotype","score_opus":0.049485525106867545,"score_gpt":0.28896140075838656,"score_spread":0.239475875651519,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077822383","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99750525,0.00013375006,0.000022832875,0.00067943457,0.000009604567,0.00013804802,0.000013188867,0.0000024742747,0.0014954084],"genre_scores_gemma":[0.9937589,0.000041483305,0.005507774,0.00022550658,0.000040826344,0.000012911459,2.3361204e-7,0.0000040276514,0.00040834665],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999183,0.000001367641,0.00017562554,0.00018446885,0.0003365921,0.00011893391],"domain_scores_gemma":[0.99962986,0.000010009425,0.00017687328,0.0000072726157,0.00015387882,0.00002208839],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003613488,0.000062387655,0.00008750391,0.0000387453,0.00015501613,0.000004990255,0.00043735193,0.000062944746,0.000001114569],"category_scores_gemma":[0.00017793936,0.000044783817,0.00008354621,0.00015229877,0.00037851027,0.000009428074,0.00011709777,0.00003756489,2.3940217e-7],"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":[0.0000035919527,0.000021652424,0.0043285782,0.000029873547,0.0000100106245,1.4189127e-9,0.0000424412,0.00052558316,0.99178,0.0023235825,0.0008664283,0.00006824739],"study_design_scores_gemma":[0.00039351493,0.00020903534,0.09764868,0.000044355293,0.000013228448,0.0002128287,0.000050800896,0.019348305,0.86046624,0.020801429,0.0006475118,0.00016407306],"about_ca_topic_score_codex":8.376177e-7,"about_ca_topic_score_gemma":1.43284815e-8,"teacher_disagreement_score":0.13131377,"about_ca_system_score_codex":0.000004349006,"about_ca_system_score_gemma":0.00002903018,"threshold_uncertainty_score":0.1826231},"labels":[],"label_agreement":null},{"id":"W2079253705","doi":"10.1111/j.1399-0004.2010.01443.x","title":"The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"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":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Methylation; Biology; Epigenetics; Differentially methylated regions; DNA methylation; Genetics; Gene; Chromosome; Placenta; Fetus; Gene expression; Pregnancy","score_opus":0.04354641001633599,"score_gpt":0.36514203586032823,"score_spread":0.32159562584399226,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2079253705","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99295527,0.0025390594,0.0034622839,0.00019477244,0.00038896443,0.000355878,0.000035356905,0.0000020770842,0.00006634643],"genre_scores_gemma":[0.9915567,0.0044205543,0.0038520866,0.000016783883,0.00005840569,0.000027248636,0.000013115485,0.000011576361,0.000043542437],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989949,0.00008457391,0.00046221237,0.00022259951,0.00009171199,0.00014403685],"domain_scores_gemma":[0.9982779,0.0009784733,0.0002356786,0.00034037887,0.00012195769,0.000045587894],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000794278,0.0000978757,0.00015641948,0.000008422612,0.00013306002,0.00000928078,0.00019455097,0.00013993075,0.00000988199],"category_scores_gemma":[0.0010634653,0.00006134138,0.00016149085,0.000040250085,0.0005816606,0.000001151722,0.00024385702,0.00009388355,4.3598047e-7],"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":[0.00010660136,0.00012625041,0.62052184,0.000030283565,0.00017186142,2.5018826e-8,0.00005995863,0.000018502216,0.20667851,0.00011845955,0.00017239679,0.17199531],"study_design_scores_gemma":[0.00075648085,0.0008154736,0.7373369,0.000005447313,0.0000922132,0.0000023138487,0.0002937187,0.009467603,0.23487698,0.0003676045,0.015863659,0.00012164661],"about_ca_topic_score_codex":0.000013285216,"about_ca_topic_score_gemma":0.00032348564,"teacher_disagreement_score":0.17187366,"about_ca_system_score_codex":0.000001395585,"about_ca_system_score_gemma":0.000031755757,"threshold_uncertainty_score":0.25014287},"labels":[],"label_agreement":null},{"id":"W2080324075","doi":"10.1016/j.placenta.2004.01.020","title":"Genes and Development—A Workshop Report","year":2004,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Calgary","funders":"","keywords":"Placenta; Biology; Function (biology); Genetically modified mouse; Phenotype; Computational biology; Transgene; Gene; Cell biology; Genetics; Pregnancy; Fetus","score_opus":0.015639742112461275,"score_gpt":0.24856034879075967,"score_spread":0.2329206066782984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080324075","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99607384,0.0010944416,0.0017475213,0.00013018887,0.000109473716,0.00006371649,5.626489e-7,0.000008341041,0.0007719131],"genre_scores_gemma":[0.9879205,0.00015197265,0.010610908,0.00010714378,0.00007391521,0.000006129044,0.000039865972,0.000011614115,0.0010779428],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99944526,0.00000555122,0.00012123963,0.00021716788,0.000059944166,0.00015081542],"domain_scores_gemma":[0.9997321,0.0000023685604,0.000036101304,0.00015510441,0.000016832277,0.00005750978],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007988973,0.00007862823,0.00006106611,0.000014063342,0.000060078124,0.000019269484,0.000060328515,0.00005593068,0.000013683877],"category_scores_gemma":[0.000030809915,0.00007569582,0.000015669466,0.000024688152,0.000023435454,0.0000012289358,0.00011526486,0.000028930881,0.000011814923],"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":[0.000018106231,0.00010345736,0.1419411,0.00004215645,0.00012537694,0.00006643418,0.00033564935,0.00020658593,0.77745295,0.00006158861,0.0010619323,0.078584686],"study_design_scores_gemma":[0.001086372,0.0000571589,0.0721109,0.000029585071,0.000011004578,0.0014442891,0.00039031578,0.0000052873306,0.5348245,0.00004666414,0.38964728,0.00034662895],"about_ca_topic_score_codex":0.000008049029,"about_ca_topic_score_gemma":0.00001854853,"teacher_disagreement_score":0.38858536,"about_ca_system_score_codex":0.0000073863844,"about_ca_system_score_gemma":0.000057038575,"threshold_uncertainty_score":0.30867857},"labels":[],"label_agreement":null},{"id":"W2080361063","doi":"10.1002/ajmg.a.36490","title":"A cryptic familial rearrangement of 11p15.5, involving both imprinting centers, in a family with a history of short stature","year":2014,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Short stature; Genomic imprinting; Family history; Genetics; Psychology; Medicine; Biology; Pediatrics; Internal medicine; Gene","score_opus":0.009875967680988498,"score_gpt":0.23778336149258597,"score_spread":0.22790739381159747,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080361063","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99411833,0.002280104,0.0029413686,0.000088599496,0.0002078659,0.00009134019,0.0000018165691,0.0000017219733,0.0002688414],"genre_scores_gemma":[0.99145633,0.0013751319,0.0067368285,0.00021340731,0.0001600038,0.0000027512096,0.0000030388837,0.00002135822,0.00003117069],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9977513,0.00016164489,0.0007993164,0.00021897217,0.00076447043,0.00030433031],"domain_scores_gemma":[0.9987331,0.00003978428,0.00056571857,0.000271461,0.00017042844,0.0002194939],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010362866,0.00016878756,0.0004930311,0.00012369567,0.000012641503,0.0000051867805,0.00038741497,0.000096166805,0.000017877906],"category_scores_gemma":[0.00024437212,0.00013944693,0.00013044069,0.00013648365,0.000410462,0.000003220148,0.0001465663,0.00026040175,2.8512085e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021222995,0.00032171627,0.15693884,0.00016559573,0.00026362124,0.000021249769,0.0010763037,0.00040199334,0.7481136,0.00001747996,0.0010276731,0.09143971],"study_design_scores_gemma":[0.0102984775,0.028228538,0.7882666,0.0035594762,0.0005249473,0.0007165035,0.010779097,0.007322967,0.037738662,0.00006868119,0.11091291,0.0015831339],"about_ca_topic_score_codex":0.000102115875,"about_ca_topic_score_gemma":0.00004067698,"teacher_disagreement_score":0.71037495,"about_ca_system_score_codex":0.000049953203,"about_ca_system_score_gemma":0.00048941525,"threshold_uncertainty_score":0.5686481},"labels":[],"label_agreement":null},{"id":"W2080675094","doi":"10.1016/j.gene.2012.01.027","title":"Loss of the Prader–Willi obesity syndrome protein necdin promotes adipogenesis","year":2012,"lang":"en","type":"article","venue":"Gene","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Canadian Institutes of Health Research; Alberta Innovates","keywords":"Adipogenesis; Biology; Obesity; Transcription factor; Endocrinology; Receptor; Internal medicine; Gene; Cell biology; Adipose tissue; Biochemistry","score_opus":0.010178052027303734,"score_gpt":0.21682648000981516,"score_spread":0.20664842798251143,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080675094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970071,0.0018076877,0.00024787092,0.00015536798,0.00018033481,0.00040126682,0.00001205602,0.0000081699445,0.0001801966],"genre_scores_gemma":[0.9970141,0.000028331147,0.0018999798,0.000053543612,0.00013510365,0.000032596847,0.000010384088,0.000023409497,0.00080253783],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989695,0.00007368938,0.0002175621,0.00022102156,0.00015673373,0.00036147734],"domain_scores_gemma":[0.9991932,0.0000046202267,0.00013015694,0.0005326488,0.000052276817,0.00008709321],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024044205,0.00014890046,0.0001548986,0.000020371785,0.00008908312,0.00000952845,0.0002924279,0.00012713103,0.00004149531],"category_scores_gemma":[0.00007574748,0.000110597175,0.0001303321,0.00011585191,0.0000849326,0.0000038252115,0.00026996256,0.0000592285,0.000015995472],"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":[0.0000010387301,0.000091747046,0.14218827,0.00003688382,0.000048122554,2.6016156e-7,0.000047764534,0.0000068578624,0.8565395,0.000020614712,0.00006230909,0.0009566289],"study_design_scores_gemma":[0.00014223071,0.00008244561,0.32430312,0.000015883841,0.000020304133,0.00013803653,0.000018669047,0.000004250896,0.6722792,0.000021320406,0.0028604784,0.00011409798],"about_ca_topic_score_codex":0.000027566888,"about_ca_topic_score_gemma":0.0000039822,"teacher_disagreement_score":0.18426034,"about_ca_system_score_codex":0.00000900058,"about_ca_system_score_gemma":0.000049382023,"threshold_uncertainty_score":0.4510022},"labels":[],"label_agreement":null},{"id":"W2080676561","doi":"10.1007/s00439-012-1207-x","title":"Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia","year":2012,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université de Sherbrooke","funders":"","keywords":"Biology; Sarcosine; Human genetics; Genetics; Gene; Molecular medicine; Metabolic disease; Computational biology; Endocrinology; Amino acid; Glycine","score_opus":0.01178772805927869,"score_gpt":0.2426123216915446,"score_spread":0.2308245936322659,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080676561","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998315,0.0008210508,0.000109340705,0.000030899315,0.000044152937,0.00028977476,0.000006976318,0.0000038894445,0.0003789382],"genre_scores_gemma":[0.997906,0.000024982703,0.0015038128,0.0001779665,0.000111426365,0.000028508397,0.00017736328,0.000025069816,0.00004485559],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989451,0.000071205286,0.00022918763,0.00020438952,0.00016456789,0.00038555503],"domain_scores_gemma":[0.99945676,0.000008361829,0.000060407307,0.00037194736,0.000041490588,0.000061012943],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018971697,0.00014899064,0.000106114596,0.00006876937,0.00007499263,0.000022522212,0.00021654452,0.00007833167,0.000019181036],"category_scores_gemma":[0.00001791259,0.00011351369,0.00003303507,0.00016847705,0.00006245988,0.0000036152817,0.00007500907,0.000096709955,0.0000088920515],"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":[0.000007037814,0.00035262,0.95945746,0.000008410754,0.000011658839,0.000001085609,0.00035773916,0.00034553467,0.03831277,0.000027333423,0.000101279475,0.0010170705],"study_design_scores_gemma":[0.00109555,0.0002557508,0.97615874,0.000010129487,0.000013513552,0.000009360037,0.00009919928,0.000022802022,0.020271692,0.0000263213,0.0018582189,0.00017872917],"about_ca_topic_score_codex":0.000020024649,"about_ca_topic_score_gemma":0.00011117733,"teacher_disagreement_score":0.01804108,"about_ca_system_score_codex":0.000016255266,"about_ca_system_score_gemma":0.00002520324,"threshold_uncertainty_score":0.4628954},"labels":[],"label_agreement":null},{"id":"W2080876236","doi":"10.1016/j.jpeds.2003.09.049","title":"Sudden death in growth hormone–treated children with Prader-Willi syndrome","year":2004,"lang":"en","type":"review","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":108,"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","funders":"","keywords":"Medicine; Autopsy; Growth hormone; Bronchopneumonia; Pediatrics; Apnea; Growth hormone treatment; Hormone; Growth retardation; Sudden death; Cause of death; Internal medicine; Disease; Pregnancy","score_opus":0.015103356636278119,"score_gpt":0.25640263626346743,"score_spread":0.2412992796271893,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080876236","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10984018,0.8895617,0.000094669784,0.00002133332,0.00007756772,0.00033978673,0.00001424352,0.000003432663,0.000047055823],"genre_scores_gemma":[0.02515113,0.97381175,0.00041164103,0.000014603177,0.00042990164,0.000004101685,0.00003694469,0.00006865492,0.00007129525],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.998102,0.00019326556,0.00078503584,0.00022473147,0.00032865803,0.0003662894],"domain_scores_gemma":[0.9983048,0.000044625573,0.0010323536,0.00035938443,0.00014079383,0.00011805882],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006420162,0.00039675366,0.0009077545,0.00024123403,0.00006172313,0.000035955913,0.0006980308,0.0003392602,0.0000043036966],"category_scores_gemma":[0.00010565698,0.00022687708,0.0002944178,0.00043321948,0.00004910147,0.000005808042,0.0001547424,0.00056987285,0.000007672176],"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":[0.00009550203,0.002853378,0.4442821,0.043092288,0.005134816,0.00064671726,0.001059101,0.0014017294,0.00023626053,0.00014094623,0.0068492116,0.49420792],"study_design_scores_gemma":[0.012217229,0.018979244,0.5397128,0.015509933,0.02841037,0.18898413,0.00031010914,0.0000026690664,0.0000903054,0.00040346652,0.18914406,0.0062356736],"about_ca_topic_score_codex":0.00005722918,"about_ca_topic_score_gemma":0.000005507119,"teacher_disagreement_score":0.48797226,"about_ca_system_score_codex":0.0000667006,"about_ca_system_score_gemma":0.00061232375,"threshold_uncertainty_score":0.9251779},"labels":[],"label_agreement":null},{"id":"W2082827707","doi":"10.1071/rd06118","title":"Gene expression and maintenance of pregnancy in bovine: roles of trophoblastic binucleate cell-specific molecules","year":2006,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":57,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; University of Calgary","funders":"","keywords":"Biology; Placentation; Placental lactogen; Pregnancy; Gene expression; Placenta; Cell biology; Microarray analysis techniques; Cell; Gene; Fetus; Genetics","score_opus":0.008195366511169309,"score_gpt":0.1976218719923018,"score_spread":0.1894265054811325,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2082827707","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9905453,0.00800655,0.0011944749,0.00001785572,0.000038205275,0.00011914876,0.0000016995184,0.000003398587,0.00007341526],"genre_scores_gemma":[0.99054015,0.0006238343,0.0086795315,0.0000020680347,0.000011175378,0.0000075078347,0.000009693166,0.000006692559,0.00011934161],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99908173,0.000026507323,0.0003158591,0.0003839238,0.000076667275,0.00011531],"domain_scores_gemma":[0.9996122,0.0000034654327,0.0000997843,0.00020655655,0.000055485627,0.000022520318],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013301508,0.00009171853,0.00013374281,0.000041952524,0.000031309544,0.0000053361414,0.00004007457,0.00005215789,0.0000037150958],"category_scores_gemma":[0.000022923268,0.00008360984,0.000016962671,0.0000540607,0.000066522996,0.000003566333,0.000082936225,0.000027682763,2.7533372e-7],"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":[0.00006763866,0.000083887455,0.020265313,0.000108420616,0.0000036726728,4.052858e-7,0.000100566875,0.00008932656,0.96907157,0.0000025520922,0.000028021615,0.0101786405],"study_design_scores_gemma":[0.00024317816,0.000049949507,0.37341684,0.000070491325,0.0000013990758,0.000003981005,0.000059660517,0.0000085639795,0.6255235,0.000028238466,0.00053748203,0.000056723293],"about_ca_topic_score_codex":0.00001416531,"about_ca_topic_score_gemma":0.0000073262413,"teacher_disagreement_score":0.35315153,"about_ca_system_score_codex":0.000007316255,"about_ca_system_score_gemma":0.000026908798,"threshold_uncertainty_score":0.34095106},"labels":[],"label_agreement":null},{"id":"W2084601112","doi":"10.1016/j.placenta.2005.07.004","title":"Unbalanced Placental Expression of Imprinted Genes in Human Intrauterine Growth Restriction","year":2005,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":300,"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","funders":"","keywords":"Genomic imprinting; Biology; MEG3; Intrauterine growth restriction; Endocrinology; Internal medicine; Placenta; Gene expression; DNA methylation; Microarray analysis techniques; Andrology; Gene; Fetus; Genetics; RNA; Medicine; Pregnancy; Long non-coding RNA","score_opus":0.0076232740461057045,"score_gpt":0.24546667790580262,"score_spread":0.2378434038596969,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084601112","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985937,0.00020413539,0.0003928359,0.000059730155,0.00009271025,0.00012692813,0.0000067433357,0.000009246217,0.0005139839],"genre_scores_gemma":[0.99757165,0.0008760379,0.0012555507,0.000025537372,0.00011762253,0.000008568803,0.00007529984,0.000013726722,0.000055987985],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99919045,0.00003265995,0.00025416794,0.00023843134,0.00009283089,0.00019147036],"domain_scores_gemma":[0.99964225,0.0000047677518,0.00009046826,0.00018775174,0.000029718716,0.000045066343],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008966644,0.00011097474,0.00012189534,0.000060112143,0.000031464308,0.000007702702,0.00013087015,0.00008758072,0.000037902664],"category_scores_gemma":[0.000023641403,0.0001100741,0.000043329488,0.00008131161,0.0000277247,0.0000045680295,0.00013875042,0.000063036816,0.0000033740546],"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":[0.00002542462,0.00008175417,0.057078347,0.000016489004,0.000005885083,5.324144e-7,0.000026405074,0.000075761905,0.94105,0.000049623108,0.00012981324,0.0014599462],"study_design_scores_gemma":[0.0009008029,0.00011313917,0.09169239,0.000031372532,0.0000034820323,0.000011327681,0.00006980498,0.00016242036,0.905726,0.00002398353,0.0011549632,0.00011028681],"about_ca_topic_score_codex":0.00008481635,"about_ca_topic_score_gemma":0.000045571844,"teacher_disagreement_score":0.035323992,"about_ca_system_score_codex":0.000023225437,"about_ca_system_score_gemma":0.000015133685,"threshold_uncertainty_score":0.44886914},"labels":[],"label_agreement":null},{"id":"W2084698702","doi":"10.1053/beog.2000.0107","title":"Confined placental mosaicism and genomic imprinting","year":2000,"lang":"en","type":"review","venue":"Best Practice & Research Clinical Obstetrics & Gynaecology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":21,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"B.C. Women's Hospital & Health Centre; University of British Columbia","funders":"","keywords":"Uniparental disomy; Genomic imprinting; Angelman syndrome; Imprinting (psychology); Genetics; Mendelian inheritance; Non-Mendelian inheritance; Beckwith–Wiedemann syndrome; Germline mosaicism; Placenta; Biology; Medicine; Chromosome; Karyotype; Fetus; Mutation; Pregnancy; Gene; DNA methylation","score_opus":0.138468466168502,"score_gpt":0.4726787761983441,"score_spread":0.3342103100298421,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084698702","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0046129744,0.97971237,0.000021242819,0.00014050287,0.0018479897,0.0015503551,0.000042375996,0.000023027458,0.012049168],"genre_scores_gemma":[0.0010905167,0.9936067,0.0017356512,0.00019543116,0.0006582288,0.00015063022,0.00021091463,0.00015739723,0.0021945378],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9900649,0.0036490276,0.002207337,0.0019161529,0.0006478856,0.001514668],"domain_scores_gemma":[0.9827821,0.013869939,0.0009074791,0.0012552282,0.0005527823,0.0006324294],"candidate_categories":["metaresearch","metaepi_narrow","research_integrity"],"consensus_categories":["research_integrity"],"category_scores_codex":[0.0067373007,0.0006602077,0.0019672043,0.0005011505,0.0004223674,0.0002642375,0.001136351,0.00212075,0.0006491406],"category_scores_gemma":[0.056064177,0.00062551623,0.00063094206,0.0007742063,0.0008119869,0.000018734407,0.002183242,0.0030830004,0.00064550765],"study_design_candidate":"design_other","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":[0.000017927452,0.0005493232,0.00027651124,0.0008623697,0.00036303798,0.00012519787,0.000012995563,6.9886465e-7,0.00001366631,0.00004938678,0.0007836634,0.9969452],"study_design_scores_gemma":[0.0010195496,0.002194454,0.00048231357,0.00015922642,0.00048918027,0.00057478197,0.00017029043,0.000016876675,0.0000031406025,0.000021337137,0.9942894,0.00057943474],"about_ca_topic_score_codex":0.00006620147,"about_ca_topic_score_gemma":0.000011467817,"teacher_disagreement_score":0.9963658,"about_ca_system_score_codex":0.00017913104,"about_ca_system_score_gemma":0.001739813,"threshold_uncertainty_score":0.9996196},"labels":[],"label_agreement":null},{"id":"W2085263711","doi":"10.1159/000118545","title":"Abnormal Food-Seeking Behavior after Surgery for Craniopharyngioma","year":2008,"lang":"en","type":"article","venue":"Neuropsychobiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Douglas Mental Health University Institute; Montreal General Hospital","funders":"","keywords":"Craniopharyngioma; Feeding behavior; Obesity; Eating behavior; Food intake; Psychology; Foraging; Medicine; Surgery; Endocrinology; Biology","score_opus":0.0212507388158746,"score_gpt":0.24675655815751413,"score_spread":0.22550581934163952,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2085263711","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996501,0.00048136624,0.0012780457,0.000069334645,0.0010921046,0.00029803268,0.000048037167,0.000024764315,0.00020727208],"genre_scores_gemma":[0.99727917,0.00014192578,0.0006435706,0.00075638515,0.0004722728,0.00023135418,0.00008629824,0.00004704191,0.00034196573],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986183,0.00006340945,0.00029641754,0.0005054832,0.000057616908,0.0004587525],"domain_scores_gemma":[0.9993458,0.000042173968,0.00008759667,0.00036441657,0.00007159348,0.00008841672],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000109491055,0.0002001555,0.00022435901,0.00006745124,0.0001239642,0.000009450036,0.00017202363,0.00018347886,0.00005649613],"category_scores_gemma":[0.00006921661,0.00019666569,0.00024152802,0.000074313015,0.0001121593,0.000003226324,0.000083993735,0.00007912577,0.000017112983],"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":[0.000115352595,0.00011737929,0.33792475,0.00001999358,0.000046318724,0.000027634045,0.000026773238,0.0000033583865,0.6543867,0.000010510655,0.0032660824,0.004055119],"study_design_scores_gemma":[0.0006920198,0.0009997735,0.9062761,0.000006841366,0.000026747628,0.001535401,0.00000903514,0.000014152649,0.015952414,0.000014308287,0.07411836,0.00035484592],"about_ca_topic_score_codex":0.0000034532698,"about_ca_topic_score_gemma":0.000004420514,"teacher_disagreement_score":0.6384343,"about_ca_system_score_codex":0.0000042309357,"about_ca_system_score_gemma":0.000041654275,"threshold_uncertainty_score":0.80197936},"labels":[],"label_agreement":null},{"id":"W2086084923","doi":"10.1007/s004280100509","title":"Promoter-specific transcription of the IGF2 gene: a novel rapid, non-radioactive and highly sensitive protocol for mRNA analysis","year":2001,"lang":"en","type":"article","venue":"Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Jewish General Hospital","funders":"Deutsche Forschungsgemeinschaft","keywords":"Biology; Molecular biology; Genomic imprinting; Gene expression; Gene; Promoter; Messenger RNA; Northern blot; RNA; Insulin-like growth factor 2; Ribonuclease; Transcription (linguistics); Genetics","score_opus":0.030873603737841742,"score_gpt":0.33033961654090543,"score_spread":0.2994660128030637,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086084923","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9280817,0.0002939103,0.048313957,0.00043661078,0.00014750255,0.021857243,0.00012155679,0.000027085664,0.0007204492],"genre_scores_gemma":[0.9791864,0.00031592563,0.01262664,0.0002995389,0.00026289737,0.0070116315,0.00014075481,0.000041406485,0.00011476155],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9972286,0.00028727,0.00067619653,0.00096337387,0.000251998,0.00059251225],"domain_scores_gemma":[0.9981791,0.00018561311,0.00046613568,0.0008342707,0.00018874709,0.00014617165],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00077244564,0.00045011914,0.0007040885,0.00017319007,0.0002486602,0.000027916589,0.00048378613,0.0003122567,0.00000779289],"category_scores_gemma":[0.00025361817,0.0003032229,0.0005032161,0.0005002865,0.00083913055,0.00001427081,0.00026185345,0.00033982488,0.0000016293884],"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":[0.00037986954,0.0002682143,0.0027703901,0.00006886318,0.00089753105,0.000005122441,0.0004756649,0.00023577492,0.9844005,0.00013800495,0.00014115675,0.010218919],"study_design_scores_gemma":[0.0066743544,0.003042133,0.22887763,0.00013133959,0.0012026458,0.000080947175,0.0010476897,0.0034301574,0.73674965,0.00090719346,0.017010067,0.0008461872],"about_ca_topic_score_codex":0.000051750667,"about_ca_topic_score_gemma":0.000019118048,"teacher_disagreement_score":0.24765083,"about_ca_system_score_codex":0.000017685652,"about_ca_system_score_gemma":0.00013402778,"threshold_uncertainty_score":0.999942},"labels":[],"label_agreement":null},{"id":"W2086493068","doi":"10.1016/j.cjca.2012.05.018","title":"Coronary Artery Dissection in Prader–Willi Syndrome: Case Report and Literature Review","year":2012,"lang":"en","type":"review","venue":"Canadian Journal of Cardiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"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; Artery dissection; Dissection (medical); Cardiology; Myocardial infarction; Internal medicine; Artery; Hypoxemia; Right coronary artery; Acute coronary syndrome; Surgery; Coronary angiography","score_opus":0.020140795290613057,"score_gpt":0.273911714645204,"score_spread":0.2537709193545909,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086493068","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0033390552,0.9951908,0.0000439445,0.00005117118,0.0008514289,0.00028953975,0.000026486578,0.0000010760037,0.00020652157],"genre_scores_gemma":[0.019724507,0.9792007,0.00007020886,0.00005671954,0.0006738432,0.000013124102,0.00011449865,0.000034682085,0.000111706744],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.998101,0.00033078293,0.0008358453,0.0002844709,0.00006287733,0.00038502656],"domain_scores_gemma":[0.9985866,0.000022107775,0.0005176547,0.00033107272,0.000107451866,0.00043514304],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007288097,0.00029192166,0.0013735584,0.00025615067,0.000053483403,0.00002425685,0.00015026926,0.0005393087,0.000007376026],"category_scores_gemma":[0.0001740914,0.0002451274,0.0003922798,0.00016133726,0.00008791665,0.000007577391,0.000038452934,0.00049579254,0.0000019134552],"study_design_candidate":"design_other","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":[8.3101816e-7,0.000003803277,0.0033831976,0.015136233,0.0006475064,0.21064785,0.000034838195,0.000004874957,0.0000066787634,0.0000041639296,0.0030483673,0.7670817],"study_design_scores_gemma":[0.00005380344,0.00008057497,0.0007349494,0.0061777825,0.00025780874,0.5140696,0.000008008725,3.2213823e-8,9.3555634e-8,0.000001902216,0.47849765,0.00011777177],"about_ca_topic_score_codex":0.000034231893,"about_ca_topic_score_gemma":0.0003187227,"teacher_disagreement_score":0.7669639,"about_ca_system_score_codex":0.00006345429,"about_ca_system_score_gemma":0.0008088448,"threshold_uncertainty_score":0.9996004},"labels":[],"label_agreement":null},{"id":"W2086864499","doi":"10.1017/s0140525x08004317","title":"Imprinting and psychiatric genetics: Beware the diagnostic phenotype","year":2008,"lang":"en","type":"article","venue":"Behavioral and Brain Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"GRASP; Imprinting (psychology); Phenotype; Psychology; Predictive power; Genomic imprinting; Genetics; Biology; Neuroscience; Gene; Computer science; Epistemology; Philosophy","score_opus":0.028770502137624013,"score_gpt":0.286319976345389,"score_spread":0.25754947420776503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086864499","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952935,0.0036092552,0.000056561064,0.0006509894,0.000111450936,0.00010771103,0.0000025753304,0.0000065971844,0.0001613521],"genre_scores_gemma":[0.9975537,0.00060230837,0.0013273497,0.00025032964,0.000114873656,0.000007906811,0.0000022788442,0.0000056964786,0.00013553094],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99920934,0.000029929943,0.00012416916,0.00030465974,0.00011811296,0.00021377896],"domain_scores_gemma":[0.99969983,0.00004075645,0.000047786434,0.00012632359,0.00002464178,0.00006068077],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002169278,0.000100764344,0.000076069795,0.000024787258,0.00056972215,0.00005308615,0.00016662381,0.00004820259,0.000008494968],"category_scores_gemma":[0.00006682685,0.0000657183,0.000028672343,0.00011806163,0.00047618506,0.0000043104915,0.00019483948,0.000050481376,0.0000020496207],"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":[0.0000017763973,0.000039172384,0.8702567,0.000008596229,0.0000044663116,0.0000023891942,0.0003133646,0.000009405686,0.06870619,0.000046562025,0.0005462695,0.060065094],"study_design_scores_gemma":[0.00023321662,0.0005017817,0.98795897,0.000007594283,0.000018115392,0.00025069626,0.00052491494,0.000075250995,0.00391595,0.00011100401,0.006196731,0.00020576784],"about_ca_topic_score_codex":0.000055897563,"about_ca_topic_score_gemma":0.000022158052,"teacher_disagreement_score":0.11770226,"about_ca_system_score_codex":0.0000014141331,"about_ca_system_score_gemma":0.000035879704,"threshold_uncertainty_score":0.43818998},"labels":[],"label_agreement":null},{"id":"W2089207825","doi":"10.1038/mp.2011.157","title":"Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder","year":2011,"lang":"en","type":"article","venue":"Molecular Psychiatry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":218,"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","funders":"","keywords":"Genome-wide association study; Single-nucleotide polymorphism; Genetic association; Genetics; Biology; SNP; Locus (genetics); Meta-analysis; Multiple comparisons problem; Candidate gene; Gene; Medicine; Genotype; Internal medicine","score_opus":0.03286568714207273,"score_gpt":0.24576275200771822,"score_spread":0.21289706486564547,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2089207825","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9836665,0.0048494264,0.010350941,0.00007639447,0.00006528123,0.000274779,0.000048822592,0.000014745506,0.00065312703],"genre_scores_gemma":[0.99717474,0.000026429732,0.0023430244,0.00012632535,0.00001988598,0.00001622673,0.0001168267,0.000044499,0.00013201982],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99828655,0.0001789585,0.00041958914,0.0005330431,0.0002983156,0.00028357693],"domain_scores_gemma":[0.99876887,0.000017196382,0.00045757878,0.000530066,0.00015258837,0.00007372656],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059146574,0.00025980023,0.00055687706,0.00014229918,0.00009783075,0.000041326453,0.00025658193,0.00009752071,0.000058112655],"category_scores_gemma":[0.0001508425,0.0002221966,0.00041199502,0.00042210333,0.000059421887,0.0000073467263,0.0001557959,0.00011080335,0.0000018871979],"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":[0.0000090133935,0.000420314,0.9223618,0.000011961062,0.058561813,0.0000020532075,0.00019455852,0.00008290451,0.018269138,0.000015628877,0.0000114326285,0.000059401696],"study_design_scores_gemma":[0.00051786524,0.00034145024,0.9632229,0.000002967826,0.03361419,0.0000016660814,0.00063008105,0.000010943412,0.001209279,0.000043693217,0.00013798181,0.00026693864],"about_ca_topic_score_codex":0.00011832818,"about_ca_topic_score_gemma":0.0012170083,"teacher_disagreement_score":0.040861163,"about_ca_system_score_codex":0.000010855681,"about_ca_system_score_gemma":0.0000400736,"threshold_uncertainty_score":0.9060914},"labels":[],"label_agreement":null},{"id":"W2089831021","doi":"10.1016/j.ygeno.2005.05.015","title":"Detailed analysis of the methylation patterns of the KvDMR1 imprinting control region of human chromosome 11","year":2005,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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","funders":"Canadian Institutes of Health Research","keywords":"Biology; Imprinting (psychology); Genetics; Genomic imprinting; Methylation; DNA methylation; Chromosome; Computational biology; Gene; Gene expression","score_opus":0.009979110336141121,"score_gpt":0.23016050058611595,"score_spread":0.22018139024997482,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2089831021","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976579,0.00011092478,0.0018907047,0.0000722374,0.00004699448,0.00014328118,0.0000132947325,0.0000013857169,0.000063285],"genre_scores_gemma":[0.9996312,0.00002413809,0.00017622976,0.00003576958,0.00005328372,0.0000027070225,0.000007612803,0.00000945663,0.00005956992],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992097,0.000065924614,0.00036887528,0.00014792744,0.00009183263,0.000115715135],"domain_scores_gemma":[0.99895585,0.000011568418,0.0004649461,0.00046655105,0.00008507368,0.00001599558],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019824342,0.00008268788,0.00020649722,0.000041068102,0.00005065397,0.000004204414,0.00027497474,0.00007578007,0.000009588025],"category_scores_gemma":[0.000039935392,0.000056837933,0.00028923684,0.00014624557,0.00004987176,0.0000016621889,0.00014676097,0.00004325334,1.794936e-7],"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":[0.0000016512321,0.000014474589,0.26888832,0.0000112825865,0.00018638131,1.5614118e-8,0.000085162865,0.0027183255,0.72718453,0.00002771666,0.0000017244387,0.0008804121],"study_design_scores_gemma":[0.00024604067,0.000025723173,0.46978933,0.0000073329697,0.00025703077,0.0000019126894,0.00006183954,0.0010077717,0.5284298,0.000009613247,0.0001176323,0.000046001885],"about_ca_topic_score_codex":0.000056478326,"about_ca_topic_score_gemma":0.0003055092,"teacher_disagreement_score":0.200901,"about_ca_system_score_codex":0.000012745801,"about_ca_system_score_gemma":0.000028023373,"threshold_uncertainty_score":0.23177835},"labels":[],"label_agreement":null},{"id":"W2090074407","doi":"10.1038/sj.ejhg.5201353","title":"Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes","year":2005,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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; Centre Hospitalier de l’Université de Montréal","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Methylation; Biology; Molar pregnancy; DNA methylation; Genetics; Reprogramming; Allele; Differentially methylated regions; Gene; Imprinting (psychology); Pregnancy; Gene expression; Gestation","score_opus":0.010379121268311238,"score_gpt":0.22698347084036158,"score_spread":0.21660434957205035,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090074407","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99666077,0.00061375217,0.0011768481,0.000020268975,0.00012475374,0.00010251842,0.000009849917,0.0000051513184,0.0012860773],"genre_scores_gemma":[0.99442625,0.00011966568,0.0043686847,0.000056194323,0.00059337483,5.677865e-7,0.00006189282,0.00005249974,0.0003208533],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9985705,0.00012928633,0.00054389215,0.00020820589,0.00028748033,0.00026064028],"domain_scores_gemma":[0.9988982,0.000004945309,0.00044224734,0.00025002754,0.0002648989,0.00013965883],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027552232,0.00020548626,0.00018199038,0.00008502957,0.00015108856,0.000038988008,0.0002983762,0.00004095281,0.000054900556],"category_scores_gemma":[0.000017729868,0.00016971995,0.000118949174,0.00004296185,0.00007817492,0.000008860742,0.00022945045,0.00011674594,0.000018702483],"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":[0.000093408315,0.00021755643,0.24720943,0.000015381664,0.00017039101,0.000010324752,0.00028861617,0.0018754003,0.69828075,0.0000027140668,0.0003686443,0.051467407],"study_design_scores_gemma":[0.0026150388,0.002860612,0.5308278,0.00003301447,0.000076529206,0.00011342821,0.00013646939,0.000115389514,0.44499385,0.0000027516073,0.017881028,0.00034406455],"about_ca_topic_score_codex":0.000001429398,"about_ca_topic_score_gemma":0.000021892578,"teacher_disagreement_score":0.2836184,"about_ca_system_score_codex":0.00003329746,"about_ca_system_score_gemma":0.000029847872,"threshold_uncertainty_score":0.69209784},"labels":[],"label_agreement":null},{"id":"W2090165161","doi":"10.1007/s10815-012-9911-y","title":"G9a co-localized with histone H3 lysine 9 monomethylation but not dimethylation in a nuclear membrane-dependent manner during mouse preimplantation embryo development","year":2012,"lang":"en","type":"article","venue":"Journal of Assisted Reproduction and Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"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":"Institute of Genetics; Institute of Genetics and Developmental Biology, Chinese Academy of Sciences; Chinese Academy of Sciences","keywords":"Histone H3; Embryo; Lysine; Histone; Cell biology; Embryogenesis; Biology; Chemistry; Genetics; Amino acid; DNA","score_opus":0.015460726796294193,"score_gpt":0.2612567741001873,"score_spread":0.24579604730389307,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090165161","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99734604,0.0007688798,0.0013110022,0.00014751632,0.00020046472,0.00015372479,0.0000021226215,0.000006275644,0.00006397818],"genre_scores_gemma":[0.98865163,0.0004439432,0.009972663,0.000018867075,0.0002592736,0.000003191153,0.000026448803,0.000024655268,0.0005993512],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99861014,0.00009524577,0.00059527915,0.00026333652,0.0002397872,0.00019622387],"domain_scores_gemma":[0.99905705,0.0000071676377,0.0004973922,0.000205403,0.00013232199,0.00010066695],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00063562,0.00014821572,0.00020219128,0.00018201975,0.000100112964,0.000032298227,0.000062093335,0.00011174335,0.000009136894],"category_scores_gemma":[0.000064154185,0.00012899419,0.00004308467,0.000110277324,0.000037578648,0.000023034963,0.0000337082,0.00012877378,0.000001943609],"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":[0.000409385,0.00015544925,0.0062861433,0.00004926912,0.0000886829,0.0000018744631,0.0005285436,0.002938321,0.9766159,0.0000018315609,0.000015270145,0.012909346],"study_design_scores_gemma":[0.0017335919,0.0002323807,0.30376282,0.000025131061,0.000048325757,0.0006337894,0.0003183065,0.0001182677,0.690489,0.0000013903816,0.0024659468,0.00017105059],"about_ca_topic_score_codex":0.000008078288,"about_ca_topic_score_gemma":0.000007305596,"teacher_disagreement_score":0.29747668,"about_ca_system_score_codex":0.00005742243,"about_ca_system_score_gemma":0.00004659456,"threshold_uncertainty_score":0.52602303},"labels":[],"label_agreement":null},{"id":"W2090557879","doi":"10.1016/j.ydbio.2007.03.371","title":"The effect of superovulation on methylation and expression of imprinted genes in pre- and post-implantation mouse embryos","year":2007,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Children's Hospital","funders":"","keywords":"Biology; Genomic imprinting; Embryo; Methylation; Andrology; Gene; DNA methylation; Imprinting (psychology); Genetics; Cell biology; Gene expression","score_opus":0.005118175458745296,"score_gpt":0.2511278387584135,"score_spread":0.2460096632996682,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090557879","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99922884,0.00024528892,0.00026983704,0.000008325951,0.00003593117,0.00016965847,0.000004019512,0.000001741159,0.00003636735],"genre_scores_gemma":[0.9991233,0.0001328905,0.00063380337,0.000008253219,0.0000073690007,0.0000047812637,0.000069377995,0.000004415671,0.00001582811],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99946475,0.000061120496,0.00020593265,0.00013766956,0.00003401227,0.00009652277],"domain_scores_gemma":[0.99975,0.00007815918,0.00007675847,0.000055269797,0.000022893111,0.00001692844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035501676,0.000070233706,0.00009164532,0.00004793197,0.000034035336,0.00000286275,0.000036399106,0.00008813531,9.79183e-7],"category_scores_gemma":[0.000073429714,0.00004869535,0.000012538311,0.000034909153,0.000055989105,0.000002236459,0.0000594884,0.000028840881,1.7753437e-7],"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":[0.00010703284,0.000004496445,0.18480824,0.000012666832,0.000006150651,5.7934795e-8,0.00008967386,0.00000240692,0.7866369,0.000010804858,3.6839558e-7,0.028321244],"study_design_scores_gemma":[0.00025974726,0.00030383072,0.44491693,0.000006383166,0.0000014886855,0.0000061669,0.00005125143,0.000008467225,0.5543881,0.0000045474667,0.000024187411,0.00002889048],"about_ca_topic_score_codex":0.000044836655,"about_ca_topic_score_gemma":0.000042137242,"teacher_disagreement_score":0.26010868,"about_ca_system_score_codex":0.0000061105193,"about_ca_system_score_gemma":0.000009233077,"threshold_uncertainty_score":0.19857389},"labels":[],"label_agreement":null},{"id":"W2091833694","doi":"10.1016/j.placenta.2009.12.003","title":"Decreased Placental Methylation at the H19/IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not Preeclampsia","year":2010,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":189,"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 British Columbia; Child and Family Research Institute","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Methylation; Placentation; DNA methylation; Intrauterine growth restriction; Biology; Preeclampsia; Imprinting (psychology); Differentially methylated regions; Epigenetics; Placenta; Andrology; Endocrinology; Candidate gene; Internal medicine; Fetus; Gene; Genetics; Gene expression; Pregnancy; Medicine","score_opus":0.0077119692239034894,"score_gpt":0.21060861554710228,"score_spread":0.2028966463231988,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2091833694","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964475,0.000033760996,0.0016968526,0.0006778027,0.00028050726,0.00045389132,0.000027595628,0.000029746687,0.00035232073],"genre_scores_gemma":[0.99846745,0.00017611349,0.00024046726,0.0004811892,0.00018599501,0.000025653224,0.00019496259,0.000036075166,0.00019212265],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986017,0.0000983395,0.00026119463,0.00044509806,0.00023131642,0.00036234842],"domain_scores_gemma":[0.99899775,0.00006786153,0.000275547,0.0003631818,0.00018891116,0.00010676458],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026909786,0.00022985724,0.00018001086,0.000044214776,0.00027813885,0.000058993755,0.00019000297,0.00020686089,0.000033329772],"category_scores_gemma":[0.00037813655,0.00017239951,0.000091137415,0.0001285513,0.000096285374,0.000010072479,0.00014807079,0.00024397268,0.000010546169],"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":[0.00021131203,0.000050930197,0.03711415,0.000008307463,0.00013917674,0.0000048049455,0.00008230153,0.00002452144,0.96065855,0.00003951145,0.00052446156,0.0011419796],"study_design_scores_gemma":[0.0031472733,0.0003302985,0.23897702,0.00002879423,0.000116293006,0.00023246692,0.00018217786,0.0020506983,0.75320286,0.000035281115,0.0013510528,0.00034581928],"about_ca_topic_score_codex":0.00030917878,"about_ca_topic_score_gemma":0.00032538368,"teacher_disagreement_score":0.20745571,"about_ca_system_score_codex":0.000051669376,"about_ca_system_score_gemma":0.000056306355,"threshold_uncertainty_score":0.7030248},"labels":[],"label_agreement":null},{"id":"W2092586481","doi":"10.1016/s0092-8674(01)00280-x","title":"Genomic Imprinting Disrupted by a Maternal Effect Mutation in the Dnmt1 Gene","year":2001,"lang":"en","type":"article","venue":"Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":686,"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 Children's Hospital","funders":"","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; DNMT1; Gene; Mutation; DNA methylation; Gene expression","score_opus":0.004131198393370567,"score_gpt":0.21747506412499282,"score_spread":0.21334386573162226,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2092586481","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99722844,0.00043010793,0.0008099716,0.00004016541,0.00007637706,0.00015429554,0.0000019240792,0.0000051056927,0.0012536114],"genre_scores_gemma":[0.99910325,0.00007416228,0.00020885341,0.00011644451,0.00008483905,0.000016038299,0.000040180556,0.000013842429,0.00034241762],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993192,0.0000663976,0.00014114384,0.00019826292,0.00006717649,0.0002078191],"domain_scores_gemma":[0.99971026,0.000011283624,0.00005226954,0.00018943568,0.000011161108,0.000025586947],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023564715,0.00009765838,0.00007486385,0.00001920031,0.00004543308,0.000034940458,0.0001676022,0.000061895196,0.000019355639],"category_scores_gemma":[0.000015418345,0.00007453588,0.000046266246,0.000057028683,0.000016990447,0.0000014449225,0.000061261686,0.00006253592,0.000027346405],"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":[0.0000052155788,0.00001592905,0.051238492,0.000009169175,0.000004503883,0.0000063869284,0.000057891615,0.000037230297,0.9445286,3.293911e-7,0.000083648694,0.0040126434],"study_design_scores_gemma":[0.0006081228,0.00016688705,0.22404943,0.0000054945276,0.000009374466,0.00015743005,0.0000708307,0.00031885138,0.76984566,0.000009773824,0.0046324437,0.00012572778],"about_ca_topic_score_codex":0.00007053188,"about_ca_topic_score_gemma":0.0000071850354,"teacher_disagreement_score":0.17468292,"about_ca_system_score_codex":0.0000082357365,"about_ca_system_score_gemma":0.000009401737,"threshold_uncertainty_score":0.3039485},"labels":[],"label_agreement":null},{"id":"W2092668546","doi":"10.1038/nature00819","title":"Placental-specific IGF-II is a major modulator of placental and fetal growth","year":2002,"lang":"en","type":"article","venue":"Nature","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1059,"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 Calgary","funders":"Biotechnology and Biological Sciences Research Council; Medical Research Council","keywords":"Placenta; Fetus; Biology; Genomic imprinting; Trophoblast; Imprinting (psychology); Fetal growth; Insulin-like growth factor 2; Endocrinology; Gene; Intrauterine growth restriction; Internal medicine; Andrology; Pregnancy; Gene expression; Genetics; Medicine; DNA methylation","score_opus":0.005329582875511895,"score_gpt":0.2037796558499418,"score_spread":0.1984500729744299,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2092668546","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98968786,0.008309079,0.00001699712,0.00026199786,0.00017123617,0.000112919246,0.00003880275,0.0000067144947,0.0013943713],"genre_scores_gemma":[0.99703896,0.00042749633,0.00084636797,0.00027636814,0.00012546525,0.000002785665,0.000022164168,0.00001839766,0.0012420135],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992272,0.000013452904,0.00014132875,0.00029592062,0.0001307758,0.00019131815],"domain_scores_gemma":[0.9996263,0.0000041474505,0.000060692768,0.0001957625,0.000042176907,0.000070919246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00004471887,0.00013665875,0.00013200185,0.00003103049,0.00007165257,0.000012693472,0.000118865435,0.00057865994,0.00016832084],"category_scores_gemma":[0.000018374893,0.00012571244,0.00007322465,0.000064594,0.00005757793,0.000002980748,0.00016732246,0.0003093508,0.0000068169725],"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":[0.000035297835,0.00016263119,0.023057919,0.00006546641,0.000096913776,0.000004214741,0.00029388382,0.0000019820907,0.93655753,0.00012489625,0.03398435,0.005614935],"study_design_scores_gemma":[0.0031608553,0.00072669314,0.0922123,0.00006000514,0.000041665502,0.0004094798,0.000338062,0.00069730775,0.80771327,0.000089748166,0.09394649,0.0006041161],"about_ca_topic_score_codex":0.000005363146,"about_ca_topic_score_gemma":0.0000023896837,"teacher_disagreement_score":0.12884423,"about_ca_system_score_codex":0.000008495697,"about_ca_system_score_gemma":0.0000073160313,"threshold_uncertainty_score":0.5126404},"labels":[],"label_agreement":null},{"id":"W2093861094","doi":"10.1111/j.1365-263x.2007.00857.x","title":"The oro‐dental phenotype in Prader–Willi syndrome: a survey of 15 patients","year":2007,"lang":"en","type":"article","venue":"International Journal of Paediatric Dentistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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; Short stature; Pediatrics; Body mass index; Oral hygiene; Overweight; Obesity; Dentistry; Internal medicine","score_opus":0.008752132501374299,"score_gpt":0.26953623670748156,"score_spread":0.26078410420610726,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2093861094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99566793,0.0012248048,0.0007525629,0.000026496924,0.0021433153,0.000055685075,0.00001870658,9.359014e-7,0.00010957537],"genre_scores_gemma":[0.9990063,0.0002872693,0.00032366373,0.00002398028,0.00020124567,5.7008396e-7,0.000026876265,0.000010608781,0.000119542274],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99852586,0.000062619685,0.0006440642,0.00011705659,0.0004751969,0.00017523159],"domain_scores_gemma":[0.9986832,0.000091099464,0.00053510896,0.0001153161,0.00051613885,0.000059093385],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001015914,0.00009319384,0.00012976456,0.00011350944,0.000028002252,0.000032799206,0.000516917,0.00008360746,0.000017758073],"category_scores_gemma":[0.00060145766,0.000074543146,0.000102997474,0.00014275176,0.000049727514,0.00000848181,0.00014658412,0.00013120678,0.0000045234074],"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":[0.000018272469,0.00012895165,0.9891585,0.000005114607,0.00009326275,0.000024057097,0.000016514563,0.000021321812,0.0025715763,0.000005158581,0.00037139838,0.007585878],"study_design_scores_gemma":[0.00089688523,0.00014884576,0.996317,0.00001593411,0.000011117486,0.00038387883,0.00007163305,0.0000068490085,0.001265994,0.000021048556,0.0007876009,0.00007316263],"about_ca_topic_score_codex":0.00007505576,"about_ca_topic_score_gemma":0.00018001547,"teacher_disagreement_score":0.0075127156,"about_ca_system_score_codex":0.000036076217,"about_ca_system_score_gemma":0.00008887664,"threshold_uncertainty_score":0.30397812},"labels":[],"label_agreement":null},{"id":"W2094145825","doi":"10.6000/2292-2598.2014.02.03.2","title":"Speech and Language Issues in Children with Prader-Willi Syndrome","year":2014,"lang":"en","type":"article","venue":"Journal of Intellectual Disability - Diagnosis and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Research Resources; National Institutes of Health","keywords":"Apraxia; Language delay; Audiology; Language development; Language disorder; Medicine; Population; Psychology; Developmental psychology; Aphasia; Cognitive psychology; Cognition; Psychiatry","score_opus":0.009846461654526276,"score_gpt":0.2559011782236664,"score_spread":0.24605471656914016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2094145825","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965465,0.0027898368,0.000028135251,0.00036877283,0.000020579471,0.00017155748,0.000004029074,0.000002020928,0.000068575646],"genre_scores_gemma":[0.99625915,0.0028207952,0.00074230967,0.000040937,0.000060023303,0.000012346429,0.0000036257982,0.0000110724095,0.000049726335],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992023,0.00007588016,0.00025548972,0.00021379569,0.00009712437,0.0001554017],"domain_scores_gemma":[0.9995454,0.000091658985,0.00009043399,0.00014953046,0.000030629653,0.00009233873],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018210743,0.00015516073,0.000265901,0.000034520937,0.000037465892,0.000036014662,0.000062568004,0.00006264479,0.000052208285],"category_scores_gemma":[0.0002494136,0.000100947844,0.000059296584,0.00005320516,0.00013701295,0.0000062808867,0.0000456177,0.00006276757,0.0000010126794],"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":[0.0000063947964,0.0004099253,0.9519922,0.000009218039,0.00013416685,0.0000013035798,0.0005615042,0.0000072306602,0.00040505474,0.0000030409312,0.000083112915,0.046386845],"study_design_scores_gemma":[0.000999462,0.0045290394,0.9863506,0.000053156422,0.00005359164,0.00086809933,0.00050939375,0.000021605612,0.0052032336,0.000028124408,0.0012550803,0.0001286265],"about_ca_topic_score_codex":0.00018532218,"about_ca_topic_score_gemma":0.00015624736,"teacher_disagreement_score":0.04625822,"about_ca_system_score_codex":0.000028283539,"about_ca_system_score_gemma":0.000016572934,"threshold_uncertainty_score":0.41165334},"labels":[],"label_agreement":null},{"id":"W2094253962","doi":"10.1002/1098-2795(200007)56:3<345::aid-mrd3>3.0.co;2-1","title":"Monoalleleic transcription of the insulin-like growth factor-II gene (Igf2) in chick embryos","year":2000,"lang":"en","type":"article","venue":"Molecular Reproduction and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Guelph","funders":"Natural Sciences and Engineering Research Council of Canada; Ontario Ministry of Agriculture, Food and Rural Affairs","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; Allele; Gene; Insulin-like growth factor 2; Embryo; Gene expression; DNA methylation","score_opus":0.009029402656602696,"score_gpt":0.20395261244627477,"score_spread":0.19492320978967206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2094253962","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975407,0.0010239535,0.000565757,0.00023382629,0.00014631651,0.00022435091,0.0000010582733,0.0000067975125,0.00025724343],"genre_scores_gemma":[0.99662197,0.00041174376,0.0020188298,0.00014586396,0.000030217678,0.000017259492,0.000015521093,0.00001395594,0.0007246359],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989105,0.00005783288,0.00028794992,0.00043623653,0.00013908821,0.00016839843],"domain_scores_gemma":[0.99954414,9.903008e-7,0.00005781675,0.0003093984,0.000046103873,0.00004154276],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019157592,0.00012899807,0.00011866865,0.000042192485,0.000091558446,0.000010386803,0.00010183012,0.00008232587,0.00003988432],"category_scores_gemma":[0.000024775385,0.00010740927,0.00004672956,0.0001220689,0.00004418419,0.0000036932918,0.000061813604,0.00007162341,0.0000029034672],"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":[0.000016127125,0.0000861221,0.0047618323,0.000022794986,0.000031352116,7.769653e-7,0.00073238905,0.00017305865,0.9425563,0.000007081847,0.000026904343,0.051585265],"study_design_scores_gemma":[0.0004701133,0.00006340003,0.28287408,0.000012598368,0.0000041553317,0.000042341304,0.000052072344,0.000012812995,0.69255674,0.000020254796,0.023749327,0.00014208567],"about_ca_topic_score_codex":0.000027915245,"about_ca_topic_score_gemma":0.000008291413,"teacher_disagreement_score":0.27811223,"about_ca_system_score_codex":0.000015320444,"about_ca_system_score_gemma":0.000068236994,"threshold_uncertainty_score":0.4380023},"labels":[],"label_agreement":null},{"id":"W2096270935","doi":"10.1111/cen.12694","title":"Growth hormone secretion decreases with age in paediatric <scp>P</scp>rader‐<scp>W</scp>illi syndrome","year":2014,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Hospital for Sick Children","keywords":"Medicine; Growth hormone deficiency; Internal medicine; Endocrinology; Bone age; Stimulation; Body mass index; Growth hormone; Pediatrics; Hormone","score_opus":0.017245802903601674,"score_gpt":0.2685242520589245,"score_spread":0.2512784491553228,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096270935","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99249357,0.001998906,0.001677797,0.0001551243,0.00037291998,0.00033090345,0.000007734594,0.00005844511,0.0029046],"genre_scores_gemma":[0.99404323,0.002331663,0.001532783,0.00055624126,0.00048442095,0.00006511409,0.00015199225,0.00006718151,0.00076739496],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.996285,0.0004726504,0.00091240153,0.0010484261,0.0002172484,0.0010642355],"domain_scores_gemma":[0.99747664,0.0010620505,0.00031879448,0.00069380703,0.000115120114,0.00033359497],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004961608,0.00040614154,0.00069536973,0.00018201277,0.00009849832,0.000038937178,0.00049938034,0.0004994182,0.000008027027],"category_scores_gemma":[0.0057719047,0.0003635871,0.00024613354,0.0003085005,0.0004516103,0.000009943222,0.00041557834,0.00052526535,0.000096264055],"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":[0.00005360326,0.0014539413,0.9345595,0.00018837453,0.0004946799,0.00082744425,0.00021487089,0.00020863127,0.034236085,0.0020531234,0.008565134,0.017144615],"study_design_scores_gemma":[0.004480789,0.00489711,0.9226924,0.000038427697,0.00012415799,0.0019033804,0.00043380275,0.00019388054,0.003960959,0.0010159692,0.060029756,0.00022934435],"about_ca_topic_score_codex":0.00006679399,"about_ca_topic_score_gemma":0.00007479907,"teacher_disagreement_score":0.05146462,"about_ca_system_score_codex":0.00002061724,"about_ca_system_score_gemma":0.00010783342,"threshold_uncertainty_score":0.9998816},"labels":[],"label_agreement":null},{"id":"W2096758563","doi":"10.1093/hmg/ddg067","title":"Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development","year":2003,"lang":"en","type":"review","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":288,"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":"Genomic imprinting; Biology; Epigenetics; Imprinting (psychology); Genetics; Beckwith–Wiedemann syndrome; DNA methylation; Allele; Gene; Locus (genetics); Gene expression","score_opus":0.02191032540696159,"score_gpt":0.2867352236854542,"score_spread":0.2648248982784926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096758563","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.013042602,0.96744454,0.016806671,0.000001982784,0.00016159592,0.0019320765,0.00008217109,0.00001511774,0.00051323697],"genre_scores_gemma":[0.035301827,0.9431829,0.018963628,0.00007157745,0.00011676164,0.0006967062,0.0006499244,0.00035135535,0.00066535326],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9960711,0.00020907298,0.0014723818,0.0009940974,0.0004283391,0.0008250027],"domain_scores_gemma":[0.9976068,0.000032007614,0.00080048287,0.0009931631,0.00033444044,0.00023311515],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00048455695,0.00086872885,0.0016916331,0.00020667876,0.00019476649,0.0000580151,0.00074773206,0.0007595005,0.000045932607],"category_scores_gemma":[0.00007240333,0.0008772303,0.0009095673,0.00017900336,0.00017368172,0.0000021932124,0.00021766737,0.00020978255,0.000021459327],"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":[0.000025302146,0.001067116,0.00036487298,0.029518917,0.006151018,0.00007778591,0.00017361031,0.0005069802,0.091529824,0.00043702233,0.0005009935,0.86964655],"study_design_scores_gemma":[0.001096609,0.0010942372,0.00018116448,0.0015515462,0.0013577644,0.0004523566,0.00003357154,0.000014489118,0.008706736,0.00010296052,0.98413706,0.0012715203],"about_ca_topic_score_codex":0.000003441855,"about_ca_topic_score_gemma":0.000008458217,"teacher_disagreement_score":0.983636,"about_ca_system_score_codex":0.000050515842,"about_ca_system_score_gemma":0.00079824874,"threshold_uncertainty_score":0.99936783},"labels":[],"label_agreement":null},{"id":"W2096765959","doi":"10.1111/j.1399-0004.2007.00793.x","title":"Toward understanding the genetic basis of neural tube defects","year":2007,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":116,"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; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Neural tube; Neurulation; Convergent extension; Biology; Neural tube defect; Genetics; Gene; Etiology; Bioinformatics; Pathology; Medicine; Embryogenesis; Embryo","score_opus":0.25823289677907457,"score_gpt":0.41922587509874265,"score_spread":0.16099297831966808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096765959","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.005356143,0.98752487,0.0047265776,0.000017076438,0.0010892574,0.0006635978,0.0000255308,0.0000117366935,0.0005852172],"genre_scores_gemma":[0.013656268,0.98328924,0.001658845,0.00013999836,0.0008973877,0.000018523668,0.000055967543,0.00011084486,0.00017295266],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99607486,0.00042269507,0.0018230395,0.00078052876,0.00031781706,0.0005810371],"domain_scores_gemma":[0.99732506,0.00041639432,0.00073949597,0.0012055535,0.00010471811,0.00020880382],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0010001768,0.00052499794,0.0013498073,0.00008670482,0.000102562575,0.000042496544,0.0009616037,0.0009093929,0.000031549112],"category_scores_gemma":[0.000484103,0.00037167335,0.0014125931,0.00029065483,0.0004641166,0.0000010701519,0.0006598768,0.0005168124,0.0000229459],"study_design_candidate":"design_other","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":[0.0000052092096,0.00009680507,0.00095567515,0.0024456498,0.0003637233,0.0000072078105,0.00001921957,0.00003706683,0.000033194083,0.0000288949,0.0005573598,0.99545],"study_design_scores_gemma":[0.00038993743,0.0009041508,0.0009364771,0.0010896566,0.001218078,0.00017670602,0.00009977037,0.00007779,0.00010347315,0.00011184955,0.99425036,0.0006417259],"about_ca_topic_score_codex":0.0000030816589,"about_ca_topic_score_gemma":0.000005744065,"teacher_disagreement_score":0.99480826,"about_ca_system_score_codex":0.000032151544,"about_ca_system_score_gemma":0.00029841872,"threshold_uncertainty_score":0.9998735},"labels":[],"label_agreement":null},{"id":"W2097248205","doi":"10.1186/1471-2156-6-s1-s160","title":"A genome scan for parent-of-origin linkage effects in alcoholism","year":2005,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research; Genome Canada; Juvenile Diabetes Research Foundation International","keywords":"Genetics; Genetic linkage; Microsatellite; Imprinting (psychology); Biology; Genomic imprinting; Locus (genetics); SNP; Single-nucleotide polymorphism; Genome Scan; Linkage (software); Complete linkage; Tag SNP; Genome; Allele; Gene; Genotype; DNA methylation","score_opus":0.02355792446827854,"score_gpt":0.28590208020858654,"score_spread":0.262344155740308,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2097248205","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.985143,0.0030972813,0.010789286,0.000026046488,0.00015651042,0.000477296,0.0000133655685,0.000006567671,0.00029061618],"genre_scores_gemma":[0.9534817,0.00023099054,0.04547701,0.00006614624,0.00033662905,0.00005999082,0.00004891014,0.000032803713,0.00026584652],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9988687,0.000036391633,0.00031955173,0.00032715482,0.00010141784,0.00034679638],"domain_scores_gemma":[0.99936825,0.000026147896,0.00009995116,0.0003675865,0.00005800549,0.000080055834],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016943627,0.00016564601,0.00019940056,0.00006692063,0.000030341836,0.000013847729,0.00022666054,0.00015165207,0.000009331051],"category_scores_gemma":[0.000072784045,0.00017361045,0.00011886063,0.00008668005,0.00004141822,0.0000014664076,0.00011027638,0.00005350585,0.0000067282986],"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":[0.000016103631,0.00012330976,0.11098968,0.00018806763,0.000028742006,4.8744084e-7,0.000111756235,0.0034936715,0.87139004,0.000045727218,0.00007161212,0.01354081],"study_design_scores_gemma":[0.0028057664,0.0007784334,0.6844927,0.00005714274,0.00004857482,0.000019241892,0.00006851968,0.0027162456,0.24615578,0.00015525152,0.062190734,0.00051161216],"about_ca_topic_score_codex":0.00000669565,"about_ca_topic_score_gemma":0.000085823995,"teacher_disagreement_score":0.62523425,"about_ca_system_score_codex":0.000015481117,"about_ca_system_score_gemma":0.00008654774,"threshold_uncertainty_score":0.7079629},"labels":[],"label_agreement":null},{"id":"W2098195823","doi":"10.1172/jci19159","title":"Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS","year":2003,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":259,"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; St. Michael's Hospital; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; U.S. Public Health Service; National Institutes of Health","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Exon; Genetics; Genomic imprinting; Biology; Locus (genetics); X chromosome; Imprinting (psychology); X-inactivation; Differentially methylated regions; DNA methylation; Molecular biology; Gene; Parathyroid hormone; Internal medicine; Medicine","score_opus":0.038505553832486036,"score_gpt":0.3210772784450016,"score_spread":0.28257172461251556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2098195823","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9929771,0.0003386095,0.006022773,0.00020492545,0.00022496496,0.00017637249,0.000005386968,0.0000026137964,0.00004726728],"genre_scores_gemma":[0.994885,0.00010353347,0.0044986773,0.00031870644,0.00010178805,0.0000028304066,0.000010091719,0.000017917966,0.000061439976],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9977956,0.0003645683,0.001129331,0.0002236312,0.00027872974,0.0002081571],"domain_scores_gemma":[0.9972793,0.00011515055,0.0017842965,0.00015256034,0.0005243608,0.00014437501],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015526358,0.00016134938,0.00044804256,0.00004980002,0.000055747663,0.000026366593,0.00012049535,0.00017865226,0.000007944328],"category_scores_gemma":[0.0013727135,0.0001211571,0.00020447557,0.000110344154,0.00014717059,0.000014148645,0.00002783274,0.00022228115,0.000001892868],"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":[0.00019762747,0.00023390862,0.15691753,0.000022034763,0.00039138668,0.000010377396,0.00029921872,0.00033108713,0.8397293,0.00006293334,0.00028138954,0.0015232305],"study_design_scores_gemma":[0.0067719463,0.005451256,0.29405922,0.00026374348,0.0002917451,0.00027482235,0.0002724117,0.0011077859,0.68958044,0.0009025217,0.00068965583,0.00033447324],"about_ca_topic_score_codex":0.000006116515,"about_ca_topic_score_gemma":0.0000042573106,"teacher_disagreement_score":0.15014887,"about_ca_system_score_codex":0.00001999118,"about_ca_system_score_gemma":0.0002487411,"threshold_uncertainty_score":0.4940643},"labels":[],"label_agreement":null},{"id":"W2099472522","doi":"10.1091/mbc.e15-01-0013","title":"Glycogen synthase kinase-3 (Gsk-3) plays a fundamental role in maintaining DNA methylation at imprinted loci in mouse embryonic stem cells","year":2015,"lang":"en","type":"article","venue":"Molecular Biology of the Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University","funders":"National Institute on Aging","keywords":"Biology; GSK-3; Embryonic stem cell; DNA methylation; GSK3B; Glycogen synthase; Cell biology; Methylation; Genetics; Glycogen debranching enzyme; Kinase; DNA; Phosphorylation; Gene; Gene expression","score_opus":0.010876007822089542,"score_gpt":0.23565132364348265,"score_spread":0.2247753158213931,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099472522","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971139,0.0012587297,0.0006201396,0.000079800295,0.00012727772,0.00035244203,0.00002219123,0.000007253242,0.00041826756],"genre_scores_gemma":[0.99885696,0.000027924985,0.00048105704,0.00010150827,0.000019203108,0.000022428289,0.000050794784,0.000030867934,0.00040922855],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982821,0.0003332215,0.00039158756,0.0004579015,0.000114404145,0.00042081747],"domain_scores_gemma":[0.99910915,0.000018217415,0.00021144791,0.00052093435,0.000047271864,0.00009299072],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005243847,0.00022492303,0.00027194797,0.000103751474,0.00004081592,0.000009346937,0.00041079632,0.00027541904,0.000012394487],"category_scores_gemma":[0.000044255074,0.00019775024,0.00014932224,0.00016686066,0.00013123456,0.0000031618567,0.0006455192,0.00015830186,0.000013166854],"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":[0.000055243792,0.00008789037,0.013152261,0.000014412366,0.000026256868,0.0000058345554,0.0001440308,0.0012621636,0.98475474,0.000017696371,0.000018559302,0.00046093168],"study_design_scores_gemma":[0.0013604431,0.00027833928,0.0012109184,0.000016596483,0.000014835242,0.000015963253,0.00055647217,0.00060237426,0.9949968,0.00009574047,0.0006439842,0.00020754423],"about_ca_topic_score_codex":0.00013345815,"about_ca_topic_score_gemma":0.00011366489,"teacher_disagreement_score":0.011941343,"about_ca_system_score_codex":0.0001130397,"about_ca_system_score_gemma":0.00009534835,"threshold_uncertainty_score":0.806402},"labels":[],"label_agreement":null},{"id":"W2099689315","doi":"10.1093/hmg/10.26.2989","title":"Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1","year":2001,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":246,"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","funders":"Hospital for Sick Children","keywords":"Imprinting (psychology); Genomic imprinting; Beckwith–Wiedemann syndrome; Biology; Wilms' tumor; Cancer research; Genetics; Uniparental disomy; DNA methylation; Gene; Chromosome; Karyotype; Gene expression","score_opus":0.02025831772675202,"score_gpt":0.25900953347926975,"score_spread":0.23875121575251773,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099689315","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98174924,0.00057719345,0.016477084,0.000028905308,0.000027850714,0.0004019037,0.000008558387,0.0000074014924,0.0007218693],"genre_scores_gemma":[0.99462163,0.000020594003,0.004923382,0.00024951837,0.000013427823,0.00004010228,0.00008246569,0.000029314504,0.000019582301],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99798715,0.00013988101,0.00062571565,0.00042156322,0.0004388825,0.00038678714],"domain_scores_gemma":[0.9988401,0.000024735567,0.00034828085,0.00047733728,0.00024350199,0.00006604567],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047340785,0.00026744523,0.00032427613,0.00012684052,0.00017153684,0.000033320117,0.0003881136,0.00012683208,0.000019236497],"category_scores_gemma":[0.00011211338,0.00023512717,0.00012623603,0.00035860768,0.00030643246,0.00000489231,0.00023041476,0.0001542588,0.000001533877],"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":[0.000008322445,0.00026979236,0.04043905,0.000050131308,0.00023014036,0.00010116626,0.0006235766,0.0030311584,0.953595,0.001460872,0.000013808085,0.00017699934],"study_design_scores_gemma":[0.0020095247,0.00089943927,0.28280744,0.00034923299,0.00016155749,0.0008072074,0.000503411,0.00045556593,0.71014225,0.00042963945,0.00074060954,0.0006941248],"about_ca_topic_score_codex":0.000017666845,"about_ca_topic_score_gemma":0.000048312566,"teacher_disagreement_score":0.24345273,"about_ca_system_score_codex":0.000031298252,"about_ca_system_score_gemma":0.0002545721,"threshold_uncertainty_score":0.95882076},"labels":[],"label_agreement":null},{"id":"W2099701757","doi":"10.1038/ng2114","title":"The imprinted gene Magel2 regulates normal circadian output","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":225,"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":"National Eye Institute; National Institute of Mental Health; National Institutes of Health","keywords":"Circadian rhythm; Biology; Suprachiasmatic nucleus; Orexin; Endocrinology; Internal medicine; Orexin-A; Hypothalamus; Phenotype; Gene; CLOCK; Cell biology; Circadian clock; Genetics; Neuropeptide; Medicine; Receptor","score_opus":0.0051499725056270125,"score_gpt":0.2351019312492238,"score_spread":0.22995195874359678,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099701757","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98488694,0.008731093,0.002081647,0.00027777837,0.00090792926,0.00020926075,0.000007068555,0.000022504873,0.0028757935],"genre_scores_gemma":[0.99086565,0.00069050444,0.004326731,0.0004050483,0.0009210633,0.0000049384666,0.000048132642,0.000046013607,0.0026919066],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9983348,0.000032824086,0.00032826004,0.00041385627,0.00024172053,0.0006485196],"domain_scores_gemma":[0.9987825,0.000028063958,0.00011294799,0.00072149816,0.0001805032,0.00017449645],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00054568646,0.00023106278,0.00013232189,0.000048156217,0.00028423392,0.00007644687,0.0005101211,0.00055554474,0.000012747197],"category_scores_gemma":[0.00013590636,0.00018323718,0.00013809837,0.00015232046,0.00012524042,0.0000018943391,0.00027087878,0.00039393557,0.00002574484],"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":[0.00003774832,0.000039292587,0.023552857,0.000015810854,0.0001371151,0.000011140255,0.00008650077,0.000081714315,0.87958556,0.000066962275,0.0037480504,0.09263722],"study_design_scores_gemma":[0.00030533012,0.00015489009,0.17900775,0.0000050320405,0.000018899587,0.0001072935,0.00007447692,0.00007041815,0.609387,0.00007806762,0.2105573,0.00023357064],"about_ca_topic_score_codex":0.0000068232534,"about_ca_topic_score_gemma":0.00007279401,"teacher_disagreement_score":0.2701986,"about_ca_system_score_codex":0.000018007937,"about_ca_system_score_gemma":0.00006810837,"threshold_uncertainty_score":0.7472195},"labels":[],"label_agreement":null},{"id":"W2100135235","doi":"10.1093/hmg/ddm225","title":"Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome","year":2007,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":198,"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":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Biology; Failure to thrive; Phenotype; Circadian rhythm; Weaning; Endocrinology; Internal medicine; Obesity; Gene; Weight gain; Genetics; Mutation; Candidate gene; Body weight; Medicine","score_opus":0.012342074490906746,"score_gpt":0.24829184261847792,"score_spread":0.23594976812757118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2100135235","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99468935,0.00028497595,0.003557514,0.0001541943,0.00008526081,0.0004352216,0.000020953767,0.000009222586,0.0007632955],"genre_scores_gemma":[0.9953657,0.000046456833,0.0037575564,0.0002958045,0.000055991244,0.000011836238,0.000054387863,0.000046836158,0.00036544053],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99812293,0.00009521225,0.0006041674,0.00042607274,0.00031415618,0.000437446],"domain_scores_gemma":[0.99882233,0.00001318065,0.0001942656,0.00072000286,0.0001494472,0.00010079289],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00051007443,0.00023161234,0.00020960465,0.00013825185,0.00009072493,0.000024745686,0.0004410384,0.0001848267,0.000006092848],"category_scores_gemma":[0.00017055587,0.00021573878,0.00012198918,0.00028866334,0.000096973694,0.000003845206,0.00034595808,0.00013563133,0.0000035174069],"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":[0.000006486674,0.00006304006,0.008456299,0.000030663636,0.000029594725,0.000005337687,0.00022227975,0.0009165836,0.9897598,0.00013274248,0.00009379067,0.0002833998],"study_design_scores_gemma":[0.0004717407,0.00029381952,0.35681134,0.000019990379,0.000012092269,0.00003975476,0.00012410586,0.000011870668,0.6408047,0.00012899356,0.0010895763,0.00019201452],"about_ca_topic_score_codex":0.000075440155,"about_ca_topic_score_gemma":0.00008966611,"teacher_disagreement_score":0.34895507,"about_ca_system_score_codex":0.00003428454,"about_ca_system_score_gemma":0.000050933624,"threshold_uncertainty_score":0.87975717},"labels":[],"label_agreement":null},{"id":"W2102400711","doi":"10.1093/hmg/ddg152","title":"Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles","year":2003,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":139,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"McGill University Health Centre; McGill University","keywords":"Biology; Genomic imprinting; Offspring; Locus (genetics); Genetics; Allele; DNA methylation; Methylation; Imprinting (psychology); Gene; Epigenetics; Pregnancy; Gene expression","score_opus":0.021386487152126706,"score_gpt":0.26424906013302246,"score_spread":0.24286257298089575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2102400711","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98570997,0.00075826433,0.01252875,0.000009867143,0.00012227733,0.00021074303,0.000013313514,0.000012983371,0.0006338227],"genre_scores_gemma":[0.9960412,0.00013503902,0.0033908589,0.000092893235,0.00006187848,0.000021235619,0.00012716549,0.00005740687,0.00007236916],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982594,0.00012060671,0.0004367219,0.0004714846,0.00024782497,0.00046393808],"domain_scores_gemma":[0.99929017,0.000004518513,0.00013336993,0.00041106204,0.00005212859,0.000108779095],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0001944785,0.00027403363,0.0002073002,0.000111090754,0.00009775504,0.00007822997,0.00026969676,0.00014005737,0.000084774016],"category_scores_gemma":[0.000020483547,0.00029867823,0.000118062846,0.00007646717,0.000053805918,0.0000045935835,0.00016463312,0.00011209794,0.000015162599],"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":[0.0000031298016,0.000050089406,0.22983803,0.000022696713,0.0000348053,0.000012345993,0.000049565617,0.00088755536,0.7677284,0.00015791926,0.0000075530697,0.0012079014],"study_design_scores_gemma":[0.0008784034,0.0002675475,0.4843801,0.00004413443,0.000018947372,0.000074131276,0.00010370701,0.00035913597,0.51144797,0.00040144788,0.0016198962,0.00040459234],"about_ca_topic_score_codex":0.00008665961,"about_ca_topic_score_gemma":0.00012829754,"teacher_disagreement_score":0.25628045,"about_ca_system_score_codex":0.000026971366,"about_ca_system_score_gemma":0.000029818986,"threshold_uncertainty_score":0.99994653},"labels":[],"label_agreement":null},{"id":"W2102431794","doi":"10.1186/1471-2164-12-204","title":"Recent acquisition of imprinting at the rodent Sfmbt2 locus correlates with insertion of a large block of miRNAs","year":2011,"lang":"en","type":"article","venue":"BMC Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Mount Sinai Hospital; Toronto Zoo; Lunenfeld-Tanenbaum Research Institute; University of Guelph; University of Toronto","funders":"Medical Research Council; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Genetics; Gene; Locus (genetics); Allele; Gene expression; DNA methylation","score_opus":0.014791571845483863,"score_gpt":0.218131124595679,"score_spread":0.20333955275019513,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2102431794","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99772257,0.0008559077,0.00084116386,0.00001030904,0.00006495541,0.0001720984,0.000010269161,0.000002263774,0.0003204368],"genre_scores_gemma":[0.99756306,0.00041919271,0.0018847836,0.000015225751,0.000020660676,0.0000048309967,0.000016497008,0.000014720502,0.00006104593],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99924815,0.00003423857,0.00031560808,0.00016586555,0.000087117296,0.00014902867],"domain_scores_gemma":[0.99916166,0.000008786827,0.00034869844,0.00031672043,0.00013826389,0.00002585829],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021697202,0.00009609816,0.00014225669,0.000024001916,0.00003664022,0.0000025836398,0.00013832877,0.0000782749,0.00003121441],"category_scores_gemma":[0.000024250203,0.000071384486,0.000069613845,0.00005893451,0.000062765095,0.0000016661453,0.00018663223,0.000038209306,0.0000018567912],"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":[0.000081385544,0.000079679034,0.106877334,0.000049541362,0.000047440142,1.2967375e-7,0.00036663865,0.00028247607,0.8909229,0.000026882963,0.000011573774,0.0012540056],"study_design_scores_gemma":[0.0004649683,0.00027562055,0.1320058,0.000026568641,0.00003951985,0.000020949381,0.0003865296,0.00015487034,0.86603934,0.000020838816,0.0004843386,0.00008063516],"about_ca_topic_score_codex":0.00006214072,"about_ca_topic_score_gemma":0.00014097051,"teacher_disagreement_score":0.025128463,"about_ca_system_score_codex":0.000014471911,"about_ca_system_score_gemma":0.00005388866,"threshold_uncertainty_score":0.2910975},"labels":[],"label_agreement":null},{"id":"W2103059889","doi":"10.1093/hmg/ddn055","title":"Superovulation alters the expression of imprinted genes in the midgestation mouse placenta","year":2008,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":216,"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 Children's Hospital","funders":"University of Pennsylvania","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Embryo; Epigenetics; Placenta; Embryogenesis; Andrology; Oocyte; DNA methylation; Genetics; Gene expression; Endocrinology; Gene; Fetus; Pregnancy","score_opus":0.020493465553971395,"score_gpt":0.2593692172811008,"score_spread":0.2388757517271294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103059889","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9948278,0.00086101587,0.0037372329,0.00006509805,0.00004467731,0.00030828905,0.0000035902146,0.000004814505,0.00014745202],"genre_scores_gemma":[0.9983742,0.00030199497,0.0009618061,0.00014007441,0.00004316539,0.000021276272,0.00007837747,0.0000228237,0.00005625677],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99884385,0.00017424981,0.00030396692,0.00024561124,0.00022867408,0.0002036268],"domain_scores_gemma":[0.9992391,0.000013830132,0.0001131488,0.0005357089,0.00006929534,0.0000289371],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020250968,0.00014373088,0.00010777999,0.000046767105,0.00013871354,0.000015805852,0.00034333693,0.000090376554,0.000009078056],"category_scores_gemma":[0.00003096102,0.00010128431,0.000084579595,0.000104409984,0.0001246855,0.000002533065,0.00011230865,0.00008790301,0.0000022085576],"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":[0.00000573454,0.00005333134,0.013503557,0.000009604695,0.000009547079,0.0000025582947,0.00047559477,0.0019270111,0.9835424,0.000033660337,0.000080352205,0.00035667393],"study_design_scores_gemma":[0.0004257196,0.00017035329,0.15017281,0.000010527314,0.000011807129,0.00004009504,0.00036531014,0.00024784287,0.8477473,0.000041154814,0.00064174156,0.00012530424],"about_ca_topic_score_codex":0.000041519008,"about_ca_topic_score_gemma":0.000027456386,"teacher_disagreement_score":0.13666926,"about_ca_system_score_codex":0.000008519178,"about_ca_system_score_gemma":0.000030593255,"threshold_uncertainty_score":0.41302544},"labels":[],"label_agreement":null},{"id":"W2103334703","doi":"10.1530/eje-10-0795","title":"Osteosclerosis in two brothers with autosomal dominant pseudohypoparathyroidism type 1b: bone histomorphometric analysis","year":2010,"lang":"en","type":"article","venue":"European Journal of Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; Health Canada","keywords":"Pseudohypoparathyroidism; Internal medicine; Endocrinology; Osteosclerosis; Parathyroid hormone; Bone histomorphometry; Hyperphosphatemia; Bone mineral; Cortical bone; Chemistry; Osteoporosis; Medicine; Anatomy; Trabecular bone; Calcium; Pathology","score_opus":0.010484899791478283,"score_gpt":0.2412951619130499,"score_spread":0.2308102621215716,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103334703","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965997,0.00092706,0.00052059605,0.00013748604,0.0003091619,0.00006550065,0.0000018937376,0.0000041329517,0.0014344981],"genre_scores_gemma":[0.99525887,0.00017351504,0.004062618,0.000083314866,0.00017362977,9.560473e-7,0.000004556624,0.00003359613,0.00020893835],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99848884,0.00022575396,0.0005038931,0.000260949,0.00013974523,0.00038078963],"domain_scores_gemma":[0.9990104,0.000021120188,0.0003771184,0.00032605967,0.00014899012,0.000116321324],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038113765,0.00017692284,0.00035936717,0.0005863953,0.00004569175,0.000022508499,0.00032428766,0.000031566804,0.000053245807],"category_scores_gemma":[0.00014453763,0.00014232096,0.00015605394,0.00069382996,0.00012992679,0.000005926894,0.0001109111,0.00034667065,0.000020349487],"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":[0.00011982956,0.00011126967,0.06032825,0.000002895148,0.00025163425,0.00030974037,0.00005675979,0.00020574138,0.9354269,0.000027901368,0.00018763896,0.0029714329],"study_design_scores_gemma":[0.0063464446,0.00363704,0.854848,0.000017588009,0.0004121404,0.0051425477,0.00017829951,0.000064075124,0.106831156,0.0000074082245,0.022063354,0.00045191494],"about_ca_topic_score_codex":0.000027664035,"about_ca_topic_score_gemma":0.000093720075,"teacher_disagreement_score":0.82859576,"about_ca_system_score_codex":0.000014129023,"about_ca_system_score_gemma":0.00006720564,"threshold_uncertainty_score":0.58036804},"labels":[],"label_agreement":null},{"id":"W2103693713","doi":"10.1093/dnares/11.6.381","title":"An Evolutionary Scenaio for Genomic Imprinting of Impact Lying between Nonimprinted Neighbors","year":2004,"lang":"en","type":"article","venue":"DNA Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Japan Society for the Promotion of Science; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Gene; Genetics; Gene duplication; Operon; Genome; DNA methylation; Gene expression","score_opus":0.0555185238834559,"score_gpt":0.396038315595073,"score_spread":0.3405197917116171,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103693713","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9935397,0.00024093216,0.005317806,0.00006548897,0.000046648893,0.00043197442,0.00003389935,0.0000110599,0.00031252447],"genre_scores_gemma":[0.9921929,0.000030417606,0.0072733597,0.000008557834,0.00029334598,0.000031926353,0.000086857195,0.000039699193,0.00004291054],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9982746,0.000085570944,0.00031262165,0.00043227914,0.00026174198,0.0006331382],"domain_scores_gemma":[0.99884975,0.000046362886,0.00008393882,0.00049845054,0.00035113236,0.00017034548],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010293395,0.00014376827,0.0001939011,0.00016330124,0.00020633206,0.000034958106,0.00042300686,0.00015654587,0.000018834824],"category_scores_gemma":[0.00025087726,0.00013795045,0.00016477227,0.00020145795,0.00013735113,0.000007134732,0.0002711034,0.0001762553,0.000008799285],"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":[0.000022585564,0.000054742413,0.06527525,0.00004390323,0.00005924745,4.8859675e-7,0.000066831,0.00045744798,0.92895705,0.000101329846,0.000024706946,0.004936411],"study_design_scores_gemma":[0.0011213555,0.0011252715,0.5571103,0.000041893563,0.000011645789,0.000015372272,0.00027682591,0.00043962605,0.4383793,0.0008146298,0.0004562545,0.00020752323],"about_ca_topic_score_codex":0.00031576253,"about_ca_topic_score_gemma":0.0000076067504,"teacher_disagreement_score":0.4918351,"about_ca_system_score_codex":0.00009089997,"about_ca_system_score_gemma":0.00036093342,"threshold_uncertainty_score":0.5625456},"labels":[],"label_agreement":null},{"id":"W2103889681","doi":"10.1097/01.asn.0000023431.16173.55","title":"Renal Abnormalities in Beckwith-Wiedemann Syndrome Are Associated with 11p15.5 Uniparental Disomy","year":2002,"lang":"en","type":"article","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"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 Cancer Institute","keywords":"Beckwith–Wiedemann syndrome; Uniparental disomy; Imprinting (psychology); Genomic imprinting; Medicine; Gigantism; Incidence (geometry); Macroglossia; Internal medicine; Gastroenterology; Pathology; Biology; Genetics; Gene; Chromosome; Karyotype","score_opus":0.012176448068181151,"score_gpt":0.22168039189991876,"score_spread":0.2095039438317376,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103889681","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99777186,0.0004591302,0.000061951614,0.0014979682,0.000048610313,0.00007028194,0.000007686215,0.0000022701574,0.000080259706],"genre_scores_gemma":[0.9974238,0.00028104984,0.0006028339,0.0013672773,0.00007027703,0.0000022317613,0.0000022024687,0.0000166369,0.00023364979],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987945,0.00014967957,0.00041521696,0.00014683616,0.00020923282,0.00028454186],"domain_scores_gemma":[0.99841905,0.000036032885,0.001164652,0.00021659349,0.00010762479,0.000056050067],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025729835,0.00014737113,0.00042101945,0.000035283047,0.00006064432,0.000008711148,0.00036818418,0.00008115063,0.00002335683],"category_scores_gemma":[0.000045496832,0.00010090297,0.00030232017,0.00022435446,0.0006096955,0.000006982244,0.00013604772,0.00022464097,6.9546684e-7],"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":[0.00014768279,0.0005876517,0.710463,0.000041336363,0.0014484243,0.000036662113,0.0014851496,0.0016039001,0.26101473,0.0000109538,0.021401687,0.0017588102],"study_design_scores_gemma":[0.0011053662,0.0016388375,0.9870305,0.000086138636,0.00006480792,0.00129539,0.0026476234,0.00016252561,0.0016768442,0.000028882348,0.0041001146,0.00016295169],"about_ca_topic_score_codex":0.000059792193,"about_ca_topic_score_gemma":0.000052944706,"teacher_disagreement_score":0.27656752,"about_ca_system_score_codex":0.000033993158,"about_ca_system_score_gemma":0.000043267533,"threshold_uncertainty_score":0.41147038},"labels":[],"label_agreement":null},{"id":"W2105964357","doi":"10.1111/j.1365-2788.2007.01004.x","title":"Facial expression of affect in children with Cornelia de Lange syndrome","year":2007,"lang":"en","type":"article","venue":"Journal of Intellectual Disability Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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":"Cornelia de Lange Syndrome; Affect (linguistics); Psychology; Facial expression; Developmental psychology; Medicine; Pediatrics; Communication","score_opus":0.036131907131039524,"score_gpt":0.3464480980124535,"score_spread":0.310316190881414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2105964357","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998613,0.00020003117,0.00072267407,0.000024499954,0.000026029618,0.00017296834,0.0000031298841,0.000001284225,0.00023636814],"genre_scores_gemma":[0.9991682,0.000053637792,0.00063660066,0.000006863607,0.000074873606,0.0000017176447,0.000002936805,0.000011796221,0.00004338077],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9984433,0.00023256084,0.00039085557,0.00017133864,0.0003967748,0.00036514053],"domain_scores_gemma":[0.99912995,0.00020386235,0.000100179255,0.00021292857,0.00023565827,0.00011743155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0032107034,0.00009445772,0.00021137128,0.00011488651,0.000038132002,0.000013835988,0.00028657072,0.00011750841,0.000098137345],"category_scores_gemma":[0.0019866633,0.00006935075,0.00009141604,0.00025254677,0.00031721077,0.0000052724135,0.0001382343,0.00036644755,0.0000034251511],"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":[0.00027740002,0.00022367909,0.6597688,0.00002331781,0.000026089163,0.000004590224,0.0003569784,0.000025167708,0.33618307,0.0000013774104,0.00016169137,0.002947798],"study_design_scores_gemma":[0.00049101224,0.001915671,0.7571038,0.00007510295,0.000004151494,0.00050574326,0.00059041823,0.000007903355,0.23912786,0.000033253484,0.00007773931,0.00006735751],"about_ca_topic_score_codex":0.000079663696,"about_ca_topic_score_gemma":0.00006708636,"teacher_disagreement_score":0.09733494,"about_ca_system_score_codex":0.000066645545,"about_ca_system_score_gemma":0.0001402185,"threshold_uncertainty_score":0.28280416},"labels":[],"label_agreement":null},{"id":"W2108321118","doi":"10.14740/jem.v4i4.235","title":"Pseudopseudohypoparathyroidism With a Novel Mutation in the GNAS Gene Showing Thin Bones of Extremities and Ossification of Entheses","year":2014,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Medicine; Exon; Ossification; Enthesis; Gene; Endocrinology; Internal medicine; Genetics; Molecular biology; Anatomy; Biology","score_opus":0.017841005248087634,"score_gpt":0.24206418267447108,"score_spread":0.22422317742638345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108321118","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9899901,0.007615401,0.0020216797,0.00015775391,0.00005223175,0.000053641354,0.0000019831039,6.16679e-7,0.00010656967],"genre_scores_gemma":[0.99600196,0.0011002906,0.0027691,0.000041206422,0.00006346558,0.000002337359,0.0000013842862,0.0000046355867,0.000015591735],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993455,0.000083024504,0.00029254664,0.000093571245,0.000080240396,0.00010513764],"domain_scores_gemma":[0.99944806,0.000052894025,0.00029607615,0.00010045429,0.00008358729,0.000018934299],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030276307,0.00007655116,0.00020292866,0.00007553194,0.00002908362,0.000007243956,0.00008708809,0.000045995657,8.1050274e-7],"category_scores_gemma":[0.00012217654,0.000048696482,0.00003318388,0.000043838234,0.00013291957,0.000008665808,0.000034848505,0.00007695132,2.8014783e-8],"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":[0.000043434153,0.000056477857,0.009146824,0.000019521905,0.000051418094,0.0000018812713,0.0008638843,0.00007954773,0.9812114,0.001699903,0.000008594088,0.0068170885],"study_design_scores_gemma":[0.001609255,0.00039117638,0.57362664,0.000037304828,0.000110755376,0.0024600509,0.002049037,0.000105278086,0.4176198,0.00068182516,0.0012050092,0.00010389271],"about_ca_topic_score_codex":0.000018027356,"about_ca_topic_score_gemma":0.0000066018324,"teacher_disagreement_score":0.56447977,"about_ca_system_score_codex":0.0000011591817,"about_ca_system_score_gemma":0.000024207102,"threshold_uncertainty_score":0.19857849},"labels":[],"label_agreement":null},{"id":"W2108580735","doi":"10.1016/j.metabol.2014.11.011","title":"Hormonal and Metabolic Responses to Endurance Exercise in Children With Prader–Willi Syndrome and Non-Syndromic Obesity","year":2014,"lang":"en","type":"article","venue":"Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Endocrinology; Internal medicine; Medicine; Hormone; Epinephrine; Endocrine system; Obesity; Lean body mass; Body weight","score_opus":0.004455833042478412,"score_gpt":0.20419753078619973,"score_spread":0.19974169774372133,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108580735","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99260557,0.0064478936,0.0003218291,0.0001156085,0.000051290244,0.00039164058,0.000012829864,0.000009933393,0.000043389067],"genre_scores_gemma":[0.99485433,0.0011907255,0.003467036,0.00014447531,0.00005551283,0.00004785012,0.000010468043,0.00003080878,0.00019878602],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.998656,0.00007929678,0.00021175199,0.0005534366,0.00014053742,0.00035900768],"domain_scores_gemma":[0.99937487,0.000011892585,0.00006468454,0.0003437195,0.000031034815,0.00017382899],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032050256,0.00024267811,0.00038358508,0.0001177801,0.00008308699,0.00004975662,0.00016092215,0.00011327984,0.0000063347134],"category_scores_gemma":[0.000055178523,0.00020851634,0.000036304707,0.00012972264,0.00008940869,0.000009569122,0.00019569354,0.0001088538,0.000007856659],"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":[0.000024078274,0.00007296821,0.870745,0.000026872976,0.00008768462,0.0000019343668,0.00017888885,0.00002609925,0.11366698,0.00008218394,0.00005023364,0.015037061],"study_design_scores_gemma":[0.00093839754,0.000113548274,0.9887928,0.000035294892,0.00005332734,0.00053155376,0.000021488193,0.00003070369,0.0065504373,0.000036142235,0.0026072592,0.00028908305],"about_ca_topic_score_codex":0.00011110131,"about_ca_topic_score_gemma":0.000017635528,"teacher_disagreement_score":0.11804775,"about_ca_system_score_codex":0.0000030315966,"about_ca_system_score_gemma":0.000030685165,"threshold_uncertainty_score":0.85030496},"labels":[],"label_agreement":null},{"id":"W2108618113","doi":"10.1210/jc.2004-1848","title":"Hypermethylation of the Promoter Region Is Associated with the Loss of <i>MEG3</i> Gene Expression in Human Pituitary Tumors","year":2005,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":209,"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 Diabetes and Digestive and Kidney Diseases; U.S. Public Health Service; National Institutes of Health; National Institute of Mental Health; Jarislowsky Foundation; Massachusetts General Hospital","keywords":"MEG3; DNA methylation; Biology; Pituitary tumors; Carcinogenesis; Gene expression; Genomic imprinting; Methylation; Cancer research; Gene isoform; Gene; Molecular biology; RNA; Endocrinology; Genetics; Long non-coding RNA","score_opus":0.025862963179958134,"score_gpt":0.3079542497951875,"score_spread":0.28209128661522936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108618113","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949756,0.0014404013,0.00016014527,0.0030557308,0.00012858711,0.00015533208,0.0000020449247,0.0000013877011,0.000080714504],"genre_scores_gemma":[0.99803996,0.0007150141,0.00032612492,0.00051965483,0.00029320747,0.0000019097345,0.0000013323645,0.000013118608,0.000089649635],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9975969,0.00080038514,0.0010175166,0.0001383748,0.00022689307,0.00021992311],"domain_scores_gemma":[0.9979039,0.00015533803,0.0012864576,0.0004200494,0.00019963934,0.000034632907],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00123089,0.00012783874,0.0004475648,0.000043310283,0.000072122544,0.000003587292,0.00054648425,0.00012612174,0.000008974964],"category_scores_gemma":[0.0003656259,0.00005695057,0.00022902682,0.00012312025,0.00043123096,0.000008113931,0.00017384617,0.00041847746,3.7039882e-7],"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":[0.00025348275,0.00039140906,0.07417209,0.000011408847,0.00027824115,0.0000068675045,0.0005871561,0.0007116157,0.9133452,0.000049374645,0.00054031773,0.009652803],"study_design_scores_gemma":[0.0017297538,0.0003656852,0.5424204,0.00007044169,0.00013960271,0.00027241127,0.00011274712,0.000021143873,0.45182326,0.00016444524,0.0028004297,0.000079690086],"about_ca_topic_score_codex":0.0000146663915,"about_ca_topic_score_gemma":0.000017801758,"teacher_disagreement_score":0.46824828,"about_ca_system_score_codex":0.0000050511985,"about_ca_system_score_gemma":0.00007976133,"threshold_uncertainty_score":0.23223768},"labels":[],"label_agreement":null},{"id":"W2108691006","doi":"10.1098/rsbl.2007.0189","title":"Virgin birth in a hammerhead shark","year":2007,"lang":"en","type":"article","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":179,"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":"Queen's University Belfast; Florida Sea Grant, University of Florida; Queen's University; Wildlife Conservation Society; National Science Foundation","keywords":"Chondrichthyes; Biology; Parthenogenesis; Vertebrate; Elasmobranchii; Zoology; Facultative; Evolutionary biology; Ecology; Fishery; Embryo; Genetics; Gene","score_opus":0.008765734897021621,"score_gpt":0.25125457054088657,"score_spread":0.24248883564386495,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108691006","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9936835,0.00032578746,0.0040982026,0.00079919543,0.0002327821,0.00009342086,0.0000037795369,0.00000979672,0.00075351784],"genre_scores_gemma":[0.9949481,0.00003123858,0.0013848725,0.0032457677,0.00017364281,0.0000063184134,0.00002997917,0.000013850894,0.00016626388],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990167,0.000043926637,0.00019979972,0.00031044384,0.00003598632,0.00039314368],"domain_scores_gemma":[0.99965537,0.000015822436,0.000045735884,0.00021821618,0.0000110884,0.000053741373],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042134305,0.00011793711,0.00011576005,0.000079841666,0.000029589384,0.0000064671854,0.00015735229,0.00013502265,0.000033624143],"category_scores_gemma":[0.000053610624,0.000112128895,0.00005522057,0.00008893136,0.00008092982,0.0000011486942,0.00008563825,0.000084057334,0.00003160265],"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":[0.000009735643,0.000014893986,0.16992056,0.00000403968,0.000011383486,0.0000048163697,0.000019396834,0.000005182775,0.82280177,0.00003811709,0.0005505035,0.0066196],"study_design_scores_gemma":[0.0009092955,0.0001889884,0.6152201,0.000012008123,0.000004238252,0.000068700676,0.00008259059,0.000020010848,0.1818201,0.000026485928,0.20131536,0.00033208393],"about_ca_topic_score_codex":0.000061752144,"about_ca_topic_score_gemma":0.00009520532,"teacher_disagreement_score":0.6409817,"about_ca_system_score_codex":0.000011232598,"about_ca_system_score_gemma":0.000014370546,"threshold_uncertainty_score":0.4572484},"labels":[],"label_agreement":null},{"id":"W2109753113","doi":"10.1002/0471695998.mgs010","title":"<scp>B</scp>eckwith‐<scp>W</scp>iedemann Syndrome and Hemihyperplasia","year":2005,"lang":"en","type":"other","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Macroglossia; Beckwith–Wiedemann syndrome; Medicine; Duodenal atresia; Polyhydramnios; Population; Incidence (geometry); Pediatrics; Endocrinology; Internal medicine; Biology; Genetics; Pathology; Pregnancy; Fetus; Gene; Tongue; Atresia","score_opus":0.006385053581246507,"score_gpt":0.22008321788003476,"score_spread":0.21369816429878827,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2109753113","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.18974485,0.014449462,0.0003486099,0.00004734826,0.0004672236,0.00053612574,0.00006315863,0.00014642706,0.7941968],"genre_scores_gemma":[0.027402762,0.0037935805,0.0044519734,0.000477129,0.0008658837,0.00004897809,0.00023611616,0.00068472297,0.9620389],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9971501,0.000055912322,0.00044823997,0.001189062,0.00030866457,0.00084799435],"domain_scores_gemma":[0.998336,0.00006765787,0.00029810457,0.0009016835,0.000055699293,0.00034086226],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00015389732,0.0007536785,0.0006694278,0.00019976204,0.00010157102,0.000108976834,0.00048544418,0.0011376311,0.000401232],"category_scores_gemma":[0.00030794452,0.0007000012,0.00022625255,0.00013775294,0.00017579336,0.0000039185315,0.0005173993,0.00029131232,0.00034771152],"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":[6.846078e-7,0.000104060535,0.002533519,0.0002392906,0.00049237744,0.000036791906,0.00007155001,0.0000091196825,0.020521251,0.0000822826,0.9717895,0.0041195857],"study_design_scores_gemma":[0.0006108442,0.00027364056,0.003090573,0.00013196912,0.000104557395,0.001276718,0.00034890903,0.000026478992,0.005112147,0.000012824942,0.9888205,0.00019084096],"about_ca_topic_score_codex":0.00009084731,"about_ca_topic_score_gemma":0.000090662725,"teacher_disagreement_score":0.16784205,"about_ca_system_score_codex":0.000017207676,"about_ca_system_score_gemma":0.00010213749,"threshold_uncertainty_score":0.9995451},"labels":[],"label_agreement":null},{"id":"W2110063687","doi":"10.1038/jhg.2014.30","title":"The imprinted gene LRRTM1 mediates schizotypy and handedness in a nonclinical population","year":2014,"lang":"en","type":"article","venue":"Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"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; Simon Fraser University","funders":"","keywords":"Single-nucleotide polymorphism; Epigenetics; Genetics; Schizotypy; Allele; DNA methylation; Biology; Schizophrenia (object-oriented programming); Genomic imprinting; Population; SNP; Genetic variation; Gene; Psychology; Genotype; Gene expression; Cognition; Neuroscience; Medicine; Psychiatry","score_opus":0.01173395077742766,"score_gpt":0.28492919129464983,"score_spread":0.27319524051722216,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2110063687","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99719644,0.0014586615,0.000880495,0.00012612862,0.00022306114,0.00006336013,5.5372294e-7,0.0000015543054,0.000049754333],"genre_scores_gemma":[0.9978197,0.0007481691,0.00094463356,0.000045803863,0.00037973467,0.000001320579,0.0000042858533,0.000014781248,0.00004153761],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989251,0.00009972208,0.0005157394,0.00013644496,0.00014518395,0.00017780732],"domain_scores_gemma":[0.9993065,0.000043606415,0.0002728496,0.0001904214,0.0001061866,0.00008041444],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007249031,0.000104488,0.00016871041,0.00004921623,0.00011001017,0.00004968664,0.0001961355,0.00010459363,0.0000034349198],"category_scores_gemma":[0.00023004595,0.000075269294,0.00006914658,0.000046810856,0.00007306552,0.0000024863045,0.00011679719,0.00014522045,8.601226e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000037919468,0.00009859011,0.3551589,0.000021619817,0.00007515771,0.0000032401367,0.000107003296,0.00022602102,0.5746575,0.00008107629,0.00009616531,0.0694368],"study_design_scores_gemma":[0.0015516046,0.0012055067,0.94334316,0.00003750044,0.000032401986,0.00016349836,0.00010296519,0.0010339139,0.04924873,0.00091178634,0.0021839992,0.0001849538],"about_ca_topic_score_codex":0.000009302672,"about_ca_topic_score_gemma":0.000096870484,"teacher_disagreement_score":0.58818424,"about_ca_system_score_codex":0.000008249499,"about_ca_system_score_gemma":0.000027134156,"threshold_uncertainty_score":0.30693927},"labels":[],"label_agreement":null},{"id":"W2111319296","doi":"10.1093/jmcb/mjq029","title":"Genome-wide Gene Expression Profiling Reveals Aberrant MAPK and Wnt Signaling Pathways Associated with Early Parthenogenesis","year":2010,"lang":"en","type":"article","venue":"Journal of Molecular Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Brock University","funders":"College of Medicine, University of Florida; Moffitt Cancer Center; University of South Florida; Cancer Research Institute","keywords":"Biology; Wnt signaling pathway; Gene expression; Parthenogenesis; Embryo; Signal transduction; MAPK/ERK pathway; Gene expression profiling; Gene; Regulation of gene expression; Genomic imprinting; Cell biology; Genetics; DNA methylation","score_opus":0.008691608230164138,"score_gpt":0.20422749012950772,"score_spread":0.1955358818993436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111319296","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9938584,0.0016857531,0.003961641,0.000037049067,0.00015919693,0.00015906054,0.0000072117246,0.000005738765,0.0001259488],"genre_scores_gemma":[0.9877438,0.00015599819,0.011741147,0.00012925718,0.00012772052,0.000005490604,0.000026829817,0.000038104332,0.000031675856],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9984935,0.00016888323,0.00049263716,0.00032924273,0.00014507642,0.0003706424],"domain_scores_gemma":[0.9987431,0.000039296712,0.00056287827,0.00024269603,0.000237551,0.00017447663],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064106716,0.0002303528,0.00034707508,0.00008859803,0.000097725126,0.0000325507,0.0002321518,0.00029991881,0.000014902637],"category_scores_gemma":[0.00018475074,0.00017487537,0.00013394759,0.00007703036,0.000083050945,0.000005389229,0.00012564589,0.00028405862,0.0000017091049],"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":[0.000037973005,0.000051380815,0.04009775,0.000012872029,0.000089251305,0.000034696208,0.000053855212,0.00008617012,0.9591188,0.0000053844606,0.0000030747228,0.0004088247],"study_design_scores_gemma":[0.00085618126,0.0009638862,0.019681817,0.000033596232,0.0000610211,0.00013267169,0.00005103722,0.000008557062,0.9775499,0.00012256889,0.00030924458,0.00022950572],"about_ca_topic_score_codex":0.0000032289358,"about_ca_topic_score_gemma":0.000002047369,"teacher_disagreement_score":0.020415934,"about_ca_system_score_codex":0.000009046833,"about_ca_system_score_gemma":0.00008942306,"threshold_uncertainty_score":0.7131211},"labels":[],"label_agreement":null},{"id":"W2111787288","doi":"10.1002/ajmg.c.30268","title":"Imprinted genes and human disease","year":2010,"lang":"en","type":"editorial","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Human genome; Disease; Phenotype; Biology; Human genetics; Human disease; Computational biology; Genetics; DNA microarray; Gene; Medical genetics; Bioinformatics; Genome; Medicine; Pathology; Gene expression","score_opus":0.006013900462875183,"score_gpt":0.2991589590729615,"score_spread":0.2931450586100863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111787288","genre_codex":"empirical","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.77647895,0.030578537,0.0006292705,0.0009751553,0.19088514,0.0002941118,0.00006006166,0.00001201102,0.00008674545],"genre_scores_gemma":[0.14056224,0.29949155,0.007260573,0.0010468841,0.5502604,0.00004698882,0.00040351605,0.0004176094,0.0005102367],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9901096,0.00047551395,0.0022164236,0.0009790731,0.005210859,0.0010085297],"domain_scores_gemma":[0.9937442,0.00044074957,0.0013470978,0.0009862665,0.00059570983,0.0028859647],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":["research_integrity"],"category_scores_codex":[0.0034413016,0.0007887172,0.0013990186,0.00033995268,0.00012924435,0.00009445781,0.002290646,0.0021554176,0.00031967385],"category_scores_gemma":[0.006381654,0.00072870497,0.0003851073,0.00034991466,0.00225469,0.0000045451334,0.0013585606,0.0034947423,0.000005999223],"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":[0.00018410935,0.00093948824,0.019977145,0.00038008104,0.00054932106,0.0011259739,0.0001898053,0.00004555905,0.011832166,0.000009262572,0.4216157,0.5431514],"study_design_scores_gemma":[0.0018735086,0.0027426719,0.0023263036,0.0013894768,0.00024055956,0.00043568318,0.0002013534,0.0002566472,0.0014972943,0.0000757141,0.9880805,0.00088029954],"about_ca_topic_score_codex":0.000043566422,"about_ca_topic_score_gemma":0.00012651434,"teacher_disagreement_score":0.6359167,"about_ca_system_score_codex":0.000047964375,"about_ca_system_score_gemma":0.0028079962,"threshold_uncertainty_score":0.9995164},"labels":[],"label_agreement":null},{"id":"W2111879149","doi":"10.1186/1756-8935-4-10","title":"Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies","year":2011,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Genomic imprinting; Differentially methylated regions; Biology; Imprinting (psychology); DNA methylation; Epigenetics; Genetics; Methylation; Gene; GNAS complex locus; Gene expression","score_opus":0.025998162810465554,"score_gpt":0.24634956916660475,"score_spread":0.2203514063561392,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111879149","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9786197,0.0015759688,0.018655313,0.000012438836,0.00010730839,0.0003628348,0.00007587804,0.000020094276,0.00057044596],"genre_scores_gemma":[0.9791731,0.00024295902,0.01983266,0.000012146766,0.000046803245,0.000017695655,0.00049752946,0.000047325073,0.00012976682],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9980266,0.00015544854,0.00086848164,0.0004281274,0.00021136987,0.00030998577],"domain_scores_gemma":[0.9985352,0.000040713716,0.00061800546,0.000542217,0.00017354701,0.000090308036],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00024793047,0.00026494,0.0004246445,0.000106094354,0.00009207019,0.000012131063,0.00033948797,0.00021058816,0.00009601602],"category_scores_gemma":[0.00015131848,0.00027260563,0.0001752156,0.00016349183,0.0001325382,0.000004619189,0.00023891915,0.000105805884,0.0000032671232],"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":[0.00001233835,0.00011947884,0.013846542,0.00006434292,0.00023733897,3.7945728e-7,0.00062265364,0.000012828327,0.9845894,0.000021320373,0.000024671222,0.00044873447],"study_design_scores_gemma":[0.0005542991,0.00027298625,0.18435113,0.000051190178,0.00006516815,0.0000010453778,0.00033534752,0.000060776267,0.81370264,0.00029804313,0.00009394544,0.00021342076],"about_ca_topic_score_codex":0.00021263974,"about_ca_topic_score_gemma":0.000023231807,"teacher_disagreement_score":0.17088673,"about_ca_system_score_codex":0.000017084161,"about_ca_system_score_gemma":0.00005343018,"threshold_uncertainty_score":0.99997264},"labels":[],"label_agreement":null},{"id":"W2112006955","doi":"10.1186/s13039-015-0109-8","title":"Functional consequences of copy number variants in miscarriage","year":2015,"lang":"en","type":"article","venue":"Molecular Cytogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"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":"Institute of Genetics; Canadian Institutes of Health Research; Michael Smith Health Research BC","keywords":"Miscarriage; Genomic imprinting; Recurrent miscarriage; Biology; Copy-number variation; Gene duplication; Gene; Genetics; Human genetics; Gene expression; Pregnancy; DNA methylation; Genome","score_opus":0.028357092811402026,"score_gpt":0.2660852716924739,"score_spread":0.2377281788810719,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2112006955","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9897062,0.0005787761,0.006027284,0.000072078816,0.00021828171,0.00013473458,0.000012125474,0.0000053742356,0.0032451537],"genre_scores_gemma":[0.9933932,0.000049756243,0.006077159,0.00014132068,0.000052684594,0.000010777399,0.00004517252,0.000023595518,0.00020637258],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99880457,0.00008687494,0.00031419485,0.0003053078,0.00023768941,0.00025137415],"domain_scores_gemma":[0.99929905,0.0000067319925,0.00009701705,0.00033400636,0.00014235385,0.000120846824],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024016228,0.00015330774,0.00017980309,0.000044979257,0.000018058146,0.000014137675,0.00018047003,0.00014503402,0.000056243254],"category_scores_gemma":[0.00013567001,0.00016143634,0.00007729536,0.00014508075,0.00013749833,0.0000017942932,0.00013178735,0.00006537698,0.000024703108],"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":[0.00001731535,0.000053186228,0.29025647,0.000011081956,0.00003420936,0.0000148089075,0.00003456131,0.0013334816,0.70724076,0.00020206891,0.00037681693,0.000425243],"study_design_scores_gemma":[0.0010652116,0.00018464385,0.029400617,0.000017781142,0.000017929522,0.00012508371,0.00011512829,0.000032826498,0.96503067,0.0006014042,0.0031909137,0.00021778821],"about_ca_topic_score_codex":0.000038565686,"about_ca_topic_score_gemma":0.000010872025,"teacher_disagreement_score":0.26085585,"about_ca_system_score_codex":0.000013841265,"about_ca_system_score_gemma":0.00019839626,"threshold_uncertainty_score":0.6583183},"labels":[],"label_agreement":null},{"id":"W2112806377","doi":"10.1038/4541054a","title":"Battle of the sexes may set the brain","year":2008,"lang":"en","type":"article","venue":"Nature","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"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","funders":"","keywords":"DISC1; Autism; Schizophrenia (object-oriented programming); Offspring; Genomic imprinting; Battle; Mental illness; Biology; Genetics; Gene; Psychology; Neuroscience; Psychiatry; Mental health; History; Gene expression; DNA methylation; Pregnancy","score_opus":0.007808402554892995,"score_gpt":0.2430938038181333,"score_spread":0.23528540126324032,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2112806377","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9944404,0.0013230062,0.000013550111,0.0026188537,0.0002499139,0.00006429867,0.0000090379945,0.0000024054145,0.0012785484],"genre_scores_gemma":[0.9960026,0.00004809614,0.00010650582,0.0011472143,0.000114044946,0.0000021519165,0.0000065076083,0.000006973916,0.0025659038],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996019,0.00003167504,0.000070685535,0.00010714186,0.0000908744,0.00009771535],"domain_scores_gemma":[0.9995919,0.000017364668,0.00004076048,0.00030997157,0.00002615728,0.000013859955],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008045618,0.000057867866,0.000051518826,0.000005508972,0.00008215289,0.000003594803,0.00023982457,0.00030956249,0.000020731628],"category_scores_gemma":[0.00012324253,0.000029923533,0.00006910263,0.000058968275,0.00007649799,5.3090804e-7,0.00011662403,0.00029525012,0.0000024586384],"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":[0.0000042381303,0.000023661752,0.057129726,0.000016546615,0.000052747593,9.450161e-7,0.00026457326,0.000051655603,0.8057346,0.00015582168,0.13400437,0.0025611133],"study_design_scores_gemma":[0.00020036587,0.000050386727,0.22908163,0.000008657884,0.000007638096,0.00012813625,0.00013665996,0.000013333994,0.38870052,0.00004311933,0.3815442,0.00008537354],"about_ca_topic_score_codex":0.000008517813,"about_ca_topic_score_gemma":0.0000077082805,"teacher_disagreement_score":0.4170341,"about_ca_system_score_codex":0.0000017495482,"about_ca_system_score_gemma":0.00002945433,"threshold_uncertainty_score":0.23876293},"labels":[],"label_agreement":null},{"id":"W2114100575","doi":"10.1093/hmg/ddm280","title":"Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development","year":2007,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":321,"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 General Medical Sciences; McGill University","keywords":"Genomic imprinting; Biology; Embryo; Imprinting (psychology); Yolk sac; Allele; Genetics; Embryogenesis; Gene expression; Locus (genetics); Gene; Andrology; DNA methylation","score_opus":0.01972676159889489,"score_gpt":0.28773413457619784,"score_spread":0.2680073729773029,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114100575","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98088753,0.00018576914,0.018315539,0.0000047299577,0.00004191127,0.00033654697,0.000009346148,0.000003583471,0.00021506517],"genre_scores_gemma":[0.9830808,0.000030638803,0.016676003,0.000020973463,0.000014410162,0.000008182443,0.000069557,0.000025846788,0.00007358727],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9984673,0.00004941275,0.00073491945,0.00028778077,0.00023533205,0.00022522693],"domain_scores_gemma":[0.9990875,0.000013123219,0.0002588848,0.0004100704,0.00016122698,0.000069191934],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032862189,0.00015604547,0.0002174763,0.00020328027,0.000033882654,0.000004348919,0.00020005899,0.0001246169,0.000007924376],"category_scores_gemma":[0.000049794657,0.00016258557,0.00006980219,0.00014260954,0.000039104674,0.0000015005008,0.00014016811,0.000054965636,0.0000014182702],"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":[0.00003470917,0.00014178234,0.004915267,0.000055390512,0.00002042004,0.0000018801521,0.0003612255,0.0026069148,0.988053,0.00004370515,0.0000070105198,0.0037586452],"study_design_scores_gemma":[0.00046650102,0.00029015512,0.21739909,0.000068322355,0.000008733869,0.0000031035188,0.00011066846,0.000022851385,0.78135586,0.000012330395,0.00013958497,0.00012278314],"about_ca_topic_score_codex":0.00002444206,"about_ca_topic_score_gemma":0.000068143105,"teacher_disagreement_score":0.21248382,"about_ca_system_score_codex":0.000015622678,"about_ca_system_score_gemma":0.000057948047,"threshold_uncertainty_score":0.6630047},"labels":[],"label_agreement":null},{"id":"W2114234140","doi":"10.1590/s1807-59322009000100008","title":"Sonographic Assessment of Renal Growth in Patients with Beckwith-Wiedemann Syndrome: The Beckwith-Wiedemann Syndrome Renal Nomogram","year":2009,"lang":"en","type":"article","venue":"Clinics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital","funders":"","keywords":"Beckwith–Wiedemann syndrome; Medicine; Nomogram; Kidney; Kidney disease; Supine position; Nephrectomy; Internal medicine; Urology; Pediatrics","score_opus":0.007847839787356698,"score_gpt":0.25937647578878575,"score_spread":0.25152863600142905,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114234140","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99735403,0.0002931628,0.0006598012,0.00028666723,0.00015734149,0.00060021435,0.000021660386,0.00001819724,0.0006089509],"genre_scores_gemma":[0.99654466,0.00015729474,0.0025563121,0.00033778543,0.00005427913,0.000031636886,0.00013886315,0.000041411582,0.00013775317],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99723446,0.0001472055,0.0008871319,0.00068445405,0.0004553595,0.00059140555],"domain_scores_gemma":[0.9982942,0.000053551335,0.0004905947,0.00079345325,0.00021996484,0.00014827374],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0007604036,0.00038795004,0.00054206175,0.00015558953,0.00014138373,0.000050565395,0.0006059845,0.00029499066,0.000019372654],"category_scores_gemma":[0.00010287355,0.00027257376,0.00025080895,0.0004471781,0.00023016115,0.000013225955,0.00018366151,0.0003703261,0.0000045982115],"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":[0.000099196935,0.0011628753,0.9900574,0.000069885835,0.00032181968,0.000040955456,0.0000916596,0.0005576175,0.0013210187,0.00021912828,0.00028380868,0.0057746265],"study_design_scores_gemma":[0.0020807101,0.004315361,0.99120855,0.00016640476,0.000090099435,0.00012847157,0.0000752988,0.00020426018,0.00033312908,0.00023461987,0.0007748923,0.000388207],"about_ca_topic_score_codex":0.000022952798,"about_ca_topic_score_gemma":0.000033925473,"teacher_disagreement_score":0.0053864196,"about_ca_system_score_codex":0.000023848668,"about_ca_system_score_gemma":0.00017071779,"threshold_uncertainty_score":0.99997264},"labels":[],"label_agreement":null},{"id":"W2114728169","doi":"10.1101/gr.111922.110","title":"A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes","year":2011,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":139,"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; Institute for Clinical Evaluative Sciences; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Hospital for Sick Children; Public Health Ontario; University of Toronto","funders":"National Institute of General Medical Sciences; Canadian Institutes of Health Research; National Institutes of Health; Hospital for Sick Children; Ministério da Ciência, Tecnologia e Ensino Superior; GlaxoSmithKline; University of Toronto; Fundação para a Ciência e a Tecnologia; McGill University","keywords":"Biology; Differentially methylated regions; Genetics; Genomic imprinting; Gene; DNA methylation; Computational biology; Gene expression","score_opus":0.11435360814045456,"score_gpt":0.31099517195343557,"score_spread":0.196641563812981,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114728169","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95588404,0.0009893853,0.03740451,0.00006304957,0.00006329135,0.00046252672,0.000013303968,0.000035939505,0.005083956],"genre_scores_gemma":[0.98146874,0.00019374058,0.0052348045,0.000019363084,0.00013217595,0.000047102323,0.00016334654,0.0000610262,0.012679692],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9976923,0.00017306666,0.00027596156,0.000642669,0.0004499047,0.0007661328],"domain_scores_gemma":[0.998559,0.00002283962,0.00009095762,0.0006560382,0.00041285757,0.00025830173],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00072292873,0.00021986211,0.00023334795,0.00019755831,0.00024135876,0.00008086786,0.0005721046,0.00022143376,0.00012744105],"category_scores_gemma":[0.00016810688,0.00018440944,0.00010774052,0.0004741049,0.00019816619,0.0000057105985,0.0005141287,0.0002890331,0.000028743638],"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":[0.000038765254,0.00021071736,0.0011883597,0.000022244787,0.00032372284,0.0000034081747,0.00041779617,0.000008864598,0.9961438,0.00008335944,0.000099702804,0.0014592691],"study_design_scores_gemma":[0.0041190563,0.0020294841,0.43911406,0.000096903066,0.00014779104,0.00023395018,0.002135262,0.0004668199,0.5429284,0.0008972249,0.006484663,0.0013463723],"about_ca_topic_score_codex":0.00091736764,"about_ca_topic_score_gemma":0.00017516145,"teacher_disagreement_score":0.4532154,"about_ca_system_score_codex":0.000031890646,"about_ca_system_score_gemma":0.00027095684,"threshold_uncertainty_score":0.7519999},"labels":[],"label_agreement":null},{"id":"W2115095020","doi":"10.1093/hmg/ddm281","title":"Coordinated diurnal regulation of genes from the Dlk1–Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes","year":2007,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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; Douglas Mental Health University Institute; McGill University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health; McGill University","keywords":"Congenic; Enhancer; Biology; Genomic imprinting; Gene; Genetics; Imprinting (psychology); Regulation of gene expression; Genome; Regulator; Chromosome; Regulatory sequence; Gene expression; DNA methylation","score_opus":0.014073947542418244,"score_gpt":0.2748342011835551,"score_spread":0.26076025364113686,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115095020","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.75245947,0.0011236388,0.24571201,0.00005114586,0.000064626496,0.00045694585,0.000049579627,0.000004509609,0.000078075755],"genre_scores_gemma":[0.9809227,0.00008479618,0.018426254,0.00003550248,0.00009193229,0.000017493932,0.00034647077,0.000040099534,0.000034744866],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99839073,0.000063825115,0.000772318,0.00033572887,0.00017088222,0.00026652936],"domain_scores_gemma":[0.9980391,0.000046138503,0.0006154399,0.00072759367,0.0005099721,0.000061707935],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038658545,0.0002000351,0.0002811347,0.00007937724,0.00011079999,0.000011507729,0.00036072388,0.00019871646,0.000009644188],"category_scores_gemma":[0.000044073677,0.00018416869,0.00022796197,0.0001738068,0.00021140279,0.0000032593582,0.00014878405,0.0000562316,3.6500697e-7],"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":[0.00003713133,0.00006562235,0.012523793,0.00004009642,0.00014136767,1.3042914e-7,0.00011011091,0.0019704518,0.97932297,0.00028352917,0.00004411823,0.005460699],"study_design_scores_gemma":[0.00057633617,0.00024498822,0.4108204,0.000021896785,0.000067276254,0.0000059206072,0.0000947613,0.0003959933,0.5863848,0.0010218266,0.0002477837,0.000118028845],"about_ca_topic_score_codex":0.0000626148,"about_ca_topic_score_gemma":0.000049818806,"teacher_disagreement_score":0.3982966,"about_ca_system_score_codex":0.000015423962,"about_ca_system_score_gemma":0.000059347665,"threshold_uncertainty_score":0.75101817},"labels":[],"label_agreement":null},{"id":"W2115123766","doi":"10.1002/ppul.10152","title":"Sleep and breathing in Prader‐Willi syndrome","year":2002,"lang":"en","type":"review","venue":"Pediatric Pulmonology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":214,"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 Children's Hospital","funders":"","keywords":"Medicine; Polysomnography; Obstructive sleep apnea; Pediatrics; Non-rapid eye movement sleep; Hypoventilation; Hypotonia; Sleep apnea; Abnormality; Excessive daytime sleepiness; Apnea; Sleep disorder; Anesthesia; Internal medicine; Insomnia; Respiratory system; Psychiatry; Electroencephalography","score_opus":0.02104118724063914,"score_gpt":0.2674210782155739,"score_spread":0.2463798909749348,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115123766","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.008759373,0.98988646,0.000036948055,0.000032711465,0.00032852346,0.00041499312,0.00001279841,0.00001688757,0.0005112918],"genre_scores_gemma":[0.0027442856,0.9956146,0.0005022791,0.000033499036,0.00039079846,0.00009113406,0.00007697969,0.000070634895,0.0004757985],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99764997,0.00017045652,0.00064825884,0.0008501258,0.00009404872,0.0005871525],"domain_scores_gemma":[0.99903536,0.00004895881,0.0003024468,0.0004804447,0.000020826752,0.00011195541],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00021859285,0.00045569174,0.0011114804,0.00035138353,0.000057739704,0.000030621093,0.00034759403,0.0009341371,0.000038354236],"category_scores_gemma":[0.00012835761,0.0004317778,0.00021110509,0.0002952706,0.000060217822,0.0000035261571,0.00042151404,0.0004170712,0.000059539365],"study_design_candidate":"design_other","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":[2.723349e-7,0.00006575765,0.0047647883,0.0037150632,0.00007782418,0.00006004064,0.000023543944,0.0000016817975,0.000004489181,0.0000150586575,0.00015875632,0.9911127],"study_design_scores_gemma":[0.00028724593,0.00023065414,0.00267815,0.00022816508,0.00037467896,0.0061452202,0.000011345268,0.000024278868,4.6273962e-7,0.000026243915,0.98936826,0.00062531896],"about_ca_topic_score_codex":0.000026484122,"about_ca_topic_score_gemma":0.000005943545,"teacher_disagreement_score":0.9904874,"about_ca_system_score_codex":0.00002994256,"about_ca_system_score_gemma":0.000068141766,"threshold_uncertainty_score":0.9998134},"labels":[],"label_agreement":null},{"id":"W2115328346","doi":"10.1002/1096-8628(20010801)102:2<161::aid-ajmg1453>3.0.co;2-o","title":"GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome","year":2001,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":129,"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 Institute for Cancer Research; Children's & Women's Health Centre of British Columbia; Hospital for Sick Children; University of British Columbia; SickKids Foundation; University of Toronto","funders":"","keywords":"Sotos syndrome; Hepatoblastoma; Genetics; Gigantism; Beckwith–Wiedemann syndrome; Exon; Biology; Medicine; Gene; Internal medicine","score_opus":0.0035735619762140244,"score_gpt":0.2290597276600335,"score_spread":0.22548616568381946,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115328346","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994666,0.0004416668,0.004522146,0.00021037045,0.00004952376,0.00006859195,0.0000045834922,8.407706e-7,0.000036314657],"genre_scores_gemma":[0.997928,0.0007354595,0.001187174,0.00007380453,0.00004504451,0.0000010638165,0.000009056996,0.000013253392,0.0000070906312],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.998196,0.000092047354,0.00061491644,0.00014607234,0.00074699725,0.00020394092],"domain_scores_gemma":[0.99871135,0.000044279495,0.0007057184,0.00023953826,0.0001743572,0.00012474827],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042969044,0.0001239628,0.0004049584,0.00015454197,0.000019159283,0.000006861939,0.00036896724,0.00006818205,0.000052349133],"category_scores_gemma":[0.00015059015,0.00008190756,0.00014157193,0.0007394589,0.00030357018,0.000003222441,0.00007529516,0.00014970705,3.2966537e-7],"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":[0.00017673415,0.00037097078,0.9612404,0.000017028038,0.0006519721,0.000024731104,0.00031248422,0.0026114618,0.0019223365,0.000005982879,0.000018620934,0.032647274],"study_design_scores_gemma":[0.0011135181,0.0042564375,0.99080104,0.000045512483,0.00025142863,0.000101504505,0.00062102743,0.0005434225,0.0019552077,0.000026393214,0.00016884957,0.000115659364],"about_ca_topic_score_codex":0.00007295013,"about_ca_topic_score_gemma":0.00005424916,"teacher_disagreement_score":0.032531615,"about_ca_system_score_codex":0.000012173153,"about_ca_system_score_gemma":0.00016234218,"threshold_uncertainty_score":0.33400932},"labels":[],"label_agreement":null},{"id":"W2116283958","doi":"10.1002/ajmg.a.31074","title":"Angelman syndrome 2005: Updated consensus for diagnostic criteria","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":646,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hamilton Health Sciences; McMaster Children's Hospital","funders":"","keywords":"Statement (logic); Consensus conference; Angelman syndrome; Scientific consensus; Salient; Scientific evidence; Management science; MEDLINE; Scientific literature; Computer science; Psychology; Medical physics; Medicine; Political science; Artificial intelligence; Epistemology; Engineering; Library science; Law","score_opus":0.00980346440927048,"score_gpt":0.2805707475976675,"score_spread":0.270767283188397,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116283958","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914501,0.0020063624,0.004094599,0.0015951068,0.0005515593,0.00015437871,0.000025520974,0.000005858511,0.00011655076],"genre_scores_gemma":[0.99097764,0.00055875955,0.006895883,0.00049108505,0.00076300546,0.000009703798,0.00004575001,0.000037760943,0.00022040651],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9979674,0.00010701332,0.00070316216,0.00024671908,0.00051663374,0.00045907512],"domain_scores_gemma":[0.9986016,0.00013666929,0.00043894493,0.00025497453,0.00021594392,0.00035185815],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007302402,0.00019336044,0.00039125586,0.00007355294,0.00006567447,0.000033096472,0.00040640848,0.00012886492,0.00016115031],"category_scores_gemma":[0.00060550903,0.00017231455,0.00019597894,0.00011473436,0.0003703017,0.000001586864,0.00010139737,0.00014986696,0.000006706444],"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":[0.00036420848,0.0014900942,0.06454708,0.00016454024,0.0012825858,0.0008105205,0.0001700421,0.0010118389,0.23040491,0.00019453836,0.5248052,0.17475449],"study_design_scores_gemma":[0.00410392,0.0070097465,0.08596705,0.00022783742,0.0002978928,0.00901484,0.00044714432,0.0009433621,0.018361578,0.00037423815,0.8724079,0.0008444605],"about_ca_topic_score_codex":0.000028553937,"about_ca_topic_score_gemma":0.00002181873,"teacher_disagreement_score":0.34760275,"about_ca_system_score_codex":0.0000129158825,"about_ca_system_score_gemma":0.00025631886,"threshold_uncertainty_score":0.7026783},"labels":[],"label_agreement":null},{"id":"W2116673901","doi":"10.1530/eje.0.1470561","title":"Parental genomic imprinting in endocrinopathies","year":2002,"lang":"en","type":"review","venue":"European Journal of Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Nesidioblastosis; Endocrinology; Internal medicine; Pseudohypoparathyroidism; Biology; Gene; Genetics; Uniparental disomy; Diabetes mellitus; Medicine; DNA methylation; Gene expression; Parathyroid hormone; Chromosome; Karyotype; Islet","score_opus":0.034659856889521126,"score_gpt":0.2815494556447907,"score_spread":0.2468895987552696,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116673901","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.012359671,0.9833452,0.00005038717,0.000011627392,0.00077687064,0.00016325565,0.0000060846596,0.0000059147214,0.003280985],"genre_scores_gemma":[0.020373292,0.97773445,0.0006988599,0.000026101978,0.00078567007,0.0000032292517,0.000013093904,0.000102020815,0.00026329717],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9964506,0.0008863076,0.0014911321,0.00040526318,0.00013162669,0.00063509686],"domain_scores_gemma":[0.9982581,0.000036538433,0.0011156781,0.00040690077,0.00006993717,0.00011285044],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00042264786,0.00043069653,0.0012038684,0.00040773585,0.000047229452,0.000035604215,0.0007998278,0.000091323745,0.00006317381],"category_scores_gemma":[0.00019443747,0.00037700293,0.0006287466,0.00013201378,0.00010227108,0.0000043882337,0.00056644774,0.0006802578,0.00010014053],"study_design_candidate":"design_other","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":[0.000003482519,0.000059154358,0.00055935077,0.00068231625,0.00015946216,0.0008462769,0.00003337521,0.0000070959823,0.0006440137,0.00001412662,0.00023910927,0.99675226],"study_design_scores_gemma":[0.0005618177,0.0004867959,0.0011651532,0.001301821,0.0001400383,0.014779384,0.00005654439,6.923792e-7,0.000060279308,0.0000029308042,0.98111373,0.00033079815],"about_ca_topic_score_codex":0.0000027044575,"about_ca_topic_score_gemma":0.0000020052441,"teacher_disagreement_score":0.99642146,"about_ca_system_score_codex":0.000044547058,"about_ca_system_score_gemma":0.00009943046,"threshold_uncertainty_score":0.9998682},"labels":[],"label_agreement":null},{"id":"W2116972945","doi":"10.1002/ajmg.a.35358","title":"Brain abnormalities in patients with Beckwith–Wiedemann syndrome","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Credit Valley Hospital; Hospital for Sick Children; University of Toronto; SickKids Foundation; Mount Sinai Hospital","funders":"","keywords":"Beckwith–Wiedemann syndrome; Dysgenesis; Genomic imprinting; Corpus callosum; Microdeletion syndrome; Genetics; Abnormality; Global developmental delay; Biology; Phenotype; Bioinformatics; Pathology; Medicine; Gene; Neuroscience; DNA methylation","score_opus":0.0063699365381236816,"score_gpt":0.2407267676707134,"score_spread":0.23435683113258973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116972945","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99763143,0.0009450829,0.0004382176,0.00053651026,0.00023678357,0.00007995026,0.0000028601778,0.0000023581977,0.00012679913],"genre_scores_gemma":[0.99714035,0.00020171917,0.0015575313,0.0007494642,0.00024134586,0.0000034857721,0.000008587472,0.000026064936,0.00007143671],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99793684,0.00013140752,0.00051410217,0.00014977578,0.00079438055,0.00047349447],"domain_scores_gemma":[0.9988568,0.000036667563,0.000340447,0.00021655139,0.00011304228,0.00043647978],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00087585195,0.00016879635,0.00033252093,0.000091254886,0.000032773863,0.00001645418,0.0003487617,0.000093359435,0.000068045534],"category_scores_gemma":[0.00020824869,0.00012920985,0.00008506868,0.00016898739,0.0002838834,0.0000070779847,0.00012159713,0.00021564249,0.0000060659786],"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":[0.00005131968,0.00025483413,0.97646487,0.000012685923,0.00010348517,0.000012799703,0.0002505596,0.00004729904,0.00019530003,0.000010423486,0.00069714134,0.02189929],"study_design_scores_gemma":[0.0016913338,0.003332262,0.9677583,0.00012092821,0.000030897154,0.00056209776,0.0007980673,0.0000130603485,0.00044384442,0.000007624105,0.024984647,0.00025692632],"about_ca_topic_score_codex":0.000015668384,"about_ca_topic_score_gemma":0.000008333684,"teacher_disagreement_score":0.024287505,"about_ca_system_score_codex":0.000015790023,"about_ca_system_score_gemma":0.00015626429,"threshold_uncertainty_score":0.52690244},"labels":[],"label_agreement":null},{"id":"W2117121254","doi":"10.1093/hmg/11.11.1317","title":"Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome","year":2002,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":332,"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","funders":"Division of Materials Research; National Cancer Institute","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Biology; Genomic imprinting; Genetics; Monozygotic twin; DNA methylation; Gene","score_opus":0.022097774345631992,"score_gpt":0.26649348897152436,"score_spread":0.24439571462589238,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117121254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9879472,0.0016821076,0.008926785,0.000055657976,0.00014608586,0.0007268405,0.000024269737,0.000014563457,0.0004764441],"genre_scores_gemma":[0.9890399,0.00016834438,0.010165074,0.00008191694,0.0000512087,0.00008217546,0.000062193794,0.00009970581,0.00024948054],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99748397,0.000076997225,0.0007750788,0.0007197784,0.0002589011,0.0006852759],"domain_scores_gemma":[0.9986309,0.000018179042,0.00027973574,0.0008278618,0.000099166624,0.00014417044],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00025010167,0.00038195337,0.0004561246,0.00016281137,0.00011446386,0.000045185956,0.00048751265,0.00012781231,0.000039272785],"category_scores_gemma":[0.00008354106,0.0003995105,0.00028934525,0.00018641462,0.00014086986,0.00000533229,0.00035062234,0.00014548723,0.000008110417],"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":[0.000006882651,0.00027277682,0.011369998,0.00015346758,0.00009694827,0.00004774434,0.00015004256,0.0011750729,0.9844055,0.0002456481,0.000067744106,0.002008129],"study_design_scores_gemma":[0.0053741164,0.004152768,0.31596544,0.00044812408,0.00029195758,0.0010206429,0.00079190504,0.011217038,0.65364724,0.0022065483,0.0026192458,0.0022649842],"about_ca_topic_score_codex":0.000033179553,"about_ca_topic_score_gemma":0.0000586713,"teacher_disagreement_score":0.3307583,"about_ca_system_score_codex":0.000026010912,"about_ca_system_score_gemma":0.000033759636,"threshold_uncertainty_score":0.9998457},"labels":[],"label_agreement":null},{"id":"W2117476997","doi":"10.1111/j.1399-0004.2010.01547.x","title":"CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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; McMaster University; Victoria General Hospital; Montreal Children's Hospital; Children's Hospital of Eastern Ontario; Alberta Children's Hospital; Diagnostic Services Manitoba","funders":"","keywords":"Uniparental disomy; Genetic testing; Prenatal diagnosis; Guideline; Medicine; Diagnostic test; Genetic counseling; Medical genetics; Genetics; Family medicine; Pediatrics; Biology; Pregnancy; Chromosome; Karyotype; Pathology","score_opus":0.06582523456584276,"score_gpt":0.3774007015368377,"score_spread":0.3115754669709949,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117476997","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99590987,0.0008073357,0.0016119214,0.0001568991,0.0008912818,0.0003736205,0.0000624221,0.000016993956,0.00016962859],"genre_scores_gemma":[0.9433632,0.00024168297,0.054619584,0.0002733995,0.0011398939,0.000032637465,0.000115484225,0.00004040498,0.00017370957],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983664,0.000030983418,0.0006322721,0.0005310336,0.00010632818,0.00033295827],"domain_scores_gemma":[0.9985549,0.0004369643,0.00013812444,0.0004099093,0.00024324667,0.00021686747],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004011742,0.00019665078,0.00021025799,0.000021881842,0.00011213357,0.000049668215,0.00024926194,0.00026450993,0.000010096669],"category_scores_gemma":[0.007404986,0.00018510419,0.00012205982,0.000057026748,0.00021935726,0.0000026299153,0.00035889164,0.00019137458,0.000006356942],"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":[0.000027198232,0.0002526713,0.6553436,0.000088121014,0.00009529079,0.000006043833,0.000025213476,0.000046082005,0.16911857,0.000070270544,0.0022662973,0.17266063],"study_design_scores_gemma":[0.004688544,0.004517307,0.8159887,0.00011699205,0.00021452748,0.00058582565,0.0002299,0.0065550245,0.056601148,0.0005391189,0.108668454,0.0012944206],"about_ca_topic_score_codex":0.0000062369495,"about_ca_topic_score_gemma":0.000022686856,"teacher_disagreement_score":0.17136621,"about_ca_system_score_codex":0.0000021704782,"about_ca_system_score_gemma":0.00008397175,"threshold_uncertainty_score":0.88649946},"labels":[],"label_agreement":null},{"id":"W2118787368","doi":"10.1111/cen.12766","title":"Metabolic profiling in Prader–Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormone","year":2015,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":39,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Ghrelin; Internal medicine; Endocrinology; Adiponectin; Leptin; Peptide YY; Medicine; Obesity; Insulin resistance; Insulin; Appetite; Hormone; Neuropeptide Y receptor; Neuropeptide","score_opus":0.025442535047017458,"score_gpt":0.2837858349495161,"score_spread":0.25834329990249866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118787368","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9846414,0.014382561,0.000034207285,0.00029980435,0.00009620103,0.00023845723,0.0000033356791,0.000006382131,0.00029767308],"genre_scores_gemma":[0.99492794,0.0041763703,0.00065635436,0.00009191451,0.000050770726,0.000021755246,0.000004121713,0.000011650983,0.0000591107],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9984314,0.00028271726,0.0005073199,0.00038968612,0.000082132894,0.0003067792],"domain_scores_gemma":[0.9992995,0.00014960379,0.00014683249,0.00025205064,0.000047671452,0.00010428916],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00049678946,0.00014785698,0.0005072261,0.000049098388,0.00003495782,0.000012393856,0.00019336867,0.00015365746,0.0000016765839],"category_scores_gemma":[0.000653594,0.00010444881,0.00006526903,0.0000685357,0.0007182068,0.000004012036,0.0004073963,0.00020181306,0.000002098997],"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":[0.00002338873,0.00009215591,0.98603207,0.000013693656,0.000087792985,0.000004403946,0.000090431306,0.0000013980049,0.0049529914,0.0027626366,0.000008176617,0.0059308745],"study_design_scores_gemma":[0.0037926575,0.0006726602,0.9853249,0.000010990972,0.000053704032,0.0008422577,0.00066184776,0.00027066102,0.003129475,0.0043768818,0.0006932084,0.00017070993],"about_ca_topic_score_codex":0.00011655119,"about_ca_topic_score_gemma":0.000014338487,"teacher_disagreement_score":0.010286572,"about_ca_system_score_codex":0.0000025264408,"about_ca_system_score_gemma":0.000059249123,"threshold_uncertainty_score":0.42592987},"labels":[],"label_agreement":null},{"id":"W2120429387","doi":"10.1136/jmg.2005.037747","title":"Phenotype of triploid embryos: Table 1","year":2005,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":160,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's & Women's Health Centre of British Columbia; University of British Columbia","funders":"","keywords":"Biology; Phenotype; Genomic imprinting; Embryo; Genetics; Ploidy; Placenta; Fetus; Imprinting (psychology); Embryogenesis; Population; Embryonic stem cell; Andrology; Gene; Pregnancy; Gene expression; DNA methylation","score_opus":0.011332655269697282,"score_gpt":0.26975413234574835,"score_spread":0.25842147707605106,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2120429387","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9862307,0.0075664236,0.00430398,0.0007358603,0.0003417973,0.00004582426,0.0000022612169,0.0000017455297,0.0007714624],"genre_scores_gemma":[0.9849305,0.0031089296,0.010174392,0.00029961,0.0011006319,5.6823603e-7,0.0000023896707,0.000017275026,0.0003656817],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9983731,0.00004442023,0.000607241,0.00011377991,0.0006601705,0.00020129673],"domain_scores_gemma":[0.99900883,0.000017374316,0.00033250655,0.00019965034,0.00021925951,0.00022239561],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006577858,0.00010317979,0.00023290486,0.000050994655,0.00002329826,0.0000099109875,0.0004193644,0.0001985178,0.0002646848],"category_scores_gemma":[0.00040269972,0.0000846693,0.00012543464,0.000091666036,0.0000787306,0.0000022877434,0.00012413975,0.00016753987,0.000006199359],"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":[0.0000664542,0.00054513634,0.007961931,0.00008515212,0.0002741014,0.000012626057,0.0001630178,0.0013163454,0.7029017,0.00007305614,0.017437845,0.26916263],"study_design_scores_gemma":[0.0034454283,0.0024635396,0.014717,0.00016712071,0.00012594966,0.0007363895,0.00029423472,0.0013457352,0.39982855,0.0001251478,0.5764066,0.00034432727],"about_ca_topic_score_codex":0.0000031637278,"about_ca_topic_score_gemma":0.0000045687816,"teacher_disagreement_score":0.5589687,"about_ca_system_score_codex":0.000008289486,"about_ca_system_score_gemma":0.00028825397,"threshold_uncertainty_score":0.3452714},"labels":[],"label_agreement":null},{"id":"W2121126641","doi":"10.1210/jc.2009-0656","title":"Cardiovascular and Metabolic Risk Profile and Acylation-Stimulating Protein Levels in Children with Prader-Willi Syndrome and Effects of Growth Hormone Treatment","year":2010,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université Laval","funders":"","keywords":"Metabolic syndrome; Acylation; Endocrinology; Internal medicine; Hormone; Growth hormone; Growth hormone treatment; Medicine; Biology; Diabetes mellitus; Biochemistry","score_opus":0.011953373926264058,"score_gpt":0.27284551506717103,"score_spread":0.260892141140907,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2121126641","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97575337,0.023376925,0.00018398195,0.00012117016,0.00006448828,0.00048496565,0.000004891939,0.0000024799172,0.000007744241],"genre_scores_gemma":[0.9899194,0.0061497944,0.0037156483,0.000021943655,0.0001541294,0.000010631668,0.0000012586803,0.000017371694,0.000009824482],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.998258,0.00044946655,0.0006697851,0.00023623626,0.00014374313,0.00024275451],"domain_scores_gemma":[0.99883777,0.00018594775,0.0005136069,0.00026448123,0.00009797394,0.000100220415],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00089324795,0.00019020498,0.00076936616,0.00007523836,0.00007111004,0.000011647047,0.0001299583,0.0001387782,0.0000015181258],"category_scores_gemma":[0.0006379488,0.00011286884,0.00013266856,0.0000743829,0.00036390318,0.000012677957,0.00011877525,0.0003965439,2.0107981e-7],"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":[0.000042238138,0.00016445544,0.83071846,0.00003134526,0.0022715875,0.0000064900496,0.0001796411,0.000055314715,0.10644398,0.00013837553,0.0000017598105,0.059946373],"study_design_scores_gemma":[0.0041035884,0.0011095488,0.97581744,0.000019552474,0.00064766756,0.0017694396,0.000026752728,0.00003348645,0.015994376,0.0001493151,0.000215245,0.0001135631],"about_ca_topic_score_codex":0.00010985229,"about_ca_topic_score_gemma":0.0000097882075,"teacher_disagreement_score":0.14509903,"about_ca_system_score_codex":0.0000015497681,"about_ca_system_score_gemma":0.00005895212,"threshold_uncertainty_score":0.46026576},"labels":[],"label_agreement":null},{"id":"W2125827772","doi":"10.1002/ajmg.a.35651","title":"Mosaicism for genome‐wide paternal uniparental disomy with features of multiple imprinting disorders: Diagnostic and management issues","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":89,"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","funders":"","keywords":"Uniparental disomy; Genetics; Biology; Genomic imprinting; Angelman syndrome; Germline mosaicism; Copy-number variation; Genome; DNA methylation; Karyotype; Chromosome; Gene; Somatic cell","score_opus":0.006956413258992593,"score_gpt":0.25851707121315376,"score_spread":0.25156065795416116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2125827772","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9852776,0.0050798757,0.008938657,0.0003340637,0.00014520506,0.00018134838,0.0000072197968,0.0000021225103,0.000033922293],"genre_scores_gemma":[0.9809134,0.007174913,0.011426904,0.000114015915,0.00029110743,0.000012138438,0.00001026774,0.000025057137,0.000032207055],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986089,0.00005364108,0.00041080004,0.00016409901,0.00041672698,0.00034587248],"domain_scores_gemma":[0.9989757,0.00011433949,0.0003801024,0.00016112399,0.00007336337,0.0002953807],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043393165,0.00016202942,0.00029288747,0.000052974203,0.00004914672,0.000016858576,0.00025598574,0.000057355133,0.0000096868935],"category_scores_gemma":[0.0002544447,0.00012366612,0.00009322642,0.00007007943,0.00029152134,0.0000050016974,0.00018383973,0.00010964994,3.3039066e-7],"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":[0.00008717613,0.00026882067,0.81099963,0.00012897872,0.0004254869,0.0000041278286,0.00044135674,0.00009900272,0.00636532,0.000021275888,0.00023149198,0.18092735],"study_design_scores_gemma":[0.002289751,0.0033024081,0.94061196,0.00025550884,0.00019986463,0.00029060172,0.0024655065,0.00010036262,0.008937396,0.000039913833,0.041167784,0.0003389176],"about_ca_topic_score_codex":0.000025881978,"about_ca_topic_score_gemma":0.000017307524,"teacher_disagreement_score":0.18058842,"about_ca_system_score_codex":0.0000067274705,"about_ca_system_score_gemma":0.000035364366,"threshold_uncertainty_score":0.50429577},"labels":[],"label_agreement":null},{"id":"W2126215378","doi":"10.1002/ajmg.a.20317","title":"X chromosome inactivation patterns in Russell–Silver syndrome patients and their mothers","year":2003,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; BC Research (Canada); University of British Columbia","funders":"","keywords":"RSS; Uniparental disomy; Genetics; Biology; X chromosome; Allele; Skewed X-inactivation; Chromosome; X-inactivation; Karyotype; Gene","score_opus":0.006809157155739113,"score_gpt":0.23384114666269604,"score_spread":0.2270319895069569,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126215378","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9983846,0.0004370445,0.0006934914,0.00017511073,0.00017109407,0.00007236768,0.0000029007626,0.0000014689244,0.000061917024],"genre_scores_gemma":[0.9978615,0.0012689095,0.00042382476,0.0003464504,0.00005512648,0.0000026049945,0.000004261781,0.000020024167,0.000017282662],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99867386,0.00014069724,0.00041797856,0.00018389587,0.00034289603,0.00024068548],"domain_scores_gemma":[0.9992606,0.000027518878,0.00027277682,0.00014375449,0.0000722413,0.00022311171],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045873068,0.00014385997,0.00026129762,0.00007855584,0.00002660534,0.000016449614,0.00018502626,0.00009202841,0.000058106863],"category_scores_gemma":[0.00021725653,0.000115442366,0.00006471307,0.00012590854,0.00014935841,0.000003888284,0.000056349727,0.0001750066,0.0000015216123],"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":[0.000031141764,0.00043281054,0.8404268,0.00003488352,0.00018261677,0.000031891734,0.00071814196,0.00013996907,0.027614748,0.000017832024,0.00024107483,0.13012812],"study_design_scores_gemma":[0.0040903846,0.0058598346,0.9231622,0.00031611882,0.000041540345,0.0014885587,0.0028028325,0.00026396802,0.029531002,0.0001266487,0.031663936,0.00065295666],"about_ca_topic_score_codex":0.000011329341,"about_ca_topic_score_gemma":0.0000067359333,"teacher_disagreement_score":0.12947515,"about_ca_system_score_codex":0.000016932612,"about_ca_system_score_gemma":0.00010932925,"threshold_uncertainty_score":0.4707603},"labels":[],"label_agreement":null},{"id":"W2126215690","doi":"10.1002/mc.20731","title":"Loss of imprinting and abnormal expression of the insulin‐like growth factor 2 gene in gastric cancer","year":2011,"lang":"en","type":"article","venue":"Molecular Carcinogenesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Saskatchewan","funders":"","keywords":"Biology; Imprinting (psychology); Genomic imprinting; Cancer; Insulin-like growth factor 2; Gene; Gene expression; Genetics; Cancer research; Growth factor; DNA methylation","score_opus":0.012808204426459757,"score_gpt":0.21367846563885082,"score_spread":0.20087026121239107,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126215690","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962653,0.0026150534,0.00076588424,0.000008769793,0.00008212741,0.00015526818,0.000015781428,0.000002548667,0.00008925581],"genre_scores_gemma":[0.9978205,0.00031919323,0.0017542348,0.00003605176,0.00001786453,0.000015367777,0.0000028321651,0.000021866941,0.0000121149515],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989638,0.00007846358,0.00030719404,0.0002800585,0.00014434833,0.0002261379],"domain_scores_gemma":[0.99934345,0.000005457471,0.0001744089,0.0003306741,0.000095548305,0.000050474442],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011257043,0.00014825616,0.00019057078,0.0000679766,0.000031710446,0.00000399177,0.00023231436,0.00011039648,0.000012113798],"category_scores_gemma":[0.000046384757,0.00011894246,0.00011009681,0.00017603,0.000094101546,0.0000031614877,0.00036513794,0.000057646084,1.815652e-7],"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":[0.000007932203,0.000020356592,0.4057142,0.000035135556,0.000012386841,0.0000014942357,0.000106466534,0.000011855086,0.5932149,0.000004164863,8.370405e-7,0.0008702551],"study_design_scores_gemma":[0.00021849354,0.00003875971,0.4545869,0.000019961857,0.0000117078725,0.000011904403,0.00002958791,0.000009916849,0.54499096,0.000008586737,0.0000063938855,0.0000668193],"about_ca_topic_score_codex":0.0004907301,"about_ca_topic_score_gemma":0.00001978981,"teacher_disagreement_score":0.048872676,"about_ca_system_score_codex":0.000008600773,"about_ca_system_score_gemma":0.000056749035,"threshold_uncertainty_score":0.48503327},"labels":[],"label_agreement":null},{"id":"W2126215730","doi":"10.1007/s00439-013-1379-z","title":"High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome","year":2013,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Calgary; SickKids Foundation; Centre Hospitalier Universitaire Sainte-Justine; University of Toronto; Hospital for Sick Children","funders":"","keywords":"Beckwith–Wiedemann syndrome; Biology; Genomic imprinting; Macroglossia; Copy-number variation; Genetics; Imprinting (psychology); Methylation; Uniparental disomy; Chromosome; Comparative genomic hybridization; DNA methylation; GiST; Gene duplication; Karyotype; Gene; Cancer research; Pathology; Medicine; Genome; Gene expression","score_opus":0.00915601971796006,"score_gpt":0.22020110568275408,"score_spread":0.21104508596479402,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126215730","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99855435,0.00009166583,0.0001435061,0.000062554565,0.00005496266,0.0005325895,0.000005820045,0.0000045299016,0.00055004226],"genre_scores_gemma":[0.99740136,0.000028940301,0.0021413383,0.00009056571,0.00003770349,0.00006674302,0.000092806804,0.000027670781,0.000112886584],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987192,0.00008716271,0.0003869441,0.00030777685,0.00020952898,0.00028937025],"domain_scores_gemma":[0.9991356,0.000012042847,0.00016207149,0.00052921084,0.00011775991,0.000043327735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000113913244,0.0001783347,0.00019888693,0.00006330055,0.000062649364,0.000029739951,0.00032856595,0.00013486989,0.00008865401],"category_scores_gemma":[0.00001927494,0.00013812387,0.000045438726,0.00019468377,0.00008760203,0.0000063513894,0.00008497234,0.00011103557,0.000020540567],"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":[0.00000303352,0.00028263952,0.9869926,0.000028249537,0.000028811466,0.0000033899553,0.00028095208,0.00014924532,0.011542777,0.00031874952,0.00013983874,0.00022969488],"study_design_scores_gemma":[0.0010307302,0.0004475744,0.99643105,0.000041253512,0.000015669419,0.00002313484,0.000090727386,0.000017886778,0.0010223421,0.0006147747,0.00007579212,0.00018904306],"about_ca_topic_score_codex":0.00038291074,"about_ca_topic_score_gemma":0.00020200024,"teacher_disagreement_score":0.010520435,"about_ca_system_score_codex":0.000018556348,"about_ca_system_score_gemma":0.00003986505,"threshold_uncertainty_score":0.5632528},"labels":[],"label_agreement":null},{"id":"W2127028166","doi":"10.1152/physiolgenomics.00163.2003","title":"A survey of genetic and epigenetic variation affecting human gene expression","year":2004,"lang":"en","type":"article","venue":"Physiological Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":262,"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; Université Laval; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; McGill University; McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Biology; Genetics; Allele; Gene; Single-nucleotide polymorphism; Epigenetics; Genetic variation; Linkage disequilibrium; Mendelian inheritance; Haplotype; Genotype","score_opus":0.02628550284291359,"score_gpt":0.2587019193799324,"score_spread":0.23241641653701883,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2127028166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99273264,0.0006014638,0.006392976,0.000005953354,0.000050137984,0.0001621895,0.000009626045,0.000007602405,0.00003741474],"genre_scores_gemma":[0.99006206,0.00023509972,0.009497874,0.000034828536,0.000082204286,0.000007170739,0.000056725927,0.000016207472,0.000007802933],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989946,0.000093807204,0.00026782142,0.00036580584,0.00006870337,0.00020929657],"domain_scores_gemma":[0.99946195,0.000017121933,0.00014656535,0.00024482413,0.00006195023,0.000067570254],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020168348,0.00014363357,0.00019529762,0.000023474922,0.000095798125,0.0000131004135,0.00013411546,0.00013378423,0.000007547543],"category_scores_gemma":[0.00011922661,0.00012571819,0.000052163276,0.00006271204,0.00007431257,0.0000017340619,0.0002219555,0.000062639345,0.0000023633665],"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":[0.0000072230064,0.000050097282,0.009169996,0.000013888585,0.000014362467,4.1977572e-7,0.00005333591,0.0026180095,0.9871821,0.000007549655,0.0000025776492,0.0008804313],"study_design_scores_gemma":[0.00032203938,0.00032497983,0.6950073,0.000007347099,0.0000067664864,0.00000788861,0.0000116396905,0.000040155737,0.30374795,0.00040224736,0.0000092971095,0.000112379515],"about_ca_topic_score_codex":0.00012390611,"about_ca_topic_score_gemma":0.00001165224,"teacher_disagreement_score":0.6858373,"about_ca_system_score_codex":0.000012320677,"about_ca_system_score_gemma":0.000029377023,"threshold_uncertainty_score":0.51266384},"labels":[],"label_agreement":null},{"id":"W2128052161","doi":"10.1016/j.jcjd.2014.07.170","title":"H19 Regulates Glucose-Induced Extracellular Matrix Protein Production in Diabetes","year":2014,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"microRNA; Medicine; Gestational diabetes; Long non-coding RNA; Genomic imprinting; Non-coding RNA; Gene; MEG3; Coding (social sciences); RNA; Diabetes mellitus; Extracellular matrix; Computational biology; Bioinformatics; Genetics; Biology; Gene expression; Pregnancy; Endocrinology; DNA methylation; Gestation","score_opus":0.006948784916698735,"score_gpt":0.20384093814396922,"score_spread":0.1968921532272705,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128052161","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99522716,0.0037702927,0.000009282824,0.00041456972,0.0003326949,0.00015740586,0.0000017131916,0.0000026183686,0.000084246254],"genre_scores_gemma":[0.99862325,0.0000061566175,0.0005845236,0.000032493448,0.00039660963,0.000006566872,0.000006318219,0.000026162357,0.00031794302],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987534,0.00009705843,0.00038296997,0.00021166357,0.00010643906,0.00044845842],"domain_scores_gemma":[0.99914616,0.000008078178,0.0002096808,0.0002123649,0.00013469109,0.00028901047],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00063478353,0.00015052948,0.00022000645,0.00020579243,0.00006825396,0.000051385003,0.00020958156,0.00013321875,0.000020758102],"category_scores_gemma":[0.00051216566,0.0001455217,0.00009682067,0.00013963722,0.00005114274,0.0000106349935,0.000019237981,0.00014906542,0.0000059517643],"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":[4.7327188e-7,0.000010876447,0.1187863,0.000028079123,0.000024163777,7.478275e-7,0.000029832921,0.00007636227,0.87264174,0.000017634615,0.000112434835,0.008271381],"study_design_scores_gemma":[0.0003455494,0.00037701154,0.11833198,0.0001472822,0.000015336878,0.0000063799894,0.000059536924,0.000105637715,0.87427115,0.00024078372,0.0058936332,0.00020573757],"about_ca_topic_score_codex":0.000086349275,"about_ca_topic_score_gemma":0.0008429316,"teacher_disagreement_score":0.008065644,"about_ca_system_score_codex":0.000034804263,"about_ca_system_score_gemma":0.00025797944,"threshold_uncertainty_score":0.59342027},"labels":[],"label_agreement":null},{"id":"W2128106580","doi":"10.1152/ajpcell.00091.2008","title":"Functional characterization of NIPA2, a selective Mg<sup>2+</sup> transporter","year":2008,"lang":"en","type":"article","venue":"American Journal of Physiology-Cell Physiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"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; University of British Columbia Hospital","funders":"Canadian Institutes of Health Research; University of British Columbia; Michael Smith Health Research BC","keywords":"Characterization (materials science); Transporter; Chemistry; Nanotechnology; Biochemistry; Materials science; Gene","score_opus":0.006838465224161937,"score_gpt":0.19976498484428376,"score_spread":0.19292651962012183,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128106580","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99863034,0.000077554905,0.00085203594,0.00007912824,0.00016578715,0.00009758844,0.000017180455,0.000005308899,0.00007504913],"genre_scores_gemma":[0.997895,0.00024321598,0.0007704359,0.00030593204,0.0004935245,0.0000063410043,0.000111519716,0.000029733132,0.00014430514],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9983648,0.00019374049,0.00061540265,0.00034618448,0.0001417819,0.00033808957],"domain_scores_gemma":[0.9983494,0.00003139284,0.0008857425,0.00026638823,0.00036346703,0.00010359058],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001238971,0.00023998384,0.0006176853,0.00011881557,0.00008571642,0.0000023708849,0.00025708,0.00012724062,0.00008673035],"category_scores_gemma":[0.00002603363,0.00021024456,0.00031349427,0.00020805953,0.00061204017,0.000011580767,0.000056249693,0.00022454474,0.00000947523],"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":[0.00029743358,0.00022466121,0.0017096886,0.000017690074,0.00017744943,0.0000014902579,0.0002762057,0.0015221498,0.99452883,0.000003221733,0.0003017091,0.00093945046],"study_design_scores_gemma":[0.0011729542,0.0035709282,0.56450176,0.000014811402,0.000056089302,0.00028694083,0.00026947982,0.00012753451,0.42807904,0.000097279364,0.0015700763,0.00025312076],"about_ca_topic_score_codex":0.000015796286,"about_ca_topic_score_gemma":4.1848824e-7,"teacher_disagreement_score":0.5664498,"about_ca_system_score_codex":0.000014954062,"about_ca_system_score_gemma":0.00018537893,"threshold_uncertainty_score":0.85735244},"labels":[],"label_agreement":null},{"id":"W2128356343","doi":"10.1158/0008-5472.can-11-2266","title":"Monoallelic Expression Determines Oncogenic Progression and Outcome in Benign and Malignant Brain Tumors","year":2011,"lang":"en","type":"article","venue":"Cancer Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"SickKids Foundation; Toronto General Hospital; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Hospital for Sick Children","keywords":"Carcinogenesis; Brain tumor; Tumor progression; Gene; IDH1; Cancer research; Biology; Cancer; Neuroblastoma; Medicine; Pathology; Genetics; Mutation","score_opus":0.09370436671842969,"score_gpt":0.39691019496942026,"score_spread":0.30320582825099057,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128356343","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958812,0.0034989496,0.000017560546,0.00012483099,0.000032565415,0.00024505408,0.0000023222526,0.000004138364,0.00019339878],"genre_scores_gemma":[0.99814403,0.0006331981,0.0006384254,0.00003893799,0.00005449497,0.00010530937,0.000003160282,0.000017425366,0.00036502807],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99884945,0.0001046184,0.0001802407,0.00038186202,0.00014727343,0.00033653804],"domain_scores_gemma":[0.9995805,0.000016373042,0.000033561802,0.00020980921,0.000051124243,0.00010859991],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000503981,0.000100455465,0.00012248155,0.00008797245,0.00007970181,0.000022954722,0.00012930103,0.000092678274,0.000025720776],"category_scores_gemma":[0.00009249352,0.000080845995,0.000021411699,0.00008446512,0.00011717215,0.000004382363,0.00035695173,0.00012227501,0.0000015461682],"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":[0.000024878082,0.000018724793,0.20433405,0.000041388543,0.000003813395,0.000007697442,0.00022256782,5.2534693e-7,0.7697162,0.000005598626,0.00007127527,0.025553254],"study_design_scores_gemma":[0.00069548155,0.00039155284,0.3408877,0.00017675657,0.00000266063,0.00004202874,0.00031282246,0.00005048439,0.6552371,0.00013200431,0.0018869555,0.00018444534],"about_ca_topic_score_codex":0.00017678949,"about_ca_topic_score_gemma":0.00007755112,"teacher_disagreement_score":0.13655365,"about_ca_system_score_codex":0.000012918399,"about_ca_system_score_gemma":0.0000522664,"threshold_uncertainty_score":0.32968038},"labels":[],"label_agreement":null},{"id":"W2130225900","doi":"10.1136/jmg.40.4.249","title":"The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"","keywords":"Genomic imprinting; Genetics; Biology; Imprinting (psychology); Epigenetics; Gene; Allele; Candidate gene; Gene cluster; Molecular biology; Gene expression; DNA methylation","score_opus":0.019663307049431717,"score_gpt":0.30436378464505703,"score_spread":0.28470047759562533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130225900","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9878468,0.0008030819,0.0077718287,0.0023065647,0.0007408575,0.00042707296,0.000007565328,0.0000064658448,0.000089755216],"genre_scores_gemma":[0.9961057,0.0007601983,0.0010207485,0.0010997526,0.00058694347,0.00002428187,0.0000107572405,0.00005294653,0.0003386759],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99725544,0.00026604877,0.0007879554,0.00035914616,0.0007776254,0.0005537826],"domain_scores_gemma":[0.9978499,0.000091935326,0.00038939744,0.0007688849,0.00032052357,0.00057934766],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017163812,0.0002783618,0.0003148235,0.000076574186,0.00036323795,0.00010109031,0.001042766,0.0002756022,0.000024785164],"category_scores_gemma":[0.00081545993,0.0001659379,0.00026628462,0.00016134612,0.00014132794,0.0000044354965,0.00018501925,0.00038614444,0.0000055876217],"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":[0.00033262122,0.0007701044,0.0012836752,0.00008455465,0.00071719184,0.00018251094,0.00057972805,0.0013747045,0.9475058,0.0005165414,0.007141694,0.03951092],"study_design_scores_gemma":[0.008007574,0.021285597,0.018194495,0.00038203975,0.0003759525,0.012950689,0.001104569,0.0030028524,0.4902933,0.00061538815,0.44252685,0.001260712],"about_ca_topic_score_codex":0.000016279493,"about_ca_topic_score_gemma":0.00007618587,"teacher_disagreement_score":0.45721248,"about_ca_system_score_codex":0.000049215854,"about_ca_system_score_gemma":0.00030291826,"threshold_uncertainty_score":0.67667514},"labels":[],"label_agreement":null},{"id":"W2130401515","doi":"10.1186/gb-2008-9-11-r160","title":"Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprinting","year":2008,"lang":"en","type":"article","venue":"Genome Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto","funders":"Ontario Ministry of Research and Innovation; Japan Society for the Promotion of Science; Hospital for Sick Children; Canadian Institutes of Health Research; Sick Kids Foundation; Genome Canada; Ontario Genomics; Ontario Genomics Institute; University of Toronto; GlaxoSmithKline","keywords":"Imprinting (psychology); Genomic imprinting; Genetics; Biology; Gene; Chemistry; Computational biology; DNA methylation; Gene expression","score_opus":0.023494236835081155,"score_gpt":0.2311479368331504,"score_spread":0.20765369999806926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130401515","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977712,0.00044450504,0.0011084456,0.000053773052,0.0002752115,0.00023905245,0.000020592202,0.00000496902,0.00008223644],"genre_scores_gemma":[0.9991035,0.0004720982,0.00008271648,0.000025584997,0.0001066296,0.0000052917203,0.000058393896,0.000017558865,0.00012823282],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989246,0.00016758847,0.00031791622,0.00027044612,0.00007897161,0.00024044992],"domain_scores_gemma":[0.99888885,0.0000097442025,0.00040249072,0.0005706574,0.00009692749,0.000031325522],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012403468,0.00015493894,0.0002188165,0.000035138517,0.000117440286,0.0000043785,0.00041062213,0.00018011035,0.000020668345],"category_scores_gemma":[0.000037904792,0.000089384754,0.00023834046,0.00014831657,0.00020342234,0.0000022278707,0.00036011444,0.00008355226,0.0000012921529],"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":[0.000011072721,0.000024229423,0.07310501,0.0000069135094,0.00005263936,2.1074784e-7,0.000084969724,0.000015098981,0.9256402,0.000010637248,0.0000043639197,0.0010446453],"study_design_scores_gemma":[0.00015280675,0.00006900489,0.4923027,0.0000049162563,0.00000620313,0.000053442378,0.0000065796876,0.0000070473666,0.50694764,0.0000144453825,0.0003774797,0.000057786954],"about_ca_topic_score_codex":0.000038253518,"about_ca_topic_score_gemma":0.0000026556127,"teacher_disagreement_score":0.41919768,"about_ca_system_score_codex":0.000012366927,"about_ca_system_score_gemma":0.00006280169,"threshold_uncertainty_score":0.36450046},"labels":[],"label_agreement":null},{"id":"W2130708302","doi":"10.1093/hmg/ddp465","title":"Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner","year":2009,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":352,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lawson Health Research Institute; Western University; Children’s Health Research Institute","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Imprinting (psychology); Biology; DNA methylation; Blastocyst; Andrology; Oocyte; Methylation; Oogenesis; Embryo; Genetics; Endocrinology; Gene; Embryogenesis; Medicine","score_opus":0.006825363874313466,"score_gpt":0.24764202968685733,"score_spread":0.24081666581254388,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130708302","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958709,0.0009814517,0.002802844,0.000014116284,0.000049856368,0.00020297305,0.0000025464067,0.0000038470985,0.000071467715],"genre_scores_gemma":[0.9985188,0.000112736525,0.0012428452,0.000027073012,0.000034181987,0.0000039784804,0.000014619267,0.000017126304,0.000028614686],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99892837,0.000066858964,0.0003756812,0.000262819,0.00018067064,0.00018561484],"domain_scores_gemma":[0.999474,0.0000056622584,0.00013553203,0.0002557983,0.0000764802,0.000052557185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012394716,0.00014976852,0.00019555933,0.00008944663,0.00002208944,0.000013104154,0.00010701346,0.0001218686,0.0000075028834],"category_scores_gemma":[0.000020115807,0.00015638107,0.000063381434,0.0000621234,0.00005671004,0.0000026900027,0.00009366351,0.00006484866,6.002847e-7],"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":[0.000012795092,0.000060550654,0.04242812,0.000060731345,0.000026681817,0.000011613643,0.00006953238,0.00048743415,0.9525532,0.00010579982,0.0000011317421,0.004182402],"study_design_scores_gemma":[0.00062995387,0.00044927496,0.47010916,0.000029466457,0.000014768964,0.000021983593,0.000007090127,0.00014375438,0.52820385,0.00029652673,0.000010098467,0.0000840739],"about_ca_topic_score_codex":0.000029396635,"about_ca_topic_score_gemma":0.000010509021,"teacher_disagreement_score":0.42768106,"about_ca_system_score_codex":0.0000072454873,"about_ca_system_score_gemma":0.000017679897,"threshold_uncertainty_score":0.6377035},"labels":[],"label_agreement":null},{"id":"W2133615187","doi":"10.1093/humrep/den009","title":"Profound phenotypic variation among mice deficient in the maintenance of genomic imprints","year":2008,"lang":"en","type":"article","venue":"Human Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital; McGill University","funders":"","keywords":"Genomic imprinting; Biology; Epigenetics; Phenotype; Embryo; Imprinting (psychology); Genetics; Somatic cell; Gestation; Fetus; Embryogenesis; Oocyte; Andrology; Gene; DNA methylation; Cell biology; Gene expression; Pregnancy","score_opus":0.018469781295581335,"score_gpt":0.23667707466583485,"score_spread":0.21820729337025352,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133615187","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984939,0.00015816474,0.00045560455,0.000045979465,0.00014133417,0.00024518912,5.186371e-7,0.0000043170157,0.00045499875],"genre_scores_gemma":[0.9991128,0.000041081104,0.0002972348,0.000017870361,0.00016216017,0.000018352102,0.000013047458,0.000008676805,0.00032878318],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99916667,0.000055984492,0.00021343776,0.00033838558,0.00009182017,0.00013368239],"domain_scores_gemma":[0.9993705,0.000002700559,0.00012812042,0.00042776976,0.000059610535,0.000011264557],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041232028,0.00007269526,0.00007594201,0.00003558806,0.00009401313,0.000006677198,0.00012487738,0.000048107107,0.000008066024],"category_scores_gemma":[0.000058646114,0.000060210867,0.000037993887,0.000074475305,0.00007218114,0.00000276674,0.000045643057,0.00006099143,0.000005062033],"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":[0.0000055376413,0.00006116555,0.03461933,0.000014681403,0.0000074074005,4.596942e-7,0.00071401533,0.00032978648,0.9632871,0.00010112288,0.000056390443,0.0008029732],"study_design_scores_gemma":[0.0001952045,0.00008080496,0.94844526,0.0000068089967,0.0000057578527,0.0000636883,0.0001651155,0.00003193767,0.050316103,0.00012116374,0.00049819297,0.00006995595],"about_ca_topic_score_codex":0.00013380789,"about_ca_topic_score_gemma":0.000036249403,"teacher_disagreement_score":0.9138259,"about_ca_system_score_codex":0.000016018606,"about_ca_system_score_gemma":0.000020043504,"threshold_uncertainty_score":0.24553278},"labels":[],"label_agreement":null},{"id":"W2133812508","doi":"10.1038/msb4100151","title":"Integrated proteomic and transcriptomic profiling of mouse lung development and Nmyc target genes","year":2007,"lang":"en","type":"article","venue":"Molecular Systems Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Ontario Genomics; Ontario Genomics Institute; Genome Canada","keywords":"Biology; Transcriptome; Gene; Gene expression profiling; Gene expression; Microarray analysis techniques; Microarray; Messenger RNA; DNA microarray; Molecular biology; Genetics; Cell biology","score_opus":0.007581777617385549,"score_gpt":0.22736491781211265,"score_spread":0.2197831401947271,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133812508","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9236998,0.00808949,0.06750279,0.000010220172,0.00012521693,0.00047870993,0.000008545759,0.000010936604,0.00007429779],"genre_scores_gemma":[0.9845002,0.00007433446,0.015152177,0.000025694248,0.000029823332,0.000029734489,0.00007129523,0.00002425737,0.0000924719],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99874115,0.00008301432,0.00042113743,0.00039010885,0.000057919562,0.0003066469],"domain_scores_gemma":[0.99951774,0.0000063400653,0.00012739435,0.00018976736,0.0000760274,0.00008275534],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046733522,0.00019105263,0.00026916544,0.00008581713,0.000052730888,0.000014279253,0.00010626887,0.0002258849,0.0000014642768],"category_scores_gemma":[0.000032060587,0.0001691681,0.00003930368,0.00006366952,0.00010541292,0.0000020550979,0.00008432131,0.00007187163,6.795221e-7],"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":[0.000017698854,0.00001528064,0.031200217,0.00013935106,0.00008601791,0.000002695049,0.000068445785,0.000013742808,0.96582854,0.00015053459,0.0000039314536,0.00247356],"study_design_scores_gemma":[0.0004607581,0.00015682398,0.0030358292,0.000030116908,0.0000136725685,0.000102149985,0.00018665855,0.0003232585,0.9934553,0.0000067211035,0.002030728,0.00019799263],"about_ca_topic_score_codex":0.00006094072,"about_ca_topic_score_gemma":0.000007888965,"teacher_disagreement_score":0.060800415,"about_ca_system_score_codex":0.0000122705405,"about_ca_system_score_gemma":0.00006429233,"threshold_uncertainty_score":0.68984747},"labels":[],"label_agreement":null},{"id":"W2134155328","doi":"10.1093/bfgp/elq017","title":"Applications of the site-specific recombinase Cre to the study of genomic imprinting","year":2010,"lang":"en","type":"review","venue":"Briefings in Functional Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 British Columbia","funders":"Canadian Institutes of Health Research; Michael Smith Health Research BC","keywords":"Biology; Recombinase; Genomic imprinting; Cre-Lox recombination; Cre recombinase; Imprinting (psychology); Genetics; Gene; Computational biology; Genome; Recombination; Transgene; Gene expression; DNA methylation","score_opus":0.024776814631630457,"score_gpt":0.26202048754038704,"score_spread":0.2372436729087566,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2134155328","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.30403322,0.69132596,0.00051170436,0.00008624867,0.00061406347,0.0030356953,0.00007040414,0.000005660805,0.00031702008],"genre_scores_gemma":[0.030126663,0.9661907,0.0011619596,0.0001981396,0.00066218927,0.00068834337,0.00012589846,0.00013158345,0.00071454345],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9983086,0.00008801296,0.0007736559,0.00046960046,0.00015364893,0.00020649303],"domain_scores_gemma":[0.99830043,0.000061365856,0.00056148705,0.0009237214,0.00011218584,0.000040825864],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047011775,0.00024679073,0.0005066557,0.00008418475,0.00012634009,0.000021631997,0.00059762324,0.00022430267,0.000023414505],"category_scores_gemma":[0.00007043913,0.00017506516,0.00029940408,0.00024726224,0.000067516026,0.0000011592533,0.00070713955,0.00035946307,0.000015028281],"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":[0.000010994075,0.0003789486,0.0007601917,0.00076618936,0.00013451751,2.496437e-7,0.00023705464,0.00043392013,0.0143226,0.00013927453,0.0007304418,0.98208565],"study_design_scores_gemma":[0.00019231594,0.00008565217,0.0034367305,0.0001469462,0.00008668385,0.000031134383,0.00011389941,0.0000026008072,0.00013448716,0.00001924468,0.9955798,0.00017051923],"about_ca_topic_score_codex":0.000111774425,"about_ca_topic_score_gemma":0.000120128156,"teacher_disagreement_score":0.9948493,"about_ca_system_score_codex":0.0000407915,"about_ca_system_score_gemma":0.00023133398,"threshold_uncertainty_score":0.713895},"labels":[],"label_agreement":null},{"id":"W2135010797","doi":"10.1530/eje-08-0462","title":"Long-acting octreotide treatment causes a sustained decrease in ghrelin concentrations but does not affect weight, behaviour and appetite in subjects with Prader–Willi syndrome","year":2008,"lang":"en","type":"article","venue":"European Journal of Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"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; BC Children's Hospital; University of British Columbia","funders":"National Institute for Health and Care Research; Yale University","keywords":"Ghrelin; Appetite; Internal medicine; Endocrinology; Affect (linguistics); Octreotide; Medicine; Obesity; Psychology; Hormone; Somatostatin","score_opus":0.014235827869000966,"score_gpt":0.23881687054280548,"score_spread":0.22458104267380452,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135010797","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99834037,0.0008356604,0.00015346837,0.0002448732,0.0000859404,0.00018150873,0.0000050279373,0.0000055244213,0.00014760584],"genre_scores_gemma":[0.9971734,0.0016477152,0.00081893837,0.00005824667,0.000076798155,0.0000041086832,0.000007461437,0.000029873423,0.00018341947],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99838257,0.00037557512,0.00045184096,0.00027591447,0.0000941481,0.00041994933],"domain_scores_gemma":[0.9992991,0.000049919276,0.00025903207,0.00017408276,0.00006786074,0.00014997159],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016669866,0.00020946968,0.00030643135,0.00017327064,0.00007408622,0.000018704171,0.00012651214,0.00003323086,0.000011295535],"category_scores_gemma":[0.00016057743,0.00015079943,0.00006326695,0.00008993194,0.00014002297,0.000012011783,0.00006758148,0.0001747562,0.000001884457],"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":[0.00004962988,0.00017322418,0.9583764,0.000013773448,0.00007436293,0.004712523,0.00023268562,0.000105816085,0.03544356,0.000012149285,0.0000047044646,0.0008011782],"study_design_scores_gemma":[0.0037337197,0.0023651016,0.9421744,0.00009743332,0.00003845967,0.020384526,0.00052963285,0.000010242057,0.030211974,0.0000017912804,0.0002520953,0.00020063753],"about_ca_topic_score_codex":0.00009441309,"about_ca_topic_score_gemma":0.0003548528,"teacher_disagreement_score":0.016202008,"about_ca_system_score_codex":0.000042459633,"about_ca_system_score_gemma":0.00015684623,"threshold_uncertainty_score":0.61494225},"labels":[],"label_agreement":null},{"id":"W2135284044","doi":"10.1002/(sici)1521-1878(200005)22:5<452::aid-bies7>3.0.co;2-k","title":"Mechanisms leading to uniparental disomy and their clinical consequences","year":2000,"lang":"en","type":"review","venue":"BioEssays","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":334,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Research (Canada)","funders":"","keywords":"Uniparental disomy; Biology; Genetics; Imprinting (psychology); Genomic imprinting; Somatic cell; Gamete; Mitotic crossover; Chromosome; Phenotype; Karyotype; Mutation; Gene","score_opus":0.06745023611415106,"score_gpt":0.3633006515805042,"score_spread":0.2958504154663531,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135284044","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0016987992,0.99563384,0.00046133288,0.000028988952,0.00035605166,0.00042736446,0.00007789306,0.000015343823,0.0013003851],"genre_scores_gemma":[0.004122103,0.9938403,0.00090961315,0.00010849064,0.00020861655,0.000042656822,0.00013871971,0.00004548215,0.00058405777],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99827284,0.00015124967,0.00051886163,0.0006638933,0.000076495475,0.00031668134],"domain_scores_gemma":[0.9992286,0.0000365972,0.00014561656,0.00037804001,0.000019323441,0.00019183809],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0002953606,0.00036812376,0.0008261137,0.000060736176,0.00008902052,0.000060599115,0.00030905177,0.0003999675,0.000048815713],"category_scores_gemma":[0.00005514013,0.0002677605,0.00030863503,0.000093029645,0.00015268016,0.0000015799035,0.0002715038,0.0001524095,0.00006542763],"study_design_candidate":"design_other","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":[0.0000019562494,0.000021641401,0.000026078887,0.00050884427,0.00009575036,0.0000024008953,0.00001160885,1.4316245e-7,0.0004514861,0.000106249754,0.00040135326,0.9983725],"study_design_scores_gemma":[0.00009967391,0.0003045864,0.000014327273,0.0011243281,0.00008842396,0.00016833373,0.000050728555,7.476194e-7,0.00019818277,0.00009152309,0.9974905,0.00036860307],"about_ca_topic_score_codex":0.000010231453,"about_ca_topic_score_gemma":0.000007284319,"teacher_disagreement_score":0.9980039,"about_ca_system_score_codex":0.000009803111,"about_ca_system_score_gemma":0.0001315056,"threshold_uncertainty_score":0.99997747},"labels":[],"label_agreement":null},{"id":"W2135374196","doi":"10.1002/ajmg.a.31404","title":"Cornelia de Lange syndrome: Parental preferences regarding the provision of medical information","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"Cornelia de Lange Syndrome Foundation","keywords":"Cornelia de Lange Syndrome; Medicine; Preference; Medical information; Health care; Health information; Information needs; Family medicine; Psychiatry; Pediatrics","score_opus":0.008614901002602688,"score_gpt":0.2598341247911243,"score_spread":0.2512192237885216,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135374196","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99509305,0.0008499641,0.0026033346,0.0009653422,0.00021630256,0.00007345467,0.0000042133997,0.000002719194,0.00019163641],"genre_scores_gemma":[0.9975325,0.0011252223,0.0008053575,0.00024701314,0.00024730866,0.0000031625714,0.000013285781,0.000008526738,0.000017634744],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9976325,0.00013180332,0.00064072566,0.00010023171,0.0012615152,0.0002332494],"domain_scores_gemma":[0.9989022,0.000046924386,0.0005416703,0.00017856118,0.00013384028,0.00019678069],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013162799,0.00011253476,0.00023849115,0.00004764205,0.00004878763,0.00002749499,0.0005932748,0.00012698935,0.00007909518],"category_scores_gemma":[0.0004093282,0.00007345044,0.00011679071,0.00012500171,0.0003507768,0.00000635077,0.00017101584,0.0002233033,0.0000031271998],"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":[0.00013476545,0.00039602016,0.34275126,0.0001419038,0.00036509332,0.00006521094,0.0008923057,0.0005905076,0.012156738,0.00016986394,0.01941592,0.6229204],"study_design_scores_gemma":[0.004371778,0.008667024,0.74979186,0.0012417485,0.00028602523,0.010514404,0.0074551157,0.005260662,0.025742825,0.00051621423,0.18531795,0.000834378],"about_ca_topic_score_codex":0.0001111199,"about_ca_topic_score_gemma":0.000019840145,"teacher_disagreement_score":0.62208605,"about_ca_system_score_codex":0.000012000147,"about_ca_system_score_gemma":0.00039295593,"threshold_uncertainty_score":0.29952222},"labels":[],"label_agreement":null},{"id":"W2135386003","doi":"10.1186/1755-8166-4-15","title":"Context-based FISH localization of genomic rearrangements within chromosome 15q11.2q13 duplicons","year":2011,"lang":"en","type":"article","venue":"Molecular Cytogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Genome Canada; Western University","funders":"Schulich School of Medicine and Dentistry; Natural Sciences and Engineering Research Council of Canada; London Health Sciences Centre","keywords":"Biology; Genetics; Pseudogene; Breakpoint; Chromosome; Context (archaeology); Fluorescence in situ hybridization; Gene dosage; Comparative genomic hybridization; Copy-number variation; Haploinsufficiency; Chromosomal rearrangement; Gene; Genome; Karyotype; Molecular biology; Phenotype; Gene expression","score_opus":0.02220257242134981,"score_gpt":0.22848057034702163,"score_spread":0.2062779979256718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135386003","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94705534,0.000446191,0.051139675,0.000022367425,0.00016813721,0.00031882644,0.00003350272,0.000016146108,0.000799805],"genre_scores_gemma":[0.9930735,0.00005540829,0.0058106384,0.00072145986,0.000039893697,0.000023034785,0.00012874289,0.0000644968,0.000082795945],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99849415,0.00007873463,0.00046597928,0.00043523908,0.00020836292,0.00031755364],"domain_scores_gemma":[0.9988138,0.0000043259606,0.00023772272,0.00065568415,0.00016624882,0.00012219835],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00016177061,0.00024281429,0.00023706739,0.00007897709,0.00006383203,0.000016540902,0.00032372007,0.00019530316,0.0001038871],"category_scores_gemma":[0.000053357806,0.00026673859,0.00015005887,0.00012489763,0.00014030024,0.000002300533,0.00016206077,0.000070702,0.000017784783],"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":[0.000022094395,0.00012472126,0.048148043,0.000048090467,0.00010947537,0.000007738461,0.00013084279,0.0016089726,0.9482438,0.000079371915,0.00013175468,0.0013451059],"study_design_scores_gemma":[0.00090819306,0.00047578098,0.010094224,0.000028149894,0.00006830968,0.00001660345,0.00007724148,0.0006972079,0.9834775,0.000060107617,0.003795177,0.00030155922],"about_ca_topic_score_codex":0.000048816313,"about_ca_topic_score_gemma":0.0000324521,"teacher_disagreement_score":0.04601818,"about_ca_system_score_codex":0.000016865717,"about_ca_system_score_gemma":0.00011702638,"threshold_uncertainty_score":0.9999785},"labels":[],"label_agreement":null},{"id":"W2135611636","doi":"10.1210/jc.2007-2633","title":"Selective Loss of MEG3 Expression and Intergenic Differentially Methylated Region Hypermethylation in the MEG3/DLK1 Locus in Human Clinically Nonfunctioning Pituitary Adenomas","year":2008,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":142,"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":"Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; Massachusetts General Hospital; National Institutes of Health; Pfizer","keywords":"MEG3; Biology; DNA methylation; Pituitary neoplasm; Pituitary tumors; Pituitary adenoma; Methylation; Adenoma; Pituitary gland; Endocrinology; Gene expression; Gene; Long non-coding RNA; RNA; Genetics; Hormone","score_opus":0.03647789990591279,"score_gpt":0.32855109320403725,"score_spread":0.2920731932981245,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135611636","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9939027,0.004068998,0.00090752484,0.00048127348,0.00036196943,0.00018141644,7.249032e-7,0.0000028431946,0.00009258011],"genre_scores_gemma":[0.99284476,0.006172217,0.00039331848,0.00018015208,0.00034889646,0.0000041343155,0.0000028925692,0.000016024625,0.00003757572],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9954517,0.0018438465,0.0019228827,0.0002603632,0.00021993427,0.0003012755],"domain_scores_gemma":[0.9978197,0.00052420184,0.0010381817,0.00033624948,0.0002196463,0.00006201954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002083466,0.00018712191,0.0006789449,0.00014812943,0.000110637375,0.0000070915494,0.0004635323,0.00024232172,0.00000907902],"category_scores_gemma":[0.0011879343,0.00011334993,0.00024847657,0.00018117731,0.00043458492,0.000015880927,0.00019841756,0.00084757805,6.6183463e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012964705,0.00066840544,0.2758974,0.000028980488,0.00039083697,0.00007830051,0.0018310801,0.00056125806,0.70626056,0.000122008096,0.0001681067,0.012696607],"study_design_scores_gemma":[0.0034321703,0.0010911329,0.9628255,0.00006909754,0.0001446397,0.0010670503,0.00040830983,0.000047389825,0.029411435,0.00077776617,0.0005738757,0.00015165079],"about_ca_topic_score_codex":0.00005114414,"about_ca_topic_score_gemma":0.000037676215,"teacher_disagreement_score":0.6869281,"about_ca_system_score_codex":0.0000073199144,"about_ca_system_score_gemma":0.000099713354,"threshold_uncertainty_score":0.4622276},"labels":[],"label_agreement":null},{"id":"W2135835560","doi":"10.1074/jbc.m112.372094","title":"Mutations in the GlyT2 Gene (SLC6A5) Are a Second Major Cause of Startle Disease","year":2012,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":84,"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":"Action Medical Research","keywords":"Gene; Disease; Genetics; Mutation; Medicine; Biology; Internal medicine","score_opus":0.023963068138088232,"score_gpt":0.26389123899218403,"score_spread":0.2399281708540958,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135835560","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972663,0.0021946025,0.00005819542,0.00014867101,0.000052905434,0.00004951339,0.00002541568,0.0000011050494,0.00020331451],"genre_scores_gemma":[0.99903035,0.00008792134,0.00038819815,0.00011487487,0.00027475596,0.0000033998297,0.000017064616,0.000005228613,0.000078213016],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992131,0.000050368613,0.0003369365,0.0000959853,0.000108465,0.00019516407],"domain_scores_gemma":[0.99932474,0.000031312018,0.00028471416,0.00016983437,0.00007379459,0.000115586525],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033573518,0.00009586318,0.00015453411,0.000014244073,0.00002774128,0.000008707223,0.00021802603,0.00010384264,0.00013819133],"category_scores_gemma":[0.00025765912,0.000058660888,0.00012871025,0.00006669484,0.00007844177,0.000003972256,0.00006105635,0.00013254424,0.0000014276832],"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":[0.00002823588,0.0001660374,0.14477502,0.000028543986,0.000032805317,0.000008814503,0.000050368482,0.000012482939,0.8545037,0.0000014714444,0.0002476005,0.00014491755],"study_design_scores_gemma":[0.00051823014,0.00011679355,0.4452008,0.000024420116,0.000031798,0.00022778117,0.0006168426,0.000004107366,0.5499971,0.00007294865,0.003074387,0.00011480932],"about_ca_topic_score_codex":0.0000013091894,"about_ca_topic_score_gemma":9.252776e-7,"teacher_disagreement_score":0.30450663,"about_ca_system_score_codex":0.000008926934,"about_ca_system_score_gemma":0.000042902975,"threshold_uncertainty_score":0.23921217},"labels":[],"label_agreement":null},{"id":"W2136629665","doi":"10.1093/hmg/ddn344","title":"Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development","year":2008,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":103,"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":"National Institute of Environmental Health Sciences; National Institute of General Medical Sciences; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute","keywords":"Biology; Gonadotropin-releasing hormone; Endocrinology; Internal medicine; Homeobox; Psychological repression; Repressor; Gene; Enhancer; Transcription factor; Gene expression; Cell biology; Hormone; Genetics; Luteinizing hormone; Medicine","score_opus":0.012659921166068804,"score_gpt":0.2227246949130071,"score_spread":0.21006477374693827,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2136629665","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9926935,0.004760795,0.0016757189,0.00004975735,0.00013528092,0.00039040612,0.0000081719845,0.000056534802,0.00022987353],"genre_scores_gemma":[0.98745537,0.0008934848,0.010298782,0.00016482658,0.000117578464,0.000040752355,0.00015132558,0.00014291944,0.0007349568],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9971374,0.000098438955,0.00061362033,0.00089107256,0.00040379772,0.0008556686],"domain_scores_gemma":[0.99845654,0.0000055428072,0.00021233001,0.0008905985,0.00013958378,0.00029539524],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00007790048,0.00049845746,0.0003605666,0.00014514581,0.00069807254,0.00007533435,0.0004820699,0.00024478926,0.000026178397],"category_scores_gemma":[0.000039116047,0.00056219293,0.0001890659,0.00019288482,0.00019690151,0.0000066948587,0.00048474988,0.00020744134,0.000036262194],"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":[0.000002979266,0.00009147455,0.007110377,0.000030475474,0.0001378636,0.00010577289,0.00015091436,0.0008489804,0.9909507,0.000013140317,0.00014662484,0.00041070068],"study_design_scores_gemma":[0.00089620496,0.00033171548,0.7074134,0.00002652347,0.00003978365,0.0021603103,0.000026742124,0.000057561265,0.28247362,0.000025948606,0.0059048655,0.00064334384],"about_ca_topic_score_codex":0.000028038203,"about_ca_topic_score_gemma":0.000010107001,"teacher_disagreement_score":0.7084771,"about_ca_system_score_codex":0.00005298819,"about_ca_system_score_gemma":0.00018897858,"threshold_uncertainty_score":0.99968296},"labels":[],"label_agreement":null},{"id":"W2136943416","doi":"10.1136/jmg.40.11.e126","title":"Identification of eight novel <i>NSD1</i> mutations in Sotos syndrome","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Health; University of Calgary","funders":"Core Research for Evolutional Science and Technology; Japan Science and Technology Corporation; Università degli Studi di Siena; Friedrich-Schiller-Universität Jena","keywords":"Sotos syndrome; Haploinsufficiency; Frontal Bossing; Gigantism; Genetics; Exon; Pituitary disorder; Point mutation; Biology; Craniofacial; Mutation; Medicine; Gene; Endocrinology; Anatomy; Phenotype","score_opus":0.012018203080545279,"score_gpt":0.27070369433063374,"score_spread":0.25868549125008844,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2136943416","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9817336,0.0015234005,0.016000591,0.00020872118,0.00032244314,0.00007540064,0.0000039047586,8.563338e-7,0.0001310877],"genre_scores_gemma":[0.99599093,0.000770405,0.003005282,0.00007646588,0.000064433545,0.0000020287732,0.000004063513,0.000012780816,0.0000735965],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982597,0.000064648004,0.00083298417,0.00012708495,0.00055085047,0.00016472823],"domain_scores_gemma":[0.99909604,0.00002591001,0.00038906242,0.0001845151,0.00016542581,0.00013907309],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00092457636,0.00009246996,0.0001963538,0.00009815842,0.000021158883,0.000011435304,0.00027528562,0.00018130436,0.000055941342],"category_scores_gemma":[0.0006652931,0.00008360681,0.000101783175,0.00015586065,0.0000823819,0.0000029411603,0.00004333435,0.00015823728,0.0000024814983],"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":[0.0000077142895,0.0004744554,0.016405819,0.00006529165,0.0000796583,0.00002312519,0.00012698006,0.0008715508,0.97692704,0.00015950404,0.0002585125,0.00460037],"study_design_scores_gemma":[0.004711424,0.0014144772,0.124833144,0.00026468423,0.00011905834,0.0052168164,0.0007515738,0.0012326055,0.8288684,0.00072085083,0.03142208,0.00044488744],"about_ca_topic_score_codex":0.00000227233,"about_ca_topic_score_gemma":0.0000039948413,"teacher_disagreement_score":0.14805862,"about_ca_system_score_codex":0.000010450967,"about_ca_system_score_gemma":0.00025868756,"threshold_uncertainty_score":0.34093866},"labels":[],"label_agreement":null},{"id":"W2137283728","doi":"10.1128/mcb.21.7.2384-2392.2001","title":"Establishment and Maintenance of DNA Methylation Patterns in Mouse <i>Ndn</i> : Implications for Maintenance of Imprinting in Target Genes of the Imprinting Center","year":2001,"lang":"en","type":"article","venue":"Molecular and Cellular Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Division of Materials Research","keywords":"Genomic imprinting; Biology; Imprinting (psychology); DNA methylation; Epigenetics; Genetics; Blastocyst; Methylation; Gene; CpG site; Bisulfite sequencing; DNA demethylation; Oocyte; RNA-Directed DNA Methylation; Molecular biology; Embryo; Embryogenesis; Gene expression","score_opus":0.007802827356174907,"score_gpt":0.22995713498546852,"score_spread":0.2221543076292936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2137283728","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96643555,0.0008927139,0.032083303,0.00013619689,0.00003645819,0.0003314867,0.000033098695,0.0000015360697,0.00004964065],"genre_scores_gemma":[0.99781907,0.0003072511,0.0017318716,0.00003862647,0.000010237852,0.000028910945,0.000030469075,0.000013109751,0.000020434549],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988934,0.00007806292,0.00044529254,0.0003004437,0.000038945884,0.0002438477],"domain_scores_gemma":[0.9993607,0.000019623883,0.00024706364,0.00026933636,0.00007683972,0.000026461841],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034055134,0.00012413476,0.00023526118,0.00006597748,0.000024420046,0.0000046539067,0.0001496126,0.0001143738,0.0000014739805],"category_scores_gemma":[0.0000863131,0.00010289071,0.00008068151,0.00010408301,0.000106934065,0.0000037172717,0.0002163888,0.00005899275,2.6404091e-8],"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":[0.000008013676,0.000025404828,0.36558652,0.000047923062,0.00001155761,1.5747933e-7,0.000034656005,0.000045043642,0.630209,0.00018990197,6.0567686e-7,0.0038412036],"study_design_scores_gemma":[0.0007562472,0.0001167866,0.118988775,0.000041305862,0.000008018511,0.0000104784385,0.0001360905,0.00020117972,0.87899,0.0003565905,0.00029717668,0.000097375516],"about_ca_topic_score_codex":0.0001242927,"about_ca_topic_score_gemma":0.00005810092,"teacher_disagreement_score":0.24878097,"about_ca_system_score_codex":0.00000728995,"about_ca_system_score_gemma":0.000020310137,"threshold_uncertainty_score":0.41957614},"labels":[],"label_agreement":null},{"id":"W2137790269","doi":"10.1002/ca.22659","title":"Angelman syndrome: A review highlighting musculoskeletal and anatomical aberrations","year":2015,"lang":"en","type":"review","venue":"Clinical Anatomy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"","keywords":"Medicine; Angelman syndrome; Physical medicine and rehabilitation; Genetics","score_opus":0.058183020319579344,"score_gpt":0.4222337289677908,"score_spread":0.3640507086482115,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2137790269","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0015189257,0.9964319,0.000022664472,0.00018591595,0.00037082695,0.0007548599,0.000032138018,0.000027373206,0.0006554132],"genre_scores_gemma":[0.00019947371,0.9973007,0.0007203146,0.00024383936,0.0004007653,0.00009132703,0.00042708195,0.00007399787,0.0005425247],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99649,0.00042885676,0.0014363467,0.0010052237,0.00022311727,0.00041644095],"domain_scores_gemma":[0.9980769,0.00009253786,0.00049919385,0.00075698725,0.00014003488,0.00043432633],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0013060337,0.0004977463,0.0019262771,0.00007218713,0.00008639019,0.000047864276,0.0004320598,0.0007069142,0.000049764734],"category_scores_gemma":[0.0007148956,0.00039930586,0.00087555044,0.00024100243,0.00023003845,0.0000049567675,0.0005992223,0.00051538146,0.00009527658],"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":[6.346277e-7,0.00007127357,0.0000827592,0.011618083,0.00025128116,0.000026671907,0.0000019499143,2.2911966e-8,7.4457904e-7,0.00007368347,0.010821982,0.9770509],"study_design_scores_gemma":[0.00024242027,0.00023595005,0.00011618099,0.0082129,0.00081453973,0.0008724075,0.0000047086023,0.0000039232705,2.2164318e-7,0.000025982137,0.98899376,0.0004769768],"about_ca_topic_score_codex":0.000005425921,"about_ca_topic_score_gemma":0.0000045382144,"teacher_disagreement_score":0.9781718,"about_ca_system_score_codex":0.00002107014,"about_ca_system_score_gemma":0.00036560628,"threshold_uncertainty_score":0.99984586},"labels":[],"label_agreement":null},{"id":"W2138958826","doi":"10.1093/toxsci/kfs303","title":"Identification of Dlk1-Dio3 Imprinted Gene Cluster Noncoding RNAs as Novel Candidate Biomarkers for Liver Tumor Promotion","year":2012,"lang":"en","type":"article","venue":"Toxicological Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":69,"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":"Cancer Research UK","keywords":"MEG3; Biology; Epigenetics; Gene expression; microRNA; Cancer research; Gene; Carcinogenesis; Genetics; RNA; Long non-coding RNA","score_opus":0.03815984994435082,"score_gpt":0.30712325360777937,"score_spread":0.2689634036634285,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2138958826","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97551376,0.00017752983,0.023253554,0.00013918093,0.00023824285,0.00036173954,0.000009604434,0.000008754674,0.00029764127],"genre_scores_gemma":[0.9951463,0.000027663287,0.004433654,0.000102385835,0.00011404461,0.00004057612,0.000011120824,0.0000052312716,0.00011905397],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989178,0.00003776606,0.00027624477,0.00029012878,0.00014732093,0.0003307279],"domain_scores_gemma":[0.9994944,0.000027618193,0.00019087733,0.00012919524,0.00006895468,0.00008896601],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000969542,0.000102101905,0.00011900783,0.00004035835,0.00014982933,0.000032216547,0.00023569632,0.00008892357,0.00004464971],"category_scores_gemma":[0.0003235183,0.00007601681,0.00007975228,0.0001423712,0.0002212891,0.000012809423,0.00013643022,0.000032500957,0.000007315015],"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":[0.000012777944,0.00012224287,0.004083348,0.000013422364,0.000014279837,8.538546e-8,0.000033936278,0.000017226634,0.99214715,0.00012390563,0.00003320471,0.0033984361],"study_design_scores_gemma":[0.0003195456,0.0006267083,0.05275334,0.00000814636,0.000015993446,0.000037543938,0.00009566572,0.0018152752,0.9433599,0.000041482985,0.0007959414,0.00013043924],"about_ca_topic_score_codex":0.000019807203,"about_ca_topic_score_gemma":0.0000055475816,"teacher_disagreement_score":0.048787218,"about_ca_system_score_codex":0.00001596986,"about_ca_system_score_gemma":0.00004055058,"threshold_uncertainty_score":0.30998757},"labels":[],"label_agreement":null},{"id":"W2139222393","doi":"10.1071/rd05118","title":"Gamete imprinting: setting epigenetic patterns for the next generation","year":2005,"lang":"en","type":"review","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":126,"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 Children's Hospital","funders":"Canadian Institutes of Health Research; McGill University; National Institutes of Health; Brandeis University","keywords":"Epigenetics; Genomic imprinting; DNA methylation; Biology; Gamete; Imprinting (psychology); Offspring; Germline; Genetics; Epigenesis; Carcinogenesis; Function (biology); Gene; Gene expression; Pregnancy","score_opus":0.11650807665525371,"score_gpt":0.32474064821823473,"score_spread":0.20823257156298103,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2139222393","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00821739,0.9809167,0.009057025,0.00011279986,0.00051962555,0.0011409406,0.000006596085,0.000016668135,0.000012299898],"genre_scores_gemma":[0.003888334,0.9879283,0.0060737724,0.00004826339,0.00089553226,0.0003669254,0.00024084562,0.00004137107,0.0005166711],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99782646,0.00008951875,0.0006561209,0.0010007174,0.00013109544,0.00029607283],"domain_scores_gemma":[0.99885565,0.000032561096,0.00027756052,0.0006665302,0.000105003564,0.00006272352],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009935901,0.00031595552,0.0004148718,0.000046603447,0.000374928,0.00010927199,0.00016648746,0.00021504765,0.000014860784],"category_scores_gemma":[0.00025234197,0.00023402242,0.00017256099,0.000064233645,0.000040376883,0.000005015199,0.00021339451,0.00013399296,0.0000073419724],"study_design_candidate":"design_other","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":[0.0000025707736,0.000018425588,0.000055922337,0.001196611,0.00010564703,5.3168318e-8,0.00005570597,0.000010873456,0.00038386104,5.8308035e-7,0.00008264194,0.9980871],"study_design_scores_gemma":[0.0001065856,0.000036869984,0.0024977971,0.00025577983,0.00012049421,0.000035281402,0.000047697897,0.00005636255,0.0016203627,0.0000017675084,0.9949377,0.00028328315],"about_ca_topic_score_codex":0.0000052181795,"about_ca_topic_score_gemma":0.00001186347,"teacher_disagreement_score":0.9978038,"about_ca_system_score_codex":0.0000412239,"about_ca_system_score_gemma":0.00023371619,"threshold_uncertainty_score":0.9543157},"labels":[],"label_agreement":null},{"id":"W2140288082","doi":"10.1242/dev.045724","title":"Activation of paternally expressed genes and perinatal death caused by deletion of the<i>Gtl2</i>gene","year":2010,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":138,"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; Division of Materials Research; Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; Massachusetts General Hospital","keywords":"Biology; Genomic imprinting; Gene; Locus (genetics); Genetics; Exon; Imprinting (psychology); Gene expression; MEG3; DNA methylation; Regulation of gene expression; Molecular biology; Long non-coding RNA; RNA","score_opus":0.007019756044616067,"score_gpt":0.2072545216897211,"score_spread":0.20023476564510503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2140288082","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99878746,0.000073355055,0.00090500433,0.000029183235,0.000071841474,0.00008196278,0.0000046862892,0.0000017560693,0.000044762386],"genre_scores_gemma":[0.9964506,0.000033598462,0.0033293902,0.000020055431,0.000014675494,0.00000804309,0.000018428162,0.000006912911,0.0001182836],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995396,0.000011007783,0.0001524777,0.00012628274,0.000089622525,0.00008097806],"domain_scores_gemma":[0.99969965,0.0000031528502,0.00009205971,0.00012779012,0.00005566667,0.00002168249],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007569311,0.00006717813,0.00006811879,0.000012323984,0.000034039713,0.0000051824936,0.00008545637,0.000057043082,0.0000074078475],"category_scores_gemma":[0.000018226006,0.000053080195,0.000019784362,0.000023045197,0.000026317935,0.0000017769784,0.00009569498,0.000032154618,2.3419858e-7],"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":[0.0000033170986,0.000012498362,0.03818097,0.000016685313,0.000015991394,4.399833e-8,0.00007091763,0.0000028441664,0.9529712,0.0000050544536,0.000017628086,0.008702816],"study_design_scores_gemma":[0.00015886434,0.000019671603,0.26333204,0.000007728414,0.0000023170185,0.0000028347897,0.000010587999,0.0000072989315,0.73142374,0.000004267931,0.004983883,0.000046743986],"about_ca_topic_score_codex":0.000017634124,"about_ca_topic_score_gemma":0.0000060066036,"teacher_disagreement_score":0.22515108,"about_ca_system_score_codex":0.0000029776768,"about_ca_system_score_gemma":0.0000464857,"threshold_uncertainty_score":0.21645476},"labels":[],"label_agreement":null},{"id":"W2140384819","doi":"10.1111/j.1469-185x.2008.00050.x","title":"Genomic imprinting in the development and evolution of psychotic spectrum conditions","year":2008,"lang":"en","type":"review","venue":"Biological reviews/Biological reviews of the Cambridge Philosophical Society","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"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","funders":"","keywords":"Genomic imprinting; Angelman syndrome; Rett syndrome; Autism; Epigenetics; Imprinting (psychology); Genetics; Psychology; Autism spectrum disorder; Neurodevelopmental disorder; Pervasive developmental disorder; Biology; Neuroscience; Gene; DNA methylation; Developmental psychology; Gene expression","score_opus":0.10805341932226731,"score_gpt":0.3308161649552741,"score_spread":0.2227627456330068,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2140384819","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.022665769,0.97366846,0.00010174135,0.00026739616,0.00015848686,0.002900669,0.00003843055,0.000007671943,0.00019136263],"genre_scores_gemma":[0.029092984,0.9687146,0.0011199813,0.00028070973,0.00031971416,0.00033453893,0.000101948135,0.000022886723,0.000012618792],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99351,0.001908666,0.0028055955,0.0009789921,0.00022434519,0.0005723733],"domain_scores_gemma":[0.9967974,0.00032221174,0.0017108277,0.0009909484,0.00005506173,0.00012357114],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0026319013,0.00073694217,0.003062594,0.000037591395,0.00022278982,0.000015544663,0.0014573879,0.0009286147,0.000015502817],"category_scores_gemma":[0.0018602489,0.00032580912,0.0025511237,0.00050278945,0.0009775251,0.0000045343395,0.0009497835,0.00081943866,0.000018335137],"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":[0.000025488866,0.001186535,0.008835198,0.018772949,0.00057498587,0.0000035519527,0.00013201637,0.000002269679,0.0054466478,0.007772728,0.0025454594,0.9547022],"study_design_scores_gemma":[0.00022275957,0.00029386277,0.015165455,0.0037874458,0.00014730223,0.00015389455,0.000015035975,0.0000022008235,0.000026508003,0.00059832376,0.9790968,0.0004904501],"about_ca_topic_score_codex":0.000005806829,"about_ca_topic_score_gemma":0.0000013615153,"teacher_disagreement_score":0.9765513,"about_ca_system_score_codex":0.00009789059,"about_ca_system_score_gemma":0.00015983557,"threshold_uncertainty_score":0.9999194},"labels":[],"label_agreement":null},{"id":"W2142247682","doi":"10.1111/j.1420-9101.2006.01091.x","title":"Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism","year":2006,"lang":"en","type":"review","venue":"Journal of Evolutionary Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":148,"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","funders":"","keywords":"Autism; Genomic imprinting; Angelman syndrome; Rett syndrome; Biology; Imprinting (psychology); Neurodevelopmental disorder; Epigenetics; Brain size; Cognition; Neuroscience; Developmental disorder; Brain development; Genetics; Gene; Psychology; Developmental psychology; DNA methylation","score_opus":0.023966328968371902,"score_gpt":0.3058627408149343,"score_spread":0.2818964118465624,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142247682","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.01310175,0.9823801,0.0031647664,0.00011857057,0.00062231306,0.0004988676,0.00006462152,0.0000033964004,0.000045626388],"genre_scores_gemma":[0.023608036,0.95382935,0.02090381,0.00006989463,0.00081147754,0.00008571579,0.00044892702,0.00006408211,0.00017873713],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9970153,0.00037643634,0.0016779078,0.0003945245,0.000097631826,0.0004381777],"domain_scores_gemma":[0.9974712,0.00034808903,0.0015823791,0.00034386266,0.00019063154,0.00006382028],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00095178484,0.0003410028,0.0011263102,0.00030685423,0.00012213599,0.0000064960354,0.0006870162,0.00063943764,0.00001822555],"category_scores_gemma":[0.0003522168,0.0002480207,0.00054919976,0.00017298118,0.00021526268,0.0000071809804,0.00023818547,0.00033070284,0.0000020520552],"study_design_candidate":"design_other","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":[0.000111978465,0.00048253656,0.008776402,0.0028423504,0.0012612181,0.0000083632485,0.00008631613,0.00061250944,0.022698632,0.0009620062,0.0035074598,0.95865023],"study_design_scores_gemma":[0.0005504448,0.00064102304,0.04629722,0.0006826203,0.00015415573,0.00092391396,0.00003426615,0.00007491603,0.00003484995,0.00032754274,0.9499705,0.00030858064],"about_ca_topic_score_codex":0.000024989904,"about_ca_topic_score_gemma":0.00001438598,"teacher_disagreement_score":0.95834166,"about_ca_system_score_codex":0.00013811405,"about_ca_system_score_gemma":0.0011337636,"threshold_uncertainty_score":0.9999972},"labels":[],"label_agreement":null},{"id":"W2142314133","doi":"10.1210/jc.2010-1733","title":"The Metabolic Phenotype of Prader-Willi Syndrome (PWS) in Childhood: Heightened Insulin Sensitivity Relative to Body Mass Index","year":2010,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":106,"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":"National Center for Research Resources; University of Alberta","keywords":"Internal medicine; Endocrinology; Adiponectin; Insulin resistance; Medicine; Resistin; Context (archaeology); Insulin; Leptin; Body mass index; Quantitative insulin sensitivity check index; Metabolic syndrome; Obesity; Biology; Insulin sensitivity","score_opus":0.014008731554147806,"score_gpt":0.30542488526259487,"score_spread":0.2914161537084471,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142314133","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99049103,0.0038331572,0.00068030105,0.0031277272,0.0013981479,0.00028117924,0.0000062941263,0.0000045922916,0.0001775587],"genre_scores_gemma":[0.9930274,0.0040994873,0.0016633758,0.00049452705,0.00059096934,0.0000049080973,0.0000016573283,0.000028842542,0.00008885461],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9958321,0.0012953284,0.0017113306,0.000296081,0.00031647077,0.0005487126],"domain_scores_gemma":[0.9968711,0.0008231963,0.0010756336,0.0007092192,0.00033553026,0.00018533542],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0031525218,0.00026005,0.000931874,0.00012102754,0.00013570386,0.000017050732,0.0007091163,0.00029226032,0.000016475928],"category_scores_gemma":[0.0036394917,0.00015143206,0.00037737007,0.0002652113,0.000495371,0.000015168788,0.0003299309,0.0014183627,0.00001168055],"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":[0.0005120882,0.0011609982,0.16085269,0.000019098923,0.002359534,0.0000607741,0.0007260092,0.00080171775,0.7201571,0.0068955375,0.00033878163,0.106115684],"study_design_scores_gemma":[0.0017395567,0.00039972272,0.95197415,0.000014754975,0.00016686763,0.0008093283,0.00013055498,0.00003821678,0.011536592,0.001637946,0.031388618,0.0001636652],"about_ca_topic_score_codex":0.000058252615,"about_ca_topic_score_gemma":0.00010403136,"teacher_disagreement_score":0.7911215,"about_ca_system_score_codex":0.00000395971,"about_ca_system_score_gemma":0.00023929763,"threshold_uncertainty_score":0.617522},"labels":[],"label_agreement":null},{"id":"W2143629379","doi":"10.1093/hmg/ddr018","title":"Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome","year":2011,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"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":"Hutchison Whampoa Limited; Ministero dell’Istruzione, dell’Università e della Ricerca; University of Cambridge; Cancer Research UK","keywords":"CTCF; Cohesin; Genomic imprinting; Biology; Beckwith–Wiedemann syndrome; Chromatin; Genetics; Epigenetics; Locus (genetics); Histone; Imprinting (psychology); DNA methylation; MEG3; Heterochromatin; Molecular biology; Enhancer; Gene; Gene expression","score_opus":0.013939239669072904,"score_gpt":0.23091790155132244,"score_spread":0.21697866188224954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143629379","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99426126,0.003534141,0.0006388161,0.000024015431,0.00008771644,0.00047001592,0.000013492305,0.000011859875,0.000958674],"genre_scores_gemma":[0.99843234,0.00035102785,0.0007020558,0.00008302936,0.000020675643,0.000028364087,0.000046654906,0.00007147228,0.00026435507],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9979742,0.00012526511,0.0005696572,0.00062237016,0.00022019449,0.00048828556],"domain_scores_gemma":[0.9986951,0.000010468284,0.00024322841,0.000846674,0.000073658695,0.00013088348],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00027770715,0.00034129136,0.00034388306,0.00011534666,0.0001311406,0.000026866768,0.00042485443,0.00024201504,0.00015131012],"category_scores_gemma":[0.00002507504,0.0003040474,0.0001596854,0.0001363928,0.00026730006,0.000004474489,0.00064759946,0.00016516355,0.000022926468],"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":[0.000015673608,0.00011931665,0.023722475,0.000056939472,0.00010434085,0.00006209847,0.00035616,0.00011168098,0.9745789,0.00013780428,0.000011040355,0.00072354934],"study_design_scores_gemma":[0.0009476176,0.0009500558,0.83017653,0.000046150923,0.000093394454,0.0010880401,0.00020855086,0.00011576964,0.16522391,0.00046367917,0.0002447056,0.00044158014],"about_ca_topic_score_codex":0.0001653437,"about_ca_topic_score_gemma":0.00017639677,"teacher_disagreement_score":0.809355,"about_ca_system_score_codex":0.00003493357,"about_ca_system_score_gemma":0.00004536189,"threshold_uncertainty_score":0.9999412},"labels":[],"label_agreement":null},{"id":"W2143659807","doi":"10.1186/1741-7007-8-105","title":"The Drosophila homolog of the mammalian imprint regulator, CTCF, maintains the maternal genomic imprint in Drosophila melanogaster","year":2010,"lang":"en","type":"article","venue":"BMC Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Allison University; Dalhousie University","funders":"Dalhousie University; Wayne State University","keywords":"CTCF; Biology; Genomic imprinting; Chromatin; Genetics; Insulator (electricity); Drosophila melanogaster; X-inactivation; Epigenetics; Regulator; DNA methylation; Heterochromatin; Gene; Imprinting (psychology); X chromosome; Gene expression; Enhancer","score_opus":0.007678675970868722,"score_gpt":0.22997203241391445,"score_spread":0.22229335644304574,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143659807","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965152,0.00024386396,0.00009969104,0.0013478821,0.0009808936,0.00037792066,0.000015105683,0.000006608403,0.00041282276],"genre_scores_gemma":[0.9984813,0.000064839856,0.0004530273,0.00022915381,0.00030264258,0.0000449105,0.000008030081,0.00002751612,0.00038862307],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.998238,0.00023292731,0.00048441137,0.00042693308,0.00009446924,0.0005232538],"domain_scores_gemma":[0.99840254,0.000055805256,0.0002510491,0.0011698923,0.000060023584,0.000060664643],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000734049,0.00023317331,0.00021857051,0.00003412462,0.00021336546,0.00003354671,0.0011149725,0.0003232843,0.00003075876],"category_scores_gemma":[0.00009752036,0.000120136225,0.00020907827,0.00009142104,0.0006797291,0.0000021785086,0.00096011726,0.00036817955,0.000014905695],"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":[0.00002564026,0.000020554762,0.22448726,0.000008041323,0.000025523072,6.3582644e-7,0.00004160841,0.000022382044,0.77016175,0.0036851873,0.000025941985,0.0014954609],"study_design_scores_gemma":[0.00047858173,0.00014282805,0.8519351,0.0000069098533,0.0000132641235,0.00021062177,0.000089105386,0.00007134851,0.13503042,0.0031456351,0.008716846,0.00015935849],"about_ca_topic_score_codex":0.00018265178,"about_ca_topic_score_gemma":0.0009219521,"teacher_disagreement_score":0.63513136,"about_ca_system_score_codex":0.00001816612,"about_ca_system_score_gemma":0.00011763156,"threshold_uncertainty_score":0.48990133},"labels":[],"label_agreement":null},{"id":"W2144824933","doi":"10.1101/gr.192278.115","title":"The landscape of genomic imprinting across diverse adult human tissues","year":2015,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"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":"Common Fund; National Institute of Biomedical Imaging and Bioengineering; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Cancer Institute; National Human Genome Research Institute; University of Miami; Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Orionin Tutkimussäätiö; Université de Genève; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Emil Aaltosen Säätiö; Israel Science Foundation; U.S. Public Health Service; Suomen Kulttuurirahasto; Roswell Park Cancer Institute; Hewlett-Packard Development Company; German-Israeli Foundation for Scientific Research and Development; Broad Institute; University of North Carolina; NIH Office of the Director; Van Andel Research Institute; National Institute on Drug Abuse; Science Applications International Corporation; University of Oxford; University of Chicago; Harvard University","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Genetics; Gene; Allele; Gene expression; Gene expression profiling; DNA methylation","score_opus":0.06576906099941318,"score_gpt":0.37813869640297826,"score_spread":0.3123696354035651,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2144824933","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9941081,0.0014331306,0.000030845844,0.00010553518,0.00006993364,0.0001735353,0.000008198305,0.000005692143,0.004065034],"genre_scores_gemma":[0.99692786,0.00027789117,0.00023497078,0.000009182949,0.00023317093,0.00001424928,0.0000180807,0.000018486036,0.0022661057],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99849397,0.00012579821,0.00022263998,0.0002730805,0.00032426967,0.0005602168],"domain_scores_gemma":[0.9987882,0.000025199563,0.00006434773,0.000499955,0.0004917771,0.00013052329],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001655284,0.00009470089,0.000115115705,0.000036864094,0.0003730592,0.00006917608,0.0005092758,0.00008621451,0.0000332481],"category_scores_gemma":[0.00021539333,0.00007256843,0.00006280274,0.000117994314,0.00021281256,0.0000018328378,0.00093995256,0.00015499924,0.00006656055],"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":[0.000014422262,0.000024759005,0.022347031,0.00002204122,0.000045416928,0.0000018612837,0.0006629752,0.000031606,0.9645222,0.0000851148,0.0005949889,0.011647593],"study_design_scores_gemma":[0.0027991172,0.0024000937,0.45606712,0.000040873114,0.000020359652,0.00008931131,0.037994843,0.00019214531,0.28653243,0.000608827,0.21256799,0.0006868992],"about_ca_topic_score_codex":0.00022280957,"about_ca_topic_score_gemma":0.00009804975,"teacher_disagreement_score":0.6779898,"about_ca_system_score_codex":0.000014260955,"about_ca_system_score_gemma":0.00008929933,"threshold_uncertainty_score":0.29592547},"labels":[],"label_agreement":null},{"id":"W2145160468","doi":"10.1093/humupd/dmh002","title":"Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology","year":2004,"lang":"en","type":"review","venue":"Human Reproduction Update","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":196,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital","funders":"","keywords":"Genomic imprinting; Reprogramming; Biology; Imprinting (psychology); Epigenetics; Germ cell; Genetics; Assisted reproductive technology; Epigenesis; DNA methylation; Infertility; Gene; Pregnancy; Gene expression","score_opus":0.023741709619292253,"score_gpt":0.29728737863305993,"score_spread":0.2735456690137677,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145160468","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.073043145,0.9232262,0.00074982416,0.00007184325,0.00082069886,0.001965216,0.00002535517,0.000060910057,0.00003683666],"genre_scores_gemma":[0.027114062,0.9645232,0.0047451737,0.0000054255465,0.0017549634,0.00037741536,0.00042309015,0.00015237238,0.00090428384],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99576664,0.0001053449,0.0009608403,0.002642553,0.00013738572,0.00038722885],"domain_scores_gemma":[0.9964268,0.000006098658,0.0012258685,0.0019463503,0.0003376138,0.000057255034],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00093487947,0.00046350318,0.0010241021,0.00035555463,0.00025989415,0.00003817524,0.00027699556,0.0004851425,0.000010027331],"category_scores_gemma":[0.00042888263,0.0004742056,0.00036605596,0.00029913272,0.00029021417,0.000007615455,0.00032758332,0.00026844812,0.000007363923],"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":[0.000016161557,0.00009817406,0.000030411415,0.008811016,0.00037053082,0.0000013966755,0.000023622968,0.000046541718,0.24572994,0.00023496467,0.000098275836,0.74453896],"study_design_scores_gemma":[0.00080637407,0.00072439417,0.00063145027,0.001952109,0.0012624807,0.0015501907,0.00008404176,0.0000018738467,0.07796788,0.0009694776,0.91294754,0.0011021628],"about_ca_topic_score_codex":0.000015077807,"about_ca_topic_score_gemma":0.0000021071362,"teacher_disagreement_score":0.9128493,"about_ca_system_score_codex":0.000066876404,"about_ca_system_score_gemma":0.00019795905,"threshold_uncertainty_score":0.99977094},"labels":[],"label_agreement":null},{"id":"W2145188829","doi":"10.1242/dev.096511","title":"The imprinted polycomb group gene <i>Sfmbt2</i> is required for trophoblast maintenance and placenta development","year":2013,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences","keywords":"Trophoblast; Biology; Genomic imprinting; Placenta; Inner cell mass; Embryonic stem cell; Embryo; Embryogenesis; Gene; Genetics; Imprinting (psychology); Parthenogenesis; Allele; Cell biology; Stem cell; Blastocyst; Gene expression; DNA methylation; Fetus; Pregnancy","score_opus":0.008274921547472978,"score_gpt":0.20902618053516658,"score_spread":0.2007512589876936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145188829","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9905065,0.0006447577,0.00717182,0.0005096544,0.00023849872,0.0006893338,0.0000038307007,0.000014473089,0.00022114784],"genre_scores_gemma":[0.95323277,0.00026850344,0.041451614,0.00078368577,0.000072014656,0.00045195856,0.00006214449,0.000039900686,0.003637387],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99850345,0.000019286626,0.00038538585,0.00043967922,0.0001425635,0.0005096226],"domain_scores_gemma":[0.99935126,0.000020585157,0.00011114746,0.00028381305,0.000104491824,0.00012872096],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023055666,0.00022412288,0.0001506877,0.000024687264,0.00039020018,0.00009704744,0.000247014,0.00009257289,0.000022556587],"category_scores_gemma":[0.00004037807,0.00016649223,0.00004984444,0.000054454,0.00007011159,0.0000047407702,0.00031544222,0.000056221703,0.000031858086],"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":[0.000042608383,0.000053603373,0.0026073854,0.000041426745,0.00021013581,7.8566273e-7,0.0008434739,0.0000013630399,0.8511358,0.000048024718,0.012048051,0.13296734],"study_design_scores_gemma":[0.0008994778,0.000093323426,0.057577755,0.00002459259,0.0000060138264,0.000033985652,0.00028515598,0.00007887493,0.5218405,0.000034326185,0.41882583,0.00030012708],"about_ca_topic_score_codex":0.000014699138,"about_ca_topic_score_gemma":0.000021998041,"teacher_disagreement_score":0.4067778,"about_ca_system_score_codex":0.000041826977,"about_ca_system_score_gemma":0.00012665824,"threshold_uncertainty_score":0.67893565},"labels":[],"label_agreement":null},{"id":"W2145709837","doi":"10.1086/497540","title":"Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor","year":2005,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"National Cancer Institute; Robert Wood Johnson Foundation; Foundation for the National Institutes of Health","keywords":"Hemihypertrophy; Wilms' tumor; Beckwith–Wiedemann syndrome; Epigenetics; Medicine; Imprinting (psychology); Genomic imprinting; Internal medicine; Pathology; DNA methylation; Biology; Genetics; Gene","score_opus":0.006669921147059524,"score_gpt":0.21626906855544475,"score_spread":0.20959914740838523,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145709837","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99648273,0.0023208729,0.00082894956,0.00016401958,0.000022358057,0.00013032957,0.0000070638002,0.000004936184,0.00003875442],"genre_scores_gemma":[0.99836725,0.00018379945,0.0009010683,0.00023592277,0.00023453748,0.0000033958463,0.0000069649655,0.000027780285,0.000039309696],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99875396,0.00009883545,0.00034515143,0.00021819831,0.00029542294,0.00028842175],"domain_scores_gemma":[0.99881846,0.000013136939,0.00061583583,0.0002524019,0.0001669168,0.00013327305],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021364093,0.00023650605,0.0003810991,0.000055760334,0.00022712657,0.00004822536,0.00028118605,0.000034329685,0.0000062305917],"category_scores_gemma":[0.000024416982,0.00013783126,0.00007480364,0.00007561095,0.0012829799,0.0000049724035,0.00009069159,0.00020110588,0.000001045073],"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":[0.00021889212,0.00044234848,0.7998426,0.000016355152,0.0018728535,0.000046010373,0.00048519447,0.0033252528,0.1857221,0.00008750436,0.00009781912,0.007843073],"study_design_scores_gemma":[0.0013759546,0.008819573,0.9671671,0.00016469393,0.00029460326,0.006142206,0.00036124574,0.000049571136,0.0150494035,0.000043481985,0.0001465617,0.0003856156],"about_ca_topic_score_codex":0.000007515097,"about_ca_topic_score_gemma":0.00002651234,"teacher_disagreement_score":0.1706727,"about_ca_system_score_codex":0.000024094295,"about_ca_system_score_gemma":0.000107009284,"threshold_uncertainty_score":0.5620596},"labels":[],"label_agreement":null},{"id":"W2145851060","doi":"10.1101/gr.2609605","title":"Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian <i>Ascl2/Mash2–Igf2–H19</i> region","year":2004,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"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; RIKEN; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; Gene; Exon; Intron; Evolutionary biology; Gene expression","score_opus":0.04462871531326501,"score_gpt":0.3041135668515461,"score_spread":0.2594848515382811,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145851060","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99528676,0.000577889,0.002017532,0.0013940723,0.00005418148,0.0003025416,0.000009495131,0.0000067750007,0.0003507666],"genre_scores_gemma":[0.99838793,0.00017157718,0.00031675055,0.00010720473,0.00013034417,0.000024918894,0.00006885427,0.0000178223,0.0007745678],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99834496,0.00014223263,0.0002552635,0.0004929841,0.0003220079,0.00044253192],"domain_scores_gemma":[0.99890494,0.000021632955,0.00006880505,0.00058512884,0.00027772537,0.00014173539],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006040167,0.00013888303,0.00020402294,0.00026219897,0.00023227169,0.00004291388,0.00027072825,0.00012716201,0.000022548971],"category_scores_gemma":[0.0001371797,0.00010471303,0.00013400239,0.0008006592,0.00020099102,0.0000030950255,0.00044501637,0.00020139827,0.000008748435],"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":[0.00022096983,0.00006916191,0.049087886,0.000071544615,0.000989017,0.000029953571,0.00091156457,0.008561533,0.92728275,0.00067416177,0.00040365066,0.011697821],"study_design_scores_gemma":[0.00074397906,0.0007790833,0.9664071,0.000016156018,0.00013796441,0.00030369277,0.00063235563,0.0001702002,0.020384477,0.00028775737,0.009865342,0.00027189145],"about_ca_topic_score_codex":0.0002596914,"about_ca_topic_score_gemma":0.00024226925,"teacher_disagreement_score":0.91731924,"about_ca_system_score_codex":0.00003376702,"about_ca_system_score_gemma":0.00010170762,"threshold_uncertainty_score":0.42700735},"labels":[],"label_agreement":null},{"id":"W2146264881","doi":"10.1146/annurev.cellbio.24.110707.175418","title":"The Evolution, Regulation, and Function of Placenta-Specific Genes","year":2008,"lang":"en","type":"review","venue":"Annual Review of Cell and Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":224,"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 Calgary","funders":"Canadian Institutes of Health Research","keywords":"Biology; Placenta; Gene; Gene family; Genetics; Function (biology); Gene expression","score_opus":0.012713991392023276,"score_gpt":0.25244370315883496,"score_spread":0.23972971176681168,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2146264881","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00076588313,0.9981303,0.00007730555,0.000008863218,0.00012939102,0.00034190566,0.000034769986,0.0000021999924,0.0005093651],"genre_scores_gemma":[0.0003272024,0.99849457,0.0005190762,0.0000292399,0.00004863118,0.000022561535,0.00023561576,0.000013033625,0.00031008114],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99866956,0.000128284,0.0006670263,0.00030957744,0.000068011555,0.00015753048],"domain_scores_gemma":[0.99920547,0.000052833897,0.0004161323,0.0001661882,0.000116122596,0.00004322717],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022003506,0.0002211062,0.0006527044,0.000036992245,0.00011156919,0.0000037749091,0.00012487538,0.00018775085,0.000011020204],"category_scores_gemma":[0.00004019009,0.0001415611,0.00013299448,0.00009689201,0.00026303128,0.0000025700917,0.00019884887,0.00006272145,0.0000035340647],"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":[0.0000042209795,0.00001397011,0.00014547406,0.011508662,0.000073391675,1.0959284e-7,0.000013638245,1.3607493e-8,0.0009727996,0.00009395598,0.0019663488,0.98520744],"study_design_scores_gemma":[0.000100615,0.00014586441,0.00034309333,0.003466464,0.000061596504,0.00013364611,0.00006506211,7.510469e-8,0.0002830647,0.000024410263,0.9952255,0.00015060711],"about_ca_topic_score_codex":0.0000056754066,"about_ca_topic_score_gemma":0.0000014697106,"teacher_disagreement_score":0.99325913,"about_ca_system_score_codex":0.000012847608,"about_ca_system_score_gemma":0.00016672543,"threshold_uncertainty_score":0.57726943},"labels":[],"label_agreement":null},{"id":"W2146975401","doi":"10.1002/ajmg.b.30934","title":"Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene <i>Magel2</i>","year":2009,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part B Neuropsychiatric Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Toronto; Hospital for Sick Children; University of Alberta","funders":"","keywords":"Circadian rhythm; Neurochemistry; Internal medicine; Endocrinology; Nucleus accumbens; Hypothalamus; Hippocampus; Neuroscience; Neurochemical; Amygdala; Biology; Dopamine; Medicine; Neurology","score_opus":0.010835415274824227,"score_gpt":0.2603576466815006,"score_spread":0.24952223140667634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2146975401","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97984916,0.0054836324,0.002775684,0.010461417,0.0008515846,0.0005232412,0.000017263344,0.000007405868,0.000030633222],"genre_scores_gemma":[0.9781339,0.008430533,0.007319755,0.004101685,0.0017532943,0.000027489488,0.000017311233,0.00006863775,0.00014735242],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9963676,0.00022866685,0.0012076633,0.0006134771,0.0008594351,0.00072321214],"domain_scores_gemma":[0.9976272,0.00013442244,0.0007766955,0.00056220236,0.00027525768,0.00062420196],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0008941597,0.00041767143,0.0005244317,0.00015298028,0.00016032481,0.0000871913,0.0009935293,0.00022193817,0.000011362662],"category_scores_gemma":[0.00042929727,0.00036419372,0.0002777022,0.00041195832,0.0004024066,0.0000063041693,0.00018654327,0.0005651996,0.0000018647352],"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":[0.00049254304,0.0009039265,0.04550569,0.00008866485,0.00024039675,0.00017417065,0.0004305481,0.0021933317,0.41495162,0.000015841275,0.01824502,0.51675826],"study_design_scores_gemma":[0.006740298,0.015128756,0.7686753,0.000114472474,0.0005302734,0.012574228,0.000592358,0.004578267,0.022629946,0.00008961582,0.16687888,0.0014675993],"about_ca_topic_score_codex":0.000011364575,"about_ca_topic_score_gemma":0.000011813078,"teacher_disagreement_score":0.7231696,"about_ca_system_score_codex":0.000018144723,"about_ca_system_score_gemma":0.00050351856,"threshold_uncertainty_score":0.999881},"labels":[],"label_agreement":null},{"id":"W2148480736","doi":"10.1038/embor.2009.98","title":"Overgrowth of a mouse model of Simpson– Golabi–Behmel syndrome is partly mediated by Indian Hedgehog","year":2009,"lang":"en","type":"article","venue":"EMBO Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":51,"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","funders":"","keywords":"Hedgehog; Indian hedgehog; Hedgehog signaling pathway; Endocrinology; Biology; Internal medicine; Null allele; Mutant; Cell biology; Genetics; Signal transduction; Medicine; Gene","score_opus":0.007241860442712335,"score_gpt":0.223233290584847,"score_spread":0.21599143014213468,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2148480736","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99792075,0.0005314335,0.00034945476,0.00007892258,0.00006175032,0.00016875626,0.000055376488,0.000011293207,0.0008222737],"genre_scores_gemma":[0.99766433,0.00013630273,0.0006331125,0.0002095353,0.000021514305,0.0000055071464,0.00011870242,0.000023696362,0.0011873209],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9983886,0.000020221867,0.0006418277,0.0004056829,0.0002470775,0.00029657784],"domain_scores_gemma":[0.99867743,0.0000065316585,0.00046662835,0.00060825684,0.000111096,0.00013005237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020930175,0.000194125,0.0003402458,0.000056865123,0.0000314862,0.000009723629,0.00014569389,0.00020781922,0.000029340505],"category_scores_gemma":[0.000118642194,0.00019190263,0.00015016716,0.00011785985,0.000059499387,0.0000052550686,0.000078620884,0.00007925481,0.0000020275359],"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":[0.000009149401,0.00015311256,0.011749002,0.000042893913,0.00006626272,0.0000270101,0.00015033493,0.00030611787,0.98346215,0.000005621373,0.0034792034,0.0005491313],"study_design_scores_gemma":[0.000422171,0.00074424245,0.008526343,0.000038988524,0.00003745851,0.0004274795,0.0000850692,0.00072559644,0.9875354,0.0002135342,0.0009137391,0.00032994154],"about_ca_topic_score_codex":0.000043605607,"about_ca_topic_score_gemma":0.0000030363503,"teacher_disagreement_score":0.0040732767,"about_ca_system_score_codex":0.00000974753,"about_ca_system_score_gemma":0.00011407502,"threshold_uncertainty_score":0.7825562},"labels":[],"label_agreement":null},{"id":"W2149392393","doi":"10.1534/genetics.107.081562","title":"Parental Effect of DNA (Cytosine-5) Methyltransferase 1 on Grandparental-Origin-Dependent Transmission Ratio Distortion in Mouse Crosses and Human Families","year":2008,"lang":"en","type":"article","venue":"Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; Hospital for Sick Children; SickKids Foundation; University of Toronto; McGill University Health Centre; McGill University","funders":"Canadian Institutes of Health Research; Ontario Genomics; Ontario Genomics Institute; Genome Canada; McGill University","keywords":"Offspring; Allele; Biology; Genetics; Mendelian inheritance; Genotype; Meiotic drive; Gene; Pregnancy","score_opus":0.011777863219230357,"score_gpt":0.2620949342952634,"score_spread":0.25031707107603307,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149392393","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997777,0.0008858297,0.0009003083,0.00001023135,0.000064597465,0.00026045585,0.000022130305,0.0000066588104,0.00007277572],"genre_scores_gemma":[0.9982538,0.0012788736,0.00018610421,0.000014609231,0.000040101237,0.00001684198,0.000086697844,0.000022494749,0.000100480574],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99891734,0.00008406019,0.00030545078,0.00032338692,0.0001668076,0.00020297522],"domain_scores_gemma":[0.99961215,0.000014819519,0.00005708741,0.00021743272,0.000024273178,0.000074219024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011668824,0.00019480202,0.00022275503,0.00007044615,0.000109877925,0.0000114794875,0.00009556305,0.000110002504,0.000008012482],"category_scores_gemma":[0.000013254987,0.00017458799,0.0000745958,0.00006198852,0.00012689289,0.0000031735883,0.00003236549,0.00007315999,0.0000010649716],"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":[0.000056841138,0.00009373841,0.14456311,0.000054847056,0.000015633846,0.000002952355,0.00016735423,0.0002843035,0.8519908,0.0000029108123,0.000014429956,0.0027530715],"study_design_scores_gemma":[0.0014316482,0.001479382,0.11321902,0.00002438242,0.000016863412,0.000027702046,0.00004726656,0.000030052966,0.8831936,0.000004925093,0.00036122213,0.00016390259],"about_ca_topic_score_codex":0.000059990343,"about_ca_topic_score_gemma":0.00006868841,"teacher_disagreement_score":0.031344086,"about_ca_system_score_codex":0.000013691766,"about_ca_system_score_gemma":0.000022438275,"threshold_uncertainty_score":0.7119491},"labels":[],"label_agreement":null},{"id":"W2149401378","doi":"10.1093/hmg/ddv159","title":"Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the<i>Magel2</i>-null mouse model of Prader–Willi syndrome","year":2015,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Women and Children’s Health Research Institute; University of Alberta","funders":"National Institutes of Health","keywords":"Leptin; Endocrinology; Internal medicine; Biology; Hypothalamus; Appetite; Leptin receptor; Obesity; Medicine","score_opus":0.030246119260698652,"score_gpt":0.2715109135179633,"score_spread":0.24126479425726466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149401378","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997028,0.00083415635,0.0013353172,0.000094384384,0.0000310538,0.00048842974,0.000039485043,0.0000059882173,0.0001431644],"genre_scores_gemma":[0.9963135,0.00004127535,0.0033209808,0.0001233318,0.000019994148,0.000020210187,0.00006992747,0.000048648842,0.00004210737],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99779445,0.0003641079,0.00060568354,0.00045478359,0.00037396408,0.00040703217],"domain_scores_gemma":[0.99873525,0.000022299204,0.00028133634,0.0007218365,0.0001509992,0.000088264496],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0007039347,0.00026996105,0.00035788878,0.00014200706,0.000029138817,0.000019093444,0.00039146226,0.0001783646,0.0000023775451],"category_scores_gemma":[0.0001603776,0.0002570811,0.00013171323,0.00019127956,0.0002201353,0.0000049053974,0.00038447918,0.00020993127,0.0000018326605],"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":[0.000006879967,0.00025523626,0.011459047,0.000048664366,0.000025421428,0.00007568631,0.0003367496,0.025279758,0.9622103,0.000041955722,0.000014816644,0.00024548318],"study_design_scores_gemma":[0.0028588688,0.0015904718,0.20864633,0.00010053218,0.00007176964,0.000837344,0.000601235,0.01818849,0.76563716,0.0007384383,0.00005965673,0.00066970725],"about_ca_topic_score_codex":0.00008900644,"about_ca_topic_score_gemma":0.000121934994,"teacher_disagreement_score":0.19718729,"about_ca_system_score_codex":0.000015942753,"about_ca_system_score_gemma":0.00013770987,"threshold_uncertainty_score":0.99998814},"labels":[],"label_agreement":null},{"id":"W2149922901","doi":"10.1136/jmg.2009.073189","title":"Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human","year":2009,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Institute of Genetics; Division of Materials Research","keywords":"GNAS complex locus; Differentially methylated regions; DNA methylation; Intracytoplasmic sperm injection; Methylation; Andrology; Epigenetics; Genomic imprinting; Biology; Pregnancy; In vitro fertilisation; Genetics; Medicine; DNA; Gene","score_opus":0.015872666162309954,"score_gpt":0.31207971366024956,"score_spread":0.2962070474979396,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149922901","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99346316,0.0008726783,0.0029107032,0.002364081,0.00014372727,0.000099812976,9.161656e-7,0.0000031944176,0.00014175697],"genre_scores_gemma":[0.99676,0.00060681027,0.0023983198,0.000063560474,0.00014669151,0.0000012196718,0.0000010887677,0.0000057081656,0.000016594482],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99826306,0.00015768831,0.00069120806,0.00020878087,0.00051793916,0.0001613515],"domain_scores_gemma":[0.99882597,0.000043977238,0.00045091406,0.00041736916,0.0002129114,0.0000488721],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0025746936,0.000101587095,0.00023237302,0.000059202892,0.000034565208,0.000011325514,0.00049714185,0.00024105063,0.000016349126],"category_scores_gemma":[0.002339131,0.00006992108,0.000097724245,0.0001587274,0.00016157376,0.0000027347714,0.00012857784,0.0002929864,3.512054e-7],"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":[0.000015545742,0.00014594267,0.0043423176,0.000010790091,0.000029598847,0.0000025949903,0.00008187497,0.00006331588,0.839981,0.000055076813,0.000056921413,0.15521501],"study_design_scores_gemma":[0.0003800391,0.0006434699,0.2584358,0.000052010433,0.000020662184,0.00007875968,0.00022263621,0.000053018142,0.73758185,0.0015410741,0.0009067093,0.00008397194],"about_ca_topic_score_codex":0.0000032693156,"about_ca_topic_score_gemma":0.0000031071,"teacher_disagreement_score":0.25409347,"about_ca_system_score_codex":0.00001718645,"about_ca_system_score_gemma":0.000115511415,"threshold_uncertainty_score":0.28512987},"labels":[],"label_agreement":null},{"id":"W2149956363","doi":"10.1093/nar/gkr871","title":"Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2","year":2011,"lang":"en","type":"article","venue":"Nucleic Acids Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"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","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genomic imprinting; Polyadenylation; Genetics; Allele; Locus (genetics); Gene; RNA interference; Imprinting (psychology); Regulation of gene expression; RNA; Gene expression; DNA methylation","score_opus":0.06589112043073807,"score_gpt":0.32226184858656487,"score_spread":0.2563707281558268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149956363","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98862237,0.0015387135,0.00027391434,0.000268426,0.00015029116,0.0004100534,0.000012443702,0.00001722803,0.008706564],"genre_scores_gemma":[0.9820202,0.00085889833,0.00070964923,0.000054167092,0.00024763143,0.000038743274,0.00006643197,0.0000493542,0.015954938],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99772346,0.00027387476,0.0002766311,0.0005898542,0.00050463586,0.00063153135],"domain_scores_gemma":[0.9986227,0.000043583543,0.00008319675,0.0008480946,0.00025472543,0.00014766025],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0008694447,0.0001933099,0.00015501799,0.000086143664,0.00053017214,0.00005447757,0.00062172743,0.00018889937,0.0015275516],"category_scores_gemma":[0.00011571625,0.00014771274,0.00008775489,0.00021341482,0.00040574322,0.0000064607207,0.0013043901,0.00024003655,0.0005474328],"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":[0.000056545286,0.000040931685,0.003640854,0.000007200611,0.000056252946,0.0000066300227,0.00053891656,0.000005436725,0.9822134,0.00006822914,0.0027918457,0.010573791],"study_design_scores_gemma":[0.0003788028,0.00031490464,0.071294144,0.0000101593905,0.000005448979,0.00007860466,0.00017707417,0.000108670356,0.8551444,0.00011910517,0.07220147,0.00016720979],"about_ca_topic_score_codex":0.00018644301,"about_ca_topic_score_gemma":0.00007660649,"teacher_disagreement_score":0.12706897,"about_ca_system_score_codex":0.0001097748,"about_ca_system_score_gemma":0.000043233344,"threshold_uncertainty_score":0.9993852},"labels":[],"label_agreement":null},{"id":"W2150199104","doi":"10.1098/rspb.2010.2627","title":"The evolutionary biology of child health","year":2011,"lang":"en","type":"review","venue":"Proceedings of the Royal Society B Biological Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Simon Fraser University","funders":"","keywords":"Biology; Epigenetics; Context (archaeology); Genomic imprinting; Offspring; Evolutionary developmental biology; Disease; Lineage (genetic); Human evolution; Developmental psychology; Evolutionary biology; Genetics; Gene; Psychology; Medicine; Pregnancy; DNA methylation","score_opus":0.043785028226027416,"score_gpt":0.3046800626499651,"score_spread":0.2608950344239377,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2150199104","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.002392427,0.9946133,0.000008165146,0.00018912448,0.00018116565,0.00036223515,0.000019116316,0.0000059272334,0.0022285755],"genre_scores_gemma":[0.008728863,0.99026364,0.0006254689,0.000082773775,0.00012438982,0.00002498877,0.0000052256537,0.000007339669,0.00013730249],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99846065,0.00004614071,0.0005386451,0.00043918003,0.00012722264,0.00038815165],"domain_scores_gemma":[0.9987713,0.000047280653,0.0008888697,0.00013902293,0.00009896558,0.000054563465],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011128242,0.00022557651,0.0005806045,0.000010779373,0.0005758569,0.000015623851,0.0014905742,0.00033217508,0.00001053278],"category_scores_gemma":[0.00023260295,0.00009233444,0.0008630486,0.00026413435,0.0019079449,0.0000016933543,0.000921737,0.00019173192,0.0000014859148],"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":[0.0000058736755,0.00016594806,0.010689047,0.0025257135,0.00039055504,1.0383387e-8,0.00010900032,0.0000011544117,0.00045769996,0.009103231,0.010018538,0.96653324],"study_design_scores_gemma":[0.000054489115,0.0006741641,0.0013448059,0.0007606977,0.00003978552,0.000011514436,0.00013701728,0.000009534853,0.00015446957,0.000545222,0.9960883,0.0001799937],"about_ca_topic_score_codex":0.000035027828,"about_ca_topic_score_gemma":2.915248e-7,"teacher_disagreement_score":0.98606974,"about_ca_system_score_codex":0.000016158636,"about_ca_system_score_gemma":0.00015963434,"threshold_uncertainty_score":0.7029903},"labels":[],"label_agreement":null},{"id":"W2151613979","doi":"10.1093/hmg/11.15.1743","title":"Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32","year":2002,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":73,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"RIKEN; Canadian Institutes of Health Research; Dunhill Medical Trust; Wellcome Trust; Howard Hughes Medical Institute","keywords":"Biology; Genomic imprinting; Genetics; Locus (genetics); Exon; Uniparental disomy; Molecular biology; Gene; Intron; Gene expression; Chromosome; Karyotype; DNA methylation","score_opus":0.015122352090671805,"score_gpt":0.25423701111710145,"score_spread":0.23911465902642964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2151613979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986418,0.00022240778,0.0004514409,0.000052723983,0.00004632429,0.00029722485,0.000009164472,0.000007547111,0.0002714003],"genre_scores_gemma":[0.9992834,0.00015213943,0.00012785615,0.0001135401,0.000060494393,0.000014693806,0.0001338386,0.00003112882,0.00008294588],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986993,0.00014004864,0.00037081476,0.00038547505,0.00019242289,0.00021191953],"domain_scores_gemma":[0.99908227,0.000004580847,0.00017399972,0.00061615184,0.000067672205,0.00005531293],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019657786,0.00017851808,0.00015265265,0.00008987925,0.00010752784,0.000056767985,0.00025644738,0.00012547975,0.000020445723],"category_scores_gemma":[0.000022265744,0.0001669151,0.000052042524,0.00012420383,0.00010937426,0.0000048274414,0.00007747871,0.00009833078,0.00000469974],"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":[0.0000016227525,0.00015485732,0.00091265043,0.000020104675,0.00001380934,0.000008114851,0.00018270513,0.00003750063,0.99651474,0.00014788791,0.0000082048655,0.0019977903],"study_design_scores_gemma":[0.00048033084,0.00055342284,0.19369127,0.000025055551,0.000023726494,0.000045044333,0.00005218321,0.00051016477,0.804017,0.000088242006,0.00031045594,0.00020308002],"about_ca_topic_score_codex":0.000011332866,"about_ca_topic_score_gemma":0.000011757483,"teacher_disagreement_score":0.19277862,"about_ca_system_score_codex":0.000008070878,"about_ca_system_score_gemma":0.00000812053,"threshold_uncertainty_score":0.68065995},"labels":[],"label_agreement":null},{"id":"W2153171596","doi":"10.1016/s1499-2671(09)33014-2","title":"Loss of the Prader-Willi Syndrome candidate gene Magel2 alters appetite energy balance","year":2009,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Appetite; Medicine; Endocrinology; Circadian rhythm; Internal medicine; Insulin resistance; Obesity; Wakefulness; Candidate gene; Failure to thrive; Hypothalamus; Gene; Biology; Psychiatry; Genetics","score_opus":0.004081531698462292,"score_gpt":0.18517318805977248,"score_spread":0.1810916563613102,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153171596","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9955632,0.002842581,0.000063076106,0.0009987886,0.00028620212,0.00004048904,0.000022498623,9.47069e-7,0.00018222847],"genre_scores_gemma":[0.99871916,0.000073891446,0.000274572,0.0005922312,0.00012865083,7.0476517e-7,0.000005465732,0.000012178153,0.00019312231],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99907154,0.000046391142,0.00029879567,0.00013048538,0.00011313913,0.00033966333],"domain_scores_gemma":[0.9991028,0.00000709859,0.00025786014,0.00026320486,0.00010146521,0.00026761225],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014674972,0.00012321163,0.00019440587,0.00007222945,0.00007308761,0.000025630725,0.0003851471,0.0000774009,0.000022529885],"category_scores_gemma":[0.00006539678,0.000095516756,0.00014347851,0.000111624686,0.00010365248,0.0000054788834,0.00002124791,0.000087291904,9.63058e-7],"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":[5.508978e-7,0.00001942117,0.65633786,0.000031218784,0.00017742284,0.000008750121,0.00008251855,0.00041986993,0.33350664,0.00008000749,0.001889626,0.007446114],"study_design_scores_gemma":[0.00046817024,0.00048205158,0.8573237,0.00016146274,0.00003963801,0.00020541337,0.00003926356,0.000037512673,0.11945216,0.00021956768,0.02135899,0.0002120613],"about_ca_topic_score_codex":0.00018155195,"about_ca_topic_score_gemma":0.00052376377,"teacher_disagreement_score":0.2140545,"about_ca_system_score_codex":0.000021643638,"about_ca_system_score_gemma":0.000379268,"threshold_uncertainty_score":0.38950604},"labels":[],"label_agreement":null},{"id":"W2153415070","doi":"10.1093/hmg/9.12.1813","title":"Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype","year":2000,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":159,"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":"University of Miami","keywords":"Imprinting (psychology); Biology; Genomic imprinting; In situ hybridization; Phenotype; Gene; Northern blot; Gene expression; Genetics; Central nervous system; Endocrinology; Molecular biology; DNA methylation","score_opus":0.0047517378301911856,"score_gpt":0.2183205789854818,"score_spread":0.21356884115529062,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153415070","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99334306,0.0052211587,0.00020188084,0.00005912445,0.00002612913,0.0003538704,0.000002822397,0.000009897481,0.0007820499],"genre_scores_gemma":[0.99621534,0.0006974534,0.0027675615,0.000065053086,0.000039942788,0.000021653615,0.000012075114,0.00004413286,0.00013678393],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99836403,0.00014694982,0.0004531584,0.0004945856,0.00016304542,0.000378252],"domain_scores_gemma":[0.99919516,0.000023263547,0.00015139724,0.0005017203,0.00004697141,0.000081510145],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037873982,0.0002479076,0.00030782897,0.00006921642,0.00013231857,0.000046956517,0.00024302595,0.00016457732,0.000045130415],"category_scores_gemma":[0.000057052046,0.00021276115,0.00007805707,0.00010613414,0.00032395485,0.000004132282,0.00040437974,0.0001790268,0.0000021749881],"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":[0.000007357861,0.000045420355,0.018160824,0.000061821906,0.00003311963,0.000007846241,0.0002977031,0.00023872884,0.9662128,0.00008970204,0.0000031689292,0.014841526],"study_design_scores_gemma":[0.0044882996,0.0006573096,0.74796593,0.00016535977,0.000085783104,0.0006676031,0.00048322944,0.0010322722,0.24145117,0.0013008659,0.0010486445,0.0006535196],"about_ca_topic_score_codex":0.000093765026,"about_ca_topic_score_gemma":0.000019778083,"teacher_disagreement_score":0.7298051,"about_ca_system_score_codex":0.000007054155,"about_ca_system_score_gemma":0.000023789118,"threshold_uncertainty_score":0.8676148},"labels":[],"label_agreement":null},{"id":"W2153563181","doi":"10.1095/biolreprod.110.085480","title":"Side-by-Side Comparison of Five Commercial Media Systems in a Mouse Model: Suboptimal In Vitro Culture Interferes with Imprint Maintenance1","year":2010,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":208,"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 Gender and Health; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; March of Dimes Foundation","keywords":"Genomic imprinting; Biology; Embryo culture; Imprinting (psychology); Blastocyst; Embryo; Epigenetics; DNA methylation; Andrology; Genetics; In vivo; Reproductive technology; Embryogenesis; Cell biology; Gene expression; Gene; Medicine","score_opus":0.012117768231121847,"score_gpt":0.2601739981159074,"score_spread":0.24805622988478557,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153563181","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99708384,0.0011131073,0.0011147653,0.000085840074,0.00025130066,0.00026894684,0.000024704827,0.000005726877,0.000051748142],"genre_scores_gemma":[0.99717575,0.00009134165,0.0024210368,0.000005430736,0.00009108241,0.00002886582,0.00009017564,0.000012448452,0.00008389312],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99879795,0.0000651606,0.00041668574,0.00045594148,0.00005951077,0.00020472682],"domain_scores_gemma":[0.99921614,0.000008961895,0.00024543068,0.0003811343,0.00011780543,0.000030506404],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030356713,0.0001393419,0.0003330585,0.000074791824,0.000016696233,0.000004254123,0.00015033665,0.00024059645,0.0000011771273],"category_scores_gemma":[0.00016743933,0.00011298946,0.00004411391,0.000076912045,0.0002030644,0.000004458512,0.00008957564,0.00021907108,4.2198369e-7],"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":[0.00021719771,0.00011161722,0.024768963,0.000031174946,0.000019728885,1.886249e-7,0.0003767624,0.0014910324,0.9676161,0.00002515004,0.000057521527,0.005284552],"study_design_scores_gemma":[0.0006303265,0.00035242413,0.008135062,0.000022909617,0.000006835802,0.000023268873,0.0006495455,0.0017143103,0.9878423,0.000028063927,0.00046072184,0.00013419808],"about_ca_topic_score_codex":0.00063555845,"about_ca_topic_score_gemma":0.0004597489,"teacher_disagreement_score":0.020226223,"about_ca_system_score_codex":0.000012100204,"about_ca_system_score_gemma":0.00004041405,"threshold_uncertainty_score":0.46075764},"labels":[],"label_agreement":null},{"id":"W2153779221","doi":"10.1136/jmg.39.2.81","title":"Current status of human chromosome 14","year":2002,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Fondation pour la Recherche Médicale; University of Alberta; March of Dimes Foundation","keywords":"Genetics; Biology; Genomic imprinting; Chromosome; Gene map; Gene; Imprinting (psychology); Gene mapping; Chromosome 21; Karyotype; Epigenetics; Uniparental disomy; Human genome; Genetic marker; Chromosome 7 (human); Genome; DNA methylation","score_opus":0.05429683282768185,"score_gpt":0.37063017859228553,"score_spread":0.3163333457646037,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153779221","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0035403261,0.994971,0.00016066877,0.000015437088,0.0009990281,0.00015092408,0.000018045523,0.000001848924,0.00014274813],"genre_scores_gemma":[0.00048081754,0.9974323,0.00045305825,0.000015747524,0.0014390767,0.0000029260525,0.000030530053,0.000053764627,0.000091782684],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99621814,0.00017709244,0.0016961471,0.0002585885,0.0011848063,0.00046523917],"domain_scores_gemma":[0.9972313,0.0000338045,0.0014936934,0.00042420684,0.0002487635,0.00056822255],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00060163025,0.00034300893,0.0013912589,0.00015597232,0.000037629838,0.000019881583,0.0008669901,0.00063670985,0.00033528992],"category_scores_gemma":[0.00042538028,0.00026223544,0.0008115578,0.00015075725,0.0001590719,0.000001379948,0.0003443961,0.000667894,0.0000091508955],"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":[8.6033816e-7,0.00018201089,0.000047644775,0.0035228706,0.00022625791,0.0000135495075,0.000016730883,0.0000015147604,0.00018703542,0.000005417537,0.0028620458,0.99293405],"study_design_scores_gemma":[0.0004335188,0.0008948887,0.000035430476,0.00561697,0.00044775187,0.00056396646,0.000009577862,0.0000049143887,0.00015249598,0.000010923999,0.99159247,0.00023707243],"about_ca_topic_score_codex":0.0000018404046,"about_ca_topic_score_gemma":0.0000012771765,"teacher_disagreement_score":0.992697,"about_ca_system_score_codex":0.000033577515,"about_ca_system_score_gemma":0.00071038917,"threshold_uncertainty_score":0.999983},"labels":[],"label_agreement":null},{"id":"W2154296562","doi":"10.1002/gene.1077","title":"Imprinting defects in mouse embryos: stochastic errors or polymorphic phenotype?","year":2001,"lang":"en","type":"article","venue":"genesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University Health Centre; Montreal Children's Hospital; Royal Victoria Hospital","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Embryo; Genetics; Phenotype; Carcinogenesis; Zygote; Gene; Embryogenesis; Gene expression; DNA methylation","score_opus":0.015466178723298314,"score_gpt":0.24311727330939673,"score_spread":0.22765109458609842,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2154296562","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953367,0.0007875896,0.0030692175,0.000055976896,0.00016292783,0.00017831929,0.0000030801577,0.000023560027,0.00038261325],"genre_scores_gemma":[0.99633205,0.000118205666,0.0010931725,0.00017795066,0.00017379457,0.000028722347,0.00001346163,0.000045384597,0.002017271],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986151,0.000049488586,0.00027663886,0.00044588602,0.0001291652,0.00048372694],"domain_scores_gemma":[0.99935085,0.000016225833,0.00008402827,0.00040491205,0.000041016552,0.00010298144],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019475624,0.00020421948,0.0001904986,0.00010802655,0.00008047531,0.000027797454,0.00022979555,0.00014804899,0.000105516316],"category_scores_gemma":[0.0001695783,0.0001884562,0.00009218444,0.00023976222,0.000036769292,0.0000036017607,0.00019265464,0.00007832443,0.00005463729],"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":[0.000045263892,0.0000702569,0.038155325,0.00002392149,0.000034007015,0.000013609583,0.00009341442,0.0017878589,0.94540894,0.000008687822,0.00007133816,0.014287353],"study_design_scores_gemma":[0.004130876,0.00096262,0.6366784,0.00012936803,0.00011314786,0.0006250518,0.0018242433,0.0031625591,0.3443998,0.000116340045,0.0058427104,0.0020148568],"about_ca_topic_score_codex":0.00020985688,"about_ca_topic_score_gemma":0.0002513572,"teacher_disagreement_score":0.60100913,"about_ca_system_score_codex":0.000019245605,"about_ca_system_score_gemma":0.00007830121,"threshold_uncertainty_score":0.768502},"labels":[],"label_agreement":null},{"id":"W2155873540","doi":"10.1016/j.rbmo.2012.03.019","title":"The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineage","year":2012,"lang":"en","type":"review","venue":"Reproductive BioMedicine Online","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"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":"Genomic imprinting; Biology; Allele; Gene; Epigenetics; Genetics; Trophoblast; Imprinting (psychology); Lineage (genetic); Function (biology); Embryonic stem cell; Placenta; DNA methylation; Gene expression; Fetus","score_opus":0.023818092567878087,"score_gpt":0.29536693831677374,"score_spread":0.27154884574889565,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2155873540","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.03076273,0.9669998,0.000093678056,0.00017444737,0.0007442243,0.001069271,0.000068849455,0.000011781609,0.00007518201],"genre_scores_gemma":[0.009128332,0.9853798,0.00023286632,0.000060113634,0.0036255042,0.00008361351,0.00079750305,0.00007062792,0.0006216134],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.997214,0.00029901558,0.0007167677,0.0009729048,0.00027047098,0.0005268025],"domain_scores_gemma":[0.99811804,0.000071059134,0.0004151057,0.0011913322,0.00009684694,0.0001076157],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0012406742,0.00050352147,0.0007092447,0.00013861859,0.00016965307,0.00003843545,0.00047142594,0.00029931767,0.000009565863],"category_scores_gemma":[0.00017407042,0.000268253,0.00022641769,0.000425326,0.00031122332,0.0000047012977,0.00041955715,0.00046032193,0.0000133741705],"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":[0.000056004068,0.0003567984,0.00019388355,0.0015144149,0.0002513364,0.0000068753575,0.00011971938,4.127523e-7,0.033593573,0.0000053077842,0.00023856827,0.9636631],"study_design_scores_gemma":[0.00054554373,0.0005458992,0.0022790702,0.00032887748,0.00044140895,0.00051338255,0.00033848442,0.0000053788735,0.00088812545,0.0000031779173,0.99379116,0.00031947187],"about_ca_topic_score_codex":0.000044935172,"about_ca_topic_score_gemma":0.000019517589,"teacher_disagreement_score":0.9935526,"about_ca_system_score_codex":0.000051426174,"about_ca_system_score_gemma":0.00012554052,"threshold_uncertainty_score":0.999977},"labels":[],"label_agreement":null},{"id":"W2157980542","doi":"10.1095/biolreprod.111.096602","title":"Loss of Genomic Imprinting in Mouse Embryos with Fast Rates of Preimplantation Development in Culture1","year":2012,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":97,"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 Gender and Health; Canadian Institutes of Health Research; Natural Sciences and Engineering Research Council of Canada; Children's Health Research Institute","keywords":"Genomic imprinting; Embryo; Biology; Imprinting (psychology); Embryogenesis; Andrology; Embryo culture; Genetics; Embryonic stem cell; Methylation; Inner cell mass; Blastocyst; Cell fate determination; Epigenetics; DNA methylation; Cell biology; Gene expression; Gene; Transcription factor","score_opus":0.01314233626520992,"score_gpt":0.2533268614587991,"score_spread":0.2401845251935892,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2157980542","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99864733,0.00080267654,0.0002935699,0.000009711956,0.00006805519,0.00014187086,0.0000017248645,0.0000016784784,0.000033353663],"genre_scores_gemma":[0.9951657,0.00011041705,0.0045817997,0.0000014265266,0.000041570867,0.000008251572,0.00003382517,0.0000058983583,0.000051109473],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992801,0.0000423066,0.0003065699,0.00020459319,0.000032639353,0.00013378466],"domain_scores_gemma":[0.9995367,0.000003946806,0.00022563581,0.00016230834,0.00005820557,0.000013229148],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034136468,0.00007147333,0.0001454193,0.00006818798,0.000009721565,8.13439e-7,0.00005546986,0.000083481,0.000002455366],"category_scores_gemma":[0.00004649144,0.000060919574,0.000018005478,0.00006452464,0.000063541185,0.0000042021943,0.00004189932,0.000038572252,4.959411e-7],"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":[0.00001963746,0.00003848869,0.41517457,0.000033790802,0.000010920069,2.495623e-8,0.0002606655,0.00007064694,0.57966214,0.000007346685,6.0307696e-7,0.004721172],"study_design_scores_gemma":[0.00018929214,0.00007369252,0.41105384,0.000011009505,0.0000019363697,0.00001565699,0.00019515779,0.0000023090452,0.5883,0.0000026903704,0.000115136296,0.00003926191],"about_ca_topic_score_codex":0.0000844556,"about_ca_topic_score_gemma":0.00003748789,"teacher_disagreement_score":0.008637891,"about_ca_system_score_codex":0.000009603987,"about_ca_system_score_gemma":0.000032923384,"threshold_uncertainty_score":0.24842282},"labels":[],"label_agreement":null},{"id":"W2158230043","doi":"10.1093/carcin/bgp254","title":"Loss of imprinting of the insulin-like growth factor II (IGF2) gene in esophageal normal and adenocarcinoma tissues","year":2009,"lang":"en","type":"article","venue":"Carcinogenesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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 Saskatchewan","funders":"Saskatchewan Health Research Foundation","keywords":"Imprinting (psychology); Internal medicine; Esophageal cancer; Genomic imprinting; Medicine; Gastroenterology; Insulin-like growth factor 2; Adenocarcinoma; Esophageal disease; Gene expression; Esophagus; Cancer; Growth factor; Biology; Gene; DNA methylation; Receptor","score_opus":0.00875851256152868,"score_gpt":0.2193568262374987,"score_spread":0.21059831367597,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2158230043","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99299544,0.0065448727,0.00004891546,0.00006682073,0.00009426082,0.00015663153,0.00001558291,0.0000038146677,0.00007366775],"genre_scores_gemma":[0.99889994,0.00026552365,0.00060611655,0.000066816094,0.000070228576,0.0000034953705,0.0000057314815,0.000015011322,0.00006715774],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99887615,0.000056602752,0.00036654863,0.00029999495,0.00014321355,0.00025748243],"domain_scores_gemma":[0.9993273,0.00001127339,0.00016157591,0.00034476235,0.00009753929,0.000057521615],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013822057,0.00016531127,0.00024778975,0.00006241984,0.000068412664,0.0000073161787,0.0002641507,0.00013020141,0.000008255603],"category_scores_gemma":[0.000067848756,0.00013780355,0.00010722695,0.00015965929,0.00010141005,0.0000044257263,0.0002954261,0.00006582351,3.964864e-7],"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":[0.000007810434,0.000027519618,0.5082873,0.000027569311,0.000012809919,0.0000014087941,0.0001792779,0.00001034037,0.48824832,0.000015011599,0.0000036463905,0.003178971],"study_design_scores_gemma":[0.0002613658,0.00013046486,0.53665555,0.000011234077,0.000011005044,0.0000233962,0.000039880524,0.000016941583,0.4627419,0.000015915659,0.0000190371,0.00007330855],"about_ca_topic_score_codex":0.00011390634,"about_ca_topic_score_gemma":0.000013095919,"teacher_disagreement_score":0.028368236,"about_ca_system_score_codex":0.000009123907,"about_ca_system_score_gemma":0.000050255505,"threshold_uncertainty_score":0.56194663},"labels":[],"label_agreement":null},{"id":"W2158310202","doi":"10.1111/j.0006-341x.2001.01074.x","title":"Statistical Analysis of Uniparental Disomy Data Using Hidden Markov Models","year":2001,"lang":"en","type":"article","venue":"Biometrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institutes of Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute for Health and Care Research; March of Dimes Foundation","keywords":"Nondisjunction; Uniparental disomy; Computer science; Crossover; Markov chain; Hidden Markov model; International HapMap Project; Set (abstract data type); Data set; Genetic genealogy; Chromosome; Genetics; Machine learning; Artificial intelligence; Biology; Single-nucleotide polymorphism; Genotype; Aneuploidy","score_opus":0.08566248651909217,"score_gpt":0.33077814357963814,"score_spread":0.24511565706054597,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2158310202","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8435324,0.0006351499,0.15497755,0.000008200712,0.00007277601,0.000056607165,0.0003505852,0.000003987232,0.00036278763],"genre_scores_gemma":[0.96615726,0.0002908495,0.03222671,0.00001799059,0.000045636272,8.4853093e-7,0.0011679459,0.000012793803,0.00007993945],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99892974,0.00003257104,0.00026670514,0.00035256366,0.00020403686,0.00021438405],"domain_scores_gemma":[0.9990313,0.000026150414,0.00010285868,0.00068700494,0.000069424816,0.00008326059],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020688427,0.0001080858,0.00020737368,0.00064319593,0.00003773622,0.000021207297,0.00039832733,0.00008970881,0.000052823485],"category_scores_gemma":[0.0001591041,0.000105224855,0.00006960697,0.0028240806,0.000061536215,0.0000052227497,0.0005086332,0.000030428102,0.0000011864626],"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":[0.000037308382,0.0004336126,0.5981001,0.00005277786,0.0022463596,0.00001270811,0.000039728417,0.0013613496,0.24939474,0.00020839769,0.0011076115,0.14700526],"study_design_scores_gemma":[0.0011620963,0.00039032524,0.48610967,0.00001856742,0.0023729154,0.00007494916,0.00037742502,0.48805714,0.007339659,0.00014231067,0.013139625,0.0008153035],"about_ca_topic_score_codex":0.0001361694,"about_ca_topic_score_gemma":0.000014404733,"teacher_disagreement_score":0.4866958,"about_ca_system_score_codex":0.000012476773,"about_ca_system_score_gemma":0.000042531883,"threshold_uncertainty_score":0.42909452},"labels":[],"label_agreement":null},{"id":"W2160062138","doi":"10.6000/2292-2598.2015.03.03.2","title":"Somatic Mosaicism as Modulator of the Global and Intellectual Phenotype in Epimutated Angelman Syndrome Patients","year":2015,"lang":"en","type":"article","venue":"Journal of Intellectual Disability - Diagnosis and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Istituto Auxologico Italiano","keywords":"Angelman syndrome; UBE3A; Genomic imprinting; Genetics; Uniparental disomy; Imprinting (psychology); Biology; Allele; Intellectual disability; Chromosome 15; Multiplex ligation-dependent probe amplification; Neurodevelopmental disorder; DNA methylation; Chromosome; Gene; Ubiquitin ligase; Karyotype; Exon; Gene expression; Ubiquitin","score_opus":0.020153219625386146,"score_gpt":0.26101897959989867,"score_spread":0.24086575997451254,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2160062138","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978482,0.0014889624,0.000010618415,0.00015095832,0.00012528201,0.0002671571,0.000016129032,0.0000016207298,0.0000910644],"genre_scores_gemma":[0.9992177,0.0005624539,0.00012485379,0.000033217493,0.000021011978,0.000011539995,0.0000037622344,0.000009314747,0.000016161011],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987823,0.00013469571,0.0005115833,0.00020860793,0.00018657673,0.00017628264],"domain_scores_gemma":[0.99917173,0.00015388356,0.00019203208,0.00019951824,0.00013565258,0.0001471795],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019739933,0.0001828086,0.00033949275,0.000028366856,0.000039301245,0.000022166745,0.00012673056,0.00008862273,0.000036475827],"category_scores_gemma":[0.0017370745,0.00011552899,0.00012061681,0.00014175108,0.00022257783,0.000008617387,0.00014226182,0.00006659714,0.0000015578398],"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":[0.0000845385,0.0012905916,0.9808611,0.000026317923,0.00017662908,0.0000025836318,0.0016902183,0.00009226961,0.00019922665,0.000007737246,0.00020502262,0.015363724],"study_design_scores_gemma":[0.0027129035,0.006055717,0.98020977,0.00014083851,0.00012612181,0.00018855915,0.0013928004,0.00031137583,0.0072322865,0.00076396606,0.00066195015,0.00020368978],"about_ca_topic_score_codex":0.00018493844,"about_ca_topic_score_gemma":0.00010120348,"teacher_disagreement_score":0.0151600335,"about_ca_system_score_codex":0.00013783367,"about_ca_system_score_gemma":0.00008644793,"threshold_uncertainty_score":0.47111353},"labels":[],"label_agreement":null},{"id":"W2160251268","doi":"10.1093/hmg/ddg194","title":"Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5","year":2003,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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":"Silencer; Biology; CTCF; Imprinting (psychology); Genomic imprinting; CpG site; Enhancer; Gene; Genetics; Insulator (electricity); Locus (genetics); Promoter; Intron; DNA methylation; Gene expression","score_opus":0.0178322690328141,"score_gpt":0.26710147119353295,"score_spread":0.24926920216071885,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2160251268","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99597156,0.00227307,0.0003678128,0.000024924817,0.00004983725,0.00024360222,0.0000017749643,0.0000046268733,0.0010627765],"genre_scores_gemma":[0.9990622,0.00020071634,0.0004682027,0.0001288382,0.00002927457,0.0000173889,0.000012503216,0.000023579774,0.000057328783],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986943,0.00016769698,0.0003342448,0.00035852476,0.00017908604,0.00026614303],"domain_scores_gemma":[0.99923915,0.0000077627465,0.00012762855,0.00050739426,0.00006436395,0.000053727275],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002463682,0.00018357717,0.00017599954,0.000065954526,0.00009500696,0.000030322799,0.0002755131,0.0001365957,0.000013612696],"category_scores_gemma":[0.00004989284,0.00015665528,0.00007391272,0.00013734821,0.00019957725,0.000002321297,0.00009655848,0.00010941679,0.0000011922156],"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":[0.0000011899539,0.000052882195,0.013893567,0.000027339645,0.00002011278,0.000011919063,0.00020630418,0.0000425375,0.9840564,0.001420136,0.000019975998,0.0002476193],"study_design_scores_gemma":[0.00097087113,0.0009871064,0.1505743,0.00006223383,0.000043415228,0.00027203513,0.0006477821,0.00003941924,0.84121233,0.0026176507,0.002136739,0.00043613074],"about_ca_topic_score_codex":0.00003223295,"about_ca_topic_score_gemma":0.000026029331,"teacher_disagreement_score":0.14284411,"about_ca_system_score_codex":0.000008160719,"about_ca_system_score_gemma":0.000039197428,"threshold_uncertainty_score":0.6388217},"labels":[],"label_agreement":null},{"id":"W2161157021","doi":"10.1210/en.2003-0591","title":"Defining Regulatory Regions in the Rat Prolactin Gene Family Locus Using a Large P1 Genomic Clone","year":2003,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Manitoba","funders":"University of Manitoba","keywords":"Biology; Pseudogene; Gene; Placental lactogen; Prolactin; Locus (genetics); Gene family; genomic DNA; Genetics; clone (Java method); Trophoblast; Molecular biology; Gene expression; Placenta; Endocrinology; Fetus; Genome; Hormone","score_opus":0.016414296249345203,"score_gpt":0.25269235302295096,"score_spread":0.23627805677360575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161157021","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9922417,0.0049162353,0.0009893291,0.00011109006,0.0002719744,0.00022634333,0.000003257139,0.000011982102,0.0012281161],"genre_scores_gemma":[0.99580497,0.00019154974,0.0031457832,0.0005536683,0.000066727516,0.000030076462,0.000015885502,0.000028458348,0.00016286923],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9983012,0.0002660286,0.00027943827,0.00041272418,0.00008786605,0.0006527473],"domain_scores_gemma":[0.9992723,0.00002472827,0.000100494784,0.0005314663,0.000027027694,0.000043968055],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027499994,0.00018068605,0.0001890253,0.00007866179,0.00015006258,0.000020117503,0.00025291461,0.00012810776,0.000016020878],"category_scores_gemma":[0.000105641164,0.00015653628,0.00008544174,0.00012843152,0.000080161495,0.0000030905012,0.0001240376,0.00020018255,0.000018566285],"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":[0.000016599724,0.0000788946,0.022316497,0.000009079141,0.000035768815,0.00004022757,0.00017774128,0.000234256,0.97186106,0.004269378,0.00037220624,0.0005882881],"study_design_scores_gemma":[0.0060112556,0.00080807804,0.23898129,0.000046372355,0.00012696565,0.0073293904,0.004538882,0.00042267973,0.45530492,0.0012942503,0.2837512,0.0013847426],"about_ca_topic_score_codex":0.000047064637,"about_ca_topic_score_gemma":0.00004199751,"teacher_disagreement_score":0.51655614,"about_ca_system_score_codex":0.000026051668,"about_ca_system_score_gemma":0.00011360176,"threshold_uncertainty_score":0.6383364},"labels":[],"label_agreement":null},{"id":"W2161327979","doi":"10.1093/hmg/ddp379","title":"The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith–Wiedemann region","year":2009,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; Ontario Institute for Cancer Research; University of Toronto; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Genetics; Epigenetics; Allele; Gene; DNA methylation; Gene expression","score_opus":0.0177984200042024,"score_gpt":0.26338588752506725,"score_spread":0.24558746752086485,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161327979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99209154,0.0015989923,0.0042401496,0.001045374,0.00007028206,0.00048794164,0.0000027667725,0.000008082581,0.00045485402],"genre_scores_gemma":[0.9978892,0.00019480019,0.00056541566,0.00071716297,0.00019519762,0.000016399625,0.00003847962,0.00002583511,0.0003575165],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986568,0.00008432589,0.00031886675,0.0004003462,0.00015020573,0.00038944252],"domain_scores_gemma":[0.9992402,0.000020812618,0.00012099272,0.00049322576,0.00006976753,0.000055008248],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034460647,0.00020306908,0.0001542487,0.00003467476,0.00030967582,0.00012802937,0.00030907444,0.0001263218,0.0000027946278],"category_scores_gemma":[0.000050280287,0.00014844965,0.00011504686,0.00008633255,0.000074412324,0.0000028842328,0.00013578933,0.00012652676,0.0000018525643],"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":[0.0000719367,0.00021515196,0.07264899,0.00010496111,0.00022316886,0.000013150395,0.0013402202,0.00016280537,0.77714247,0.0021661106,0.005061379,0.14084965],"study_design_scores_gemma":[0.0020941086,0.0020237912,0.8284943,0.000086824504,0.0001862193,0.000073506424,0.0011574832,0.0005308098,0.071924865,0.0062291943,0.086505204,0.00069368485],"about_ca_topic_score_codex":0.000013501651,"about_ca_topic_score_gemma":0.000045253677,"teacher_disagreement_score":0.7558453,"about_ca_system_score_codex":0.000010650106,"about_ca_system_score_gemma":0.000017182181,"threshold_uncertainty_score":0.6053601},"labels":[],"label_agreement":null},{"id":"W2161352411","doi":"10.1128/mcb.01435-10","title":"An Extended Domain of <i>Kcnq1ot1</i> Silencing Revealed by an Imprinted Fluorescent Reporter","year":2011,"lang":"en","type":"article","venue":"Molecular and Cellular Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Biology; Gene silencing; Genomic imprinting; DNA methylation; Reporter gene; Molecular biology; Transgene; Genetics; Green fluorescent protein; Gene; Gene expression","score_opus":0.00792062358987711,"score_gpt":0.22517100009757526,"score_spread":0.21725037650769816,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161352411","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95733273,0.0012101482,0.040619813,0.000012375435,0.00009846309,0.00020823044,0.000014448145,0.000015451142,0.0004883696],"genre_scores_gemma":[0.9933568,0.00007230645,0.0060113557,0.00017260863,0.00003995778,0.00001568548,0.00025535954,0.000035937413,0.000039963572],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9981987,0.00022161263,0.000447882,0.00066354586,0.000086295324,0.00038194653],"domain_scores_gemma":[0.99879897,0.0000032892526,0.00019628885,0.0007186373,0.00008954477,0.00019325953],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036441107,0.00024466333,0.00029389377,0.000054255266,0.000063585605,0.00001169919,0.00025787496,0.0002756116,0.000047911977],"category_scores_gemma":[0.000025800102,0.00022916196,0.00010853618,0.00006927971,0.0001798617,0.0000054227226,0.00014563993,0.00009137497,0.0000015373272],"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":[0.00003391255,0.0001605895,0.0072358744,0.000020524232,0.00005997165,0.000015048559,0.0001581533,6.8764695e-7,0.98821086,0.0001431519,0.00002578227,0.0039354335],"study_design_scores_gemma":[0.00055239635,0.0013829311,0.0038879476,0.000010387663,0.00003300004,0.00009781994,0.00022869481,0.00005296106,0.9922333,0.00052057754,0.0007148816,0.00028512502],"about_ca_topic_score_codex":0.00012543872,"about_ca_topic_score_gemma":0.000008684186,"teacher_disagreement_score":0.036024123,"about_ca_system_score_codex":0.0000060288294,"about_ca_system_score_gemma":0.00003693568,"threshold_uncertainty_score":0.93449533},"labels":[],"label_agreement":null},{"id":"W2161588299","doi":"10.1186/1756-8935-4-7","title":"Extensive epigenetic reprogramming in human somatic tissues between fetus and adult","year":2011,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"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; Pacific Centre for Reproductive Medicine; University of British Columbia","funders":"National Institutes of Health; Michael Smith Health Research BC; Canadian Institute for Advanced Research","keywords":"Reprogramming; Biology; Somatic cell; Epigenetics; Human genetics; Fetus; Epigenesis; Cell biology; Genetics; DNA methylation; Pregnancy; Gene; Gene expression","score_opus":0.023080123668449908,"score_gpt":0.2659722796408841,"score_spread":0.2428921559724342,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161588299","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994971,0.002078711,0.0010750085,0.00003461106,0.00007478537,0.0004258724,0.0000060094367,0.000028939863,0.0013050986],"genre_scores_gemma":[0.9778134,0.00031247927,0.021235796,0.00006150699,0.00016466681,0.000047959384,0.000052331572,0.00006325564,0.00024855763],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99778956,0.000119216886,0.00064940157,0.0006829296,0.00018810523,0.00057076116],"domain_scores_gemma":[0.9988294,0.000022860842,0.00021039553,0.0006465022,0.00011395158,0.00017686078],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0002794628,0.00032450166,0.00037832835,0.000115819246,0.00013938086,0.00004772351,0.0002830382,0.0002270021,0.000046445246],"category_scores_gemma":[0.0001802186,0.0003433826,0.00008281828,0.00015746226,0.00016111044,0.0000049937953,0.0002965468,0.00013923549,0.000020562766],"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":[0.0000062631725,0.00014225174,0.4488494,0.00017434964,0.000105618674,0.000023919494,0.0022566312,0.000017812888,0.49549085,0.000096298,0.000074700016,0.052761897],"study_design_scores_gemma":[0.00068915344,0.0006088474,0.69711924,0.000106734005,0.00004599366,0.000038438848,0.0006282174,0.000063138774,0.29880035,0.00074022746,0.0006850259,0.0004746178],"about_ca_topic_score_codex":0.000289031,"about_ca_topic_score_gemma":0.00012878535,"teacher_disagreement_score":0.24826984,"about_ca_system_score_codex":0.000017052454,"about_ca_system_score_gemma":0.000037165137,"threshold_uncertainty_score":0.99990183},"labels":[],"label_agreement":null},{"id":"W2163441749","doi":"10.1002/ajmg.a.20370","title":"Unexpected death and critical illness in Prader–Willi syndrome: Report of ten individuals","year":2003,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":122,"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":"","keywords":"Medicine; Demise; Pediatrics; Adrenal insufficiency; Autopsy; Intensive care medicine; Internal medicine","score_opus":0.012020472643480135,"score_gpt":0.29602827211050986,"score_spread":0.2840077994670297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2163441749","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953143,0.0024097573,0.0012460393,0.00059835945,0.00020119405,0.00007517372,0.000003124449,0.0000019203653,0.0001501509],"genre_scores_gemma":[0.9925698,0.0013314717,0.005832329,0.0001461528,0.00006565262,0.0000037535676,0.0000036648078,0.000020754735,0.00002640506],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9975884,0.0002354248,0.00089938694,0.00025568265,0.0006984477,0.00032268593],"domain_scores_gemma":[0.9986988,0.00009586314,0.00042751405,0.0002539584,0.00016701114,0.000356887],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012292349,0.00016381108,0.00048004446,0.00011618569,0.000033401175,0.000015924788,0.00026052954,0.00014689377,0.000053466865],"category_scores_gemma":[0.0024224168,0.00014162608,0.00009446952,0.00023026361,0.0005150976,0.000003604016,0.0001098492,0.00024541127,6.2499646e-7],"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":[0.00000869092,0.00042322776,0.95475644,0.000069221904,0.00025337233,0.00044323935,0.00045618584,0.00005338625,0.012217564,0.00021364485,0.00038131166,0.030723691],"study_design_scores_gemma":[0.0025519305,0.004768396,0.8845989,0.0004756501,0.00017332031,0.049540423,0.0032590502,0.00009004808,0.016276497,0.0004628698,0.03710554,0.000697359],"about_ca_topic_score_codex":0.00001604757,"about_ca_topic_score_gemma":0.0000041527355,"teacher_disagreement_score":0.07015755,"about_ca_system_score_codex":0.00000967555,"about_ca_system_score_gemma":0.00034505152,"threshold_uncertainty_score":0.5775344},"labels":[],"label_agreement":null},{"id":"W2164252048","doi":"10.1210/jc.2003-030222","title":"A Pituitary-Derived MEG3 Isoform Functions as a Growth Suppressor in Tumor Cells","year":2003,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":448,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"U.S. Public Health Service; National Institutes of Health; Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; Massachusetts General Hospital","keywords":"Pituitary tumors; Biology; Tumor suppressor gene; Corticotropic cell; Pituitary adenoma; Gene isoform; Cancer research; Ectopic expression; MEG3; Gene; Gene expression; Somatic cell; Pituitary gland; Adenoma; Molecular biology; Carcinogenesis; Genetics; Endocrinology; Downregulation and upregulation; Hormone","score_opus":0.022547382130748375,"score_gpt":0.3100039637456756,"score_spread":0.28745658161492726,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164252048","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9925312,0.0031141427,0.00040977617,0.00092767563,0.0014032216,0.00015038175,0.0000041735243,0.0000047235217,0.0014547388],"genre_scores_gemma":[0.99458534,0.0022000812,0.0010837102,0.0012404047,0.00048042703,0.000005844214,0.000001970204,0.000023287288,0.00037894511],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9970319,0.0007499479,0.0012868033,0.00023549826,0.00018892485,0.0005069123],"domain_scores_gemma":[0.99843425,0.0002369182,0.0005708313,0.0003923372,0.00021235441,0.00015334086],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014293574,0.00020297615,0.0006062499,0.000100048856,0.00009024022,0.00001403026,0.00048629823,0.00014363373,0.00015116531],"category_scores_gemma":[0.0017347605,0.00013731702,0.00037022933,0.00013529001,0.00026470653,0.000009832524,0.00013699352,0.0006314882,0.00004303964],"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":[0.00059721136,0.0009675008,0.0144693395,0.000027086355,0.0008355235,0.00013306907,0.0003211753,0.00029167678,0.96923286,0.0022866873,0.0048094797,0.0060283644],"study_design_scores_gemma":[0.008773423,0.001921846,0.23559691,0.00004172064,0.0005572483,0.0054485346,0.0012855341,0.000023678194,0.45215327,0.004222505,0.28943086,0.0005444623],"about_ca_topic_score_codex":0.000043509157,"about_ca_topic_score_gemma":0.000019661999,"teacher_disagreement_score":0.5170796,"about_ca_system_score_codex":0.000006150143,"about_ca_system_score_gemma":0.00022607011,"threshold_uncertainty_score":0.5599626},"labels":[],"label_agreement":null},{"id":"W2164283721","doi":"10.1186/gb-2011-12-3-r25","title":"Genome-wide assessment of imprinted expression in human cells","year":2011,"lang":"en","type":"article","venue":"Genome biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":71,"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 and Génome Québec Innovation Centre","funders":"Canadian Institutes of Health Research; Canada Research Chairs; Genome Canada","keywords":"Biology; Human genetics; Genome Biology; Human genome; Genome; Computational biology; Genomic imprinting; Genetics; Genomics; Computational genomics; Personal genomics; Evolutionary biology; Gene expression; Gene; DNA methylation","score_opus":0.01911953228187124,"score_gpt":0.27028552359692853,"score_spread":0.2511659913150573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164283721","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99233043,0.00027479455,0.0030641637,0.0000065551058,0.00011745668,0.00017764568,0.000009502498,0.0000065018767,0.0040129554],"genre_scores_gemma":[0.9941224,0.00009630237,0.0054147574,0.00004601859,0.00004965028,0.000018844572,0.00007757504,0.000017447413,0.00015701367],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99882114,0.00008734072,0.00036528835,0.00036939548,0.000045437137,0.00031138692],"domain_scores_gemma":[0.999343,0.000007294501,0.00014757302,0.0003939828,0.000047975114,0.000060223523],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022485167,0.00014752062,0.00022434405,0.00009355398,0.000034347835,0.0000032117084,0.00028174958,0.00019128078,0.00021449609],"category_scores_gemma":[0.000015930333,0.00013663137,0.00007865831,0.000073029485,0.000089521556,0.0000015424217,0.00029810067,0.00008783508,0.0000063802227],"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":[0.0000044994945,0.00006689164,0.108307414,0.000012805015,0.000016415726,9.513351e-7,0.00007623051,0.000007857528,0.8912864,0.000030625106,0.000003052144,0.00018689063],"study_design_scores_gemma":[0.0002968651,0.0003280452,0.543187,0.0000047788117,0.0000038314065,0.000003362577,0.00005418944,0.000003631573,0.45380622,0.00009191524,0.0021062614,0.00011391206],"about_ca_topic_score_codex":0.000055964454,"about_ca_topic_score_gemma":0.00001573558,"teacher_disagreement_score":0.43748015,"about_ca_system_score_codex":0.000015534075,"about_ca_system_score_gemma":0.000043371216,"threshold_uncertainty_score":0.5571665},"labels":[],"label_agreement":null},{"id":"W2164504762","doi":"10.1002/ajmg.a.32332","title":"Beckwith‐Wiedemann syndrome in adults: Observations from one family and recommendations for care","year":2008,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"","keywords":"Malignancy; Medicine; Beckwith–Wiedemann syndrome; Infertility; Pediatrics; Pregnancy; Internal medicine","score_opus":0.05160115333471197,"score_gpt":0.3286387192876364,"score_spread":0.2770375659529244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164504762","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0343421,0.96365935,0.0007290232,0.00042270598,0.00030639596,0.00036861657,0.00015182131,0.00000287532,0.000017138698],"genre_scores_gemma":[0.0013180001,0.9835368,0.0140181715,0.00023887845,0.0003680616,0.000054805892,0.00038334887,0.000054748045,0.000027192622],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9974917,0.00016644436,0.0012009426,0.00038479493,0.00044096695,0.00031514993],"domain_scores_gemma":[0.99811876,0.00015744091,0.00087945175,0.00031063458,0.00020287205,0.00033082417],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00026863493,0.000310501,0.001241758,0.00014755144,0.000073837335,0.00002379758,0.00050382415,0.0003083276,0.00001968519],"category_scores_gemma":[0.00035961153,0.0002795383,0.00034485993,0.00022421847,0.0002546771,0.0000034562813,0.00018085464,0.00038025947,0.0000022837598],"study_design_candidate":"design_other","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":[0.000008052908,0.000080959246,0.00027259224,0.00054695853,0.00027149246,0.000018635257,0.00018729661,0.000002230876,0.000008594415,0.0000025700135,0.0013446443,0.997256],"study_design_scores_gemma":[0.00074265583,0.0012154111,0.0015661891,0.0076653133,0.0002451589,0.00070965424,0.00078659994,0.000012005749,0.0000023037617,0.000013510295,0.9867251,0.0003161067],"about_ca_topic_score_codex":0.000060934686,"about_ca_topic_score_gemma":0.000046278634,"teacher_disagreement_score":0.99693984,"about_ca_system_score_codex":0.00003396238,"about_ca_system_score_gemma":0.0007203339,"threshold_uncertainty_score":0.99996567},"labels":[],"label_agreement":null},{"id":"W2164643560","doi":"10.1152/physiolgenomics.00071.2005","title":"Genome-wide analysis of gene transcription in the hypothalamus","year":2005,"lang":"en","type":"article","venue":"Physiological Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Biology; Gene; Genetics; Candidate gene; Phenotype; Human genome; Genome; Gene expression; Hypothalamus; Population; Gene expression profiling; Computational biology; Neuroscience; Medicine","score_opus":0.02244686644299496,"score_gpt":0.23842578624586838,"score_spread":0.21597891980287343,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164643560","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99801505,0.0004714601,0.0008671564,0.000108183005,0.000020016663,0.000115961724,0.000010549375,0.0000031666273,0.00038844478],"genre_scores_gemma":[0.99738806,0.0003366632,0.0016388535,0.00039340474,0.00009800989,0.000011588989,0.00010016571,0.000006408021,0.000026865564],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9991554,0.000073830495,0.00025885776,0.00024597795,0.00007353165,0.00019240011],"domain_scores_gemma":[0.9995701,0.000017709435,0.000074426476,0.00028635896,0.000024482713,0.000026953496],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020629376,0.00010637034,0.00020305773,0.00005665145,0.00003075499,0.000008673383,0.00027278808,0.00009013906,0.000031467524],"category_scores_gemma":[0.000033238834,0.000073745105,0.0001970149,0.00023750254,0.000057824254,0.0000016832414,0.000038513044,0.00006802135,0.0000050207173],"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":[0.000008595835,0.00007887259,0.0042064115,0.0000027125136,0.000103942555,2.7232738e-7,0.0001318836,0.014913405,0.97915447,0.000017383374,0.000008235315,0.0013738013],"study_design_scores_gemma":[0.00020628201,0.00014671861,0.9482552,8.666022e-7,0.0001042051,0.0000026199941,0.00014169033,0.0009018666,0.046386324,0.000063790045,0.0036738396,0.00011660436],"about_ca_topic_score_codex":0.000009427696,"about_ca_topic_score_gemma":0.000017627866,"teacher_disagreement_score":0.94404876,"about_ca_system_score_codex":0.000011741227,"about_ca_system_score_gemma":0.000013148486,"threshold_uncertainty_score":0.3007238},"labels":[],"label_agreement":null},{"id":"W2164748186","doi":"10.1186/1471-2156-6-s1-s159","title":"A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkage","year":2005,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill Genome Centre; McGill University Health Centre","funders":"Canadian Institutes of Health Research","keywords":"Imprinting (psychology); Genetic linkage; Genetics; Biology; Linkage (software); Genomic imprinting; Nonparametric statistics; Null hypothesis; Gene; Candidate gene; Statistical hypothesis testing; Evolutionary biology; Statistics; Mathematics","score_opus":0.016057938750947385,"score_gpt":0.29067779830599755,"score_spread":0.27461985955505014,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164748186","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9850708,0.00060801883,0.011518583,0.00013507158,0.00006973526,0.0019297714,0.000009822429,0.000011298403,0.0006468523],"genre_scores_gemma":[0.9416542,0.0001119559,0.05675273,0.000571051,0.00020474258,0.00019267955,0.000010343216,0.00005185952,0.0004504068],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982157,0.00007595174,0.00045262327,0.00052644766,0.00022621284,0.0005031017],"domain_scores_gemma":[0.99859905,0.0004042517,0.00018381937,0.0006178556,0.00010869058,0.00008630429],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041447786,0.00026560234,0.00025700557,0.00008236225,0.00007792704,0.00004576579,0.0005846103,0.0002106013,0.00002069502],"category_scores_gemma":[0.0023105976,0.00020123427,0.00014962803,0.0003957518,0.000054724354,0.0000047951266,0.00021312259,0.00013011455,0.000040297098],"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":[0.00013545342,0.0009769652,0.05340463,0.0010455173,0.000078561316,0.000004608863,0.0033442576,0.03358206,0.8866986,0.000060793107,0.00078764546,0.019880934],"study_design_scores_gemma":[0.0026834714,0.0045388318,0.04015737,0.00016957463,0.00007518066,0.00007747087,0.002077153,0.016040651,0.88679993,0.0002683814,0.04641738,0.0006946164],"about_ca_topic_score_codex":0.00005510405,"about_ca_topic_score_gemma":0.00018363917,"teacher_disagreement_score":0.045629736,"about_ca_system_score_codex":0.000018761617,"about_ca_system_score_gemma":0.00015955254,"threshold_uncertainty_score":0.82060957},"labels":[],"label_agreement":null},{"id":"W2164973887","doi":"10.1371/journal.pgen.1001251","title":"Thymus-Associated Parathyroid Hormone Has Two Cellular Origins with Distinct Endocrine and Immunological Functions","year":2010,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Medical Research Council; National Institutes of Health; National Institute of Allergy and Infectious Diseases; Deutsches Krebsforschungszentrum; Leukemia and Lymphoma Society","keywords":"Biology; Parathyroid hormone; Internal medicine; Endocrinology; Parathyroid chief cell; Parathyroid gland; Homeostasis; Organogenesis; Endocrine system; Hormone; Calcium; Gene; Genetics; Medicine","score_opus":0.013944757147507127,"score_gpt":0.21808840830861723,"score_spread":0.2041436511611101,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164973887","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99559414,0.0028438729,0.0004767064,0.00012182171,0.000110043424,0.00021978108,0.000028699109,0.000033894707,0.00057104416],"genre_scores_gemma":[0.99711096,0.00037036728,0.0016406334,0.00004697228,0.0001921716,0.000031537966,0.00014232505,0.0000385939,0.00042641372],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99871665,0.000042418487,0.00022500605,0.00044504972,0.0001612599,0.00040961918],"domain_scores_gemma":[0.99916863,0.000018916939,0.000099973855,0.00045781088,0.00011581622,0.00013886843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008298421,0.0002477037,0.00020721395,0.000034836343,0.00024117353,0.00008365441,0.00018627108,0.00014377186,0.000034604163],"category_scores_gemma":[0.00008071051,0.00020283407,0.000057127025,0.00010910093,0.00025150657,0.000002823517,0.00020229725,0.00026375326,0.00001955536],"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":[0.000017534807,0.00020071269,0.009776465,0.0000042020843,0.00012009508,0.000006510305,0.000027168437,0.000016605425,0.9882717,0.000030075413,0.000088582245,0.0014403069],"study_design_scores_gemma":[0.0032643867,0.002961246,0.093622,0.000014537843,0.00025407903,0.00024610801,0.000158956,0.00132738,0.8293826,0.000114589435,0.06780548,0.000848635],"about_ca_topic_score_codex":0.00001814354,"about_ca_topic_score_gemma":0.00013133147,"teacher_disagreement_score":0.15888913,"about_ca_system_score_codex":0.000010316059,"about_ca_system_score_gemma":0.00006586075,"threshold_uncertainty_score":0.8271333},"labels":[],"label_agreement":null},{"id":"W2165425175","doi":"10.1016/j.devcel.2009.12.017","title":"ATRX Partners with Cohesin and MeCP2 and Contributes to Developmental Silencing of Imprinted Genes in the Brain","year":2010,"lang":"en","type":"article","venue":"Developmental Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":178,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lawson Health Research Institute; University Health Network; Western University; Children’s Health Research Institute; Mental Health Commission of Canada","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; International Rett Syndrome Foundation","keywords":"Biology; Genomic imprinting; ATRX; Gene silencing; Cohesin; MECP2; Genetics; Gene; Cell biology; Meiosis; DNA methylation; Mutation; Phenotype; Gene expression","score_opus":0.0060567624258092605,"score_gpt":0.2207533121127046,"score_spread":0.21469654968689533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2165425175","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985459,0.0001686316,0.0001414953,0.00020778838,0.000031613203,0.00023524364,0.0000034047614,0.0000030402894,0.00066286867],"genre_scores_gemma":[0.987012,0.00002560841,0.012475524,0.00034262022,0.000010051057,0.000018068115,0.000014129485,0.000010698022,0.0000912948],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99925464,0.000024707184,0.00018908558,0.00024570344,0.000088475346,0.0001973689],"domain_scores_gemma":[0.9997614,0.000029660067,0.000046429974,0.00008091094,0.000028070112,0.00005354656],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026989376,0.00012952882,0.00012484925,0.00004660079,0.000060169925,0.000025179645,0.000115657334,0.00006493662,0.0000072871967],"category_scores_gemma":[0.000037600224,0.000095303825,0.0000131562065,0.00009757992,0.00008125256,0.0000032176797,0.00015462226,0.00007497288,0.0000015268566],"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":[0.000013916191,0.000017160939,0.1338366,0.000017080396,0.000013205696,0.0000016735703,0.0005140452,9.587047e-7,0.8620722,0.000014063802,0.000064463165,0.003434631],"study_design_scores_gemma":[0.0005182891,0.00007665845,0.33203098,0.000014973533,0.000004225407,0.000081987484,0.002149522,0.000006941861,0.6621117,0.000007263012,0.0028705595,0.0001268628],"about_ca_topic_score_codex":0.000056934594,"about_ca_topic_score_gemma":0.000358113,"teacher_disagreement_score":0.19996049,"about_ca_system_score_codex":0.000008678871,"about_ca_system_score_gemma":0.000086017535,"threshold_uncertainty_score":0.3886377},"labels":[],"label_agreement":null},{"id":"W2165496628","doi":"10.1242/dev.057778","title":"Depletion of <i>Kcnq1ot1</i> non-coding RNA does not affect imprinting maintenance in stem cells","year":2011,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":62,"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; Lawson Health Research Institute; Western University","funders":"Institute of Gender and Health; National Institutes of Health; National Cancer Institute; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Lawson Health Research Institute","keywords":"Biology; Genomic imprinting; Non-coding RNA; DNA methylation; Embryonic stem cell; Gene silencing; Gene; Genetics; Imprinting (psychology); Epigenetics; RNA; microRNA; Long non-coding RNA; Transcription (linguistics); Regulation of gene expression; Cell biology; Gene expression","score_opus":0.015480516245157524,"score_gpt":0.21382991729323395,"score_spread":0.1983494010480764,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2165496628","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99273884,0.000031834596,0.0055972775,0.000009641251,0.00022271399,0.00017541474,0.0000013545136,0.000006363674,0.0012165693],"genre_scores_gemma":[0.9864284,0.000055052747,0.0130906785,0.000058163343,0.0000250948,0.000021090194,0.000003975509,0.000017434424,0.00030011445],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99891615,0.000025408694,0.00035494074,0.00030063713,0.000109675275,0.0002931856],"domain_scores_gemma":[0.9995582,0.0000061496776,0.00014314841,0.00019913483,0.00004786898,0.0000454716],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003749897,0.00014055306,0.00016671338,0.00005809094,0.000038445072,0.000008384369,0.00016731852,0.000084954474,0.000014204594],"category_scores_gemma":[0.00001347906,0.00011737294,0.000051311432,0.00007607515,0.00002542035,0.0000031858842,0.00018493636,0.00006469951,0.000009066737],"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":[0.00000992112,0.00003360136,0.030758938,0.00005861295,0.000018970597,0.0000021392984,0.0005396244,0.0000074749323,0.9490432,0.000011331306,0.000019440424,0.019496746],"study_design_scores_gemma":[0.00029888714,0.00003989249,0.15053591,0.0000764601,0.0000026393302,0.000004673787,0.0002097258,0.000030927007,0.84801984,0.000004211986,0.0006313609,0.00014549379],"about_ca_topic_score_codex":0.000040831437,"about_ca_topic_score_gemma":0.000036125293,"teacher_disagreement_score":0.11977698,"about_ca_system_score_codex":0.000023352386,"about_ca_system_score_gemma":0.00006288291,"threshold_uncertainty_score":0.47863296},"labels":[],"label_agreement":null},{"id":"W2166152082","doi":"10.1210/jc.2012-3888","title":"Growth Hormone Research Society Workshop Summary: Consensus Guidelines for Recombinant Human Growth Hormone Therapy in Prader-Willi Syndrome","year":2013,"lang":"en","type":"review","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":380,"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":"Cliniques Universitaires Saint-Luc; Children's Hospital of Pittsburgh; National Institute of Diabetes and Digestive and Kidney Diseases; Erasmus Universitair Medisch Centrum Rotterdam; Sahlgrenska Akademin; Medical Research Council; Centre hospitalier universitaire Sainte-Justine; Istituto Auxologico Italiano; National Institutes of Health; Massachusetts General Hospital; Istituto Ortopedico Rizzoli di Bologna; Institut National de la Santé et de la Recherche Médicale; University of New South Wales; Aarhus Universitetshospital; Johns Hopkins Children's Center; Imperial College London; Helsingin Yliopisto; Novo Nordisk; Aarhus Universitet; Göteborgs Universitet; McMaster University; University of Sydney; Johns Hopkins University; Foundation for Prader-Willi Research; Hospital for Sick Children; Université de Montréal; Pfizer; Eli Lilly and Company","keywords":"Human growth hormone; Recombinant DNA; Growth hormone; Hormone therapy; Hormone; Medicine; Endocrinology; Internal medicine; Biology; Biochemistry; Gene","score_opus":0.32844551305299874,"score_gpt":0.4977400659301458,"score_spread":0.16929455287714706,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2166152082","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.057468522,0.9363464,0.000068993315,0.0033767244,0.0011161153,0.001547645,0.000017862982,0.000009865754,0.000047847177],"genre_scores_gemma":[0.002074674,0.9916175,0.00277104,0.0004403783,0.0019323878,0.00013194006,0.000042977434,0.00013776557,0.00085131585],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9892939,0.0030676415,0.00495138,0.000759057,0.00057546294,0.0013525856],"domain_scores_gemma":[0.9916655,0.002211053,0.0025694317,0.0009849962,0.002281516,0.00028753962],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.009854251,0.00073992444,0.003956181,0.0003027432,0.00031832166,0.00006755975,0.0019880289,0.0011792567,0.000013929029],"category_scores_gemma":[0.005539715,0.0004509988,0.0023266529,0.00045677906,0.0010236787,0.000012458515,0.0006786276,0.0027925433,0.000014355659],"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":[0.00012854666,0.0010561603,0.00021083315,0.0009727134,0.0045067626,0.000048982638,0.00011257592,0.0000049335285,0.0017980284,0.00065368146,0.2808558,0.709651],"study_design_scores_gemma":[0.003939982,0.0021126887,0.0028217435,0.00077163806,0.00070466223,0.0025603508,0.00019918046,0.0000049665955,0.000046088928,0.0017043102,0.9845923,0.000542092],"about_ca_topic_score_codex":0.00009509809,"about_ca_topic_score_gemma":0.000007747163,"teacher_disagreement_score":0.7091089,"about_ca_system_score_codex":0.000036982,"about_ca_system_score_gemma":0.0007816441,"threshold_uncertainty_score":0.9997942},"labels":[],"label_agreement":null},{"id":"W2167980095","doi":"10.1016/j.ajpath.2011.07.002","title":"Silencing of the Imprinted DLK1-MEG3 Locus in Human Clinically Nonfunctioning Pituitary Adenomas","year":2011,"lang":"en","type":"article","venue":"American Journal Of Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":95,"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 Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; Jarislowsky Foundation","keywords":"MEG3; Gene silencing; Genomic imprinting; Cancer research; Medicine; Biology; Genetics; Gene; DNA methylation; RNA","score_opus":0.013938040122147638,"score_gpt":0.25486389720499514,"score_spread":0.2409258570828475,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2167980095","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997265,0.00018356947,0.0015646827,0.000041644846,0.0002217157,0.000052659143,9.552681e-7,0.0000015862835,0.0006681777],"genre_scores_gemma":[0.99696463,0.000054048756,0.002686099,0.00014964033,0.000098293174,0.000001416675,5.841522e-7,0.000013670872,0.000031638632],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986192,0.00019695163,0.00071117363,0.00016734448,0.00009686705,0.00020845287],"domain_scores_gemma":[0.9987317,0.000022615692,0.0007885008,0.00027230984,0.00013130308,0.0000536265],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00057383685,0.00010659679,0.00029415273,0.00007865243,0.000042014606,0.0000032077473,0.00033652564,0.00007200111,0.00003011676],"category_scores_gemma":[0.00019804816,0.000080479556,0.0001726233,0.0001389053,0.00033844984,0.0000034754257,0.00016304075,0.00023684025,0.0000011539386],"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":[0.000034052573,0.00007262616,0.20131972,0.0000057245734,0.00003670572,0.000030596544,0.0005013651,0.00004615725,0.7876178,0.000016971988,0.000011173158,0.0103070745],"study_design_scores_gemma":[0.00084557966,0.004079497,0.8627287,0.0000880931,0.000048097252,0.0018750123,0.002520562,0.00001569323,0.12733376,0.0001677317,0.00011696907,0.00018029637],"about_ca_topic_score_codex":0.00008427671,"about_ca_topic_score_gemma":0.000022122264,"teacher_disagreement_score":0.66140896,"about_ca_system_score_codex":0.000011778761,"about_ca_system_score_gemma":0.00009011363,"threshold_uncertainty_score":0.32818612},"labels":[],"label_agreement":null},{"id":"W2168910284","doi":"10.1093/nar/gkh671","title":"Tissue-specific and imprinted epigenetic modifications of the human NDN gene","year":2004,"lang":"en","type":"article","venue":"Nucleic Acids Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":51,"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":"Natural Sciences and Engineering Research Council of Canada; Alberta Heritage Foundation for Medical Research; Fondation pour la Recherche Médicale; Canadian Institutes of Health Research; University of Miami","keywords":"Biology; Epigenetics of physical exercise; Epigenetics; Cancer epigenetics; DNA methylation; Epigenomics; Histone methylation; Histone; Epigenetic regulation of neurogenesis; Histone code; Histone H2A; Genetics; Genomic imprinting; Molecular biology; Histone methyltransferase; Gene; Gene expression; Nucleosome","score_opus":0.048756542291033524,"score_gpt":0.3367287096033134,"score_spread":0.28797216731227987,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2168910284","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954001,0.00094327604,0.0009790413,0.0003719798,0.00004776037,0.00028207747,0.0000073072074,0.0000059163076,0.0019625432],"genre_scores_gemma":[0.9972466,0.0003544055,0.001625161,0.00001698777,0.00007716684,0.000020565107,0.00000828691,0.000023408851,0.000627373],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99874353,0.00009239898,0.00021916273,0.00033397126,0.0002878567,0.0003230851],"domain_scores_gemma":[0.9989553,0.000011609262,0.000048794023,0.0006981181,0.00020057346,0.00008559666],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038963824,0.00010109161,0.00010954614,0.00006588803,0.0002886323,0.00003184834,0.00042449275,0.00011415987,0.000041510048],"category_scores_gemma":[0.000079849386,0.00008080539,0.000051926374,0.0002308304,0.00039866424,0.0000021441097,0.0004567926,0.0001779349,0.000015982858],"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":[0.0000021940557,0.000046057634,0.002635918,0.000012790178,0.000014758356,3.542003e-7,0.00010681946,0.000037800673,0.99121153,0.0007155487,0.00008727438,0.005128938],"study_design_scores_gemma":[0.00037467256,0.00017224083,0.16804253,0.000015493368,0.000003904668,0.00002037993,0.00013813585,0.000009575816,0.8220023,0.00084320264,0.008289076,0.000088511326],"about_ca_topic_score_codex":0.00007462625,"about_ca_topic_score_gemma":0.000013174178,"teacher_disagreement_score":0.16920926,"about_ca_system_score_codex":0.00002086724,"about_ca_system_score_gemma":0.00007018007,"threshold_uncertainty_score":0.3295148},"labels":[],"label_agreement":null},{"id":"W2170120898","doi":"10.1038/ng.3274","title":"Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":230,"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","funders":"National Institute on Drug Abuse; National Human Genome Research Institute; National Institute of General Medical Sciences; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Cancer Institute; National Institutes of Health","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Epigenetics; Genetics; Gene; Gene expression; DNA methylation","score_opus":0.01847355808492379,"score_gpt":0.2810012463782578,"score_spread":0.262527688293334,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2170120898","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98640734,0.012552146,0.000072036906,0.000022295788,0.00011831678,0.00025707125,0.000010022442,0.000007241798,0.00055351877],"genre_scores_gemma":[0.99181014,0.0008392194,0.0069100466,0.000051862084,0.000116067895,0.000008458233,0.000037742033,0.000039139097,0.00018733495],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9985038,0.00006974089,0.0004622937,0.00045566304,0.00015934433,0.00034914791],"domain_scores_gemma":[0.9992188,0.000008779818,0.0001358431,0.00041606047,0.00010812667,0.000112342816],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026731478,0.00020511905,0.00026445894,0.00016285235,0.000025659476,0.000022689133,0.00024404856,0.00046067336,0.000007525119],"category_scores_gemma":[0.000056860343,0.00022316442,0.00003584506,0.00017234485,0.00008166372,0.0000021654334,0.00026107405,0.00032348195,0.000003152916],"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":[0.000011083034,0.00004528635,0.0937305,0.000025314548,0.000009577962,0.0000047133594,0.00018834215,0.0002744117,0.9017474,0.000013205829,0.00017925314,0.003770917],"study_design_scores_gemma":[0.0018975653,0.0004627507,0.50253195,0.00003049291,0.0000098838145,0.000057742356,0.0002385942,0.0001156574,0.46137577,0.00015415017,0.03275256,0.00037291978],"about_ca_topic_score_codex":0.00004192281,"about_ca_topic_score_gemma":0.00013184766,"teacher_disagreement_score":0.44037163,"about_ca_system_score_codex":0.000028687708,"about_ca_system_score_gemma":0.000063682746,"threshold_uncertainty_score":0.91003805},"labels":[],"label_agreement":null},{"id":"W2171385037","doi":"10.1016/j.placenta.2005.12.001","title":"Characterization of the Placenta Specific Bovine Mammalian Achaete Scute-like Homologue 2 (Mash2) Gene","year":2006,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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; Cegep de Saint Hyacinthe","funders":"Institute of Human Development, Child and Youth Health; Natural Sciences and Engineering Research Council of Canada","keywords":"Biology; Trophoblast; Placenta; Gene; Genomic imprinting; Messenger RNA; Gene expression; Molecular biology; Genetics; DNA methylation; Fetus","score_opus":0.007069917725459457,"score_gpt":0.19461328874034348,"score_spread":0.18754337101488402,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2171385037","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973142,0.00027367618,0.0006771623,0.00021783465,0.0005570003,0.00024957664,0.0000841957,0.000010036357,0.0006163274],"genre_scores_gemma":[0.99555564,0.00014865752,0.00043190215,0.00012476469,0.0002839701,0.000009241183,0.00055649126,0.00002802769,0.0028613224],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99887824,0.000061856816,0.00029262484,0.00032384568,0.00016145225,0.00028198006],"domain_scores_gemma":[0.9992152,0.000005314024,0.00017971643,0.00050602626,0.000048986018,0.000044753655],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012255034,0.0001688055,0.00015140283,0.000032173208,0.000093782925,0.000021984764,0.00031118383,0.00012087033,0.00007941572],"category_scores_gemma":[0.00001096572,0.00013790285,0.0001128778,0.00011601135,0.00008271798,0.0000041048315,0.0002408318,0.000075218886,0.000017521414],"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":[0.000022181843,0.00006012929,0.03215999,0.000017507951,0.000017624297,0.000001411579,0.000016420208,0.000019144041,0.9658628,0.00003315961,0.0012480475,0.0005415916],"study_design_scores_gemma":[0.00055949076,0.00009225049,0.21441503,0.000016143926,0.000017051041,0.00005704459,0.000026720018,0.000043598982,0.72296107,0.000011421195,0.061636895,0.0001633138],"about_ca_topic_score_codex":0.00007383494,"about_ca_topic_score_gemma":0.00003774767,"teacher_disagreement_score":0.24290174,"about_ca_system_score_codex":0.000018124216,"about_ca_system_score_gemma":0.000033265453,"threshold_uncertainty_score":0.5623515},"labels":[],"label_agreement":null},{"id":"W2172727295","doi":"10.1089/153623003769645866","title":"Growth Restricted <i>In Vitro</i> Culture Conditions Alter the Imprinted Gene Expression Patterns of Mouse Embryonic Stem Cells","year":2003,"lang":"en","type":"article","venue":"Cloning and Stem Cells","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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","funders":"","keywords":"Biology; Genomic imprinting; Reprogramming; Epigenetics; Embryonic stem cell; DNA methylation; Cell biology; Gene expression; Gene; Regulation of gene expression; Genetics","score_opus":0.0075259584323903814,"score_gpt":0.21312907612889587,"score_spread":0.2056031176965055,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2172727295","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977439,0.0009369323,0.00073199306,0.000019062092,0.0001379274,0.0002015418,0.000043093125,0.000008285351,0.00017724339],"genre_scores_gemma":[0.9962834,0.0005635495,0.00029673177,0.00006645042,0.000029385606,0.000016197851,0.00002252644,0.00002089732,0.002700825],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988769,0.00014823541,0.0002737289,0.00033173888,0.00010196815,0.000267408],"domain_scores_gemma":[0.9993773,0.000024932593,0.00013964588,0.0003199408,0.00006826411,0.000069878995],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014163424,0.0001711439,0.00018712619,0.00003768785,0.00010533882,0.000030310306,0.00014852271,0.00014630322,0.000006512777],"category_scores_gemma":[0.000006171433,0.00012560785,0.0000792397,0.00008801632,0.000045179248,0.000003853194,0.00008901804,0.00013745432,0.0000026942043],"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":[0.0000088325005,0.000034944584,0.0018150709,0.000037234702,0.000018419369,0.0000021425562,0.00016938595,0.00007576208,0.997513,0.000011121978,0.00017445098,0.00013966755],"study_design_scores_gemma":[0.00057713204,0.000099064375,0.00069317676,0.00004916487,0.000016125909,0.000032600565,0.0005949943,0.000046781428,0.9969392,0.000004648586,0.00079573627,0.00015141541],"about_ca_topic_score_codex":0.000019073257,"about_ca_topic_score_gemma":0.0000020866996,"teacher_disagreement_score":0.0025235815,"about_ca_system_score_codex":0.000008643903,"about_ca_system_score_gemma":0.000031402004,"threshold_uncertainty_score":0.51221395},"labels":[],"label_agreement":null},{"id":"W2173045156","doi":"10.1186/s13148-015-0143-8","title":"Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci","year":2015,"lang":"en","type":"review","venue":"Clinical Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":214,"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; Assistance publique-Hôpitaux de Paris; Bundesministerium für Bildung und Forschung; Seconda Università degli Studi di Napoli; Institute of Genetics; Institut National de la Santé et de la Recherche Médicale; European Cooperation in Science and Technology; Instituto de Salud Carlos III; National Institute for Health and Care Research","keywords":"Genomic imprinting; Epigenetics; Human genetics; Imprinting (psychology); Biology; Genetics; DNA methylation; Gene; Molecular genetics; Disease; Bioinformatics; Computational biology; Medicine; Gene expression; Internal medicine","score_opus":0.037804355574652976,"score_gpt":0.34524692443060395,"score_spread":0.307442568855951,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2173045156","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.1639068,0.8238315,0.010390771,0.000010780042,0.00034590665,0.0011429358,0.00008258499,0.00002040053,0.00026833126],"genre_scores_gemma":[0.1308015,0.8661162,0.0024371175,0.00001680205,0.00020474766,0.000043528362,0.00018969548,0.00016043657,0.0000299373],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99580514,0.00043472854,0.0017531086,0.0009996017,0.00039082786,0.0006166087],"domain_scores_gemma":[0.9964565,0.00022116778,0.0017714374,0.0010578181,0.00024840893,0.00024468722],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.001146428,0.00069388654,0.0022408161,0.00013991845,0.000053087802,0.000027148933,0.00070586783,0.0008135786,0.000013297355],"category_scores_gemma":[0.00069834915,0.00060226925,0.0009037301,0.00027107078,0.00032906822,0.0000035265225,0.0011276944,0.00050718174,0.0000031023958],"study_design_candidate":"design_other","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":[0.000013042419,0.00024855646,0.008270466,0.005864956,0.0009289524,0.000002170148,0.000041377793,0.000024839375,0.0009942465,0.0000130828985,0.00000494072,0.98359334],"study_design_scores_gemma":[0.008231008,0.02002874,0.012504903,0.026570415,0.00873314,0.00019852855,0.0019378888,0.00037268008,0.0052025183,0.0004225531,0.90886533,0.0069322656],"about_ca_topic_score_codex":0.00008414442,"about_ca_topic_score_gemma":0.0002297124,"teacher_disagreement_score":0.9766611,"about_ca_system_score_codex":0.000022890414,"about_ca_system_score_gemma":0.00028956044,"threshold_uncertainty_score":0.99964285},"labels":[],"label_agreement":null},{"id":"W2174847659","doi":"10.1002/ajmg.a.37402","title":"Severe connective tissue laxity including aortic dilatation in Sotos syndrome","year":2015,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Canadian Institutes of Health Research; McGill University","keywords":"Boycott; Medicine; Library science; Family medicine; Sociology; Political science; Law; Politics","score_opus":0.027509324616941874,"score_gpt":0.3173268875463814,"score_spread":0.2898175629294395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2174847659","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954394,0.0008843661,0.0024964947,0.00059050036,0.0003298752,0.000100324345,0.0000024941453,0.000003256758,0.00015330121],"genre_scores_gemma":[0.99691045,0.00047480065,0.0020503367,0.00028505444,0.0002091176,0.000004560098,0.0000068748445,0.000020347517,0.000038432074],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99800754,0.00018302891,0.00058077055,0.00021585796,0.0007133062,0.00029950272],"domain_scores_gemma":[0.99873155,0.000045163677,0.00038663164,0.00019412368,0.00019507512,0.0004474474],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011204361,0.00014964571,0.0003449952,0.000093451796,0.000031986212,0.000021274696,0.00034892157,0.00011325642,0.000037676335],"category_scores_gemma":[0.0009103099,0.00013628024,0.00007158639,0.00022333983,0.000211533,0.0000055217306,0.00019045986,0.00024057424,0.000009283658],"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":[0.00027586697,0.0007965169,0.36676994,0.00009876922,0.0005711444,0.00065829884,0.0037201,0.0036886276,0.0534792,0.0000633538,0.0036813696,0.5661968],"study_design_scores_gemma":[0.016707327,0.031431552,0.7191625,0.0016111152,0.00038276386,0.025992306,0.02056814,0.006704677,0.063180834,0.001964429,0.10933013,0.0029642282],"about_ca_topic_score_codex":0.000042822405,"about_ca_topic_score_gemma":0.00003204803,"teacher_disagreement_score":0.5632326,"about_ca_system_score_codex":0.000040739124,"about_ca_system_score_gemma":0.0004284119,"threshold_uncertainty_score":0.55573475},"labels":[],"label_agreement":null},{"id":"W2180090034","doi":"10.1155/2015/278287","title":"Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome","year":2015,"lang":"en","type":"article","venue":"Case Reports in Neurological Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital; University of Toronto; University Health Network","funders":"","keywords":"Medicine; Sleep (system call); Pediatrics; Psychiatry","score_opus":0.02798860704608892,"score_gpt":0.26900204877914535,"score_spread":0.24101344173305644,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2180090034","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9644891,0.030910194,0.00032927445,0.0030880463,0.00019522873,0.0006185978,0.000002371273,0.000019577192,0.00034763172],"genre_scores_gemma":[0.9929275,0.0042618522,0.0007693343,0.0018298908,0.00007132071,0.000041043426,0.000024932478,0.000030990435,0.000043171618],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9974383,0.00010091778,0.00087692577,0.0008046544,0.00038896734,0.00039024724],"domain_scores_gemma":[0.9982275,0.00006742906,0.00046530864,0.0006933912,0.00016808104,0.00037833655],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010358258,0.0003108559,0.00070096937,0.00009821871,0.00004245915,0.000008864786,0.00011313433,0.00019621123,0.000039486138],"category_scores_gemma":[0.002146236,0.00020953265,0.000060599177,0.00032623688,0.00048121676,0.000008014916,0.0002225569,0.00028613908,8.2677917e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000018717834,0.00046270463,0.8862744,0.0047247987,0.00018737822,0.089700125,0.00012452852,0.00010507878,0.0031653456,0.00009389129,0.0027866743,0.012356339],"study_design_scores_gemma":[0.0011836871,0.0060189622,0.3031405,0.001891477,0.00014349591,0.67466813,0.000050722814,0.00011250887,0.00006954375,0.0003302806,0.012026223,0.00036448034],"about_ca_topic_score_codex":0.00005573844,"about_ca_topic_score_gemma":0.000015631804,"teacher_disagreement_score":0.58496803,"about_ca_system_score_codex":0.0000072959688,"about_ca_system_score_gemma":0.000082328814,"threshold_uncertainty_score":0.85444933},"labels":[],"label_agreement":null},{"id":"W2206303315","doi":"10.1210/jc.2015-3895","title":"Resting Energy Expenditure Is Decreased in Pseudohypoparathyroidism Type 1A","year":2015,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"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; University of Toronto; Université de Montréal; SickKids Foundation; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; National Center for Advancing Translational Sciences; Johns Hopkins University","keywords":"Resting energy expenditure; GNAS complex locus; Medicine; Endocrine system; Endocrinology; Internal medicine; Pseudohypoparathyroidism; Body mass index; Neurocognitive; Obesity; Hormone; Cohort; Energy expenditure; Pediatrics; Parathyroid hormone; Biology; Psychiatry","score_opus":0.06503032546723593,"score_gpt":0.3617859862144264,"score_spread":0.2967556607471905,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2206303315","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9797389,0.016538104,0.00032182081,0.0013778635,0.0012608572,0.000055776847,0.0000012502119,0.0000044034514,0.00070100644],"genre_scores_gemma":[0.991288,0.0035071617,0.0014148842,0.0019237872,0.0014875281,0.0000017554132,0.0000029193425,0.0000217878,0.00035216962],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9972705,0.00069672853,0.0011764157,0.00021945081,0.00022960655,0.00040724964],"domain_scores_gemma":[0.9982665,0.00017269034,0.0006314419,0.00042953133,0.0002698895,0.00022992014],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001604701,0.0001827377,0.00054981356,0.00008115052,0.000048716156,0.000014327037,0.00059435185,0.00020829003,0.000020056732],"category_scores_gemma":[0.0018518395,0.00012239069,0.00020672246,0.00013403223,0.00018504506,0.000008003607,0.0002179242,0.0004819967,0.000011938895],"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":[0.00641527,0.0022411002,0.16440399,0.000033974924,0.0020609167,0.0007297311,0.0025164005,0.0026649039,0.46714792,0.004672047,0.19172224,0.1553915],"study_design_scores_gemma":[0.010201004,0.0021814639,0.18065177,0.00004916497,0.00034337284,0.0046179215,0.0012447477,0.00020182674,0.052306253,0.004662538,0.74295074,0.0005891762],"about_ca_topic_score_codex":0.00008668832,"about_ca_topic_score_gemma":0.000022111068,"teacher_disagreement_score":0.5512285,"about_ca_system_score_codex":0.0000069685793,"about_ca_system_score_gemma":0.0003143518,"threshold_uncertainty_score":0.49909472},"labels":[],"label_agreement":null},{"id":"W2219501799","doi":"10.1016/j.appet.2015.12.021","title":"A review of chemosensory perceptions, food preferences and food-related behaviours in subjects with Prader–Willi Syndrome","year":2015,"lang":"en","type":"review","venue":"Appetite","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture Food and Rural Development; University of Alberta","funders":"Canadian Institutes of Health Research; University of Alberta","keywords":"Perception; Food choice; Dysfunctional family; Psychology; Preference; Obesity; Food preference; Developmental psychology; Medicine; Clinical psychology; Neuroscience; Biology; Food science; Endocrinology","score_opus":0.031317537572964606,"score_gpt":0.2854373369697193,"score_spread":0.25411979939675466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2219501799","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.080960736,0.91787213,0.0000018786541,0.000016594202,0.000043988257,0.0008107287,0.00005395788,0.000008174432,0.00023181857],"genre_scores_gemma":[0.0067897746,0.9922746,0.0003064259,0.000029118239,0.000020010657,0.00008610969,0.00032028236,0.000051605428,0.00012211743],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9982384,0.00015344245,0.00059636927,0.0005506293,0.00017606354,0.00028510386],"domain_scores_gemma":[0.99893755,0.00001618708,0.00039475478,0.00045965487,0.0000845837,0.00010728923],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0003276025,0.00038237483,0.0011316423,0.00010686837,0.000026737107,0.000015423117,0.00022936518,0.0003497676,0.000021051645],"category_scores_gemma":[0.000055514352,0.0002985645,0.00016319838,0.00023602322,0.00013152747,0.0000040632353,0.0001622883,0.00023061167,0.0000058591345],"study_design_candidate":"design_other","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":[0.0000015130861,0.00034719962,0.007926934,0.23761502,0.000883955,0.0000052902565,0.00016279094,9.0393695e-7,0.00009443914,0.000043336815,0.00066352065,0.7522551],"study_design_scores_gemma":[0.00076211576,0.0037314491,0.007854812,0.33458865,0.00087592186,0.0023269444,0.0001253819,5.862762e-7,0.000011909723,0.000023989684,0.64868,0.0010182394],"about_ca_topic_score_codex":0.000015779144,"about_ca_topic_score_gemma":0.000039320577,"teacher_disagreement_score":0.75123686,"about_ca_system_score_codex":0.000018987406,"about_ca_system_score_gemma":0.00024881357,"threshold_uncertainty_score":0.99994665},"labels":[],"label_agreement":null},{"id":"W2232856929","doi":"10.1101/gr.196139.115","title":"Pervasive polymorphic imprinted methylation in the human placenta","year":2016,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":143,"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":"Medical Research Council; Canadian Institutes of Health Research; Child and Family Research Institute","keywords":"Differentially methylated regions; Genomic imprinting; Biology; DNA methylation; Imprinting (psychology); Methylation; Germline; Epigenetics; Genetics; Bisulfite sequencing; Placenta; Gene; Gene expression; Fetus; Pregnancy","score_opus":0.06737292024968491,"score_gpt":0.3631432697790212,"score_spread":0.29577034952933634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2232856929","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99568975,0.0004899978,0.0002679202,0.0011056525,0.000027309308,0.00026116354,0.00000454211,0.000003709204,0.0021499405],"genre_scores_gemma":[0.99824864,0.00015938825,0.000076886616,0.000046235262,0.00014306433,0.000039375715,0.00001640876,0.000013782983,0.0012562006],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9985101,0.00033065194,0.00015964177,0.00029513924,0.00028577851,0.0004186804],"domain_scores_gemma":[0.99933493,0.000052717547,0.000028136797,0.00043412842,0.00010063059,0.000049450187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015184785,0.00008315175,0.000077020646,0.0001088602,0.0001427913,0.000032931188,0.000402257,0.00008494484,0.00011963084],"category_scores_gemma":[0.00017120651,0.000049251626,0.000048510323,0.0001968994,0.00010358935,0.0000026115356,0.00023641903,0.00013233665,0.000074349344],"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":[0.0000047565186,0.000024284307,0.009661045,0.0000055594987,0.000010354269,0.0000021149456,0.00014557155,0.0000013784158,0.984839,0.00010429881,0.00007054752,0.005131068],"study_design_scores_gemma":[0.0010964194,0.00046773703,0.6838883,0.000028924953,0.0000044808153,0.000049891692,0.0010454522,0.000008116177,0.2865108,0.0006640775,0.02601814,0.00021766358],"about_ca_topic_score_codex":0.000108636945,"about_ca_topic_score_gemma":0.00005836595,"teacher_disagreement_score":0.69832826,"about_ca_system_score_codex":0.000031491145,"about_ca_system_score_gemma":0.000059100348,"threshold_uncertainty_score":0.2008423},"labels":[],"label_agreement":null},{"id":"W2254272094","doi":"10.1038/srep10596","title":"Assisted reproduction causes placental maldevelopment and dysfunction linked to reduced fetal weight in mice","year":2015,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":105,"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 Key Research and Development Program of China; Institute of Genetics and Developmental Biology, Chinese Academy of Sciences; Chinese Academy of Sciences; Institute of Genetics; National Natural Science Foundation of China","keywords":"Offspring; Maldevelopment; Genomic imprinting; Placenta; Fetus; Placentation; Biology; Andrology; In utero; Pregnancy; Low birth weight; Embryo; Imprinting (psychology); Birth weight; Epigenetics; Downregulation and upregulation; Endocrinology; Cell biology; Medicine; Genetics; Gene expression; DNA methylation; Gene; Anatomy","score_opus":0.02024845168967122,"score_gpt":0.24717084596980682,"score_spread":0.2269223942801356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2254272094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9940269,0.00020360883,0.00008301781,0.0002079094,0.004837728,0.00025455435,5.642479e-7,0.0000127527455,0.00037294396],"genre_scores_gemma":[0.99278384,0.000005947217,0.0022196681,0.000023417353,0.000112183545,0.00001895447,0.00009273274,0.0000110354395,0.004732205],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99838734,0.00003439875,0.00033113654,0.0008265877,0.00020950606,0.00021101176],"domain_scores_gemma":[0.9992491,0.0000019261972,0.00011529711,0.00037295377,0.00011753,0.00014318775],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009838768,0.000109256696,0.000108322936,0.0001051065,0.00008717333,0.00009089016,0.000049495327,0.000074548196,0.0000064088426],"category_scores_gemma":[0.0002744168,0.00010614417,0.000025049038,0.00022281747,0.000054658085,0.0000075637827,0.00013679033,0.000049215836,0.000009410901],"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":[0.000015420579,0.000042535554,0.02861156,0.00000800625,0.000010182041,0.000021624834,0.00019257369,0.000049003676,0.9616602,7.570732e-7,0.004761564,0.0046265423],"study_design_scores_gemma":[0.000525853,0.00017460789,0.3808349,0.00004553506,0.000014405218,0.002070456,0.0005736534,0.000045486795,0.5270113,0.00009826752,0.08826316,0.00034240802],"about_ca_topic_score_codex":0.000036850695,"about_ca_topic_score_gemma":0.000060738228,"teacher_disagreement_score":0.43464896,"about_ca_system_score_codex":0.000045115718,"about_ca_system_score_gemma":0.00014267088,"threshold_uncertainty_score":0.4328434},"labels":[],"label_agreement":null},{"id":"W2256023856","doi":"10.1172/jci80937","title":"TGF-β/β2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome","year":2016,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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 Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute on Alcohol Abuse and Alcoholism; University of Texas MD Anderson Cancer Center; Directorate for Biological Sciences; George Washington University; American Cancer Society; U.S. Department of Veterans Affairs; National Cancer Institute; National Institutes of Health","keywords":"Beckwith–Wiedemann syndrome; CTCF; Medicine; Spectrin; Biology; Cancer research; Immunology; Genetics; Cell; Gene; Transcription factor","score_opus":0.030103862795979115,"score_gpt":0.31492420656648573,"score_spread":0.28482034377050663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2256023856","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99779713,0.00029782957,0.0004944323,0.0007080784,0.00039969553,0.00013827569,0.0000023790708,0.00000595656,0.0001562347],"genre_scores_gemma":[0.9978942,0.000110547975,0.0007061647,0.0001742131,0.00026118415,0.0000031321078,0.000006575483,0.000024926183,0.000819001],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9973204,0.00027960638,0.0015818044,0.00029478243,0.0002705047,0.00025287142],"domain_scores_gemma":[0.998262,0.000095971234,0.0009695957,0.00027962946,0.0001702006,0.0002226286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013456189,0.0001709312,0.00040717554,0.000105909225,0.000059323123,0.000028196953,0.00026707212,0.0002209193,0.000049602502],"category_scores_gemma":[0.00030432522,0.00011520469,0.00022032417,0.00012646739,0.00014973868,0.000020558551,0.000101591904,0.00022896884,0.0000112850075],"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":[0.000042617106,0.00016495807,0.30598143,0.000030158286,0.000040016224,0.000026913618,0.000037879992,0.00009256763,0.68702996,0.00003522673,0.0009748054,0.0055434946],"study_design_scores_gemma":[0.0035131637,0.0016379397,0.8065271,0.00044059262,0.000044065077,0.00026787794,0.00008425464,0.00009894042,0.18208858,0.0011155838,0.003890447,0.00029149748],"about_ca_topic_score_codex":0.000010979666,"about_ca_topic_score_gemma":0.000012247864,"teacher_disagreement_score":0.50494134,"about_ca_system_score_codex":0.00002078797,"about_ca_system_score_gemma":0.00013760338,"threshold_uncertainty_score":0.46979108},"labels":[],"label_agreement":null},{"id":"W2267339756","doi":"","title":"발달장애 아동의 기능적응을 위한 감각치료에 관한 연구","year":2013,"lang":"ko","type":"article","venue":"한국유아교육·보육복지연구","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Focus (optics); Occupational therapy; Psychology; Medicine; Physical medicine and rehabilitation; Physical therapy","score_opus":0.007234114929904836,"score_gpt":0.22078330178963093,"score_spread":0.2135491868597261,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2267339756","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9794132,0.0036886032,0.00079847814,0.0016361144,0.0017211204,0.00074831024,0.000042948555,0.000049844548,0.0119013665],"genre_scores_gemma":[0.9780357,0.0010806995,0.0018749855,0.0013022731,0.0012936783,0.00008449361,0.00014917795,0.00012898324,0.016049996],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99617165,0.00017044248,0.00078425405,0.001188178,0.000402962,0.0012824889],"domain_scores_gemma":[0.9974535,0.000038886345,0.00031516352,0.0014031775,0.0002985395,0.0004907192],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00034340378,0.0006780209,0.0005718258,0.00011285249,0.00029170825,0.00029726676,0.00081551116,0.0007460475,0.0028347517],"category_scores_gemma":[0.00021469983,0.00067649654,0.0004441104,0.00024885277,0.00023330715,0.000017077658,0.0007581852,0.0004124302,0.0032069718],"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":[0.00002527106,0.000524718,0.07688129,0.0003669867,0.0006261798,0.00002758812,0.0004589556,0.00006807173,0.75819165,0.00030625545,0.055639833,0.106883235],"study_design_scores_gemma":[0.0038029759,0.0020716093,0.3893648,0.00037503632,0.0003568705,0.0005560291,0.0015700241,0.0012407537,0.21293527,0.0014529615,0.38300717,0.0032664917],"about_ca_topic_score_codex":0.00044640206,"about_ca_topic_score_gemma":0.000037906466,"teacher_disagreement_score":0.5452563,"about_ca_system_score_codex":0.000046215206,"about_ca_system_score_gemma":0.00021714994,"threshold_uncertainty_score":0.99956864},"labels":[],"label_agreement":null},{"id":"W2267376195","doi":"10.1038/ncomms10207","title":"NSD1 mutations generate a genome-wide DNA methylation signature","year":2015,"lang":"en","type":"article","venue":"Nature Communications","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":211,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; University of Toronto; University of New Brunswick; University of Alberta; Child and Family Research Institute; Canada Research Chairs; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Rare Disease Foundation","keywords":"Epigenetics; Genetics; Methyltransferase; Biology; Genome; Gene; Histone; DNA methylation; Phenotype; Methylation; dNaM; Computational biology; Gene expression","score_opus":0.02523140765637531,"score_gpt":0.2936934390081372,"score_spread":0.2684620313517619,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2267376195","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9394017,0.03341246,0.0057249726,0.005940477,0.00046587092,0.0005537182,0.000056650613,0.00008090487,0.014363252],"genre_scores_gemma":[0.97590727,0.00034369386,0.021025442,0.00073654216,0.0001306489,0.000046885743,0.0010783444,0.00002644196,0.00070470886],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990453,0.00014974229,0.00021858538,0.00024693273,0.00014577074,0.00019364005],"domain_scores_gemma":[0.99797857,0.000039726718,0.00011025766,0.0013912843,0.00035148067,0.00012867518],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029313934,0.00014208647,0.000114419745,0.00006936254,0.00020997426,0.00004925863,0.0007001038,0.00037668354,0.000011130572],"category_scores_gemma":[0.0004719003,0.0001420773,0.00007989463,0.00024232044,0.000081491184,0.000007303413,0.0003746249,0.00041584577,0.00003250575],"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":[0.000015874692,0.0002635085,0.016225154,0.000014890034,0.00025409294,0.000001391068,0.0008203517,0.0020034716,0.95278573,0.0027891637,0.017839104,0.0069872444],"study_design_scores_gemma":[0.0009700146,0.00017820664,0.07972185,0.000013688669,0.00008831507,0.00004270777,0.00056018255,0.0012704461,0.04603298,0.0010721292,0.86950254,0.0005469356],"about_ca_topic_score_codex":0.000008078331,"about_ca_topic_score_gemma":0.000112643625,"teacher_disagreement_score":0.90675277,"about_ca_system_score_codex":0.0000273447,"about_ca_system_score_gemma":0.00014225744,"threshold_uncertainty_score":0.57937443},"labels":[],"label_agreement":null},{"id":"W2274471732","doi":"10.3109/14767058.2016.1138465","title":"Epigenetic Dysregulation of Insulin-like Growth Factor (IGF)-related Genes and Adverse Pregnancy Outcomes: A Systematic Review","year":2016,"lang":"en","type":"review","venue":"The Journal of Maternal-Fetal & Neonatal Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Epigenetics; Low birth weight; Small for gestational age; Observational study; Medicine; Birth weight; Bioinformatics; Genomic imprinting; Pregnancy; DNA methylation; Oncology; Genetics; Internal medicine; Biology; Gene","score_opus":0.01592236954165377,"score_gpt":0.2814813707652216,"score_spread":0.26555900122356785,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2274471732","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.009963467,0.9879436,0.000267547,0.000115500035,0.00054282486,0.0011126285,0.00003440813,0.000004408498,0.000015625978],"genre_scores_gemma":[0.012489376,0.986735,0.00008641488,0.000054030745,0.00011697246,0.000010634014,0.000017790295,0.00005894501,0.00043085995],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.99603695,0.0005443935,0.002365556,0.00025350894,0.0005327077,0.00026687354],"domain_scores_gemma":[0.9956335,0.00019624022,0.0031898401,0.0005293146,0.00029985677,0.00015123968],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00097152713,0.0005099885,0.0025638554,0.00015470349,0.000051511848,0.0000071714203,0.00064401777,0.00023210564,0.000062939325],"category_scores_gemma":[0.0005812677,0.00023552768,0.00046692902,0.00014005648,0.00022968437,0.000013930254,0.00023848734,0.00022685574,0.000010219898],"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":[0.000018920298,0.000035709716,0.00016689667,0.68301207,0.0018192733,0.000027194907,0.00013712083,8.559731e-7,0.0011924193,0.000009982682,0.00003433121,0.31354523],"study_design_scores_gemma":[0.0013717996,0.0009384965,0.001172495,0.9786178,0.0050152144,0.004269409,0.000043886794,0.00000272401,0.0002504975,0.000066521345,0.007854632,0.00039654452],"about_ca_topic_score_codex":0.000016955564,"about_ca_topic_score_gemma":0.0000015523541,"teacher_disagreement_score":0.3131487,"about_ca_system_score_codex":0.000032363365,"about_ca_system_score_gemma":0.00012745507,"threshold_uncertainty_score":0.960454},"labels":[],"label_agreement":null},{"id":"W2283197660","doi":"10.71781/3667","title":"Study of imprinted genes in bovine embryos produced by assisted reproductive technologies","year":2008,"lang":"en","type":"dissertation","venue":"Open MIND","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Conselho Nacional de Desenvolvimento Científico e Tecnológico","keywords":"Embryo; Genomic imprinting; Andrology; Biology; Gene; Genetics; Biotechnology; Medicine; Gene expression","score_opus":0.0258992838831357,"score_gpt":0.3096075164327498,"score_spread":0.2837082325496141,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2283197660","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949084,0.0016307689,0.0000012681704,0.000021859003,0.00016865658,0.0014594418,0.000019625326,0.0000025148076,0.0017874485],"genre_scores_gemma":[0.98982555,0.00026211375,0.0007309266,0.0000014521822,0.0000307638,0.00012109163,0.00063478114,0.00003721629,0.008356123],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9980321,0.00006454031,0.0005166511,0.0010086676,0.00015369432,0.00022436665],"domain_scores_gemma":[0.99849695,0.0000057278717,0.00040249623,0.0008875898,0.000184783,0.000022437587],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00021571355,0.0002722938,0.00044221804,0.00011901233,0.000049908733,0.000029985451,0.0006695318,0.00032987507,0.000033803284],"category_scores_gemma":[0.00029957303,0.00026466223,0.00005926796,0.00023139128,0.000039989645,0.000004376952,0.00033069946,0.00017609466,0.000006917839],"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":[0.00009702804,0.0005973024,0.004825597,0.000023496752,0.00012395084,0.000006053463,0.00050475483,0.0000028859336,0.89382684,8.4765e-8,0.00024205078,0.099749945],"study_design_scores_gemma":[0.0008358407,0.0010053931,0.032796636,0.00005963842,0.000038774895,0.000020241301,0.012207146,0.0000018486154,0.9502549,0.00000189794,0.0024750766,0.00030256488],"about_ca_topic_score_codex":0.00019842171,"about_ca_topic_score_gemma":0.00038674232,"teacher_disagreement_score":0.09944738,"about_ca_system_score_codex":0.000017009263,"about_ca_system_score_gemma":0.00014123962,"threshold_uncertainty_score":0.99998057},"labels":[],"label_agreement":null},{"id":"W2314857307","doi":"10.1097/00001577-200001220-00006","title":"Prader-Willi Syndrome","year":2000,"lang":"en","type":"article","venue":"Pediatric Physical Therapy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Intervention (counseling); Medicine; Family medicine; Association (psychology); MEDLINE; Pediatrics; Physical therapy; Psychology; Nursing; Political science","score_opus":0.01033319299372057,"score_gpt":0.24615006921483973,"score_spread":0.23581687622111916,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2314857307","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99618477,0.0010087816,0.00006171029,0.00011179118,0.00007838728,0.00013336849,0.0000044166677,0.000024284187,0.0023925],"genre_scores_gemma":[0.9944137,0.0026042715,0.0002037335,0.00024887302,0.0010818662,0.000020339263,0.000017895427,0.000027782557,0.0013815546],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9990787,0.00003622628,0.00012951602,0.00032313715,0.00014259563,0.00028986222],"domain_scores_gemma":[0.9995295,0.00001147494,0.000036188056,0.00030920948,0.000020283658,0.00009337157],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000058119305,0.00015768244,0.00015230376,0.000021551234,0.00006662421,0.000022575095,0.00019541926,0.000070472735,0.00024512803],"category_scores_gemma":[0.000008785064,0.0001346965,0.00013859141,0.00014194033,0.000030501255,0.0000030838455,0.000029687099,0.00007990715,0.00021080459],"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":[0.000024948837,0.0018148024,0.09392411,0.00004884768,0.00027535643,0.000008170062,0.00041907633,0.00044177813,0.20821616,0.00015118325,0.007686309,0.68698925],"study_design_scores_gemma":[0.0028634032,0.00223887,0.71281856,0.0000059830163,0.000055002944,0.00022347675,0.000033302975,0.00031282924,0.014404041,0.0018304503,0.26409078,0.001123307],"about_ca_topic_score_codex":0.000006917615,"about_ca_topic_score_gemma":1.5476508e-7,"teacher_disagreement_score":0.68586594,"about_ca_system_score_codex":0.0000044185917,"about_ca_system_score_gemma":0.000028103117,"threshold_uncertainty_score":0.5492764},"labels":[],"label_agreement":null},{"id":"W2315270862","doi":"10.15331/jdsm.3900","title":"Macroglossia and Down Syndrome: Don't Be Fooled","year":2014,"lang":"en","type":"article","venue":"Journal of Dental Sleep Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 of Alberta","funders":"","keywords":"Macroglossia; Medicine; Philosophy; Linguistics; Tongue","score_opus":0.005697273049798441,"score_gpt":0.23590983015897382,"score_spread":0.23021255710917538,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2315270862","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952499,0.0013957821,0.00094241294,0.0010444785,0.0003792594,0.000053375472,6.538541e-7,0.0000022498468,0.00093183405],"genre_scores_gemma":[0.99774325,0.00021565706,0.00081882824,0.00061087287,0.00040691282,8.545023e-7,0.0000045451147,0.000013416888,0.00018564392],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99908394,0.00004107844,0.00034424473,0.00013978388,0.00022042671,0.00017050965],"domain_scores_gemma":[0.9993968,0.000014476495,0.00022339729,0.00014043142,0.0000535105,0.00017135844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038071457,0.00012127151,0.00024106662,0.000050055343,0.00004820483,0.000012700819,0.00014727424,0.000080324004,0.00010964669],"category_scores_gemma":[0.00015131077,0.000088197405,0.00006657833,0.000059036214,0.000115238865,0.0000040737405,0.000103381404,0.000112094276,0.0000022028448],"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":[0.00012763415,0.00013807956,0.2430699,0.00006888359,0.0003332136,0.000108446424,0.00016966625,0.00002707156,0.6781857,0.000044972334,0.006835983,0.07089044],"study_design_scores_gemma":[0.012233017,0.013630886,0.746319,0.0003541968,0.0004394712,0.048114218,0.0012402934,0.00036879975,0.028090984,0.00029159785,0.14826109,0.0006564755],"about_ca_topic_score_codex":0.000010079857,"about_ca_topic_score_gemma":0.000007211592,"teacher_disagreement_score":0.65009475,"about_ca_system_score_codex":0.00000963382,"about_ca_system_score_gemma":0.000010373504,"threshold_uncertainty_score":0.35965857},"labels":[],"label_agreement":null},{"id":"W2315847851","doi":"10.1016/s1499-2671(08)24294-2","title":"Pseudohypoparathyroidism type 1a and the GNAS p.R231H mutation: somatic and gonadal mosaicism in a mother with 2 affected sons","year":2008,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Gs alpha subunit; Short stature; Endocrinology; Internal medicine; Brachydactyly; Mutation; Somatic cell; Adenylyl cyclase; Parathyroid hormone; Obesity; Receptor; Genetics; Gene; Biology","score_opus":0.005658972180609143,"score_gpt":0.18260078256213375,"score_spread":0.1769418103815246,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2315847851","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9932777,0.005985077,0.000013000758,0.0004944051,0.00004060853,0.000080040336,0.0000026046143,7.3877175e-7,0.00010577144],"genre_scores_gemma":[0.99926674,0.000059534043,0.0003573123,0.0001648529,0.000047164627,0.0000020681978,0.0000021534815,0.000010542028,0.00008964113],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994969,0.000048626094,0.00014006782,0.000086909095,0.000053652166,0.0001738385],"domain_scores_gemma":[0.9996205,0.000017953405,0.00007931215,0.000080780104,0.000053282572,0.00014820116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013109212,0.00008266622,0.00013726142,0.000055594133,0.000083920524,0.000024324316,0.0000696478,0.00004583775,0.0000057006296],"category_scores_gemma":[0.0000734944,0.00005518651,0.000020969954,0.000075141244,0.00016253412,0.000004666247,0.000009977514,0.000077746336,5.160108e-7],"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":[0.000033556233,0.00004827264,0.87726384,0.00007021325,0.00042000329,0.00010429123,0.0040724277,0.00045772744,0.108611465,0.00020370106,0.003068624,0.0056458716],"study_design_scores_gemma":[0.0033251038,0.00073108997,0.9886129,0.00007583736,0.000048124857,0.0008040943,0.0006098302,0.00042454054,0.003675347,0.0003267668,0.0011438132,0.00022256745],"about_ca_topic_score_codex":0.00020547105,"about_ca_topic_score_gemma":0.0023520116,"teacher_disagreement_score":0.11134903,"about_ca_system_score_codex":0.000008160832,"about_ca_system_score_gemma":0.00025272978,"threshold_uncertainty_score":0.22504404},"labels":[],"label_agreement":null},{"id":"W2318267505","doi":"10.1038/sj.mp.4001098","title":"Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4","year":2002,"lang":"en","type":"article","venue":"Molecular Psychiatry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Health Sciences Centre; University of Manitoba; Centre for Addiction and Mental Health; University of Toronto","funders":"","keywords":"Genetics; Transmission disequilibrium test; Bipolar disorder; Allele; Biology; Linkage disequilibrium; Dopamine; Genomic imprinting; Gene; Haplotype; Endocrinology","score_opus":0.009990049899582775,"score_gpt":0.24030591042897598,"score_spread":0.2303158605293932,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2318267505","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8385622,0.15925397,0.001333573,0.0003730803,0.00013463772,0.00027395904,0.000013604641,0.0000060095135,0.000048963106],"genre_scores_gemma":[0.983994,0.0029603234,0.012599861,0.00012635367,0.00007985764,0.000046454432,0.000020987367,0.00003539174,0.000136755],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99889004,0.000042761945,0.00029878507,0.0004001067,0.00010358697,0.00026473458],"domain_scores_gemma":[0.9994134,0.0000128403735,0.00010356446,0.00035372115,0.000044265635,0.00007223688],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014472255,0.00017577475,0.00019523672,0.00007625436,0.000041827967,0.000015238659,0.00016766277,0.00010689917,0.000025352696],"category_scores_gemma":[0.00009088627,0.0001811538,0.00010229924,0.00013360767,0.000063115716,0.000004825175,0.00010259218,0.00005925349,0.0000032284186],"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":[0.000020689244,0.0001290999,0.05870943,0.000094974464,0.000029434252,6.0379773e-7,0.000028003815,0.00006937572,0.9136014,0.00007490128,0.000119880104,0.027122201],"study_design_scores_gemma":[0.0049274643,0.0026315064,0.035252042,0.0005075186,0.00013182194,0.00015831707,0.0004694722,0.006495975,0.8196757,0.00077059004,0.12767144,0.0013081962],"about_ca_topic_score_codex":0.00004563712,"about_ca_topic_score_gemma":0.000043797743,"teacher_disagreement_score":0.15629365,"about_ca_system_score_codex":0.0000051956426,"about_ca_system_score_gemma":0.00002310504,"threshold_uncertainty_score":0.7387237},"labels":[],"label_agreement":null},{"id":"W2322812678","doi":"10.12703/p7-20","title":"Sublingual thyroid ectopy: similarities and differences with Kallmann syndrome","year":2015,"lang":"en","type":"review","venue":"F1000Prime Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; HEC Montréal","funders":"Canadian Institutes of Health Research; Centre hospitalier universitaire Sainte-Justine","keywords":"Thyroid; Ectopic thyroid; Medicine; Congenital hypothyroidism; Internal medicine; Endocrinology; Thyroid disease; Pathology","score_opus":0.031505076523798234,"score_gpt":0.2891671972331874,"score_spread":0.25766212070938915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2322812678","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.035632275,0.96174574,0.000021579539,0.000010806393,0.00026578867,0.0005049287,0.000016868835,0.000033807864,0.0017681955],"genre_scores_gemma":[0.013895754,0.98221403,0.0005613689,0.000022228638,0.0003003362,0.00006341243,0.00027825497,0.0001056934,0.002558938],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9974599,0.000094975454,0.0006887581,0.0009448581,0.00035311517,0.00045842663],"domain_scores_gemma":[0.99821275,0.000021457992,0.0005782497,0.0008061706,0.00014756856,0.00023378184],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004347787,0.0005907105,0.0013535346,0.0001358131,0.00010129346,0.00012799402,0.00021875901,0.00048470285,0.000022034903],"category_scores_gemma":[0.000106187086,0.0004316226,0.00021537661,0.00015246219,0.00019109457,0.0000051442767,0.0003804083,0.00025057877,0.000006631585],"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":[0.000018655672,0.0002691955,0.011601243,0.023225574,0.002336598,0.0037810619,0.00020541805,0.0000029989676,0.00018027509,0.00004014995,0.004785692,0.95355314],"study_design_scores_gemma":[0.00013940403,0.00063225284,0.00084587216,0.002024342,0.00044679813,0.027494492,0.000045195262,6.510616e-7,0.000033596785,0.00004315445,0.96759117,0.0007030731],"about_ca_topic_score_codex":0.0000468211,"about_ca_topic_score_gemma":0.000009741754,"teacher_disagreement_score":0.96280545,"about_ca_system_score_codex":0.000026075286,"about_ca_system_score_gemma":0.00064351154,"threshold_uncertainty_score":0.99981356},"labels":[],"label_agreement":null},{"id":"W2323605318","doi":"10.2174/1573400510666140319234658","title":"Prader-Willi Syndrome: Genetics, Phenotype, and Management","year":2014,"lang":"en","type":"article","venue":"Current Psychiatry Reviews","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster Children's Hospital; McMaster University","funders":"","keywords":"Hypotonia; Psychosis; Intellectual disability; Medicine; Failure to thrive; Autism; Neurodevelopmental disorder; Autism spectrum disorder; Psychiatry; Phenotype; Psychology; Genetics; Pediatrics; Biology; Gene","score_opus":0.019588437047842914,"score_gpt":0.28202949986877685,"score_spread":0.26244106282093393,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2323605318","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.49516273,0.48424992,0.009100853,0.00063731085,0.0044121016,0.0013983598,0.0000070173132,0.00003399005,0.004997716],"genre_scores_gemma":[0.5425795,0.410816,0.04190525,0.0012666566,0.0015045272,0.00024747488,0.00017574013,0.00012553466,0.0013792968],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99859446,0.00010002149,0.00038905657,0.0005127863,0.00010862542,0.00029504654],"domain_scores_gemma":[0.999122,0.0000033547014,0.00015207188,0.0005695217,0.00002285576,0.00013018846],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003328372,0.00023505744,0.0002690662,0.000039569735,0.00009074,0.000038789913,0.00022420904,0.00007178786,0.00002966606],"category_scores_gemma":[0.000023711895,0.00020609566,0.00011621956,0.000090121495,0.000053065763,0.0000028044626,0.00019736766,0.0000918609,0.00009226579],"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":[0.0000013013116,0.00018544252,0.12211565,0.0017621479,0.00008606897,1.444564e-7,0.000022527773,0.0000060313123,0.00096214283,0.0017511602,0.027380014,0.8457274],"study_design_scores_gemma":[0.00035230644,0.00014772844,0.11616982,0.00018294834,0.000058140617,0.00003944542,0.000009120609,0.0000379293,0.000027549384,0.00023007883,0.882492,0.00025291252],"about_ca_topic_score_codex":7.168911e-7,"about_ca_topic_score_gemma":0.000003419918,"teacher_disagreement_score":0.855112,"about_ca_system_score_codex":0.0000045562797,"about_ca_system_score_gemma":0.000014349139,"threshold_uncertainty_score":0.8404337},"labels":[],"label_agreement":null},{"id":"W2325566001","doi":"10.1139/gen-2013-0062","title":"Comparative analysis of the <i>IGF2</i> and <i>ZBED6</i> gene variants and haplotypes reveals significant effect of growth traits in cattle","year":2013,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"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":"Biology; Haplotype; Genetics; Linkage disequilibrium; Single-nucleotide polymorphism; Allele; Heterozygote advantage; Gene; Genotype","score_opus":0.007202621978442396,"score_gpt":0.2202007359054904,"score_spread":0.212998113927048,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2325566001","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99841,0.0010363739,0.000053539057,0.000035387176,0.00001530995,0.00023822348,0.00002435483,0.0000011960308,0.00018563175],"genre_scores_gemma":[0.999531,0.000120256176,0.00023360738,0.00003499798,0.0000103905095,0.000012427879,0.00000839839,0.0000054168313,0.000043542295],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99929065,0.000096887554,0.00021154412,0.0002034983,0.00006679679,0.0001306158],"domain_scores_gemma":[0.99962306,0.00003129311,0.00010795392,0.00015674693,0.000043813186,0.000037121554],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018688953,0.00009898545,0.00031178238,0.000053507112,0.000023333703,0.00000812859,0.000102769634,0.000054307537,0.0000090872345],"category_scores_gemma":[0.000028958944,0.00006877569,0.00005812033,0.00021086918,0.00010086866,0.0000024870728,0.00010379255,0.000036529545,6.759378e-7],"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":[0.0000051957268,0.000013932512,0.079334006,0.000028942557,0.00016816685,9.392919e-8,0.00018084672,0.00006523881,0.9200254,0.000007859724,0.000006632968,0.00016370241],"study_design_scores_gemma":[0.0002387647,0.00015280269,0.7891098,0.0000063210823,0.00011125035,0.0000027009744,0.00003846221,0.000047038913,0.21019328,0.000022043292,0.000015502514,0.000061980485],"about_ca_topic_score_codex":0.0001804197,"about_ca_topic_score_gemma":0.000023794928,"teacher_disagreement_score":0.70983213,"about_ca_system_score_codex":0.000002392716,"about_ca_system_score_gemma":0.000012354208,"threshold_uncertainty_score":0.28045914},"labels":[],"label_agreement":null},{"id":"W2327465536","doi":"10.1017/s0317167100022599","title":"DIETARY TREATMENT OF EPILEPSY. PRACTICAL IMPLEMENTATION OF KETOGENIC THERAPY. 2012. Edited by Elizabeth Neal. Published by Wiley-Blackwell. 241 pages. C$80 approx.","year":2013,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Ketogenic diet; Approx; Action (physics); Epilepsy; Gerontology; Psychology; Medicine; Neuroscience; Computer science; Physics; Computer security","score_opus":0.02968155150110296,"score_gpt":0.2838706410746815,"score_spread":0.25418908957357855,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2327465536","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98822665,0.007863933,0.00004284396,0.0028559586,0.00045642376,0.00027541516,0.000031543015,0.000004060367,0.00024316674],"genre_scores_gemma":[0.9889207,0.008755441,0.0013219584,0.0007684857,0.00018100067,0.0000074564446,0.000005721447,0.000012567899,0.000026660604],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.996272,0.0006854972,0.0010222459,0.0005095509,0.00055396307,0.00095674256],"domain_scores_gemma":[0.99694085,0.00016777772,0.0011468306,0.00019712148,0.0005124839,0.0010349299],"candidate_categories":["sts"],"consensus_categories":[],"category_scores_codex":[0.0015895078,0.0003090082,0.0004845164,0.0003149998,0.0006023431,0.00029071607,0.0010242916,0.00021002482,0.00035543615],"category_scores_gemma":[0.00048583216,0.0002059844,0.00025776547,0.0005780095,0.0028305585,0.00018974795,0.000058869064,0.00033174123,0.0000012088199],"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":[0.000061219136,0.00017407889,0.87370116,0.000011803159,0.00008923916,0.00009863071,0.00024105128,0.0002442557,0.051758096,0.000017209843,0.041983265,0.03161998],"study_design_scores_gemma":[0.0029327783,0.34746295,0.5011618,0.00006398492,0.00016592165,0.010609171,0.001998634,0.00088618015,0.08111727,0.003308775,0.049066678,0.0012258362],"about_ca_topic_score_codex":0.00335147,"about_ca_topic_score_gemma":0.006693624,"teacher_disagreement_score":0.37253937,"about_ca_system_score_codex":0.00006398752,"about_ca_system_score_gemma":0.001643541,"threshold_uncertainty_score":0.9998832},"labels":[],"label_agreement":null},{"id":"W2328600316","doi":"10.1016/j.jcjd.2013.03.337","title":"Investigating Food Choice and Food-Related Problems in Individuals Living with Prader-Willi Syndrome","year":2013,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Kelowna General Hospital","funders":"","keywords":"Medicine; Obesity; Food choice; Caloric theory; Disease; Developmental psychology; Clinical psychology; Psychology; Endocrinology; Internal medicine","score_opus":0.009067810950848488,"score_gpt":0.18552140524191701,"score_spread":0.17645359429106852,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2328600316","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965642,0.002736945,0.000005170149,0.00035434403,0.000057777743,0.00017175959,0.0000044998596,0.0000020071227,0.000103296836],"genre_scores_gemma":[0.9991227,0.0000102154745,0.0006183555,0.00014363095,0.000035761645,0.00000905681,0.0000030850688,0.000024076598,0.000033131426],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989364,0.00005764746,0.00034092233,0.00017068782,0.00009473736,0.00039960412],"domain_scores_gemma":[0.9990918,0.00004328237,0.00022856756,0.00011899318,0.0000928865,0.00042446825],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026255238,0.00014383771,0.00020573463,0.00017186056,0.0000737555,0.000103245955,0.0001621601,0.000114923605,0.000025697509],"category_scores_gemma":[0.00035214477,0.00012493176,0.000035166006,0.0001527587,0.00010688004,0.000020091518,0.00003216162,0.0001847535,0.0000016142517],"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":[3.4403405e-10,0.000005483935,0.99567544,0.000033601227,0.00008718527,3.162936e-8,0.00021794312,0.000115258605,0.002987222,0.000004664747,0.000066085704,0.0008070776],"study_design_scores_gemma":[0.00033763022,0.0011380558,0.99692655,0.00043508993,0.000017045213,0.000062259605,0.00023779285,0.000034964618,0.00015910303,0.00016092046,0.00032269408,0.00016788124],"about_ca_topic_score_codex":0.00030477025,"about_ca_topic_score_gemma":0.0033266717,"teacher_disagreement_score":0.0030219012,"about_ca_system_score_codex":0.000019171444,"about_ca_system_score_gemma":0.00030480407,"threshold_uncertainty_score":0.5094569},"labels":[{"model":"gemma","categories":[],"domain":null,"study_design":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"low"},{"model":"gpt","categories":[],"domain":null,"study_design":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"low"}],"label_agreement":"agree"},{"id":"W2334848682","doi":"10.1515/jpem.2004.17.9.1215","title":"Lack of Association of Birth Size with Polymorphisms of Two Imprinted Genes, IGF2R and GRB10","year":2004,"lang":"en","type":"article","venue":"Journal of Pediatric Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Genomic imprinting; Linkage disequilibrium; Allele; Genetics; Single-nucleotide polymorphism; SNP; Imprinting (psychology); Genotype; Gene; Medicine; Genetic association; Insulin-like growth factor 2 receptor; Biology; Insulin-like growth factor 1 receptor","score_opus":0.009059304429495851,"score_gpt":0.24769438171630606,"score_spread":0.23863507728681022,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2334848682","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98434544,0.014811326,0.00045371478,0.0001181789,0.00015132077,0.000060688755,0.00001029161,0.0000013027935,0.00004776024],"genre_scores_gemma":[0.98191065,0.013095364,0.0046509462,0.000027503944,0.00023459256,7.9885064e-7,0.0000011321952,0.000009431787,0.000069603746],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.998988,0.00005422223,0.0005020535,0.0001292053,0.00014026627,0.00018627921],"domain_scores_gemma":[0.9985533,0.000043090855,0.0009568981,0.0001177449,0.00026767506,0.00006129104],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021978129,0.00011523435,0.00040422223,0.000116913965,0.000021815747,0.0000030677584,0.00010053546,0.000096135576,0.000006660128],"category_scores_gemma":[0.0001696703,0.00009080773,0.00008050273,0.00011185784,0.00008749828,0.000006927339,0.00007542258,0.00011712244,1.1991331e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009640015,0.00012828378,0.36046773,0.00008843528,0.0003298533,0.0000065573636,0.00013350646,0.0000789282,0.6341284,0.0005536795,0.000020673595,0.0039675366],"study_design_scores_gemma":[0.0052341186,0.0007728011,0.63775074,0.000013752079,0.00047505132,0.00052739575,0.00012071315,0.0000017942386,0.35349628,0.00042267173,0.0010446198,0.00014004667],"about_ca_topic_score_codex":0.00005031391,"about_ca_topic_score_gemma":0.000008888992,"teacher_disagreement_score":0.28063214,"about_ca_system_score_codex":0.000005658988,"about_ca_system_score_gemma":0.00012199458,"threshold_uncertainty_score":0.37030315},"labels":[],"label_agreement":null},{"id":"W2342794187","doi":"10.14740/jem.v6i2.337","title":"Clinical and Genetic Study of Pseudohypoparathyroidism Type 1b in Hong Kong Chinese","year":2016,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Uniparental disomy; Imprinting (psychology); Multiplex ligation-dependent probe amplification; Genetics; Chinese population; Locus (genetics); Gene; Bioinformatics; Chromosome; Internal medicine; Parathyroid hormone; Karyotype; Biology; Genotype; Exon","score_opus":0.016792506397998935,"score_gpt":0.30657542035166213,"score_spread":0.2897829139536632,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2342794187","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9873995,0.01193276,0.0000494922,0.00009967693,0.00038854804,0.00008394798,9.17313e-7,0.0000010785923,0.000044061788],"genre_scores_gemma":[0.9924235,0.006566751,0.0006898479,0.000033400942,0.00020321137,0.0000011349503,1.6753633e-7,0.0000086537275,0.000073382645],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99882805,0.00015676115,0.00057271484,0.00018272466,0.00007234611,0.00018739217],"domain_scores_gemma":[0.9993855,0.000043159307,0.00025106812,0.00015280306,0.00009298965,0.000074524876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002263506,0.00011464057,0.00037606515,0.00009899993,0.000023368937,0.0000049928085,0.000115882314,0.00008669865,0.0000039703064],"category_scores_gemma":[0.00026378376,0.000071437906,0.000054774388,0.00006294901,0.00013696152,0.0000061567303,0.00013476139,0.00011937931,5.9664626e-7],"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":[0.000057018166,0.00020662132,0.83142936,0.0000042963757,0.000089395675,0.000040981242,0.000087687506,0.0000024338713,0.15104331,0.00002841369,0.00004067506,0.016969824],"study_design_scores_gemma":[0.0036106377,0.00083078374,0.9906474,0.000011163951,0.00004739674,0.0009917886,0.00016568373,0.0000012134227,0.0023541076,0.0001763942,0.0010800884,0.00008339137],"about_ca_topic_score_codex":0.00000768867,"about_ca_topic_score_gemma":0.000016811598,"teacher_disagreement_score":0.15921801,"about_ca_system_score_codex":0.000001396644,"about_ca_system_score_gemma":0.00003582349,"threshold_uncertainty_score":0.29131532},"labels":[],"label_agreement":null},{"id":"W2343776705","doi":"10.1016/j.soard.2016.04.023","title":"Sleeve gastrectomy leads to weight loss in the Magel2 knockout mouse","year":2016,"lang":"en","type":"article","venue":"Surgery for Obesity and Related Diseases","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Medicine; Weight loss; Internal medicine; Obesity; Sleeve gastrectomy; Endocrinology; Lean body mass; Knockout mouse; Weight gain; Body weight; Gastric bypass","score_opus":0.006801932565752736,"score_gpt":0.2175652416658789,"score_spread":0.21076330910012617,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2343776705","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972135,0.0010345273,0.00012981768,0.0010633058,0.000142811,0.00024540076,0.00006943555,0.000011259609,0.000089958136],"genre_scores_gemma":[0.9978967,0.000515641,0.000040774874,0.00017565148,0.000080519836,0.000039341307,0.000040236573,0.0000143864245,0.0011967956],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99909896,0.00006319009,0.00018685703,0.0002914716,0.00007796506,0.00028157662],"domain_scores_gemma":[0.9994677,0.0001186887,0.000044105836,0.00022739865,0.000033216646,0.00010891083],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018978777,0.00013121261,0.00014970831,0.000055583718,0.00009728144,0.000020493138,0.0001108601,0.00010050931,0.00002846837],"category_scores_gemma":[0.0001888868,0.00007672402,0.00013669462,0.00008841127,0.000066846405,0.0000051003626,0.000069143534,0.00003779025,0.0000130573435],"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":[0.00010417625,0.0001880864,0.9290797,0.00006297646,0.000064906766,0.000015254622,0.00009846071,0.000012385403,0.04667326,0.000074147785,0.005272217,0.01835443],"study_design_scores_gemma":[0.0010359203,0.00019563788,0.9290436,0.00013109871,0.00007793314,0.00007745011,0.000112090434,0.00000959376,0.04348039,0.0005315126,0.024877328,0.0004274428],"about_ca_topic_score_codex":0.000009553217,"about_ca_topic_score_gemma":0.000008451648,"teacher_disagreement_score":0.01960511,"about_ca_system_score_codex":0.000006344477,"about_ca_system_score_gemma":0.00003853539,"threshold_uncertainty_score":0.3128715},"labels":[],"label_agreement":null},{"id":"W2344998708","doi":"10.1242/dev.129.7.1657","title":"Disruption of mesodermal enhancers for<i>Igf2</i>in the minute mutant","year":2002,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"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 Joseph's Health Care; Lawson Health Research Institute","funders":"","keywords":"Biology; Genomic imprinting; Enhancer; DNA methylation; Genetics; Methylation; Gene silencing; Mutant; Gene; Cell biology; Gene expression","score_opus":0.019845530644543925,"score_gpt":0.2398604491141757,"score_spread":0.22001491846963178,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2344998708","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99580073,0.0003189824,0.0027058455,0.00014517906,0.000072467585,0.00018062223,0.000001916578,0.0000018175391,0.0007724252],"genre_scores_gemma":[0.9944369,0.00007012479,0.0049864114,0.00012633593,0.000030069637,0.00004790705,0.000016952992,0.000006224097,0.00027905434],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999426,0.000015462887,0.0001814073,0.00014109982,0.00008519319,0.00015081537],"domain_scores_gemma":[0.9997776,0.000007477663,0.000048928618,0.00012704093,0.000022720636,0.000016244809],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015617507,0.00007028134,0.00007127348,0.000018889454,0.00003427343,0.000006530655,0.00011782854,0.00004051065,0.000018619556],"category_scores_gemma":[0.000017558084,0.00005316853,0.00003693322,0.000045686967,0.000018750343,0.0000011139543,0.000033358727,0.000023454253,0.0000037942252],"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":[0.000012799665,0.00013063542,0.006261596,0.00006299125,0.000054039938,0.0000017429422,0.0030716415,0.00008606959,0.8793507,0.00007373022,0.0012239687,0.109670095],"study_design_scores_gemma":[0.0007621032,0.00014203192,0.076699115,0.000028505412,0.000010030505,0.00003059169,0.00057794066,0.00038076512,0.7870757,0.00002851639,0.13405626,0.00020844275],"about_ca_topic_score_codex":0.0000032907324,"about_ca_topic_score_gemma":0.000014777136,"teacher_disagreement_score":0.13283227,"about_ca_system_score_codex":0.0000089353325,"about_ca_system_score_gemma":0.000018499335,"threshold_uncertainty_score":0.21681497},"labels":[],"label_agreement":null},{"id":"W2345654030","doi":"10.1371/journal.pgen.1005993","title":"Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders","year":2016,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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; Centre for Addiction and Mental Health","funders":"European Commission; Canadian Institutes of Health Research; National Institute for Health and Care Research; Innovative Medicines Initiative; Genetics Society; National Institute of Mental Health; Medical Research Council; European Federation of Pharmaceutical Industries and Associations","keywords":"Biology; Gene duplication; Angelman syndrome; Genetics; Copy-number variation; Offspring; Population; Schizophrenia (object-oriented programming); Autism; Segmental duplication; Neurodevelopmental disorder; Gene; Pregnancy; Genome; Psychology; Medicine; Psychiatry","score_opus":0.01100033361773941,"score_gpt":0.2301001261174353,"score_spread":0.21909979249969588,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2345654030","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99850017,0.0002758215,0.00014883536,0.000079590965,0.00005663874,0.00013181401,0.000014216525,0.0000057675074,0.0007871514],"genre_scores_gemma":[0.9977481,0.00047660962,0.0013095487,0.000017826955,0.000028545217,0.000013789576,0.000009981647,0.000025628426,0.00037001082],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993012,0.00001859031,0.00018956156,0.0002538052,0.000074891235,0.00016197446],"domain_scores_gemma":[0.9996749,0.000008808772,0.000057875113,0.00018709303,0.000015231086,0.000056093224],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000029072244,0.00010718952,0.00009896223,0.00004764932,0.000027112932,0.0000054209368,0.00011072318,0.000058757363,0.000059857302],"category_scores_gemma":[0.000027609321,0.00009039357,0.000027951732,0.000050874263,0.00010320915,0.0000016166895,0.00022751468,0.000025130104,0.000011720582],"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":[0.000012861563,0.000061006685,0.21816443,0.000009923164,0.000016977863,2.5487498e-7,0.000037443744,0.000003313304,0.7742665,0.000021521537,0.00007045354,0.0073353346],"study_design_scores_gemma":[0.0018614746,0.00035430642,0.42511752,0.00006383883,0.000019916406,0.000026410451,0.000073835174,0.0001841856,0.5653243,0.00009393422,0.0065653548,0.00031492073],"about_ca_topic_score_codex":0.0000050473664,"about_ca_topic_score_gemma":0.00014656386,"teacher_disagreement_score":0.20894219,"about_ca_system_score_codex":0.000012321924,"about_ca_system_score_gemma":0.00002840497,"threshold_uncertainty_score":0.36861432},"labels":[],"label_agreement":null},{"id":"W2345760292","doi":"10.1007/s00439-016-1675-5","title":"The expanding phenotypic spectrum of female SLC9A6 mutation carriers: a case series and review of the literature","year":2016,"lang":"en","type":"review","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"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; Mount Sinai Hospital; Lakeridge Health; Hospital for Sick Children","funders":"","keywords":"Biology; Intellectual disability; Phenotype; Microcephaly; Genetics; Mutation; Angelman syndrome; Rett syndrome; Fragile X syndrome; UBE3A; Gene","score_opus":0.02066044893561742,"score_gpt":0.30338355180319254,"score_spread":0.2827231028675751,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2345760292","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.009589078,0.98949265,0.000015751977,0.000022739872,0.00015620548,0.0005357744,0.00005773544,0.0000023877446,0.00012769866],"genre_scores_gemma":[0.0055132704,0.9935612,0.00010990597,0.000016378197,0.00016025541,0.000026693175,0.000031426087,0.00003530264,0.000545578],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9986402,0.00017402496,0.00056790485,0.00028661342,0.00013192742,0.00019937012],"domain_scores_gemma":[0.9985635,0.000029292954,0.0005815619,0.00068980595,0.000093069735,0.000042735923],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026261996,0.0002584776,0.0005439244,0.0000296027,0.000197397,0.000032399166,0.0002874234,0.00018579226,0.000010116803],"category_scores_gemma":[0.0000936014,0.00013637976,0.00028039058,0.00012447152,0.0002187833,0.0000021143878,0.00028259825,0.00011744873,6.2054465e-7],"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":[0.0000048642314,0.000030349203,0.00012245736,0.12095343,0.0004821665,0.000029773204,0.0004734812,7.698122e-7,0.0027004713,0.0003151297,0.0003874621,0.8744996],"study_design_scores_gemma":[0.00022692932,0.000386099,0.00005452214,0.08696345,0.0006599866,0.0044969344,0.00017621937,3.8939626e-7,0.0033909194,0.00018884073,0.9030567,0.00039901905],"about_ca_topic_score_codex":0.0000023738585,"about_ca_topic_score_gemma":0.000014260102,"teacher_disagreement_score":0.90266925,"about_ca_system_score_codex":0.00001190408,"about_ca_system_score_gemma":0.00010708486,"threshold_uncertainty_score":0.55614054},"labels":[],"label_agreement":null},{"id":"W2346557592","doi":"10.1186/s13148-016-0215-4","title":"Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation","year":2016,"lang":"en","type":"article","venue":"Clinical Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University Health Centre","funders":"Studienstiftung des Deutschen Volkes; Bundesministerium für Bildung und Forschung","keywords":"CTCF; Genomic imprinting; DNA methylation; Biology; Transcription factor; Epigenetics; Imprinting (psychology); Chromatin; CRISPR; Methylation; Genetics; Chromatin immunoprecipitation; Enhancer; Promoter; Gene; Gene expression","score_opus":0.03547001202568329,"score_gpt":0.3256148072426463,"score_spread":0.290144795216963,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2346557592","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9720106,0.00081694144,0.025593333,0.0008146915,0.00027777633,0.0001382868,0.000015181522,0.000013248343,0.00031994915],"genre_scores_gemma":[0.9935526,0.00096109224,0.0037159855,0.00014248875,0.0004414654,0.000008585501,0.000041770443,0.000022317035,0.0011136784],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99858016,0.000102234335,0.0005398309,0.00041669377,0.0001325921,0.00022849343],"domain_scores_gemma":[0.99924916,0.00008679517,0.00014083623,0.00028485185,0.00011341125,0.00012496552],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005116112,0.00014226415,0.00018402684,0.000027355063,0.00008691378,0.000017917555,0.0001239545,0.00022103029,0.00007837804],"category_scores_gemma":[0.00043109746,0.00010658709,0.00010589297,0.00004736688,0.00021656138,0.000003962089,0.0001025661,0.000068072266,0.00001527107],"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":[0.0000139346685,0.000053998567,0.07645347,0.000011870938,0.000038076952,4.2819445e-7,0.000015619618,0.000019340107,0.82647735,0.00070521847,0.00043919313,0.0957715],"study_design_scores_gemma":[0.0013009993,0.00054544664,0.91776186,0.000039607774,0.000033970275,0.000008995771,0.000011709502,0.00012529896,0.0511629,0.006182379,0.022573967,0.00025285117],"about_ca_topic_score_codex":0.000004295686,"about_ca_topic_score_gemma":0.00002264955,"teacher_disagreement_score":0.8413084,"about_ca_system_score_codex":0.0000068818917,"about_ca_system_score_gemma":0.000032625187,"threshold_uncertainty_score":0.43464953},"labels":[],"label_agreement":null},{"id":"W2360837375","doi":"10.1016/j.fertnstert.2016.04.036","title":"Altered DNA methylation and expression of PLAGL1 in cord blood from assisted reproductive technology pregnancies compared with natural conceptions","year":2016,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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 British Columbia","funders":"Division of Materials Research; Canadian Institutes of Health Research","keywords":"DNA methylation; Genomic imprinting; Cord blood; Epigenetics; Biology; Andrology; Methylation; Methylated DNA immunoprecipitation; Placenta; Differentially methylated regions; Molecular biology; Genetics; Gene expression; Gene; Fetus; Pregnancy; Medicine","score_opus":0.016758465906837137,"score_gpt":0.24634008863740597,"score_spread":0.22958162273056884,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2360837375","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99819267,0.0008901189,0.0005146559,0.00009728968,0.000041231637,0.00018520532,0.00004878729,0.000008194946,0.00002182444],"genre_scores_gemma":[0.998777,0.00003021817,0.0011111306,0.0000053527624,0.000011226361,0.000013493907,0.000022772107,0.0000040480104,0.000024762765],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99911124,0.000083503364,0.00021343525,0.00041689238,0.00005871475,0.000116221665],"domain_scores_gemma":[0.9994674,0.0000237349,0.00009352182,0.00031610215,0.000071120165,0.000028122115],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012450758,0.000099348144,0.00018850168,0.000029526373,0.000041443585,0.0000069445277,0.000058217156,0.000097564734,0.0000067766446],"category_scores_gemma":[0.00012738461,0.00006743607,0.000017776003,0.000059632384,0.00029147076,0.000008805165,0.000117192685,0.00004923781,1.0215823e-7],"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":[0.001135485,0.000050451647,0.13638587,0.000018167984,0.000015692003,1.9764312e-7,0.00009821988,2.5870537e-7,0.8536342,9.16751e-7,0.0000010407754,0.008659516],"study_design_scores_gemma":[0.00059652043,0.00015693225,0.62837404,0.00006323215,0.000008900615,0.0000031610243,0.00013545211,0.0000074064064,0.37044814,0.00012392037,0.000027300852,0.000054985685],"about_ca_topic_score_codex":0.00005813542,"about_ca_topic_score_gemma":0.00017414513,"teacher_disagreement_score":0.49198818,"about_ca_system_score_codex":0.0000054639318,"about_ca_system_score_gemma":0.000017714336,"threshold_uncertainty_score":0.27499634},"labels":[],"label_agreement":null},{"id":"W2375961688","doi":"10.1038/ejhg.2016.45","title":"EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome","year":2016,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto","funders":"Bundesministerium für Bildung und Forschung","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Guideline; Best practice; Genetic testing; Context (archaeology); Snapshot (computer storage); Genomic imprinting; Medicine; Psychology; Computer science; Genetics; Biology; Political science; Pathology; Gene; Law","score_opus":0.053850792924303593,"score_gpt":0.3185356653326078,"score_spread":0.2646848724083042,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2375961688","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97948265,0.010836793,0.008500203,0.00055246835,0.00013320238,0.0002527817,0.000004343619,0.0000050991475,0.00023248255],"genre_scores_gemma":[0.931631,0.0015309938,0.06626911,0.00012586196,0.0002816813,0.0000026385455,9.112176e-7,0.000070143724,0.000087648266],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9969424,0.0001613741,0.0019697929,0.0003550802,0.00024477518,0.00032658692],"domain_scores_gemma":[0.9951488,0.000187787,0.0030410846,0.0004034719,0.0010915166,0.00012735045],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022122297,0.00025573673,0.00036447594,0.00007350974,0.00021719468,0.000071090064,0.00034364258,0.000055992205,0.000004263045],"category_scores_gemma":[0.0068637077,0.0001686294,0.00014693341,0.000085070176,0.0002021323,0.000013689226,0.00036226743,0.00011810442,7.8091114e-7],"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":[0.000011246919,0.000054751777,0.007411796,0.00008078099,0.0001826097,0.000043406115,0.0001125897,0.00021361238,0.9188233,0.000009763315,0.000087728215,0.07296844],"study_design_scores_gemma":[0.012413423,0.032212526,0.4106406,0.004162689,0.0032800876,0.042540796,0.006364081,0.0018027289,0.42380026,0.001445443,0.05798335,0.003353991],"about_ca_topic_score_codex":0.0000065576196,"about_ca_topic_score_gemma":0.000002781753,"teacher_disagreement_score":0.495023,"about_ca_system_score_codex":0.000008007078,"about_ca_system_score_gemma":0.00006270446,"threshold_uncertainty_score":0.8216995},"labels":[],"label_agreement":null},{"id":"W2395063123","doi":"10.1371/journal.pgen.1006062","title":"Angelman Syndrome Protein Ube3a Regulates Synaptic Growth and Endocytosis by Inhibiting BMP Signaling in Drosophila","year":2016,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"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 Natural Science Foundation of China; Ministry of Science and Technology; National Science Foundation; National Institutes of Health; Chinese Academy of Sciences","keywords":"UBE3A; Biology; Cell biology; Ubiquitin ligase; Angelman syndrome; Bone morphogenetic protein; Ubiquitin; Endocytosis; F-box protein; BMPR2; Genetics; Receptor","score_opus":0.00981467043920895,"score_gpt":0.2027767330921121,"score_spread":0.19296206265290317,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2395063123","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967848,0.0022194583,0.000096052136,0.00029730887,0.000033184213,0.00038956595,0.000021193122,0.000021903872,0.00013652343],"genre_scores_gemma":[0.99782866,0.00030496603,0.0014797924,0.00006686573,0.00006874933,0.000059851096,0.000016541964,0.000060108476,0.00011443284],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982288,0.00008022759,0.00040019286,0.0005925562,0.00018877069,0.0005094396],"domain_scores_gemma":[0.9993649,0.000032818843,0.00012917799,0.00027854042,0.000055476703,0.00013907913],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015767073,0.00027259171,0.0002615606,0.00008679335,0.000085926265,0.00004725134,0.00019855342,0.00019429166,0.000015138264],"category_scores_gemma":[0.00015984676,0.00023218797,0.00006133001,0.00012420515,0.00012184096,0.0000067356827,0.0002661362,0.00009150363,0.0000062388453],"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":[0.0000061335213,0.000061769744,0.017621234,0.00007068132,0.000053526957,0.00000938496,0.000035506073,0.0000050536128,0.9811111,0.000018140818,0.000017764545,0.0009897238],"study_design_scores_gemma":[0.00075004675,0.0004261468,0.0026223764,0.00025715417,0.000026442074,0.00011460482,0.000049884442,0.00013560223,0.9948563,0.00029560263,0.0001031787,0.00036264458],"about_ca_topic_score_codex":0.000009037122,"about_ca_topic_score_gemma":0.0000068450663,"teacher_disagreement_score":0.014998857,"about_ca_system_score_codex":0.000019030918,"about_ca_system_score_gemma":0.000033096854,"threshold_uncertainty_score":0.94683504},"labels":[],"label_agreement":null},{"id":"W2402010036","doi":"10.1016/j.jtho.2016.05.010","title":"ITPKA Gene Body Methylation Regulates Gene Expression and Serves as an Early Diagnostic Marker in Lung and Other Cancers","year":2016,"lang":"en","type":"article","venue":"Journal of Thoracic Oncology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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 Cancer Agency","funders":"National Cancer Institute","keywords":"Medicine; Methylation; Gene; DNA methylation; Lung cancer; Gene expression; Cancer research; Lung; Genetics; Pathology; Internal medicine; Biology","score_opus":0.010288991759806392,"score_gpt":0.3360287557402515,"score_spread":0.3257397639804451,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2402010036","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99611443,0.0028602362,0.00038403037,0.00032032508,0.00015489347,0.00009027005,0.000002953399,0.0000019397432,0.00007091256],"genre_scores_gemma":[0.994622,0.00085390505,0.0040539615,0.00010625276,0.00017307531,0.00000406936,0.0000012558194,0.000016145792,0.0001693433],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999017,0.00021518373,0.00031257625,0.00019593896,0.00008601933,0.00017328367],"domain_scores_gemma":[0.9993298,0.000094859926,0.0002694169,0.00012728275,0.000070207374,0.00010844711],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005220039,0.00011016767,0.0002103049,0.000084689396,0.000037122238,0.000017695495,0.00009000949,0.0001733315,0.000026656622],"category_scores_gemma":[0.00024024185,0.00007633449,0.000035233563,0.00004140668,0.00006641505,0.000017105978,0.00007960494,0.00007455663,6.333151e-7],"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":[0.000118770855,0.000024040948,0.12673984,0.000012159421,0.00002733379,0.000012070871,0.00009759455,0.0000139725435,0.8404329,0.0000016177033,0.00003429516,0.03248542],"study_design_scores_gemma":[0.0006071422,0.0010440467,0.47627556,0.00009528726,0.000037088448,0.00038709122,0.00008764905,0.000038664835,0.51965165,0.00022260536,0.0014318774,0.000121310666],"about_ca_topic_score_codex":0.000052443283,"about_ca_topic_score_gemma":0.00003689491,"teacher_disagreement_score":0.34953573,"about_ca_system_score_codex":0.000044634853,"about_ca_system_score_gemma":0.00009186012,"threshold_uncertainty_score":0.311283},"labels":[],"label_agreement":null},{"id":"W2403173295","doi":"10.1038/gim.2016.53","title":"The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families","year":2016,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":122,"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; Children's & Women's Health Centre of British Columbia; Centre Hospitalier Universitaire de Sherbrooke","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Intellectual and Developmental Disabilities Research Center; Foundation for Prader-Willi Research","keywords":"Genetics; Hypotonia; Phenotype; Allele; Autism spectrum disorder; Intellectual disability; Disease; Context (archaeology); Biology; Gene; Medicine; Autism; Internal medicine","score_opus":0.013843740163734906,"score_gpt":0.2566116621732599,"score_spread":0.24276792200952502,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2403173295","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9859538,0.009176656,0.0020117117,0.0014590581,0.0004981606,0.00023554693,0.000014391839,0.000009831664,0.0006408211],"genre_scores_gemma":[0.99224955,0.004801,0.0015160401,0.000119582655,0.0003503319,0.000009261544,0.000023261577,0.000030824816,0.00090012955],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9983514,0.00009711858,0.00047440923,0.0003858789,0.00029629344,0.00039490726],"domain_scores_gemma":[0.99886566,0.00011663832,0.00017786724,0.0006754132,0.00005227378,0.00011216253],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004037049,0.00021122297,0.0003081808,0.00008343524,0.0000667404,0.000010478093,0.00047342642,0.00016043778,0.00015848274],"category_scores_gemma":[0.00044620552,0.00012446949,0.000060178983,0.00019211431,0.00030293022,0.000002149622,0.00024647987,0.00010153646,0.000014158423],"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":[0.000019372714,0.000041546697,0.115430795,0.00002100786,0.00014982831,0.0000051541538,0.00026730399,0.000025685007,0.8078168,0.00009820232,0.0041630627,0.07196126],"study_design_scores_gemma":[0.0030261357,0.0009327136,0.7925478,0.0003492651,0.000066382636,0.000041535186,0.00044435117,0.000022888482,0.17426099,0.0035700824,0.024414351,0.0003234801],"about_ca_topic_score_codex":0.00018846581,"about_ca_topic_score_gemma":0.00016529305,"teacher_disagreement_score":0.67711705,"about_ca_system_score_codex":0.000015590467,"about_ca_system_score_gemma":0.0000935438,"threshold_uncertainty_score":0.5075718},"labels":[],"label_agreement":null},{"id":"W246072","doi":"10.1385/1-59259-300-3:291","title":"Molecular Detection of Uniparental Disomy","year":2003,"lang":"en","type":"article","venue":"Molecular Cytogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Uniparental disomy; Genetics; Biology; Genotyping; Microsatellite; Imprinting (psychology); Karyotype; Genomic imprinting; DNA methylation; Chromosome; Genotype; Gene; Allele","score_opus":0.007801442593724252,"score_gpt":0.22665746649278531,"score_spread":0.21885602389906106,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W246072","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9281463,0.001563854,0.067953005,0.000010892193,0.00016913241,0.000188344,0.0000069296457,0.000010563103,0.0019509918],"genre_scores_gemma":[0.9959122,0.00008918162,0.003721255,0.00009252169,0.000022730816,0.000015364703,0.000027387496,0.000051583193,0.000067778514],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986178,0.00011555339,0.0003238732,0.0003859759,0.00022875892,0.00032802625],"domain_scores_gemma":[0.99909383,0.0000045680094,0.00012559647,0.000553972,0.000109003995,0.00011305446],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013930476,0.00022012035,0.00018806053,0.000067800574,0.000051385265,0.000017369914,0.00020281546,0.00016617897,0.000019515683],"category_scores_gemma":[0.000112778675,0.00024237891,0.00018474432,0.00018108527,0.00009245759,0.0000017078761,0.000105192434,0.000078034165,0.000008623824],"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":[0.0000047281655,0.000060768973,0.014592672,0.000019091214,0.00006368022,0.0000061823157,0.00001334836,0.00094379194,0.98165774,0.00040407927,0.000007204,0.0022267061],"study_design_scores_gemma":[0.00048463934,0.0003157145,0.0025235463,0.000009662589,0.00004179701,0.000079343736,0.000058080674,0.000033534805,0.9867412,0.00017032264,0.009283389,0.0002587697],"about_ca_topic_score_codex":0.0000069133403,"about_ca_topic_score_gemma":0.000004235804,"teacher_disagreement_score":0.06776591,"about_ca_system_score_codex":0.000012570957,"about_ca_system_score_gemma":0.000061388506,"threshold_uncertainty_score":0.9883925},"labels":[],"label_agreement":null},{"id":"W2464134108","doi":"10.2217/epi-2016-0007","title":"Phenotypic Spectrum and Extent of DNA Methylation Defects Associated with Multilocus Imprinting Disturbances","year":2016,"lang":"en","type":"article","venue":"Epigenomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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","keywords":"Biology; Imprinting (psychology); DNA methylation; Genetics; Phenotype; Genomic imprinting; Epigenetics; Methylation; DNA; Computational biology; Evolutionary biology; Gene; Gene expression","score_opus":0.00778595025884418,"score_gpt":0.2124860684525933,"score_spread":0.20470011819374911,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2464134108","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9927352,0.00072984165,0.0060768044,0.00004446083,0.00005947548,0.00011584306,0.0000075149337,0.000005862112,0.00022497385],"genre_scores_gemma":[0.9983492,0.00017802982,0.0011920953,0.000011566591,0.00005163997,0.0000039598444,0.000007188613,0.000016811304,0.00018953963],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992449,0.000039371324,0.00020720289,0.00025098302,0.00007283971,0.00018469724],"domain_scores_gemma":[0.99949485,0.000031431366,0.00019788636,0.00019149501,0.000041311527,0.000043006334],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023067102,0.0001114756,0.00014982536,0.000019120194,0.000046850037,0.000011755192,0.00007995982,0.000064367494,0.000005368048],"category_scores_gemma":[0.00013684407,0.00007517998,0.00004245186,0.000033471686,0.00006366639,0.000003070397,0.00007980334,0.000028875864,0.0000012470045],"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":[0.000014955419,0.000023654125,0.06216007,0.000009348631,0.000061524624,3.4204115e-7,0.00006136866,0.00003219775,0.9153804,0.00007665341,0.000005230381,0.022174262],"study_design_scores_gemma":[0.00059427274,0.00023136147,0.47927025,0.000030664083,0.000023064338,0.0000040215573,0.00003805713,0.0000554106,0.51877964,0.00015895233,0.000663391,0.00015093395],"about_ca_topic_score_codex":0.000020935846,"about_ca_topic_score_gemma":0.000045956403,"teacher_disagreement_score":0.41711017,"about_ca_system_score_codex":0.000015830512,"about_ca_system_score_gemma":0.000022633225,"threshold_uncertainty_score":0.30657506},"labels":[],"label_agreement":null},{"id":"W2465632847","doi":"10.1080/02701367.2016.1182113","title":"A Characterization of Movement Skills in Obese Children With and Without Prader-Willi Syndrome","year":2016,"lang":"en","type":"article","venue":"Research Quarterly for Exercise and Sport","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Francis Xavier University","funders":"California State University, Fullerton","keywords":"Normative; Gross motor skill; Motor skill; Movement assessment; Medicine; Psychology; Motor function; Developmental psychology; Physical therapy; Audiology; Physical medicine and rehabilitation","score_opus":0.010247144788470131,"score_gpt":0.2747624842016629,"score_spread":0.2645153394131928,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2465632847","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9987488,0.00016533627,0.00027326072,0.0000832104,0.0000094315365,0.0006823934,0.000020536907,0.0000027351468,0.000014341569],"genre_scores_gemma":[0.99832195,0.00077788846,0.0002506275,0.000008725225,0.000018325449,0.00008977963,0.000041674324,0.000016141676,0.0004748587],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99905443,0.000014946769,0.00018801613,0.0003015621,0.00016663072,0.00027439406],"domain_scores_gemma":[0.9995839,0.000005852968,0.000053864787,0.0001910988,0.0000835801,0.000081722486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038093558,0.00009974607,0.00018529115,0.00010007029,0.000042803473,0.00001780295,0.000074003576,0.000070674316,0.0000044130948],"category_scores_gemma":[0.000008247273,0.000066688,0.000023265293,0.00007435892,0.0001059232,0.0000100151865,0.000032633798,0.000039547438,6.0074285e-7],"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":[0.00002297521,0.000087217944,0.6616528,0.000053087577,0.000024265728,5.157137e-7,0.00015354458,9.700011e-8,0.29063,0.000024333709,0.000004608965,0.04734653],"study_design_scores_gemma":[0.0012305446,0.0018431172,0.974103,0.0002475525,0.000008457237,0.000034509318,0.00009856555,0.0000075056796,0.022075672,0.00008216569,0.00015692694,0.00011198376],"about_ca_topic_score_codex":0.00004489522,"about_ca_topic_score_gemma":0.00002563248,"teacher_disagreement_score":0.3124502,"about_ca_system_score_codex":0.000006345673,"about_ca_system_score_gemma":0.00004290523,"threshold_uncertainty_score":0.27194577},"labels":[],"label_agreement":null},{"id":"W2465667391","doi":"10.1093/hmg/ddw181","title":"Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder","year":2016,"lang":"en","type":"review","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":237,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Douglas Mental Health University Institute; McGill University Health Centre; Montreal Neurological Institute and Hospital; Dalhousie University","funders":"Common Fund; National Institute of Neurological Disorders and Stroke; National Cancer Institute; NIH Office of the Director; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Drug Abuse; University of Miami; National Alliance for Research on Schizophrenia and Depression; National Institutes of Health; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; University of Louisville; Ministry of Education, India; Broad Institute; Johns Hopkins University; National Center for Advancing Translational Sciences; National Human Genome Research Institute; Wellcome Trust; University of Pennsylvania; Wayne State University","keywords":"Genome-wide association study; Bipolar disorder; Genetics; Heritability; Biology; Odds ratio; Genetic association; Genotype; Medicine; Single-nucleotide polymorphism; Internal medicine; Gene; Lithium (medication); Endocrinology","score_opus":0.021665797165333386,"score_gpt":0.2920494485161157,"score_spread":0.2703836513507823,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2465667391","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.38383597,0.61408913,0.00067323196,0.0000037505927,0.00008398224,0.0010735146,0.00014763793,0.000017169885,0.00007561005],"genre_scores_gemma":[0.10746244,0.88874084,0.0002955024,0.00004895328,0.00019515869,0.00020335102,0.0013011472,0.00035889752,0.0013937071],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.995867,0.00042766874,0.0012050947,0.0010097258,0.0007909295,0.0006995916],"domain_scores_gemma":[0.99651515,0.00008637684,0.0016981225,0.0011581477,0.00039716376,0.00014501532],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006523337,0.0007898154,0.0015039908,0.00026324714,0.0001976946,0.00011216252,0.00082302146,0.0006130679,0.00005578346],"category_scores_gemma":[0.00035250047,0.0006583688,0.0004696777,0.0003470007,0.00010545186,0.0000049637133,0.0005866277,0.00030065692,0.000016346958],"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":[0.000046341687,0.015427841,0.41135013,0.013357093,0.053288437,0.00013029932,0.0024306278,0.0010980573,0.17713685,0.00007975115,0.0014712651,0.3241833],"study_design_scores_gemma":[0.0042053303,0.0028079238,0.066794425,0.0029296821,0.0041216146,0.00002042709,0.00022655883,0.0000019912388,0.0011194336,0.00005132354,0.9154599,0.0022614433],"about_ca_topic_score_codex":0.000034225475,"about_ca_topic_score_gemma":0.00011208353,"teacher_disagreement_score":0.9139886,"about_ca_system_score_codex":0.000119375996,"about_ca_system_score_gemma":0.00020409163,"threshold_uncertainty_score":0.99958676},"labels":[],"label_agreement":null},{"id":"W2472443615","doi":"10.1037/bne0000150","title":"Dopamine pathway imbalance in mice lacking Magel2, a Prader-Willi syndrome candidate gene.","year":2016,"lang":"en","type":"article","venue":"Behavioral Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"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":"Stollery Children’s Hospital Foundation","keywords":"Dopaminergic; Dopamine; Binge eating; Dopaminergic pathways; Appetite; Psychology; Neuroscience; Eating disorders; Endocrinology; Internal medicine; Medicine; Psychiatry","score_opus":0.02205572228013147,"score_gpt":0.2701116726898296,"score_spread":0.24805595040969813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2472443615","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99824876,0.00013539837,0.00070728816,0.0002651827,0.00036594202,0.00018705244,0.000027691956,0.000018878975,0.000043834607],"genre_scores_gemma":[0.9978778,0.00012309132,0.0006745756,0.00022029756,0.000044908975,0.000026536478,0.0000051869274,0.000024164063,0.0010034513],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9982368,0.000055555363,0.0002673735,0.0006927522,0.00021210838,0.0005354254],"domain_scores_gemma":[0.99934447,0.000007694389,0.00010491807,0.00038652998,0.000035083234,0.00012130484],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018406639,0.00019607187,0.00016226192,0.000069639085,0.000086131375,0.00005005094,0.00043590137,0.000085146115,0.0000120226805],"category_scores_gemma":[0.000069874724,0.00015293882,0.000059330807,0.00023329876,0.00016752075,0.000016723052,0.0002694233,0.000080613856,0.0000147592555],"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":[9.68106e-7,0.000044753433,0.18324411,0.0000036008541,3.9840307e-7,0.000023413604,0.000008921711,0.000007356633,0.8120335,0.0000031616387,0.000016574617,0.0046132565],"study_design_scores_gemma":[0.0005335947,0.00037956936,0.7648167,0.00003672256,0.0000040354307,0.0005394079,0.0000131839815,0.00003739979,0.22833955,0.0000073983992,0.0050077867,0.00028465939],"about_ca_topic_score_codex":0.0000750508,"about_ca_topic_score_gemma":0.000053863267,"teacher_disagreement_score":0.5836939,"about_ca_system_score_codex":0.000021540453,"about_ca_system_score_gemma":0.000075050404,"threshold_uncertainty_score":0.62366647},"labels":[],"label_agreement":null},{"id":"W2473766466","doi":"10.1007/978-1-62703-011-3_8","title":"Engineering of Large Deletions and Duplications In Vivo","year":2012,"lang":"en","type":"article","venue":"Methods in molecular biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Limiting; Subcloning; Biology; Insertional mutagenesis; Transgene; Gene; Computational biology; Genetics; Stem cell; Cell biology; Genome; Engineering; Recombinant DNA","score_opus":0.012458061833912133,"score_gpt":0.35242424333669076,"score_spread":0.33996618150277863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2473766466","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5649387,0.0012703269,0.43344945,0.00003326032,0.000047366422,0.00007078152,0.0000037943746,0.0000022020922,0.00018409325],"genre_scores_gemma":[0.60263723,0.00008113895,0.39716512,0.00004630321,0.000015535508,0.00002311211,0.0000064392166,0.000008466067,0.00001667192],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999169,0.00016330503,0.00020920485,0.0001749362,0.000021202752,0.0002623594],"domain_scores_gemma":[0.9996609,0.00003081846,0.00004241225,0.00020684497,0.000017596445,0.00004144755],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006896855,0.00008505004,0.00014175616,0.00010377352,0.00001196122,0.0000020720965,0.00008524977,0.00013435479,0.000014280709],"category_scores_gemma":[0.00029172646,0.000089216315,0.000034400506,0.00013352933,0.000035257228,0.0000014981283,0.0001278718,0.00007003158,5.5085525e-7],"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":[9.734946e-7,0.000037322763,0.06601699,0.000009500875,0.000008293114,1.743452e-7,0.000037430487,0.00004721319,0.93001246,0.0023407054,0.000003290674,0.001485621],"study_design_scores_gemma":[0.00040546904,0.00006638546,0.06620741,0.000012713302,0.000008243455,0.00002807196,0.000060927745,0.00041186836,0.9201255,0.00026305515,0.012247935,0.0001624501],"about_ca_topic_score_codex":0.000019073068,"about_ca_topic_score_gemma":0.0000075625217,"teacher_disagreement_score":0.037698492,"about_ca_system_score_codex":0.0000058946903,"about_ca_system_score_gemma":0.000011683176,"threshold_uncertainty_score":0.36381358},"labels":[],"label_agreement":null},{"id":"W2473891204","doi":"10.1002/ajmg.a.37819","title":"Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell–Silver syndrome","year":2016,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Centre for Global Health Research; SickKids Foundation; Mount Sinai Hospital; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Epigenetics; Genetics; Biology; Phenotype; DNA methylation; Etiology; Gene; Medicine; Internal medicine; Gene expression","score_opus":0.013388694992727183,"score_gpt":0.27735202652610513,"score_spread":0.263963331533378,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2473891204","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954688,0.002442964,0.0010530304,0.0006837567,0.00011432161,0.00021054348,0.0000060999787,0.0000010592543,0.000019428944],"genre_scores_gemma":[0.9948502,0.00342479,0.0014053838,0.00018796106,0.000088004854,0.000012422669,7.8605865e-7,0.000021703287,0.000008703505],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9978064,0.00014525196,0.00090458774,0.00023582461,0.00052644475,0.00038153474],"domain_scores_gemma":[0.9985244,0.0001883176,0.0006939408,0.0003463031,0.00012160468,0.00012542152],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012401552,0.0001674267,0.00046910526,0.000108115186,0.000016281534,0.000008342627,0.00072850776,0.000091352646,0.000031683958],"category_scores_gemma":[0.0005521112,0.00010533596,0.00018586211,0.00021638001,0.00036067923,0.000005734739,0.00015193933,0.00014987942,0.0000019199276],"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":[0.00015297187,0.00024327896,0.5589651,0.00007106526,0.00013923175,0.000030423453,0.0009822451,0.00007436947,0.37704948,0.000011664344,0.00003865075,0.062241506],"study_design_scores_gemma":[0.0042930255,0.0057559935,0.95318717,0.0019369732,0.00009704999,0.001640511,0.0039565824,0.00035916883,0.02414679,0.00027721692,0.0039160857,0.00043342632],"about_ca_topic_score_codex":0.00007449965,"about_ca_topic_score_gemma":0.00006613,"teacher_disagreement_score":0.39422208,"about_ca_system_score_codex":0.000021807165,"about_ca_system_score_gemma":0.0002597333,"threshold_uncertainty_score":0.42954758},"labels":[],"label_agreement":null},{"id":"W2485121654","doi":"10.1016/j.yapd.2016.04.005","title":"Prader Willi Syndrome","year":2016,"lang":"en","type":"review","venue":"Advances in Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":83,"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 Hospital; University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; Canadian Institutes of Health Research","keywords":"Medicine; Insulin resistance; Obesity; Disease; Hypotonia; Bioinformatics; Metabolic syndrome; Diabetes mellitus; Type 2 diabetes; Epidemiology; Internal medicine; Endocrinology; Intensive care medicine; Biology","score_opus":0.01318526558406407,"score_gpt":0.3115986136356986,"score_spread":0.2984133480516345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2485121654","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00008310989,0.99695635,0.00035938842,0.000007726408,0.00080460054,0.00034287744,0.0000354633,0.000011901442,0.0013985902],"genre_scores_gemma":[0.0000675791,0.99705595,0.00088804174,0.000024504912,0.00059420103,0.000076820885,0.00007881367,0.00007128687,0.0011427926],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9981372,0.000078389916,0.00055333955,0.0006206475,0.0001695897,0.00044086008],"domain_scores_gemma":[0.9989758,0.00005769942,0.0003143894,0.00053482136,0.00003364028,0.000083608174],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0001892679,0.00037891607,0.0007390543,0.00016222426,0.000043278902,0.000019220743,0.00043779745,0.00042674446,0.000032455602],"category_scores_gemma":[0.00018364062,0.00028773677,0.0002733836,0.0002855253,0.00005315076,0.000007534505,0.000262978,0.00019584746,0.000107351596],"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":[1.3202289e-7,0.000021432445,0.0005165463,0.003029417,0.000014611074,0.000005376823,0.0000026605321,0.000002255771,0.0000010296997,0.000021374317,0.0003486897,0.99603647],"study_design_scores_gemma":[0.00014749423,0.000093402276,0.00006245556,0.0009757875,0.000078437595,0.00024239394,0.0000039696956,1.9827246e-7,7.261821e-7,0.00006557699,0.99792886,0.0004006784],"about_ca_topic_score_codex":0.0000010626786,"about_ca_topic_score_gemma":0.0000030701053,"teacher_disagreement_score":0.9975802,"about_ca_system_score_codex":0.000033842,"about_ca_system_score_gemma":0.00017613346,"threshold_uncertainty_score":0.9999575},"labels":[],"label_agreement":null},{"id":"W2492410565","doi":"10.1093/hmg/ddw225","title":"Muscle dysfunction caused by loss of<i>Magel2</i>in a mouse model of Prader-Willi and Schaaf-Yang syndromes","year":2016,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"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":"Hypotonia; Internal medicine; Endocrinology; Atrophy; Phenotype; Sarcopenia; Biology; Obesity; Lean body mass; Medicine; Gene; Body weight; Genetics","score_opus":0.014592802896699009,"score_gpt":0.23441282972254737,"score_spread":0.21982002682584836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2492410565","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9805004,0.0011970366,0.017852178,0.0000613373,0.000030585772,0.00021470123,0.00004580781,0.000007651185,0.00009028479],"genre_scores_gemma":[0.99703205,0.00058535207,0.0018094237,0.00004409097,0.000017627997,0.000013814263,0.00002153689,0.000047253874,0.00042885588],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99859995,0.00006214073,0.00042061508,0.00042445696,0.00019643632,0.00029637598],"domain_scores_gemma":[0.99914837,0.000008983437,0.0001839134,0.00048171473,0.00009089369,0.000086137276],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015391987,0.00021188502,0.00026477568,0.000090843234,0.00003940021,0.000011669886,0.00018004588,0.00016387644,0.000009775273],"category_scores_gemma":[0.000042495656,0.00019040915,0.00009060193,0.00007754737,0.00018871178,0.0000048268594,0.00018269608,0.000061418585,0.0000015889218],"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":[0.000002207877,0.0000674139,0.007682269,0.00005846351,0.00004065472,0.0000010125818,0.0000517751,0.0003764386,0.98968977,0.00004733848,0.000053068736,0.0019295872],"study_design_scores_gemma":[0.0013984119,0.00048060087,0.026727466,0.00006568709,0.00003710742,0.000011268917,0.000045040975,0.000557755,0.96972847,0.0002505855,0.00039003982,0.00030757213],"about_ca_topic_score_codex":0.000016843695,"about_ca_topic_score_gemma":0.000014787614,"teacher_disagreement_score":0.019961307,"about_ca_system_score_codex":0.000011920651,"about_ca_system_score_gemma":0.000042099575,"threshold_uncertainty_score":0.77646595},"labels":[],"label_agreement":null},{"id":"W2503979078","doi":"10.1002/ajmg.a.37876","title":"Maternal uniparental disomy for chromosome 6 in a patient with IUGR, ambiguous genitalia, and persistent mullerian structures","year":2016,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto; University of Alberta; SickKids Foundation; Mount Sinai Hospital","funders":"","keywords":"Uniparental disomy; Karyotype; Biology; SNP array; Testis determining factor; Ambiguous genitalia; Vagina; Chromosome; Genetics; Gynecology; Y chromosome; Medicine; Anatomy; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.014196344817869353,"score_gpt":0.2866293410021264,"score_spread":0.27243299618425704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2503979078","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.35836798,0.6408379,0.00016253663,0.00005726412,0.0002352811,0.0002800068,0.00004816655,0.0000015318706,0.000009318694],"genre_scores_gemma":[0.06164097,0.9361731,0.0015389364,0.0000710422,0.00042289845,0.000032823707,0.000025179708,0.00006379182,0.000031288262],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99760944,0.00013521292,0.0008824734,0.0003791536,0.000572156,0.00042156357],"domain_scores_gemma":[0.99835914,0.000029501593,0.0008371354,0.00025123273,0.00009350828,0.0004295071],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026672456,0.0003827106,0.0011248778,0.00012560003,0.000044158012,0.00004152338,0.0004306067,0.0002058184,0.00004054755],"category_scores_gemma":[0.000079302576,0.00024024118,0.00038176196,0.00009728346,0.0004048652,0.0000026482744,0.00020708393,0.00023236484,0.000001152847],"study_design_candidate":"design_other","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":[0.000029022964,0.000051637926,0.00029602624,0.0005343664,0.00037771463,0.000066066284,0.000064873675,0.000003282886,0.000069307855,0.0000016492189,0.0000803923,0.99842566],"study_design_scores_gemma":[0.0014356471,0.0061506582,0.0004994686,0.005578997,0.00040723765,0.007840746,0.00036782128,0.000012013632,0.00008715977,0.000010787379,0.9770658,0.00054368644],"about_ca_topic_score_codex":0.000024936251,"about_ca_topic_score_gemma":0.000016475662,"teacher_disagreement_score":0.99788195,"about_ca_system_score_codex":0.000039326565,"about_ca_system_score_gemma":0.00044580415,"threshold_uncertainty_score":0.9796751},"labels":[],"label_agreement":null},{"id":"W2510138868","doi":"10.1086/377956","title":"<i>Genomic Imprinting and Kinship</i>. <i>The Rutgers Series in Human Evolution. By </i>David Haig. <i>New Brunswick (New Jersey): Rutgers University Press</i>. $65.00 (hardcover); $29.00 (paper). xiii + 218 p; ill.; index. ISBN: 0–8135–3026–1 (hc); 0–8135–3027–X (pb). 2002.","year":2003,"lang":"en","type":"review","venue":"The Quarterly Review of Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Kinship; Library science; Index (typography); History; Genealogy; Anthropology; Sociology; Media studies; Computer science","score_opus":0.012061909293222477,"score_gpt":0.2500481354270149,"score_spread":0.2379862261337924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2510138868","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005113425,0.9926535,0.00029242583,0.00053068413,0.00047514177,0.0021264097,0.00013041565,0.000030936455,0.0032491444],"genre_scores_gemma":[0.00067294156,0.99371886,0.00027191226,0.0008954239,0.00037744798,0.000028797349,0.00030314224,0.00012280978,0.0036086608],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9935097,0.0016757948,0.0018585133,0.0014880197,0.00027991936,0.001188039],"domain_scores_gemma":[0.9957866,0.00016584333,0.0017273519,0.0018195614,0.00018171415,0.0003189064],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0016257063,0.0011970601,0.0026757533,0.00016480016,0.00040033905,0.000081904276,0.0017930106,0.0009960468,0.00013603439],"category_scores_gemma":[0.00011773597,0.0008857401,0.0008849841,0.000515492,0.00081298914,0.00003850429,0.00046722108,0.0009844546,0.000034169643],"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":[0.000096030766,0.00025692765,0.0005660405,0.03741687,0.0018547238,0.00001848824,0.0005044332,0.0000050644853,0.06799338,0.0011578954,0.10222711,0.787903],"study_design_scores_gemma":[0.00089798274,0.00087557844,0.00003608443,0.005787711,0.0006634992,0.0002951902,0.000101700694,0.000001318108,0.00034055868,0.00008764593,0.9899867,0.00092601473],"about_ca_topic_score_codex":0.0019526393,"about_ca_topic_score_gemma":0.000068992435,"teacher_disagreement_score":0.8877596,"about_ca_system_score_codex":0.00015338988,"about_ca_system_score_gemma":0.0012905177,"threshold_uncertainty_score":0.9993593},"labels":[],"label_agreement":null},{"id":"W2510213943","doi":"10.1016/j.placenta.2016.06.204","title":"The expression of imprinted genes in the preeclamptic placenta","year":2016,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"","keywords":"Medicine; Randomized controlled trial; Abdominal aortic aneurysm; Ultrasonography; Surgery; Abdominal ultrasonography; Radiology; Internal medicine; Aneurysm","score_opus":0.009860331585256224,"score_gpt":0.23785578526263287,"score_spread":0.22799545367737664,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2510213943","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99757916,0.00081894116,0.00029226605,0.0004503747,0.00011994859,0.00018881602,0.000004815904,0.0000032482042,0.0005424172],"genre_scores_gemma":[0.99868083,0.00058390154,0.00012747527,0.00004937498,0.00005266706,0.000018996752,0.0000046290456,0.000009551829,0.00047258678],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991558,0.00012482742,0.00019507315,0.0001831725,0.00012732392,0.00021380749],"domain_scores_gemma":[0.9993479,0.00009191935,0.000080883205,0.00043037173,0.000024092213,0.000024813487],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003749642,0.00009349922,0.0000768419,0.0000153529,0.00007850427,0.0000146013235,0.0003804366,0.00005878085,0.000019741297],"category_scores_gemma":[0.00012427103,0.000041275733,0.00004933185,0.000049555667,0.00007497991,0.0000021167396,0.00017217937,0.000050320923,0.000007319667],"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":[0.000026501113,0.000029542321,0.032665778,0.000006489258,0.000008015175,3.564186e-7,0.00007067084,0.0000026885834,0.9584546,0.000026739399,0.0005521678,0.008156422],"study_design_scores_gemma":[0.00076677697,0.00011369208,0.056492236,0.000056089564,0.0000070127394,0.000023782253,0.00053953903,0.000018587829,0.91966593,0.00004972385,0.022163972,0.00010266884],"about_ca_topic_score_codex":0.0000187918,"about_ca_topic_score_gemma":0.000041929386,"teacher_disagreement_score":0.03878871,"about_ca_system_score_codex":0.000007881761,"about_ca_system_score_gemma":0.000024394936,"threshold_uncertainty_score":0.16831756},"labels":[],"label_agreement":null},{"id":"W2513703067","doi":"10.1017/s0033291716001598","title":"Maternal prenatal depression is associated with decreased placental expression of the imprinted gene <i>PEG3</i>","year":2016,"lang":"en","type":"article","venue":"Psychological Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":56,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Douglas Mental Health University Institute","funders":"National Institute of Mental Health; Medical Research Council; Directorate for Biological Sciences; NIHR Imperial Biomedical Research Centre; National Institutes of Health; Imperial College London; National Institute for Health and Care Research; Biotechnology and Biological Sciences Research Council; Genesis Research Trust","keywords":"Genomic imprinting; Human placental lactogen; Pregnancy; Edinburgh Postnatal Depression Scale; Antenatal depression; Placenta; Depression (economics); Obstetrics; Cohort; Offspring; Fetus; Placental lactogen; Endocrinology; Medicine; Internal medicine; Biology; Andrology; Gene expression; Gene; Postpartum depression; Genetics; Diabetes mellitus; DNA methylation; Depressive symptoms","score_opus":0.011479190111584775,"score_gpt":0.2627150293439754,"score_spread":0.2512358392323906,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2513703067","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967153,0.00018572097,0.0015475537,0.00050566165,0.00017301533,0.00017733,0.000023638546,0.000012002549,0.0006597982],"genre_scores_gemma":[0.9987778,0.000051013554,0.00026285296,0.00047801834,0.00009833096,0.000012460284,0.000013529825,0.000013885275,0.0002921158],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99883366,0.000084450185,0.00024779065,0.0003565041,0.00024977836,0.00022784657],"domain_scores_gemma":[0.99921274,0.000041309773,0.00018575513,0.00039183616,0.000065802495,0.00010257753],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015889252,0.00015395405,0.00018332167,0.000018360424,0.00005193539,0.000003331936,0.00029640054,0.00014665112,0.00022220488],"category_scores_gemma":[0.00033978242,0.000059675665,0.000062403946,0.00007616326,0.0002384668,0.0000024072444,0.00016247938,0.00007479867,0.0000032349703],"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":[0.00011863274,0.000080426995,0.082381144,0.0000043966165,0.000020244244,0.0000020830125,0.000014295058,3.7391948e-7,0.9114499,0.0000010739108,0.0006198357,0.005307591],"study_design_scores_gemma":[0.001816357,0.00045165565,0.3654758,0.00030471833,0.000013070462,0.00007281096,0.000011955833,0.00000267365,0.6316103,0.00001849387,0.00015093315,0.00007127566],"about_ca_topic_score_codex":0.000009368936,"about_ca_topic_score_gemma":0.0000018568713,"teacher_disagreement_score":0.28309464,"about_ca_system_score_codex":0.000008944768,"about_ca_system_score_gemma":0.0000064262986,"threshold_uncertainty_score":0.2433503},"labels":[],"label_agreement":null},{"id":"W2514989011","doi":"10.1016/j.placenta.2016.08.093","title":"DNA methylation-associated repression of MEST/PEG1 expression contributes to the invasion of extravillous trophoblast cells","year":2016,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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":"National Natural Science Foundation of China","keywords":"Gene knockdown; DNA methylation; Biology; Decidua; Cell migration; Trophoblast; Cell biology; Bisulfite sequencing; Cancer research; Molecular biology; Matrigel; Placenta; Cell culture; Gene expression; Fetus; Angiogenesis; Gene; Genetics","score_opus":0.009354382557413556,"score_gpt":0.23024272581077976,"score_spread":0.2208883432533662,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2514989011","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965544,0.00034552172,0.002226719,0.00027578665,0.0001714738,0.00023828875,0.000036609665,0.000004997075,0.00014625298],"genre_scores_gemma":[0.99898005,0.00015212965,0.00032230714,0.000043374293,0.0000275056,0.00000921563,0.000017201233,0.000012948921,0.00043530096],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990246,0.00010759689,0.0003055352,0.00023930274,0.00015263309,0.00017031892],"domain_scores_gemma":[0.99916345,0.00007838202,0.00021944502,0.00037657854,0.00011330514,0.00004886233],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002898209,0.00010700364,0.00016774892,0.000033271383,0.000052770887,0.0000064816604,0.00020832456,0.0001060658,0.00003636633],"category_scores_gemma":[0.0003850132,0.000060279115,0.000078258665,0.000086943415,0.00004151188,0.000002810957,0.00020466966,0.00003263898,0.000005715547],"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":[0.000046973793,0.000053199023,0.004750008,0.000008916888,0.000024329782,1.5879537e-7,0.000057439203,0.00004320063,0.9898376,0.000004843011,0.0018130305,0.0033603236],"study_design_scores_gemma":[0.00071179704,0.0001659946,0.02348512,0.00017311506,0.000016032387,0.0000013037516,0.00008474687,0.000015415686,0.9715615,0.000024987774,0.0036816618,0.000078337616],"about_ca_topic_score_codex":0.000025330331,"about_ca_topic_score_gemma":0.00001227796,"teacher_disagreement_score":0.018735113,"about_ca_system_score_codex":0.000013093271,"about_ca_system_score_gemma":0.000030806164,"threshold_uncertainty_score":0.2458111},"labels":[],"label_agreement":null},{"id":"W2515063230","doi":"10.1016/j.placenta.2015.07.303","title":"Transient and placenta-specific imprinting in human development","year":2015,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Placenta; Biology; Cell biology; Pregnancy; Genetics; Fetus; Gene expression; DNA methylation; Gene","score_opus":0.0282525145561611,"score_gpt":0.2527833168940993,"score_spread":0.22453080233793818,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2515063230","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99694484,0.00064014434,0.00025864594,0.000058032558,0.000096154756,0.00013920189,8.9531335e-7,0.000008989115,0.0018530894],"genre_scores_gemma":[0.9977421,0.00006944585,0.0017433651,0.000060004888,0.00006852918,0.000010599097,0.000028055802,0.00001604766,0.00026184524],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990359,0.000031162523,0.00022245267,0.00031315567,0.00011453454,0.0002827782],"domain_scores_gemma":[0.9996357,0.000004248626,0.000042012394,0.00017086405,0.000023621933,0.0001235839],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030188114,0.0001268945,0.00012407293,0.00004518921,0.00005400319,0.000032061293,0.00011041968,0.00007058417,0.00001346236],"category_scores_gemma":[0.000017119763,0.00012964469,0.000022262137,0.00005324401,0.000030345402,0.0000026384287,0.00014204282,0.00007612265,0.000008066034],"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":[0.000046805206,0.00018536045,0.31703138,0.00005779653,0.000043833887,0.000009128248,0.001998845,0.00012977533,0.65215576,0.00009643199,0.0032278844,0.025017012],"study_design_scores_gemma":[0.006363999,0.00033440965,0.37460285,0.00009693939,0.0000105844665,0.00012606867,0.0022007914,0.0001458473,0.3180255,0.00003863161,0.29734743,0.00070694106],"about_ca_topic_score_codex":0.00002390272,"about_ca_topic_score_gemma":0.000052652333,"teacher_disagreement_score":0.33413023,"about_ca_system_score_codex":0.00003037541,"about_ca_system_score_gemma":0.0000420563,"threshold_uncertainty_score":0.52867573},"labels":[],"label_agreement":null},{"id":"W2520543312","doi":"10.1155/2016/7645938","title":"The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?","year":2016,"lang":"en","type":"article","venue":"Case Reports in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster Children's Hospital; McMaster University","funders":"","keywords":"Medicine; Macrocephaly; GNAS complex locus; Calcinosis cutis; Hydrocephalus; Pediatrics; Pseudohypoparathyroidism; Congenital hypothyroidism; Hyperphosphatemia; Osteodystrophy; Family history; Parathyroid hormone; Internal medicine; Endocrinology; Calcinosis; Surgery; Calcification; Thyroid","score_opus":0.01281899398824794,"score_gpt":0.2843591662796567,"score_spread":0.27154017229140875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2520543312","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99759734,0.0007476681,0.00018975604,0.0006435827,0.0002110832,0.00014685316,5.775583e-7,0.0000040767723,0.00045904488],"genre_scores_gemma":[0.9982,0.0005599633,0.00019199184,0.000056545687,0.00011248467,0.000005874987,0.0000068389445,0.000008187725,0.00085809623],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.99914515,0.00004189412,0.0003675894,0.00014465261,0.00015981024,0.00014088434],"domain_scores_gemma":[0.9990675,0.0000559141,0.00036805173,0.00029920347,0.0001734774,0.000035844387],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00074478384,0.00008034382,0.00014222268,0.000025577196,0.000051471907,0.0000047069625,0.000043685854,0.00008005505,0.000011420355],"category_scores_gemma":[0.00094353023,0.00003669655,0.000014824598,0.00013732586,0.000070316106,0.000004001899,0.00003796495,0.000054481712,0.0000013858415],"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":[0.0005382286,0.00009397598,0.34862748,0.000103755185,0.00019473307,0.011311824,0.0009952942,0.00007521855,0.5551372,0.00011715364,0.0074612047,0.07534391],"study_design_scores_gemma":[0.0062278653,0.009590609,0.34866843,0.0015915846,0.0003068506,0.40998137,0.002994761,0.00043273554,0.12997589,0.000603708,0.08862341,0.0010027973],"about_ca_topic_score_codex":0.00007156237,"about_ca_topic_score_gemma":0.00026038007,"teacher_disagreement_score":0.42516136,"about_ca_system_score_codex":0.000029204934,"about_ca_system_score_gemma":0.00009550774,"threshold_uncertainty_score":0.1496442},"labels":[],"label_agreement":null},{"id":"W2520927888","doi":"10.1186/s12859-016-1238-8","title":"A haplotype-based normalization technique for the analysis and detection of allele specific expression","year":2016,"lang":"en","type":"article","venue":"BMC Bioinformatics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Institute of Cancer Research; University of Toronto; Ontario Institute for Cancer Research; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"Medical Research Council; Partenariat Canadien Contre Le Cancer; Fonds Québécois de la Recherche sur la Nature et les Technologies; Ontario Institute for Cancer Research","keywords":"Haplotype; DNA microarray; Normalization (sociology); Allele; Genetics; Computational biology; Biology; Haplotype estimation; Gene expression; Gene","score_opus":0.011896984848092967,"score_gpt":0.22670366014951726,"score_spread":0.2148066753014243,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2520927888","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.08400572,0.00011189303,0.9155435,0.000017285327,0.000021320711,0.00025811122,0.000009065185,0.0000048267657,0.000028307742],"genre_scores_gemma":[0.91166157,0.00011409342,0.08807881,0.000017321805,0.000023532884,0.000042593303,0.000017945806,0.000006615208,0.000037500406],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995582,0.000011857949,0.00020316598,0.00007531186,0.000062649815,0.00008880679],"domain_scores_gemma":[0.9995365,0.000034232726,0.00013326302,0.00020768307,0.00006803511,0.000020242605],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001798138,0.00006577624,0.000079850695,0.000055831348,0.000058791866,0.000010775249,0.00007246593,0.0000708359,0.000004763287],"category_scores_gemma":[0.000056238227,0.000036996436,0.000071626426,0.00010354157,0.00004008318,0.0000044184517,0.000037739122,0.000013058408,6.2911784e-7],"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":[0.000019545218,0.000009340624,0.004288824,0.000055413635,0.000035107827,5.9658256e-9,0.000026200745,0.00026750425,0.9809696,0.000009686512,0.00004669762,0.014272054],"study_design_scores_gemma":[0.00034281358,0.00011666528,0.01400849,0.000015136926,0.000058669008,0.0000022368827,0.000065621614,0.018942334,0.9626242,0.000014572081,0.0037347118,0.00007456444],"about_ca_topic_score_codex":0.0000027714173,"about_ca_topic_score_gemma":0.000013145659,"teacher_disagreement_score":0.82765585,"about_ca_system_score_codex":0.0000040444465,"about_ca_system_score_gemma":0.000016176422,"threshold_uncertainty_score":0.15086709},"labels":[],"label_agreement":null},{"id":"W2524086747","doi":"10.1002/uog.15631","title":"EP09.34: Prenatal diagnosis of Prader‐Willi syndrome","year":2015,"lang":"en","type":"article","venue":"Ultrasound in Obstetrics and Gynecology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire de Sherbrooke","funders":"","keywords":"Medicine; Polyhydramnios; Obstetrics; Context (archaeology); Fetus; Prenatal diagnosis; Amniotic fluid index; Amniotic fluid; Pregnancy; Pediatrics; Gynecology","score_opus":0.015170379970124947,"score_gpt":0.2403481506961012,"score_spread":0.22517777072597625,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2524086747","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9923341,0.005693389,0.00007029552,0.000065476415,0.0006039192,0.0001883198,0.000019220402,0.000005832324,0.0010194482],"genre_scores_gemma":[0.9958325,0.0027435962,0.000986711,0.00009139076,0.000026623817,0.00003376645,0.000044163255,0.000018642217,0.0002226043],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987552,0.000074333955,0.00035407633,0.00036277281,0.00012776777,0.00032584617],"domain_scores_gemma":[0.9974847,0.0018765887,0.00012934717,0.0002800992,0.00009377497,0.00013553064],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.0002838029,0.0001556832,0.00027156802,0.0001376283,0.000032109645,0.000017638062,0.00018258845,0.00025033922,0.000030306885],"category_scores_gemma":[0.017152296,0.00015828549,0.00005468426,0.00026274295,0.00013587889,0.000006073675,0.00015076753,0.00011177677,0.0000056596155],"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":[0.0000023917821,0.00025860014,0.97069544,0.00007061783,0.00006836022,0.000011361444,0.0002559246,0.000120665594,0.006218112,0.0003185939,0.0005825405,0.021397417],"study_design_scores_gemma":[0.0038047172,0.0031276713,0.7829796,0.000050257262,0.000059497263,0.000865862,0.0014812975,0.000100563346,0.01538571,0.0012279805,0.19015445,0.00076240813],"about_ca_topic_score_codex":0.000059310434,"about_ca_topic_score_gemma":0.00003680572,"teacher_disagreement_score":0.1895719,"about_ca_system_score_codex":0.000029862025,"about_ca_system_score_gemma":0.0000828949,"threshold_uncertainty_score":0.99112666},"labels":[],"label_agreement":null},{"id":"W2526178173","doi":"10.1002/uog.15630","title":"EP09.33: Early prenatal diagnosis of Golabi syndrome","year":2015,"lang":"en","type":"article","venue":"Ultrasound in Obstetrics and Gynecology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Polyhydramnios; Organomegaly; Prenatal diagnosis; Amniotic fluid index; Pediatrics; Failure to thrive; Obstetrics; Amniotic fluid; Fetus; Pregnancy; Gynecology; Pathology; Polyneuropathy","score_opus":0.012948194397463421,"score_gpt":0.23281580499516968,"score_spread":0.21986761059770626,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2526178173","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99500966,0.003234684,0.000047201207,0.000032904645,0.0005620097,0.00016865783,0.00002666128,0.0000055341598,0.00091269275],"genre_scores_gemma":[0.9972788,0.0015406157,0.0007612999,0.00006421992,0.000023952467,0.00002946359,0.000031151576,0.000017996439,0.00025248597],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99880964,0.00007007244,0.0003362725,0.00034546363,0.00012170258,0.00031684976],"domain_scores_gemma":[0.9976572,0.0017162275,0.00011646217,0.00027399816,0.000101394675,0.00013472216],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.00027520128,0.00014835584,0.00026051735,0.0001333881,0.000029249659,0.000020204723,0.00018462342,0.00023833764,0.00002328869],"category_scores_gemma":[0.014506327,0.0001526504,0.000053550037,0.00026305803,0.00012456365,0.000006289172,0.00015106046,0.00010933041,0.0000070469996],"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":[0.000008113147,0.00020291313,0.96954864,0.0000499897,0.000058429054,0.000023373083,0.00029564422,0.00006910407,0.008207113,0.00025067586,0.00030055727,0.02098542],"study_design_scores_gemma":[0.0025538302,0.002551789,0.9094763,0.000030464795,0.00003663132,0.00041732218,0.0005417563,0.00003663067,0.012946381,0.00079817214,0.07011936,0.0004913831],"about_ca_topic_score_codex":0.000096484044,"about_ca_topic_score_gemma":0.000034989294,"teacher_disagreement_score":0.0698188,"about_ca_system_score_codex":0.000024446119,"about_ca_system_score_gemma":0.00007220335,"threshold_uncertainty_score":0.9937949},"labels":[],"label_agreement":null},{"id":"W2527298399","doi":"10.1101/076794","title":"Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility","year":2016,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; University of Toronto; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; Centre for Global Health Research","funders":"","keywords":"Mendelian randomization; Menarche; Biology; Heritability; Population; Prostate cancer; Genetics; Physiology; Endocrinology; Genotype; Oncology; Demography; Gene; Cancer; Medicine; Genetic variants","score_opus":0.03228565572964071,"score_gpt":0.2978485590993267,"score_spread":0.265562903369686,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2527298399","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9934348,0.0027088355,0.0015163299,0.00007449258,0.0005478718,0.0014097359,0.00027061705,0.000028784001,0.000008558899],"genre_scores_gemma":[0.99741733,0.000822617,0.00084617425,0.00008966315,0.00030931202,0.0003416606,0.0000024056985,0.00011895598,0.000051853713],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9965127,0.00020395908,0.0007127762,0.0015164907,0.0003930599,0.00066098245],"domain_scores_gemma":[0.99731934,0.0001157505,0.00077692274,0.0012298344,0.00027119956,0.00028692605],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0008230196,0.00061609916,0.0007579551,0.00021335029,0.00016742093,0.00009912724,0.0005679165,0.00071122247,0.000036716112],"category_scores_gemma":[0.00029604827,0.00054402126,0.00031899143,0.00011092688,0.00018864844,0.000008592796,0.0017945557,0.00031477623,0.000008573738],"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":[0.00006350519,0.00010139023,0.03138071,0.0010467464,0.0005676878,0.00000875777,0.000015162822,0.00007355641,0.9666175,0.000008540019,0.00008592256,0.000030471481],"study_design_scores_gemma":[0.0007698669,0.0001753254,0.29536402,0.000348208,0.00020397038,5.4928602e-8,0.0000031306074,0.00003192793,0.70239216,0.000006487508,0.0002507774,0.00045406565],"about_ca_topic_score_codex":0.00008011171,"about_ca_topic_score_gemma":0.000034634682,"teacher_disagreement_score":0.2642254,"about_ca_system_score_codex":0.00023797278,"about_ca_system_score_gemma":0.00033827478,"threshold_uncertainty_score":0.99970114},"labels":[],"label_agreement":null},{"id":"W2530594373","doi":"10.1182/blood.v112.11.202.202","title":"An Upstream Insulator Element Regulates DLK1 Imprinting in AML","year":2008,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Princess Margaret Cancer Centre","funders":"","keywords":"Biology; Genomic imprinting; MEG3; CpG site; DNA methylation; Methylation; Imprinting (psychology); Molecular biology; Promoter; Genetics; Cancer research; Gene; Uniparental disomy; Gene expression; Downregulation and upregulation; Long non-coding RNA; Chromosome","score_opus":0.008113948638552441,"score_gpt":0.22598488199235234,"score_spread":0.2178709333537999,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2530594373","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99892056,0.00027032057,0.00005703557,0.000025417032,0.000053965337,0.000117663556,0.0000023570622,0.000014722788,0.00053796277],"genre_scores_gemma":[0.9971552,0.000100948,0.002365069,0.000058011872,0.00014105404,0.000012983087,0.000026044243,0.000021671045,0.00011904006],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990217,0.000031285006,0.00023294211,0.0003278999,0.00009430665,0.00029183627],"domain_scores_gemma":[0.9994547,0.0000036116212,0.000062842264,0.00037173,0.000031258885,0.00007586459],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001295313,0.00013050932,0.00012242743,0.000043687716,0.00006888067,0.000013972263,0.00017029875,0.00009421903,0.000022810133],"category_scores_gemma":[0.000031742442,0.00013045034,0.000053378215,0.00007871985,0.000034773107,0.0000032066846,0.000101092184,0.00006302336,0.000008842793],"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":[0.0000023689813,0.00024132601,0.35466307,0.000006805813,0.000020935606,0.000006148831,0.0000792509,0.000045787267,0.64285564,0.000013194555,0.000017405828,0.0020480254],"study_design_scores_gemma":[0.001001463,0.00022777538,0.42570633,0.000010566371,0.000009100022,0.00011518682,0.00008244731,0.00006794536,0.5714699,0.000025871623,0.0011169006,0.00016653264],"about_ca_topic_score_codex":0.000058201276,"about_ca_topic_score_gemma":0.00002013201,"teacher_disagreement_score":0.07138577,"about_ca_system_score_codex":0.0000053330587,"about_ca_system_score_gemma":0.000040094914,"threshold_uncertainty_score":0.5319611},"labels":[],"label_agreement":null},{"id":"W2538843384","doi":"10.1016/j.molmet.2016.10.004","title":"Targeting the endocannabinoid/CB1 receptor system for treating obesity in Prader–Willi syndrome","year":2016,"lang":"en","type":"article","venue":"Molecular Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":74,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; Israel Science Foundation; National Institute for Health and Care Research; Canadian Institutes of Health Research; Foundation for Prader-Willi Research","keywords":"Endocannabinoid system; Cannabinoid receptor; Rimonabant; Medicine; Receptor; Obesity; 2-Arachidonoylglycerol; Internal medicine; Endocrinology; Neuroscience; Pharmacology; Biology; Agonist","score_opus":0.006027089376842569,"score_gpt":0.2170869620226673,"score_spread":0.21105987264582474,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2538843384","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97533023,0.0035729657,0.019088184,0.0005997896,0.00043505948,0.00071733986,0.000027785403,0.00002906959,0.0001995423],"genre_scores_gemma":[0.9950281,0.000089423425,0.0038084663,0.00014279337,0.0001886705,0.00023124022,0.000026422329,0.000058930513,0.00042597138],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99801254,0.00020179641,0.00043385878,0.00057014305,0.00019534466,0.0005863083],"domain_scores_gemma":[0.9990774,0.00003799269,0.00018018612,0.00051620643,0.000096055606,0.00009219183],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00062874245,0.00027373258,0.00031828228,0.00006626877,0.00016080287,0.000045235898,0.0003839252,0.00013410105,0.000012469627],"category_scores_gemma":[0.00038372184,0.00017445527,0.0002075706,0.00015255355,0.00006981643,0.0000071876507,0.00018310688,0.00008923454,0.000016065878],"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":[0.0000035423295,0.000031874988,0.003213777,0.000050143084,0.00006136203,0.0000034414181,0.00006042916,0.00005939978,0.9907959,0.00055115024,0.00023150975,0.0049374597],"study_design_scores_gemma":[0.0031376549,0.00020414885,0.04512828,0.0002117779,0.00011274114,0.0002483688,0.00065464334,0.00021668001,0.8571512,0.00015622513,0.091961056,0.00081720925],"about_ca_topic_score_codex":0.000054574517,"about_ca_topic_score_gemma":0.000005708753,"teacher_disagreement_score":0.1336447,"about_ca_system_score_codex":0.000033814107,"about_ca_system_score_gemma":0.0000660542,"threshold_uncertainty_score":0.71140796},"labels":[],"label_agreement":null},{"id":"W2539027126","doi":"10.1111/pde.13014","title":"Pilomatricoma Associated with Kabuki Syndrome","year":2016,"lang":"en","type":"article","venue":"Pediatric Dermatology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université Laval; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Pilomatricoma; Medicine; Kabuki; Wnt signaling pathway; Kabuki syndrome; Carcinogenesis; Dermatology; Pathology; Genetics; Internal medicine; Biology; Signal transduction; Cancer; Pediatrics","score_opus":0.006316566195172781,"score_gpt":0.20570764664078797,"score_spread":0.19939108044561518,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2539027126","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9955851,0.0007672345,0.0018606395,0.00047112675,0.00017561983,0.00013398449,0.000009744687,0.000043942244,0.0009526437],"genre_scores_gemma":[0.9983244,0.00047458682,0.00037539515,0.0001391473,0.00010464833,0.000025143829,0.00001970794,0.000033906043,0.000503097],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99867785,0.00007636727,0.00025793418,0.0003871776,0.00013457687,0.0004661019],"domain_scores_gemma":[0.9992599,0.000055101475,0.00014889184,0.00034235395,0.000078208686,0.00011556749],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008975933,0.00019117448,0.00023352345,0.000097906,0.00007646735,0.000013359275,0.00023463782,0.00019239061,0.00006578415],"category_scores_gemma":[0.00017864334,0.00012676253,0.00006932806,0.00019478847,0.000069232294,0.000004235164,0.00013044135,0.000056744342,0.000113038885],"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":[0.000015316069,0.0001087183,0.97832435,0.000020931782,0.00010766295,0.00013290883,0.000011727611,0.0000023667233,0.013240049,0.000057931706,0.004327583,0.0036504504],"study_design_scores_gemma":[0.0035862005,0.00084599416,0.9608713,0.0000309361,0.00017639468,0.010858675,0.000024456556,0.0000142098415,0.009281801,0.00021568917,0.013293127,0.00080124283],"about_ca_topic_score_codex":0.0000040680447,"about_ca_topic_score_gemma":0.0000071127965,"teacher_disagreement_score":0.01745308,"about_ca_system_score_codex":0.00001312609,"about_ca_system_score_gemma":0.00008073938,"threshold_uncertainty_score":0.5169226},"labels":[],"label_agreement":null},{"id":"W2539704783","doi":"10.1093/biolreprod/81.s1.266","title":"Investigating the Molecular Effects of Superovulation and Embryo Culture on Genomic Imprinting in a Mouse Model System.","year":2009,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Epigenetics; DNA methylation; Embryo; Genetics; Embryonic stem cell; Methylation; Embryo culture; Gene; Embryogenesis; Gene expression","score_opus":0.007152254045509899,"score_gpt":0.22713766172061434,"score_spread":0.21998540767510444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2539704783","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969998,0.0015595703,0.0009961614,0.00010299216,0.000058379625,0.00021969642,9.2294545e-7,0.000005856459,0.000056600442],"genre_scores_gemma":[0.9976365,0.00008908128,0.0021462669,0.000022188657,0.00004909278,0.000005537313,0.000009099192,0.0000060715847,0.000036157962],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992411,0.00007484046,0.00022241271,0.00031462393,0.000039448183,0.00010757122],"domain_scores_gemma":[0.9995062,0.0000069256994,0.00014670489,0.00028093287,0.00004346498,0.000015820615],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029051013,0.000088213004,0.00013243439,0.000040613177,0.000034664743,0.000003459983,0.00006798367,0.000112184265,9.6741594e-8],"category_scores_gemma":[0.00022150653,0.00006796694,0.0000349598,0.00005484947,0.000069320595,0.0000024166072,0.000038128073,0.000066588764,1.6669888e-7],"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":[0.0000045423644,0.000014612791,0.005057236,0.00006178061,0.0000100862735,5.8039017e-8,0.00014011144,0.0024661762,0.9851074,0.0008455032,0.0000019463623,0.006290539],"study_design_scores_gemma":[0.00024818402,0.00033675545,0.03593156,0.000041719788,0.000008352459,0.000013514137,0.00013451086,0.0020339987,0.9609144,0.0002478134,0.000018770144,0.0000704729],"about_ca_topic_score_codex":0.000023284845,"about_ca_topic_score_gemma":0.0000013062936,"teacher_disagreement_score":0.030874325,"about_ca_system_score_codex":0.000008736006,"about_ca_system_score_gemma":0.000018698367,"threshold_uncertainty_score":0.27716115},"labels":[],"label_agreement":null},{"id":"W2551400455","doi":"10.1186/s13072-016-0104-2","title":"Widespread recovery of methylation at gametic imprints in hypomethylated mouse stem cells following rescue with DNMT3A2","year":2016,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"Medical Research Council; Cereal Partners Worldwide; Ulster University","keywords":"Biology; Methylation; DNA methylation; Stem cell; Genetics; Human genetics; Computational biology; Gene; Gene expression","score_opus":0.0101238654089752,"score_gpt":0.2261453435508654,"score_spread":0.2160214781418902,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2551400455","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954442,0.0006679038,0.0030640054,0.000040278348,0.0001688115,0.0003833017,0.000023188204,0.00001721163,0.0001910913],"genre_scores_gemma":[0.9917048,0.00032025282,0.0059998776,0.000022780358,0.000038536804,0.00002675764,0.00001671952,0.00006626164,0.0018039797],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9978381,0.00018987045,0.000663445,0.00056389155,0.00028952313,0.00045521287],"domain_scores_gemma":[0.99872035,0.000109122404,0.00027053594,0.0006964511,0.00009036921,0.00011320002],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005211671,0.0002882614,0.00038498623,0.0001552643,0.000051942436,0.000018395562,0.00028109903,0.0002269082,0.00003825522],"category_scores_gemma":[0.00011696877,0.00022205239,0.00015227159,0.00025451827,0.000083233106,0.000008330555,0.00024528793,0.000077009,0.000029607474],"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":[0.000038993712,0.000058966292,0.01147124,0.00004098365,0.00008433764,0.0000037940179,0.00009578924,0.0006267236,0.97355664,0.0000018071144,0.000032941978,0.013987778],"study_design_scores_gemma":[0.0012915969,0.00061302236,0.026692467,0.00018040539,0.00003330193,0.000009202119,0.0000606452,0.000073646916,0.9703683,0.00003532259,0.00032860582,0.00031343367],"about_ca_topic_score_codex":0.00008149625,"about_ca_topic_score_gemma":0.00012496192,"teacher_disagreement_score":0.015221227,"about_ca_system_score_codex":0.00007931458,"about_ca_system_score_gemma":0.00009089053,"threshold_uncertainty_score":0.90550333},"labels":[],"label_agreement":null},{"id":"W2551678515","doi":"10.1055/s-0036-1593840","title":"An Update on Molecular Diagnostic Testing of Human Imprinting Disorders","year":2016,"lang":"en","type":"review","venue":"Journal of Pediatric Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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; McMaster University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Molecular imprinting; Gene; Biology; Computational biology; Genetics; Bioinformatics; Gene expression; DNA methylation; Biochemistry","score_opus":0.02148006789144498,"score_gpt":0.31226309378601164,"score_spread":0.29078302589456667,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2551678515","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.1259957,0.8723943,0.0007886338,0.000006814705,0.00040702248,0.000261624,0.000023955205,0.000004690064,0.000117234136],"genre_scores_gemma":[0.033051297,0.96158963,0.003554475,0.000015097858,0.0016378852,0.000006010988,0.000018513005,0.00011010421,0.000016959586],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.996963,0.00022588632,0.0015667493,0.0004124795,0.0004037116,0.00042812878],"domain_scores_gemma":[0.99614596,0.0001888888,0.0024840264,0.0006496016,0.00031496404,0.0002165671],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006010991,0.00047632202,0.0010982677,0.0003430234,0.00007560027,0.00003748081,0.0008250901,0.00040137017,0.000015502188],"category_scores_gemma":[0.0009365772,0.00036892339,0.0006428014,0.00027754897,0.000060791135,0.000004408903,0.00021961893,0.00034113548,0.000007021046],"study_design_candidate":"design_other","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":[0.0000023392695,0.00021366517,0.002477764,0.002364893,0.00021901354,0.000014921074,0.000011338201,0.00013245814,0.004522311,0.000011899896,0.000122003235,0.9899074],"study_design_scores_gemma":[0.0034419182,0.018745473,0.004118916,0.01068611,0.008230625,0.0010430769,0.00010151383,0.000029447769,0.0073748864,0.0007701593,0.9415472,0.003910681],"about_ca_topic_score_codex":0.000002280249,"about_ca_topic_score_gemma":8.8841875e-7,"teacher_disagreement_score":0.9859967,"about_ca_system_score_codex":0.000027329856,"about_ca_system_score_gemma":0.00036435222,"threshold_uncertainty_score":0.99987626},"labels":[],"label_agreement":null},{"id":"W2558344898","doi":"10.1182/blood.v114.22.379.379","title":"Necdin Regulates Hematopoietic Stem Cell Quiescence and Sensitivity to Genotoxic Stress.","year":2009,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Haematopoiesis; Biology; Stem cell; Null cell; Bone marrow; Stromal cell; Transplantation; Myeloid; Cancer research; Cell biology; Immunology; Cell culture; Genetics; Internal medicine; Medicine","score_opus":0.005984711559342947,"score_gpt":0.20369361230941213,"score_spread":0.1977089007500692,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2558344898","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99803704,0.00086173374,0.00027434173,0.00015700473,0.00003282827,0.00015023525,0.0000058799083,0.000013910445,0.00046702757],"genre_scores_gemma":[0.9979557,0.000070039896,0.001245382,0.00022495264,0.00006941586,0.0000030898616,0.0000055495534,0.000011326077,0.00041455321],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991721,0.000033764038,0.00013275704,0.0003316214,0.00008397249,0.00024576476],"domain_scores_gemma":[0.9995233,0.0000073493848,0.00004038753,0.00028039576,0.000030697076,0.00011790093],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010825085,0.00013324028,0.00012795765,0.000024105486,0.000063116655,0.000034659315,0.00006236164,0.00008216332,0.000003993299],"category_scores_gemma":[0.0000114985105,0.00013150506,0.00003844123,0.00005966108,0.00002393575,0.0000019625159,0.000095440046,0.00004462687,0.000009078322],"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":[0.0000027108083,0.0000969916,0.0040723933,0.000020645824,0.000009356354,0.000007950459,0.00010827001,0.000021721275,0.99145645,0.000010218294,0.00005490267,0.0041383663],"study_design_scores_gemma":[0.00039542443,0.00030253746,0.061777256,0.000024961235,0.00002071261,0.00014457083,0.00012693678,0.000021372864,0.9365962,0.00002522191,0.00038406654,0.00018073905],"about_ca_topic_score_codex":0.000006161241,"about_ca_topic_score_gemma":0.0000065356576,"teacher_disagreement_score":0.057704862,"about_ca_system_score_codex":0.0000025755353,"about_ca_system_score_gemma":0.000017824968,"threshold_uncertainty_score":0.53626204},"labels":[],"label_agreement":null},{"id":"W2559984380","doi":"10.1142/9789813144279_0007","title":"Genetic and Epigenetic Variation at the <i>H19</i> Imprinted Region and Its Effect on Birth Weight","year":2016,"lang":"en","type":"book-chapter","venue":"WORLD SCIENTIFIC eBooks","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Health Centre; McGill University; Jewish General Hospital","funders":"Health Science Center, University of Tennessee; National Institutes of Health; National Institute of Child Health and Human Development; Mitacs","keywords":"Epigenetics; Genomic imprinting; Variation (astronomy); Imprinting (psychology); Biology; Genetics; Evolutionary biology; DNA methylation; Physics; Gene; Astrophysics","score_opus":0.009343419746129364,"score_gpt":0.2054754599127091,"score_spread":0.19613204016657973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2559984380","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.587376,0.0070394147,0.00020337754,0.00032599474,0.0019822998,0.0016266133,0.0000581907,0.000044059936,0.40134406],"genre_scores_gemma":[0.3168653,0.000075369666,0.000031722684,0.00010030229,0.00020469149,0.000023063225,0.000014063457,0.000053321717,0.6826322],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9978826,0.000080249556,0.0003316261,0.0010615966,0.00028347698,0.00036044786],"domain_scores_gemma":[0.99866015,0.0000665249,0.00025468416,0.00078257255,0.00008880847,0.00014729035],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00042085993,0.00041453535,0.00028217057,0.00016679906,0.00047938045,0.00014467699,0.0002487564,0.0002349203,0.00006418055],"category_scores_gemma":[0.000025193161,0.0002744281,0.00012287972,0.000027934237,0.00035666596,0.0000018763183,0.00046769972,0.00016789474,0.00009065648],"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":[0.00010989251,0.000018256362,0.00078654237,0.0002574463,0.00028480196,0.000020245181,0.00020193467,0.0000044764615,0.8911741,0.006463532,0.0046659554,0.09601284],"study_design_scores_gemma":[0.00091980083,0.00056229817,0.00526591,0.0003715702,0.00014528389,0.00017452004,0.000002036673,0.00004854801,0.088305004,0.0013469686,0.90213627,0.0007218041],"about_ca_topic_score_codex":0.0000015657531,"about_ca_topic_score_gemma":0.00016818046,"teacher_disagreement_score":0.8974703,"about_ca_system_score_codex":0.000032525066,"about_ca_system_score_gemma":0.000052151136,"threshold_uncertainty_score":0.9999708},"labels":[],"label_agreement":null},{"id":"W2560135976","doi":"10.1681/asn.2016010069","title":"Genetic Variants Associated with Circulating Parathyroid Hormone","year":2016,"lang":"en","type":"article","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":70,"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 Center for Research Resources; U.S. National Library of Medicine; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Institutes of Health; Ministry of Cultural Affairs; Roche Diabetes Care; Abbott Diabetes Care; Universitair Medisch Centrum Groningen; Göteborgs Läkaresällskap; Siemens; Vetenskapsrådet; Novo Nordisk; Bundesministerium für Bildung und Forschung; Vrije Universiteit Amsterdam; Stiftelsen för Strategisk Forskning; National Center for Advancing Translational Sciences; Leids Universitair Medisch Centrum; Universiteit Leiden; Insulet Corporation; Nipro; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; European Commission; Universität Greifswald; Johns Hopkins University; Eli Lilly and Company; Novo Nordisk Fonden; Foundation for the National Institutes of Health","keywords":"Parathyroid hormone; CYP24A1; Single-nucleotide polymorphism; Internal medicine; Endocrinology; Vitamin D and neurology; Minor allele frequency; Biology; Secondary hyperparathyroidism; SNP; Calcitriol receptor; Medicine; Genotype; Genetics; Calcium; Gene","score_opus":0.009539322404251978,"score_gpt":0.22858521971117188,"score_spread":0.2190458973069199,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2560135976","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99476075,0.00037253345,0.0035897235,0.001149663,0.000035309386,0.00005592804,0.0000035216644,0.0000020400237,0.000030499421],"genre_scores_gemma":[0.9934917,0.00030347667,0.0047319387,0.0012244626,0.00015831702,0.0000011143349,3.414902e-7,0.00001677669,0.00007186985],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989779,0.00012528064,0.00034752628,0.00013838004,0.00017539952,0.00023552697],"domain_scores_gemma":[0.9982827,0.00005438436,0.0011784823,0.0002483395,0.00018135968,0.000054789187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026762433,0.00011591696,0.0002951435,0.00001574616,0.00006136059,0.000005328066,0.00031619237,0.00006648774,0.000005120562],"category_scores_gemma":[0.00010084134,0.00006187043,0.0002755565,0.00013920083,0.0004521126,0.0000034322607,0.00011269974,0.00009458889,6.9015806e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000032725235,0.00003720601,0.016445879,0.0000016330699,0.00033893477,0.0000012723599,0.00006723892,0.000071250586,0.9764915,0.0000013541279,0.0032877398,0.003223246],"study_design_scores_gemma":[0.0009987943,0.0014862906,0.9872022,0.000024293964,0.000071658,0.000443442,0.00014307078,0.000041310373,0.0075799627,0.00007714168,0.0018257246,0.000106098094],"about_ca_topic_score_codex":0.00001326643,"about_ca_topic_score_gemma":0.0000027889348,"teacher_disagreement_score":0.97075635,"about_ca_system_score_codex":0.000019520685,"about_ca_system_score_gemma":0.00010786239,"threshold_uncertainty_score":0.2523003},"labels":[],"label_agreement":null},{"id":"W2560187753","doi":"10.1172/jci88648","title":"Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome","year":2016,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":176,"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 Sherbrooke","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Prohormone convertase; Endocrinology; Prohormone; Internal medicine; Biology; Proinsulin; Knockout mouse; Hormone; Gene; Medicine; Insulin; Genetics","score_opus":0.0408665860268086,"score_gpt":0.3312495679486059,"score_spread":0.2903829819217973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2560187753","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99660224,0.0008190908,0.0006925953,0.0014444144,0.00015596159,0.00021066717,0.000001294131,0.0000036521567,0.00007006462],"genre_scores_gemma":[0.9967717,0.00026351152,0.0025423076,0.00017658618,0.00013130684,0.0000075997004,0.0000033772178,0.00001626591,0.00008734686],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99746186,0.00019026997,0.0015736179,0.00026416522,0.00024629149,0.0002638148],"domain_scores_gemma":[0.9986336,0.000060135695,0.00080542866,0.00016799061,0.00016110134,0.00017171833],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020413175,0.00013994737,0.00035410412,0.00013320237,0.00002795335,0.000024099789,0.00020111223,0.00022556349,0.0000072788207],"category_scores_gemma":[0.0018714366,0.00009622261,0.000117859425,0.00017956499,0.0001770654,0.00003271372,0.000061510036,0.0002335212,0.000005083976],"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":[0.000020462034,0.00021295817,0.8078134,0.00005120884,0.000011764986,0.000014909134,0.00010440923,0.000040349725,0.15734869,0.0000149285415,0.00017299021,0.034193914],"study_design_scores_gemma":[0.0021920884,0.0011887157,0.986733,0.00036873342,0.000015733185,0.00028544082,0.000085643806,0.00022601838,0.0074702753,0.0008491676,0.00041193148,0.00017325772],"about_ca_topic_score_codex":0.000009658543,"about_ca_topic_score_gemma":0.000020671489,"teacher_disagreement_score":0.17891958,"about_ca_system_score_codex":0.000030247844,"about_ca_system_score_gemma":0.00037821522,"threshold_uncertainty_score":0.3923844},"labels":[],"label_agreement":null},{"id":"W2573478446","doi":"10.1016/j.metabol.2017.01.020","title":"The use of magnetic resonance imaging to characterize abnormal body composition phenotypes in youth with Prader–Willi syndrome","year":2017,"lang":"en","type":"article","venue":"Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Concordia University; University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Medicine; Interquartile range; Magnetic resonance imaging; Anthropometry; Adipose tissue; Skeletal muscle; Internal medicine; Nuclear medicine; Radiology","score_opus":0.01666072822338955,"score_gpt":0.22725242028795406,"score_spread":0.21059169206456452,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2573478446","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99696106,0.0020616397,0.00017794494,0.0003100152,0.00014893927,0.00022123464,0.00003103762,0.000004507729,0.000083605184],"genre_scores_gemma":[0.9978245,0.0001840045,0.0015835433,0.00011637616,0.000062010055,0.000015950767,0.000020825228,0.000019440096,0.00017334681],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990834,0.00004916482,0.00021327358,0.00025290984,0.00013171762,0.00026955473],"domain_scores_gemma":[0.9991247,0.000009856713,0.0001437532,0.00060585095,0.00006217783,0.000053660147],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016327895,0.00013468298,0.00017698805,0.000033341024,0.00020068315,0.00012562897,0.000309524,0.000041499246,0.0000044744247],"category_scores_gemma":[0.000057474223,0.000098067976,0.00004052394,0.000044697546,0.00010755174,0.000014853222,0.00017784587,0.00007127022,0.000003540008],"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":[0.000057900263,0.000118871336,0.20125867,0.000027547787,0.00003535092,0.000008408105,0.0006974811,0.00008603331,0.7250754,0.00020043521,0.000070118076,0.07236373],"study_design_scores_gemma":[0.00046342664,0.00009237874,0.97213924,0.00004424634,0.000020622838,0.000048115064,0.00004798706,0.00008994314,0.009227187,0.0000060658767,0.017681452,0.00013933454],"about_ca_topic_score_codex":0.0002195668,"about_ca_topic_score_gemma":0.000032648742,"teacher_disagreement_score":0.7708806,"about_ca_system_score_codex":0.0000041134094,"about_ca_system_score_gemma":0.000025127028,"threshold_uncertainty_score":0.39990962},"labels":[],"label_agreement":null},{"id":"W2580576361","doi":"10.1136/archdischild-2016-311298","title":"Longitudinal evaluation of sleep disordered breathing in infants with Prader-Willi syndrome","year":2017,"lang":"en","type":"article","venue":"Archives of Disease in Childhood","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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; University of Toronto","funders":"","keywords":"Medicine; Polysomnography; Interquartile range; Pediatrics; Obstructive sleep apnea; Sleep study; Retrospective cohort study; Tonsillectomy; Sleep disordered breathing; Breathing; Internal medicine; Apnea; Surgery; Anesthesia","score_opus":0.013089762812245529,"score_gpt":0.2662526455727095,"score_spread":0.25316288276046395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2580576361","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982371,0.00059459,0.00008803125,0.00009491399,0.000029312861,0.00031710477,0.000019820238,0.0000020656128,0.0006170805],"genre_scores_gemma":[0.9990888,0.0000782479,0.0007336848,0.0000060800594,0.000016160433,0.000022379887,0.000033320215,0.000014973717,0.0000063096877],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99893117,0.0000737898,0.00027057345,0.0003011074,0.00023040405,0.00019295447],"domain_scores_gemma":[0.9990797,0.00002047417,0.00023205034,0.000567054,0.000030098363,0.00007060295],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019923241,0.00012823592,0.00019185407,0.00009519357,0.000054406388,0.000015254915,0.00029512608,0.00003605654,0.0000072888865],"category_scores_gemma":[0.0002810588,0.00011723369,0.0000652987,0.000041824107,0.00013926484,0.00001071939,0.00017392007,0.00006924632,4.0302953e-7],"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":[0.00001581415,0.00030125078,0.9820004,0.000057581103,0.000045576337,0.0000016442535,0.00035645725,0.0016457214,0.0027337712,0.0000130609715,5.4885857e-7,0.012828172],"study_design_scores_gemma":[0.0020332881,0.00020704152,0.9942719,0.0003204203,0.000044924713,0.000010908078,0.00008106303,0.0011539428,0.0010243279,0.0007140095,0.0000029280006,0.00013527926],"about_ca_topic_score_codex":0.00013311178,"about_ca_topic_score_gemma":0.00013072125,"teacher_disagreement_score":0.012692893,"about_ca_system_score_codex":0.0000042919064,"about_ca_system_score_gemma":0.00012498457,"threshold_uncertainty_score":0.47806513},"labels":[],"label_agreement":null},{"id":"W2581843842","doi":"10.1016/j.fertnstert.2006.07.506","title":"P-159","year":2006,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine","score_opus":0.008495560238070469,"score_gpt":0.2201083053447275,"score_spread":0.21161274510665704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2581843842","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952558,0.00038787478,0.00075821264,0.00007070944,0.000069478025,0.00007313889,0.000008558123,0.000010146244,0.003366054],"genre_scores_gemma":[0.9988802,0.000007158106,0.00035188705,0.00006896946,0.000049977436,0.000004688326,0.000025373998,0.0000047783833,0.0006069391],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99935853,0.000034300192,0.00013930454,0.00026120502,0.00005387793,0.00015275647],"domain_scores_gemma":[0.9996596,0.0000037836787,0.000023245166,0.00024831522,0.000025522555,0.00003954451],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015225209,0.00008239274,0.00008569724,0.000007867761,0.0000672148,0.000021937482,0.00005928785,0.00006910281,0.00003255623],"category_scores_gemma":[0.000023413359,0.00007678053,0.000039633705,0.00002511228,0.00006962195,0.0000017970586,0.00010067039,0.0000341704,0.00000478625],"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":[0.00086478906,0.00020246772,0.5026648,0.00010779488,0.0000280435,0.0000014553457,0.00004964557,0.000010300045,0.46359393,0.000035550096,0.0007206542,0.03172059],"study_design_scores_gemma":[0.00015824966,0.00005995251,0.97195494,0.0000021829226,0.0000035542862,0.0000048826487,0.0000147128485,0.00004654825,0.014572443,0.00040350188,0.012696768,0.000082266044],"about_ca_topic_score_codex":0.00015608202,"about_ca_topic_score_gemma":0.00009148235,"teacher_disagreement_score":0.46929014,"about_ca_system_score_codex":0.000003230114,"about_ca_system_score_gemma":0.000011521955,"threshold_uncertainty_score":0.31310192},"labels":[],"label_agreement":null},{"id":"W2585315210","doi":"10.1038/gim.2016.220","title":"Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing","year":2017,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":140,"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; McGill University Health Centre","funders":"Société Française de Dermatologie et de Pathologie Sexuellement Transmissible; Université de Bourgogne; Agence Nationale de la Recherche","keywords":"Phenotype; Allele; Medicine; Genetic testing; Mutation; Mutant; Genetic heterogeneity; Genetic diagnosis; Allelic heterogeneity; DNA sequencing; Bioinformatics; Genetics; Pathology; Biology; Internal medicine; Gene","score_opus":0.01962944552466315,"score_gpt":0.2875711897181372,"score_spread":0.26794174419347405,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2585315210","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963489,0.0013862884,0.00036213637,0.0009141826,0.00020007974,0.00044691123,0.000012102261,0.0000029867629,0.00032638217],"genre_scores_gemma":[0.98972636,0.0010883001,0.008888928,0.00009256572,0.00005496693,0.00006172785,0.0000395326,0.000026028696,0.000021595784],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987133,0.000037138885,0.00048606956,0.0003674736,0.000119228214,0.00027678997],"domain_scores_gemma":[0.99910396,0.000050415252,0.00025940628,0.0004380514,0.00008173851,0.00006641171],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028751523,0.00015826728,0.00025546702,0.000108328866,0.000083993415,0.000014203069,0.00025392126,0.00012615167,0.00001038874],"category_scores_gemma":[0.0010306488,0.0001574922,0.000032676257,0.00008849312,0.00015918528,0.000003016056,0.00019905767,0.00008825006,4.0902137e-7],"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":[0.000008850942,0.00007593147,0.9417109,0.00005832849,0.000020480653,0.0000015694593,0.00010316642,0.0001455479,0.035625387,0.000037328246,0.00009499793,0.022117523],"study_design_scores_gemma":[0.002751129,0.0009792448,0.96119565,0.00020738452,0.000029273791,0.0000057846814,0.0000692945,0.0009230003,0.03158285,0.0014346367,0.00063515175,0.00018660037],"about_ca_topic_score_codex":0.00013760861,"about_ca_topic_score_gemma":0.00009607641,"teacher_disagreement_score":0.021930924,"about_ca_system_score_codex":0.000013903186,"about_ca_system_score_gemma":0.000031446674,"threshold_uncertainty_score":0.64223456},"labels":[],"label_agreement":null},{"id":"W2592165355","doi":"10.1159/000454805","title":"Hormonal and Metabolic Responses to a Single Bout of Resistance Exercise in Prader-Willi Syndrome","year":2017,"lang":"en","type":"article","venue":"Hormone Research in Paediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"U.S. Army","keywords":"Resistance training; Hormone; Metabolic syndrome; Endocrinology; Internal medicine; Insulin resistance; Medicine; Physiology; Obesity","score_opus":0.05309056597284074,"score_gpt":0.33803158660827926,"score_spread":0.2849410206354385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2592165355","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.965184,0.03351057,0.000029568646,0.0004697199,0.00003972695,0.0003945711,0.000019477973,0.0000031349755,0.00034927216],"genre_scores_gemma":[0.9843239,0.013216498,0.0017721708,0.0000093178805,0.000052225023,0.000057388967,0.0000052869023,0.000023409615,0.0005397971],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9979119,0.00016835329,0.00036387055,0.0004651177,0.00044123406,0.0006495614],"domain_scores_gemma":[0.9987804,0.0000897973,0.000108788794,0.0007058305,0.00014238448,0.00017275845],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020366348,0.00014476162,0.00029003195,0.0004466757,0.00014389293,0.0000859764,0.0004867719,0.00016522026,0.0000017113136],"category_scores_gemma":[0.0014226676,0.00014758967,0.000049243332,0.00032687653,0.00020436663,0.000012316321,0.0006911005,0.00025045025,0.0000054658626],"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":[0.00027719338,0.0005210133,0.48790023,0.00023404592,0.000039960818,0.00007472732,0.0005327221,0.000024039151,0.48896024,0.00021183194,0.0021148191,0.019109199],"study_design_scores_gemma":[0.00078013295,0.00038612413,0.9870549,0.000056602832,0.000006734289,0.00002105404,0.00020751073,0.000014227617,0.0070495065,0.00032346035,0.003915064,0.00018467051],"about_ca_topic_score_codex":0.00018265891,"about_ca_topic_score_gemma":0.00014127363,"teacher_disagreement_score":0.4991547,"about_ca_system_score_codex":0.000026693815,"about_ca_system_score_gemma":0.00017428753,"threshold_uncertainty_score":0.60185325},"labels":[],"label_agreement":null},{"id":"W2593243414","doi":"10.3390/ijms18030517","title":"Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome: A Case Study","year":2017,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Glenrose Rehabilitation Hospital; University of Alberta","funders":"Canadian Institutes of Health Research; Stollery Children’s Hospital Foundation; Children's Hospital Foundation; University of Alberta; Women and Children's Health Research Institute; Children's Health Research Institute","keywords":"Autism Diagnostic Observation Schedule; Autism spectrum disorder; Autism; Intellectual disability; Vineland Adaptive Behavior Scale; Psychology; Clinical psychology; Rating scale; Observational study; Pediatrics; Pervasive developmental disorder; Social skills; Medicine; Psychiatry; Developmental psychology; Internal medicine","score_opus":0.012001346830556767,"score_gpt":0.2852279803621676,"score_spread":0.27322663353161086,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2593243414","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986535,0.00022933983,0.00023452289,0.00038354803,0.00021632318,0.00013362184,0.0000016194064,0.0000022357335,0.00014534016],"genre_scores_gemma":[0.99830055,0.000012581723,0.0015628262,0.00006173645,0.000029768335,0.0000028156478,0.000001040339,0.0000090838075,0.000019621108],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986848,0.00006605361,0.00035474094,0.00023729923,0.00048533286,0.00017175544],"domain_scores_gemma":[0.9990439,0.000007517067,0.00054034527,0.00020343676,0.00012797327,0.00007681771],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006156753,0.000117840944,0.00013952891,0.0001449492,0.00017708424,0.00024408789,0.0008933148,0.00005050042,0.0000061349715],"category_scores_gemma":[0.00017578421,0.000091901486,0.00006168605,0.00007617522,0.0002728397,0.000028467219,0.00021534505,0.00013436661,0.0000010897921],"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":[6.604241e-7,0.00010322111,0.9825036,9.4159344e-7,0.00022867946,0.0005607501,0.00020192261,0.0010858647,0.011696774,0.00003455987,0.0000031364355,0.0035798785],"study_design_scores_gemma":[0.0013905099,0.0012160653,0.93070966,0.00007850085,0.00002585435,0.06338191,0.00077131693,0.00020676761,0.0019135989,0.00013220008,0.000017074655,0.00015652852],"about_ca_topic_score_codex":0.00022039448,"about_ca_topic_score_gemma":0.00004646646,"teacher_disagreement_score":0.06282116,"about_ca_system_score_codex":0.000015841195,"about_ca_system_score_gemma":0.00016445531,"threshold_uncertainty_score":0.37476337},"labels":[],"label_agreement":null},{"id":"W2595510945","doi":"10.1093/biolreprod/81.s1.142","title":"Characterization of the Mouse Kcnq1ot1 Non-Coding RNA.","year":2009,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Non-coding RNA; Genetics; Gene; Epigenetics; DNA methylation; Gene silencing; Regulation of gene expression; RNA; Gene expression; Computational biology","score_opus":0.009590569694354392,"score_gpt":0.23234196752874567,"score_spread":0.22275139783439127,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2595510945","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99676573,0.00014895968,0.0022206304,0.0003170143,0.0002583381,0.00011162012,0.0000028801992,0.0000037841264,0.00017106108],"genre_scores_gemma":[0.99883723,0.00018790891,0.00034852716,0.000024276907,0.00017710436,0.000001789276,0.000035935827,0.0000042343145,0.00038297471],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99943113,0.000038654955,0.00017963187,0.00022871309,0.000035402285,0.00008645323],"domain_scores_gemma":[0.9993588,0.0000015437685,0.00018646535,0.00037089264,0.00007143033,0.00001086828],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020313577,0.000060359194,0.000093527575,0.000023028886,0.000034872442,0.0000018089073,0.0001013622,0.000085990505,0.0000045400925],"category_scores_gemma":[0.000106955624,0.000046066565,0.000056207416,0.00006948016,0.00006113176,0.000002035903,0.00003694596,0.00003313275,7.727255e-7],"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":[0.000005678674,0.000021420517,0.004231524,0.0000064471433,0.000009360555,9.051115e-9,0.000023523287,0.0000060873567,0.9695327,0.000036238573,0.000022412714,0.026104573],"study_design_scores_gemma":[0.00009024378,0.00014546007,0.12411581,0.000005281705,0.00000522551,0.000008009496,0.000012457286,0.000010097544,0.8728409,0.000033276287,0.002691576,0.000041657597],"about_ca_topic_score_codex":0.00000680051,"about_ca_topic_score_gemma":4.9807437e-7,"teacher_disagreement_score":0.11988429,"about_ca_system_score_codex":0.0000032209614,"about_ca_system_score_gemma":0.000016094024,"threshold_uncertainty_score":0.187854},"labels":[],"label_agreement":null},{"id":"W2597256494","doi":"10.1200/jco.2007.25.18_suppl.21178","title":"A novel case of Silver Russell Syndrome (SRS) and male breast cancer","year":2007,"lang":"en","type":"article","venue":"Journal of Clinical Oncology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Windsor Regional Hospital","funders":"","keywords":"Medicine; Breast cancer; Cancer; Biopsy; Oncology; Pathology; Internal medicine","score_opus":0.046802345447217196,"score_gpt":0.40222441366332434,"score_spread":0.35542206821610717,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2597256494","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962542,0.00086805155,0.0010931765,0.00042418644,0.0005603471,0.00005894871,0.000011216425,0.0000010035534,0.00072886725],"genre_scores_gemma":[0.9925926,0.00062341715,0.00570507,0.0003637181,0.000418843,5.5951654e-7,6.9064095e-7,0.000011797066,0.00028332046],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9981354,0.00006603164,0.0013134206,0.00016814073,0.00010853102,0.00020850725],"domain_scores_gemma":[0.9981804,0.00020029576,0.0010024927,0.00014240421,0.000250577,0.00022384267],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021623971,0.000101379126,0.00056958024,0.000052972373,0.000026379868,0.000004925356,0.00012894216,0.00033214872,0.00011271823],"category_scores_gemma":[0.00036853243,0.000081419064,0.00022065055,0.00006027478,0.00017497667,0.000004652213,0.00010863393,0.00025931373,0.0000014089708],"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":[0.00091674173,0.0016173887,0.34558082,0.00010465539,0.00068460737,0.0034839672,0.00010497626,0.00006822475,0.3629683,0.00009015269,0.0015334055,0.28284675],"study_design_scores_gemma":[0.003396523,0.0042298576,0.80122566,0.000048062586,0.00015178716,0.17207675,0.0002312899,0.000031141284,0.0026518863,0.00003295174,0.015767522,0.0001565539],"about_ca_topic_score_codex":0.00009066045,"about_ca_topic_score_gemma":0.00011729661,"teacher_disagreement_score":0.45564485,"about_ca_system_score_codex":0.000013168829,"about_ca_system_score_gemma":0.0003315647,"threshold_uncertainty_score":0.3320173},"labels":[],"label_agreement":null},{"id":"W2605138257","doi":"10.1093/pch/10.4.221a","title":"Case 2: I don't like your tone","year":2005,"lang":"en","type":"article","venue":"Paediatrics & Child Health","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Tone (literature); Medicine; Audiology; Philosophy; Linguistics","score_opus":0.013154947667769023,"score_gpt":0.2805507150368905,"score_spread":0.26739576736912146,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2605138257","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97756,0.013083645,0.0012084157,0.0045051607,0.00044806994,0.0002990129,0.00003377854,0.000035937832,0.002825975],"genre_scores_gemma":[0.9848741,0.0036293273,0.005181153,0.0035856627,0.0021347424,0.000010100023,0.00005743203,0.000035928628,0.0004915272],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9985283,0.000052909985,0.00034624722,0.00040464834,0.0001513804,0.00051650923],"domain_scores_gemma":[0.9990963,0.000010339232,0.00014841389,0.00041091666,0.00005437069,0.00027966808],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037144867,0.00017810769,0.00018238802,0.000070434566,0.0002925596,0.000026717078,0.00015718126,0.00013098755,0.000041102572],"category_scores_gemma":[0.0000555883,0.00017760188,0.00010769045,0.00015772365,0.000026634487,0.0000031448226,0.00014616775,0.00017151679,0.00005426228],"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":[0.00006116378,0.0013429384,0.1317974,0.00057691254,0.00027175382,0.0003060083,0.0022240162,0.0015266113,0.0071440805,0.0006761224,0.11217381,0.7418992],"study_design_scores_gemma":[0.0017983251,0.0008058703,0.031118633,0.00002069041,0.000040469593,0.0080591785,0.00040309574,0.00031313984,0.0019097999,0.00003427357,0.95475805,0.00073846587],"about_ca_topic_score_codex":0.00017285507,"about_ca_topic_score_gemma":0.00010855731,"teacher_disagreement_score":0.84258425,"about_ca_system_score_codex":0.000034336186,"about_ca_system_score_gemma":0.00014886534,"threshold_uncertainty_score":0.72423947},"labels":[],"label_agreement":null},{"id":"W2611012165","doi":"10.1016/j.celrep.2017.04.020","title":"Large-Scale Analysis of Loss of Imprinting in Human Pluripotent Stem Cells","year":2017,"lang":"en","type":"article","venue":"Cell Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":104,"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":"Azrieli Foundation; Rosetrees Trust","keywords":"Induced pluripotent stem cell; Imprinting (psychology); Genomic imprinting; Biology; Germline; Embryonic stem cell; DNA methylation; Somatic cell; Genetics; Epigenetics; Stem cell; Gene; Gene expression","score_opus":0.009685806512709946,"score_gpt":0.24803655244467748,"score_spread":0.23835074593196753,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2611012165","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969467,0.00014474322,0.0003583733,0.000004934515,0.000103884864,0.00009046235,0.0000036238166,0.0000021079736,0.0023451552],"genre_scores_gemma":[0.9988477,0.000031767213,0.00029538988,0.0000048078737,0.000022272749,0.0000030524516,0.000011359231,0.000011420676,0.0007721854],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99878675,0.00001942471,0.000545698,0.00031705247,0.00012534799,0.00020575327],"domain_scores_gemma":[0.99814767,0.0000036478261,0.00077929057,0.00094513793,0.00007883232,0.00004542479],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004231393,0.00010265552,0.00029904695,0.000092495044,0.000070028276,0.000015198069,0.00017920912,0.00009641505,0.000019382993],"category_scores_gemma":[0.000017481218,0.000103066355,0.00020723866,0.000076314565,0.00005836479,0.0000024445267,0.00028100496,0.000050697632,3.7439946e-7],"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":[9.708947e-7,0.000056914374,0.34144887,0.000034772485,0.00006253399,0.000015057477,0.000079218014,0.00032370441,0.65771073,0.0000012963724,0.0000060489647,0.00025987308],"study_design_scores_gemma":[0.00013746541,0.0000383719,0.27684253,0.000014325183,0.00008998336,0.000007515488,0.0001361166,0.00013713633,0.722104,0.000008069645,0.00040221642,0.000082225204],"about_ca_topic_score_codex":0.00012608756,"about_ca_topic_score_gemma":0.000085443244,"teacher_disagreement_score":0.06460634,"about_ca_system_score_codex":0.0000063261564,"about_ca_system_score_gemma":0.000027686287,"threshold_uncertainty_score":0.4202924},"labels":[],"label_agreement":null},{"id":"W2612348400","doi":"10.14288/1.0340922","title":"Detailed phenotyping and next-generation sequencing for characterization of rare overgrowth syndromes","year":2017,"lang":"en","type":"article","venue":"Open Collections","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"DNA sequencing; Computer science; Computational biology; Medicine; Biology; Genetics; Gene","score_opus":0.05838203144902022,"score_gpt":0.27657928565151435,"score_spread":0.21819725420249414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2612348400","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9857506,0.00004032621,0.0093708765,0.0000836693,0.00018126091,0.00052655453,0.000031414264,0.0000036554025,0.0040116515],"genre_scores_gemma":[0.9885352,0.00007422281,0.0020458072,0.000028054848,0.000096148535,0.00007719189,0.00008704351,0.000012564432,0.009043768],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995176,0.000014785701,0.00013918136,0.00019315815,0.000036384772,0.00009887989],"domain_scores_gemma":[0.9994853,0.0000054527945,0.00015502497,0.00023436303,0.000090899295,0.000028948116],"candidate_categories":["sts"],"consensus_categories":[],"category_scores_codex":[0.00010358691,0.00007043156,0.00010799257,0.000018717343,0.0014800546,0.00060093123,0.00015613696,0.00005815356,0.000018866487],"category_scores_gemma":[0.00012388096,0.000074334515,0.000032540738,0.000042120642,0.000030314093,0.000021786593,0.00015755881,0.000021286403,2.0622095e-7],"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":[0.000008532091,0.000009699513,0.00089986017,0.000016581535,0.000031129588,7.6056e-8,0.00003825122,0.000010137694,0.99712163,0.000024991952,0.00027935015,0.0015597772],"study_design_scores_gemma":[0.002196014,0.0006244976,0.049372267,0.00010306898,0.00009941832,0.00008965773,0.00026795288,0.012384465,0.92233026,0.00023422235,0.011855884,0.0004422868],"about_ca_topic_score_codex":0.00023230303,"about_ca_topic_score_gemma":0.00024590938,"teacher_disagreement_score":0.07479135,"about_ca_system_score_codex":0.000011764149,"about_ca_system_score_gemma":0.00007611597,"threshold_uncertainty_score":0.9998199},"labels":[],"label_agreement":null},{"id":"W2613710287","doi":"10.5489/cuaj.4297","title":"Recurrent, bilateral, and metastatic pheochromocytoma in a young patient with Beckwith-Wiedemann syndrome: A genetic link?","year":2017,"lang":"en","type":"article","venue":"Canadian Urological Association Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"","keywords":"Beckwith–Wiedemann syndrome; Pheochromocytoma; Paraganglioma; Histopathology; Comparative genomic hybridization; Medicine; Pathology; Genotyping; Bioinformatics; Genetics; Biology; Chromosome; Gene; Genotype","score_opus":0.008952839217501106,"score_gpt":0.2179903056821508,"score_spread":0.20903746646464968,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2613710287","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99653614,0.00048255583,0.00006013397,0.0022247878,0.0001584896,0.00015817578,0.000013443824,0.0000033794852,0.00036287511],"genre_scores_gemma":[0.9982035,0.00016096022,0.0010931637,0.0003183627,0.00009045872,0.000013152066,0.000009264366,0.000014184943,0.00009695238],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99866074,0.000117300144,0.00028886987,0.00028753455,0.00017386643,0.00047170988],"domain_scores_gemma":[0.9989504,0.000013972635,0.00035912325,0.0002067177,0.000102197984,0.00036755248],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003153724,0.0001613817,0.0002121117,0.00009286966,0.00040763308,0.0002811369,0.00020428839,0.00014832102,0.00004694954],"category_scores_gemma":[0.00034766216,0.00012853452,0.000054640055,0.000050882154,0.00005706246,0.00001184077,0.00006334153,0.00025527301,0.0000060517355],"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":[0.000018788014,0.000027732574,0.9857885,0.000006736445,0.00010123317,0.0003097513,0.00010985117,0.00006162685,0.00088384474,0.0000073692295,0.00024599058,0.012438552],"study_design_scores_gemma":[0.00078238826,0.0010304772,0.9905331,0.000025648344,0.000031114218,0.0041963514,0.00005233292,0.0002037842,0.000076737815,0.00017043242,0.0026998965,0.00019770036],"about_ca_topic_score_codex":0.00093741925,"about_ca_topic_score_gemma":0.006195673,"teacher_disagreement_score":0.012240852,"about_ca_system_score_codex":0.00011945045,"about_ca_system_score_gemma":0.00019550101,"threshold_uncertainty_score":0.5241486},"labels":[],"label_agreement":null},{"id":"W2615109464","doi":"10.1034/j.1399-0004.2001.600302.2.x","title":"Discoveries in Charcot–Marie–Tooth disease, Crohn's disease and Bardet–Biedl syndrome 4","year":2001,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Pacific Centre for Reproductive Medicine; University of British Columbia","funders":"","keywords":"Medicine","score_opus":0.05614264677642138,"score_gpt":0.36644885646761083,"score_spread":0.31030620969118944,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2615109464","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.030312503,0.96761864,0.000100098485,0.000054349985,0.00060041546,0.0009158249,0.00021111363,0.00001740412,0.00016964039],"genre_scores_gemma":[0.003089353,0.99293303,0.00052333885,0.00017068755,0.00048952847,0.000118667216,0.00054310093,0.00014544705,0.0019868694],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9956738,0.0003552873,0.0015539926,0.0014292223,0.0002758772,0.00071185385],"domain_scores_gemma":[0.99718684,0.0001779629,0.00041699395,0.0012684572,0.000058967773,0.0008908014],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00047518293,0.0007417077,0.0016323023,0.00011779546,0.00010052052,0.00013833304,0.00061793975,0.00062429317,0.00007460699],"category_scores_gemma":[0.00090876577,0.0006654756,0.00074631063,0.00025323665,0.0005061279,0.0000051103716,0.0010342185,0.00050123304,0.000042052485],"study_design_candidate":"design_other","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":[0.000042321786,0.0003836795,0.018315313,0.0052051377,0.00027732376,0.0005145006,0.000008087868,0.000018746034,0.0000024649817,0.00002820668,0.0005784275,0.97462577],"study_design_scores_gemma":[0.00046293458,0.00026173092,0.074462585,0.0020674823,0.0006232665,0.00006240433,0.000008846965,0.00003161315,4.6164385e-7,0.000118668424,0.92110527,0.00079471443],"about_ca_topic_score_codex":0.0000066882976,"about_ca_topic_score_gemma":0.00001417016,"teacher_disagreement_score":0.97383106,"about_ca_system_score_codex":0.000024806368,"about_ca_system_score_gemma":0.0006195232,"threshold_uncertainty_score":0.99957967},"labels":[],"label_agreement":null},{"id":"W2619988375","doi":"10.1093/molehr/gax029","title":"Intergenerational impact of paternal lifetime exposures to both folic acid deficiency and supplementation on reproductive outcomes and imprinted gene methylation","year":2017,"lang":"en","type":"article","venue":"Molecular Human Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":125,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Health Canada; McGill University; William Osler Health System; McGill University Health Centre","funders":"Canadian Institutes of Health Research","keywords":"Biology; Methylation; Folic acid; Folic acid supplementation; Genomic imprinting; DNA methylation; Endocrinology; Genetics; Imprinting (psychology); Gene; Internal medicine; Pregnancy; Gene expression","score_opus":0.016662114616363265,"score_gpt":0.31959485427291484,"score_spread":0.3029327396565516,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2619988375","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954171,0.0001739125,0.003659206,0.00024156936,0.0001276343,0.000307045,0.0000104154815,0.000007052619,0.000056075707],"genre_scores_gemma":[0.99761695,0.000027887281,0.001955853,0.000023948545,0.00014729255,0.000022666176,0.00007422064,0.000018743764,0.0001124538],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986709,0.000060944145,0.00027221348,0.0006917712,0.00015581133,0.00014839292],"domain_scores_gemma":[0.99887156,0.0000024374563,0.00023398643,0.00070770126,0.00012490698,0.000059383143],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003542916,0.00015786393,0.00015547067,0.00009345945,0.00023695779,0.00007341768,0.000107366606,0.000058138972,0.0000121610965],"category_scores_gemma":[0.00027854403,0.00014597304,0.00007546728,0.00003098514,0.00006954111,0.000012112934,0.00015790998,0.000051821855,0.0000010084032],"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":[0.000029162129,0.000041791263,0.098281756,0.000008872502,0.00006123453,4.5022608e-7,0.00013896266,0.00021340717,0.89594734,0.000060323673,0.000021932043,0.0051947534],"study_design_scores_gemma":[0.0002355001,0.0005836794,0.477142,0.0000057641355,0.000013684641,0.000013902313,0.00001528695,0.000014611004,0.5217672,0.00010878387,0.000016474178,0.00008312092],"about_ca_topic_score_codex":0.0002064675,"about_ca_topic_score_gemma":0.000018106886,"teacher_disagreement_score":0.37886027,"about_ca_system_score_codex":0.000019830324,"about_ca_system_score_gemma":0.00002066094,"threshold_uncertainty_score":0.5952608},"labels":[],"label_agreement":null},{"id":"W2624029039","doi":"10.1096/fj.201700229r","title":"<i>In vivo</i> imaging of prodromal hippocampus CA1 subfield oxidative stress in models of Alzheimer disease and Angelman syndrome","year":2017,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":36,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Kingston Health Sciences Centre; Queen's University","funders":"National Eye Institute; National Institute on Aging; Research to Prevent Blindness","keywords":"Oxidative stress; Angelman syndrome; Hippocampus; Disease; Neuroscience; In vivo; Medicine; Pathology; Biology; Internal medicine; Biochemistry; Genetics","score_opus":0.01481228296134809,"score_gpt":0.2531388628538565,"score_spread":0.2383265798925084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2624029039","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972761,0.0019696523,0.00007044048,0.00023545891,0.00007066046,0.00011663154,0.000018649469,6.7793127e-7,0.00024169504],"genre_scores_gemma":[0.99951524,0.00022187413,0.00014999782,0.000030727977,0.000034994944,0.000003081088,0.0000014849346,0.00000949226,0.00003309984],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992595,0.00005974055,0.00024987725,0.00014374463,0.000106524065,0.00018066162],"domain_scores_gemma":[0.9993121,0.000009799406,0.00025792405,0.00030690365,0.000043737302,0.00006953808],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030624281,0.00009842346,0.00016108804,0.000046615907,0.00008365218,0.000028284228,0.00025883855,0.00003551829,0.000011364827],"category_scores_gemma":[0.0000477515,0.00007472394,0.00005318094,0.000024351557,0.00014621027,0.000016920621,0.00016730462,0.00012136934,1.5798963e-7],"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":[0.000042910113,0.000074270654,0.19362682,0.000029263496,0.000059489932,0.000055673176,0.00027782295,0.00041598323,0.8038985,0.000031340176,0.000035167406,0.0014527747],"study_design_scores_gemma":[0.0010474665,0.00015011647,0.24700856,0.00022228954,0.00006795048,0.00041745006,0.00044517592,0.0013857423,0.7473084,0.0017677267,0.000008987854,0.00017012794],"about_ca_topic_score_codex":0.00012248126,"about_ca_topic_score_gemma":0.00003808693,"teacher_disagreement_score":0.056590088,"about_ca_system_score_codex":0.0000039752726,"about_ca_system_score_gemma":0.000052518004,"threshold_uncertainty_score":0.3047154},"labels":[],"label_agreement":null},{"id":"W2629299361","doi":"10.1007/s00439-017-1824-5","title":"Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion","year":2017,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"HEC Montréal; McGill University","funders":"","keywords":"Biology; Imprinting (psychology); Allele; Genetics; Genomic imprinting; Genetic model; Gene; Gene expression","score_opus":0.05227242962283838,"score_gpt":0.3248412895296295,"score_spread":0.2725688599067911,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2629299361","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6327415,0.0004570825,0.36623323,0.0000026129687,0.0000348169,0.00048738075,0.000032828146,0.0000027084907,0.000007825655],"genre_scores_gemma":[0.9719798,0.00006845736,0.02759088,0.0000031544673,0.000083147905,0.00005183258,0.00013302229,0.000031207594,0.000058472662],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99881244,0.000028210046,0.00042968284,0.0003717162,0.00012860839,0.0002293693],"domain_scores_gemma":[0.9986913,0.000018155293,0.00047240328,0.0005818293,0.00017270529,0.0000635583],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024985182,0.00018869751,0.0003725801,0.00009019419,0.00029867687,0.000029616684,0.00018862958,0.00010837698,0.000003517986],"category_scores_gemma":[0.00002129963,0.00016596568,0.00028159143,0.00005118454,0.00007699863,0.0000033339372,0.0000628308,0.000035788547,4.9565955e-8],"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":[0.000080684695,0.00010041989,0.012518235,0.00022681682,0.00055025425,9.263221e-7,0.00020702438,0.087763086,0.8736024,0.0000119870065,0.000011340025,0.024926823],"study_design_scores_gemma":[0.0019201628,0.0014683933,0.009355719,0.000056591238,0.0015162254,0.000018683148,0.00010943933,0.42752084,0.5574413,0.000016081305,0.00030195247,0.00027465157],"about_ca_topic_score_codex":0.000020931704,"about_ca_topic_score_gemma":0.000028837605,"teacher_disagreement_score":0.33975774,"about_ca_system_score_codex":0.000020920541,"about_ca_system_score_gemma":0.00004297025,"threshold_uncertainty_score":0.6767884},"labels":[],"label_agreement":null},{"id":"W2724568932","doi":"10.5038/2074-1235.41.2.1026","title":"Hybridization from Possible Sexual Mis-imprinting: Molecular Characterization of Hybridization Between Brown Sula Leucogaster and Blue-footed Boobies S Nebouxii","year":2013,"lang":"en","type":"article","venue":"Marine ornithology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Natural Sciences and Engineering Research Council of Canada; McGill University","keywords":"Ornithology; Imprinting (psychology); Seabird; Biology; Zoology; Genetics; Ecology; Gene; Southern Hemisphere","score_opus":0.007862932673764039,"score_gpt":0.21035160640327727,"score_spread":0.20248867372951324,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2724568932","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9809074,0.000043425407,0.018109934,0.00017046709,0.00009794213,0.00030085392,0.00002595832,0.000023359773,0.00032065884],"genre_scores_gemma":[0.9955604,0.000028331517,0.0019608529,0.00014093757,0.00014853763,0.000021671565,0.0015958544,0.000041778836,0.000501644],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99857515,0.00012143537,0.00043517776,0.00047206998,0.00011524511,0.00028090162],"domain_scores_gemma":[0.99909705,0.000018524428,0.00026699025,0.0003426268,0.00019399522,0.00008079557],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012337716,0.00021839599,0.00028488308,0.00010330177,0.00006804258,0.00005439231,0.00014955463,0.00018256227,0.00013963113],"category_scores_gemma":[0.00011322539,0.00022842966,0.000042638047,0.00011429067,0.00011493086,0.000016733602,0.00032997102,0.00009183114,0.000012701241],"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":[0.000006250903,0.000021508398,0.2449171,0.000022934679,0.000047090987,0.0000012406178,0.000051740517,0.00002348552,0.7424843,0.000008021697,0.000017632212,0.012398749],"study_design_scores_gemma":[0.0005167545,0.00019414579,0.60543483,0.000008792415,0.00004175205,0.000029163313,0.000064046566,0.00030336215,0.3923123,0.00006641629,0.0008445996,0.00018382227],"about_ca_topic_score_codex":0.00019239642,"about_ca_topic_score_gemma":0.0000097187985,"teacher_disagreement_score":0.36051777,"about_ca_system_score_codex":0.0000081081,"about_ca_system_score_gemma":0.000033730503,"threshold_uncertainty_score":0.93150914},"labels":[],"label_agreement":null},{"id":"W2734652700","doi":"10.1038/ejhg.2017.102","title":"Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines","year":2017,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Beckwith–Wiedemann syndrome; Methylation; Wilms' tumor; Wilms tumour; Imprinting (psychology); Uniparental disomy; Genomic imprinting; Medicine; DNA methylation; Oncology; Biology; Internal medicine; Karyotype; Cancer research; Genetics; Chromosome; Gene","score_opus":0.026596188275592715,"score_gpt":0.2868495838775544,"score_spread":0.26025339560196165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2734652700","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961005,0.0027349384,0.00022703822,0.00017357453,0.00012738083,0.000085812375,0.0000037517543,0.0000026227804,0.00054441486],"genre_scores_gemma":[0.9956001,0.00061973784,0.0032490455,0.000020904035,0.00031173686,1.9734317e-7,0.0000046981795,0.000042958683,0.00015059636],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9980185,0.00024420486,0.001004026,0.0002618147,0.00020884907,0.0002626083],"domain_scores_gemma":[0.9977297,0.000016433714,0.0014220051,0.00037848335,0.00035236074,0.00010099261],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017793459,0.00019313842,0.0003468673,0.000088541354,0.00021609712,0.00007501873,0.00044929667,0.000046167374,0.00001078108],"category_scores_gemma":[0.00049583905,0.00018408432,0.00011771739,0.00003736665,0.000112594316,0.000010185164,0.00051044347,0.00014125786,0.0000022836864],"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":[0.000009242457,0.00001701042,0.3142587,0.00006533483,0.000038968163,0.00007875603,0.00012166993,0.0003079003,0.68085825,0.0000060319057,0.000047344285,0.0041908184],"study_design_scores_gemma":[0.0010124103,0.0003981949,0.92113304,0.00035279003,0.00002664372,0.0007843525,0.00017200055,0.00014989992,0.075058416,0.000025690515,0.00064815953,0.00023839343],"about_ca_topic_score_codex":0.000007885257,"about_ca_topic_score_gemma":0.000019172508,"teacher_disagreement_score":0.60687435,"about_ca_system_score_codex":0.000014478231,"about_ca_system_score_gemma":0.000028416598,"threshold_uncertainty_score":0.750674},"labels":[],"label_agreement":null},{"id":"W2738352505","doi":"10.1080/17476348.2017.1355241","title":"<i>DLK1-DIO3</i>imprinted locus deregulation in development, respiratory disease, and cancer","year":2017,"lang":"en","type":"review","venue":"Expert Review of Respiratory Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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","keywords":"Medicine; Internal medicine; Locus (genetics); Oncology; Intensive care medicine; Genetics; Gene; Biology","score_opus":0.08602050507173746,"score_gpt":0.4124554655017475,"score_spread":0.32643496043001,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2738352505","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00021840149,0.9979423,0.000033758253,0.00008003167,0.0003104006,0.0010768968,0.000009208843,0.000008760285,0.00032022625],"genre_scores_gemma":[0.00004281345,0.99746406,0.00012042984,0.0011214431,0.0006136981,0.00034727744,0.000068920395,0.000068488764,0.00015285396],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99681336,0.00030790255,0.0014354693,0.0007680312,0.00033374992,0.00034148552],"domain_scores_gemma":[0.9973989,0.000036018235,0.0010885926,0.0010697374,0.00015881816,0.00024792814],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0010820164,0.0005468524,0.0019585292,0.0001921416,0.00009378136,0.000011677799,0.00049895747,0.00027864813,0.0000828407],"category_scores_gemma":[0.00088380196,0.00041405053,0.00022333502,0.00016132931,0.00028016543,0.000007748328,0.0003113119,0.00022503395,0.0000046500622],"study_design_candidate":"design_other","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":[0.0000036237896,0.000024365198,0.00023989019,0.048275564,0.000098968114,0.000006537392,0.000025689234,7.7145074e-8,0.00045207594,0.000003612768,0.0024971492,0.9483724],"study_design_scores_gemma":[0.00035239712,0.00009068277,0.0008575466,0.15314628,0.00015272545,0.000007669545,0.0000058095916,2.043666e-7,0.00009461344,8.947452e-7,0.84495556,0.00033564214],"about_ca_topic_score_codex":0.00002675925,"about_ca_topic_score_gemma":0.000024612178,"teacher_disagreement_score":0.9480368,"about_ca_system_score_codex":0.00006007029,"about_ca_system_score_gemma":0.00086167903,"threshold_uncertainty_score":0.99983114},"labels":[],"label_agreement":null},{"id":"W2743543325","doi":"10.1038/gim.2017.105","title":"Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction","year":2017,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":137,"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":"Université Pierre et Marie Curie; Institut National de la Santé et de la Recherche Médicale; European Commission; Rare Disease Foundation; Agence Nationale de la Recherche; Children’s Hospital of Wisconsin Research Institute; Seattle Children's Research Institute","keywords":"HMGA2; Fetal growth; Genetics; Biology; Genomic imprinting; CRISPR; Intrauterine growth restriction; Fetus; Cancer research; Medicine; Gene; DNA methylation; Pregnancy; microRNA; Gene expression","score_opus":0.01962991651978447,"score_gpt":0.28069400855638804,"score_spread":0.2610640920366036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2743543325","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99482834,0.0019259243,0.0007116931,0.00044029698,0.0008708211,0.00026610272,0.000007749062,0.0000050848107,0.00094396615],"genre_scores_gemma":[0.9945666,0.00379023,0.00080489484,0.00009294429,0.0004904183,0.00001505875,0.000012447544,0.000025907259,0.00020145578],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99852777,0.00008191178,0.00044390207,0.00036692547,0.0002939123,0.00028559536],"domain_scores_gemma":[0.99841815,0.000016340953,0.0003456106,0.0010324658,0.000116379306,0.000071074435],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003102522,0.00018663384,0.00023305803,0.0000642954,0.00020371105,0.000018800423,0.00060374243,0.00017292901,0.000019370009],"category_scores_gemma":[0.0005047394,0.00013794005,0.000090857495,0.00009678672,0.00035407156,0.0000033735591,0.0003392015,0.00014411043,0.0000036062634],"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":[0.000012800388,0.000047353267,0.30080828,0.000039034483,0.000032299195,0.0000032176927,0.000104237,0.00011580375,0.68747085,0.00006039747,0.00022846153,0.011077287],"study_design_scores_gemma":[0.0009240018,0.00036264796,0.85025704,0.000092401,0.000039504837,0.00004383935,0.000116588344,0.00015372965,0.1456345,0.00045515012,0.0017665611,0.00015405356],"about_ca_topic_score_codex":0.0002469714,"about_ca_topic_score_gemma":0.00021666681,"teacher_disagreement_score":0.5494487,"about_ca_system_score_codex":0.000021373995,"about_ca_system_score_gemma":0.00008448019,"threshold_uncertainty_score":0.5625032},"labels":[],"label_agreement":null},{"id":"W2743664205","doi":"10.1016/j.jmoldx.2017.07.002","title":"Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders","year":2017,"lang":"en","type":"article","venue":"Journal of Molecular Diagnostics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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; London Health Sciences Centre; Western University","funders":"","keywords":"DNA methylation; Imprinting (psychology); Genomic imprinting; Biology; Genetics; Genome; Methylation; Computational biology; DNA; Gene; Gene expression","score_opus":0.01812132853283012,"score_gpt":0.3117323569973819,"score_spread":0.2936110284645518,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2743664205","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8107854,0.0010713823,0.18732178,0.00019725302,0.00028021305,0.00024503842,0.000012056255,0.0000015720592,0.00008527903],"genre_scores_gemma":[0.97833544,0.0020676532,0.019347763,0.000054618624,0.00012102311,0.00001218333,0.000019839545,0.000036207784,0.000005274157],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9979349,0.00016226937,0.0011459003,0.00023203965,0.00029954777,0.00022539188],"domain_scores_gemma":[0.9960606,0.00037634833,0.0022439007,0.0005611834,0.0006520603,0.00010588648],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.001680054,0.00017663695,0.00044970843,0.00010022967,0.00008896136,0.000046976664,0.00050440506,0.00020979921,0.0000057566535],"category_scores_gemma":[0.012945752,0.00017558502,0.0005550783,0.000052894782,0.00013629212,0.00001581744,0.00019866986,0.00013640002,4.8016017e-7],"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":[0.000036870817,0.00027326657,0.3558012,0.00013347357,0.0004205218,0.000005700492,0.000041662963,0.002227101,0.613191,0.00009410884,0.00007598899,0.027699083],"study_design_scores_gemma":[0.0012377966,0.0009385355,0.16568975,0.00011163935,0.00027633138,0.000010657756,0.00005442543,0.000119338605,0.8291537,0.0008458174,0.0013764832,0.00018548213],"about_ca_topic_score_codex":0.000008266399,"about_ca_topic_score_gemma":0.0000027294568,"teacher_disagreement_score":0.21596271,"about_ca_system_score_codex":0.000011999957,"about_ca_system_score_gemma":0.00012262826,"threshold_uncertainty_score":0.9953686},"labels":[],"label_agreement":null},{"id":"W2751630511","doi":"10.1111/gbb.12422","title":"Dopaminergic and behavioural changes in a loss‐of‐imprinting model of <i>Cdkn1c</i>","year":2017,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":31,"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; Medical Research Council Canada; Wellcome Trust","keywords":"Imprinting (psychology); Dopaminergic; Neuroscience; Psychology; Biology; Dopamine; Genetics","score_opus":0.029026630276423243,"score_gpt":0.27406393081868946,"score_spread":0.24503730054226622,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2751630511","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988736,0.00056119286,0.000078263016,0.00012963313,0.00007351138,0.00018062662,0.000020611054,0.0000038063802,0.00007877823],"genre_scores_gemma":[0.9969105,0.0002047535,0.0024703175,0.000031346484,0.000038389524,0.000034330416,0.00001183066,0.00002228594,0.00027625146],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990399,0.000023084107,0.00027168635,0.00030739157,0.00010910349,0.0002488278],"domain_scores_gemma":[0.99909747,0.000010104202,0.00024367851,0.00053122465,0.000060351213,0.000057145407],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023385565,0.00015329206,0.0002331859,0.00006069081,0.000077151635,0.00002329536,0.00029144145,0.00012740097,0.000006209808],"category_scores_gemma":[0.00008394439,0.00015517724,0.00006667936,0.000029447738,0.00017570752,0.0000052696487,0.00039510083,0.000061507264,4.3801208e-7],"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":[0.0000041670432,0.000040864506,0.33432886,0.000018825038,0.000004363788,0.000001915921,0.000069442016,0.00003123868,0.64725333,0.000009228402,0.000005429172,0.018232355],"study_design_scores_gemma":[0.0006358987,0.0001435357,0.5167273,0.000036836173,0.00003241717,0.000033376684,0.0001071797,0.00033526574,0.4816623,0.000009592354,0.00009513632,0.00018112351],"about_ca_topic_score_codex":0.00021888319,"about_ca_topic_score_gemma":0.0002672563,"teacher_disagreement_score":0.18239848,"about_ca_system_score_codex":0.0000045658508,"about_ca_system_score_gemma":0.000033994485,"threshold_uncertainty_score":0.63279444},"labels":[],"label_agreement":null},{"id":"W2754709583","doi":"10.1002/uog.18555","title":"EP14.39: Should we consider prenatal diagnosis of Silver–Russell syndrome?","year":2017,"lang":"en","type":"article","venue":"Ultrasound in Obstetrics and Gynecology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Intrauterine growth restriction; Amniocentesis; Pediatrics; Gestational age; Birth weight; Short stature; Failure to thrive; Prenatal diagnosis; Obstetrics; Amniotic fluid; Abdomen; Small for gestational age; Achondroplasia; Fetus; Pregnancy; Surgery","score_opus":0.022237382162049894,"score_gpt":0.26910150174397557,"score_spread":0.24686411958192567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2754709583","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9912542,0.0060901404,0.000024921676,0.00021678099,0.0007784663,0.00021606626,0.000033475368,0.0000051698753,0.0013807458],"genre_scores_gemma":[0.98467803,0.014128021,0.0006233578,0.00011388614,0.000029709081,0.00003054567,0.000022287682,0.00002231674,0.00035185408],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99859357,0.0000579274,0.00038504388,0.00045792706,0.00012224745,0.0003832788],"domain_scores_gemma":[0.99609625,0.0028251458,0.00025994444,0.00063702173,0.00008000306,0.00010161076],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.00024532693,0.00019809311,0.00035019024,0.000118659955,0.00016371523,0.00006049541,0.00035182366,0.00033997433,0.000104478466],"category_scores_gemma":[0.019270135,0.00019879304,0.00008840871,0.00008830024,0.00031045396,0.000010170007,0.0002826728,0.00015667765,0.000006650239],"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":[0.000007801022,0.000248915,0.92697257,0.00013528406,0.00011470804,0.00005003184,0.00016521866,0.000037868493,0.029451208,0.0004231273,0.00048063218,0.041912645],"study_design_scores_gemma":[0.0023888343,0.0010599509,0.8301407,0.00007132355,0.00006462025,0.0004657347,0.00038552686,0.000049757633,0.046315543,0.0011765865,0.1172706,0.00061083375],"about_ca_topic_score_codex":0.000093501905,"about_ca_topic_score_gemma":0.000089177935,"teacher_disagreement_score":0.11678997,"about_ca_system_score_codex":0.0000179281,"about_ca_system_score_gemma":0.00006446414,"threshold_uncertainty_score":0.98899096},"labels":[],"label_agreement":null},{"id":"W2762704796","doi":"10.1093/eep/dvx015","title":"Maintenance of Mest imprinted methylation in blastocyst-stage mouse embryos is less stable than other imprinted loci following superovulation or embryo culture","year":2017,"lang":"en","type":"review","venue":"Current Zoology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"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 Health Research Institute; Western University","funders":"","keywords":"Genomic imprinting; Methylation; Blastocyst; Biology; Imprinting (psychology); DNA methylation; Andrology; Embryo; Insulin-like growth factor 2 receptor; Epigenetics; Embryo culture; Genetics; Embryogenesis; Gene; Growth factor; Gene expression; Medicine","score_opus":0.08081879887219379,"score_gpt":0.36886258394210114,"score_spread":0.28804378506990735,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2762704796","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.08524142,0.9075807,0.0040852022,0.000014295419,0.0011125013,0.0015047541,0.00020579995,0.000025408499,0.0002299333],"genre_scores_gemma":[0.024470007,0.9670557,0.0005249255,0.000020547488,0.00022116468,0.0001814057,0.0007805959,0.00014226895,0.0066034147],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9968431,0.00029567446,0.0010977213,0.00094741577,0.00019721763,0.00061886746],"domain_scores_gemma":[0.99760234,0.0000348802,0.0010091435,0.001083328,0.00016695028,0.00010335708],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005023057,0.00061762513,0.0015871295,0.0001914124,0.00010520723,0.000047596037,0.0007011958,0.00080858916,0.00007388054],"category_scores_gemma":[0.0003543323,0.00049287674,0.0006639738,0.00018542935,0.0001273645,0.000015346928,0.00044598684,0.00048753148,0.000018035606],"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":[0.000100823636,0.000442391,0.0038970965,0.013637674,0.001008622,0.000015855687,0.0005753763,0.000057980942,0.04587594,0.00012236075,0.0004401994,0.9338257],"study_design_scores_gemma":[0.001725549,0.00040002327,0.0010168778,0.004068308,0.00045842267,0.000057364763,0.00025039067,0.00030226726,0.007073943,0.000021464426,0.9835468,0.0010786066],"about_ca_topic_score_codex":0.00018100603,"about_ca_topic_score_gemma":0.0003591054,"teacher_disagreement_score":0.98310655,"about_ca_system_score_codex":0.000091327965,"about_ca_system_score_gemma":0.00034742893,"threshold_uncertainty_score":0.9997523},"labels":[],"label_agreement":null},{"id":"W2768805139","doi":"10.1098/rsbl.2017.0643","title":"Associations between imprinted gene expression in the placenta, human fetal growth and preeclampsia","year":2017,"lang":"en","type":"article","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Simon Fraser University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Gene; Placenta; Preeclampsia; Genetics; Microarray; Fetus; Microarray analysis techniques; Gene expression; Gene expression profiling; Pregnancy; DNA methylation","score_opus":0.017628612096924578,"score_gpt":0.2753254026786517,"score_spread":0.2576967905817271,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2768805139","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99732673,0.000067000794,0.00053022144,0.0016193159,0.000070904156,0.00013658797,0.000020670195,0.0000044968797,0.00022404428],"genre_scores_gemma":[0.998582,0.000017073717,0.0005949873,0.00044888625,0.00017958546,0.000012020626,0.00014225279,0.000008153303,0.000015019389],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99923,0.000117285475,0.00014889952,0.0002536902,0.000042791802,0.00020730963],"domain_scores_gemma":[0.9994768,0.000020765603,0.00012794591,0.0003358502,0.000010471875,0.000028197126],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025654573,0.000101863654,0.00011646369,0.00002422339,0.00031735084,0.00004380753,0.00032331567,0.0001277184,0.000002809001],"category_scores_gemma":[0.00010751639,0.000077059565,0.00004154808,0.000014295703,0.00013625986,0.0000035093349,0.00021130507,0.00009838863,0.0000017715374],"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":[8.174791e-7,0.000005547616,0.4382651,0.0000011915502,0.000010791423,4.2786647e-7,0.000032842938,1.4125749e-7,0.56134826,0.00001010215,0.00008781303,0.00023701777],"study_design_scores_gemma":[0.00036182848,0.0000489211,0.84545785,0.000004631263,0.000008383662,0.000005848219,0.000019691133,0.000001745351,0.15367731,0.00004464755,0.00028068293,0.00008847412],"about_ca_topic_score_codex":0.00011399652,"about_ca_topic_score_gemma":0.000027291626,"teacher_disagreement_score":0.40767092,"about_ca_system_score_codex":0.0000060823527,"about_ca_system_score_gemma":0.0000077381765,"threshold_uncertainty_score":0.3142398},"labels":[],"label_agreement":null},{"id":"W2772621846","doi":"10.1002/pd.5198","title":"Nonisolated diaphragmatic hernia in Simpson‐Golabi‐Behmel syndrome","year":2017,"lang":"en","type":"article","venue":"Prenatal Diagnosis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Congenital diaphragmatic hernia; Medicine; Prenatal diagnosis; Autopsy; Fetus; Diaphragmatic hernia; Omphalocele; Genetic testing; Pathology; Hernia; Surgery; Pregnancy; Internal medicine; Biology; Genetics","score_opus":0.010382595637977698,"score_gpt":0.2536748326890288,"score_spread":0.2432922370510511,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2772621846","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970933,0.0009042506,0.00006454374,0.00022571745,0.00022655564,0.00026421688,0.0000266826,0.000017105878,0.0011775781],"genre_scores_gemma":[0.9983742,0.00054605707,0.0004251733,0.00009587069,0.000053624273,0.00015506166,0.000045270444,0.000036084388,0.0002686433],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99866545,0.00004259334,0.0002851799,0.00045324067,0.00014256916,0.00041095322],"domain_scores_gemma":[0.998797,0.000024715258,0.00015962406,0.0008655376,0.000036979287,0.00011615306],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001809381,0.00021453996,0.00023461215,0.0000599667,0.00020136301,0.00015442321,0.0005960727,0.00017803008,0.00009380373],"category_scores_gemma":[0.00038729032,0.00021399475,0.00010902032,0.00005308555,0.00008499527,0.000013945965,0.00048009036,0.00012412923,0.00009332946],"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":[0.000012778056,0.00024853204,0.9575514,0.00013659633,0.000094623814,0.000076439326,0.000101559745,0.0001248258,0.018952763,0.000017831431,0.00047518883,0.02220742],"study_design_scores_gemma":[0.00089176156,0.00021067668,0.95676076,0.0001475656,0.000020954198,0.00010324584,0.00003339882,0.00042876395,0.038844638,0.00007443474,0.0021352193,0.00034858577],"about_ca_topic_score_codex":0.00032328384,"about_ca_topic_score_gemma":0.00021042161,"teacher_disagreement_score":0.021858834,"about_ca_system_score_codex":0.000017828754,"about_ca_system_score_gemma":0.00003552635,"threshold_uncertainty_score":0.87264526},"labels":[],"label_agreement":null},{"id":"W2784138807","doi":"10.1098/rsbl.2017.0694","title":"A genetic locus for paranoia","year":2018,"lang":"en","type":"article","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta; Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Paranoia; Biology; Autism; Locus (genetics); Genetics; Single-nucleotide polymorphism; Psychosis; Phenotype; Autism spectrum disorder; Genomic imprinting; Gene; Population; Genotype; Psychology; Developmental psychology; Gene expression; Psychiatry; Medicine","score_opus":0.010290541977726157,"score_gpt":0.2522138954187322,"score_spread":0.24192335344100602,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2784138807","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9518626,0.00026344226,0.046228305,0.0007926416,0.00042106546,0.00018717545,0.000009127687,0.000012232507,0.00022344635],"genre_scores_gemma":[0.9860271,0.000017775546,0.009448938,0.0033516805,0.0009220612,0.00004465596,0.00002914023,0.00001857915,0.0001400533],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99915427,0.000036327703,0.00014343699,0.0003277861,0.000026450243,0.00031174492],"domain_scores_gemma":[0.9995831,0.0000120172,0.00004899664,0.00026503144,0.00004252304,0.00004827844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010731998,0.00011711825,0.000105459985,0.000027360164,0.000082807484,0.000009694804,0.00017246096,0.000115970004,0.000027067934],"category_scores_gemma":[0.00005951254,0.000106688676,0.0000807754,0.00003629896,0.00019017069,6.881111e-7,0.00006771695,0.00002877532,0.00004200598],"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":[0.000012149904,0.000008985397,0.01564397,0.000004887455,0.000035861096,2.9731956e-7,0.000013386135,0.000002342065,0.97099733,0.00003510587,0.0058811544,0.0073645455],"study_design_scores_gemma":[0.0015403577,0.0014166448,0.08759956,0.000010538172,0.000043345142,0.0001021758,0.000027556684,0.00013915166,0.33706903,0.00028548206,0.57121277,0.00055339123],"about_ca_topic_score_codex":0.000010322653,"about_ca_topic_score_gemma":0.000007665742,"teacher_disagreement_score":0.6339283,"about_ca_system_score_codex":0.0000046383116,"about_ca_system_score_gemma":0.000018366924,"threshold_uncertainty_score":0.4350638},"labels":[],"label_agreement":null},{"id":"W2785962058","doi":"10.1159/000484532","title":"A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing","year":2018,"lang":"en","type":"review","venue":"Molecular Syndromology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"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; University of British Columbia","funders":"","keywords":"Medicine; Massive parallel sequencing; Mendelian inheritance; Phenotype; DNA sequencing; Bioinformatics; Biology; Genetics; Gene","score_opus":0.052388509760893036,"score_gpt":0.35853683278497234,"score_spread":0.3061483230240793,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2785962058","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.010996308,0.98658663,0.0005559862,0.00005662173,0.00027752717,0.001132086,0.000036810245,0.000005913046,0.00035210027],"genre_scores_gemma":[0.0026600263,0.99239784,0.003853476,0.0004527229,0.000085033935,0.00014141104,0.00028025114,0.00008004308,0.00004916782],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.993737,0.0020870774,0.002381366,0.00090671325,0.0003441077,0.00054374966],"domain_scores_gemma":[0.9966635,0.00012752014,0.0014704224,0.0014708121,0.00018217364,0.00008556463],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0020618865,0.0005889266,0.0029180741,0.00013944655,0.000037116297,0.000010433993,0.0013153647,0.00082811364,0.0000533467],"category_scores_gemma":[0.00075737276,0.00043414166,0.0014372558,0.0004522656,0.0004727516,0.000003320182,0.00048248906,0.0005677299,0.00001971424],"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":[0.00007948421,0.0012930947,0.0007341993,0.43318823,0.0061053056,0.0065949983,0.00024287579,0.000020711064,0.0017953714,0.002976952,0.0066446126,0.54032415],"study_design_scores_gemma":[0.0016121565,0.0036377453,0.00032315953,0.11244431,0.0024061848,0.042199638,0.000042128,0.0000123441305,0.00015974243,0.00041761075,0.8351951,0.0015498837],"about_ca_topic_score_codex":0.00006598212,"about_ca_topic_score_gemma":0.0000076201195,"teacher_disagreement_score":0.82855046,"about_ca_system_score_codex":0.00003350989,"about_ca_system_score_gemma":0.0007300768,"threshold_uncertainty_score":0.99981105},"labels":[],"label_agreement":null},{"id":"W2789571584","doi":"10.4274/jcrpe.0029","title":"Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life","year":2018,"lang":"en","type":"article","venue":"Journal of Clinical Research in Pediatric Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Hospital for Sick Children","keywords":"Medicine; Hypotonia; Pediatrics; Polyhydramnios; Confounding; Retrospective cohort study; Obstetrics; Pregnancy; Fetus; Internal medicine","score_opus":0.10396025017628574,"score_gpt":0.4276925213637875,"score_spread":0.32373227118750175,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2789571584","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9832528,0.004902785,0.000033420267,0.010709589,0.00059327105,0.0004125861,0.000009747544,0.0000010464646,0.000084753156],"genre_scores_gemma":[0.9935815,0.0045141554,0.00015985114,0.00017555358,0.0014575975,0.000034244487,3.1658575e-7,0.000016031308,0.000060779465],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9967581,0.00083210185,0.0012316701,0.0002311363,0.00040886857,0.0005381358],"domain_scores_gemma":[0.99412304,0.003868541,0.0007944653,0.00060750503,0.00053661707,0.00006982754],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.003772316,0.00012615435,0.00036274368,0.000107393615,0.0003485876,0.0000237896,0.0013145305,0.00015856954,0.000014179766],"category_scores_gemma":[0.011781321,0.000054697357,0.00039860912,0.0003755445,0.0010775897,0.000006559188,0.00081605295,0.00095579616,0.0000010153262],"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":[0.00017112,0.00030698776,0.9772317,0.00022536963,0.0002790135,0.000115039235,0.0002800567,0.00009807798,0.00019778701,0.00021526772,0.0063514537,0.014528147],"study_design_scores_gemma":[0.0013910166,0.001904854,0.97289175,0.00004206314,0.0000682749,0.005106477,0.00083554885,0.00002437783,0.0010824472,0.0004044721,0.01616398,0.00008474656],"about_ca_topic_score_codex":0.000059678383,"about_ca_topic_score_gemma":0.00024113982,"teacher_disagreement_score":0.0144434,"about_ca_system_score_codex":0.000013835463,"about_ca_system_score_gemma":0.0003607541,"threshold_uncertainty_score":0.9965429},"labels":[],"label_agreement":null},{"id":"W2790406623","doi":"10.1242/jeb.164517","title":"Genomic imprinting, growth and maternal–fetal interactions","year":2018,"lang":"en","type":"review","venue":"Journal of Experimental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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; Medical Research Council Canada; Society for Endocrinology","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Insulin-like growth factor 2 receptor; Genetics; Gene; Placenta; Fetus; Growth factor; Pregnancy; Insulin-like growth factor 1 receptor; Receptor; DNA methylation; Gene expression","score_opus":0.022620177964341927,"score_gpt":0.33288154678861287,"score_spread":0.31026136882427097,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790406623","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.09559514,0.90297616,0.000054815988,0.000010730878,0.000927787,0.00011301508,0.0000097631655,0.0000025323454,0.00031004247],"genre_scores_gemma":[0.057935074,0.9395575,0.0013176261,0.000037335707,0.0010082534,0.0000069717735,0.000020966609,0.00003679491,0.000079483994],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9985843,0.00012439137,0.0007028898,0.0002857859,0.0000546331,0.0002480224],"domain_scores_gemma":[0.99881494,0.000017525683,0.00080788584,0.0001788535,0.00006327319,0.000117519936],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016648446,0.00028384157,0.0007226669,0.0001333899,0.00006732858,0.00003539047,0.00030280958,0.00024370171,0.000062000545],"category_scores_gemma":[0.00004803786,0.00021768444,0.00039331065,0.00003959133,0.00016227034,0.0000042133133,0.00040445567,0.00020429258,0.000016175994],"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":[0.000017638782,0.0001462094,0.0011716421,0.00077723165,0.001057523,0.000013929328,0.000074428484,2.9016713e-8,0.78565097,0.00006294526,0.0005907631,0.21043672],"study_design_scores_gemma":[0.00030153268,0.0010404468,0.00006431685,0.00059430633,0.00013996898,0.005281926,0.000075807584,6.342776e-7,0.029505223,0.000012286826,0.9627071,0.0002764206],"about_ca_topic_score_codex":0.000005976623,"about_ca_topic_score_gemma":7.83628e-7,"teacher_disagreement_score":0.96211636,"about_ca_system_score_codex":0.000028241311,"about_ca_system_score_gemma":0.00009476032,"threshold_uncertainty_score":0.8876914},"labels":[],"label_agreement":null},{"id":"W2790585426","doi":"10.1007/978-1-4939-7710-9_14","title":"A Protocol for Epigenetic Imprinting Analysis with RNA-Seq Data","year":2018,"lang":"en","type":"article","venue":"Methods in molecular biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Saskatchewan Research Council (Canada); National Research Council Canada","funders":"","keywords":"Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Arabidopsis; Genetics; Gene; Computational biology; Transcriptome; DNA methylation; Gene expression","score_opus":0.059478134429637106,"score_gpt":0.4539570101624232,"score_spread":0.39447887573278606,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790585426","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.027465746,0.000042490934,0.9523415,0.00006886257,0.000060573428,0.01945726,0.000015300315,0.000013254961,0.000535012],"genre_scores_gemma":[0.018602163,0.0000025461245,0.9521511,0.00023184127,0.00016545136,0.028588895,0.000119323515,0.00004313184,0.00009550593],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99740714,0.0004990632,0.00043405293,0.0010342919,0.00007430351,0.00055113435],"domain_scores_gemma":[0.9980673,0.0000580137,0.00019449557,0.0014471309,0.00015188757,0.000081182014],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016503171,0.00025827994,0.00039191364,0.0002068786,0.00008422984,0.000029048595,0.0007829217,0.000246537,0.000036774712],"category_scores_gemma":[0.000559056,0.00021598031,0.00012809651,0.0005327618,0.00023976143,0.0000028767895,0.0006677042,0.00010796006,0.0000026536559],"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":[0.000055413228,0.00004872564,0.014097147,0.000029026065,0.00036385338,0.0000016533417,0.000021636784,0.0000693853,0.9446118,0.00011489845,0.00002005269,0.040566433],"study_design_scores_gemma":[0.0021329317,0.0017974704,0.0063528516,0.000024486455,0.0002491202,0.00003126652,0.000060309194,0.005770297,0.9364708,0.0010231265,0.045503862,0.0005834871],"about_ca_topic_score_codex":0.0000631808,"about_ca_topic_score_gemma":0.0001132814,"teacher_disagreement_score":0.045483813,"about_ca_system_score_codex":0.000012199017,"about_ca_system_score_gemma":0.00009846793,"threshold_uncertainty_score":0.88074213},"labels":[],"label_agreement":null},{"id":"W2790668598","doi":"10.1016/j.jpeds.2017.12.083","title":"Pseudopseudohypoparathyroidism: A Diagnostic Consideration in a Patient with Brachydactyly","year":2018,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Montreal Children's Hospital","funders":"","keywords":"Medicine; GNAS complex locus; Brachydactyly; Pseudohypoparathyroidism; Parathyroid hormone; Physical examination; Short stature; Pediatrics; Anatomy; Surgery; Internal medicine","score_opus":0.006819442429877253,"score_gpt":0.22325190541952158,"score_spread":0.21643246298964433,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790668598","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963949,0.0012868966,0.0017378621,0.00018997086,0.00012915437,0.00008713492,0.0000010661912,0.0000012208724,0.00017183827],"genre_scores_gemma":[0.99772346,0.0004865883,0.0010420587,0.00018139853,0.0005346613,0.0000011608557,0.0000010205506,0.000009875098,0.000019768413],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992671,0.00008300747,0.0002756204,0.00007487805,0.00015594657,0.00014342934],"domain_scores_gemma":[0.9992767,0.000093420786,0.00025172046,0.00014174255,0.00018999155,0.000046437686],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034930938,0.00008250042,0.00009948643,0.00005472133,0.000055833774,0.000019732322,0.00011922377,0.000046125682,0.0000053447147],"category_scores_gemma":[0.00044506826,0.000050825678,0.000030087496,0.00012875446,0.000058675378,0.0000047331055,0.000044890923,0.00010436847,0.000004882608],"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":[0.00091898633,0.0009010802,0.48961344,0.0001094567,0.00010320388,0.00028227537,0.0078027393,0.0058451933,0.44148064,0.00014726282,0.03372995,0.019065777],"study_design_scores_gemma":[0.009682591,0.03535487,0.6930747,0.00014250209,0.000850341,0.025622506,0.005775274,0.0005175124,0.21717341,0.0014074683,0.00881617,0.00158264],"about_ca_topic_score_codex":0.000012147565,"about_ca_topic_score_gemma":0.000044402426,"teacher_disagreement_score":0.22430722,"about_ca_system_score_codex":0.000010179276,"about_ca_system_score_gemma":0.000119694065,"threshold_uncertainty_score":0.2072611},"labels":[],"label_agreement":null},{"id":"W2790744144","doi":"10.3945/an.117.016253","title":"Energy Metabolism Profile in Individuals with Prader-Willi Syndrome and Implications for Clinical Management: A Systematic Review","year":2017,"lang":"en","type":"review","venue":"Advances in Nutrition","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":55,"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":"Body mass index; Thermogenesis; Resting energy expenditure; Endocrinology; Lean body mass; Energy expenditure; Medicine; Weight management; Internal medicine; Weight loss; Obesity; Weight gain; Body weight","score_opus":0.04971778163201943,"score_gpt":0.39853241773752535,"score_spread":0.3488146361055059,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790744144","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000017036298,0.9952648,0.00043042688,0.000046541598,0.00006324291,0.0039606574,0.0000867598,0.0000052947366,0.00012521542],"genre_scores_gemma":[0.00008521225,0.98741025,0.0043662405,0.000068209505,0.000050400584,0.0073506883,0.0005488224,0.00003444969,0.000085739],"study_design_codex":"systematic_review","study_design_gemma":"not_applicable","domain_scores_codex":[0.9980158,0.00018240027,0.0009117461,0.0005751211,0.000080522375,0.00023439244],"domain_scores_gemma":[0.9985697,0.00006485095,0.0006906263,0.0005872351,0.000040650648,0.000046881272],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055776304,0.00026871936,0.0014747982,0.00012250862,0.00006102254,0.00003433138,0.00029673812,0.00020540184,0.0000010855184],"category_scores_gemma":[0.00011543313,0.00021424158,0.00017216634,0.00012511248,0.00006805615,0.000016338785,0.00011484632,0.00010335912,0.0000010089144],"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":[3.0291736e-7,0.00010683539,0.000145589,0.7726304,0.00010273317,7.048804e-7,0.0000014218974,8.1495486e-8,2.2208117e-7,0.0002980135,0.00006550214,0.22664818],"study_design_scores_gemma":[0.00049973244,0.00010564741,0.00039444506,0.3152272,0.0006198267,0.00017320423,0.0000063030006,6.227236e-7,3.3119298e-7,0.00023702951,0.6825074,0.00022826955],"about_ca_topic_score_codex":0.0000017252516,"about_ca_topic_score_gemma":0.000011923259,"teacher_disagreement_score":0.6824419,"about_ca_system_score_codex":0.000014676978,"about_ca_system_score_gemma":0.000036281017,"threshold_uncertainty_score":0.8736518},"labels":[],"label_agreement":null},{"id":"W2792735683","doi":"10.1097/bpo.0000000000001123","title":"Growth Friendly Surgery and Serial Cast Correction in the Treatment of Early-onset Scoliosis for Patients With Prader-Willi Syndrome","year":2018,"lang":"en","type":"article","venue":"Journal of Pediatric Orthopaedics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Izaak Walton Killam Health Centre; Dalhousie University","funders":"","keywords":"Medicine; Scoliosis; Kyphosis; Body mass index; Surgery; Nuclear medicine; Internal medicine; Radiography","score_opus":0.008634636247402688,"score_gpt":0.22499391837269508,"score_spread":0.2163592821252924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2792735683","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998499,0.00034839078,0.00022677143,0.000036250738,0.00065989344,0.00020787034,0.000014189863,9.853508e-7,0.0000066984044],"genre_scores_gemma":[0.9977342,0.0010214053,0.0004143189,0.000015503754,0.0007794347,0.000006509208,0.0000068170125,0.00001222941,0.000009570695],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99911684,0.000054956407,0.00036421698,0.00012526156,0.00017763312,0.00016110708],"domain_scores_gemma":[0.99912363,0.0000633272,0.00040328922,0.000101117395,0.00025512875,0.000053499964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002600062,0.00011160293,0.00020598983,0.00012515429,0.000056475274,0.000017986633,0.00006885809,0.000079398764,0.0000021744063],"category_scores_gemma":[0.00013329549,0.00007139889,0.00010310273,0.0001770105,0.000055866327,0.000008471664,0.000014019198,0.000047129906,1.9587453e-7],"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":[0.00004506061,0.00023280655,0.99742204,0.000022784963,0.000039071445,0.0000015096515,0.00019139747,0.0000026145078,0.00003685487,2.4953738e-7,0.0003558345,0.0016497509],"study_design_scores_gemma":[0.0013242585,0.009845804,0.98744285,0.000017585573,0.0001367338,0.0002217895,0.00013347509,0.0000058088226,0.00024265057,0.000004952351,0.00053482264,0.000089287976],"about_ca_topic_score_codex":0.000021310283,"about_ca_topic_score_gemma":0.00002395906,"teacher_disagreement_score":0.009979235,"about_ca_system_score_codex":0.000013441843,"about_ca_system_score_gemma":0.000119664495,"threshold_uncertainty_score":0.29115623},"labels":[],"label_agreement":null},{"id":"W2793616120","doi":"10.1016/j.ymgme.2018.02.018","title":"Chronic diazoxide treatment decreases fat mass and improves endurance capacity in an obese mouse model of Prader-Willi syndrome","year":2018,"lang":"en","type":"article","venue":"Molecular Genetics and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"University of Alberta; Foundation for Prader-Willi Research","keywords":"Diazoxide; Endocrinology; Internal medicine; Medicine; Fat mass; Obesity; Metabolic syndrome; Insulin","score_opus":0.018840384411991713,"score_gpt":0.2380819341873577,"score_spread":0.219241549775366,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2793616120","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9820939,0.014244861,0.0031589894,0.000033861746,0.0000611931,0.00032147506,0.000039926876,0.000007527082,0.000038289734],"genre_scores_gemma":[0.9858672,0.00419434,0.009601058,0.00006917313,0.000088634966,0.000037487534,0.000020587606,0.000041440024,0.00008009602],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99850065,0.00007557729,0.00032341172,0.0005721084,0.00014049452,0.00038778444],"domain_scores_gemma":[0.9990929,0.000006215528,0.00011544476,0.0004966851,0.000086371976,0.00020242597],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0001086191,0.00029506756,0.0003569464,0.000085489686,0.00006519611,0.000037872353,0.0001534074,0.00017047995,0.0000031277714],"category_scores_gemma":[0.000030025902,0.00027386867,0.00007486288,0.000080180886,0.00026249047,0.000008433876,0.00012372433,0.00006365831,6.3356083e-7],"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":[0.0000032764688,0.00006991298,0.0036489062,0.000031952648,0.00005252438,0.000001402222,0.00012956206,0.0002976746,0.98746616,0.00008879875,0.0000012481617,0.008208566],"study_design_scores_gemma":[0.001283924,0.00073901087,0.069966234,0.000021025542,0.00008059779,0.000039414077,0.00006011937,0.0066263117,0.9197052,0.00037997338,0.0007500812,0.00034811013],"about_ca_topic_score_codex":0.0001296258,"about_ca_topic_score_gemma":0.00014089436,"teacher_disagreement_score":0.06776098,"about_ca_system_score_codex":0.00001538442,"about_ca_system_score_gemma":0.0000742499,"threshold_uncertainty_score":0.99997133},"labels":[],"label_agreement":null},{"id":"W2797591163","doi":"10.1681/asn.2018030288","title":"Using Large Datasets to Understand CKD","year":2018,"lang":"en","type":"letter","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Children’s Health Research Institute; Western University","funders":"Canadian Institutes of Health Research","keywords":"Medicine; Computer science; Intensive care medicine","score_opus":0.03024405026960725,"score_gpt":0.299838997234843,"score_spread":0.2695949469652357,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2797591163","genre_codex":"empirical","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"commentary","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8001005,0.00043403116,0.005982088,0.19254479,0.0004951666,0.0001655181,0.00024056374,0.0000021853862,0.0000351449],"genre_scores_gemma":[0.03938374,0.00029587338,0.020344181,0.93418276,0.0054937312,6.926575e-7,0.000050414164,0.0000616011,0.00018697567],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99845964,0.00016608107,0.00047712203,0.00023781785,0.00026680564,0.0003925387],"domain_scores_gemma":[0.9977055,0.000029761539,0.0014542635,0.0005688781,0.00017979987,0.0000617744],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037444299,0.0002134722,0.000542499,0.00004065939,0.0000916949,0.000013523867,0.00080096704,0.00028826174,0.000023670149],"category_scores_gemma":[0.000048364876,0.0001580559,0.00060648716,0.00015830007,0.00051247247,0.000002593478,0.0005293752,0.00054392096,0.0000021835892],"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":[0.000016113705,0.000015411108,0.00017684577,0.000020948106,0.00034692703,0.0000027443573,0.00007993704,0.000018463832,0.17506823,2.4948466e-7,0.824105,0.00014912289],"study_design_scores_gemma":[0.00032123362,0.0008810641,0.0018810423,0.000038339535,0.00014806708,0.00054622634,0.00041817446,0.000028779465,0.0023095314,0.00003724797,0.99322087,0.00016945355],"about_ca_topic_score_codex":0.00004164341,"about_ca_topic_score_gemma":0.0000045999795,"teacher_disagreement_score":0.7607168,"about_ca_system_score_codex":0.000039381415,"about_ca_system_score_gemma":0.0002067237,"threshold_uncertainty_score":0.6445333},"labels":[],"label_agreement":null},{"id":"W2797685235","doi":"10.1016/j.jpsychires.2018.04.012","title":"The impact of body mass index in gene expression of reelin pathway mediators in individuals with schizophrenia and mood disorders: A post-mortem study","year":2018,"lang":"en","type":"article","venue":"Journal of Psychiatric Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University Health Network; McMaster University; University of Toronto","funders":"National Institute of Mental Health","keywords":"Reelin; Schizophrenia (object-oriented programming); Body mass index; Hippocampus; Internal medicine; Medicine; Mood disorders; Psychology; Oncology; Endocrinology; Bioinformatics; Psychiatry; Biology; Receptor","score_opus":0.012338122558814299,"score_gpt":0.33025873478642914,"score_spread":0.31792061222761486,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2797685235","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9983629,0.0010517015,0.000033789525,0.00006773545,0.00004117834,0.0002931996,0.000003454926,5.3566436e-7,0.00014548865],"genre_scores_gemma":[0.9983382,0.0004555216,0.0010541003,9.256165e-7,0.000110421715,0.0000046840087,6.681694e-7,0.00001806422,0.000017420978],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9981875,0.00033243923,0.0005514408,0.00017357146,0.00049218483,0.00026287796],"domain_scores_gemma":[0.9989745,0.000060253224,0.00034791304,0.00026330823,0.00026992674,0.00008408185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002229086,0.00010460258,0.0002254001,0.00043687827,0.00005112841,0.000020068397,0.00031699342,0.00008774119,0.000009072302],"category_scores_gemma":[0.00023640983,0.00005995413,0.00006275906,0.00051859114,0.00013906407,0.0000061887476,0.00013460788,0.00026207019,3.1465223e-7],"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":[0.0003196932,0.0002475722,0.8550038,0.000010901014,0.00004761388,0.0000010802972,0.0002082516,0.000018668727,0.14256784,0.0000013706785,0.00004075382,0.001532457],"study_design_scores_gemma":[0.0029510737,0.006267983,0.97462577,0.0000479025,0.0000062231725,0.000019346868,0.0018841071,0.000025319174,0.013969584,0.00012309845,0.000012193211,0.00006741345],"about_ca_topic_score_codex":0.00019735756,"about_ca_topic_score_gemma":0.00033499982,"teacher_disagreement_score":0.12859826,"about_ca_system_score_codex":0.000013515377,"about_ca_system_score_gemma":0.00032311594,"threshold_uncertainty_score":0.24448586},"labels":[],"label_agreement":null},{"id":"W2799463622","doi":"10.1111/gbb.12483","title":"Distinct chromatin structures at the monoamine oxidase‐A promoter correlate with allele‐specific expression in SH‐SY5Y cells","year":2018,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute for Health and Care Research; Medical Research Council Canada; University of Liverpool; Wellcome Trust","keywords":"Epigenetics; Allele; Biology; Monoamine oxidase A; Genetics; Promoter; DNA methylation; Transcription factor; Gene; Gene expression","score_opus":0.009971459689510477,"score_gpt":0.23516728401833578,"score_spread":0.22519582432882532,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2799463622","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99802476,0.0006689706,0.00030576106,0.00010785271,0.00018262325,0.000544719,0.000021251053,0.000016079215,0.00012798871],"genre_scores_gemma":[0.99473345,0.000048408812,0.0023544335,0.000113613736,0.00025953466,0.00010740156,0.000117063006,0.00005184185,0.0022142236],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.998438,0.00009422871,0.00029968383,0.00055515574,0.00019371648,0.00041919135],"domain_scores_gemma":[0.999041,0.000021290685,0.0001314076,0.00065897265,0.00006169611,0.000085599895],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017645904,0.00027736987,0.0001939631,0.000040434858,0.00019649637,0.00005066833,0.00032275228,0.00016596573,0.00035838704],"category_scores_gemma":[0.000018737448,0.0001808113,0.00007283329,0.0001061753,0.00022322619,0.000004695661,0.00033387498,0.00011189041,0.00004035047],"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":[0.000032712447,0.00005947914,0.01152915,0.000007684713,0.000009086202,0.000009859893,0.00022688482,0.000011793144,0.9720793,0.0000012598874,0.0018014701,0.014231347],"study_design_scores_gemma":[0.00059572526,0.00037929823,0.33501884,0.000023848947,0.000016004822,0.0000786979,0.00011192524,0.00003244948,0.64380264,0.000003825268,0.019695891,0.00024084502],"about_ca_topic_score_codex":0.000028652745,"about_ca_topic_score_gemma":0.00019274825,"teacher_disagreement_score":0.32827663,"about_ca_system_score_codex":0.000024861565,"about_ca_system_score_gemma":0.000031443582,"threshold_uncertainty_score":0.7373271},"labels":[],"label_agreement":null},{"id":"W2799899236","doi":"10.5206/uwomj.v86is1.2108","title":"Decreased level of consciousness in a toddler with overgrowth syndrome","year":2018,"lang":"en","type":"article","venue":"University of Western Ontario Medical Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Toddler; Medicine; Pediatrics; Disease; Exome; Exome sequencing; Intensive care medicine; Mutation; Bioinformatics; Psychology; Genetics; Internal medicine; Developmental psychology; Gene; Biology","score_opus":0.018023905711904882,"score_gpt":0.21929992530296719,"score_spread":0.2012760195910623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2799899236","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946804,0.000025183455,0.0046360986,0.00008420237,0.000055503304,0.000043302196,0.00000310428,0.0000012256746,0.00047097143],"genre_scores_gemma":[0.99807584,0.000021125317,0.0012763834,0.000050429408,0.000029225272,3.1625888e-8,0.0000032096689,0.0000053113413,0.00053845946],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992122,0.00003848886,0.00016375635,0.00013415048,0.00028803648,0.00016334637],"domain_scores_gemma":[0.9994337,0.000010301328,0.00013761957,0.00012458765,0.00012153318,0.00017225674],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022011093,0.00008072018,0.00018641712,0.00006713187,0.000042479165,0.0000049179544,0.0002566849,0.00011098696,0.00036072114],"category_scores_gemma":[0.0000351864,0.000073708994,0.000053577707,0.000057148955,0.00028846815,0.000005253497,0.000103632236,0.00014456523,0.000002133578],"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":[0.00017478486,0.00012185811,0.99222934,0.000014722665,0.00008410033,0.000158851,0.0006232335,0.0000035570008,0.005247416,0.000005999264,0.0000681725,0.0012679502],"study_design_scores_gemma":[0.002334391,0.0012309239,0.98961884,0.00022587084,0.000025614714,0.001922278,0.00044487684,0.000009423864,0.0020278406,0.000014893993,0.0020348907,0.00011014684],"about_ca_topic_score_codex":0.008162951,"about_ca_topic_score_gemma":0.15611103,"teacher_disagreement_score":0.14794807,"about_ca_system_score_codex":0.00003281323,"about_ca_system_score_gemma":0.0006428996,"threshold_uncertainty_score":0.99844176},"labels":[],"label_agreement":null},{"id":"W2800622687","doi":"10.1530/rep-18-0051","title":"Imprint stability and plasticity during development","year":2018,"lang":"en","type":"review","venue":"Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Terry Fox Research Institute","funders":"Biotechnology and Biological Sciences Research Council; Economic and Social Research Council; Medical Research Council","keywords":"Genomic imprinting; Imprinting (psychology); Biology; DNA methylation; Genome; Locus (genetics); Evolutionary biology; Genetics; Computational biology; Gene; Gene expression","score_opus":0.03589163940571044,"score_gpt":0.2837698675764381,"score_spread":0.24787822817072763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2800622687","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.18389447,0.81533086,0.00009958799,0.000003718132,0.00028635087,0.00029819747,0.0000021445253,0.000014027815,0.00007066553],"genre_scores_gemma":[0.0042576203,0.9933163,0.001257526,0.0000013817036,0.0007477026,0.00004029439,0.000039596358,0.00003013833,0.00030947253],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99836785,0.000059678587,0.0003595184,0.0009284805,0.00008859953,0.0001958574],"domain_scores_gemma":[0.99923205,0.000004315379,0.00017716523,0.00046431518,0.000063918524,0.000058202382],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030830406,0.00022456406,0.00037560763,0.00003937032,0.00011788869,0.000025248311,0.00008849737,0.00019331332,0.000018076245],"category_scores_gemma":[0.00020132899,0.00019898333,0.000092586655,0.000062183724,0.00006138638,0.000001743952,0.0002830307,0.00010255616,0.000018253517],"study_design_candidate":"design_other","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":[0.0000032662508,0.00003548504,0.00016429524,0.0072787046,0.00011598503,4.1152526e-7,0.000033275486,3.381583e-7,0.0042621624,0.0000018997163,0.000032885608,0.98807126],"study_design_scores_gemma":[0.00006783153,0.00005185395,0.00206697,0.00057383836,0.00007199743,0.00022374891,0.000010315908,4.33677e-7,0.017451556,0.0000020493105,0.97922486,0.00025454123],"about_ca_topic_score_codex":0.0000039783213,"about_ca_topic_score_gemma":0.0000032050527,"teacher_disagreement_score":0.98781675,"about_ca_system_score_codex":0.00004006529,"about_ca_system_score_gemma":0.00013869029,"threshold_uncertainty_score":0.81143045},"labels":[],"label_agreement":null},{"id":"W2804089987","doi":"10.1016/j.yhbeh.2018.05.011","title":"Wnt-2b in the intermediate hyperpallium apicale of the telencephalon is critical for the thyroid hormone-mediated opening of the sensitive period for filial imprinting in domestic chicks (Gallus gallus domesticus)","year":2018,"lang":"en","type":"article","venue":"Hormones and Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"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":"Institute of Musculoskeletal Health and Arthritis; Japan Society for the Promotion of Science; Foundation for Promotion of Cancer Research; Ministry of Education, Culture, Sports, Science and Technology; National Cancer Institute; Japan Foundation of Applied Enzymology; Uehara Memorial Foundation; Naito Foundation","keywords":"Imprinting (psychology); Cerebrum; Wnt signaling pathway; Period (music); Hatching; Internal medicine; Triiodothyronine; Endocrinology; Hormone; Biology; Chemistry; Cell biology; Central nervous system; Animal science; Gene; Biochemistry; Medicine; Signal transduction","score_opus":0.012110408448500833,"score_gpt":0.2824105187629376,"score_spread":0.2703001103144368,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2804089987","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99693096,0.0006445238,0.00034162725,0.00066076306,0.00021887626,0.0011157646,0.000060835613,0.000002742771,0.000023924704],"genre_scores_gemma":[0.99897295,0.00011379565,0.00033334768,0.00016218484,0.00016833136,0.00019329823,0.0000068616177,0.000020069752,0.00002917837],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99858326,0.00009888611,0.00044218966,0.0003269243,0.0001823601,0.0003663599],"domain_scores_gemma":[0.99896806,0.000289754,0.00015922604,0.00038227654,0.00016329033,0.00003738528],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055782654,0.00019490482,0.00025404684,0.000031427153,0.00021715071,0.000041882606,0.00048480043,0.00015122177,0.0000035880855],"category_scores_gemma":[0.0006954261,0.00009638255,0.0001746717,0.00015790005,0.00065332046,0.000007979106,0.00035012877,0.0001770161,3.99973e-7],"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":[0.0001447272,0.00018168389,0.025969906,0.00006351775,0.00002688876,0.000002476237,0.0025670922,0.0000058767837,0.96315086,0.00006094937,0.00006166378,0.007764336],"study_design_scores_gemma":[0.0014200984,0.0008340487,0.93944144,0.000079913116,0.00016683724,0.00011289457,0.003611854,0.0010594882,0.05288283,0.00005445834,0.00014560501,0.00019054294],"about_ca_topic_score_codex":0.00012392539,"about_ca_topic_score_gemma":0.000118293014,"teacher_disagreement_score":0.9134715,"about_ca_system_score_codex":0.000010418133,"about_ca_system_score_gemma":0.00007194393,"threshold_uncertainty_score":0.39303663},"labels":[],"label_agreement":null},{"id":"W2808484533","doi":"10.1186/s12864-018-4835-2","title":"Development and application of an integrated allele-specific pipeline for methylomic and epigenomic analysis (MEA)","year":2018,"lang":"en","type":"article","venue":"BMC Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"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's Michael Smith Genome Sciences Centre; Simon Fraser University; University of British Columbia","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Killam Trusts; U.S. Department of Veterans Affairs","keywords":"Epigenomics; Biology; Indel; Allele; Genetics; Computational biology; DNA methylation; Epigenome; Gene; Gene expression; Single-nucleotide polymorphism; Genotype","score_opus":0.01811735396814028,"score_gpt":0.25624073942530323,"score_spread":0.23812338545716294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2808484533","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7336602,0.000470509,0.26564422,0.0000050487306,0.000018745344,0.00017515305,0.000013947449,0.000003424577,0.000008728289],"genre_scores_gemma":[0.80941343,0.00014468998,0.19004925,0.000020060928,0.000076759316,0.000017936141,0.00023954337,0.000013887171,0.000024444022],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99921083,0.000020035812,0.0002589838,0.0003290413,0.000040774103,0.0001403311],"domain_scores_gemma":[0.9994838,0.000008693758,0.00011445026,0.0002363304,0.00009555086,0.00006117515],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024562253,0.0001118862,0.00017314577,0.000072675786,0.000061717925,0.000018789231,0.00011194125,0.00008571952,0.0000024702124],"category_scores_gemma":[0.000014143835,0.00011090292,0.00004396341,0.00007804521,0.00007599058,0.0000019475858,0.00008408998,0.000021404863,9.914415e-7],"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":[0.0000443955,0.000026081114,0.0024638737,0.000016040924,0.00013443168,3.2381177e-8,0.00028405298,0.00009771138,0.8275405,0.000022845934,0.000017187866,0.1693528],"study_design_scores_gemma":[0.0010956893,0.0002754616,0.0440014,0.0000035019561,0.00019491896,0.000009719596,0.00070308935,0.021172369,0.7953445,0.00009821053,0.13673674,0.0003644057],"about_ca_topic_score_codex":0.000026740896,"about_ca_topic_score_gemma":0.00034603948,"teacher_disagreement_score":0.16898839,"about_ca_system_score_codex":0.000014132139,"about_ca_system_score_gemma":0.000055619523,"threshold_uncertainty_score":0.452249},"labels":[],"label_agreement":null},{"id":"W2809162318","doi":"10.1016/j.rehab.2018.06.001","title":"Test-retest reliability of the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition for youth with Prader-Willi syndrome","year":2018,"lang":"en","type":"letter","venue":"Annals of Physical and Rehabilitation Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"St. Francis Xavier University","funders":"","keywords":"Test (biology); Psychology; Reliability (semiconductor); Developmental psychology; Audiology; Physical medicine and rehabilitation; Medicine; Physics","score_opus":0.01625771701906824,"score_gpt":0.26988096203585055,"score_spread":0.2536232450167823,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2809162318","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93908834,0.00012819207,0.000057933536,0.05917901,0.000113740396,0.000904721,0.00043937928,0.0000039827496,0.00008470254],"genre_scores_gemma":[0.99420834,0.000017848217,0.0004996993,0.003818061,0.00092633575,0.00004589556,0.0001955999,0.000025932572,0.0002622814],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9983972,0.00007576689,0.0005387059,0.0004391841,0.00033934915,0.00020983156],"domain_scores_gemma":[0.9971327,0.0008625791,0.0006333528,0.00049080345,0.0008347391,0.000045823923],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039859238,0.00023216351,0.00054028054,0.00005406251,0.00005338672,0.0000033154047,0.00021211708,0.0002668776,0.000011589265],"category_scores_gemma":[0.0025293492,0.00013278278,0.000183163,0.00014748887,0.0015689872,0.000006876285,0.00007144243,0.00020285352,2.3834447e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006517328,0.0015890757,0.08101098,0.015729915,0.00032424444,5.0031997e-7,0.0070980354,0.000019524326,0.6890919,0.000055825883,0.20313008,0.0018847416],"study_design_scores_gemma":[0.0027762237,0.08393845,0.78833514,0.0036189188,0.00051499106,0.00003336015,0.0018132757,0.0002548391,0.0859108,0.0027728837,0.029262787,0.000768352],"about_ca_topic_score_codex":0.000027288235,"about_ca_topic_score_gemma":0.0000026770822,"teacher_disagreement_score":0.70732415,"about_ca_system_score_codex":0.0000039117276,"about_ca_system_score_gemma":0.00008964089,"threshold_uncertainty_score":0.57809985},"labels":[],"label_agreement":null},{"id":"W2810557264","doi":"10.3390/languages3030023","title":"The Narrative Abilities of an English-Spanish Bilingual with Prader-Willi Syndrome","year":2018,"lang":"en","type":"article","venue":"Languages","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Wilfrid Laurier University; University of Ottawa","funders":"Universidad El Bosque","keywords":"Narrative; Linguistics; Psychology; History; Philosophy","score_opus":0.005002492442178484,"score_gpt":0.24713342296892962,"score_spread":0.24213093052675114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2810557264","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99770945,0.00056752533,0.000039321792,0.00004871893,0.00010152801,0.00012159378,0.0000075202656,0.000013723973,0.0013906193],"genre_scores_gemma":[0.9975846,0.000022870627,0.0013253278,0.000046732584,0.00024250944,0.000008086618,0.000014952738,0.000017166187,0.00073775713],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99927527,0.000060266193,0.0001374556,0.00021884574,0.00011111766,0.00019703347],"domain_scores_gemma":[0.99931026,0.000025426283,0.00007709449,0.00037750503,0.00016705068,0.00004268882],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016872969,0.00010903391,0.00010975296,0.00001400775,0.00013589559,0.00002975279,0.00019110933,0.000055957677,0.000028092652],"category_scores_gemma":[0.00013505184,0.00006747638,0.00003491055,0.000057760702,0.00034253896,0.0000040586856,0.00006797456,0.000050351922,0.0000017565108],"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":[0.00005924882,0.0004579064,0.1028343,0.00021429583,0.00084701605,0.00001508567,0.13538511,0.00010465546,0.7236099,0.0012552559,0.000857111,0.034360062],"study_design_scores_gemma":[0.0012959635,0.009123984,0.25698626,0.00009310607,0.000063773026,0.0004301882,0.24286501,0.00008338145,0.46626967,0.00014039534,0.02195234,0.0006959257],"about_ca_topic_score_codex":0.000056047294,"about_ca_topic_score_gemma":0.00026946943,"teacher_disagreement_score":0.25734028,"about_ca_system_score_codex":0.000003646087,"about_ca_system_score_gemma":0.000061580104,"threshold_uncertainty_score":0.27516067},"labels":[],"label_agreement":null},{"id":"W284515077","doi":"10.1016/b978-0-444-52014-2.00012-4","title":"Benign hereditary chorea","year":2011,"lang":"en","type":"review","venue":"Handbook of clinical neurology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"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; University of Toronto","funders":"","keywords":"Haploinsufficiency; Chorea; Phenotype; Pathology; Neuroscience; Medicine; Psychology; Biology; Genetics; Gene","score_opus":0.11223752989189935,"score_gpt":0.39036854470936766,"score_spread":0.2781310148174683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W284515077","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00059558667,0.99539244,0.00013712498,0.00001367391,0.001304645,0.0003587384,0.000027227714,0.000011451964,0.0021590942],"genre_scores_gemma":[0.0000888845,0.99732935,0.0006181717,0.00031731717,0.0010613245,0.000031212203,0.00012252433,0.00007454119,0.00035665213],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9964149,0.00052175083,0.001744974,0.0008367212,0.00010257466,0.00037907876],"domain_scores_gemma":[0.9978398,0.00019120143,0.0008009102,0.0009205183,0.00007565468,0.00017192497],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.0005736457,0.000393815,0.0020719094,0.00006879578,0.0000323934,0.000005332018,0.0006263049,0.0013120392,0.00015963738],"category_scores_gemma":[0.0005032429,0.00032692688,0.0012028632,0.00006397681,0.00033230416,0.0000012929611,0.0004714358,0.00055067317,0.00008065677],"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":[0.000025385818,0.00011795661,0.00023002944,0.0012291617,0.00023992632,0.00001549045,0.000002779124,2.2290867e-7,0.000015072628,0.000024079287,0.002867695,0.9952322],"study_design_scores_gemma":[0.0003365505,0.0016887975,0.00021014438,0.00069392874,0.00031559012,0.0002692468,5.626474e-7,9.539117e-7,0.000034533125,0.000057737092,0.9961324,0.0002595906],"about_ca_topic_score_codex":0.00001185514,"about_ca_topic_score_gemma":0.0000063894186,"teacher_disagreement_score":0.9949726,"about_ca_system_score_codex":0.0000013153276,"about_ca_system_score_gemma":0.0002566626,"threshold_uncertainty_score":0.99998444},"labels":[],"label_agreement":null},{"id":"W2855880246","doi":"10.1038/s41467-018-05208-2","title":"Nucleoporin 107, 62 and 153 mediate Kcnq1ot1 imprinted domain regulation in extraembryonic endoderm stem cells","year":2018,"lang":"en","type":"article","venue":"Nature Communications","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"Canadian Institutes of Health Research; Lawson Health Research Institute; Magee-Womens Research Institute; Children's Health Research Institute; Natural Sciences and Engineering Research Council of Canada; University of Pittsburgh","keywords":"Genomic imprinting; Nucleoporin; Biology; Epigenetics; Endoderm; Cell biology; Genetics; Cellular differentiation; DNA methylation; Transcription factor; Gene; Gene expression; Nuclear protein","score_opus":0.01128368231826908,"score_gpt":0.2644159377348545,"score_spread":0.2531322554165854,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2855880246","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99233973,0.0037253,0.00026410754,0.00059877883,0.00016991582,0.00023825512,0.000009162607,0.0000160928,0.0026386809],"genre_scores_gemma":[0.9931231,0.0010400169,0.005141523,0.00016285216,0.000093072355,0.00002257088,0.000054434393,0.000022197837,0.0003402446],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990164,0.00012439552,0.00026136969,0.00028515424,0.00009306831,0.00021962382],"domain_scores_gemma":[0.9984259,0.000044105866,0.000106670224,0.0012495656,0.000105105646,0.00006862793],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027291413,0.00013735071,0.00013001577,0.00007545048,0.00015452006,0.00003162448,0.0005142753,0.00032271483,0.000024392499],"category_scores_gemma":[0.00004111677,0.00014041005,0.000044899924,0.00017015249,0.00018815136,0.0000063858383,0.0005030105,0.0003220576,0.000015407057],"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":[0.000009506044,0.00007122417,0.009385353,0.0000121414405,0.00002935861,3.414822e-7,0.0002642551,0.0000031817153,0.9809065,0.0016301941,0.0003845754,0.0073033795],"study_design_scores_gemma":[0.0018453503,0.0003146526,0.42274314,0.00009014534,0.000038467493,0.00008016697,0.0005878199,0.001649065,0.3685169,0.0009226358,0.20256394,0.0006477266],"about_ca_topic_score_codex":0.000019742594,"about_ca_topic_score_gemma":0.000688534,"teacher_disagreement_score":0.6123896,"about_ca_system_score_codex":0.00002147321,"about_ca_system_score_gemma":0.000046558413,"threshold_uncertainty_score":0.57257557},"labels":[],"label_agreement":null},{"id":"W2883447942","doi":"10.1136/jmedgenet-2018-105328","title":"Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay","year":2018,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Uniparental disomy; Genetics; Biology; Genomic imprinting; Exome sequencing; Imprinting (psychology); Karyotype; SNP array; Chromosome; DNA methylation; Phenotype; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.01000815464124764,"score_gpt":0.248395496992991,"score_spread":0.23838734235174336,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883447942","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99648356,0.002615811,0.0005402847,0.00012844204,0.00012480584,0.000071764836,0.0000040266414,9.154749e-7,0.000030412912],"genre_scores_gemma":[0.99516356,0.0010067773,0.0035471471,0.0000518695,0.000193806,0.0000010011048,0.0000031831535,0.000014219488,0.000018457144],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985355,0.00005772004,0.0005401322,0.00015003257,0.000517144,0.00019944672],"domain_scores_gemma":[0.99923795,0.000019375153,0.00030229831,0.0001127296,0.000119975586,0.00020768071],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003612664,0.00013384376,0.00027701852,0.00008966713,0.000024444285,0.000008953565,0.00026618977,0.00015779122,0.000036541293],"category_scores_gemma":[0.0001341915,0.00009904055,0.00005905451,0.00010955197,0.00031215427,0.0000035877365,0.0001624771,0.00017172874,4.1594004e-7],"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":[0.000169341,0.00041581524,0.8327725,0.00015681636,0.00025855287,0.0000771786,0.00086416106,0.00006479823,0.1448156,0.0000135390455,0.00024777217,0.020143906],"study_design_scores_gemma":[0.0036625273,0.0052256426,0.8394528,0.0006401164,0.00007142022,0.0051438934,0.0009598035,0.00023375473,0.14305127,0.00006684105,0.0012206321,0.00027129622],"about_ca_topic_score_codex":0.000029458315,"about_ca_topic_score_gemma":0.000084894586,"teacher_disagreement_score":0.01987261,"about_ca_system_score_codex":0.000019515312,"about_ca_system_score_gemma":0.00038404722,"threshold_uncertainty_score":0.40387565},"labels":[],"label_agreement":null},{"id":"W2884634246","doi":"10.1016/j.cobeha.2018.05.008","title":"Autism, psychosis, and genomic imprinting: recent discoveries and conundrums","year":2018,"lang":"en","type":"article","venue":"Current Opinion in Behavioral Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Genomic imprinting; Autism; Imprinting (psychology); Psychosis; Offspring; Phenotype; Schizophrenia (object-oriented programming); SNP; Psychology; Biology; Gene; Genetics; Neuroscience; Developmental psychology; DNA methylation; Psychiatry; Gene expression; Single-nucleotide polymorphism; Pregnancy","score_opus":0.06942812654723494,"score_gpt":0.3792514506696602,"score_spread":0.30982332412242525,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2884634246","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99422044,0.0035818114,0.00005803048,0.00023718,0.0016749479,0.0001216599,0.000004080916,0.0000053325502,0.00009652248],"genre_scores_gemma":[0.995076,0.0042417645,0.0005003235,0.000014719094,0.00013201682,0.000010891552,0.0000069226194,0.0000050614062,0.000012299961],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990945,0.00002559913,0.00016870789,0.00038776288,0.0000940756,0.00022934446],"domain_scores_gemma":[0.9997411,0.000003600019,0.000060316266,0.000109958426,0.000018958537,0.00006611105],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021163558,0.00010513544,0.00009103417,0.00004481671,0.00015197488,0.00009055261,0.00012888978,0.000045768196,0.000020304615],"category_scores_gemma":[0.00001243124,0.000091361755,0.00001702069,0.00010615097,0.00058118446,0.0000095576825,0.000222291,0.00005088514,0.000002255351],"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":[0.000004786416,0.00006758804,0.7962942,0.000021145108,0.0000020128496,4.673445e-8,0.00018193865,8.704256e-7,0.06288391,0.00038871248,0.00024227823,0.13991249],"study_design_scores_gemma":[0.0003342609,0.00054840546,0.91114914,0.000069641785,0.00000435893,0.000021629423,0.0002640838,0.00005452674,0.0036890486,0.00020220356,0.0834434,0.00021927406],"about_ca_topic_score_codex":0.00004910445,"about_ca_topic_score_gemma":0.000020212077,"teacher_disagreement_score":0.13969322,"about_ca_system_score_codex":0.0000062081426,"about_ca_system_score_gemma":0.000030980547,"threshold_uncertainty_score":0.37256244},"labels":[],"label_agreement":null},{"id":"W2886227808","doi":"10.1371/journal.pgen.1007587","title":"Transcription factor ASCL2 is required for development of the glycogen trophoblast cell lineage","year":2018,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Biology; Trophoblast; Gene silencing; Genetics; Genomic imprinting; Transcription factor; Cellular differentiation; Cell biology; DNA methylation; Gene expression; Gene; Placenta","score_opus":0.02991959982545794,"score_gpt":0.24483939453820877,"score_spread":0.21491979471275083,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2886227808","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99549484,0.0003336098,0.0031969575,0.000040051058,0.0002300295,0.00037688328,0.00005706674,0.000005780178,0.0002647583],"genre_scores_gemma":[0.9848262,0.000041101186,0.01401421,0.0001221045,0.00024413147,0.000023967179,0.000021412654,0.000031196032,0.00067567173],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989931,0.000022635966,0.0003170839,0.0002742226,0.0001523438,0.00024062658],"domain_scores_gemma":[0.99925935,0.000006109985,0.00012609968,0.0003776295,0.00017716996,0.000053664924],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000061784136,0.00014778589,0.00013232818,0.000020280031,0.00012108546,0.000013927061,0.0002792556,0.00012812616,0.000043195527],"category_scores_gemma":[0.000022652108,0.00011850357,0.0001232929,0.00006223665,0.00008368616,0.0000010927979,0.00009401364,0.00003733076,0.000008644088],"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":[0.000015256157,0.0000782234,0.00063241343,0.00005290621,0.000040213625,2.8503266e-8,0.00051191956,0.000004032558,0.99628276,0.0000010630514,0.0002842026,0.002096966],"study_design_scores_gemma":[0.00048224043,0.0003732893,0.0022910575,0.00001698573,0.000032037802,0.0000016957438,0.00006122803,0.0003517733,0.9538005,0.000008378694,0.04243644,0.00014440478],"about_ca_topic_score_codex":0.0000010143656,"about_ca_topic_score_gemma":0.000013652326,"teacher_disagreement_score":0.042482305,"about_ca_system_score_codex":0.000010446072,"about_ca_system_score_gemma":0.00010587046,"threshold_uncertainty_score":0.48324355},"labels":[],"label_agreement":null},{"id":"W2887748933","doi":"10.1098/rsbl.2018.0523","title":"Paranoia, autism and the architecture of genomic conflicts: a reply to Abu-Akel 2018","year":2018,"lang":"en","type":"letter","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"","keywords":"Biology; Paranoia; Autism; Architecture; Evolutionary biology; Cognitive science; Developmental psychology; Psychology; Psychiatry; Archaeology","score_opus":0.008545336770511492,"score_gpt":0.22327213291760564,"score_spread":0.21472679614709414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2887748933","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.4339873,0.0015900631,0.0012921612,0.5616816,0.0006074856,0.0005423112,0.00008184314,0.00001094966,0.00020630658],"genre_scores_gemma":[0.04696368,0.00020811247,0.0016295891,0.94771326,0.002334767,0.0000674814,0.00024371891,0.000062102845,0.00077727006],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9980273,0.0002843368,0.00041122944,0.00071325013,0.000087555076,0.00047633194],"domain_scores_gemma":[0.9987132,0.000076396645,0.00026992778,0.0008468025,0.000035780176,0.000057927326],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00037573412,0.00035578996,0.00048974616,0.000088868816,0.0000941494,0.000021064896,0.0005309093,0.0006354284,0.000026980055],"category_scores_gemma":[0.0001002584,0.00024889017,0.00018720314,0.00005071915,0.0009865706,8.093284e-7,0.00039301568,0.0004386727,0.000028276228],"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":[0.000047502726,0.000004711115,0.000436079,0.000060960923,0.00026678893,0.0000056115814,0.00020344293,0.0000031960253,0.43746328,0.000011730761,0.5604509,0.0010458068],"study_design_scores_gemma":[0.000831604,0.00025878084,0.0036084566,0.00003592048,0.000069687056,0.00015500459,0.000008604921,0.0000023225987,0.003819373,0.000068673726,0.9908314,0.00031016849],"about_ca_topic_score_codex":0.00016779479,"about_ca_topic_score_gemma":0.0000072041703,"teacher_disagreement_score":0.4336439,"about_ca_system_score_codex":0.0000104770215,"about_ca_system_score_gemma":0.00004114308,"threshold_uncertainty_score":0.9999963},"labels":[],"label_agreement":null},{"id":"W2889225402","doi":"10.1242/dmm.035832","title":"Fetal growth restriction in a genetic model of sporadic Beckwith–Wiedemann syndrome","year":2018,"lang":"en","type":"article","venue":"Disease Models & Mechanisms","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Directorate for Biological Sciences; Biotechnology and Biological Sciences Research Council; Cardiff University; Waterloo Foundation","keywords":"Beckwith–Wiedemann syndrome; Fetal growth; Fetus; Biology; Genetics; Medicine; Pregnancy; Gene; DNA methylation","score_opus":0.014868693476616793,"score_gpt":0.22317470204802578,"score_spread":0.208306008571409,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2889225402","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.79083806,0.00027884633,0.2082731,0.000033566776,0.00010107537,0.00023346377,0.000029417477,0.000013897805,0.00019854581],"genre_scores_gemma":[0.9887939,0.00018276337,0.010625364,0.000096596494,0.000058784826,0.000042410724,0.000052938653,0.000043026805,0.00010420156],"study_design_codex":"bench_or_experimental","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9984422,0.000043543634,0.00036847213,0.0005260461,0.00025707216,0.00036267994],"domain_scores_gemma":[0.9990893,0.000003481366,0.00012793986,0.00044952484,0.00012566977,0.00020410771],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015127262,0.00021969328,0.00022545845,0.00013834696,0.00006442082,0.00001621971,0.0002494109,0.00013229092,0.000014708213],"category_scores_gemma":[0.00003222163,0.00022838933,0.00013288484,0.00017733657,0.000075841956,0.000010324901,0.00015509529,0.000068044086,0.000008874552],"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":[0.00030246936,0.00078645995,0.006579614,0.00028064864,0.00016264341,0.00006896929,0.00035440442,0.066257514,0.9003019,0.022691317,0.00014488031,0.0020692348],"study_design_scores_gemma":[0.0015060202,0.0009325342,0.03381212,0.00012505645,0.00012763556,0.000054174943,0.00012219069,0.74570173,0.047647074,0.16927253,0.0000123739555,0.0006865346],"about_ca_topic_score_codex":0.00006972025,"about_ca_topic_score_gemma":0.00001706263,"teacher_disagreement_score":0.85265476,"about_ca_system_score_codex":0.00002034023,"about_ca_system_score_gemma":0.00016489322,"threshold_uncertainty_score":0.9313446},"labels":[],"label_agreement":null},{"id":"W2889619667","doi":"10.1111/ijpo.12462","title":"Changes in cardiometabolic markers in children with Prader–Willi syndrome and nonsyndromic obesity following participation in a home‐based physical activity intervention","year":2018,"lang":"en","type":"article","venue":"Pediatric Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Canadian Institutes of Health Research; U.S. Army","keywords":"Medicine; Insulin resistance; Obesity; Internal medicine; Childhood obesity; Endocrinology; Physical activity; Homeostatic model assessment; Body fat percentage; Metabolic syndrome; Body mass index; Physical therapy; Overweight","score_opus":0.007160991952919399,"score_gpt":0.25131436931593265,"score_spread":0.24415337736301326,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2889619667","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99908704,0.00018645854,0.00016544868,0.000032129803,0.00006962514,0.0004295015,0.0000060728244,0.00001012956,0.000013611001],"genre_scores_gemma":[0.9995311,0.00006476949,0.00017918195,0.000011403363,0.000119291515,0.00005003111,0.000018353148,0.000017797725,0.000008067538],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99863917,0.00017733935,0.00016888136,0.00049066526,0.00015258671,0.0003713702],"domain_scores_gemma":[0.9995607,0.000017756654,0.00009956102,0.00022822904,0.00002129183,0.00007244355],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004230566,0.0001920869,0.0003190656,0.00027669335,0.000049814316,0.000025800535,0.00011015019,0.00012165762,0.0000035463772],"category_scores_gemma":[0.000060795042,0.00019169656,0.00007333413,0.00051691046,0.000052789954,0.000016712089,0.00012136323,0.00014394522,0.0000030843848],"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":[0.00001024003,0.0005070388,0.995487,0.000034556982,0.000022442007,0.000002740639,0.000067811394,0.00003338738,0.0014942486,5.590775e-7,0.0000017239048,0.0023382588],"study_design_scores_gemma":[0.0017133997,0.00047991142,0.99544847,0.000026774824,0.00005313565,0.000022738928,0.000026605672,0.00075755414,0.0012313284,0.0000092501805,0.0000030727451,0.00022775959],"about_ca_topic_score_codex":0.00068704487,"about_ca_topic_score_gemma":0.001796604,"teacher_disagreement_score":0.0021104992,"about_ca_system_score_codex":0.000046413254,"about_ca_system_score_gemma":0.000047958543,"threshold_uncertainty_score":0.78171587},"labels":[],"label_agreement":null},{"id":"W2892128276","doi":"10.1002/ajmg.a.40491","title":"Dietary intake in youth with prader‐willi syndrome","year":2018,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Canadian Institutes of Health Research; Women and Children's Health Research Institute; Foundation for Prader-Willi Research","keywords":"Medicine; Nutrient; Nutrient density; Obesity; Interquartile range; Food group; Micronutrient; Energy density; Vitamin; Vitamin D and neurology; Environmental health; Internal medicine; Biology","score_opus":0.015055089745961904,"score_gpt":0.2649318630061272,"score_spread":0.2498767732601653,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2892128276","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99713504,0.0007446322,0.0008634549,0.00070522574,0.00025889915,0.000073351934,0.0000036902195,0.000003085335,0.00021259773],"genre_scores_gemma":[0.99455446,0.0008406019,0.0034467007,0.00061938,0.00045707394,0.0000020094126,0.0000068475106,0.000028215982,0.000044710745],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99803376,0.000112314076,0.0005394453,0.00024713526,0.00069675886,0.00037059505],"domain_scores_gemma":[0.9988584,0.000019455234,0.0003425635,0.0002770481,0.00014534812,0.0003571737],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00062346325,0.00017728911,0.00035097043,0.000094665775,0.000039752114,0.00001948248,0.0004654479,0.000105462335,0.00008609873],"category_scores_gemma":[0.00015459885,0.00013517513,0.00008839929,0.000277491,0.00069771847,0.0000032297764,0.00013956946,0.0002654154,0.000008824504],"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":[0.00011208857,0.00078145426,0.4935746,0.000048416867,0.0007478986,0.00022732088,0.0032263575,0.00021818801,0.018192722,0.000011118279,0.0020443383,0.4808155],"study_design_scores_gemma":[0.0050403555,0.04064439,0.866599,0.0008731394,0.00023114096,0.010918771,0.008675603,0.00047255188,0.007917042,0.00007455468,0.0573784,0.0011750393],"about_ca_topic_score_codex":0.00003325317,"about_ca_topic_score_gemma":0.000058044803,"teacher_disagreement_score":0.47964045,"about_ca_system_score_codex":0.0000129992695,"about_ca_system_score_gemma":0.0002929422,"threshold_uncertainty_score":0.55122817},"labels":[],"label_agreement":null},{"id":"W2894420738","doi":"10.1101/430694","title":"Conserved mechanism of nucleoporin regulation of the <i>Kcnq1ot1</i> imprinted domain with divergence in embryonic and trophoblast stem cells","year":2018,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Lawson Health Research Institute; Western University","funders":"Canadian Institutes of Health Research; Magee-Womens Research Institute; University of Pittsburgh","keywords":"Nucleoporin; Biology; CTCF; Cell biology; Genomic imprinting; Embryonic stem cell; Genetics; DNA methylation; Gene; Cell nucleus; Gene expression; Nuclear transport","score_opus":0.006623870198471408,"score_gpt":0.18194872419563224,"score_spread":0.17532485399716083,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2894420738","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976738,0.00029796013,0.0010327768,0.000031313095,0.00031860932,0.0005652398,0.00006475979,0.000010642325,0.0000048760626],"genre_scores_gemma":[0.99729514,0.00016816177,0.002365546,0.000022848235,0.000055234843,0.000030184925,1.780951e-7,0.00005357222,0.000009157941],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9981785,0.0001451381,0.000493804,0.0006593786,0.00022710384,0.00029607804],"domain_scores_gemma":[0.9979132,0.000016553302,0.00065099297,0.0010284254,0.0003084748,0.00008239474],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00039193095,0.0003288146,0.00041400304,0.00008613402,0.00005797267,0.00002478733,0.00044254898,0.00035442243,0.00001171617],"category_scores_gemma":[0.000026930722,0.00027532617,0.000100457095,0.00023749536,0.00026796025,0.0000050030385,0.00085390505,0.00021079116,0.000001351263],"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":[0.00004160044,0.000050249826,0.021610014,0.00026280744,0.000072667994,9.1359186e-7,0.000012138271,0.000045107903,0.977754,0.00013833545,0.000010673989,0.0000014981214],"study_design_scores_gemma":[0.0005386976,0.00018483584,0.17326388,0.00034589003,0.00003686623,7.882923e-8,0.000012438539,0.00013296348,0.825131,0.0000047352805,0.000101468635,0.0002471728],"about_ca_topic_score_codex":0.00007358333,"about_ca_topic_score_gemma":0.000020716747,"teacher_disagreement_score":0.15262301,"about_ca_system_score_codex":0.00003464023,"about_ca_system_score_gemma":0.00029129058,"threshold_uncertainty_score":0.9999699},"labels":[],"label_agreement":null},{"id":"W2894978875","doi":"10.1016/j.jcjd.2018.08.097","title":"Fetal Serum Phosphorus is Set Independently of Maternal Serum Phosphorus and Phosphorus Intake","year":2018,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Phosphorus; Endocrinology; Parathyroid hormone; Fetus; Medicine; Phosphorus deficiency; Internal medicine; Black phosphorus; Calcium; Pregnancy; Biology; Chemistry","score_opus":0.007867445049499868,"score_gpt":0.2129977249535344,"score_spread":0.2051302799040345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2894978875","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9911013,0.0072994037,0.000013683226,0.00022319096,0.00069054187,0.0000945864,0.00016567943,0.0000024862904,0.00040908097],"genre_scores_gemma":[0.998225,0.00021293538,0.00045427278,0.0004559339,0.00028067676,0.0000015886743,0.0000060055086,0.000037120168,0.0003264932],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99837303,0.000038795133,0.00052617805,0.00027114112,0.00020591274,0.00058493897],"domain_scores_gemma":[0.9984031,0.0000112662265,0.00037188557,0.0002805469,0.00032044246,0.00061277486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003377837,0.00024253545,0.0003533015,0.00014076509,0.00013408964,0.00008211342,0.00038006436,0.00020690967,0.00022705302],"category_scores_gemma":[0.00008433005,0.00023276382,0.00015225509,0.00012737991,0.00028791805,0.000014976605,0.00009201321,0.00018688496,0.000011386854],"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":[0.000006083458,0.000012351158,0.9388004,0.000024433342,0.00020472766,0.000007694088,0.00027730904,0.000002695215,0.020115059,0.000010839902,0.001745895,0.03879249],"study_design_scores_gemma":[0.0006817472,0.0007973653,0.60867167,0.00008867053,0.0000535727,0.000092643364,0.0002961452,0.000029968753,0.37061542,0.00010844213,0.01833809,0.00022626051],"about_ca_topic_score_codex":0.0008845793,"about_ca_topic_score_gemma":0.0010141894,"teacher_disagreement_score":0.35050038,"about_ca_system_score_codex":0.000035143486,"about_ca_system_score_gemma":0.00053972244,"threshold_uncertainty_score":0.94918334},"labels":[],"label_agreement":null},{"id":"W2897168131","doi":"10.7554/elife.42368","title":"The discovery and importance of genomic imprinting","year":2018,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":75,"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":"Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Genetics; Gene; DNA methylation; Gene expression","score_opus":0.006511186296832042,"score_gpt":0.23186166614246737,"score_spread":0.22535047984563533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2897168131","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975178,0.001065931,0.0003213642,0.000061972285,0.00009773636,0.000046271056,0.0000013152068,0.0000022332463,0.00088535546],"genre_scores_gemma":[0.9985111,0.00025815272,0.0005442322,0.000088553374,0.00020798609,0.000002123845,0.0000015029899,0.0000076253878,0.0003787354],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995544,0.000010762072,0.00012880923,0.00013128963,0.00005144869,0.00012330328],"domain_scores_gemma":[0.99965924,0.000008241635,0.000068629146,0.0002035985,0.000037643124,0.000022624294],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016627596,0.000052643507,0.000054359138,0.00000609359,0.00008790743,0.000020964007,0.00009498058,0.000030162424,0.0000034838022],"category_scores_gemma":[0.000062109946,0.000037745962,0.000026469455,0.000018509762,0.00012194484,0.0000014607604,0.00015808266,0.000023983754,0.0000032813455],"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":[0.000003211334,0.000003544009,0.1337346,0.0000043467394,0.000015730622,8.636032e-8,0.000027546372,5.95776e-7,0.86116236,0.00011400993,0.00017728691,0.004756698],"study_design_scores_gemma":[0.00016756776,0.00013653243,0.604194,0.0000061439223,0.0000060927414,0.000017453636,0.00013983906,0.00005330676,0.3744693,0.00004853412,0.020674711,0.000086549124],"about_ca_topic_score_codex":0.000008875654,"about_ca_topic_score_gemma":0.000020006368,"teacher_disagreement_score":0.48669305,"about_ca_system_score_codex":0.000001783332,"about_ca_system_score_gemma":0.000020745281,"threshold_uncertainty_score":0.15392357},"labels":[],"label_agreement":null},{"id":"W2898659056","doi":"10.1016/j.transci.2018.10.008","title":"Introduction to part two of a three-part theme on hereditary bleeding disorders","year":2018,"lang":"en","type":"editorial","venue":"Transfusion and Apheresis Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland","funders":"","keywords":"Medicine; Wish; Associate editor; Hemostasis; Hematologist; Library science; Internal medicine; Sociology; Computer science","score_opus":0.008644078713782387,"score_gpt":0.25106347197528345,"score_spread":0.24241939326150105,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2898659056","genre_codex":"empirical","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"editorial","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.68305564,0.00026298602,0.00036182549,0.0005821586,0.3138108,0.00037610426,0.000050380855,0.000016150194,0.0014839504],"genre_scores_gemma":[0.16084917,0.0029958368,0.001351149,0.00011955991,0.83293545,0.000044319087,0.00008689624,0.00007252642,0.0015450894],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99792546,0.000026660508,0.00028288132,0.0008615594,0.00056855055,0.0003348638],"domain_scores_gemma":[0.9991384,0.000028738505,0.0000966467,0.0004208231,0.0001679684,0.0001473862],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006006772,0.00023278165,0.00023551671,0.00010456828,0.00023617882,0.000046775454,0.00037675456,0.0002064798,0.00016291118],"category_scores_gemma":[0.00024137321,0.0002007927,0.00008347705,0.0002940437,0.00041037766,0.0000073060937,0.00013492328,0.00015180816,0.000009740987],"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":[0.000071742215,0.000067420835,0.00015504565,0.00006231792,0.00002331615,3.361863e-7,0.00009651179,0.000036208123,0.2559107,0.000015384448,0.7271558,0.01640522],"study_design_scores_gemma":[0.0004951215,0.00113524,0.0005136763,0.00017115596,0.000035212703,0.0000035499945,0.00013300264,0.000042454638,0.04196866,0.00006366621,0.955095,0.00034328448],"about_ca_topic_score_codex":0.0001292916,"about_ca_topic_score_gemma":0.00038975762,"teacher_disagreement_score":0.5222065,"about_ca_system_score_codex":0.000011880961,"about_ca_system_score_gemma":0.00014640554,"threshold_uncertainty_score":0.81880885},"labels":[],"label_agreement":null},{"id":"W2899340054","doi":"10.1210/jc.2018-01504","title":"Hypermethylator Phenotype and Ectopic GIP Receptor in GNAS Mutation-Negative Somatotropinomas","year":2018,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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; Centre Hospitalier de l’Université de Montréal","funders":"Fondation pour la Recherche Médicale","keywords":"Acromegaly; GNAS complex locus; Gigantism; Biology; Endocrinology; Internal medicine; Ectopic expression; Phenotype; Allele; Somatotropic cell; DNA methylation; Gene expression; Genetics; Gene; Pituitary gland; Hormone; Medicine; Growth hormone","score_opus":0.027076818027284785,"score_gpt":0.33598587923603895,"score_spread":0.30890906120875417,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2899340054","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99429464,0.0030256691,0.0002710884,0.0011303554,0.0009085356,0.000099723606,0.0000016101819,0.0000031010995,0.00026524704],"genre_scores_gemma":[0.9930361,0.0019596685,0.002889638,0.00058253406,0.0013867943,0.0000019777488,0.0000010086069,0.000014227292,0.0001280844],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.998044,0.0005099804,0.0008622762,0.00018443748,0.00011867343,0.00028060778],"domain_scores_gemma":[0.99875253,0.0002478189,0.00046240079,0.0002390748,0.00020648848,0.00009170274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00076227786,0.0001370428,0.00043136236,0.00006669599,0.000072198876,0.00001152557,0.0002836914,0.00013293893,0.00005889537],"category_scores_gemma":[0.0014020544,0.00009159991,0.00012087565,0.00009069938,0.0004934,0.0000075556677,0.00014518386,0.00032306492,0.00001748263],"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":[0.0013881403,0.0007223432,0.22325979,0.000057623936,0.0015436691,0.000063655294,0.0026161044,0.00009039196,0.33915204,0.004074818,0.0020507362,0.4249807],"study_design_scores_gemma":[0.0029220092,0.0009615243,0.92910755,0.000021535538,0.00010657698,0.00052391423,0.00028561935,0.000048360256,0.028370999,0.002181802,0.03529981,0.00017030872],"about_ca_topic_score_codex":0.000028566365,"about_ca_topic_score_gemma":0.000023123603,"teacher_disagreement_score":0.70584774,"about_ca_system_score_codex":0.0000041268563,"about_ca_system_score_gemma":0.00011100261,"threshold_uncertainty_score":0.37353358},"labels":[],"label_agreement":null},{"id":"W2908470212","doi":"10.1101/gad.320069.118","title":"ZNF445 is a primary regulator of genomic imprinting","year":2019,"lang":"en","type":"article","venue":"Genes & Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":224,"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; Medical Research Council Canada; European Commission; Wellcome Trust; Gebert Rüf Stiftung; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Science Foundation","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Reprogramming; Epigenetics; DNA methylation; Penetrance; Genetics; Regulator; Regulation of gene expression; Zinc finger; Gene; Phenotype; Gene expression; Cell biology; Transcription factor","score_opus":0.005898302427109366,"score_gpt":0.20275046994225154,"score_spread":0.19685216751514217,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908470212","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99613386,0.0012642653,0.0003151794,0.00003401187,0.00021732126,0.00020435743,0.0000020126058,0.000008438575,0.0018205284],"genre_scores_gemma":[0.97677934,0.00013551037,0.020901546,0.0002368461,0.00006445347,0.000012147118,0.000026831982,0.000026777947,0.0018165716],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988517,0.00001582425,0.00034711807,0.0003594136,0.00014802012,0.00027793014],"domain_scores_gemma":[0.9993558,0.000004239822,0.00013879412,0.00037328433,0.00006899908,0.000058880632],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019367115,0.00015372034,0.00018882149,0.000043911266,0.00004309413,0.000012381426,0.0002143825,0.00009598674,0.00013604166],"category_scores_gemma":[0.000006376206,0.00015266013,0.00007888006,0.000053634616,0.000022427645,0.0000019399888,0.00036541163,0.000040096013,0.00011253791],"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":[0.0000048652246,0.000018035671,0.0569596,0.00006362505,0.00006200391,2.3573531e-7,0.0001552628,0.000019231478,0.8865772,0.000009337624,0.000123253,0.056007367],"study_design_scores_gemma":[0.00026856255,0.00004487702,0.3399546,0.000016905578,0.0000059724134,0.00001476699,0.000062970656,0.000011412097,0.5814118,0.000008817078,0.078032,0.00016735861],"about_ca_topic_score_codex":0.0000068773365,"about_ca_topic_score_gemma":0.000001427111,"teacher_disagreement_score":0.30516544,"about_ca_system_score_codex":0.000024288065,"about_ca_system_score_gemma":0.00021585567,"threshold_uncertainty_score":0.6225299},"labels":[],"label_agreement":null},{"id":"W2908503642","doi":"10.1111/cge.13151","title":"Are all Xq26.2 duplications overlapping <i>GPC3</i> on array‐CGH a cause of Simpson‐Golabi‐Behmel syndrome? When do we need transcript analysis?","year":2018,"lang":"en","type":"letter","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Genetics; Biology; Gene duplication; Gene","score_opus":0.06180763596712226,"score_gpt":0.33024938877234566,"score_spread":0.2684417528052234,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908503642","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8674764,0.009465576,0.008026099,0.108652,0.0023682883,0.0017761193,0.0010553417,0.000099732715,0.0010804428],"genre_scores_gemma":[0.64549404,0.018195326,0.014736491,0.3007653,0.0091871135,0.00024398012,0.0027715294,0.00066387147,0.007942355],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9942365,0.00034008827,0.0021165388,0.0017517098,0.00064005697,0.0009150961],"domain_scores_gemma":[0.99456346,0.00023567128,0.0016276311,0.0027833746,0.00048222448,0.00030762766],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.0006295399,0.0008208628,0.001590386,0.00030669718,0.00013398183,0.000106342864,0.0012927699,0.0023797126,0.00016029464],"category_scores_gemma":[0.0004497137,0.00082177774,0.0015728247,0.00048582724,0.00053482817,0.0000044891726,0.00028339511,0.0013383131,0.00008310646],"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":[0.00007249107,0.0009546095,0.029584123,0.00062586524,0.010470213,0.000116708004,0.0002611463,0.00054729776,0.034581278,0.000008988196,0.9190842,0.0036931036],"study_design_scores_gemma":[0.0010949319,0.0015492615,0.020334508,0.0002862059,0.0034099198,0.00006777297,0.00010327144,0.00015757802,0.003248623,0.00016963265,0.96845376,0.0011245103],"about_ca_topic_score_codex":0.000018184439,"about_ca_topic_score_gemma":0.000030469855,"teacher_disagreement_score":0.22198237,"about_ca_system_score_codex":0.000035557554,"about_ca_system_score_gemma":0.00019781211,"threshold_uncertainty_score":0.9994233},"labels":[],"label_agreement":null},{"id":"W2908505564","doi":"10.1111/ijpo.12493","title":"Obestatin and adropin in Prader‐Willi syndrome and nonsyndromic obesity: Associations with weight, BMI‐z, and HOMA‐IR","year":2018,"lang":"en","type":"article","venue":"Pediatric Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research","keywords":"Obestatin; Ghrelin; Medicine; Endocrinology; Internal medicine; Obesity; Childhood obesity; Hormone; Overweight","score_opus":0.005525405858576366,"score_gpt":0.21257506939000162,"score_spread":0.20704966353142526,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908505564","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99738276,0.001718246,0.00018364482,0.00016560197,0.00007210898,0.0002728625,0.000025802252,0.00001556449,0.00016342342],"genre_scores_gemma":[0.99525905,0.0016979707,0.002553958,0.00008631677,0.00017221314,0.000013020474,0.000023518458,0.000023326329,0.00017064963],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99865943,0.00007641207,0.0002388672,0.00053287036,0.00013834563,0.00035405534],"domain_scores_gemma":[0.99939555,0.000038134545,0.00012806096,0.00022522037,0.00006199219,0.00015102806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023819218,0.00021722741,0.00026308093,0.00010879706,0.00019153407,0.00005788284,0.00009626766,0.0001733009,0.0000122266065],"category_scores_gemma":[0.000089522226,0.00020350765,0.00002453351,0.00019799429,0.00015057727,0.000013562777,0.0002225402,0.00013218215,0.0000066562393],"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":[0.0000022841843,0.0000859269,0.99808335,0.00005119037,0.000022959388,0.000005725365,0.000119377575,6.556764e-7,0.0009675678,0.000020048901,0.0001441761,0.0004967623],"study_design_scores_gemma":[0.0009120517,0.0005342109,0.9969653,0.000014408141,0.00006624685,0.00037038376,0.000067664994,0.00008967542,0.00029599227,0.00009811769,0.00030790354,0.000278056],"about_ca_topic_score_codex":0.00018765568,"about_ca_topic_score_gemma":0.0003283796,"teacher_disagreement_score":0.002370313,"about_ca_system_score_codex":0.00001885178,"about_ca_system_score_gemma":0.00007712302,"threshold_uncertainty_score":0.82988006},"labels":[],"label_agreement":null},{"id":"W2910777113","doi":"10.1111/cen.13933","title":"Hormonal and metabolic effects of carbohydrate restriction in children with Prader‐Willi syndrome","year":2019,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta Hospital; University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Child Health and Human Development; Foundation for Prader-Willi Research","keywords":"Postprandial; Internal medicine; Endocrinology; Carbohydrate; Ghrelin; Adiponectin; Insulin; Calorie; Meal; Glucagon-like peptide-1; Medicine; Hormone; Insulin resistance; Type 2 diabetes; Diabetes mellitus","score_opus":0.007751614674323291,"score_gpt":0.25926566326243433,"score_spread":0.25151404858811105,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2910777113","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975888,0.0017322962,0.000037517784,0.00006190112,0.00015730267,0.00029971942,0.0000020301984,0.0000061383703,0.00011429479],"genre_scores_gemma":[0.997627,0.0018012787,0.00035381457,0.000067257,0.000043291304,0.000013902948,0.00001369003,0.0000142597455,0.00006546778],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99882716,0.000115809984,0.00034008845,0.00038218184,0.00006577649,0.00026900467],"domain_scores_gemma":[0.9994701,0.000057983518,0.00012319749,0.00026510438,0.0000258466,0.00005773846],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010062969,0.00012366008,0.00032585298,0.00006498734,0.000014390158,0.0000045665306,0.00011117755,0.00014284265,0.0000050756785],"category_scores_gemma":[0.000118349584,0.00010350048,0.00005583396,0.00009535339,0.00014028004,0.0000029671903,0.00013305772,0.00016155862,0.0000062895547],"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":[0.0000053353397,0.00006817295,0.97296774,0.00001675461,0.00010210321,0.0000021775752,0.0000046475834,0.000018450857,0.023698572,0.00016161164,0.000007009108,0.0029474136],"study_design_scores_gemma":[0.0015219768,0.0014808552,0.9922285,0.000014635857,0.000033312863,0.00024033869,0.000008837931,0.000019366558,0.0038899565,0.00005074018,0.00039559335,0.00011587167],"about_ca_topic_score_codex":0.000057646448,"about_ca_topic_score_gemma":0.000007860512,"teacher_disagreement_score":0.019808615,"about_ca_system_score_codex":0.0000025980228,"about_ca_system_score_gemma":0.000039488077,"threshold_uncertainty_score":0.4220627},"labels":[],"label_agreement":null},{"id":"W2914071115","doi":"10.1177/2050312118823585","title":"Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes","year":2019,"lang":"en","type":"review","venue":"SAGE Open Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada","keywords":"Angelman syndrome; UBE3A; Genomic imprinting; Rett syndrome; Neurodevelopmental disorder; Phenotype; Epigenetics; MECP2; Medicine; Chromosome 15; Genetics; Endocrinology; Gene; Biology; DNA methylation; Chromosome; Gene expression","score_opus":0.10410958322111684,"score_gpt":0.3669626128591385,"score_spread":0.26285302963802165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2914071115","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.05716754,0.9394597,0.00049803883,0.00021054504,0.00014453592,0.0023796575,0.00009822444,0.0000036593806,0.000038110462],"genre_scores_gemma":[0.019214245,0.9777165,0.0017811614,0.000102352846,0.00020098085,0.00024412552,0.00027391073,0.00005871421,0.00040797496],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99790597,0.00015231954,0.0005841801,0.0009135311,0.00012919742,0.00031481707],"domain_scores_gemma":[0.9988459,0.00023497542,0.00023550677,0.0004884771,0.00003141418,0.00016372456],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00024655848,0.00044781272,0.0012247785,0.00010204366,0.00009916275,0.000114556715,0.00033789108,0.00026213366,0.000037158217],"category_scores_gemma":[0.0001973456,0.00033923393,0.0000678883,0.00007676113,0.0001567159,0.000010274626,0.00061554555,0.00015000788,0.0000016982215],"study_design_candidate":"design_other","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":[0.00000546544,0.000031774853,0.0019674124,0.004259402,0.0002529091,0.000002474899,0.00018127444,7.723001e-7,0.0012155669,0.0000079442025,0.000114955146,0.99196005],"study_design_scores_gemma":[0.0074209166,0.009179173,0.12370409,0.08701202,0.005398624,0.0007993258,0.0004921197,0.00028063703,0.000332794,0.00068813603,0.7617615,0.0029306544],"about_ca_topic_score_codex":0.00014086977,"about_ca_topic_score_gemma":0.0001999158,"teacher_disagreement_score":0.9890294,"about_ca_system_score_codex":0.000015509728,"about_ca_system_score_gemma":0.000080299484,"threshold_uncertainty_score":0.99990594},"labels":[],"label_agreement":null},{"id":"W2915087909","doi":"10.1101/560474","title":"BORIS/CTCFL promotes a switch from a proliferative towards an invasive phenotype in melanoma cell lines","year":2019,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University Health Centre; McGill University; Jewish General Hospital","funders":"Canadian Institutes of Health Research; McGill University; Israel Cancer Research Fund","keywords":"Reprogramming; Melanoma; Phenotype; Biology; Cancer research; Transcriptome; Phenotypic switching; Regulator; Transcriptional regulation; Cell; Transcription factor; Gene expression; Genetics; Gene","score_opus":0.011951469963488203,"score_gpt":0.22359190229947656,"score_spread":0.21164043233598837,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2915087909","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9945755,0.0022032845,0.0005101156,0.00010137027,0.0008385955,0.0013756737,0.00028514274,0.00007108233,0.00003924058],"genre_scores_gemma":[0.99058515,0.0002975921,0.007578715,0.00018168638,0.00087231846,0.00027863463,0.0000118119015,0.00017527604,0.000018808838],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9963134,0.00023588288,0.00068438146,0.0017336417,0.00033207372,0.0007006461],"domain_scores_gemma":[0.9970662,0.000029139506,0.0004796815,0.0016474058,0.00051290717,0.0002646641],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00041109178,0.00077023916,0.00075020513,0.00018657855,0.00008710136,0.00022469026,0.00082590105,0.00097005046,0.000038654267],"category_scores_gemma":[0.00030033104,0.0007984893,0.00018419127,0.0002638106,0.00008323517,0.000018506182,0.0010213348,0.0006626125,0.00005422295],"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":[0.000032699587,0.0002679651,0.06399271,0.0002449669,0.0001258519,0.000019219924,0.00006914385,0.00013149179,0.93503475,0.000009218953,0.000063063446,0.000008915712],"study_design_scores_gemma":[0.000836563,0.00033921574,0.21637654,0.0002563503,0.000067906025,3.672735e-8,0.000025237367,0.00037313337,0.78010654,0.000005907848,0.0007295946,0.0008829431],"about_ca_topic_score_codex":0.000536307,"about_ca_topic_score_gemma":0.000068277,"teacher_disagreement_score":0.15492818,"about_ca_system_score_codex":0.00009783843,"about_ca_system_score_gemma":0.0014989665,"threshold_uncertainty_score":0.9994466},"labels":[],"label_agreement":null},{"id":"W2917246659","doi":"10.1002/ajmg.a.61071","title":"Disruption of the PTHLH regulatory landscape results in features consistent with hyperparathyroid disease","year":2019,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Science and Engineering Research Board","keywords":"Enhancer; Regulatory sequence; Parathyroid hormone; Coding region; Cancer research; Biology; Transcription factor; Medicine; Endocrinology; Internal medicine; Genetics; Gene","score_opus":0.005481013258852192,"score_gpt":0.23679842735114648,"score_spread":0.23131741409229428,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2917246659","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966425,0.0019362065,0.00003395266,0.000936495,0.0001788169,0.0000996958,0.000006138952,0.0000011074297,0.00016509555],"genre_scores_gemma":[0.99856573,0.0006125957,0.0003077383,0.00022758592,0.00011480245,0.0000016592329,0.000004413727,0.000012177585,0.00015328228],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9984779,0.00011872796,0.0004354354,0.00016763665,0.0006231299,0.00017720884],"domain_scores_gemma":[0.9989099,0.000028495971,0.00042443213,0.00033927316,0.000100795776,0.00019712676],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047507722,0.000110535424,0.00024015985,0.000040648865,0.000018719264,0.000008846247,0.00032177113,0.00005800495,0.000017139406],"category_scores_gemma":[0.00017374424,0.00006731822,0.00011103952,0.00013932212,0.00027103306,0.0000018742949,0.00010450236,0.00017320192,0.0000016845217],"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":[0.001444685,0.0004761103,0.8555893,0.00007552791,0.00028841564,0.000045258654,0.0005336244,0.004407556,0.08186712,0.00004766049,0.004564642,0.050660107],"study_design_scores_gemma":[0.0019957717,0.0015223997,0.98082036,0.00023088885,0.00004866456,0.00025826835,0.00061947166,0.00014676715,0.0047314833,0.000011874112,0.009462712,0.00015136518],"about_ca_topic_score_codex":0.0000073912256,"about_ca_topic_score_gemma":0.000016021959,"teacher_disagreement_score":0.12523104,"about_ca_system_score_codex":0.000007742701,"about_ca_system_score_gemma":0.0003128748,"threshold_uncertainty_score":0.27451572},"labels":[],"label_agreement":null},{"id":"W2922146825","doi":"10.1016/j.psychres.2019.03.019","title":"Genetic variation of UBE3A is associated with schizotypy in a population of typical individuals","year":2019,"lang":"en","type":"article","venue":"Psychiatry Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta; Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"UBE3A; Angelman syndrome; Psychosis; Genetics; Schizotypy; Biology; Autism; Population; Schizophrenia (object-oriented programming); Haplotype; Penetrance; Genotype; Psychology; Phenotype; Medicine; Psychiatry; Gene","score_opus":0.02140425203211636,"score_gpt":0.31709655928177666,"score_spread":0.2956923072496603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2922146825","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989208,0.0002250494,0.000045919758,0.00012323212,0.00007108601,0.00026656676,0.0000091038855,0.0000020423997,0.0003361856],"genre_scores_gemma":[0.99788296,0.000022786071,0.0018839613,0.000014047084,0.000033688055,0.000007887401,0.000029368923,0.000013530556,0.00011177281],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99879295,0.00015276945,0.00026683253,0.00023557823,0.00033384262,0.00021805894],"domain_scores_gemma":[0.99941015,0.00002311802,0.00010699017,0.00027342318,0.00015247836,0.000033853736],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006055426,0.00007173581,0.00015001354,0.00014292056,0.000021064698,0.000008016339,0.00015246647,0.0001365374,0.0000733917],"category_scores_gemma":[0.00010767136,0.00006483386,0.000036791163,0.00034129017,0.000036122256,0.0000028516097,0.00007727158,0.00012578444,0.0000071830746],"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":[0.000042056265,0.000112793474,0.9607613,0.000040181054,0.000039894392,6.6464786e-8,0.000052620177,0.000053454896,0.038368836,0.000092821465,0.000034068136,0.00040189122],"study_design_scores_gemma":[0.0007325661,0.00056730205,0.99663943,0.00007254521,0.0000059954227,0.0000024338235,0.000052644707,0.00018839777,0.0012662217,0.00037367136,0.000028925611,0.000069866306],"about_ca_topic_score_codex":0.00015606357,"about_ca_topic_score_gemma":0.00008899198,"teacher_disagreement_score":0.037102614,"about_ca_system_score_codex":0.000010895937,"about_ca_system_score_gemma":0.00011742683,"threshold_uncertainty_score":0.26438484},"labels":[],"label_agreement":null},{"id":"W2922220912","doi":"10.1016/j.omtm.2019.03.001","title":"Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis","year":2019,"lang":"en","type":"review","venue":"Molecular Therapy — Methods & Clinical Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"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","keywords":"Endophenotype; Medicine; Clinical trial; Context (archaeology); Bioinformatics; Translational research; Disease; Preclinical research; Neuroscience; Biology; Internal medicine; Pathology; Cognition; Psychiatry","score_opus":0.39317348149902526,"score_gpt":0.51069152147912,"score_spread":0.11751803998009475,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2922220912","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.016425766,0.9436634,0.038553238,0.000025117775,0.00013351487,0.0010621011,0.000014581521,0.000010300559,0.00011197684],"genre_scores_gemma":[0.0010449127,0.66521925,0.33331987,0.000083032435,0.000025532876,0.000072481176,0.00013135391,0.0000616607,0.00004188233],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99236816,0.0023016613,0.0030972124,0.0013723896,0.00038220783,0.00047836316],"domain_scores_gemma":[0.997087,0.00089930627,0.0009453945,0.00074294733,0.00014086283,0.0001844624],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0052365884,0.00063915947,0.0030285937,0.00029839942,0.00004787175,0.000036094683,0.0005126529,0.000932285,0.000029285047],"category_scores_gemma":[0.0006073421,0.0005570397,0.0011419657,0.0008263121,0.00014936535,0.000007094006,0.0003120838,0.000540409,0.000004146169],"study_design_candidate":"design_other","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":[0.000006385705,0.0002096463,0.0030326638,0.0017085873,0.002372217,0.0000040062114,0.00003035111,0.00009992799,0.00018923775,0.000033536682,0.0000018657989,0.9923116],"study_design_scores_gemma":[0.004543749,0.0025953855,0.106428936,0.009187574,0.00561108,0.0003029927,0.00003530644,0.002505188,0.00047117512,0.0011264627,0.8634536,0.0037385179],"about_ca_topic_score_codex":0.000008781471,"about_ca_topic_score_gemma":0.0000032349355,"teacher_disagreement_score":0.9885731,"about_ca_system_score_codex":0.000023626866,"about_ca_system_score_gemma":0.00081295456,"threshold_uncertainty_score":0.9996881},"labels":[],"label_agreement":null},{"id":"W2923698345","doi":"","title":"Kane and Able","year":2017,"lang":"en","type":"article","venue":"Dalhousie review","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Geology","score_opus":0.0179352793432706,"score_gpt":0.28720217669327835,"score_spread":0.26926689735000775,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2923698345","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5279742,0.44584024,0.00017346098,0.0015030247,0.00021071211,0.00038895223,0.000006865986,0.000014092641,0.023888486],"genre_scores_gemma":[0.55491525,0.43901828,0.0013177333,0.0012298084,0.00017048811,0.000018936295,0.000018640663,0.00002261756,0.0032882488],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995057,0.000013562015,0.0001092823,0.00018886753,0.000047607587,0.00013497239],"domain_scores_gemma":[0.999293,0.0000020309149,0.00008319757,0.00054584065,0.00002309696,0.00005279788],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016619194,0.00007870019,0.00013783961,0.000005290524,0.00014894258,0.000041558425,0.00017363485,0.000037971862,0.000041435727],"category_scores_gemma":[0.00013078704,0.000067138135,0.000042757867,0.000009543711,0.000044064844,0.0000019253753,0.00020612295,0.000030875144,0.000027704413],"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":[0.000002747107,0.000049872222,0.028183682,0.0035261132,0.000098560995,0.000009514775,0.000022763217,7.130334e-7,0.10868195,0.00024108458,0.019683499,0.8394995],"study_design_scores_gemma":[0.00015858532,0.00005991054,0.036691952,0.00053646637,0.000031268108,0.000097887314,0.0000025844972,0.0000047265376,0.0029236889,0.000026758826,0.95932513,0.0001410361],"about_ca_topic_score_codex":0.000016014645,"about_ca_topic_score_gemma":0.0000053707568,"teacher_disagreement_score":0.93964165,"about_ca_system_score_codex":0.0000011592069,"about_ca_system_score_gemma":0.000015018875,"threshold_uncertainty_score":0.2737814},"labels":[],"label_agreement":null},{"id":"W2944830605","doi":"10.1080/17518423.2019.1619857","title":"Using Behavioral Approaches to Assess Memory, Imitation and Motor Performance in Children with Angelman Syndrome: Results of a Pilot Study","year":2019,"lang":"en","type":"article","venue":"Developmental Neurorehabilitation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"Angelman Syndrome Foundation","keywords":"Angelman syndrome; Psychology; Imitation; Developmental psychology; Physical medicine and rehabilitation; Clinical psychology; Cognitive psychology; Medicine; Neuroscience","score_opus":0.0843971213659254,"score_gpt":0.2692353614891771,"score_spread":0.18483824012325167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2944830605","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99872684,0.000008282534,0.00002510804,0.000010350229,0.000034150347,0.0011400541,0.000006612964,0.0000043756995,0.000044193475],"genre_scores_gemma":[0.987889,0.0000012844097,0.011987049,0.0000081881435,0.0000046758587,0.000036199686,0.00003620076,0.000015813643,0.0000216224],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99906,0.000059797163,0.000256049,0.0003528343,0.0001391734,0.00013217799],"domain_scores_gemma":[0.99971044,0.000011676788,0.00007918141,0.00012949824,0.00003187943,0.000037330574],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021318725,0.0001182402,0.00012830297,0.00010099305,0.000029574525,0.0000140225175,0.00007174411,0.000025040545,0.0000013105778],"category_scores_gemma":[0.000025885367,0.00011262763,0.000011037722,0.00014841057,0.00002882642,0.00001407808,0.00007902778,0.000042585816,0.0000014489358],"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":[0.00010382383,0.00025963454,0.85267156,0.000021448514,0.000010889339,2.6491887e-7,0.0006226941,0.00032052613,0.14433731,5.1227516e-7,3.960275e-7,0.0016509144],"study_design_scores_gemma":[0.001250565,0.0071545052,0.9832066,0.000029098817,0.000008503933,0.00004042759,0.0014634018,0.00016358317,0.0065444256,7.1523203e-7,0.0000018329523,0.00013629252],"about_ca_topic_score_codex":0.000065549924,"about_ca_topic_score_gemma":0.00003776599,"teacher_disagreement_score":0.13779289,"about_ca_system_score_codex":0.000022637487,"about_ca_system_score_gemma":0.000040610383,"threshold_uncertainty_score":0.45928216},"labels":[],"label_agreement":null},{"id":"W2946589254","doi":"10.1016/j.evolhumbehav.2019.05.003","title":"Response to vocal music in Angelman syndrome contrasts with Prader-Willi syndrome","year":2019,"lang":"en","type":"article","venue":"Evolution and Human Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Harvard University","keywords":"Angelman syndrome; Offspring; Genomic imprinting; Imprinting (psychology); Psychology; Parent–offspring conflict; Developmental psychology; Parental investment; Biology; Genetics; Gene; Pregnancy","score_opus":0.010116746861948031,"score_gpt":0.24203751178537003,"score_spread":0.231920764923422,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2946589254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988856,0.00012921375,0.00008773829,0.000106797575,0.000093388335,0.00056804763,0.000008689675,0.000016092486,0.000104464794],"genre_scores_gemma":[0.9976373,0.0000021809653,0.00024771842,0.00011457169,0.00001867208,0.000067943205,0.000022394484,0.00002683722,0.0018624151],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99881005,0.00007727037,0.00020704196,0.00044186693,0.00014321748,0.00032057043],"domain_scores_gemma":[0.9994631,0.0000073431697,0.000053296946,0.00030102828,0.000037129103,0.00013813286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023064559,0.0001747527,0.00019805043,0.0001319538,0.00008244003,0.000034168275,0.0001138888,0.00012471717,0.00010597132],"category_scores_gemma":[0.000013866376,0.00016483999,0.00003949338,0.00011286906,0.00006118564,0.00000742543,0.0000938948,0.000103821054,0.000047367434],"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":[0.000024796316,0.00013611745,0.6886234,0.00001566535,0.000012599623,0.000019277024,0.00012362856,0.000015094683,0.31050947,0.00009113416,0.000112501686,0.00031627243],"study_design_scores_gemma":[0.0011923756,0.0017223608,0.99353755,0.000050207862,0.000019101984,0.0008207802,0.00019799647,0.0000059273852,0.00040142421,0.0000058919873,0.0017952283,0.00025116152],"about_ca_topic_score_codex":0.000091341106,"about_ca_topic_score_gemma":0.0002958299,"teacher_disagreement_score":0.31010807,"about_ca_system_score_codex":0.000039138296,"about_ca_system_score_gemma":0.00004354826,"threshold_uncertainty_score":0.672198},"labels":[],"label_agreement":null},{"id":"W2949563565","doi":"","title":"305 CHYLOTHORAX IN AN INFANT WITH FEATURES OF PETERS PLUS SYNDROME.","year":2007,"lang":"en","type":"article","venue":"Journal of Investigative Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine; Polyhydramnios; Ductus arteriosus; Etiology; Chylothorax; Cardiology; Internal medicine; Pathology; Gestation; Pregnancy","score_opus":0.019585386787861404,"score_gpt":0.2785593719628053,"score_spread":0.25897398517494385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2949563565","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99746394,0.00084221334,0.00057656557,0.00048479682,0.00010094853,0.00008860466,0.0000010352558,0.0000013338524,0.00044056104],"genre_scores_gemma":[0.994618,0.000049868784,0.004848221,0.00025878559,0.00014694694,7.074954e-7,0.0000044750495,0.000014096962,0.00005889969],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99882996,0.0000601197,0.0005027733,0.00013948538,0.00027362106,0.00019404416],"domain_scores_gemma":[0.9989239,0.000024806774,0.00046696505,0.00015962479,0.00023495966,0.00018976761],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008964031,0.00013656703,0.00034592234,0.00018243957,0.000019232586,0.0000042201104,0.00018200821,0.00007210529,0.000011698364],"category_scores_gemma":[0.00031189894,0.00008813978,0.000042120097,0.00019303412,0.0004732046,0.000007772138,0.000033583317,0.0001907399,2.1259885e-7],"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":[0.000116180025,0.00004071629,0.069098294,0.000042658106,0.000074450785,0.000114798866,0.0010869853,0.00014462518,0.9276248,0.000064085325,0.0001994131,0.0013929815],"study_design_scores_gemma":[0.0018816788,0.005312781,0.7694665,0.0004652079,0.000032935848,0.0015137818,0.0021676412,0.000008622583,0.21855795,0.00013944192,0.00033166652,0.00012177155],"about_ca_topic_score_codex":0.00005480026,"about_ca_topic_score_gemma":0.00010452035,"teacher_disagreement_score":0.70906687,"about_ca_system_score_codex":0.000022644945,"about_ca_system_score_gemma":0.00013824915,"threshold_uncertainty_score":0.35942358},"labels":[],"label_agreement":null},{"id":"W2956085547","doi":"10.7554/elife.45282","title":"Fetal and trophoblast PI3K p110α have distinct roles in regulating resource supply to the growing fetus in mice","year":2019,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"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":"Erasmus+; Biotechnology and Biological Sciences Research Council; Royal Society; Medical Research Council; European Cooperation in Science and Technology; Wellcome Trust","keywords":"Trophoblast; Conceptus; Biology; Placenta; Fetus; Cell biology; Phenotype; Embryonic stem cell; Genetics; Gene; Pregnancy","score_opus":0.0045721865324490595,"score_gpt":0.21024307467844808,"score_spread":0.20567088814599901,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2956085547","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99810773,0.00045953784,0.000036462086,0.00060938916,0.000052485877,0.00019838852,0.0000047258345,0.0000043449318,0.00052694895],"genre_scores_gemma":[0.99857485,0.000013665272,0.00047874483,0.00037015905,0.00010961511,0.0000105609115,0.000014244182,0.000018682904,0.00040946744],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999026,0.00005864699,0.00021197442,0.0003198856,0.00011288576,0.00027060573],"domain_scores_gemma":[0.9996426,0.000023409993,0.000045313584,0.00021891361,0.000015662326,0.00005409246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026458956,0.000121530305,0.00013364851,0.00004057124,0.00004548474,0.000035036424,0.00014887795,0.00007102811,0.000010615437],"category_scores_gemma":[0.00010470272,0.00009982945,0.00003608736,0.00007982279,0.00002245333,0.000004285261,0.00019323853,0.000101601705,0.000011608125],"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":[0.00003382141,0.000023047207,0.48630774,0.000020536836,0.000011488866,0.000002788663,0.0005619985,0.0012953948,0.5012259,0.000011137334,0.00027401812,0.010232146],"study_design_scores_gemma":[0.0007333231,0.00016550889,0.9284317,0.00009051227,0.000004558493,0.000028417277,0.0015644239,0.0012268478,0.048408795,0.000005198096,0.019125983,0.00021474838],"about_ca_topic_score_codex":0.00016173623,"about_ca_topic_score_gemma":0.00053090684,"teacher_disagreement_score":0.4528171,"about_ca_system_score_codex":0.0000125338975,"about_ca_system_score_gemma":0.000017643506,"threshold_uncertainty_score":0.4070927},"labels":[],"label_agreement":null},{"id":"W2961087513","doi":"10.1097/mph.0000000000001555","title":"Challenges in the Diagnosis of Medulloblastoma Recurrence at an Unusual Site in a Patient With Prader-Willi Syndrome","year":2019,"lang":"en","type":"article","venue":"Journal of Pediatric Hematology/Oncology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"Brain Tumour Charity","keywords":"Medulloblastoma; Medicine; Pediatrics; Histology; Biopsy; Pathology","score_opus":0.024332796119822298,"score_gpt":0.2818840949584432,"score_spread":0.2575512988386209,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2961087513","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99151945,0.006780063,0.000009332294,0.0008875375,0.00022554839,0.0002737268,0.000003487076,0.0000017221563,0.0002991489],"genre_scores_gemma":[0.9944624,0.0045973435,0.0007155134,0.00009373346,0.000082085506,0.00002480318,0.0000038667185,0.000015035722,0.000005230807],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9978063,0.00048814042,0.0008035449,0.00030562133,0.00024121616,0.00035516926],"domain_scores_gemma":[0.99841833,0.00022357654,0.00083184097,0.00030855613,0.0001300586,0.000087636865],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008791808,0.0001853674,0.0005909796,0.00026694126,0.0000237702,0.00000538387,0.00037906243,0.0003116938,0.00001994035],"category_scores_gemma":[0.0001808325,0.00012645904,0.00009498701,0.00026793932,0.00008495376,0.000013027282,0.00013947116,0.0003141726,0.0000071069285],"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":[0.000052756037,0.000797984,0.9871144,0.00012151769,0.00004861928,0.00022565098,0.0022290016,0.00015261576,0.0013009869,0.000049540868,0.00017600632,0.007730908],"study_design_scores_gemma":[0.004270964,0.029705456,0.90815353,0.00012735426,0.0001347187,0.03954112,0.006107725,0.000052906944,0.0029303473,0.00010066926,0.00841697,0.00045821656],"about_ca_topic_score_codex":0.000013492852,"about_ca_topic_score_gemma":0.00033148786,"teacher_disagreement_score":0.07896086,"about_ca_system_score_codex":0.00006184302,"about_ca_system_score_gemma":0.00028660832,"threshold_uncertainty_score":0.51568496},"labels":[],"label_agreement":null},{"id":"W2964455242","doi":"10.1101/723254","title":"Evolution of imprinting via lineage-specific insertion of retroviral promoters","year":2019,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Biology; Genomic imprinting; Genetics; Endogenous retrovirus; Germline; Gene; Epigenetics; DNA methylation; Allele; Imprinting (psychology); CRISPR; Transcription (linguistics); Genome; Gene expression","score_opus":0.00872867119547473,"score_gpt":0.20293498455257641,"score_spread":0.19420631335710167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2964455242","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97736514,0.0014854237,0.01963772,0.00001781222,0.0008082353,0.00058697094,0.000051691743,0.00003490301,0.000012083152],"genre_scores_gemma":[0.9921562,0.00022305801,0.00715769,0.0000125648485,0.0003189855,0.000029533208,0.0000016659588,0.00009348802,0.0000068112854],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9974711,0.00011430177,0.0008393072,0.0008564432,0.00030950477,0.0004093227],"domain_scores_gemma":[0.9970014,0.00001141147,0.00097564893,0.0013515672,0.0005586476,0.00010132243],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005966495,0.0004084964,0.0005467518,0.00020301105,0.000050967872,0.00003342522,0.0004987573,0.00065638096,0.00001266277],"category_scores_gemma":[0.00014390936,0.00045911464,0.0002795874,0.00024279181,0.000149782,0.0000089477835,0.00074514665,0.00036764055,0.0000103093125],"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":[0.000022627875,0.000088572015,0.035015285,0.000553414,0.00009929028,8.7757434e-7,0.000005263094,0.00048664844,0.96364623,0.000039278217,0.000028615174,0.000013910265],"study_design_scores_gemma":[0.0003727212,0.00020822664,0.22974266,0.0002571309,0.0000443576,4.254527e-8,0.0000046843775,0.00080176676,0.7677245,9.4895205e-7,0.00048554337,0.00035741745],"about_ca_topic_score_codex":0.00006586049,"about_ca_topic_score_gemma":8.6547607e-7,"teacher_disagreement_score":0.19592172,"about_ca_system_score_codex":0.000101121244,"about_ca_system_score_gemma":0.00034062323,"threshold_uncertainty_score":0.9997861},"labels":[],"label_agreement":null},{"id":"W2965756418","doi":"10.1101/717868","title":"Imprinted maternally-expressed microRNAs antagonize paternally-driven gene programs in neurons","year":2019,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Cancer Institute; Fonds de Recherche du Québec - Santé; Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology","keywords":"Genomic imprinting; Biology; microRNA; Gene; Gene cluster; Genetics; Psychological repression; Regulation of gene expression; Gene expression; DNA methylation","score_opus":0.013708305574120259,"score_gpt":0.21355734898681256,"score_spread":0.1998490434126923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2965756418","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949436,0.0007220983,0.0013940794,0.000098989425,0.0013817811,0.0011870231,0.00014938472,0.00011229822,0.000010739677],"genre_scores_gemma":[0.99189484,0.0007389671,0.006215378,0.00021074696,0.00043923402,0.00021086146,0.0000068544823,0.00024789877,0.00003520822],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9958321,0.00017914783,0.00086417637,0.0017452113,0.00035884563,0.0010205129],"domain_scores_gemma":[0.9968414,0.000012644509,0.00055878866,0.0019702641,0.0003361309,0.00028082277],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00037783725,0.0008282387,0.0007223062,0.00023579001,0.00008147831,0.00030659724,0.0012360397,0.00085376704,0.00003008267],"category_scores_gemma":[0.000088811685,0.0009062825,0.00030564668,0.00023815034,0.00011241295,0.00001104765,0.0018536827,0.00076078635,0.00008716727],"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":[0.00003577027,0.00018325109,0.16540824,0.0002364082,0.00014267968,0.000049105383,0.000006537105,0.00022044522,0.8336689,0.000004023908,0.000035875477,0.000008749055],"study_design_scores_gemma":[0.00097439735,0.00018035504,0.31791526,0.00028031337,0.000048835325,3.0674715e-7,0.0000024557048,0.00033899845,0.6764073,5.567925e-7,0.0030301001,0.00082114164],"about_ca_topic_score_codex":0.00018506449,"about_ca_topic_score_gemma":0.000011395627,"teacher_disagreement_score":0.15726165,"about_ca_system_score_codex":0.00010584753,"about_ca_system_score_gemma":0.0004848996,"threshold_uncertainty_score":0.9993388},"labels":[],"label_agreement":null},{"id":"W2968123855","doi":"10.1186/s13072-019-0295-4","title":"ZFP57 regulation of transposable elements and gene expression within and beyond imprinted domains","year":2019,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":67,"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":"Biotechnology and Biological Sciences Research Council; Medical Research Council; Wellcome Trust; Wellcome","keywords":"Biology; DNA methylation; Genomic imprinting; Genetics; Transposable element; Chromatin; Differentially methylated regions; Epigenetics; RNA-Directed DNA Methylation; Epigenomics; Regulation of gene expression; Epigenetics of physical exercise; Gene; Genome; Gene expression","score_opus":0.004894203272541832,"score_gpt":0.21827363984481293,"score_spread":0.2133794365722711,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2968123855","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970958,0.00076204614,0.0011269281,0.000024198567,0.00009497901,0.00030605908,0.000014916811,0.000007738636,0.0005672886],"genre_scores_gemma":[0.9629774,0.00022661606,0.03629152,0.00003308223,0.000035362646,0.0000074193836,0.00005744238,0.000025511681,0.00034565642],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988707,0.00004720711,0.00038927913,0.00034641413,0.00014726337,0.00019919284],"domain_scores_gemma":[0.999347,0.000012033542,0.00018795808,0.00032071758,0.00005420822,0.00007812116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021283292,0.00016029298,0.0001930923,0.000043261727,0.000052220563,0.000018931043,0.000099172205,0.00012789792,0.00004321823],"category_scores_gemma":[0.000023539735,0.00015585446,0.00003825615,0.00005937558,0.00006568324,0.000004406673,0.00011876906,0.000052083946,0.0000030203964],"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":[0.000010674394,0.000026041387,0.06697577,0.00007238369,0.000024721196,1.8442863e-7,0.00018278378,0.000074742486,0.9313835,0.000036986323,0.000018625296,0.0011935993],"study_design_scores_gemma":[0.000818193,0.0003223554,0.13216582,0.000041529813,0.000017884839,0.000013524948,0.00011214847,0.0012566352,0.86461663,0.00013548779,0.0003410394,0.0001587401],"about_ca_topic_score_codex":0.000007188253,"about_ca_topic_score_gemma":0.000006682811,"teacher_disagreement_score":0.066766836,"about_ca_system_score_codex":0.000006022538,"about_ca_system_score_gemma":0.000028015167,"threshold_uncertainty_score":0.63555604},"labels":[],"label_agreement":null},{"id":"W2969359780","doi":"10.1093/biolre/ioz168","title":"Resiliency of equid H19 imprint to somatic cell reprogramming by oocyte nuclear transfer and genetically induced pluripotency†","year":2019,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Reprogramming; Somatic cell nuclear transfer; Biology; Genomic imprinting; Imprinting (psychology); Epigenetics; Induced pluripotent stem cell; DNA methylation; Somatic cell; Genetics; Embryonic stem cell; Differentially methylated regions; Cell biology; Methylation; Embryo; Gene; Gene expression; Blastocyst; Embryogenesis","score_opus":0.0069012412677957975,"score_gpt":0.22639805056229148,"score_spread":0.2194968092944957,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2969359780","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966312,0.001617601,0.00078758074,0.00015099214,0.00020019228,0.00037787794,0.0000035780058,0.000009701745,0.00022128636],"genre_scores_gemma":[0.9950539,0.00028134478,0.0044079716,0.000018529563,0.000057062956,0.000007235572,0.000012212174,0.000018399516,0.00014335554],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985974,0.000061366874,0.0003791963,0.00067232456,0.0000738879,0.0002158511],"domain_scores_gemma":[0.9991371,0.000006649116,0.00009515421,0.00060465443,0.000095516516,0.000060929542],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034917615,0.0001321047,0.00023777559,0.000054848617,0.0000304449,0.0000052101036,0.00013605611,0.00017584083,0.000020839785],"category_scores_gemma":[0.00010037878,0.00012614402,0.00006574063,0.000088073386,0.000081761056,0.0000031760121,0.000117923235,0.0000655535,0.0000070186666],"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":[0.000042331976,0.00005240865,0.006734207,0.000080539634,0.000021949962,7.0137254e-8,0.00011179279,0.000008044556,0.9502374,0.000026359625,0.000020419035,0.042664472],"study_design_scores_gemma":[0.00035779737,0.0017197593,0.023717895,0.000018326638,0.000016502208,0.000023807448,0.00014665318,0.000018528694,0.9687963,0.000051861156,0.00498571,0.00014686286],"about_ca_topic_score_codex":0.00005561769,"about_ca_topic_score_gemma":0.0000013330961,"teacher_disagreement_score":0.04251761,"about_ca_system_score_codex":0.000006662522,"about_ca_system_score_gemma":0.000028317221,"threshold_uncertainty_score":0.5144004},"labels":[],"label_agreement":null},{"id":"W2972063248","doi":"10.1016/j.stem.2019.06.013","title":"Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells","year":2019,"lang":"en","type":"article","venue":"Cell stem cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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":"Azrieli Foundation; Israel Science Foundation; United States-Israel Binational Science Foundation; New York State Stem Cell Science","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Epigenetics; Embryonic stem cell; Induced pluripotent stem cell; Genetics; Reprogramming; X-inactivation; DNA methylation; Gene; Gene expression; X chromosome","score_opus":0.007473356786152542,"score_gpt":0.2000458829801031,"score_spread":0.19257252619395054,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2972063248","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99364007,0.005169797,0.00009469312,0.000004654085,0.00012230735,0.0003640306,0.000010621986,0.000009604279,0.00058422494],"genre_scores_gemma":[0.9981001,0.0002288368,0.000105425024,0.000014483998,0.000039746217,0.000007757877,0.00002180384,0.000037284666,0.0014445566],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986607,0.00007906847,0.00031604263,0.0005091006,0.00013381691,0.00030128149],"domain_scores_gemma":[0.99921703,0.000026561836,0.0002369472,0.0003632135,0.000050055794,0.00010618784],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015225331,0.00023614676,0.00026819788,0.000053499905,0.00008619592,0.000043821565,0.00014561186,0.00016525063,0.000026090116],"category_scores_gemma":[0.0000013912379,0.00022518984,0.00007777246,0.00006225891,0.00006235911,0.0000033258877,0.00023053604,0.00008808944,0.000008443184],"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":[0.000005151603,0.0000409118,0.05601779,0.00033304913,0.000018131144,4.562891e-7,0.000084391104,0.000054374636,0.9403462,0.0000029006496,0.0000124277,0.003084244],"study_design_scores_gemma":[0.00089170993,0.00042321198,0.07147279,0.000036800935,0.000049877002,0.0000052044,0.00020724596,0.00046353808,0.9258552,0.000007944099,0.00032670176,0.00025975492],"about_ca_topic_score_codex":0.000010877443,"about_ca_topic_score_gemma":0.000005421772,"teacher_disagreement_score":0.015454999,"about_ca_system_score_codex":0.0000062873314,"about_ca_system_score_gemma":0.000022812603,"threshold_uncertainty_score":0.91829747},"labels":[],"label_agreement":null},{"id":"W2978823510","doi":"10.1038/s41436-019-0657-0","title":"Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency","year":2019,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; McGill University; SickKids Foundation; Dalhousie University; University of Toronto; Montreal Children's Hospital; Izaak Walton Killam Health Centre","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; Center for Individualized Medicine, Mayo Clinic; Institut National de la Santé et de la Recherche Médicale; Assistance Publique - Hôpitaux de Paris; National Institute for Health and Care Research; Cleveland Clinic; Wellcome Trust; Assistance publique-Hôpitaux de Paris; Agence Nationale de la Recherche","keywords":"Haploinsufficiency; Missense mutation; Genetics; Transactivation; Biology; Phenotype; Transcription factor; Bioinformatics; Gene","score_opus":0.010466189557652297,"score_gpt":0.27111945980091945,"score_spread":0.2606532702432672,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2978823510","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99665326,0.0013136024,0.0005069877,0.00047231663,0.00047651585,0.00039537775,0.0000029777457,0.0000027864503,0.00017620609],"genre_scores_gemma":[0.9966958,0.00040120413,0.0023815082,0.00029539116,0.00005422391,0.000004720038,0.000003050385,0.00002283799,0.0001412507],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983272,0.00008740572,0.00064929697,0.00039642083,0.00027626895,0.0002634089],"domain_scores_gemma":[0.99918324,0.000037472062,0.00016296282,0.00048195585,0.00005471727,0.00007967565],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003979624,0.00016087834,0.00036293277,0.00008282234,0.00002440831,0.000004606726,0.00038541504,0.000106280975,0.000034200337],"category_scores_gemma":[0.0001986283,0.000120429155,0.000062237894,0.00022160282,0.00021633522,0.0000013457313,0.0005244193,0.00012485658,0.0000033643787],"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":[0.000014450096,0.00008095217,0.90993905,0.000053353306,0.000031931584,0.00000495285,0.00023897462,0.0003444656,0.08225112,0.000011199166,0.00006344929,0.006966135],"study_design_scores_gemma":[0.0009840506,0.0010246708,0.9901816,0.0001322844,0.000021578266,0.00015204964,0.00020629153,0.00023967488,0.006266227,0.00005443304,0.0006022633,0.00013482677],"about_ca_topic_score_codex":0.000058433172,"about_ca_topic_score_gemma":0.00007465313,"teacher_disagreement_score":0.08024263,"about_ca_system_score_codex":0.000006876069,"about_ca_system_score_gemma":0.000076961966,"threshold_uncertainty_score":0.49109584},"labels":[],"label_agreement":null},{"id":"W2982377894","doi":"10.1186/s13059-019-1833-x","title":"Endogenous retroviral insertions drive non-canonical imprinting in extra-embryonic tissues","year":2019,"lang":"en","type":"article","venue":"Genome biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":96,"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":"European Research Council; Medical Research Council; Fondazione Pierfranco e Luisa Mariani; Bundesministerium für Bildung und Forschung; E-Rare; Agence Nationale de la Recherche; Biotechnology and Biological Sciences Research Council; Ministero della Salute","keywords":"Biology; Endogenous retrovirus; Imprinting (psychology); Embryonic stem cell; Genomic imprinting; Genetics; Computational biology; Human genetics; Endogeny; Evolutionary biology; Cell biology; Genome; Gene; DNA methylation; Gene expression","score_opus":0.014500278220783753,"score_gpt":0.24514050205476504,"score_spread":0.23064022383398128,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2982377894","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99352276,0.0011636381,0.0002635531,0.00010366294,0.00034039537,0.00032014895,0.0000101685055,0.000014565118,0.004261107],"genre_scores_gemma":[0.9973358,0.00022813077,0.0010748445,0.00017398594,0.00020703136,0.000028657289,0.0001026787,0.00002967116,0.00081920275],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9983122,0.00008499421,0.000337101,0.0005975221,0.00006169408,0.00060653116],"domain_scores_gemma":[0.99925524,0.000018464663,0.000104785395,0.000489955,0.000045685076,0.00008587837],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024051503,0.00020810137,0.000286054,0.000099595796,0.000061930325,0.000018447305,0.00033082755,0.00030011008,0.00014717372],"category_scores_gemma":[0.00005716111,0.00020621225,0.000116672025,0.0001342899,0.0000838522,0.000003592824,0.00032497768,0.00018777962,0.00025155395],"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":[0.000008735418,0.000033598546,0.12780045,0.000011512484,0.000027769645,0.0000026866771,0.00006633796,0.00003398247,0.8697997,0.00010606506,0.000009738489,0.0020994528],"study_design_scores_gemma":[0.0026587022,0.002541556,0.76785445,0.00003495148,0.00003186819,0.0003840937,0.0005115856,0.00018700844,0.14394315,0.00035236188,0.08043092,0.0010693555],"about_ca_topic_score_codex":0.00012344898,"about_ca_topic_score_gemma":0.000070584174,"teacher_disagreement_score":0.72585654,"about_ca_system_score_codex":0.000038415325,"about_ca_system_score_gemma":0.00013062784,"threshold_uncertainty_score":0.8409091},"labels":[],"label_agreement":null},{"id":"W2983259024","doi":"10.1002/ajmg.c.31754","title":"PRC2‐complex related dysfunction in overgrowth syndromes: A review of <i>EZH2</i>, <i>EED</i>, and <i>SUZ12</i> and their syndromic phenotypes","year":2019,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":77,"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; University of British Columbia","funders":"Canadian Institutes of Health Research; BC Children's Hospital","keywords":"Phenotype; Medicine; EZH2; PRC2; Genetics; Biology; Epigenetics","score_opus":0.021459204881092188,"score_gpt":0.308190557840712,"score_spread":0.28673135295961977,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2983259024","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.05714274,0.94112504,0.00010630628,0.00035620463,0.00053898105,0.0006123014,0.000027009994,0.0000050438944,0.00008637546],"genre_scores_gemma":[0.0059649944,0.99162084,0.0012432586,0.0007132697,0.00020809313,0.000021405145,0.00007475419,0.000117304364,0.0000360568],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99234396,0.0008995806,0.0034444826,0.00086181937,0.0017098307,0.00074030546],"domain_scores_gemma":[0.9957095,0.00045762167,0.0020955312,0.0007120335,0.00019016815,0.0008351863],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0036923157,0.0008130785,0.003702789,0.00040283808,0.00004109385,0.000027449205,0.001150913,0.0009797262,0.00014885576],"category_scores_gemma":[0.0016765798,0.00064722676,0.00048253706,0.00081422646,0.0012752059,0.00000781363,0.0008274609,0.0014606887,0.00000408833],"study_design_candidate":"design_other","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":[0.000022127622,0.00023375837,0.000908386,0.017030615,0.00034195534,0.000102304,0.00010597155,0.0000066776256,0.00011260356,0.0000049564424,0.0011535956,0.9799771],"study_design_scores_gemma":[0.0019302202,0.004545422,0.00057120796,0.17329353,0.0006802075,0.01043276,0.00032125483,0.00028025833,0.000053267926,0.000057360146,0.8068408,0.0009937375],"about_ca_topic_score_codex":0.000018304576,"about_ca_topic_score_gemma":0.000012631438,"teacher_disagreement_score":0.9789833,"about_ca_system_score_codex":0.00006748523,"about_ca_system_score_gemma":0.0015646283,"threshold_uncertainty_score":0.9995979},"labels":[],"label_agreement":null},{"id":"W2987490438","doi":"10.1111/gtc.12736","title":"Characterization of genetic‐origin‐dependent monoallelic expression in mouse embryonic stem cells","year":2019,"lang":"en","type":"article","venue":"Genes to Cells","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Japan Society for the Promotion of Science; Takeda Medical Research Foundation","keywords":"Biology; Epigenetics; Embryonic stem cell; Genetics; Genomic imprinting; Retrotransposon; Gene; Allele; Induced pluripotent stem cell; X-inactivation; DNA methylation; Gene expression; X chromosome; Transposable element; Genome","score_opus":0.008496817429384778,"score_gpt":0.216265221183739,"score_spread":0.20776840375435424,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2987490438","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99745363,0.000255402,0.0012992516,0.000017917535,0.00035740173,0.0004692611,0.00001843294,0.0000073468673,0.000121346035],"genre_scores_gemma":[0.9921801,0.00049424253,0.001331197,0.00007899249,0.00007675441,0.000021492557,0.000024549126,0.000033477223,0.005759199],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99873555,0.000053414347,0.0003306039,0.00042924625,0.00015964874,0.00029153842],"domain_scores_gemma":[0.99922997,0.000005270153,0.00013017323,0.0004931719,0.00005369813,0.00008770872],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012005649,0.00017291281,0.00020884194,0.0000850458,0.00001968527,0.000019280425,0.00025605576,0.0001414149,0.000061885745],"category_scores_gemma":[0.0000018700973,0.00017347856,0.00007046556,0.00009405426,0.000011822426,0.0000041165,0.00021528245,0.00005254519,0.00013309882],"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":[0.00001433262,0.000047558104,0.008330541,0.000048726535,0.000009270889,7.440077e-7,0.00007417329,0.0021511558,0.9842962,7.542705e-7,0.00002754672,0.004999005],"study_design_scores_gemma":[0.0003987265,0.00021367011,0.011642845,0.000025879628,0.000004491254,0.0000028072975,0.00006577207,0.00012901051,0.98039836,9.80728e-7,0.006922842,0.00019463935],"about_ca_topic_score_codex":0.000018223116,"about_ca_topic_score_gemma":0.000008957862,"teacher_disagreement_score":0.0068952953,"about_ca_system_score_codex":0.000016022428,"about_ca_system_score_gemma":0.000045814148,"threshold_uncertainty_score":0.70742506},"labels":[],"label_agreement":null},{"id":"W2989504433","doi":"10.1139/cjas-2018-0253","title":"Analysis of porcine <i>OSBPL5</i> gene allelic expression in skeletal muscle and association of a single-nucleotide polymorphism in the coding region with production traits","year":2019,"lang":"en","type":"article","venue":"Canadian Journal of Animal Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Biology; Single-nucleotide polymorphism; Genotype; Allele; SNP; Genetics; Imprinting (psychology); Gene; Genomic imprinting; Coding region; Gene expression; Molecular biology; DNA methylation","score_opus":0.010079440442688062,"score_gpt":0.2072850765852229,"score_spread":0.19720563614253483,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2989504433","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99940634,0.00018721331,0.000022748292,0.00023815938,0.00002866483,0.00006004534,0.0000010547376,1.9245314e-7,0.00005558598],"genre_scores_gemma":[0.999715,0.000023729097,0.00020240131,0.000026022602,0.000021876092,2.9252232e-7,6.988809e-7,0.000002476844,0.000007509901],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993256,0.000034552697,0.0002059429,0.00012402458,0.00015868887,0.00015121375],"domain_scores_gemma":[0.9994817,0.000007795777,0.00026926937,0.00007283553,0.00010320629,0.00006521134],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007131051,0.000047259207,0.00012276208,0.00025667358,0.00002914501,0.000013184066,0.00013259123,0.00003085153,0.0000021660767],"category_scores_gemma":[0.00010793855,0.000034456232,0.000030456576,0.00055472227,0.00007593754,0.000016210626,0.000011405989,0.000053183678,3.880772e-8],"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":[0.0000055021433,0.00000858184,0.18075281,0.0000036923884,0.000007753132,0.0000019612646,0.00029055664,0.00013688236,0.8182146,0.0000020566843,0.0000039878623,0.0005716384],"study_design_scores_gemma":[0.00018825373,0.00050285563,0.9295164,0.000045900873,0.000022779324,0.000039245748,0.0003949642,0.000076320444,0.06912077,0.00000185816,0.00005008786,0.000040594972],"about_ca_topic_score_codex":0.00055480184,"about_ca_topic_score_gemma":0.0033003695,"teacher_disagreement_score":0.7490938,"about_ca_system_score_codex":0.000039872535,"about_ca_system_score_gemma":0.00021729522,"threshold_uncertainty_score":0.18416837},"labels":[],"label_agreement":null},{"id":"W2990673862","doi":"10.6000/2292-2598.2019.07.04.4","title":"Outstretched Index Finger - A Pointer is Peculiar Behaviour Characteristic of Angelman Syndrome in Adults – A Case Series Study","year":2019,"lang":"en","type":"article","venue":"Journal of Intellectual Disability - Diagnosis and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Angelman syndrome; Pointer (user interface); Index (typography); Psychology; Series (stratigraphy); Index finger; Audiology; Computer science; Medicine; Artificial intelligence; Geology; Anatomy; World Wide Web","score_opus":0.013684549450089727,"score_gpt":0.2602945599648094,"score_spread":0.24661001051471965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2990673862","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988252,0.00033710367,0.0000031653567,0.00020035531,0.00010071642,0.00048371434,0.000026920254,0.0000017801888,0.00002105914],"genre_scores_gemma":[0.9994249,0.00035269238,0.000050459093,0.00002359539,0.000027605016,0.000035602792,0.000004490191,0.000015515612,0.00006513495],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99860936,0.000098385266,0.00064683397,0.00030593883,0.00014257645,0.0001969088],"domain_scores_gemma":[0.9991846,0.000088184555,0.0002484933,0.00027410293,0.0001062081,0.00009840002],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019353144,0.00022530426,0.00048284492,0.00006920831,0.000025964842,0.000026319152,0.000098505996,0.00009171421,0.0004360573],"category_scores_gemma":[0.00019183713,0.00016983543,0.00019799198,0.0000865061,0.00009576907,0.000013117111,0.00009450187,0.00009616545,0.0000037872244],"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":[0.0002455816,0.002854341,0.9846908,0.000051680694,0.00020637808,0.00018246738,0.0072378204,0.0000030744438,0.00038686438,2.5878737e-7,0.00003897598,0.0041017462],"study_design_scores_gemma":[0.0028168454,0.012621077,0.9655178,0.00018776786,0.00011125362,0.003322027,0.011178006,0.000031875632,0.0039215744,0.000009086919,0.00009139538,0.00019125533],"about_ca_topic_score_codex":0.00044542082,"about_ca_topic_score_gemma":0.00045674542,"teacher_disagreement_score":0.019172976,"about_ca_system_score_codex":0.00006606367,"about_ca_system_score_gemma":0.000038709397,"threshold_uncertainty_score":0.6925688},"labels":[],"label_agreement":null},{"id":"W2991788166","doi":"","title":"Characterizing the phenotypic spectrum of Peters anomaly: from mild to severe disease","year":2015,"lang":"en","type":"article","venue":"Investigative Ophthalmology & Visual Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"","keywords":"Anomaly (physics); Spectrum (functional analysis); Phenotype; Disease; Clinical phenotype; Medicine; Genetics; Biology; Internal medicine; Physics; Gene","score_opus":0.038259411159624904,"score_gpt":0.303362438156321,"score_spread":0.26510302699669613,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2991788166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977481,0.00012531268,0.000014592154,0.0010733648,0.00028411348,0.00020433191,0.000019672043,0.0000061020633,0.0005244294],"genre_scores_gemma":[0.99798024,0.0000019279462,0.0011215791,0.0006207026,0.00012304218,0.000016639671,0.000013192683,0.000012186612,0.00011050974],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99849653,0.000110386936,0.0002202068,0.0005336157,0.00025741284,0.0003818609],"domain_scores_gemma":[0.9988866,0.000027278345,0.00013536449,0.00037428518,0.00011884792,0.00045766597],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043791073,0.00016443263,0.00016590317,0.00005677617,0.00015024544,0.00003326042,0.0006223179,0.000054687614,0.00002657449],"category_scores_gemma":[0.0005908536,0.00012610188,0.000053718188,0.00035222326,0.0012186848,0.000012826605,0.00051217765,0.00008797352,0.000026527168],"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":[0.000021836697,0.000026284499,0.111747496,0.0000028094412,0.000013582649,0.0000061361943,0.00048546077,0.00003464011,0.88751674,0.000021192298,0.00003336077,0.00009044791],"study_design_scores_gemma":[0.00016284044,0.00038239406,0.5501616,0.000018368866,0.000010954394,0.00003378366,0.0003482624,0.00007227948,0.44767144,0.0008333888,0.00016036684,0.00014432435],"about_ca_topic_score_codex":0.00020789824,"about_ca_topic_score_gemma":0.0000044068165,"teacher_disagreement_score":0.4398453,"about_ca_system_score_codex":0.000026570102,"about_ca_system_score_gemma":0.00040263787,"threshold_uncertainty_score":0.5142285},"labels":[],"label_agreement":null},{"id":"W2996944597","doi":"10.1111/obr.12992","title":"Current and emerging therapies for managing hyperphagia and obesity in Prader‐Willi syndrome: A narrative review","year":2019,"lang":"en","type":"review","venue":"Obesity Reviews","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":89,"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":"Millendo Therapeutics","keywords":"Medicine; Appetite; Weight gain; Weight loss; Obesity; Narrative review; Clinical trial; Intensive care medicine; Pediatrics; Internal medicine; Body weight","score_opus":0.04305196452338748,"score_gpt":0.34376366903967015,"score_spread":0.30071170451628265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2996944597","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0014557226,0.9936921,0.000103171245,0.00007195923,0.00021309874,0.004379053,0.000019599975,0.00000797554,0.000057313253],"genre_scores_gemma":[0.000052790674,0.99808645,0.0008336339,0.00012190917,0.00007458435,0.00040441027,0.00013736398,0.00005405622,0.00023481717],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99715596,0.00040973327,0.0009241919,0.0009683291,0.00011863503,0.00042317252],"domain_scores_gemma":[0.99862796,0.000048641254,0.00058289245,0.0005863254,0.000048619797,0.00010553666],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0011907412,0.0006207353,0.0025465272,0.00010019296,0.00012894448,0.000054130018,0.00028566926,0.00022701349,0.000014973395],"category_scores_gemma":[0.00019197872,0.00049423066,0.00044948273,0.00019546984,0.00007211907,0.000010417618,0.00035806868,0.00029484063,0.000013820727],"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":[2.611939e-7,0.000039025992,0.0007240752,0.13687892,0.00007798921,6.4932345e-7,0.000084329564,3.9840266e-8,0.000005828865,0.000014449179,0.0006130747,0.86156136],"study_design_scores_gemma":[0.00019739172,0.00010814411,0.0006932425,0.066491224,0.00050432316,0.00020982901,0.000029688346,0.000003455958,6.874765e-7,0.000025000349,0.9312341,0.00050286856],"about_ca_topic_score_codex":0.0000071966956,"about_ca_topic_score_gemma":0.000011827466,"teacher_disagreement_score":0.9306211,"about_ca_system_score_codex":0.000031157768,"about_ca_system_score_gemma":0.000091070535,"threshold_uncertainty_score":0.9997509},"labels":[],"label_agreement":null},{"id":"W2997229123","doi":"10.1002/wsbm.1476","title":"The evolution of genomic imprinting: Epigenetic control of mammary gland development and postnatal resource control","year":2019,"lang":"en","type":"review","venue":"WIREs Systems Biology and Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Medical Research Council; Medical Research Council Canada; Federation of European Biochemical Societies","keywords":"Genomic imprinting; Imprinting (psychology); Offspring; Biology; Epigenetics; Lactation; DNA methylation; Pregnancy; Endocrinology; Genetics; Gene; Gene expression","score_opus":0.012919201667696521,"score_gpt":0.26518524002958843,"score_spread":0.25226603836189193,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2997229123","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.021651851,0.97550595,0.0015545172,0.000030293071,0.0003136108,0.00080023735,0.00002583519,0.0000036099718,0.00011410355],"genre_scores_gemma":[0.33560377,0.66391546,0.000031424555,0.000009064655,0.0001699227,0.00003070424,0.000051429473,0.000016241327,0.00017196874],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99809575,0.0002988727,0.0008676519,0.0003953345,0.00008060787,0.0002617556],"domain_scores_gemma":[0.99856377,0.00018955038,0.0007144847,0.00038397874,0.000076903394,0.0000713369],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086410483,0.00028151117,0.0011976588,0.0000820297,0.0000943911,0.0000062882273,0.0002381663,0.0003993947,9.560488e-7],"category_scores_gemma":[0.00012908755,0.00016703401,0.00009099409,0.000044572935,0.0003839958,0.0000012710051,0.0001567462,0.00012591877,9.216669e-7],"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":[0.000103063496,0.00004061805,0.008159245,0.021939836,0.0023001912,0.000004481039,0.0001970898,0.000008331177,0.04224063,0.001603453,0.00014824474,0.9232548],"study_design_scores_gemma":[0.0019499596,0.0008032956,0.004952519,0.0030977232,0.0005175836,0.0005613439,0.00021431118,0.000059613707,0.000076558055,0.000007381068,0.9874852,0.00027456207],"about_ca_topic_score_codex":0.00010544044,"about_ca_topic_score_gemma":0.0000060767934,"teacher_disagreement_score":0.98733693,"about_ca_system_score_codex":0.00002016951,"about_ca_system_score_gemma":0.00022677853,"threshold_uncertainty_score":0.68114495},"labels":[],"label_agreement":null},{"id":"W2997372936","doi":"10.1558/jmbs.v1i2.11878","title":"Grammatical Gender in Atypical Language Development","year":2019,"lang":"en","type":"article","venue":"Journal of Monolingual and Bilingual Speech","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Neuroscience of multilingualism; Linguistics; Psychology; Grammatical gender; Noun; Sentence; Task (project management); Population; Preference; Typically developing; Developmental psychology; Sociology; Mathematics","score_opus":0.011580703515498798,"score_gpt":0.2640288862382522,"score_spread":0.25244818272275343,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2997372936","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99841356,0.00094707904,0.00008599279,0.000029420315,0.00017750135,0.00008164044,4.5938455e-7,0.0000023512102,0.0002619649],"genre_scores_gemma":[0.9903946,0.0000588543,0.009035375,0.000071777904,0.00022740196,4.1643713e-7,0.0000025605755,0.000011241023,0.00019776539],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989906,0.00003199015,0.00043163556,0.0001649983,0.00016896393,0.00021183296],"domain_scores_gemma":[0.99959224,0.000017685647,0.00012241956,0.000107196975,0.00006836026,0.00009206951],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004339802,0.00011533311,0.00020669459,0.00007705572,0.000020255324,0.000022590337,0.00012022785,0.00011716312,0.000027297709],"category_scores_gemma":[0.00012622404,0.00008948156,0.00006249357,0.00006239443,0.00002554293,0.0000036425993,0.00010256113,0.00017110274,0.000008676184],"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":[0.00018370236,0.0002187451,0.13000363,0.00009135572,0.00008845776,0.00011154303,0.0034935863,0.00007173492,0.70441616,0.00003623575,0.000031481577,0.16125336],"study_design_scores_gemma":[0.0035214273,0.0011789353,0.27389458,0.00013783047,0.000033921526,0.002765461,0.0037659237,0.00026115592,0.70241094,0.00044092312,0.010984284,0.0006046518],"about_ca_topic_score_codex":0.0000061788787,"about_ca_topic_score_gemma":0.00001222912,"teacher_disagreement_score":0.16064872,"about_ca_system_score_codex":0.000013338613,"about_ca_system_score_gemma":0.00015924667,"threshold_uncertainty_score":0.3648952},"labels":[],"label_agreement":null},{"id":"W3000225091","doi":"10.1038/s41420-019-0235-x","title":"BORIS/CTCFL promotes a switch from a proliferative towards an invasive phenotype in melanoma cells","year":2020,"lang":"en","type":"article","venue":"Cell Death Discovery","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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; Jewish General Hospital","funders":"Canadian Institutes of Health Research; McGill University; Israel Cancer Research Fund","keywords":"Reprogramming; Melanoma; Phenotype; Biology; Phenotypic switching; Cancer research; Transcriptome; Regulator; Cell biology; Gene expression; Genetics; Cell; Gene","score_opus":0.016438551772940478,"score_gpt":0.23310696395937022,"score_spread":0.21666841218642974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3000225091","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9960063,0.00066394993,0.0008868135,0.00016342454,0.00012582279,0.00039957577,0.00006522781,0.00001390858,0.0016749951],"genre_scores_gemma":[0.99676985,0.00010295915,0.0016787446,0.0006205336,0.00032740063,0.000039924587,0.00020130488,0.000038802722,0.00022045875],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99851555,0.000084453124,0.00027103277,0.00064808404,0.00014625011,0.0003346102],"domain_scores_gemma":[0.99935776,0.000014639968,0.000096549804,0.00032088102,0.000047736314,0.00016240742],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007470036,0.00024906278,0.00025565075,0.000027890545,0.000049569942,0.00011054784,0.00027784336,0.00015497059,0.00003807287],"category_scores_gemma":[0.000071397204,0.00023030848,0.000089463734,0.00010975732,0.000033543,0.000022482534,0.0002234029,0.00014335505,0.000030499594],"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":[0.0000454828,0.00014263194,0.033033933,0.000043766326,0.00003356629,0.000018874536,0.0012724965,0.00008176749,0.96437037,0.0000149895295,0.0001486422,0.0007934949],"study_design_scores_gemma":[0.0008351691,0.0007471698,0.043720216,0.00002851778,0.00002601343,0.0000027810522,0.0006835398,0.00033699753,0.95224315,0.000183763,0.00083365926,0.00035902386],"about_ca_topic_score_codex":0.00026951692,"about_ca_topic_score_gemma":0.00008240145,"teacher_disagreement_score":0.012127204,"about_ca_system_score_codex":0.000017380373,"about_ca_system_score_gemma":0.0002572829,"threshold_uncertainty_score":0.93917066},"labels":[],"label_agreement":null},{"id":"W3001089571","doi":"10.1038/s41398-020-0720-2","title":"Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome","year":2020,"lang":"en","type":"article","venue":"Translational Psychiatry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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; Toronto Centre for Phenogenomics; Hospital for Sick Children","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; National Institute of Neurological Disorders and Stroke; Foundation for Angelman Syndrome Therapeutics","keywords":"UBE3A; Angelman syndrome; Microcephaly; Intellectual disability; Ataxia; Neurodevelopmental disorder; Ubiquitin ligase; Genetics; Biology; Neuroscience; Psychology; Ubiquitin; Gene","score_opus":0.018486156859936896,"score_gpt":0.2455962153933495,"score_spread":0.2271100585334126,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3001089571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9793546,0.0005028663,0.016759833,0.0027222624,0.00005769167,0.00034369197,0.000117652904,0.0000071389723,0.00013423164],"genre_scores_gemma":[0.9693177,0.000011017246,0.03024418,0.00014290075,0.00004878508,0.000019308256,0.00016806087,0.000020537991,0.000027545315],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9987247,0.000039166298,0.00053503073,0.00029202236,0.00024295921,0.00016613194],"domain_scores_gemma":[0.99957424,0.000008187066,0.0001367856,0.00014492765,0.00006548155,0.000070365575],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012833906,0.0001567209,0.00025051113,0.000067233814,0.000024774181,0.000004580729,0.00014500707,0.0001313155,0.000039838866],"category_scores_gemma":[0.0000130613535,0.00016388764,0.00016728378,0.00013572974,0.000051755378,0.000007909705,0.000014877401,0.00008802415,0.0000022132135],"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":[0.00013107587,0.00019227594,0.08790084,0.00017620108,0.000056359593,5.4765854e-7,0.00018305653,0.02297791,0.8869779,0.0009218639,0.0000238653,0.0004581225],"study_design_scores_gemma":[0.009731223,0.002031289,0.5739785,0.00027348666,0.00014941425,0.00008592714,0.00022113438,0.07958393,0.32296774,0.009465545,0.00023637933,0.0012754772],"about_ca_topic_score_codex":0.000008544267,"about_ca_topic_score_gemma":0.000037491827,"teacher_disagreement_score":0.56401014,"about_ca_system_score_codex":0.0000027217668,"about_ca_system_score_gemma":0.00017152504,"threshold_uncertainty_score":0.6683144},"labels":[],"label_agreement":null},{"id":"W3001510942","doi":"10.3390/genes11020128","title":"Prader–Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion","year":2020,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Stollery Children's Hospital; University of Saskatchewan; University of Alberta Hospital; University of Alberta","funders":"Canadian Institutes of Health Research; Alberta Innovates; W. Garfield Weston Foundation; BC Children's Hospital","keywords":"Exome sequencing; Phenotype; Genetics; Short stature; Biology; Phenocopy; Locus (genetics); Small nucleolar RNA; Hypotonia; Exome; Gene; Long non-coding RNA; Endocrinology; RNA","score_opus":0.015961166765606563,"score_gpt":0.2368240721635669,"score_spread":0.22086290539796033,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3001510942","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99215007,0.002001089,0.0045281085,0.0009079147,0.00014551,0.00011648243,0.000014305524,0.00002594248,0.000110589426],"genre_scores_gemma":[0.995871,0.00021984748,0.0015432235,0.0014794606,0.0003824391,0.000008290219,0.0002150648,0.000029333576,0.0002513504],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99907047,0.00004525583,0.00015981508,0.0003925733,0.000095420844,0.00023647422],"domain_scores_gemma":[0.9995207,0.0000030086446,0.000049117818,0.00023278104,0.000043030315,0.00015136233],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000055285414,0.00013922532,0.00011818005,0.000010346369,0.00006979309,0.000030400575,0.00016936829,0.00013171742,0.00006165904],"category_scores_gemma":[0.00002447259,0.00013701839,0.000056950325,0.000059598562,0.000036141213,0.0000031445581,0.00009214646,0.000059030226,0.00005320345],"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":[0.0000064960213,0.000028807646,0.0042610574,0.000012858704,0.000022199662,3.9846864e-7,0.000064008564,0.00004470192,0.9781662,0.0000064905107,0.006604767,0.010781973],"study_design_scores_gemma":[0.00070329895,0.00072028436,0.027674355,0.000006073461,0.0000329313,0.00001570069,0.0001762846,0.00076311006,0.4630325,0.000027084481,0.5064197,0.00042865728],"about_ca_topic_score_codex":0.000011473401,"about_ca_topic_score_gemma":0.0000068503837,"teacher_disagreement_score":0.51513374,"about_ca_system_score_codex":0.000004563277,"about_ca_system_score_gemma":0.000032005904,"threshold_uncertainty_score":0.5587447},"labels":[],"label_agreement":null},{"id":"W3003079370","doi":"10.3389/fendo.2019.00940","title":"Why and How Imprinted Genes Drive Fetal Programming","year":2020,"lang":"en","type":"article","venue":"Frontiers in Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":36,"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":"Natural Sciences and Engineering Research Council of Canada; Simon Fraser University","keywords":"Genomic imprinting; Offspring; Intrauterine growth restriction; Biology; Fetus; Disease; Imprinting (psychology); Endocrinology; Internal medicine; Gene; Bioinformatics; Pregnancy; Physiology; Genetics; Gene expression; Medicine; DNA methylation","score_opus":0.0096604366547733,"score_gpt":0.21931681166894307,"score_spread":0.20965637501416978,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3003079370","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9610166,0.004069628,0.029437527,0.0046128966,0.00042502288,0.00023265161,0.0000034623745,0.000024960464,0.00017727744],"genre_scores_gemma":[0.9632117,0.0006647306,0.034816444,0.000990173,0.00015425945,0.000028265258,0.000020579175,0.000022608947,0.0000912285],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.9989118,0.000053417083,0.00012746247,0.00043440293,0.00005639389,0.00041650448],"domain_scores_gemma":[0.9996582,0.0000042458546,0.00005324271,0.00015921198,0.000027200771,0.00009784885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000035254823,0.00015345956,0.00020245141,0.000053175143,0.00004152361,0.000024936277,0.0001628744,0.00010330022,0.0000053655936],"category_scores_gemma":[0.00008272482,0.00015800456,0.000050455743,0.000087228305,0.00013334778,0.0000035988433,0.00026088726,0.00012115077,0.000001579547],"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":[0.00003957498,0.000039182374,0.42701596,0.00005658497,0.00013830727,0.000045394896,0.00024568487,0.000024114417,0.25967655,0.000055971886,0.0076600933,0.30500257],"study_design_scores_gemma":[0.0023239567,0.0010478717,0.04445406,0.00001531037,0.000038690152,0.00032482034,0.002353184,0.001730341,0.13666713,0.00009238679,0.81033087,0.00062138936],"about_ca_topic_score_codex":0.00001543634,"about_ca_topic_score_gemma":0.000013127612,"teacher_disagreement_score":0.8026708,"about_ca_system_score_codex":0.00000775297,"about_ca_system_score_gemma":0.000020024028,"threshold_uncertainty_score":0.64432395},"labels":[],"label_agreement":null},{"id":"W3004450975","doi":"10.1016/j.molcel.2020.01.020","title":"Imprinted Maternally Expressed microRNAs Antagonize Paternally Driven Gene Programs in Neurons","year":2020,"lang":"en","type":"article","venue":"Molecular Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Eye Institute; National Institutes of Health; National Cancer Institute; Fonds de Recherche du Québec - Santé; Natural Sciences and Engineering Research Council of Canada","keywords":"Biology; Genomic imprinting; microRNA; Gene silencing; Genetics; Gene; Regulation of gene expression; Gene expression; Gene cluster; Psychological repression; DNA methylation","score_opus":0.013404715163751761,"score_gpt":0.20686282610414045,"score_spread":0.19345811094038867,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3004450975","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9920025,0.00028909268,0.0063306154,0.00035083716,0.000095874086,0.000328183,0.000008936178,0.000027929167,0.0005660506],"genre_scores_gemma":[0.99344397,0.000084055646,0.0049712993,0.0011056956,0.00007730494,0.000028067056,0.00008575436,0.00006518623,0.00013866214],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9983521,0.000075913435,0.00033761258,0.000613301,0.00016694407,0.00045411277],"domain_scores_gemma":[0.9992671,0.0000026515586,0.00010871973,0.00037587946,0.000054369037,0.00019125684],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000067521294,0.0002563652,0.0002111372,0.000038852606,0.00003337632,0.00007284741,0.0004448697,0.00013763255,0.000028685721],"category_scores_gemma":[0.000022733262,0.0002684964,0.00014502725,0.00012503765,0.000040742103,0.0000033927638,0.00036041762,0.00015356623,0.000045377987],"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":[0.000030568142,0.000086339074,0.024619322,0.00003710392,0.00002299903,0.00013713873,0.00009550455,0.00016908541,0.973196,0.0000015015553,0.00003647635,0.0015679131],"study_design_scores_gemma":[0.0011328328,0.00042737348,0.011272733,0.000015237241,0.000014604558,0.000027787746,0.000034583794,0.00046891658,0.9797903,0.0000076059487,0.006499358,0.0003087252],"about_ca_topic_score_codex":0.000048356593,"about_ca_topic_score_gemma":0.000007293065,"teacher_disagreement_score":0.013346588,"about_ca_system_score_codex":0.00001003865,"about_ca_system_score_gemma":0.00005394565,"threshold_uncertainty_score":0.9999767},"labels":[],"label_agreement":null},{"id":"W3005197391","doi":"10.1016/j.psychres.2020.112858","title":"Does SNORD116 mediate aspects of psychosis in Prader-Willi syndrome? Evidence from a non-clinical population","year":2020,"lang":"en","type":"article","venue":"Psychiatry Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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; Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Epigenetics; Genetics; Locus (genetics); Psychosis; Biology; Autism; Phenotype; Genomic imprinting; Population; Single-nucleotide polymorphism; Haplotype; Gene; Allele; Psychology; Gene expression; DNA methylation; Genotype; Developmental psychology; Medicine; Psychiatry","score_opus":0.08071746153591641,"score_gpt":0.40203637846510015,"score_spread":0.32131891692918374,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3005197391","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99078244,0.0011487462,0.00017985063,0.0066609466,0.0006046739,0.00036502743,0.000014872749,0.000007652228,0.00023577276],"genre_scores_gemma":[0.9949273,0.0010617306,0.0032673161,0.00015021837,0.0004633341,0.000031125724,0.000036402344,0.000027399707,0.000035182806],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9974453,0.00033923163,0.00062149623,0.00069556636,0.0004857512,0.00041266807],"domain_scores_gemma":[0.998922,0.00012460968,0.0001354056,0.00049181265,0.00011801557,0.00020818661],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010086119,0.00015109166,0.0002996759,0.00009525735,0.000059317874,0.000030274805,0.00047578497,0.0002263684,0.00010218278],"category_scores_gemma":[0.0008404003,0.000114632436,0.0001327613,0.00044927697,0.000109565066,0.000009554137,0.00025824556,0.00038132438,0.00003812432],"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":[0.000018624169,0.00011434481,0.97929883,0.000089474655,0.000046776502,0.0000011169692,0.000100571975,0.000018896571,0.017608285,0.000009455271,0.0006849829,0.002008667],"study_design_scores_gemma":[0.0005879622,0.0006987801,0.9956597,0.00021354429,0.000010709195,0.0000036080953,0.00020804754,0.00042223866,0.0009617484,0.0007152121,0.0003632797,0.00015518135],"about_ca_topic_score_codex":0.00087774906,"about_ca_topic_score_gemma":0.0005446182,"teacher_disagreement_score":0.016646536,"about_ca_system_score_codex":0.000011625189,"about_ca_system_score_gemma":0.00014252962,"threshold_uncertainty_score":0.4674575},"labels":[],"label_agreement":null},{"id":"W3006415667","doi":"10.1186/s12863-020-0809-x","title":"The effects of the DNA Demethylating reagent, 5-azacytidine on SMCHD1 genomic localization","year":2020,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"DNA methylation; Biology; Chromatin; Epigenetics; RNA-Directed DNA Methylation; Genomic imprinting; Genetics; Epigenomics; Gene; Methylation; Molecular biology; Gene expression","score_opus":0.01324606570476634,"score_gpt":0.22662208433280492,"score_spread":0.2133760186280386,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3006415667","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9898353,0.0017076832,0.007372917,0.00015522241,0.00027954904,0.00033692285,0.000002663069,0.0000071323825,0.00030257352],"genre_scores_gemma":[0.99786437,0.0004111045,0.00091277866,0.0004293848,0.00022106718,0.000009756674,0.000007069369,0.000028590608,0.00011587702],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989934,0.00011991688,0.00026823295,0.00025127528,0.00015766812,0.00020952291],"domain_scores_gemma":[0.9992102,0.0000705815,0.00017096425,0.00043355313,0.000052184627,0.00006252267],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013305062,0.00013824171,0.00011150153,0.000009402669,0.00018080902,0.000022760973,0.00034894818,0.000086150656,0.00000303048],"category_scores_gemma":[0.00055669085,0.0000909281,0.000113056914,0.000120439894,0.00007330299,7.4840557e-7,0.00026424378,0.000071959636,0.0000061626088],"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":[0.00001170819,0.000019325618,0.025138507,0.00008850093,0.000034720586,1.777772e-7,0.000097402364,0.004150917,0.9648688,0.00005124882,0.00045909645,0.005079606],"study_design_scores_gemma":[0.00045487224,0.0005257763,0.060657986,0.0000289818,0.00004184676,0.0000035115404,0.000076357646,0.004594231,0.9173399,0.000050610553,0.016074851,0.00015107651],"about_ca_topic_score_codex":0.000003729287,"about_ca_topic_score_gemma":0.000009507563,"teacher_disagreement_score":0.047528893,"about_ca_system_score_codex":0.0000080670015,"about_ca_system_score_gemma":0.000063493855,"threshold_uncertainty_score":0.37079403},"labels":[],"label_agreement":null},{"id":"W3010580726","doi":"10.1016/j.physbeh.2020.112864","title":"Disentangling ingestive behavior-related phenotypes in Prader–Willi syndrome: Integrating information from nonclinical studies and clinical trials to better understand the pathophysiology of hyperphagia and obesity","year":2020,"lang":"en","type":"review","venue":"Physiology & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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","funders":"Canadian Institutes of Health Research","keywords":"Obesity; Medicine; Phenotype; Clinical trial; Endocrine system; Bioinformatics; Candidate gene; Animal studies; Gene; Internal medicine; Biology; Genetics; Hormone","score_opus":0.10035659614918822,"score_gpt":0.41738866921887036,"score_spread":0.3170320730696821,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3010580726","genre_codex":"empirical","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6585579,0.34001032,0.00001264117,0.00006941636,0.00024865154,0.0010051631,0.00008774081,0.0000067344445,0.0000014457456],"genre_scores_gemma":[0.26365623,0.7346841,0.0008073463,0.00020866658,0.00013540786,0.00020359425,0.00026779104,0.000034109573,0.0000027645094],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9953629,0.0015041566,0.0020352828,0.0006909161,0.00011267248,0.00029407715],"domain_scores_gemma":[0.99737716,0.0010432246,0.0010063526,0.00036465027,0.00009193975,0.000116702024],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0011143618,0.0004596946,0.002575502,0.00008592025,0.00010214509,0.000023996852,0.00027264238,0.00065889105,0.000006198384],"category_scores_gemma":[0.0017711661,0.00030845543,0.00036674787,0.00016481492,0.0005071036,0.000014470806,0.0007256371,0.0006497312,0.0000049630444],"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":[0.000022670976,0.000174773,0.030836763,0.0006403386,0.00064558134,0.000008676934,0.0007771662,0.0000010865855,0.0023709335,0.000009393672,0.000032491283,0.9644801],"study_design_scores_gemma":[0.003122718,0.0032661888,0.9568741,0.0058102906,0.009277809,0.0001601282,0.0046232888,0.000043702992,0.00013933501,0.00046870104,0.014528563,0.0016852053],"about_ca_topic_score_codex":0.00003421177,"about_ca_topic_score_gemma":0.000020470186,"teacher_disagreement_score":0.9627949,"about_ca_system_score_codex":0.000030648192,"about_ca_system_score_gemma":0.00011651818,"threshold_uncertainty_score":0.99993676},"labels":[],"label_agreement":null},{"id":"W3014418129","doi":"10.1089/biores.2020.0004","title":"Klotho Pathways, Myelination Disorders, Neurodegenerative Diseases, and Epigenetic Drugs","year":2020,"lang":"en","type":"review","venue":"BioResearch open access","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Eye Institute","keywords":"Klotho; Remyelination; Neuroscience; Medicine; Myelin; Disease; Bioinformatics; Central nervous system; Biology; Internal medicine","score_opus":0.09038504095882766,"score_gpt":0.42740823788262605,"score_spread":0.3370231969237984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3014418129","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00054212956,0.99564147,0.00018736112,0.00023422013,0.00016316271,0.0022483352,0.00031228628,0.0000142096405,0.00065681443],"genre_scores_gemma":[0.0017887518,0.9955806,0.00026204681,0.00007909462,0.00037575158,0.00043297355,0.0008749668,0.0001088237,0.00049694785],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.996814,0.00055483484,0.0004992407,0.0012454933,0.00036585357,0.0005205581],"domain_scores_gemma":[0.99851555,0.0000585162,0.00024698462,0.00065799383,0.00011976279,0.0004012093],"candidate_categories":["metaepi_narrow","scholarly_communication"],"consensus_categories":[],"category_scores_codex":[0.00034327523,0.0004878595,0.00088980614,0.00013751956,0.00025648248,0.0014870786,0.002605266,0.00027150277,0.000074376105],"category_scores_gemma":[0.00034606922,0.00041598515,0.00022385216,0.0004064413,0.0001682952,0.00003036271,0.0067816586,0.00030373473,0.000036894173],"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":[0.0000068572535,0.000058715337,0.00019492015,0.001825085,0.00010281522,0.0000044433223,0.00002112135,7.3266074e-7,0.00013371359,0.000052690484,0.0017229116,0.995876],"study_design_scores_gemma":[0.0003088799,0.00023813684,0.0011984751,0.00057075557,0.00012894628,0.000010418868,0.000025684283,0.000033758024,0.00011396011,0.00009093179,0.99677706,0.0005029821],"about_ca_topic_score_codex":0.00010675884,"about_ca_topic_score_gemma":0.000028469416,"teacher_disagreement_score":0.995373,"about_ca_system_score_codex":0.00003349515,"about_ca_system_score_gemma":0.0007396239,"threshold_uncertainty_score":0.9998292},"labels":[],"label_agreement":null},{"id":"W3019737162","doi":"10.1371/journal.pgen.1008709","title":"Placental imprinting: Emerging mechanisms and functions","year":2020,"lang":"en","type":"review","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":81,"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":"Alberta Children's Hospital Research Institute; BC Children's Hospital","keywords":"Placentation; Biology; Imprinting (psychology); Epigenome; Genomic imprinting; Placenta; Trophoblast; Epigenetics; Epigenesis; Pregnancy; Genetics; Bioinformatics; Evolutionary biology; Cell biology; DNA methylation; Gene; Fetus; Gene expression","score_opus":0.029202394456767252,"score_gpt":0.2746002806374351,"score_spread":0.24539788618066782,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3019737162","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00084166514,0.9967674,0.0010007863,0.000025171248,0.00030979942,0.00048437758,0.000047721194,0.000030231506,0.0004928643],"genre_scores_gemma":[0.00039302986,0.99518234,0.003191073,0.000048020436,0.00042088502,0.000053987194,0.00019689,0.00012167509,0.00039212435],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99814993,0.00007251931,0.00047335518,0.00073938665,0.00017723479,0.00038755118],"domain_scores_gemma":[0.99905807,0.000016445592,0.00023426683,0.0004365663,0.00004472007,0.00020995174],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00008073839,0.00046258667,0.00073790556,0.000071112765,0.00013827477,0.000071887414,0.00027939735,0.00036807667,0.00004038275],"category_scores_gemma":[0.00006915952,0.00045046178,0.00028612054,0.0001350603,0.00005174598,0.0000013880677,0.00069237174,0.000255173,0.00006429734],"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":[0.0000015695165,0.000064200074,0.000024861793,0.0033739223,0.0004771637,0.0000058450123,0.000032681215,0.000004068813,0.008544778,0.000033298467,0.00037124357,0.9870664],"study_design_scores_gemma":[0.00015657718,0.00022821593,0.0000031981872,0.00060502754,0.00061046024,0.0001784318,0.00006758742,0.00016918528,0.0015411947,0.000017878792,0.9959266,0.00049565185],"about_ca_topic_score_codex":9.520282e-7,"about_ca_topic_score_gemma":0.0000017484412,"teacher_disagreement_score":0.99555534,"about_ca_system_score_codex":0.000017853503,"about_ca_system_score_gemma":0.00013708009,"threshold_uncertainty_score":0.9997947},"labels":[],"label_agreement":null},{"id":"W3029749726","doi":"10.1111/gbb.12679","title":"Mice lacking paternal expression of imprinted <i>Grb10</i> are risk‐takers","year":2020,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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; Leverhulme Trust; Medical Research Council Canada; Wellcome Trust","keywords":"Task (project management); Reinforcement; Genomic imprinting; Psychology; Developmental psychology; Social psychology; Biology; Genetics; Gene; Gene expression; Economics","score_opus":0.01825033895365077,"score_gpt":0.2499651888315403,"score_spread":0.23171484987788954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3029749726","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970877,0.00066020986,0.0015735031,0.00021977436,0.00014991843,0.00019966239,0.000047263824,0.000019771549,0.000042176165],"genre_scores_gemma":[0.9961001,0.0001428869,0.0029521887,0.00039316877,0.00019990599,0.000025147676,0.000039745933,0.00003767757,0.00010914883],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987189,0.0000780411,0.0003208358,0.00043560384,0.00016694015,0.00027968816],"domain_scores_gemma":[0.99917424,0.000016370308,0.00027349353,0.00030347827,0.00008643834,0.00014596712],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001317123,0.00019080627,0.00020715524,0.00002564464,0.00007302874,0.000021622305,0.000288232,0.00014518958,0.000060297964],"category_scores_gemma":[0.00014570565,0.00018470375,0.0001589736,0.00008897771,0.000053986703,0.0000036723713,0.00027761582,0.00011240426,0.00001353454],"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":[0.00001700501,0.000037723425,0.15790966,0.000020329528,0.000011757537,0.0000035475955,0.00012020836,0.000038543112,0.82671314,3.8638504e-7,0.00037858568,0.014749107],"study_design_scores_gemma":[0.00051245245,0.00020097513,0.1496738,0.000031448824,0.000034925546,0.000016437429,0.0003212228,0.00004118608,0.84230745,0.0000014637243,0.0066579073,0.00020075541],"about_ca_topic_score_codex":0.000047132016,"about_ca_topic_score_gemma":0.0000076212277,"teacher_disagreement_score":0.015594276,"about_ca_system_score_codex":0.000006344325,"about_ca_system_score_gemma":0.00003304961,"threshold_uncertainty_score":0.7532},"labels":[],"label_agreement":null},{"id":"W3030349097","doi":"10.1097/md.0000000000019965","title":"Identification of a novel mutation in pseudohypoparathyroidism type Ia in a Chinese family","year":2020,"lang":"en","type":"article","venue":"Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Artificial Intelligence in Medicine (Canada)","funders":"","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Endocrinology; Internal medicine; Brachydactyly; Parathyroid hormone; Short stature; Hypoparathyroidism; Genetics; Gene; Biology; Calcium","score_opus":0.018241394745705165,"score_gpt":0.29234828736636614,"score_spread":0.27410689262066096,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3030349097","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963617,0.00087537157,0.0015520866,0.0008874558,0.000070067465,0.00010619904,0.0000012246046,0.0000024010465,0.00014354764],"genre_scores_gemma":[0.9993536,0.00007447537,0.00019739823,0.00022703777,0.0000777877,0.0000048037723,0.00002979415,0.0000066435755,0.000028474242],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993914,0.000015515903,0.0002753672,0.00015981188,0.00007744095,0.00008046389],"domain_scores_gemma":[0.99975336,0.000005505906,0.00007319384,0.00010316143,0.00003566127,0.000029126539],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001500256,0.000062019324,0.00011804124,0.000044894812,0.0000058909727,0.0000017906478,0.000073598654,0.00004452014,0.0000041094004],"category_scores_gemma":[0.00030520034,0.00005271445,0.000013989353,0.00025566784,0.00002808724,0.0000016613728,0.000027381762,0.00004310757,0.000002612826],"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":[0.000013950477,0.000028541108,0.015645461,0.000015650077,0.0000031484271,0.0000016464489,0.00043546798,0.00021300197,0.98289794,0.000008198958,0.00010486263,0.0006321505],"study_design_scores_gemma":[0.0023910608,0.0004864568,0.95299476,0.000034256267,0.000007253987,0.000015984115,0.00049546774,0.0069428603,0.036128026,0.000042098512,0.00035565897,0.00010612882],"about_ca_topic_score_codex":0.00007051386,"about_ca_topic_score_gemma":0.000021438384,"teacher_disagreement_score":0.9467699,"about_ca_system_score_codex":0.000004432159,"about_ca_system_score_gemma":0.000021162852,"threshold_uncertainty_score":0.2149633},"labels":[],"label_agreement":null},{"id":"W3035437525","doi":"10.1007/s00439-020-02193-9","title":"The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry","year":2020,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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","funders":"Canadian Institutes of Health Research","keywords":"Interactome; Biology; Protein–protein interaction; Biotinylation; PRC2; Gene; Ubiquitin ligase; Ubiquitin; Genetics; Loss function; Cell biology; Computational biology; Molecular biology; Epigenetics; Phenotype; Histone H3","score_opus":0.027086289820761538,"score_gpt":0.28755874619843247,"score_spread":0.2604724563776709,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3035437525","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9916514,0.0051683844,0.002595064,0.00008655547,0.000092740636,0.0003362047,0.0000064564865,0.0000054151055,0.000057771103],"genre_scores_gemma":[0.99658746,0.00039239207,0.002784162,0.000040535226,0.00012642205,0.000005471906,0.000009933239,0.00001666597,0.00003696868],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99905044,0.00009843011,0.00023938742,0.0002644438,0.00015371596,0.00019359002],"domain_scores_gemma":[0.9994232,0.000049937353,0.0001635195,0.00023520086,0.00006336417,0.00006476498],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017846285,0.00013958024,0.00011711493,0.000023315404,0.0003295654,0.00008098741,0.00016605978,0.00007355109,0.0000031027985],"category_scores_gemma":[0.0001284513,0.00009980677,0.00004011837,0.000081359634,0.00016334509,0.000003894818,0.0002305313,0.00011301123,5.1564103e-7],"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":[0.0000051613033,0.000015923806,0.01414304,0.000107891814,0.000027795904,4.153992e-7,0.00023968247,0.00009526711,0.9839363,0.000024763616,0.0000053447184,0.0013983998],"study_design_scores_gemma":[0.00042042256,0.00067467015,0.041365854,0.000030503083,0.00007300413,0.000009989688,0.00036134684,0.0038867795,0.9529183,0.00006317958,0.00006447205,0.00013149803],"about_ca_topic_score_codex":0.000006344369,"about_ca_topic_score_gemma":0.000007649719,"teacher_disagreement_score":0.031018034,"about_ca_system_score_codex":0.0000084293415,"about_ca_system_score_gemma":0.000030731124,"threshold_uncertainty_score":0.4070002},"labels":[],"label_agreement":null},{"id":"W3041261123","doi":"10.1002/ajmg.a.61740","title":"A novel intronic variant in <scp><i>UBE3A</i></scp> identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome","year":2020,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Children's Hospital of Eastern Ontario; SickKids Foundation; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Angelman syndrome; UBE3A; Genetics; Neurodevelopmental disorder; Biology; RNA splicing; Allele; Genetic testing; Presentation (obstetrics); RNA; Medicine; Gene","score_opus":0.012480952546646067,"score_gpt":0.24690597599017483,"score_spread":0.23442502344352875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3041261123","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99218196,0.00075412216,0.0065036383,0.00031787556,0.00006016381,0.00015332742,0.000009665097,0.0000022664306,0.00001695593],"genre_scores_gemma":[0.9955027,0.0003745291,0.003600892,0.00037774877,0.0000882869,0.000006856377,0.000019926036,0.000024954552,0.000004119892],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9977133,0.00016147459,0.00080334,0.00029924582,0.00068216765,0.00034046543],"domain_scores_gemma":[0.9987499,0.00004876407,0.00050939573,0.00018973228,0.000101838545,0.00040035983],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047416988,0.0001689206,0.00042620418,0.00009116345,0.0000180683,0.000019780795,0.00038269671,0.00010512554,0.000014615101],"category_scores_gemma":[0.0003626795,0.00014721674,0.00007229163,0.00033668723,0.00022115266,0.0000085757065,0.00013294692,0.00030177904,9.607219e-7],"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":[0.00027035663,0.0006916289,0.026905593,0.000112406444,0.00029248468,0.0008002296,0.0052833757,0.007176765,0.937629,0.000014946811,0.0002621283,0.020561075],"study_design_scores_gemma":[0.029534107,0.11516579,0.55763537,0.0020439741,0.0005979495,0.033185728,0.060658257,0.043439567,0.13115247,0.00017596266,0.024452573,0.001958256],"about_ca_topic_score_codex":0.00007883043,"about_ca_topic_score_gemma":0.00007361949,"teacher_disagreement_score":0.80647653,"about_ca_system_score_codex":0.000043071715,"about_ca_system_score_gemma":0.00044611772,"threshold_uncertainty_score":0.60033244},"labels":[],"label_agreement":null},{"id":"W3041895066","doi":"10.1111/cen.14279","title":"Dietary macronutrient regulation of acyl and desacyl ghrelin concentrations in children with Prader‐Willi syndrome (PWS)","year":2020,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta Hospital; University of Alberta","funders":"","keywords":"Internal medicine; Endocrinology; Ghrelin; Orexigenic; Appetite; Medicine; Meal; Insulin; Hormone; Neuropeptide Y receptor; Receptor; Neuropeptide","score_opus":0.027591795270119828,"score_gpt":0.29000655695067773,"score_spread":0.2624147616805579,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3041895066","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973852,0.0007434905,0.00039538898,0.0010755854,0.000048466474,0.0002738023,0.000009170807,0.000008658651,0.00006020322],"genre_scores_gemma":[0.9970827,0.0007094084,0.0016929266,0.00034629033,0.00006586262,0.000011614333,0.0000586539,0.000013144265,0.000019371333],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986891,0.00009716008,0.0004884724,0.00040692266,0.000068645866,0.00024970787],"domain_scores_gemma":[0.99947125,0.00003930109,0.00014281065,0.00020404896,0.00003932289,0.00010327342],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008176934,0.00012215778,0.0002714719,0.000024091285,0.000029871886,0.0000061580395,0.0001215206,0.00012393824,0.00001920165],"category_scores_gemma":[0.00018968777,0.0001094685,0.00005493806,0.000087752225,0.0002665994,0.0000039276533,0.00014178902,0.00015152634,0.0000038075357],"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":[0.000013929902,0.000085843996,0.9773261,0.000013398943,0.000078202655,0.0000015949078,0.000034407407,0.00013799149,0.015808053,0.000093870745,0.000057676247,0.0063489256],"study_design_scores_gemma":[0.0015508119,0.0013711975,0.99137187,0.000013060884,0.000029231058,0.00022115537,0.0000493134,0.00025726092,0.004142889,0.00006139406,0.0008070531,0.00012478238],"about_ca_topic_score_codex":0.00002238046,"about_ca_topic_score_gemma":0.000014712607,"teacher_disagreement_score":0.014045747,"about_ca_system_score_codex":0.000003939359,"about_ca_system_score_gemma":0.00005201496,"threshold_uncertainty_score":0.44639957},"labels":[],"label_agreement":null},{"id":"W3047935522","doi":"10.3390/genes11080904","title":"The Gut Microbiota Profile in Children with Prader–Willi Syndrome","year":2020,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"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":"W. Garfield Weston Foundation; Children's Health Research Institute; Women and Children's Health Research Institute; Foundation for Prader-Willi Research","keywords":"Biology; Feces; Gut flora; Microbiome; Metagenomics; Disease; Zoology; Microbiology; Physiology; Immunology; Genetics; Internal medicine; Medicine; Gene","score_opus":0.006564377946100264,"score_gpt":0.19878761642997406,"score_spread":0.1922232384838738,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3047935522","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958982,0.0021841766,0.00007597729,0.0013563124,0.00003660366,0.00026343117,0.000007767321,0.000009187812,0.0001683513],"genre_scores_gemma":[0.99809,0.0002478856,0.00091876404,0.00029158618,0.00008831273,0.000022652508,0.000034098943,0.000020772866,0.00028588925],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992342,0.000029574156,0.0001345446,0.0002844622,0.000069504014,0.00024772342],"domain_scores_gemma":[0.99964136,0.000004189368,0.00004787793,0.00022772668,0.000021015414,0.000057816676],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000064589,0.00012025165,0.00009695023,0.000011285838,0.0000859155,0.000036236248,0.00022295945,0.00006476443,0.000014292286],"category_scores_gemma":[0.000019017843,0.00008047391,0.000036759073,0.00009913642,0.000057347203,0.0000016151849,0.00012824027,0.00006261156,0.000026249281],"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":[0.0000029397333,0.000021702104,0.4490447,0.00001177422,0.00008200267,0.0000011199809,0.00006852475,0.00007428169,0.54093367,0.000010739547,0.00077453826,0.008973981],"study_design_scores_gemma":[0.00045871676,0.0003345984,0.9490521,0.000009618592,0.000011128121,0.00029424074,0.000116166164,0.000037686397,0.029333796,0.0000056251824,0.020149658,0.00019668906],"about_ca_topic_score_codex":0.000020240253,"about_ca_topic_score_gemma":0.000019992069,"teacher_disagreement_score":0.5115999,"about_ca_system_score_codex":0.0000037582502,"about_ca_system_score_gemma":0.00004433445,"threshold_uncertainty_score":0.3281631},"labels":[],"label_agreement":null},{"id":"W3080176413","doi":"10.3390/genes11090984","title":"A 24-Week Physical Activity Intervention Increases Bone Mineral Content without Changes in Bone Markers in Youth with PWS","year":2020,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Medical Research and Materiel Command","keywords":"Medicine; Bone mineral; Bone mineral content; Internal medicine; Bone remodeling; Endocrinology; N-terminal telopeptide; Bone density; Alkaline phosphatase; Osteoporosis; Osteocalcin; Chemistry; Enzyme","score_opus":0.03726872326891207,"score_gpt":0.24791540877408969,"score_spread":0.21064668550517762,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3080176413","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99861217,0.0005946262,0.00013981079,0.00033296985,0.000036598416,0.00021096376,0.000016273689,0.000009218029,0.00004738562],"genre_scores_gemma":[0.9991679,0.00007807738,0.00030824041,0.00011914895,0.00013676558,0.000030014035,0.000047124973,0.000018906156,0.00009381767],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999122,0.000075616575,0.0001258765,0.0003425745,0.0001008517,0.00023302787],"domain_scores_gemma":[0.9996737,0.0000054302895,0.000077324185,0.00014069199,0.000026207219,0.00007660354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000095657735,0.00015626877,0.00022827131,0.000042839263,0.00001869954,0.000018979292,0.00007950635,0.000060036204,0.000006310545],"category_scores_gemma":[0.00004352144,0.00013509051,0.00006438225,0.00010741453,0.00004502242,0.0000045827546,0.00011947069,0.00007472988,0.0000023133666],"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":[0.00040537314,0.0004076724,0.14565551,0.000060644048,0.00003745441,0.000015656215,0.00047344118,0.000059822578,0.81865305,0.0000013743417,0.000028982804,0.03420102],"study_design_scores_gemma":[0.004570992,0.002758658,0.7143294,0.00017532885,0.00005509036,0.000062490944,0.003189416,0.0016891663,0.27203357,0.0000055784762,0.0005644983,0.00056577387],"about_ca_topic_score_codex":0.0006789231,"about_ca_topic_score_gemma":0.0013495809,"teacher_disagreement_score":0.5686739,"about_ca_system_score_codex":0.000011673604,"about_ca_system_score_gemma":0.000021912054,"threshold_uncertainty_score":0.5508831},"labels":[],"label_agreement":null},{"id":"W3087985205","doi":"10.1016/j.theriogenology.2020.09.027","title":"Specific imprinted genes demethylation in association with oocyte donor’s age and culture conditions in bovine embryos assessed at day 7 and 12 post insemination","year":2020,"lang":"en","type":"article","venue":"Theriogenology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"L'Alliance Boviteq; Université Laval","funders":"Fonds de recherche du Québec – Nature et technologies; Natural Sciences and Engineering Research Council of Canada; Fiona Stanley Hospital; Lyda Hill Foundation","keywords":"Genomic imprinting; Andrology; Biology; Oocyte; Embryo; Embryo culture; Insemination; Embryogenesis; Methylation; Estrous cycle; Human fertilization; DNA methylation; Genetics; Endocrinology; Gene expression; Gene; Pregnancy; Medicine","score_opus":0.010519241186511614,"score_gpt":0.22725927063183748,"score_spread":0.21674002944532586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3087985205","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974461,0.0010934144,0.00034287758,0.0006397466,0.000029411363,0.00020908185,0.000014394531,0.000008650723,0.00021630489],"genre_scores_gemma":[0.9980421,0.00085135334,0.00052282773,0.00016915408,0.000043918644,0.000016923379,0.00021790717,0.000014245053,0.00012157683],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99920624,0.00010327444,0.00017740384,0.00028633932,0.000056453784,0.00017025929],"domain_scores_gemma":[0.99969476,0.00001854192,0.00010542155,0.00009424273,0.000045185283,0.000041869815],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013840037,0.00011607501,0.00015212139,0.000053008916,0.00004678101,0.00001802375,0.000054722725,0.0001859239,0.00002320276],"category_scores_gemma":[0.00006868109,0.00010792896,0.000015429516,0.00010123976,0.00004445465,0.000006782843,0.0000879419,0.00008395638,0.0000026388661],"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":[0.00004812144,0.000017283006,0.15454568,0.000010188377,0.000021259299,0.000005710389,0.0006047042,0.000019760166,0.84301466,0.000017855147,0.000017554108,0.0016772492],"study_design_scores_gemma":[0.0011415739,0.00048092986,0.8895227,0.000010894999,0.000012536613,0.000028427672,0.00027368942,0.00018375799,0.10439022,0.00004127498,0.0037560249,0.00015803007],"about_ca_topic_score_codex":0.000058531303,"about_ca_topic_score_gemma":0.0006008781,"teacher_disagreement_score":0.7386244,"about_ca_system_score_codex":0.000041598356,"about_ca_system_score_gemma":0.000020334684,"threshold_uncertainty_score":0.44012153},"labels":[],"label_agreement":null},{"id":"W3088182247","doi":"10.1016/j.neuron.2020.08.023","title":"Parental Bias Has Benefits","year":2020,"lang":"en","type":"letter","venue":"Neuron","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Toronto","funders":"","keywords":"Homogeneous; Biology; Psychology; Neuroscience; Expression (computer science); Evolutionary biology; Developmental psychology; Genetics; Computer science","score_opus":0.046770615314432544,"score_gpt":0.23405310633725476,"score_spread":0.1872824910228222,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3088182247","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.28104118,0.0018300638,0.000039142622,0.71075773,0.0022202497,0.00042527495,0.00014322033,0.00006855966,0.0034746],"genre_scores_gemma":[0.21252726,0.0002469401,0.00018187644,0.7772911,0.0061521493,0.000019880068,0.0012745305,0.0001298726,0.0021763623],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9986134,0.000053965676,0.00020803827,0.00060223415,0.00018965689,0.00033267718],"domain_scores_gemma":[0.9993784,0.000009151886,0.00011227527,0.00040799202,0.00002805578,0.00006414782],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000024671244,0.0002777596,0.00020914324,0.000029135274,0.00007613082,0.000074671814,0.00031210604,0.0004094704,0.00006266374],"category_scores_gemma":[0.00006246224,0.00028024788,0.00017363945,0.00004929231,0.00005099557,8.936656e-7,0.00026854346,0.00052442093,0.00013795114],"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":[0.000002171346,0.000007498427,0.00079097867,0.000045042714,0.000026144106,0.000050317958,0.0000089350015,0.000007845778,0.019747533,5.5379235e-7,0.975549,0.0037639888],"study_design_scores_gemma":[0.00017293864,0.00029318302,0.002858273,0.000018426821,0.000025883328,0.00008535622,0.0000036867646,0.000014090557,0.008728704,0.000005584041,0.9875172,0.0002766913],"about_ca_topic_score_codex":0.000014792658,"about_ca_topic_score_gemma":0.0000026852433,"teacher_disagreement_score":0.068513915,"about_ca_system_score_codex":0.0000060846637,"about_ca_system_score_gemma":0.000057603782,"threshold_uncertainty_score":0.99996495},"labels":[],"label_agreement":null},{"id":"W3089698622","doi":"10.1108/amhid-04-2020-0009","title":"The use of the Montreal Cognitive Assessment (MoCA) to assess cognitive impairment in Prader-Willi syndrome","year":2020,"lang":"en","type":"article","venue":"Advances in Mental Health and Intellectual Disabilities","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Montreal Cognitive Assessment; Normative; Psychology; Cognition; Population; Neuropsychological assessment; Cronbach's alpha; Developmental psychology; Clinical psychology; Neuropsychology; Psychometrics; Psychiatry; Medicine; Cognitive impairment","score_opus":0.042927487114125196,"score_gpt":0.33232331579522195,"score_spread":0.28939582868109676,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3089698622","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99367166,0.0031611056,0.00019697346,0.0016289173,0.00012131275,0.0009700304,0.00007010695,0.000003536296,0.00017633197],"genre_scores_gemma":[0.9937856,0.0043459716,0.00017011425,0.0014816686,0.0000186304,0.00009499391,0.00002465932,0.000011878716,0.00006648114],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99851143,0.0002332569,0.0004086129,0.000331809,0.00017262502,0.00034223864],"domain_scores_gemma":[0.9990577,0.0005568916,0.0000883218,0.00011589834,0.00003829922,0.000142867],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019014427,0.00016158604,0.00021859197,0.000022860962,0.00015080802,0.000028946622,0.0001377776,0.00004326155,0.000012120053],"category_scores_gemma":[0.0011497926,0.00010792872,0.00005347635,0.0001648825,0.00033133323,0.00001845846,0.00026121517,0.00014175395,0.0000012140474],"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":[0.000489622,0.0008279166,0.7633691,0.00089547306,0.0001227753,0.0000011667927,0.063099906,0.0003861161,0.0013115854,0.00021662685,0.0013803086,0.16789943],"study_design_scores_gemma":[0.003031242,0.011723767,0.5949224,0.0011161049,0.000018803932,0.00007211858,0.36164057,0.0014912795,0.004383526,0.00026001935,0.020685209,0.00065492536],"about_ca_topic_score_codex":0.00018065891,"about_ca_topic_score_gemma":0.00069682184,"teacher_disagreement_score":0.29854065,"about_ca_system_score_codex":0.000054802822,"about_ca_system_score_gemma":0.00013952242,"threshold_uncertainty_score":0.44012055},"labels":[],"label_agreement":null},{"id":"W3090851569","doi":"10.1097/yct.0000000000000722","title":"Transcranial Direct Current Stimulation for Prader-Willi Syndrome","year":2020,"lang":"en","type":"article","venue":"Journal of Ect","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 of Toronto; Centre for Addiction and Mental Health","funders":"","keywords":"Transcranial direct-current stimulation; Craving; Food craving; Dorsolateral prefrontal cortex; Stimulation; Medicine; Prefrontal cortex; Physical medicine and rehabilitation; Population; Psychology; Neuroscience; Cognition","score_opus":0.029014499696601376,"score_gpt":0.28049495448517736,"score_spread":0.251480454788576,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3090851569","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9806557,0.001579792,0.016596783,0.0005850858,0.00034405527,0.00013755258,0.000007515995,0.0000030843976,0.00009040818],"genre_scores_gemma":[0.997384,0.00014861935,0.0018248577,0.000095504874,0.0005069354,0.0000019874972,0.000006649455,0.000013919101,0.0000175396],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.999348,0.000025769792,0.00027503268,0.00011724075,0.0001062558,0.00012769655],"domain_scores_gemma":[0.9995695,0.000015023446,0.00016848958,0.0000646372,0.00009027682,0.00009210702],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014304054,0.000085582986,0.00016228281,0.00002329447,0.000035201632,0.00001767444,0.00010886202,0.00005048655,0.000015250879],"category_scores_gemma":[0.00013727363,0.000073272924,0.00019217632,0.00004811758,0.00001225664,0.000003975217,0.00001485836,0.000071585215,0.0000017793639],"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":[0.000065479195,0.0001559435,0.015726905,0.00019358816,0.00025909924,0.0000042903503,0.00034072396,0.0031295028,0.9279555,0.000015763237,0.004500732,0.047652442],"study_design_scores_gemma":[0.011043218,0.01608301,0.38733518,0.00026626987,0.00052397005,0.0014110918,0.00020118823,0.005693719,0.09725286,0.0002572621,0.47891212,0.0010201014],"about_ca_topic_score_codex":6.147568e-7,"about_ca_topic_score_gemma":5.035225e-7,"teacher_disagreement_score":0.83070266,"about_ca_system_score_codex":0.0000060905913,"about_ca_system_score_gemma":0.000060052233,"threshold_uncertainty_score":0.29879832},"labels":[],"label_agreement":null},{"id":"W3093643846","doi":"10.1002/aur.2418","title":"<scp>CIM6P</scp>/<scp>IGF</scp>‐2 Receptor Ligands Reverse Deficits in Angelman Syndrome Model Mice","year":2020,"lang":"en","type":"article","venue":"Autism Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"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 Guelph","funders":"National Institute on Aging; National Institute of Mental Health; Foundation for Angelman Syndrome Therapeutics","keywords":"UBE3A; Angelman syndrome; Insulin-like growth factor 2 receptor; Neuroscience; Neurodevelopmental disorder; Psychology; Ataxia; Receptor; Insulin-like growth factor 1 receptor; Endocrinology; Internal medicine; Medicine; Autism; Growth factor; Chemistry; Developmental psychology; Biochemistry","score_opus":0.04950761889439175,"score_gpt":0.30504289158893755,"score_spread":0.2555352726945458,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3093643846","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99045306,0.0020971342,0.00027249378,0.0010105325,0.00012557805,0.0004959133,0.000041243587,0.000037507743,0.005466538],"genre_scores_gemma":[0.9893023,0.001134971,0.0016309322,0.0004703627,0.00012388157,0.000071423536,0.00009946964,0.00008618861,0.0070804767],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99634945,0.00020729682,0.00047449037,0.001025302,0.000668324,0.0012751481],"domain_scores_gemma":[0.9984494,0.00020362204,0.00009637413,0.00062442216,0.00015763594,0.00046856722],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0010795862,0.00032025122,0.00037312225,0.00020838736,0.00020908883,0.00011012715,0.0008114829,0.0004403127,0.000021523754],"category_scores_gemma":[0.0019471486,0.00033929583,0.00015716699,0.0007377717,0.00017994466,0.000015926524,0.0009189899,0.0007272753,0.00039150123],"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":[0.000007245789,0.00015346037,0.0054779793,0.00017043114,0.00008007324,0.00009625401,0.0012017417,0.00071291014,0.9302859,0.00025347644,0.060124803,0.0014357715],"study_design_scores_gemma":[0.005479362,0.003936002,0.077771746,0.00047288206,0.00007386252,0.00057273096,0.006685379,0.034372915,0.5370156,0.0013506345,0.331584,0.00068486796],"about_ca_topic_score_codex":0.00013781621,"about_ca_topic_score_gemma":0.000036415127,"teacher_disagreement_score":0.39327025,"about_ca_system_score_codex":0.00005446145,"about_ca_system_score_gemma":0.00031150703,"threshold_uncertainty_score":0.9999059},"labels":[],"label_agreement":null},{"id":"W3108052922","doi":"10.3389/fcell.2020.583801","title":"mTORC1 Transcriptional Regulation of Ribosome Subunits, Protein Synthesis, and Molecular Transport in Primary Human Trophoblast Cells","year":2020,"lang":"en","type":"article","venue":"Frontiers in Cell and Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Western University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health","keywords":"mTORC1; Biology; Cell biology; Ribosome biogenesis; Ribosomal protein; Ribosomal protein s6; Gene; TOR signaling; PI3K/AKT/mTOR pathway; P70-S6 Kinase 1; Signal transduction; Ribosome; Genetics; RNA","score_opus":0.006403641789978965,"score_gpt":0.18128965346610146,"score_spread":0.1748860116761225,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3108052922","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966056,0.001131543,0.0015406662,0.000058269343,0.00004173608,0.00021808357,0.00001754479,0.000003230304,0.0003833322],"genre_scores_gemma":[0.9886373,0.00018503149,0.01089823,0.000097777935,0.000013658112,0.000020891895,0.00010087505,0.000010927955,0.000035261633],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999109,0.00005096461,0.00029448664,0.00032011783,0.00005214212,0.00017324067],"domain_scores_gemma":[0.9998135,0.000004017822,0.00005634422,0.000053628475,0.000012881547,0.00005963032],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009393359,0.000133766,0.00022157803,0.00006895727,0.000026907614,0.000003642876,0.00007579367,0.00014811258,0.00001110276],"category_scores_gemma":[0.000006194103,0.00013776695,0.000028623701,0.00008347785,0.000118483884,0.000004239,0.000038723763,0.00007108794,4.1197612e-7],"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":[0.00004111165,0.000031732372,0.097333394,0.00008584113,0.000011650394,0.000001851538,0.00016697972,0.000006720848,0.90101814,0.000019819407,0.000030753614,0.0012519917],"study_design_scores_gemma":[0.00076111575,0.00017345617,0.2253285,0.00002609018,0.0000060625157,0.0000053478425,0.00026148965,0.000020810288,0.7718832,0.0001189013,0.0012375995,0.00017744674],"about_ca_topic_score_codex":0.000018931565,"about_ca_topic_score_gemma":0.0000067614537,"teacher_disagreement_score":0.12913498,"about_ca_system_score_codex":0.000015373036,"about_ca_system_score_gemma":0.000048332982,"threshold_uncertainty_score":0.5617973},"labels":[],"label_agreement":null},{"id":"W3113794034","doi":"10.1097/brs.0000000000003879","title":"The Association of Scoliosis and NSD1 Gene Deletion in Sotos Syndrome Patients","year":2020,"lang":"en","type":"article","venue":"Spine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Sotos syndrome; Scoliosis; Medicine; Haploinsufficiency; Pediatrics; Genetics; Phenotype; Gene; Biology; Surgery","score_opus":0.005035252808327655,"score_gpt":0.20247464127393064,"score_spread":0.197439388465603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3113794034","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990477,0.00028442062,0.00006340152,0.0003923664,0.000036425554,0.000108665925,0.0000024429357,0.0000017981514,0.000062769075],"genre_scores_gemma":[0.9994103,0.00021023666,0.00019453105,0.00011086085,0.000022548751,0.0000059757053,0.000011847152,0.0000053653052,0.0000283495],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995697,0.000020756524,0.00013224824,0.00011124784,0.000069758695,0.00009626793],"domain_scores_gemma":[0.9997905,0.0000025228628,0.00007470695,0.000067406625,0.000039008024,0.000025842179],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000094895695,0.000044904013,0.00006706138,0.000010090722,0.000026796219,0.000008109046,0.000050840572,0.000048436727,0.0000013891276],"category_scores_gemma":[0.00013759226,0.00003834516,0.000020610614,0.00006233744,0.000011636725,0.0000012511988,0.000061051214,0.000028695702,0.000001433581],"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":[0.000008643712,0.000032786927,0.5688971,0.00003199083,0.0000308839,4.3171454e-7,0.00006557794,0.00003939929,0.4221668,0.000012578614,0.00009232457,0.008621476],"study_design_scores_gemma":[0.00046836358,0.00027267603,0.9590436,0.000010030816,0.0000058194414,0.0000016200934,0.000017317016,0.00012353156,0.038709883,0.000006345271,0.0012888678,0.000051897838],"about_ca_topic_score_codex":0.000009224612,"about_ca_topic_score_gemma":0.0000095327305,"teacher_disagreement_score":0.39014652,"about_ca_system_score_codex":0.0000070155793,"about_ca_system_score_gemma":0.000009914181,"threshold_uncertainty_score":0.15636702},"labels":[],"label_agreement":null},{"id":"W3113925640","doi":"","title":"Evidence for a cilia component in Axenfeld-Rieger Syndrome","year":2019,"lang":"en","type":"article","venue":"Investigative Ophthalmology & Visual Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Alberta","funders":"","keywords":"Component (thermodynamics); Cilium; Biology; Physics; Cell biology","score_opus":0.06236117749293582,"score_gpt":0.3516625539148661,"score_spread":0.2893013764219303,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3113925640","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980415,0.00028902598,0.000022267483,0.00021640894,0.00037260717,0.0006438212,0.0000044357307,0.000008166039,0.0004017355],"genre_scores_gemma":[0.9969722,0.0000089481155,0.0022111603,0.000228477,0.000034939247,0.00008641908,0.000008094576,0.000015879796,0.0004338828],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99787307,0.00009371716,0.00031407466,0.000865104,0.00024513074,0.0006088889],"domain_scores_gemma":[0.99907583,0.000099307654,0.00013074749,0.00035364888,0.00015757002,0.0001829109],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009634536,0.00020636695,0.00025623423,0.00013040133,0.00012587868,0.000039647068,0.0005672245,0.00013613142,0.00007443686],"category_scores_gemma":[0.000790368,0.00019582987,0.00007552175,0.0004461339,0.0011999503,0.00002373812,0.00037571564,0.00012508109,0.00006668327],"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":[0.000012789402,0.000040749685,0.17777853,0.000019237707,0.0000072081634,0.0000113314045,0.000093626906,0.00006910361,0.82177895,0.000038780363,0.000015251655,0.00013441301],"study_design_scores_gemma":[0.0004617277,0.0014580558,0.6225073,0.00012462802,0.000005628027,0.0005517662,0.00013973138,0.0006296671,0.37300995,0.0006926163,0.00014473259,0.00027422968],"about_ca_topic_score_codex":0.00007626323,"about_ca_topic_score_gemma":0.000004513902,"teacher_disagreement_score":0.448769,"about_ca_system_score_codex":0.000053344094,"about_ca_system_score_gemma":0.0003586106,"threshold_uncertainty_score":0.79857105},"labels":[],"label_agreement":null},{"id":"W3115333912","doi":"10.6215/fjpt.2018.75.p60","title":"【論文摘要】以家庭為中心概念執行普瑞德威利症候群嬰兒早期介入：個案報告","year":2018,"lang":"zh","type":"article","venue":"物理治療","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Computer science","score_opus":0.01052740576619488,"score_gpt":0.248949996840862,"score_spread":0.23842259107466712,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3115333912","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8346301,0.0042438284,0.0016105608,0.00086834974,0.0024309433,0.00032191756,0.000059856775,0.00003544101,0.15579906],"genre_scores_gemma":[0.978566,0.0005299357,0.0015803362,0.0008710718,0.002914796,0.000010778828,0.000057738787,0.00007096193,0.015398375],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9976954,0.00008643985,0.00042463565,0.0007803252,0.00024138972,0.0007717961],"domain_scores_gemma":[0.998425,0.000013343907,0.00016855811,0.0009316088,0.00021481607,0.0002466778],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00028374285,0.00037330692,0.0002967935,0.00006087943,0.00024799083,0.000105147126,0.0004792949,0.0004128201,0.0011268749],"category_scores_gemma":[0.00014718935,0.00037958453,0.00022621844,0.00018404894,0.00034193313,0.0000044617577,0.00047452256,0.00017240792,0.001163491],"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":[0.000063757136,0.00036365696,0.022915559,0.0001768266,0.00054120965,0.000020355475,0.00068534934,0.000009453557,0.77394176,0.002180115,0.058328785,0.14077316],"study_design_scores_gemma":[0.0012159013,0.001782575,0.031932406,0.000099350145,0.00011563648,0.00018950357,0.00030367865,0.0002616223,0.12062807,0.0006614004,0.84190637,0.0009034746],"about_ca_topic_score_codex":0.00006863247,"about_ca_topic_score_gemma":0.00003965988,"teacher_disagreement_score":0.7835776,"about_ca_system_score_codex":0.000023252287,"about_ca_system_score_gemma":0.00015946731,"threshold_uncertainty_score":0.9998656},"labels":[],"label_agreement":null},{"id":"W3124329809","doi":"10.3390/genes12020172","title":"Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome","year":2021,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Uniparental disomy; Genomic imprinting; Genetics; Biology; Beckwith–Wiedemann syndrome; Imprinting (psychology); DNA methylation; Epigenetics; Locus (genetics); SNP array; Differentially methylated regions; Chromosome; Single-nucleotide polymorphism; Karyotype; Gene; Genotype","score_opus":0.005121358447455173,"score_gpt":0.19804596692051832,"score_spread":0.19292460847306314,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3124329809","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99722856,0.0018770676,0.000032015498,0.00022074838,0.00012393243,0.00010347436,0.000016667142,0.000003163467,0.00039438644],"genre_scores_gemma":[0.99890447,0.000119385746,0.00020388863,0.0000464191,0.000049784885,0.000012226175,0.000036197718,0.000016480803,0.000611146],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991762,0.000041966454,0.00018191102,0.0002632774,0.00013277409,0.00020387459],"domain_scores_gemma":[0.99950236,0.0000029044988,0.00007712467,0.0003410901,0.000038883732,0.000037635895],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000052188436,0.00012308855,0.00014700669,0.000020122803,0.000053547672,0.0000148054005,0.00019375308,0.00006510198,0.000037845955],"category_scores_gemma":[0.000010113963,0.00008576941,0.00007913593,0.00013366567,0.00006794062,0.0000024335952,0.00022836865,0.00006077202,0.0000026173307],"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":[0.000009397646,0.00012142109,0.55389416,0.000059588423,0.00007985312,0.000042770884,0.00009712451,0.00021339764,0.44313788,0.000018760129,0.00002562246,0.002300012],"study_design_scores_gemma":[0.000698102,0.00019537528,0.57907975,0.00014379849,0.000022083377,0.0017791567,0.00035360194,0.000024394882,0.41502747,0.000022363756,0.0024716617,0.00018224561],"about_ca_topic_score_codex":0.000046634035,"about_ca_topic_score_gemma":0.00025855782,"teacher_disagreement_score":0.028110407,"about_ca_system_score_codex":0.0000068203017,"about_ca_system_score_gemma":0.00006620362,"threshold_uncertainty_score":0.34975752},"labels":[],"label_agreement":null},{"id":"W3129589084","doi":"10.1093/cdn/nzab016","title":"Effect of High-Protein Diet on Postprandial Energy Expenditure in Children with Prader-Willi Syndrome: A Pilot and Feasibility Study","year":2021,"lang":"en","type":"article","venue":"Current Developments in Nutrition","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Saudi Arabian Cultural Bureau; Saudi Arabian Cultural Mission; Women and Children's Health Research Institute; Children's Health Research Institute","keywords":"Postprandial; Energy expenditure; Medicine; Internal medicine; Endocrinology; Pediatrics; Gerontology; Insulin","score_opus":0.012751954866017457,"score_gpt":0.27128064610643127,"score_spread":0.25852869124041383,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3129589084","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99799466,0.0010296277,0.000026983618,0.000013154203,0.00009394576,0.0008140526,0.000013055966,0.0000039653023,0.000010562094],"genre_scores_gemma":[0.99906224,0.0002224746,0.00024320382,0.000007996259,0.000023019704,0.00017674574,0.0002475395,0.000013115168,0.0000036694116],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99868596,0.00022485631,0.00026340276,0.000464085,0.00016973105,0.00019199289],"domain_scores_gemma":[0.9996422,0.000012569292,0.00007946648,0.00019062549,0.000032086216,0.000043051565],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021810166,0.000177264,0.00024634527,0.00008722401,0.00003323874,0.000015607562,0.0000795918,0.000068047884,0.000004512179],"category_scores_gemma":[0.0000519536,0.00015687205,0.000021249425,0.00015190072,0.000032942447,0.0000056441604,0.0000992389,0.00010506466,4.0914952e-7],"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":[0.00029757697,0.0021748333,0.97939503,0.0001744727,0.000055674434,0.0000048326074,0.00006415207,0.0000057286875,0.010899788,0.000008023225,0.000009267255,0.006910595],"study_design_scores_gemma":[0.006632416,0.008576079,0.960826,0.00040023235,0.000010838979,0.00003305432,0.000048068887,0.0000011770051,0.02322308,0.00002436622,0.00004538496,0.0001793344],"about_ca_topic_score_codex":0.000036442718,"about_ca_topic_score_gemma":0.00007094907,"teacher_disagreement_score":0.018569088,"about_ca_system_score_codex":0.000033502598,"about_ca_system_score_gemma":0.000052450832,"threshold_uncertainty_score":0.6397056},"labels":[],"label_agreement":null},{"id":"W3133907890","doi":"10.1073/pnas.2015505118","title":"<i>Dlk1</i> dosage regulates hippocampal neurogenesis and cognition","year":2021,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"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; Banco Bilbao Vizcaya Argentaria; Generalitat Valenciana; Ministerio de Economía y Competitividad; European Commission; Ministerio de Ciencia e Innovación; Wellcome Trust; Fundación BBVA","keywords":"Neurogenesis; Subgranular zone; Subventricular zone; Dentate gyrus; Hippocampal formation; Hippocampus; Neuroscience; Lateral ventricles; Biology; Cognition; Neural stem cell; Psychology; Stem cell; Cell biology","score_opus":0.022141435783407437,"score_gpt":0.2672747866014067,"score_spread":0.24513335081799925,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3133907890","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967909,0.00049436564,9.1247296e-7,0.0008150775,0.000011251725,0.00004516873,0.000005316114,0.0000017877031,0.0018352241],"genre_scores_gemma":[0.998377,0.00014454186,0.0010769085,0.00024615484,0.00004511826,0.000002399591,3.6261787e-7,0.0000026357982,0.0001048291],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99930865,0.0000047831254,0.0001404154,0.00018459663,0.00027846327,0.0000831192],"domain_scores_gemma":[0.999659,0.000014336001,0.0001311466,0.0000058732226,0.00016942395,0.000020238147],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031349174,0.00005211013,0.000066391636,0.000024515719,0.000092673006,0.000016108603,0.00016633332,0.000051221676,0.000005015692],"category_scores_gemma":[0.0002718715,0.000039198967,0.0000398728,0.00019082525,0.00028364357,0.000008643364,0.00015924615,0.000034833858,2.1341455e-7],"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":[0.0000015196347,0.000011696111,0.008071988,0.000020414018,0.000008136346,2.5987172e-9,0.000015130965,0.000007332891,0.9903207,0.00065386965,0.00010541973,0.00078383536],"study_design_scores_gemma":[0.00008911417,0.000026294545,0.1485268,0.000020204174,0.0000087166345,0.000037914124,0.00006988059,0.000057255573,0.8467373,0.0041517005,0.00023508289,0.000039713806],"about_ca_topic_score_codex":7.2093985e-7,"about_ca_topic_score_gemma":2.853619e-8,"teacher_disagreement_score":0.14358333,"about_ca_system_score_codex":0.0000017744734,"about_ca_system_score_gemma":0.000019266865,"threshold_uncertainty_score":0.15984875},"labels":[],"label_agreement":null},{"id":"W3142078217","doi":"10.4021/jem198w","title":"Pseudopseudohypoparathyroidism With a Novel Mutation in the GNAS Gene Showing Thin Bones of Extremities and Ossification of Entheses","year":2013,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"National Center for Global Health and Medicine","keywords":"GNAS complex locus; Medicine; Ossification; Heterotopic ossification; Osteodystrophy; Pseudohypoparathyroidism; Internal medicine; Short stature; Endocrinology; Gene; Anatomy; Parathyroid hormone; Genetics; Biology","score_opus":0.01863866593083609,"score_gpt":0.23944879154916862,"score_spread":0.22081012561833252,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3142078217","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9878867,0.011042092,0.0006411204,0.00021137348,0.00004648923,0.000086756154,0.0000020303876,6.0988503e-7,0.0000827953],"genre_scores_gemma":[0.99564236,0.0014684682,0.0027671538,0.000040060146,0.000048071328,0.000005222812,0.0000013604445,0.0000046483265,0.000022669537],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993542,0.000060486564,0.00030352117,0.00009131885,0.00007909362,0.00011137185],"domain_scores_gemma":[0.99944496,0.000040806266,0.00028741977,0.00009599879,0.00011025793,0.000020537376],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017978626,0.00007819929,0.0001945445,0.00007669814,0.000027780436,0.00000999021,0.000087452216,0.000046684796,0.0000023807922],"category_scores_gemma":[0.00007830906,0.000048826154,0.00003286837,0.000046370424,0.00013528483,0.000013572467,0.00003717716,0.00007864356,6.824223e-8],"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":[0.000021504908,0.000054168653,0.008882326,0.000015538873,0.00005273771,0.0000021276858,0.00084856624,0.000040794162,0.9843627,0.0005998327,0.0000164974,0.0051031816],"study_design_scores_gemma":[0.0011073959,0.00024480035,0.6685542,0.000027454242,0.00007379384,0.0020959717,0.0030255332,0.00005149539,0.3238202,0.00053890055,0.00037696326,0.000083287065],"about_ca_topic_score_codex":0.00004807651,"about_ca_topic_score_gemma":0.0000056158206,"teacher_disagreement_score":0.66054255,"about_ca_system_score_codex":0.0000013124536,"about_ca_system_score_gemma":0.000028532926,"threshold_uncertainty_score":0.19910727},"labels":[],"label_agreement":null},{"id":"W3148518460","doi":"10.1002/epi4.12484","title":"Seizures in Sotos syndrome: Phenotyping in 49 patients","year":2021,"lang":"en","type":"article","venue":"Epilepsia Open","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan; McGill University Health Centre; Université de Sherbrooke; McGill University; Montreal Children's Hospital","funders":"Medical Research Council; National Health and Medical Research Council; McGill University; McGill University Health Centre; Citizens United for Research in Epilepsy","keywords":"Sotos syndrome; Epilepsy; Pediatrics; Medicine; Epilepsy syndromes; Seizure types; Levetiracetam; Semiology; Macrocephaly; Psychiatry","score_opus":0.011955994704059449,"score_gpt":0.2639440680920125,"score_spread":0.25198807338795304,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3148518460","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9925972,0.0002922356,0.000038648937,0.00013619689,0.0001477798,0.00030139508,0.0000050390754,0.000003290513,0.006478206],"genre_scores_gemma":[0.99756217,0.000067121546,0.0010677589,0.00034894567,0.00002599567,0.000043032058,0.0000970717,0.000020761405,0.00076714833],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988451,0.00008745331,0.00027492305,0.00040500495,0.00009186574,0.00029567542],"domain_scores_gemma":[0.99950635,0.000010132486,0.00005574764,0.0003325266,0.00004271064,0.000052527976],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018969638,0.00012502172,0.00019281621,0.000045321685,0.000037606027,0.000072154595,0.00034499043,0.00010532093,0.00011758669],"category_scores_gemma":[0.00015030592,0.00013496295,0.000041936415,0.00018058106,0.000018626777,0.000007259164,0.0006866446,0.00010224921,0.000038033515],"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":[0.00001955489,0.00030592518,0.9461476,0.00003735137,0.000030235686,0.000108136745,0.00021492047,0.00023528167,0.036398973,0.000069300266,0.0010386097,0.015394089],"study_design_scores_gemma":[0.001448827,0.000088458786,0.97147715,0.000085276006,0.0000037049906,0.000056272587,0.00018240353,0.00007904318,0.013620892,0.00012450342,0.012598737,0.00023476049],"about_ca_topic_score_codex":0.00015332665,"about_ca_topic_score_gemma":0.00033104792,"teacher_disagreement_score":0.025329502,"about_ca_system_score_codex":0.000020257208,"about_ca_system_score_gemma":0.00009768733,"threshold_uncertainty_score":0.55036294},"labels":[],"label_agreement":null},{"id":"W3151565048","doi":"10.14740/jem235w","title":"Erratum to: Pseudopseudohypoparathyroidism With a Novel Mutation in the GNAS Gene Showing Thin Bones of Extremities and Ossification of Entheses","year":2014,"lang":"en","type":"erratum","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Medicine; Exon; Ossification; Gene; Endocrinology; Internal medicine; Genetics; Anatomy; Biology","score_opus":0.01898992797138789,"score_gpt":0.25264973405704977,"score_spread":0.2336598060856619,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3151565048","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9671446,0.029522227,0.0010112155,0.00033617407,0.0011754032,0.00016585254,0.000017449445,0.0000012984301,0.00062577834],"genre_scores_gemma":[0.9915017,0.0047420426,0.0022837538,0.000104324325,0.00040795072,0.000008788012,0.000018670291,0.000017963272,0.0009148213],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99867606,0.00013748943,0.0005860182,0.00021583616,0.00017702236,0.0002075593],"domain_scores_gemma":[0.99875516,0.00005714107,0.00072501774,0.00021933028,0.00019812414,0.00004524207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040266343,0.00020348639,0.0005426513,0.00021083407,0.00004639456,0.0000181402,0.00021775404,0.00020636858,0.0000013857778],"category_scores_gemma":[0.00022288364,0.0001355517,0.000081359525,0.00008830465,0.00017886849,0.00000950443,0.000095393116,0.00032369804,8.11795e-8],"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":[0.00021011163,0.00022455133,0.0024239314,0.00025764966,0.0004604967,0.000023351846,0.0032215114,0.0001648112,0.9705344,0.0011110095,0.012587281,0.008780882],"study_design_scores_gemma":[0.0056990013,0.0028391748,0.58219117,0.00091949484,0.0013700229,0.014437316,0.007928754,0.00014185072,0.24421474,0.0016530659,0.13751678,0.0010886074],"about_ca_topic_score_codex":0.0000409436,"about_ca_topic_score_gemma":0.00002731454,"teacher_disagreement_score":0.7263197,"about_ca_system_score_codex":0.0000038140643,"about_ca_system_score_gemma":0.00011999106,"threshold_uncertainty_score":0.55276376},"labels":[],"label_agreement":null},{"id":"W3159797256","doi":"10.1210/jendso/bvab048.1403","title":"Topline Results of the CARE-PWS Phase 3 Study: Intranasal Carbetocin Improves Hyperphagia and Anxiety and Distress Symptoms in Prader-Willi Syndrome (PWS)","year":2021,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Placebo; Clinical endpoint; Anxiety; Internal medicine; Tolerability; Distress; Randomized controlled trial; Pediatrics; Adverse effect; Psychiatry; Clinical psychology","score_opus":0.005396942329276989,"score_gpt":0.2542645968719744,"score_spread":0.2488676545426974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3159797256","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954202,0.0031283086,0.000013397703,0.00093803025,0.0002355991,0.00020167182,0.000034981855,0.0000014314398,0.00002638306],"genre_scores_gemma":[0.99858725,0.00078619877,0.00029655374,0.00009196489,0.000101840495,0.0000027613792,0.0000039542774,0.000013762365,0.00011573549],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9987732,0.00011940256,0.00047985697,0.00022242773,0.00020576808,0.00019935078],"domain_scores_gemma":[0.99912953,0.00002668831,0.00031193768,0.00033099338,0.00013988608,0.0000609612],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002414593,0.00015146758,0.00027812002,0.000011915215,0.00008871959,0.00003202594,0.00024305526,0.00007378661,0.0000017638739],"category_scores_gemma":[0.00014273103,0.000093134826,0.00022655558,0.00013381074,0.00012560892,0.0000074730165,0.00040512698,0.00031825592,2.9538203e-8],"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":[0.00004053843,0.000601613,0.2920535,0.0001822663,0.00059123774,0.0000137891475,0.0037437826,0.00014531077,0.68464404,0.0000057640673,0.0005801668,0.017398007],"study_design_scores_gemma":[0.012584181,0.0012389673,0.84468025,0.00017842483,0.00028843456,0.0027350092,0.013446212,0.00020888483,0.11992367,0.000030294688,0.0043800157,0.00030564514],"about_ca_topic_score_codex":0.000050644012,"about_ca_topic_score_gemma":0.00004495809,"teacher_disagreement_score":0.5647204,"about_ca_system_score_codex":0.000021062784,"about_ca_system_score_gemma":0.00009828211,"threshold_uncertainty_score":0.3797928},"labels":[],"label_agreement":null},{"id":"W3163620746","doi":"10.1093/jas/skab140","title":"Genetic potential for residual feed intake and diet fed during early- to mid-gestation influences post-natal DNA methylation of imprinted genes in muscle and liver tissues in beef cattle","year":2021,"lang":"en","type":"article","venue":"Journal of Animal Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Agriculture and Agri-Food Canada","funders":"Alberta Livestock and Meat Agency","keywords":"Biology; Residual feed intake; DNA methylation; Genomic imprinting; Beef cattle; Epigenetics; Offspring; Gestation; Methylation; Animal science; Genetics; Andrology; Endocrinology; Gene; Pregnancy; Feed conversion ratio; Gene expression; Body weight; Medicine","score_opus":0.010010109750430523,"score_gpt":0.26452106651556917,"score_spread":0.25451095676513863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3163620746","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998892,0.00078914117,0.00009991128,0.000089596186,0.000039009105,0.00008312614,0.000003833531,6.15169e-7,0.0000027836063],"genre_scores_gemma":[0.9936615,0.0001514004,0.0061313226,0.000010221288,0.000034769848,0.0000013306624,8.940285e-7,0.0000037723462,0.0000047852805],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99925923,0.000027363618,0.000264652,0.000173114,0.00013898662,0.00013662459],"domain_scores_gemma":[0.9995216,0.000013410363,0.0001264888,0.000052032105,0.0002286325,0.00005779789],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031443324,0.00006024378,0.00011024754,0.000112568756,0.00004511986,0.000045291,0.000088545115,0.000037963313,0.0000021810854],"category_scores_gemma":[0.00024227174,0.00005705497,0.00002010973,0.00015504207,0.00008645141,0.00002066474,0.00011172367,0.00004068694,8.666653e-8],"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":[0.00011267912,0.000016130098,0.028957687,0.000020749607,0.0000037752388,0.000004840357,0.00038847025,0.000112633556,0.96520305,0.0000016500936,2.4000636e-7,0.005178102],"study_design_scores_gemma":[0.00024608677,0.000652368,0.56969565,0.000021230026,0.0000038416974,0.000039078022,0.00030002894,0.00007084439,0.4289204,0.000008480422,0.000004254901,0.000037736743],"about_ca_topic_score_codex":0.00014079285,"about_ca_topic_score_gemma":0.0001804201,"teacher_disagreement_score":0.540738,"about_ca_system_score_codex":0.000012118889,"about_ca_system_score_gemma":0.00008917246,"threshold_uncertainty_score":0.23266341},"labels":[],"label_agreement":null},{"id":"W3164396936","doi":"10.14218/jcth.2021.00016","title":"Identification of Expression Pattern and Clinical Significance of the Small Cajal Body-specific RNA SCARNA16 in Hepatocellular Carcinoma","year":2021,"lang":"en","type":"article","venue":"Journal of Clinical and Translational Hepatology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pancreas Centre (Canada)","funders":"National Natural Science Foundation of China","keywords":"Clinical significance; Hepatocellular carcinoma; Biomarker; Identification (biology); Messenger RNA; RNA; Small nucleolar RNA; Potency","score_opus":0.039646243047157886,"score_gpt":0.31139116357049795,"score_spread":0.2717449205233401,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3164396936","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942144,0.002616435,0.0022605855,0.00048814696,0.00031226102,0.000076031916,0.000010001864,4.6472428e-7,0.000021675267],"genre_scores_gemma":[0.9978,0.0015110031,0.0004893917,0.00004434391,0.00012546641,9.894693e-7,0.0000045056886,0.0000063573584,0.000017964361],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99753207,0.00037282988,0.0016430876,0.00021122,0.00014059611,0.000100209945],"domain_scores_gemma":[0.9986801,0.00021180903,0.00065989554,0.00015721357,0.00022769823,0.0000632716],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009430709,0.0000846965,0.00039317991,0.000031333097,0.00002844418,0.0000056053773,0.00012430933,0.00019971833,0.000008975508],"category_scores_gemma":[0.00018278953,0.00006334036,0.00021410809,0.000065924534,0.0002994827,0.000005336136,0.00005165974,0.0002124635,1.4735821e-7],"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":[0.000060075017,0.0001294244,0.8704553,0.00003181588,0.000030084864,0.000006574285,0.000023191637,0.000008083655,0.115867436,0.00005065911,0.000009753365,0.013327564],"study_design_scores_gemma":[0.0012313289,0.00016578093,0.93134975,0.000045407356,0.000028906783,0.00012172349,0.00003116145,0.00058216363,0.06548591,0.00046776523,0.00043036623,0.000059755657],"about_ca_topic_score_codex":0.000009459416,"about_ca_topic_score_gemma":0.000024338935,"teacher_disagreement_score":0.060894396,"about_ca_system_score_codex":0.0000013467123,"about_ca_system_score_gemma":0.00016688839,"threshold_uncertainty_score":0.2582945},"labels":[],"label_agreement":null},{"id":"W3165895781","doi":"10.1016/j.aace.2021.06.003","title":"A Case Report of Hyperestrogenism in Prader-Willi Syndrome","year":2021,"lang":"en","type":"article","venue":"AACE Clinical Case Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University","funders":"","keywords":"Medicine; Hyperandrogenism; Polycystic ovary; Estrogen; Concomitant; Hormone replacement therapy (female-to-male); Estrone; Internal medicine; Endocrinology; Pediatrics; Insulin; Testosterone (patch); Insulin resistance","score_opus":0.04309169645467011,"score_gpt":0.34307316042811864,"score_spread":0.29998146397344855,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3165895781","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972992,0.0014578825,0.000071487986,0.00013598104,0.0004210071,0.00016708535,0.0000058112173,0.000009000397,0.00043254343],"genre_scores_gemma":[0.9960144,0.00013270174,0.0030625465,0.000093815055,0.00009080938,0.000013604618,0.000048075864,0.000027435264,0.0005166134],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99712485,0.00015425395,0.0015270868,0.00073829904,0.00016014445,0.00029535242],"domain_scores_gemma":[0.9980338,0.00007439273,0.00051640876,0.001030501,0.00017206832,0.00017281223],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010649611,0.00017068407,0.00042703518,0.00003638786,0.00004364303,0.0000151258055,0.000045802342,0.00029466377,0.000044506214],"category_scores_gemma":[0.0021376212,0.00017349885,0.00029203529,0.00016367104,0.00011122741,0.000003797761,0.0002517594,0.00019774976,0.0000028640738],"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":[0.000001003191,0.00018760459,0.1617001,0.00002855302,0.000054258777,0.83276325,0.000012263267,0.000019793944,0.0041870726,0.0000041997823,0.00012565605,0.00091622246],"study_design_scores_gemma":[0.00032031987,0.00021155494,0.026462546,0.000028998944,0.00004253884,0.96307725,0.00017010262,0.000020304018,0.005091228,0.00005487659,0.0043376046,0.00018267187],"about_ca_topic_score_codex":0.00015340142,"about_ca_topic_score_gemma":0.00015772473,"teacher_disagreement_score":0.13523756,"about_ca_system_score_codex":0.000009240729,"about_ca_system_score_gemma":0.0003290136,"threshold_uncertainty_score":0.7075078},"labels":[],"label_agreement":null},{"id":"W3166105596","doi":"10.1093/nar/gkab475","title":"The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome","year":2021,"lang":"en","type":"article","venue":"Nucleic Acids Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institutes of Health; Alex's Lemonade Stand Foundation for Childhood Cancer; National Cancer Institute; Damon Runyon Cancer Research Foundation","keywords":"CTCF; Genomic imprinting; Biology; Chromatin; Imprinting (psychology); Genetics; DNA methylation; Chromosome conformation capture; Bivalent chromatin; Gene silencing; Gene; Transcription factor; Gene expression; Chromatin remodeling; Enhancer","score_opus":0.011294666021898632,"score_gpt":0.28726603073821144,"score_spread":0.2759713647163128,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3166105596","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970761,0.0005289093,0.000049628874,0.0006477275,0.00005870526,0.00016589789,0.0000032269108,0.0000014772974,0.0014683502],"genre_scores_gemma":[0.999371,0.00023353408,0.000118995136,0.00003312378,0.000037576814,0.000006371044,0.000008426401,0.000013640105,0.00017734584],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99853086,0.00044952618,0.00023362694,0.00017617285,0.0003514666,0.00025834737],"domain_scores_gemma":[0.9988493,0.00008539321,0.00007108073,0.0006019398,0.00036914827,0.000023144948],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00084098,0.00006835144,0.00009369052,0.000032197648,0.00013232206,0.00003298069,0.00063200435,0.00006903916,0.00005385697],"category_scores_gemma":[0.0007798891,0.00003703676,0.000058594753,0.0007306944,0.00019505281,0.000002436626,0.0005398503,0.00021245805,0.0000049806836],"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":[0.00000568024,0.00005210932,0.04369988,0.0000107820115,0.000019218667,7.171114e-7,0.0005436678,0.0000052050145,0.94774485,0.0003216035,0.00007234412,0.007523973],"study_design_scores_gemma":[0.00029062523,0.00009060105,0.29281902,0.000026377216,0.0000039085185,0.000035574125,0.0078106313,0.00008492251,0.6779438,0.00042718108,0.020408101,0.000059235183],"about_ca_topic_score_codex":0.000048215425,"about_ca_topic_score_gemma":0.000035963483,"teacher_disagreement_score":0.26980102,"about_ca_system_score_codex":0.000016019378,"about_ca_system_score_gemma":0.00013801428,"threshold_uncertainty_score":0.15103152},"labels":[],"label_agreement":null},{"id":"W3169291890","doi":"10.1080/08880018.2021.1933281","title":"Allogeneic hematopoietic stem cell transplantation in an adolescent with Prader-Willi syndrome – unique considerations","year":2021,"lang":"en","type":"letter","venue":"Pediatric Hematology and Oncology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; SickKids Foundation; Hospital for Sick Children; London Health Sciences Centre; University of Toronto","funders":"","keywords":"Medicine; Hematopoietic stem cell transplantation; Stem cell; Transplantation; Haematopoiesis; Oncology; Immunology; Cancer research; Internal medicine; Genetics; Biology","score_opus":0.01613634671782262,"score_gpt":0.24855339131535653,"score_spread":0.2324170445975339,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3169291890","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9559402,0.0063794167,0.0007785727,0.035661455,0.00030386428,0.0006445666,0.000036362857,0.000025939074,0.0002296287],"genre_scores_gemma":[0.93221,0.0047251736,0.0018751291,0.059196196,0.0005551564,0.00018883163,0.00090491585,0.00008748706,0.0002570535],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9970732,0.0006077357,0.0006144171,0.00096259435,0.00014281968,0.0005992521],"domain_scores_gemma":[0.9988875,0.00013993656,0.00030265536,0.00043489708,0.00011063836,0.0001244074],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.00022654176,0.0004394286,0.00078131835,0.00022796226,0.00012544236,0.00003486248,0.00016952849,0.0018686058,0.000048823236],"category_scores_gemma":[0.000015203596,0.00042297662,0.00008353701,0.00015983307,0.0001583361,0.000008457868,0.00008540477,0.00093570456,0.000007170262],"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":[0.000038951213,0.0016061882,0.8505051,0.008632159,0.00040327135,0.012069396,0.0023106334,0.00031383475,0.0045051924,0.00033616557,0.11780402,0.0014750693],"study_design_scores_gemma":[0.017272959,0.015089044,0.35359353,0.0006819138,0.0036921722,0.31910324,0.0030477867,0.00013324335,0.0123895025,0.0011731836,0.2658807,0.007942718],"about_ca_topic_score_codex":0.0000177085,"about_ca_topic_score_gemma":0.0002590712,"teacher_disagreement_score":0.49691162,"about_ca_system_score_codex":0.000041728323,"about_ca_system_score_gemma":0.0007411664,"threshold_uncertainty_score":0.9998222},"labels":[],"label_agreement":null},{"id":"W3185059072","doi":"10.1038/s41598-021-93885-3","title":"Human placental piwi-interacting RNA transcriptome is characterized by expression from the DLK1-DIO3 imprinted region","year":2021,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Capital District Health Authority; BC Cancer Agency; Izaak Walton Killam Health Centre; BC Children's Hospital; Dalhousie University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Genomic imprinting; Transcriptome; Piwi-interacting RNA; RNA; Biology; Computational biology; Gene expression; Genetics; Gene; DNA methylation; RNA interference","score_opus":0.013299611721513357,"score_gpt":0.24977501692902992,"score_spread":0.23647540520751656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3185059072","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99429256,0.00060973415,0.0007426521,0.00028558326,0.0033815345,0.00021678946,0.000013126759,0.000022197002,0.0004358151],"genre_scores_gemma":[0.9921498,0.000019847621,0.00022970459,0.00020431483,0.00022171944,0.000021763453,0.00058387395,0.000027318316,0.0065416927],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9977779,0.000097874305,0.00049427984,0.0009778657,0.00030821943,0.00034388519],"domain_scores_gemma":[0.9984041,0.000012848663,0.0003213485,0.0010159739,0.00013775464,0.00010799019],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003957408,0.00019644294,0.0001867994,0.000025305295,0.0004829501,0.00033786093,0.00021842307,0.00012258104,0.00024609707],"category_scores_gemma":[0.000088073364,0.0001562459,0.00020025253,0.00014115688,0.00011354658,0.000013254966,0.00022400022,0.00015578463,0.000009936264],"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":[0.000005516289,0.000051578405,0.0045361076,0.000008008591,0.000029374727,0.000056559053,0.00027220396,5.743486e-7,0.9802411,3.8619828e-7,0.013359057,0.0014395278],"study_design_scores_gemma":[0.00025627553,0.000023685472,0.0041996813,0.00007204816,0.000016594953,0.0003620664,0.0004543082,0.000014903771,0.87381184,0.000040671912,0.12056836,0.00017957408],"about_ca_topic_score_codex":0.000045385972,"about_ca_topic_score_gemma":0.000007922564,"teacher_disagreement_score":0.1072093,"about_ca_system_score_codex":0.000018738132,"about_ca_system_score_gemma":0.00007339124,"threshold_uncertainty_score":0.63715225},"labels":[],"label_agreement":null},{"id":"W3186869997","doi":"10.1101/2021.07.17.452734","title":"Genome-Wide Detection of Imprinted Differentially Methylated Regions Using Nanopore Sequencing","year":2021,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"University of British Columbia; Canada Research Chairs","keywords":"Genomic imprinting; Imprinting (psychology); Differentially methylated regions; Biology; DNA methylation; Nanopore sequencing; Genetics; Methylated DNA immunoprecipitation; CpG site; Genome; Computational biology; Epigenetics; Germline; Methylation; Gene; Gene expression","score_opus":0.016228537565887033,"score_gpt":0.22196470451478623,"score_spread":0.20573616694889918,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3186869997","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9489431,0.0016626397,0.04801681,0.000016678763,0.00079381623,0.00044945074,0.000043805798,0.00006916741,0.000004536618],"genre_scores_gemma":[0.9907192,0.0003883502,0.008408867,0.00004072787,0.0002434077,0.000038644423,0.000003843269,0.00015071723,0.000006232896],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9969477,0.00021083413,0.000805524,0.001155925,0.00030799865,0.0005720181],"domain_scores_gemma":[0.99668694,0.000020626507,0.00075704977,0.0014761158,0.00084819476,0.00021106491],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000408162,0.0005745054,0.0006603539,0.00022810939,0.00016390053,0.00012700664,0.0005019742,0.000835865,0.00002728952],"category_scores_gemma":[0.000345955,0.00066154054,0.00037506476,0.00034111025,0.00012589885,0.000009325184,0.0010812207,0.00051292556,0.0000029164548],"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":[0.00000995556,0.00005366704,0.0035054653,0.00029179233,0.00037791466,0.000012415047,0.000011391355,0.00040621992,0.9953229,0.000004082583,0.0000010721467,0.0000031649447],"study_design_scores_gemma":[0.00034015518,0.0000777712,0.0894644,0.0002450665,0.00019306812,2.606151e-7,0.000019856518,0.000622596,0.9082811,9.5358064e-7,0.00016000647,0.00059479545],"about_ca_topic_score_codex":0.00016115031,"about_ca_topic_score_gemma":0.000014366814,"teacher_disagreement_score":0.087041795,"about_ca_system_score_codex":0.00018560197,"about_ca_system_score_gemma":0.0008976084,"threshold_uncertainty_score":0.9995836},"labels":[],"label_agreement":null},{"id":"W3191261968","doi":"10.1017/cjn.2019.150","title":"P.050 Epilepsy phenotypes in patients with Sotos syndrome","year":2019,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Saskatoon Medical Imaging; Sherbrooke O.E.M (Canada)","funders":"","keywords":"Sotos syndrome; Epilepsy; Macrocephaly; Medicine; Pediatrics; Levetiracetam; Epilepsy syndromes; Lamotrigine; Psychiatry","score_opus":0.009925297653657796,"score_gpt":0.21445863963426312,"score_spread":0.20453334198060533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3191261968","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99738514,0.00037624023,0.0000105295185,0.00043317245,0.0004911482,0.00017995649,0.000004617411,0.0000036085582,0.0011155779],"genre_scores_gemma":[0.9976322,0.00008716191,0.0010886758,0.0010674981,0.000076070086,0.0000014556931,6.382761e-7,0.000011618927,0.000034688102],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99705815,0.00036752762,0.0005666425,0.00048938394,0.0004914321,0.0010268873],"domain_scores_gemma":[0.9982345,0.00007875493,0.00044877653,0.00016088529,0.00026174504,0.0008153462],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016927193,0.00025277224,0.00035712094,0.00048755016,0.00060862245,0.0002849695,0.001346009,0.00015845564,0.00013726029],"category_scores_gemma":[0.00049517635,0.00016566974,0.00012188525,0.00066335953,0.0018372742,0.00008051684,0.00007618987,0.00055861456,0.0000061172905],"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":[0.000037840495,0.000024050854,0.9959448,0.0000037052673,0.000008433554,0.00029165932,0.000048904665,0.0024694614,0.00010242958,0.000049143553,0.000056493333,0.00096308714],"study_design_scores_gemma":[0.0005042351,0.056228377,0.9370071,0.000027586004,0.00000889446,0.0043160096,0.00008234667,0.00009183915,0.00008270695,0.0006420471,0.000786923,0.000221895],"about_ca_topic_score_codex":0.00054405705,"about_ca_topic_score_gemma":0.018830797,"teacher_disagreement_score":0.05893765,"about_ca_system_score_codex":0.00006322624,"about_ca_system_score_gemma":0.0014466093,"threshold_uncertainty_score":0.99907297},"labels":[],"label_agreement":null},{"id":"W3192140173","doi":"10.1530/ec-21-0277","title":"Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre","year":2021,"lang":"en","type":"article","venue":"Endocrine Connections","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","keywords":"Medicine; Pediatrics; Early adulthood; Young adult; Obstetrics; Gerontology","score_opus":0.015467305862803928,"score_gpt":0.25314786956654034,"score_spread":0.2376805637037364,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3192140173","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970985,0.0004088391,0.00028366168,0.001180012,0.00028022518,0.00017158006,0.00003147333,0.000015873078,0.0005298589],"genre_scores_gemma":[0.9961367,0.00005785227,0.002457173,0.00025126842,0.000074214906,0.00005437189,0.00005920254,0.000022416405,0.0008867951],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99869984,0.00006480377,0.00025962273,0.00051124307,0.00009236072,0.00037212495],"domain_scores_gemma":[0.9994087,0.000027288419,0.000036857557,0.00035428238,0.0000510321,0.00012180986],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00003608504,0.00014785951,0.00017347389,0.00009819328,0.000053634263,0.00003299224,0.00012865785,0.000054992448,0.00026605916],"category_scores_gemma":[0.00037082942,0.00016959393,0.00006222747,0.00038015418,0.000022112436,0.000005962471,0.00017993407,0.000111244655,0.000038640115],"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":[0.000006605787,0.00054128,0.3321798,0.000020552789,0.000044238106,0.00015941699,0.0021221372,0.0006077799,0.6604075,0.00019942231,0.0005325987,0.0031786696],"study_design_scores_gemma":[0.002089634,0.00029485777,0.77466774,0.00013933406,0.000011177384,0.00058822735,0.010260645,0.00010201152,0.107114285,0.00019638598,0.10394535,0.000590347],"about_ca_topic_score_codex":0.00035549948,"about_ca_topic_score_gemma":0.00252843,"teacher_disagreement_score":0.55329317,"about_ca_system_score_codex":0.000036684403,"about_ca_system_score_gemma":0.000071293,"threshold_uncertainty_score":0.691584},"labels":[],"label_agreement":null},{"id":"W3192601169","doi":"10.1002/epi4.12528","title":"Response: Sotos Syndrome and the added value of genetic workup in epilepsy surgery","year":2021,"lang":"en","type":"letter","venue":"Epilepsia Open","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University; McGill University Health Centre; Montreal Children's Hospital","funders":"Savoy Foundation; LivaNova; Biogen","keywords":"Sotos syndrome; Epilepsy; Levetiracetam; Medicine; Pediatrics; Malignancy; Epilepsy surgery; Epileptogenesis; Epilepsy syndromes; Surgery; Pathology; Psychiatry","score_opus":0.01718373920330835,"score_gpt":0.2508722893739756,"score_spread":0.23368855017066725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3192601169","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8954188,0.005047381,0.000052640487,0.09704709,0.0004696597,0.001309699,0.000050991035,0.000006033064,0.0005976694],"genre_scores_gemma":[0.81032276,0.0027873698,0.0034342182,0.17225984,0.00090923475,0.000598665,0.0006884505,0.00025136772,0.00874807],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99603593,0.0014227652,0.0008697328,0.0008485555,0.00028491882,0.00053811364],"domain_scores_gemma":[0.9976261,0.00058656826,0.00042847556,0.0012108069,0.00008388456,0.00006415164],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0017580118,0.0004112569,0.0010214042,0.00013656482,0.00008626616,0.00015097398,0.0009870272,0.0007711498,0.00017121468],"category_scores_gemma":[0.0007171144,0.00033428354,0.00027966526,0.00025818343,0.00032819386,0.0000051415723,0.0014515888,0.00067831523,0.000010408136],"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":[0.0008166524,0.00010556863,0.060605947,0.00046574947,0.0006570434,0.0010621353,0.00028126893,0.00008171571,0.009251579,0.000033941207,0.9212663,0.005372067],"study_design_scores_gemma":[0.0026974233,0.00023579816,0.401433,0.0008241621,0.0001273057,0.0013329235,0.00016360395,0.000056627538,0.0021726377,0.00023086392,0.58983874,0.0008869303],"about_ca_topic_score_codex":0.00025880002,"about_ca_topic_score_gemma":0.000020927353,"teacher_disagreement_score":0.34082705,"about_ca_system_score_codex":0.000019719788,"about_ca_system_score_gemma":0.0004274949,"threshold_uncertainty_score":0.9999109},"labels":[],"label_agreement":null},{"id":"W3196779067","doi":"10.1523/jneurosci.0925-21.2021","title":"Excessive Laughter-like Vocalizations, Microcephaly, and Translational Outcomes in the<i>Ube3a</i>Deletion Rat Model of Angelman Syndrome","year":2021,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research; National Institute of Mental Health; Deutsche Forschungsgemeinschaft; Foundation for Angelman Syndrome Therapeutics; Ontario Brain Institute","keywords":"Laughter; Angelman syndrome; UBE3A; Neuroscience; Psychology; Neurodevelopmental disorder; Intellectual disability; Microcephaly; Disease; Phenotype; Fragile X syndrome; Developmental psychology; Medicine; Autism; Biology; Psychiatry; Genetics; Pathology","score_opus":0.018091002529620027,"score_gpt":0.2606791225541923,"score_spread":0.24258812002457225,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3196779067","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99159306,0.0004458005,0.007156355,0.000609252,0.000120799676,0.000039499115,0.0000053011204,5.8038745e-7,0.000029377014],"genre_scores_gemma":[0.9981057,0.00026193942,0.0010722213,0.00045301064,0.000013677757,8.375145e-7,0.0000021069575,0.000004208529,0.00008627785],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99924386,0.000057529338,0.0002759204,0.00013481526,0.00018934863,0.00009852416],"domain_scores_gemma":[0.9995809,0.000016349775,0.00016393776,0.000101776495,0.00010640276,0.000030637966],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020418028,0.00006646969,0.00012032215,0.000048482067,0.00004533299,0.000025445563,0.00016057046,0.00003504608,0.0000016302237],"category_scores_gemma":[0.00007669092,0.00004955969,0.000055850818,0.00013796867,0.00007650952,0.000012941549,0.000035725443,0.00006713395,8.695059e-8],"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":[0.0000030280792,0.00006041815,0.031203976,0.000011386612,0.000002394596,0.000013207437,0.00011173731,0.0022480327,0.9659913,0.000026956586,0.00004668652,0.00028084853],"study_design_scores_gemma":[0.0012307217,0.0004580127,0.8831634,0.00007368913,0.000039383274,0.004347148,0.0003692039,0.009025032,0.098556116,0.0005657287,0.0019397534,0.00023183943],"about_ca_topic_score_codex":0.0000011648483,"about_ca_topic_score_gemma":0.0000052627074,"teacher_disagreement_score":0.8674352,"about_ca_system_score_codex":0.0000020475532,"about_ca_system_score_gemma":0.000088460045,"threshold_uncertainty_score":0.20209855},"labels":[],"label_agreement":null},{"id":"W3203823955","doi":"10.1016/j.stemcr.2021.09.002","title":"Large-scale analysis of imprinting in naive human pluripotent stem cells reveals recurrent aberrations and a potential link to FGF signaling","year":2021,"lang":"en","type":"article","venue":"Stem Cell Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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":"Azrieli Foundation; Israel Science Foundation; Rosetrees Trust","keywords":"Biology; Imprinting (psychology); Genomic imprinting; Induced pluripotent stem cell; DNA methylation; Reprogramming; Genetics; Embryonic stem cell; Epigenetics; Genomics; Computational biology; Gene; Genome; Gene expression","score_opus":0.009291860211971608,"score_gpt":0.24166990324657212,"score_spread":0.2323780430346005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3203823955","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99597573,0.0007297743,0.0025323944,0.000044568806,0.00018084416,0.00021651892,0.000011109454,0.0000060414304,0.000303041],"genre_scores_gemma":[0.99768656,0.000056055687,0.0011689344,0.00003190338,0.00006043693,0.00001540487,0.000050314386,0.000017983964,0.000912402],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9980234,0.00009024269,0.0007816782,0.00061111804,0.0001899439,0.0003036554],"domain_scores_gemma":[0.9988713,0.000010002105,0.00035820814,0.0004515231,0.0001883674,0.000120548655],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00052679685,0.00016376442,0.00036375097,0.0001565251,0.00009584647,0.00004027518,0.00007218283,0.00012106123,0.00002157194],"category_scores_gemma":[0.000011345093,0.00017683064,0.00019260688,0.00039494742,0.00001866144,0.0000037339998,0.00028077827,0.00009661028,8.0923957e-7],"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":[0.0000025148815,0.00006795318,0.02425927,0.000062833205,0.00013699324,0.00006052175,0.0005964821,0.0029618936,0.9701701,0.0000022772683,0.00001663207,0.0016625698],"study_design_scores_gemma":[0.00025998914,0.00013571024,0.04809282,0.00009212025,0.00031951375,0.00006621224,0.002108325,0.00047479934,0.9474938,0.000017212582,0.0006610394,0.00027843885],"about_ca_topic_score_codex":0.000027212407,"about_ca_topic_score_gemma":0.000085524356,"teacher_disagreement_score":0.023833549,"about_ca_system_score_codex":0.000018670144,"about_ca_system_score_gemma":0.00006605008,"threshold_uncertainty_score":0.7210944},"labels":[],"label_agreement":null},{"id":"W3207949079","doi":"","title":"Unique Circumstances and Family Stress: Having a Sibling with Prader-Willi Syndrome","year":2021,"lang":"en","type":"article","venue":"Student Research Proceedings","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"MacEwan University","funders":"","keywords":"Psychology; Sister; Sibling; Developmental psychology; Context (archaeology); Anxiety; Depression (economics); Neglect; Clinical psychology; Medicine; Psychiatry","score_opus":0.04991309114187602,"score_gpt":0.3578921124897909,"score_spread":0.3079790213479149,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3207949079","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9928803,0.002634884,0.000112052185,0.0003420247,0.00003354921,0.0003256676,0.0000039801507,0.000018475675,0.0036490567],"genre_scores_gemma":[0.9958008,0.0012782064,0.0014606976,0.00006785161,0.00009570366,0.00007574522,0.000011280915,0.000033506916,0.0011762268],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99782974,0.000040089326,0.00020322087,0.00067541463,0.0006414739,0.00061006227],"domain_scores_gemma":[0.9989105,0.000025253557,0.000059362934,0.00018146272,0.0006550034,0.00016845547],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00067814376,0.00017716945,0.00018921579,0.000114725466,0.00029776085,0.00032437156,0.00027038672,0.00010998871,0.000011612303],"category_scores_gemma":[0.00017354079,0.00015486339,0.000037605663,0.0004187687,0.00018813326,0.0000155165,0.00059272564,0.0003011012,0.0000029889015],"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":[0.0000030683698,0.00012025582,0.51214355,0.00024151342,0.00013054059,0.000022155156,0.0009612945,0.0000053127756,0.48421595,0.0003485751,0.00031841503,0.0014893848],"study_design_scores_gemma":[0.0011363678,0.0013921685,0.897342,0.000669779,0.000028731978,0.0007664105,0.02622557,0.000039639577,0.061523955,0.00027316101,0.010065909,0.000536288],"about_ca_topic_score_codex":0.00004272681,"about_ca_topic_score_gemma":0.000033338732,"teacher_disagreement_score":0.422692,"about_ca_system_score_codex":0.000025514602,"about_ca_system_score_gemma":0.00017412724,"threshold_uncertainty_score":0.63151455},"labels":[],"label_agreement":null},{"id":"W35139074","doi":"10.1371/journal.pgen.1009644","title":"人CYP17基因启动子5＇上游-34碱基处T→C突变与复发性流产","year":2010,"lang":"en","type":"article","venue":"现代妇产科进展","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; National Institute of General Medical Sciences; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Geology","score_opus":0.005039009677445543,"score_gpt":0.22708826777008523,"score_spread":0.22204925809263967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W35139074","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9816131,0.0001481689,0.0004507167,0.00021675885,0.0007142208,0.00009876837,0.0000043324076,0.000022526505,0.016731393],"genre_scores_gemma":[0.9920297,0.000031610394,0.0031308706,0.0003449079,0.0005063297,0.000011771631,0.000031334053,0.00002704794,0.0038863793],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99910647,0.000016193762,0.00016058139,0.0003140984,0.000107553744,0.00029513513],"domain_scores_gemma":[0.9993037,0.0000065521353,0.000050874278,0.00048005793,0.000050690545,0.0001081507],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014509915,0.00013683485,0.000108517,0.00002881382,0.00007996759,0.000033450346,0.00023506228,0.00016292802,0.00027487383],"category_scores_gemma":[0.00009657119,0.00012916868,0.000092026356,0.00006255624,0.00006158287,0.0000018893534,0.00015091735,0.00015121543,0.00016842467],"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":[0.0000030338958,0.000027329406,0.008989731,0.000006540136,0.000017911481,0.0000016076672,0.00002199665,0.0000037158516,0.97366834,0.00022729533,0.0033796548,0.013652817],"study_design_scores_gemma":[0.00056589075,0.00016169436,0.06915268,0.0000060439284,0.000015001639,0.00013050469,0.00005539805,0.000062012085,0.34666932,0.00024213271,0.58260465,0.0003346529],"about_ca_topic_score_codex":0.00001995096,"about_ca_topic_score_gemma":0.00003754655,"teacher_disagreement_score":0.626999,"about_ca_system_score_codex":0.0000027056196,"about_ca_system_score_gemma":0.00004158961,"threshold_uncertainty_score":0.5267346},"labels":[],"label_agreement":null},{"id":"W4051065","doi":"10.2105/ajph.75.11.1288","title":"Maintenance of germ line and somatic DNA methylation during mouse development","year":2003,"lang":"en","type":"article","venue":"American journal of public health","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Genomic imprinting; DNA methylation; Biology; Imprinting (psychology); Genetics; Methylation; RNA-Directed DNA Methylation; Transgene; Epigenetics; Gene; Gene expression","score_opus":0.019194254761217444,"score_gpt":0.2721981206192444,"score_spread":0.253003865858027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4051065","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9859894,0.00046179414,0.01289997,0.00051365007,0.000038365593,0.000049603274,6.6861077e-7,0.0000014220456,0.000045132194],"genre_scores_gemma":[0.98022586,0.00036712753,0.019173075,0.00012842633,0.000028094219,9.560528e-7,0.0000013474555,0.000009331708,0.00006578493],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989438,0.00013870659,0.0004778827,0.000099307654,0.00012167269,0.00021860847],"domain_scores_gemma":[0.9988818,0.000011259356,0.00069969735,0.00010365615,0.00013229485,0.00017130178],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010037769,0.000074830044,0.00021840153,0.00007382814,0.000047343834,0.0000111680665,0.000072951254,0.000019924772,0.000005404106],"category_scores_gemma":[0.00026268035,0.00006378868,0.00003620127,0.00010476003,0.00006616244,0.0000052945015,0.000025410136,0.00006203053,3.0538453e-7],"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":[0.000011457084,0.0001621551,0.03521393,0.0001933072,0.00015164143,0.0000021211356,0.0015410736,0.00006387634,0.5445891,0.00010516772,0.00005203072,0.41791412],"study_design_scores_gemma":[0.0022897571,0.0031269637,0.49068245,0.00016971848,0.000017528904,0.0011526941,0.0055483007,0.000059924172,0.4731208,0.00007206456,0.023323113,0.00043667216],"about_ca_topic_score_codex":0.000010418761,"about_ca_topic_score_gemma":0.0000042637844,"teacher_disagreement_score":0.4554685,"about_ca_system_score_codex":0.000027615455,"about_ca_system_score_gemma":0.00047567248,"threshold_uncertainty_score":0.2601227},"labels":[],"label_agreement":null},{"id":"W4200396616","doi":"10.1007/s11657-021-01040-2","title":"Publisher Correction: Exercise for improving age-related hyperkyphosis: a systematic review and meta-analysis with GRADE assessment","year":2021,"lang":"en","type":"review","venue":"Archives of Osteoporosis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Research Institute for Aging; University of Waterloo","funders":"","keywords":"Meta-analysis; Medicine; Physical therapy; Physical medicine and rehabilitation; Gerontology; Internal medicine","score_opus":0.03151592619834888,"score_gpt":0.30105692603731293,"score_spread":0.26954099983896407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4200396616","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0000100781635,0.99656856,0.0004602035,0.000038686776,0.00010168081,0.0025816886,0.00004529826,0.000009433149,0.00018439635],"genre_scores_gemma":[0.00019675666,0.9876534,0.0070478665,0.00004652879,0.0000113408105,0.0015958757,0.0006435666,0.00006536694,0.002739303],"study_design_codex":"systematic_review","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9973543,0.00026181745,0.0011198628,0.00079191005,0.00019231018,0.00027976756],"domain_scores_gemma":[0.9976634,0.00014232678,0.0010954416,0.0008869327,0.000100428406,0.00011151061],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00038691223,0.00050175906,0.005327642,0.00019307106,0.00009053699,0.00009738241,0.00031807652,0.00017184688,0.000024715364],"category_scores_gemma":[0.00013204741,0.00033861512,0.0026182386,0.00043098905,0.00010558937,0.000007423248,0.00024900155,0.00015385868,3.3828186e-7],"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":[0.0000015023687,0.000091716705,0.000007698519,0.85517436,0.11744789,0.000002769794,0.000063167085,0.0000049793116,0.000033656645,0.0000066047537,0.00022738997,0.02693825],"study_design_scores_gemma":[0.00019489991,0.000253177,0.000009936165,0.027195828,0.9637047,0.00011188992,0.00011268834,0.000013132984,0.000019526758,0.0000067620026,0.007901751,0.00047569026],"about_ca_topic_score_codex":0.000034202127,"about_ca_topic_score_gemma":0.000015515561,"teacher_disagreement_score":0.84625685,"about_ca_system_score_codex":0.0000094891975,"about_ca_system_score_gemma":0.00016530894,"threshold_uncertainty_score":0.9999066},"labels":[],"label_agreement":null},{"id":"W4206219844","doi":"10.1038/npg.els.0005823","title":"Chromosome 14","year":2006,"lang":"en","type":"other","venue":"Encyclopedia of Life Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Chromosome; Centromere; Gene; Genetics; Biology; Chromosome 22; Genome","score_opus":0.008982955648986138,"score_gpt":0.2428887717947663,"score_spread":0.23390581614578018,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206219844","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.014139311,0.0064749606,0.00008095463,0.000045760447,0.0006740329,0.00012656115,0.00002478995,0.00001794412,0.97841567],"genre_scores_gemma":[0.020271288,0.004003671,0.005271177,0.00011216394,0.0017053629,0.0000133322055,0.000055543434,0.00015817837,0.9684093],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99883765,0.000027331816,0.00023210162,0.000403768,0.00025231685,0.0002468164],"domain_scores_gemma":[0.9993927,0.000007448455,0.00023947602,0.0002702028,0.000021717025,0.000068489746],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016953266,0.00017879458,0.00022521423,0.00010630876,0.000043171643,0.000010148804,0.00043212547,0.00020521818,0.00028609033],"category_scores_gemma":[0.000099961886,0.00015396712,0.000091245296,0.00014649902,0.00032463064,0.0000012752125,0.00014343517,0.000054403197,0.000027802063],"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":[6.1898214e-7,0.00003206655,0.008178872,0.00005449739,0.000024287392,5.498497e-7,0.000009210222,0.000014058257,0.003283193,0.00003513187,0.98659587,0.0017716383],"study_design_scores_gemma":[0.00012396772,0.00014531934,0.0022306256,0.000046952366,0.00001023952,0.0000038816615,0.00002121321,0.0000032432342,0.00070659636,0.000026998683,0.9964702,0.00021074539],"about_ca_topic_score_codex":0.00022137773,"about_ca_topic_score_gemma":0.00010520703,"teacher_disagreement_score":0.010006404,"about_ca_system_score_codex":0.0000023492603,"about_ca_system_score_gemma":0.0002053363,"threshold_uncertainty_score":0.6278597},"labels":[],"label_agreement":null},{"id":"W4206265803","doi":"10.1101/2022.01.10.21268493","title":"Network-based integrative analysis of lithium response in bipolar disorder using transcriptomic and GWAS data","year":2022,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Center for Advancing Translational Sciences; National Institute of Mental Health; National Institutes of Health; Genome Atlantic; University of California, San Diego; Dalhousie University; Research Nova Scotia; U.S. Department of Veterans Affairs; Paul G. Allen Frontiers Group; Georgia Clinical and Translational Science Alliance; Dalhousie Medical Research Foundation; JPB Foundation; Canadian Institutes of Health Research; American Heart Association","keywords":"Genome-wide association study; Transcriptome; Computational biology; Biology; Bipolar disorder; Candidate gene; Gene; Gene expression profiling; Gene regulatory network; Genetics; Lithium (medication); Single-nucleotide polymorphism; Gene expression; Endocrinology; Genotype","score_opus":0.032882806206032476,"score_gpt":0.29736505055948925,"score_spread":0.2644822443534568,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206265803","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9820587,0.010329622,0.006785118,0.000088589964,0.00017913421,0.00023642757,0.00030313228,0.000005174056,0.00001412186],"genre_scores_gemma":[0.9956934,0.00036124804,0.0029128012,0.00006924659,0.000037147245,0.000017457603,0.0008304085,0.000030406762,0.000047889298],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9977448,0.00056861585,0.0004662902,0.0007950629,0.00016275127,0.00026249755],"domain_scores_gemma":[0.9983777,0.000058401383,0.00023487622,0.0012251788,0.000049188766,0.000054693694],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0013264634,0.00026069707,0.00053204305,0.0003052254,0.00005612422,0.000023543724,0.00062007445,0.00021855801,0.000060184113],"category_scores_gemma":[0.00020183933,0.00025337486,0.00015403409,0.0004922164,0.00010668246,0.0000025144955,0.0012403259,0.0003530565,1.3620084e-7],"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":[0.00031136812,0.00008879947,0.7509672,0.00009010918,0.00078590534,0.000004675098,0.000283167,0.10011063,0.14637108,0.0000032169512,0.00002558252,0.0009582307],"study_design_scores_gemma":[0.00090588845,0.00032817014,0.80536926,0.00014499057,0.0014389186,0.0000052862574,0.00046782268,0.1706382,0.0050156857,0.000045881945,0.014951466,0.0006884553],"about_ca_topic_score_codex":0.0004678348,"about_ca_topic_score_gemma":0.00039305206,"teacher_disagreement_score":0.1413554,"about_ca_system_score_codex":0.000022024873,"about_ca_system_score_gemma":0.00021949796,"threshold_uncertainty_score":0.99999183},"labels":[],"label_agreement":null},{"id":"W4210561741","doi":"10.1096/fasebj.22.1_supplement.306.2","title":"Glucose transporter type 2 (GLUT2) genotype is associated with higher intakes of sugars in two distinct populations","year":2008,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"GLUT2; Allele; Population; Type 2 diabetes; Genotype; Biology; Medicine; Food intake; Endocrinology; Diabetes mellitus; Internal medicine; Physiology; Genetics; Glucose transporter; Insulin; Gene; Environmental health","score_opus":0.026378080613727255,"score_gpt":0.25799924830692544,"score_spread":0.23162116769319818,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210561741","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988009,0.00037716184,0.0001508771,0.00010949295,0.00011071568,0.000058833382,0.000007796664,0.0000025602237,0.00038166012],"genre_scores_gemma":[0.9989392,0.00007577292,0.00035495553,0.00008365761,0.00007257584,0.000001031635,0.000022788823,0.000014076167,0.00043593725],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993269,0.000049540584,0.00022331432,0.000104899686,0.00012514545,0.00017023741],"domain_scores_gemma":[0.99957764,0.000007728458,0.00013285429,0.00015248156,0.0000846424,0.000044622553],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015432076,0.00009328322,0.00012361736,0.000032060274,0.00010125048,0.000008243983,0.00013786781,0.00004182945,0.00013259],"category_scores_gemma":[0.000020063348,0.00006110615,0.00005615467,0.00012371884,0.00007417139,0.0000031375594,0.000016818864,0.00012763232,0.0000026695823],"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":[0.000056793782,0.00008406201,0.62070805,0.0000032615085,0.000095147334,0.000021382855,0.0003983818,0.00023825753,0.377254,0.000015699663,0.00021179162,0.0009131663],"study_design_scores_gemma":[0.0007921445,0.00020404457,0.9407444,0.000026701671,0.000032658074,0.00024592402,0.000055840956,0.000037158294,0.05736476,0.00006212911,0.00032801332,0.0001062234],"about_ca_topic_score_codex":0.00006306607,"about_ca_topic_score_gemma":0.0001697286,"teacher_disagreement_score":0.32003635,"about_ca_system_score_codex":0.000012015621,"about_ca_system_score_gemma":0.00006325474,"threshold_uncertainty_score":0.24918362},"labels":[],"label_agreement":null},{"id":"W4210836986","doi":"10.3410/f.1007260.264660","title":"Faculty Opinions recommendation of Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion.","year":2004,"lang":"en","type":"dataset","venue":"Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Breakpoint; Sotos syndrome; Genetics; Haploinsufficiency; Gene; Biology; Craniofacial; Chromosome; Phenotype","score_opus":0.010268431137120185,"score_gpt":0.28909266394488126,"score_spread":0.2788242328077611,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210836986","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0022522702,0.000490061,0.000067516696,0.013720088,0.00035382417,0.0017745073,0.98132366,0.0000082369315,0.000009838112],"genre_scores_gemma":[0.005904874,0.000172205,0.00041004858,0.00041581382,0.000044162523,0.00018090305,0.99263424,0.000030081475,0.00020768933],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9960374,0.00032673994,0.0018091823,0.00066536514,0.000877123,0.00028418124],"domain_scores_gemma":[0.99283594,0.000028952829,0.0021401357,0.0012154682,0.003654161,0.00012533153],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00096592394,0.00041840348,0.000791695,0.0003704549,0.000106486696,0.000056395114,0.0009918128,0.000624895,0.000053781878],"category_scores_gemma":[0.0014516588,0.00030867374,0.00033946504,0.001238339,0.0002297733,0.000043489705,0.0003365232,0.0004696018,0.0000067417295],"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":[0.000028115097,0.0007793277,0.0006297245,0.0054234937,0.0001466116,1.1328215e-7,0.00006724958,0.0000019895742,0.000116423995,0.000031461244,0.9913722,0.0014032688],"study_design_scores_gemma":[0.0017458266,0.00046206047,0.123496436,0.0073098848,0.00013455101,0.000027114162,0.000022398237,0.0000055616138,0.00041715382,0.000020317057,0.86602974,0.00032895076],"about_ca_topic_score_codex":0.000105907246,"about_ca_topic_score_gemma":0.000019399487,"teacher_disagreement_score":0.12534247,"about_ca_system_score_codex":0.0001017474,"about_ca_system_score_gemma":0.0003611153,"threshold_uncertainty_score":0.9999365},"labels":[],"label_agreement":null},{"id":"W4210985019","doi":"10.1101/2022.02.11.479460","title":"BORIS/CTCFL-mediated chromatin accessibility alterations promote a pro-invasive transcriptional signature in melanoma cells","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University; Jewish General Hospital","funders":"","keywords":"Ectopic expression; Chromatin; Melanoma; Biology; Transcription factor; Reprogramming; Promoter; Cancer research; Chromatin immunoprecipitation; Phenotype; Transcriptional regulation; Bivalent chromatin; Gene; Cell biology; Gene expression; Chromatin remodeling; Genetics","score_opus":0.011069053623991035,"score_gpt":0.2273465842418269,"score_spread":0.2162775306178359,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210985019","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9943444,0.0015685207,0.00050966174,0.00018496212,0.00093929865,0.0015642544,0.0007867408,0.00008553087,0.000016614133],"genre_scores_gemma":[0.9942226,0.00024384446,0.0040194443,0.00018366978,0.00037607827,0.00079081766,0.000024054798,0.000119015014,0.000020502146],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9962439,0.00031320538,0.0008083507,0.0015349572,0.0004508991,0.00064870314],"domain_scores_gemma":[0.99776506,0.000034712117,0.0004412226,0.0012267242,0.00030829443,0.00022400254],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00068520254,0.0006212929,0.0005420914,0.00022211194,0.00021714832,0.00018740864,0.00079617556,0.00072818104,0.0002528221],"category_scores_gemma":[0.00027701992,0.0006958261,0.00024883106,0.00044511657,0.000102820086,0.000017269964,0.000723797,0.0010085376,0.000016102258],"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":[0.000019531293,0.0002800644,0.007985557,0.0003370928,0.00011617876,0.000024076262,0.000030142151,0.00033506678,0.99066556,0.000020750409,0.00018304246,0.0000029188748],"study_design_scores_gemma":[0.0009007437,0.00021504718,0.20190172,0.00018082155,0.000064245534,1.16393515e-7,0.000013737468,0.00040622285,0.7907313,0.000004059307,0.004695034,0.00088693015],"about_ca_topic_score_codex":0.000055273136,"about_ca_topic_score_gemma":0.000027067064,"teacher_disagreement_score":0.19993424,"about_ca_system_score_codex":0.00019901495,"about_ca_system_score_gemma":0.0013302555,"threshold_uncertainty_score":0.99954927},"labels":[],"label_agreement":null},{"id":"W4211064310","doi":"10.1002/ajmg.c.30267","title":"Beckwith–Wiedemann syndrome","year":2010,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":297,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Imprinting (psychology); Epigenetics; Genetics; Biology; Gene; Untranslated region; Gene expression; Messenger RNA; DNA methylation","score_opus":0.017864193219866785,"score_gpt":0.33544943385092874,"score_spread":0.31758524063106197,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4211064310","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.029837968,0.9660722,0.0004924682,0.00036421735,0.002513486,0.00044462833,0.000023745602,0.0000110345045,0.00024022309],"genre_scores_gemma":[0.0010803642,0.990546,0.0053554755,0.0006032016,0.0017975509,0.000038597238,0.00008235056,0.00022947708,0.00026699787],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.988449,0.00083429366,0.0037614142,0.0010448615,0.004581993,0.0013284635],"domain_scores_gemma":[0.9933464,0.00039728204,0.0023146,0.0013011863,0.00031629825,0.0023242685],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":["research_integrity"],"category_scores_codex":[0.0046100076,0.0010838214,0.0036240565,0.00054064445,0.000101093865,0.000078536665,0.003853887,0.0024080302,0.0008143939],"category_scores_gemma":[0.0031948658,0.00090657827,0.0011904588,0.000911309,0.0018306092,0.000004965726,0.0012310522,0.0036700747,0.000060452636],"study_design_candidate":"design_other","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":[0.000010019732,0.00033657785,0.00031973928,0.0008539776,0.00030386596,0.00088747847,0.000053134667,0.000007693172,0.00001981311,0.000003595976,0.0026627393,0.99454135],"study_design_scores_gemma":[0.00077999354,0.002733636,0.00009972197,0.012602078,0.00052071176,0.017953383,0.00015548592,0.000061481165,0.000034299308,0.00002388031,0.9641468,0.00088851695],"about_ca_topic_score_codex":0.000011141162,"about_ca_topic_score_gemma":0.000037144488,"teacher_disagreement_score":0.9936528,"about_ca_system_score_codex":0.00007915745,"about_ca_system_score_gemma":0.003969116,"threshold_uncertainty_score":0.9993385},"labels":[],"label_agreement":null},{"id":"W4211087283","doi":"10.1002/mgg3.1843","title":"A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome","year":2022,"lang":"en","type":"review","venue":"Molecular Genetics & Genomic Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Foundation for Angelman Syndrome Therapeutics; Angelman Syndrome Foundation","keywords":"Medicine; Health care; Angelman syndrome; Intervention (counseling); Multidisciplinary approach; Psychiatry; Psychology; Family medicine","score_opus":0.029301818757621393,"score_gpt":0.33384397302053886,"score_spread":0.3045421542629175,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4211087283","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.012313875,0.9778894,0.005207979,0.000028326724,0.0002096655,0.0029968189,0.00065405865,0.000011197453,0.00068865676],"genre_scores_gemma":[0.002935352,0.9768571,0.017722022,0.00005098949,0.000106152926,0.0005111752,0.0010932373,0.0002724423,0.00045152547],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99696666,0.0001738475,0.000961951,0.0009984304,0.00041419372,0.00048494237],"domain_scores_gemma":[0.9981705,0.000040538627,0.0004610756,0.00089168356,0.00015377782,0.0002824406],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00062690844,0.00056904135,0.0015283751,0.0002711264,0.00010200516,0.00001609447,0.0004452329,0.00023619855,0.00007336081],"category_scores_gemma":[0.00015992823,0.0005277719,0.00027479703,0.00020148189,0.00017430312,6.313297e-7,0.0008963725,0.00015154116,0.0000010659951],"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":[0.00006337296,0.00015273664,0.000044906734,0.034516912,0.0013228046,0.00006963625,0.001479635,0.00046256784,0.020996798,0.00005370704,0.0019724562,0.93886447],"study_design_scores_gemma":[0.0009265384,0.0024777863,0.00004006086,0.0009185238,0.0008291692,0.00031937548,0.00087188074,0.00002615211,0.0002052925,0.000009383225,0.9928567,0.0005191668],"about_ca_topic_score_codex":0.000023676814,"about_ca_topic_score_gemma":0.0000075227867,"teacher_disagreement_score":0.9908842,"about_ca_system_score_codex":0.00010936262,"about_ca_system_score_gemma":0.0004632863,"threshold_uncertainty_score":0.99971735},"labels":[],"label_agreement":null},{"id":"W4211106289","doi":"10.1007/978-3-319-68192-4_9","title":"Syndromic Obesity","year":2017,"lang":"en","type":"book-chapter","venue":"Contemporary Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Alberta Hospital","funders":"","keywords":"Obesity; Medicine; Genetic syndromes; Mutation; Internal medicine; Genetics; Pediatrics; Bioinformatics; Biology; Gene","score_opus":0.03242328646650253,"score_gpt":0.2538936169145437,"score_spread":0.22147033044804118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4211106289","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.016536016,0.011700606,0.000082977866,0.00020876118,0.0011753978,0.00039936692,0.00006203368,0.000047144014,0.9697877],"genre_scores_gemma":[0.44929326,0.0008978022,0.00010368799,0.00016333439,0.00039716225,0.000012521369,0.00024399684,0.000078758276,0.54880947],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9981345,0.000028789424,0.00040567323,0.0008460513,0.00012717521,0.00045778978],"domain_scores_gemma":[0.99780613,0.000012762132,0.00043312358,0.0015258709,0.00008984343,0.00013229784],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000085140375,0.00048409327,0.0005777043,0.000097160526,0.00019784967,0.00004285575,0.00076969893,0.0006006635,0.00025203134],"category_scores_gemma":[0.00006061663,0.0005157361,0.00031310672,0.00000405478,0.0003243513,0.000003921719,0.00073506526,0.0003588139,0.00041269878],"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":[0.00033946714,0.0004526794,0.038866412,0.00108304,0.0063128946,0.0039063552,0.00018461874,0.000013829356,0.123122044,0.14239565,0.5227043,0.16061874],"study_design_scores_gemma":[0.0005974237,0.00035781952,0.0021858271,0.000069522364,0.000039396164,0.00085285003,0.0000053134104,0.0000018708586,0.002095426,0.002181979,0.9910316,0.0005810022],"about_ca_topic_score_codex":0.000032880223,"about_ca_topic_score_gemma":0.000016757465,"teacher_disagreement_score":0.46832728,"about_ca_system_score_codex":0.000019526547,"about_ca_system_score_gemma":0.0002819201,"threshold_uncertainty_score":0.9997294},"labels":[],"label_agreement":null},{"id":"W4214511712","doi":"10.1210/clinem/dgac105","title":"The Efficacy, Safety, and Pharmacology of a Ghrelin O-Acyltransferase Inhibitor for the Treatment of Prader-Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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 Universitaire Sainte-Justine; University of Alberta; Centre Hospitalier de l’Université de Montréal","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; Eli Lilly and Company","keywords":"Placebo; Medicine; Adverse effect; Pharmacodynamics; Internal medicine; Pharmacokinetics; Ghrelin; Appetite; Crossover study; Endocrinology; Obesity; Clinical trial; Pharmacology; Hormone","score_opus":0.03070680707183707,"score_gpt":0.3471978001677184,"score_spread":0.3164909930958813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4214511712","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96317315,0.028626401,0.00039396028,0.0058177733,0.0014806332,0.00046450592,0.000028977945,0.0000018688853,0.000012708877],"genre_scores_gemma":[0.9517108,0.047131065,0.00023323871,0.0002551569,0.00051486806,0.000022063246,0.0000024071724,0.000017023382,0.000113342125],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99721515,0.0007771362,0.0013593321,0.00016707239,0.0001767573,0.00030454248],"domain_scores_gemma":[0.9966544,0.0020289184,0.000776572,0.00032837354,0.0001441242,0.00006760405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015698301,0.00015917189,0.00061829237,0.000037136153,0.00031948133,0.000005430555,0.0005297066,0.00007248072,0.000030928335],"category_scores_gemma":[0.00031002436,0.00007749,0.00043089397,0.00007821498,0.00065698184,0.0000029787577,0.00016636656,0.00028125237,3.2022515e-7],"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":[0.005542777,0.004145585,0.009014182,0.00009334459,0.009087158,0.00002438982,0.0018018795,0.004268082,0.5027909,0.0016321903,0.0034960792,0.45810342],"study_design_scores_gemma":[0.011921603,0.009940615,0.09941381,0.000009484332,0.0016271438,0.0023122309,0.0009453251,0.00012716078,0.05111878,0.00025441317,0.82215,0.00017941378],"about_ca_topic_score_codex":0.000016340386,"about_ca_topic_score_gemma":0.000004450573,"teacher_disagreement_score":0.81865394,"about_ca_system_score_codex":0.000006545371,"about_ca_system_score_gemma":0.00015355901,"threshold_uncertainty_score":0.31599507},"labels":[],"label_agreement":null},{"id":"W4224224823","doi":"10.3390/jcm11082268","title":"Serum Asprosin Concentrations in Children with Prader–Willi Syndrome: Correlations with Metabolic Parameters","year":2022,"lang":"en","type":"article","venue":"Journal of Clinical Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Stollery Children’s Hospital Foundation; Canadian Institutes of Health Research; Women and Children's Health Research Institute; Foundation for Prader-Willi Research","keywords":"Medicine; Postprandial; Internal medicine; Endocrinology; Overweight; Obesity; Insulin resistance; Insulin; Leptin; Metabolic syndrome; Adipose tissue","score_opus":0.023468248629222126,"score_gpt":0.31687579950565775,"score_spread":0.2934075508764356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224224823","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99487644,0.0010327034,0.0011361617,0.0023664238,0.00023712301,0.00021212544,0.0000058254327,0.0000025071765,0.00013068222],"genre_scores_gemma":[0.9965184,0.000260273,0.0023735675,0.0005396602,0.00016429373,0.000009142246,0.000015118177,0.000015484455,0.00010407194],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9982546,0.00020141718,0.0008350464,0.00018894135,0.00033370877,0.00018629368],"domain_scores_gemma":[0.99890643,0.00008376439,0.0005783642,0.00019458745,0.000095894604,0.00014097453],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00091310096,0.000116392606,0.00041248163,0.000077195626,0.00008548854,0.000008058984,0.00018799448,0.000058230587,0.00007857253],"category_scores_gemma":[0.00035728115,0.000076327466,0.00007644645,0.00023692436,0.00018297593,0.0000065222293,0.000053524993,0.00045526537,7.490466e-7],"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":[0.000019343204,0.00014250097,0.9935623,0.000002526848,0.00020581105,0.000007000493,0.00004875984,0.002529602,0.00047803117,0.000032365762,0.00027487223,0.0026969132],"study_design_scores_gemma":[0.003500899,0.004770618,0.9846579,0.00005187724,0.00013930685,0.0026562891,0.00032366082,0.00008362127,0.00010550735,0.00002609225,0.0035797367,0.000104500294],"about_ca_topic_score_codex":0.000017048815,"about_ca_topic_score_gemma":0.000013435269,"teacher_disagreement_score":0.008904383,"about_ca_system_score_codex":0.000009531369,"about_ca_system_score_gemma":0.00022446588,"threshold_uncertainty_score":0.31125435},"labels":[],"label_agreement":null},{"id":"W4225123264","doi":"10.1371/journal.pgen.1010186","title":"Subnuclear localisation is associated with gene expression more than parental origin at the imprinted Dlk1-Dio3 locus","year":2022,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Medical Research Council; Canadian Institutes of Health Research; Deutsche Forschungsgemeinschaft; Wellcome Trust","keywords":"Biology; Imprinting (psychology); Genomic imprinting; Allele; Locus (genetics); Genetics; Gene; Mutant; Gene expression; Cell biology; DNA methylation","score_opus":0.01517431627127163,"score_gpt":0.22800009878546648,"score_spread":0.21282578251419484,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4225123264","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982036,0.00062570936,0.00018601459,0.00024213911,0.00013557992,0.00033892767,0.00009236827,0.000026305393,0.00014939118],"genre_scores_gemma":[0.99784964,0.0000825068,0.00021025084,0.00037489773,0.00010799153,0.0000651461,0.00037847683,0.00006624062,0.0008648219],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982732,0.0001409111,0.0002561559,0.0004842443,0.00046209464,0.0003833818],"domain_scores_gemma":[0.9990157,0.000016434933,0.00018462272,0.00059140276,0.00009494682,0.00009692948],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016144132,0.00023426318,0.00017040482,0.000034464392,0.0004944027,0.00003970537,0.00037141275,0.00010238912,0.0003195217],"category_scores_gemma":[0.000034976158,0.00018163519,0.0000961,0.00016661808,0.00011382988,0.0000026065175,0.0007294163,0.00017676325,0.000014505205],"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":[0.000043430435,0.00014507443,0.032729276,0.0000074729187,0.00011944909,0.000004752372,0.00037098056,0.0013485898,0.96370554,0.0000013250901,0.0011409521,0.00038313292],"study_design_scores_gemma":[0.0007593186,0.00058290304,0.007527724,0.000015150676,0.00006771209,0.000069478716,0.00063870294,0.002802659,0.9795673,0.000009960407,0.0076493914,0.0003097011],"about_ca_topic_score_codex":0.000016445656,"about_ca_topic_score_gemma":0.000029924946,"teacher_disagreement_score":0.02520155,"about_ca_system_score_codex":0.000092810384,"about_ca_system_score_gemma":0.000071443246,"threshold_uncertainty_score":0.7406868},"labels":[],"label_agreement":null},{"id":"W4225308711","doi":"10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a3002","title":"The Presence of 14 and 6 Hz Spike Wave Activity in Children with Prader Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; SickKids Foundation","funders":"","keywords":"Spike (software development); Audiology; Computer science; Psychology; Neuroscience; Medicine","score_opus":0.006450644347144715,"score_gpt":0.20544277638527714,"score_spread":0.19899213203813243,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4225308711","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99882406,0.00029585962,0.00010063056,0.00017383047,0.000021826398,0.00019272698,0.0000040349005,0.0000024806964,0.0003845602],"genre_scores_gemma":[0.99895364,0.000074938245,0.00026141372,0.000028403341,0.000007424852,0.000023026178,0.0000036303436,0.000008077378,0.00063946715],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993933,0.00005115634,0.00009027487,0.0002014786,0.00011152016,0.0001522643],"domain_scores_gemma":[0.9996717,0.000012811621,0.000052926618,0.00022277133,0.000014016995,0.000025786372],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001688265,0.000073817886,0.00008247857,0.00001609781,0.00009732318,0.0000106820235,0.0001086513,0.000026122618,0.000018792232],"category_scores_gemma":[0.000021030335,0.00004974548,0.000019311497,0.00007204706,0.00007767704,0.0000018974357,0.00029167178,0.00007982909,1.9699152e-7],"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":[0.000007891795,0.00008853541,0.89234465,0.000010803103,0.000086129636,0.000001008014,0.00008035174,0.00020594033,0.09772906,0.00007601795,0.00012852845,0.009241093],"study_design_scores_gemma":[0.00033345952,0.00042804985,0.9868886,0.0000033744193,0.000005963982,0.00039091494,0.00013516948,0.00012212995,0.010584488,0.000021682257,0.0009976246,0.00008858171],"about_ca_topic_score_codex":0.0001075888,"about_ca_topic_score_gemma":0.000042630083,"teacher_disagreement_score":0.09454392,"about_ca_system_score_codex":0.000004401768,"about_ca_system_score_gemma":0.000030018724,"threshold_uncertainty_score":0.20285617},"labels":[],"label_agreement":null},{"id":"W4229587581","doi":"10.1139/gen-44-3-311","title":"Imprinting and deviation from Mendelian transmission ratios","year":2001,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Imprinting (psychology); Biology; Mendelian inheritance; Genetics; Genomic imprinting; Evolutionary biology; Gene; DNA methylation","score_opus":0.009623054575879447,"score_gpt":0.22403843145084426,"score_spread":0.2144153768749648,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4229587581","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97554684,0.0010437213,0.022150796,0.00015177242,0.00004435858,0.000083688275,0.0000026647444,0.000008971577,0.00096720736],"genre_scores_gemma":[0.99411446,0.0004209904,0.0048309783,0.000110266825,0.00015067031,0.0000047971353,0.00006277857,0.000011959231,0.00029310165],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994246,0.000017640177,0.0001302872,0.00022633561,0.00005677332,0.00014439554],"domain_scores_gemma":[0.99973917,0.0000035620014,0.00003878006,0.00013634117,0.000022112865,0.000060024155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000080568665,0.000082053884,0.00006976405,0.000020205316,0.00007230582,0.000025728365,0.000061218656,0.00006694754,0.00006690858],"category_scores_gemma":[0.000011718091,0.00007952226,0.000028239916,0.000038736493,0.000012781815,0.000002449762,0.00004729089,0.000034564473,0.000010373731],"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":[0.000002784864,0.0000062842632,0.0066789766,0.000003224028,0.000012006816,6.068798e-7,0.00006658158,0.000021059635,0.95249695,0.0000063203547,0.0000053830267,0.040699843],"study_design_scores_gemma":[0.0010422688,0.00021439907,0.69938016,0.000019798166,0.000033999157,0.00006904512,0.00030138163,0.0006975173,0.1297409,0.00046908052,0.16759625,0.00043523507],"about_ca_topic_score_codex":0.000037807542,"about_ca_topic_score_gemma":0.000006423074,"teacher_disagreement_score":0.82275605,"about_ca_system_score_codex":0.0000045185875,"about_ca_system_score_gemma":0.000013878834,"threshold_uncertainty_score":0.32428235},"labels":[],"label_agreement":null},{"id":"W4232227875","doi":"10.14740/jem337w","title":"Clinical and Genetic Study of Pseudohypoparathyroidism Type 1b in Hong Kong Chinese","year":2016,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Imprinting (psychology); Uniparental disomy; Multiplex ligation-dependent probe amplification; Genetics; Chinese population; Locus (genetics); Gene; Bioinformatics; Chromosome; Parathyroid hormone; Internal medicine; Karyotype; Biology; Genotype; Exon","score_opus":0.016792506397998935,"score_gpt":0.30657542035166213,"score_spread":0.2897829139536632,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4232227875","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9873995,0.01193276,0.0000494922,0.00009967693,0.00038854804,0.00008394798,9.17313e-7,0.0000010785923,0.000044061788],"genre_scores_gemma":[0.9924235,0.006566751,0.0006898479,0.000033400942,0.00020321137,0.0000011349503,1.6753633e-7,0.0000086537275,0.000073382645],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99882805,0.00015676115,0.00057271484,0.00018272466,0.00007234611,0.00018739217],"domain_scores_gemma":[0.9993855,0.000043159307,0.00025106812,0.00015280306,0.00009298965,0.000074524876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002263506,0.00011464057,0.00037606515,0.00009899993,0.000023368937,0.0000049928085,0.000115882314,0.00008669865,0.0000039703064],"category_scores_gemma":[0.00026378376,0.000071437906,0.000054774388,0.00006294901,0.00013696152,0.0000061567303,0.00013476139,0.00011937931,5.9664626e-7],"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":[0.000057018166,0.00020662132,0.83142936,0.0000042963757,0.000089395675,0.000040981242,0.000087687506,0.0000024338713,0.15104331,0.00002841369,0.00004067506,0.016969824],"study_design_scores_gemma":[0.0036106377,0.00083078374,0.9906474,0.000011163951,0.00004739674,0.0009917886,0.00016568373,0.0000012134227,0.0023541076,0.0001763942,0.0010800884,0.00008339137],"about_ca_topic_score_codex":0.00000768867,"about_ca_topic_score_gemma":0.000016811598,"teacher_disagreement_score":0.15921801,"about_ca_system_score_codex":0.000001396644,"about_ca_system_score_gemma":0.00003582349,"threshold_uncertainty_score":0.29131532},"labels":[],"label_agreement":null},{"id":"W4235369933","doi":"10.1139/gen-43-2-285","title":"Varied expression of a Y-linked P[&lt;i&gt;w&lt;/i&gt;&lt;sup&gt;+&lt;/sup&gt;] insert due to imprinting in &lt;i&gt;Drosophila melanogaster&lt;/i&gt;","year":2000,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Drosophila melanogaster; Genetics; Molecular biology; Imprinting (psychology); Gene","score_opus":0.009955639820608242,"score_gpt":0.22337404346120782,"score_spread":0.21341840364059958,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4235369933","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9832891,0.004364947,0.00090759876,0.0004287801,0.00048287836,0.0014456507,0.00015282522,0.00012155935,0.008806612],"genre_scores_gemma":[0.9856079,0.0009396441,0.006319705,0.00057074585,0.0008421534,0.00022277805,0.00038975835,0.00027866015,0.004828659],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9918477,0.00043703863,0.0021931508,0.0023388774,0.0009790576,0.0022041905],"domain_scores_gemma":[0.99561346,0.00011309753,0.0006827321,0.0023880429,0.00040019245,0.000802455],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["metaepi_narrow"],"category_scores_codex":[0.0013087739,0.0012861299,0.0015587275,0.0005771165,0.00045030887,0.00020233355,0.0017108204,0.0011272507,0.0009320793],"category_scores_gemma":[0.0003359295,0.0013407322,0.00066649873,0.00094232487,0.00030271919,0.00005994503,0.0014666924,0.00053850847,0.00039334898],"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":[0.00022982844,0.00040195163,0.0005597153,0.00020045332,0.00017253311,0.00008430449,0.0012821425,0.0021179975,0.98628545,0.00017878991,0.00050160824,0.0079852035],"study_design_scores_gemma":[0.008566283,0.002553163,0.15704167,0.00089331385,0.00032294288,0.00080813025,0.0002028078,0.0018472428,0.34083432,0.00064713904,0.4822187,0.004064289],"about_ca_topic_score_codex":0.00003787252,"about_ca_topic_score_gemma":0.00016499375,"teacher_disagreement_score":0.6454512,"about_ca_system_score_codex":0.00018198288,"about_ca_system_score_gemma":0.00039514087,"threshold_uncertainty_score":0.99998903},"labels":[],"label_agreement":null},{"id":"W4239765192","doi":"10.3410/f.717960858.793463732","title":"Faculty Opinions recommendation of Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus.","year":2012,"lang":"en","type":"dataset","venue":"Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Locus (genetics); Homeotic gene; Genetics; Transformation (genetics); Biology; Computational biology; Gene","score_opus":0.022390570867623954,"score_gpt":0.30961445852962904,"score_spread":0.2872238876620051,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4239765192","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00017207183,0.0010911059,0.00007239624,0.054605957,0.0004569062,0.0015639798,0.9419729,0.000010425158,0.00005425684],"genre_scores_gemma":[0.00071713753,0.00027581197,0.00013059167,0.0021260935,0.00017854942,0.00019048706,0.99549747,0.000029671904,0.0008541995],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99685454,0.0004100576,0.0010320456,0.00047779782,0.0008414199,0.0003841195],"domain_scores_gemma":[0.9955625,0.000044648263,0.0010643007,0.0011288895,0.0019851988,0.00021446223],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014182411,0.00042402753,0.00055720494,0.00014406558,0.00025904257,0.000073638934,0.0010688932,0.00047774529,0.00030109935],"category_scores_gemma":[0.0017702205,0.00023587274,0.00035933388,0.00086134044,0.00020102167,0.000026899908,0.00042108246,0.00042164107,0.000046765035],"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":[0.0000140232005,0.00017591359,0.000027849384,0.0013975032,0.00022951711,3.0766792e-8,0.00011540404,9.902382e-7,0.00010927607,0.000006603759,0.9959599,0.0019630394],"study_design_scores_gemma":[0.0006610073,0.0003046649,0.0071948776,0.0024976353,0.00024326595,0.000026997006,0.000031572166,0.000003248387,0.00022507127,0.00000172366,0.98854,0.00026995954],"about_ca_topic_score_codex":0.000029911704,"about_ca_topic_score_gemma":0.000020712097,"teacher_disagreement_score":0.053524554,"about_ca_system_score_codex":0.0000973551,"about_ca_system_score_gemma":0.00018993785,"threshold_uncertainty_score":0.9618611},"labels":[],"label_agreement":null},{"id":"W4243593601","doi":"10.3410/f.13491969.14870064","title":"Faculty Opinions recommendation of Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome.","year":2012,"lang":"en","type":"dataset","venue":"Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"","keywords":"Phenotype; Neuroscience; Computational biology; Biology; Psychology; Genetics; Gene","score_opus":0.02783178862621694,"score_gpt":0.3116417928913443,"score_spread":0.28381000426512737,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4243593601","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00036808633,0.00074439123,0.00021471489,0.018362606,0.0005988378,0.001086013,0.9785887,0.000014174946,0.00002247498],"genre_scores_gemma":[0.0007829419,0.00007507281,0.0010617888,0.002160882,0.00017867461,0.000071063994,0.99521685,0.000043988417,0.00040877025],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99670565,0.00036739281,0.0010019751,0.0006479106,0.0008391097,0.00043795994],"domain_scores_gemma":[0.99452996,0.00004292528,0.0011415206,0.0012172326,0.002760626,0.0003077287],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0007894249,0.0004975037,0.00073294877,0.0001915055,0.00018988812,0.000080662314,0.0010370072,0.00061399565,0.00023038956],"category_scores_gemma":[0.0031938425,0.0003381278,0.00038851707,0.0011109317,0.0001870351,0.000028317767,0.0006275359,0.00048542922,0.0000222202],"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":[0.000007542087,0.00026488747,0.000037359605,0.0013180512,0.00022975531,2.0789872e-7,0.000038578277,0.0000026117043,0.00048378922,0.0000063716234,0.997119,0.0004918115],"study_design_scores_gemma":[0.00048127936,0.00027441018,0.003924807,0.003878168,0.0002581236,0.000057312318,0.000019171475,0.000009803375,0.00037368987,0.0000019042816,0.990347,0.00037428446],"about_ca_topic_score_codex":0.000048043756,"about_ca_topic_score_gemma":0.0000073184074,"teacher_disagreement_score":0.016628116,"about_ca_system_score_codex":0.00006223691,"about_ca_system_score_gemma":0.0003607388,"threshold_uncertainty_score":0.9999071},"labels":[],"label_agreement":null},{"id":"W4245234573","doi":"10.1172/jci200319159","title":"Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS","year":2003,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"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; St. Michael's Hospital; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Imprinting (psychology); Genomic imprinting; Genetics; Biology; Endocrinology; Internal medicine; Medicine; Gene; Parathyroid hormone","score_opus":0.038505553832486036,"score_gpt":0.3210772784450016,"score_spread":0.28257172461251556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4245234573","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9929771,0.0003386095,0.006022773,0.00020492545,0.00022496496,0.00017637249,0.000005386968,0.0000026137964,0.00004726728],"genre_scores_gemma":[0.994885,0.00010353347,0.0044986773,0.00031870644,0.00010178805,0.0000028304066,0.000010091719,0.000017917966,0.000061439976],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9977956,0.0003645683,0.001129331,0.0002236312,0.00027872974,0.0002081571],"domain_scores_gemma":[0.9972793,0.00011515055,0.0017842965,0.00015256034,0.0005243608,0.00014437501],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015526358,0.00016134938,0.00044804256,0.00004980002,0.000055747663,0.000026366593,0.00012049535,0.00017865226,0.000007944328],"category_scores_gemma":[0.0013727135,0.0001211571,0.00020447557,0.000110344154,0.00014717059,0.000014148645,0.00002783274,0.00022228115,0.000001892868],"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":[0.00019762747,0.00023390862,0.15691753,0.000022034763,0.00039138668,0.000010377396,0.00029921872,0.00033108713,0.8397293,0.00006293334,0.00028138954,0.0015232305],"study_design_scores_gemma":[0.0067719463,0.005451256,0.29405922,0.00026374348,0.0002917451,0.00027482235,0.0002724117,0.0011077859,0.68958044,0.0009025217,0.00068965583,0.00033447324],"about_ca_topic_score_codex":0.000006116515,"about_ca_topic_score_gemma":0.0000042573106,"teacher_disagreement_score":0.15014887,"about_ca_system_score_codex":0.00001999118,"about_ca_system_score_gemma":0.0002487411,"threshold_uncertainty_score":0.4940643},"labels":[],"label_agreement":null},{"id":"W4245280555","doi":"10.1002/ajmg.c.30058","title":"Beckwith–Wiedemann syndrome","year":2005,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":261,"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":"","keywords":"Beckwith–Wiedemann syndrome; Epigenetics; Genomic imprinting; Biology; Genetics; Monozygotic twin; Wilms' tumor; Phenotype; Bioinformatics; DNA methylation; Gene","score_opus":0.008731687724892948,"score_gpt":0.28627210111506673,"score_spread":0.27754041339017377,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4245280555","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9771259,0.014764931,0.0024038544,0.0042315377,0.00080329785,0.00016643143,0.0000053654476,0.000009910802,0.00048876647],"genre_scores_gemma":[0.9447152,0.03646382,0.014239596,0.002789759,0.0013865374,0.000011187172,0.00001511029,0.00008368009,0.00029510938],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99293226,0.00035149232,0.0018277547,0.00057872833,0.0033673146,0.0009424787],"domain_scores_gemma":[0.9966421,0.00015482152,0.00072382804,0.0006622903,0.0002522838,0.001564677],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0030489133,0.0004461472,0.00086812826,0.00025289698,0.00008123642,0.000043284366,0.0018050815,0.0005668621,0.00094312715],"category_scores_gemma":[0.001656095,0.0004040984,0.00031869518,0.0005259535,0.0010828123,0.0000069607167,0.00058505934,0.00096606463,0.000047581474],"study_design_candidate":"design_other","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":[0.00007675746,0.0008836991,0.039692935,0.00005168484,0.00028132013,0.000697284,0.00039449515,0.0009862053,0.0037696678,0.000019033418,0.011628142,0.9415188],"study_design_scores_gemma":[0.0061644255,0.011910856,0.041635085,0.0021054032,0.00025326444,0.025453731,0.0023354087,0.0063201436,0.012738574,0.00017323664,0.8890368,0.0018730831],"about_ca_topic_score_codex":0.000011741995,"about_ca_topic_score_gemma":0.00005146817,"teacher_disagreement_score":0.9396457,"about_ca_system_score_codex":0.00006110506,"about_ca_system_score_gemma":0.0010184469,"threshold_uncertainty_score":0.99997014},"labels":[],"label_agreement":null},{"id":"W4245435215","doi":"10.1016/j.jpeds.2008.12.032","title":"Reply","year":2009,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Observational study; Jury; Clinical endpoint; Randomized controlled trial; Pediatrics; Body mass index; Idiopathic short stature; Obesity; Food and drug administration; Clinical trial; Growth hormone; Short stature; Internal medicine; Hormone; Medical emergency","score_opus":0.008040849730539847,"score_gpt":0.23761835483085902,"score_spread":0.22957750510031918,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4245435215","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9940555,0.0022614296,0.0016946039,0.0010246921,0.00018573414,0.000024811312,3.996243e-7,0.0000013038398,0.0007515229],"genre_scores_gemma":[0.99552405,0.0013658911,0.00097334926,0.00090669945,0.0009792475,4.828737e-8,4.536637e-7,0.000004228223,0.00024601817],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995265,0.000032249387,0.00018756375,0.000041106294,0.00011284783,0.00009972127],"domain_scores_gemma":[0.9995317,0.000011453471,0.00017557379,0.00014863387,0.00009301291,0.000039651757],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004537506,0.000049437127,0.00006383928,0.000024640916,0.00003763602,0.0000093216295,0.00019743413,0.000030488969,0.000005563106],"category_scores_gemma":[0.00013629928,0.00003099055,0.000058940343,0.000066307744,0.000011862877,0.0000013943588,0.00002537342,0.000079514764,0.0000035922155],"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":[0.00013767426,0.00023661542,0.030332051,0.000040663814,0.000038015718,0.00001849733,0.0005968769,0.0013931979,0.7095523,0.00014011646,0.15816164,0.09935238],"study_design_scores_gemma":[0.003213893,0.008732364,0.56987554,0.000026813348,0.000664325,0.005231445,0.0010919033,0.000051745363,0.12326859,0.003535283,0.28348753,0.0008205375],"about_ca_topic_score_codex":0.000001267466,"about_ca_topic_score_gemma":1.7176852e-7,"teacher_disagreement_score":0.5862837,"about_ca_system_score_codex":0.0000034093434,"about_ca_system_score_gemma":0.000042320473,"threshold_uncertainty_score":0.1263758},"labels":[],"label_agreement":null},{"id":"W4249491592","doi":"10.1126/science.330.6005.771","title":"2010 Grand Prize Winner","year":2010,"lang":"en","type":"article","venue":"Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Philosophy","score_opus":0.006707372463534485,"score_gpt":0.239318066395827,"score_spread":0.23261069393229253,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4249491592","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99490386,0.00004769463,0.00027987367,0.00015192297,0.0008245226,0.000049218692,8.220048e-7,0.000005956967,0.0037360988],"genre_scores_gemma":[0.99431735,0.0000087920025,0.0034880324,0.00013121324,0.000120216406,0.0000027366007,0.0000013421737,0.0000047409067,0.0019255657],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993287,0.0000040947352,0.00006971249,0.00025412638,0.00012711463,0.00021630796],"domain_scores_gemma":[0.9995341,0.000002216575,0.000024203551,0.00030215422,0.00005753139,0.000079828555],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028849734,0.000056385914,0.00004124556,0.000025468838,0.00012629837,0.0000428242,0.00029842954,0.000043044078,0.000052010913],"category_scores_gemma":[0.00013380541,0.0000469275,0.000024545436,0.00012613124,0.00032667318,0.0000032083872,0.0001389112,0.00006909887,0.00003548097],"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":[5.1730694e-7,0.0000065520435,0.006454644,0.0000010096082,8.778165e-7,1.7337709e-7,0.000012750018,0.0000013907088,0.9882735,0.00004494978,0.00023163264,0.004972007],"study_design_scores_gemma":[0.0001659338,0.00006164695,0.23378007,0.0000020002624,0.0000021294136,0.00004657529,0.000016135125,0.000049511094,0.68251175,0.00015190117,0.083091654,0.00012071635],"about_ca_topic_score_codex":0.0000056577715,"about_ca_topic_score_gemma":0.000013460785,"teacher_disagreement_score":0.30576175,"about_ca_system_score_codex":0.0000014053527,"about_ca_system_score_gemma":0.00008284612,"threshold_uncertainty_score":0.1913648},"labels":[],"label_agreement":null},{"id":"W4252671102","doi":"10.1136/adc.88.suppl_1.a70","title":"Metabolic diseases","year":2003,"lang":"en","type":"article","venue":"Archives of Disease in Childhood","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Medicine; Hypotonia; Internal medicine; Endocrinology; Cytochrome c oxidase; Muscle biopsy; Mitochondrion; Biopsy; Biochemistry; Biology","score_opus":0.004642183146264477,"score_gpt":0.2188441076969611,"score_spread":0.21420192455069664,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4252671102","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9911587,0.00545762,0.0001571519,0.00003624059,0.00005263687,0.00012926338,0.000028555125,0.0000050104195,0.0029748161],"genre_scores_gemma":[0.9983848,0.00043267626,0.0009397854,0.00006801868,0.00003721951,0.000014301105,0.000030810254,0.00001546475,0.00007697643],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992278,0.00006810427,0.0001818757,0.00024334107,0.00008037086,0.00019847516],"domain_scores_gemma":[0.9994605,0.000018783932,0.0000506946,0.00031425618,0.000007860258,0.00014791638],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00003503598,0.00011038541,0.00013149285,0.000063240244,0.000024855664,0.0000065864556,0.00014472826,0.000020362215,0.000023889008],"category_scores_gemma":[0.00020768851,0.00010649137,0.00012552117,0.0000683458,0.0000685545,0.0000019455802,0.00006533206,0.000038396218,0.0000031256238],"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":[0.000028242654,0.00072067755,0.9524561,0.00004419521,0.00007701111,0.0000028634295,0.00017922388,0.00038505718,0.031019468,0.0025828173,0.000048943042,0.0124553805],"study_design_scores_gemma":[0.0005992717,0.00005425732,0.979528,0.000026480788,0.000025224157,0.0000019742338,0.00004315373,0.000013843771,0.013911492,0.0028322751,0.002831821,0.0001321894],"about_ca_topic_score_codex":0.000005776806,"about_ca_topic_score_gemma":0.0000027240865,"teacher_disagreement_score":0.027071897,"about_ca_system_score_codex":8.2060484e-7,"about_ca_system_score_gemma":0.00008830976,"threshold_uncertainty_score":0.4342592},"labels":[],"label_agreement":null},{"id":"W4255496423","doi":"10.1016/s1701-2163(16)35026-5","title":"San Pedro","year":2011,"lang":"en","type":"article","venue":"Journal of Obstetrics and Gynaecology Canada","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Pregnancy; Obstetrics; Pediatrics; Gestational age; Macroglossia; Prenatal diagnosis; Epidemiology; Population; Live birth; Fetus; Internal medicine; Tongue; Pathology","score_opus":0.01296928004640372,"score_gpt":0.20728454478738376,"score_spread":0.19431526474098004,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4255496423","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9892128,0.0034903495,0.00009828246,0.000027671938,0.0037983605,0.000030608953,0.0000023576877,6.6935803e-7,0.0033389153],"genre_scores_gemma":[0.9981347,0.00014991673,0.0012810214,0.00020709599,0.00003066779,4.918387e-7,0.0000010748522,0.000007748347,0.00018731177],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99936706,0.000025198322,0.00024634527,0.000098499295,0.00009719623,0.00016570429],"domain_scores_gemma":[0.9993842,0.00006426344,0.00019141757,0.00010073052,0.00013789254,0.00012150074],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013236333,0.00007877052,0.00013969628,0.000056680343,0.000046123525,0.0000069112184,0.00013145736,0.000081744,0.00015469982],"category_scores_gemma":[0.00080942205,0.000068336,0.000040292118,0.00007495334,0.000032988188,0.000002148148,0.000060694,0.00009546917,3.3179316e-7],"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":[0.000004141686,0.00009968258,0.7986909,0.000031265874,0.0002556723,0.0005178604,0.00016520223,0.00001617901,0.0057307486,0.00017696503,0.0072628413,0.18704854],"study_design_scores_gemma":[0.0007721218,0.0006355223,0.94410706,0.0000016202164,0.00003285711,0.0002303198,0.00027905699,0.0000087625185,0.0039256983,0.00010904396,0.049756773,0.00014118744],"about_ca_topic_score_codex":0.003681207,"about_ca_topic_score_gemma":0.007779894,"teacher_disagreement_score":0.18690735,"about_ca_system_score_codex":0.000042448497,"about_ca_system_score_gemma":0.0005453732,"threshold_uncertainty_score":0.55649084},"labels":[],"label_agreement":null},{"id":"W4280526296","doi":"10.1101/2022.04.21.488764","title":"Conservation and divergence of canonical and non-canonical imprinting in murids","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"NODAI Genome Research Center, Tokyo University of Agriculture; Japan Society for the Promotion of Science; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Provincial Health Services Authority; Children's Hospital Foundation; Keio University; Fondation pour la Recherche Médicale; Tokyo University of Agriculture; BC Children's Hospital; Sumitomo Foundation","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Gene; Genetics; DNA methylation; Promoter; Genome; Epigenetics; Gene expression","score_opus":0.009617956130026048,"score_gpt":0.22313069120822085,"score_spread":0.2135127350781948,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4280526296","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975849,0.0013247035,0.0002990978,0.00009973401,0.000279386,0.00034047518,0.00004643996,0.000013286236,0.000011983394],"genre_scores_gemma":[0.9955994,0.00086315157,0.0032435139,0.000088381326,0.00008771958,0.00006819324,7.6324505e-7,0.000044472374,0.000004401785],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99804646,0.00009968663,0.0005194724,0.00080358895,0.00019051004,0.00034026752],"domain_scores_gemma":[0.9988367,0.000030742667,0.0002912762,0.00058309623,0.00012611056,0.00013210354],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006069568,0.00029110114,0.00039508098,0.000111427915,0.00008531387,0.00004490987,0.0002746977,0.00033520916,0.000024050752],"category_scores_gemma":[0.00023894891,0.00034100303,0.00006949906,0.00016361705,0.00016426377,0.000005697422,0.0018674496,0.00040834583,6.3531684e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00000866889,0.000034722467,0.36014298,0.00017673933,0.000034118275,0.0000043568884,0.0000061455107,0.000035393805,0.6394907,0.000043631542,0.000015365717,0.0000071794325],"study_design_scores_gemma":[0.0004688515,0.000111975896,0.8607996,0.000111495385,0.00003207973,1.1580315e-7,0.000010477308,0.00049317116,0.13661937,0.0000013958279,0.0009947643,0.00035668205],"about_ca_topic_score_codex":0.00038806826,"about_ca_topic_score_gemma":0.000021553697,"teacher_disagreement_score":0.50287133,"about_ca_system_score_codex":0.000042219726,"about_ca_system_score_gemma":0.00047498778,"threshold_uncertainty_score":0.9999042},"labels":[],"label_agreement":null},{"id":"W4281258467","doi":"10.1002/ajmg.a.62782","title":"A 79‐kb paternally inherited 7q32.2 microdeletion involving <scp><i>MEST</i></scp> in a patient with a <scp>Silver‐Russell</scp> syndrome‐like phenotype","year":2022,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Children's Hospital of Eastern Ontario; Hospital for Sick Children; University of Ottawa","funders":"","keywords":"Phenotype; Genetics; Genomic imprinting; Uniparental disomy; Biology; Imprinting (psychology); Gene; Chromosome; DNA methylation; Karyotype; Gene expression","score_opus":0.007081262859299045,"score_gpt":0.2201342164133504,"score_spread":0.21305295355405135,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4281258467","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9938008,0.004097616,0.0010282294,0.00022848089,0.00044862882,0.00024669347,0.000015128064,0.0000115748735,0.00012281747],"genre_scores_gemma":[0.9928954,0.001850933,0.003324773,0.0014170532,0.00018373241,0.000039116065,0.000034250912,0.000081991704,0.00017272038],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99553806,0.00047859855,0.0010684083,0.0005575562,0.0015808224,0.0007765386],"domain_scores_gemma":[0.9976201,0.00013491612,0.0009825429,0.00044739823,0.00024145222,0.00057357573],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0010934916,0.0003881018,0.0006486912,0.00025246645,0.00016193149,0.00006696025,0.0008184309,0.0001510739,0.000048070455],"category_scores_gemma":[0.00047716624,0.00035357408,0.00021081346,0.0006672087,0.00032431044,0.000009858622,0.0005684151,0.0008075743,0.000006540972],"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":[0.00025981775,0.0036394217,0.23002844,0.00030920393,0.0019499804,0.006273177,0.012000624,0.01650646,0.5024719,0.000029930427,0.019606479,0.20692456],"study_design_scores_gemma":[0.012423164,0.050818127,0.13236031,0.0014180015,0.00058093655,0.049113262,0.033942472,0.0063416087,0.026735723,0.00022294176,0.68494666,0.0010968244],"about_ca_topic_score_codex":0.0001363394,"about_ca_topic_score_gemma":0.000062048166,"teacher_disagreement_score":0.6653401,"about_ca_system_score_codex":0.000087533284,"about_ca_system_score_gemma":0.0006854938,"threshold_uncertainty_score":0.99989164},"labels":[],"label_agreement":null},{"id":"W4281559669","doi":"10.1101/2022.05.24.493320","title":"Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; University of British Columbia; BC Cancer Agency","funders":"Canadian Institutes of Health Research; Terry Fox Research Institute; University of British Columbia; Canada Research Chairs","keywords":"Autosome; Genetics; Biology; Haplotype; DNA methylation; DNA sequencing; Indel; Allele; Chromosome; DNA; Gene; Genotype; Single-nucleotide polymorphism","score_opus":0.023002636170163467,"score_gpt":0.2474176973530804,"score_spread":0.22441506118291693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4281559669","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98711985,0.003112085,0.0087177735,0.000012477301,0.0005000282,0.00043265894,0.00005776107,0.000043007512,0.0000043272976],"genre_scores_gemma":[0.9938843,0.0006383073,0.0051147784,0.000020100953,0.00021064038,0.00004320296,0.0000015972493,0.00008428903,0.0000027385825],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9979213,0.00013874497,0.00048185608,0.00087428675,0.00022546915,0.00035834158],"domain_scores_gemma":[0.99867433,0.000018883442,0.00043539674,0.0005646947,0.0001593281,0.00014736463],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005241292,0.0003837022,0.0004131137,0.0001653313,0.00022462284,0.00009874924,0.00018363344,0.00036470956,0.000024792036],"category_scores_gemma":[0.000083109684,0.00045506717,0.00009905244,0.00018694495,0.00011131698,0.000014344452,0.0006113861,0.0003425799,5.213015e-7],"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":[0.000012037914,0.000019302503,0.031425677,0.0003509082,0.000104921455,0.000003172811,0.000017531525,0.00045149372,0.9675313,0.000005101968,6.935623e-7,0.0000778536],"study_design_scores_gemma":[0.000549693,0.00015440711,0.21636271,0.00023807981,0.00018014497,6.1382576e-7,0.000030156723,0.0028303573,0.778596,0.0000026535402,0.0004114088,0.00064378005],"about_ca_topic_score_codex":0.000117370386,"about_ca_topic_score_gemma":0.000010067049,"teacher_disagreement_score":0.18893531,"about_ca_system_score_codex":0.00011606051,"about_ca_system_score_gemma":0.0002597625,"threshold_uncertainty_score":0.99979013},"labels":[],"label_agreement":null},{"id":"W4281695503","doi":"10.1042/bsr20220610","title":"Proteins and proteases of Prader–Willi syndrome: a comprehensive review and perspectives","year":2022,"lang":"en","type":"review","venue":"Bioscience Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; SickKids Foundation; University of Ottawa; Hospital for Sick Children; University of Toronto","funders":"Foundation for Prader-Willi Research","keywords":"Hypotonia; Short stature; Disease; Bioinformatics; Genomic imprinting; Imprinting (psychology); Medicine; Biology; Genetics; Internal medicine; DNA methylation; Gene","score_opus":0.0536649125002168,"score_gpt":0.3146451358547597,"score_spread":0.2609802233545429,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4281695503","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0030393212,0.9946818,0.000007861134,0.000039291786,0.00006586374,0.0020633792,0.000018403101,0.0000074868144,0.00007664717],"genre_scores_gemma":[0.0012422695,0.9975761,0.0006498896,0.00003051571,0.000018358267,0.00028328254,0.000021864951,0.000023513654,0.00015419675],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99798006,0.00012095127,0.00056570885,0.0008584521,0.00023546,0.00023936406],"domain_scores_gemma":[0.99852085,0.000018198609,0.00077132514,0.000514696,0.000069005226,0.00010593124],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033083776,0.00029507148,0.00095320126,0.00007996708,0.00013186433,0.000025169238,0.00015549872,0.00011564629,0.000031639476],"category_scores_gemma":[0.0003869981,0.00023812242,0.00016930416,0.0002523239,0.00036933634,0.000004943659,0.00054703857,0.00012902415,2.8432183e-7],"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":[4.7764235e-7,0.00020060189,0.0006220283,0.12781635,0.00025053573,0.00011520623,0.00012767514,1.903257e-7,0.0016577749,0.000022715018,0.00029897186,0.8688875],"study_design_scores_gemma":[0.00003760242,0.00036237584,0.00094256434,0.0053534606,0.0003048624,0.014612785,0.000116720774,2.1929768e-7,0.00002651861,0.0000061820106,0.97793734,0.0002993533],"about_ca_topic_score_codex":0.000020305386,"about_ca_topic_score_gemma":5.401818e-7,"teacher_disagreement_score":0.97763836,"about_ca_system_score_codex":0.000016770206,"about_ca_system_score_gemma":0.00035153626,"threshold_uncertainty_score":0.971035},"labels":[],"label_agreement":null},{"id":"W4282546381","doi":"10.1186/s13073-022-01064-4","title":"Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Genome Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"BC Children's Hospital","funders":"Center for Individualized Medicine, Mayo Clinic; Deutsche Forschungsgemeinschaft","keywords":"Loss function; Phenotype; Imprinting (psychology); Biology; Genetics; Genomic imprinting; Intellectual disability; Bioinformatics; Neuroscience; Gene; Computational biology; DNA methylation; Gene expression","score_opus":0.010608952852647662,"score_gpt":0.2157817611501218,"score_spread":0.20517280829747414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4282546381","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9889483,0.0024126903,0.0078654755,0.00035200332,0.00015041664,0.00018794337,0.000020900641,0.000006602698,0.000055696037],"genre_scores_gemma":[0.9990542,0.00014462891,0.00010632487,0.000101893595,0.00008880926,0.000017986466,0.0001634551,0.000016010441,0.0003067264],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99912155,0.000036690475,0.0002448041,0.00028632834,0.0001538779,0.00015676882],"domain_scores_gemma":[0.99957055,0.000010792676,0.00016348924,0.00014677714,0.000051057366,0.000057343244],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043729364,0.000109720815,0.0001579238,0.00006594925,0.0001275277,0.0000052002742,0.000061043225,0.000053284093,0.000054946362],"category_scores_gemma":[0.00006137099,0.00010935049,0.000017510762,0.00010627245,0.000042232117,0.000004142054,0.00019048578,0.000070802926,4.5116815e-7],"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":[0.00001298182,0.000022615819,0.0012665498,0.000048877842,0.000042923955,6.407982e-7,0.00022070015,0.00020207277,0.99747276,0.00005443392,0.000036861707,0.0006186076],"study_design_scores_gemma":[0.004692869,0.0033672948,0.9582456,0.000058894126,0.00023053741,0.0011921993,0.0013172226,0.006389108,0.017123643,0.0004240014,0.006416724,0.0005419014],"about_ca_topic_score_codex":0.000039841896,"about_ca_topic_score_gemma":0.0000013111259,"teacher_disagreement_score":0.98034906,"about_ca_system_score_codex":0.000013426194,"about_ca_system_score_gemma":0.00001567196,"threshold_uncertainty_score":0.44591835},"labels":[],"label_agreement":null},{"id":"W4282842119","doi":"10.1002/mrd.23621","title":"IGF2R, KCNQ1, PLAGL1, and SNRPN DNA methylation is completed in bovine by the early antral follicle stage","year":2022,"lang":"en","type":"article","venue":"Molecular Reproduction and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Biology; Antral follicle; Methylation; DNA methylation; Follicle; Genetics; Andrology; DNA; Molecular biology; Endocrinology; Gene; Ovary","score_opus":0.012465995144153839,"score_gpt":0.22961667399872293,"score_spread":0.2171506788545691,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4282842119","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99521613,0.0014943732,0.0018535202,0.000983969,0.00009187828,0.00023942719,0.0000066740436,0.000008406737,0.00010559335],"genre_scores_gemma":[0.99764735,0.00006408311,0.0008577649,0.00036340827,0.00001900925,0.000042308176,0.00006076427,0.000013713208,0.0009316195],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989003,0.000086006155,0.0002090637,0.0004712137,0.00015687334,0.00017657361],"domain_scores_gemma":[0.99962515,0.0000033864485,0.00006621809,0.0002381906,0.000024611323,0.000042425152],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004004313,0.00011243617,0.00009824459,0.000041032425,0.00022666597,0.000033979508,0.0000714295,0.000033889053,0.000030227013],"category_scores_gemma":[0.000026698795,0.00010235042,0.000020137933,0.00011406896,0.0000357934,0.0000040066975,0.000214513,0.000088894376,9.636916e-7],"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":[0.00003875707,0.00006317217,0.00913892,0.000015508369,0.00005197148,0.0000035179007,0.00079529744,0.00008285373,0.9543819,0.00005244287,0.00096788275,0.034407794],"study_design_scores_gemma":[0.0010436625,0.0002763549,0.14322114,0.000005116334,0.000009689792,0.00010311598,0.0007511879,0.00022646488,0.5376275,0.000026824691,0.3163988,0.00031009156],"about_ca_topic_score_codex":0.000052627813,"about_ca_topic_score_gemma":0.000004131151,"teacher_disagreement_score":0.41675434,"about_ca_system_score_codex":0.000020001944,"about_ca_system_score_gemma":0.00003638201,"threshold_uncertainty_score":0.4173729},"labels":[],"label_agreement":null},{"id":"W4283726389","doi":"10.1016/j.jbiomech.2022.111213","title":"Lower extremity coordination and joint kinetic distribution during gait in adults with and without Prader-Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"Journal of Biomechanics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Western University","funders":"California State University, Fullerton; California State University","keywords":"Ankle; Gait; Medicine; Biomechanics; Physical medicine and rehabilitation; Obesity; Gait analysis; Physical therapy; Anatomy; Internal medicine","score_opus":0.006387930685537412,"score_gpt":0.20440844168734199,"score_spread":0.19802051100180457,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283726389","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99724805,0.0008101751,0.0015111333,0.00019271235,0.00010177221,0.00011563942,0.000012379362,0.0000021954215,0.000005912857],"genre_scores_gemma":[0.9992257,0.00021706847,0.00044161282,0.000019863019,0.000027357428,0.0000046413084,0.00001484184,0.000012070305,0.000036844038],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99917173,0.000049072856,0.00027606232,0.00017520739,0.00017458673,0.0001533317],"domain_scores_gemma":[0.99951166,0.0000036935025,0.00025732548,0.00009739634,0.00006317422,0.00006675314],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002928138,0.0001045783,0.00016523643,0.00008685843,0.00008531946,0.000021356695,0.0000614863,0.000051867064,0.000009146504],"category_scores_gemma":[0.000035516085,0.00009280276,0.00003168039,0.00012964295,0.000024130832,0.000007830389,0.0001450255,0.00014375547,1.18661696e-7],"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":[0.00014812949,0.00029749944,0.052159376,0.00023378203,0.00010592755,0.000046302943,0.0002819371,0.00011962058,0.9296705,0.000036344187,0.000074228556,0.016826319],"study_design_scores_gemma":[0.012421961,0.008423223,0.8735591,0.00068983535,0.00015399493,0.033301365,0.0025470247,0.011062014,0.052152142,0.00045771906,0.0042002057,0.0010313764],"about_ca_topic_score_codex":0.000008663615,"about_ca_topic_score_gemma":0.0000053345443,"teacher_disagreement_score":0.8775184,"about_ca_system_score_codex":0.000038904276,"about_ca_system_score_gemma":0.00003276608,"threshold_uncertainty_score":0.37843868},"labels":[],"label_agreement":null},{"id":"W4283735939","doi":"10.1136/jmedgenet-2021-108288","title":"A 132 bp deletion affecting the <i>KCNQ1OT1</i> gene associated with Silver-Russell syndrome clinical phenotype","year":2022,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University; Nova Scotia Health Authority; Izaak Walton Killam Health Centre; Vitalité Health Network; Atlantic Cancer Research Institute; Université de Moncton","funders":"Fondation de la recherche en santé du Nouveau-Brunswick","keywords":"Genomic imprinting; Genetics; Proband; Biology; Phenotype; Gene; Imprinting (psychology); Copy-number variation; Epigenetics; X-inactivation; X chromosome; DNA methylation; Mutation; Gene expression; Genome","score_opus":0.017521788524396117,"score_gpt":0.2809629543558431,"score_spread":0.263441165831447,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283735939","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99280775,0.002485225,0.0023277542,0.0012810096,0.00081850006,0.00015457676,0.000005830267,0.0000066179905,0.0001127658],"genre_scores_gemma":[0.99608713,0.0008043471,0.0010572001,0.0013112644,0.0005452772,0.000005632963,0.000016144768,0.00003907846,0.00013393127],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9965807,0.00057875435,0.0008071054,0.0002664133,0.0013981481,0.0003688541],"domain_scores_gemma":[0.99833864,0.00017363066,0.0006917909,0.00032370453,0.00020021145,0.0002720089],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0037011087,0.00018823156,0.000342357,0.000049828217,0.0002865685,0.00003846441,0.00075600855,0.00020633808,0.0001884374],"category_scores_gemma":[0.00087330485,0.00012899861,0.0002425288,0.00023171165,0.0001557116,0.0000031377165,0.00043571484,0.00082696625,0.0000035416],"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":[0.001206019,0.006784499,0.34521854,0.00020347706,0.0068685887,0.002544891,0.0018981624,0.02962197,0.268587,0.00010929879,0.06240348,0.27455407],"study_design_scores_gemma":[0.0218276,0.048325777,0.48465014,0.0005899048,0.0019740295,0.039938338,0.0048785843,0.010182567,0.02839099,0.0005052948,0.3560945,0.002642255],"about_ca_topic_score_codex":0.0000061487244,"about_ca_topic_score_gemma":0.000010819037,"teacher_disagreement_score":0.29369104,"about_ca_system_score_codex":0.00003908181,"about_ca_system_score_gemma":0.0004501663,"threshold_uncertainty_score":0.5260411},"labels":[],"label_agreement":null},{"id":"W4283805795","doi":"10.7554/elife.77898","title":"Genome-wide detection of imprinted differentially methylated regions using nanopore sequencing","year":2022,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":52,"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's Michael Smith Genome Sciences Centre; University of British Columbia; BC Cancer Agency","funders":"University of British Columbia Graduate School; Canada Research Chairs","keywords":"Differentially methylated regions; Genomic imprinting; Biology; DNA methylation; Imprinting (psychology); Nanopore sequencing; Bisulfite sequencing; Genome; Illumina Methylation Assay; Genetics; Computational biology; Germline; Epigenetics; CpG site; Genomics; DNA sequencing; Methylation; Gene; Gene expression","score_opus":0.019000132591906076,"score_gpt":0.24200954668157332,"score_spread":0.22300941408966724,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283805795","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9826865,0.00032378314,0.016509285,0.000018110906,0.00020078737,0.00012657452,0.000007672881,0.000013728361,0.000113560156],"genre_scores_gemma":[0.99860644,0.00003129329,0.0010041783,0.000060505237,0.00005514997,0.000010829044,0.000040463117,0.000023805545,0.0001673525],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990393,0.00008621417,0.00025443683,0.00024986253,0.00017265561,0.00019753771],"domain_scores_gemma":[0.9994247,0.000007703137,0.00015904092,0.00027582995,0.000082555285,0.000050182905],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018729275,0.00010882527,0.00013686334,0.00006660024,0.0001868515,0.000008912666,0.00015615157,0.00005687126,0.000065510205],"category_scores_gemma":[0.00007037848,0.00011832097,0.000103873,0.00013057496,0.00003061833,0.0000017155913,0.00031180002,0.00010572287,0.0000013502597],"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":[0.000007839494,0.000016550963,0.0021342111,0.000009631489,0.00005261622,0.0000011743678,0.00007263587,0.0010049215,0.99627244,0.0000034299271,0.0000038037856,0.00042073752],"study_design_scores_gemma":[0.00030023186,0.00019940495,0.023159362,0.0000051604807,0.000030287698,0.000058855123,0.0003756286,0.0009948,0.97265047,0.000022084036,0.002049503,0.00015421274],"about_ca_topic_score_codex":0.000095698844,"about_ca_topic_score_gemma":0.000014917641,"teacher_disagreement_score":0.023621978,"about_ca_system_score_codex":0.000047847905,"about_ca_system_score_gemma":0.00009597834,"threshold_uncertainty_score":0.4824989},"labels":[],"label_agreement":null},{"id":"W4285188752","doi":"10.1007/978-1-0716-2533-0_18","title":"Tools and Techniques for Genomic Imprinting","year":2022,"lang":"en","type":"book-chapter","venue":"Springer protocols handbooks/Springer protocols","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Computational biology; Biology; Genetics; Computer science; Evolutionary biology; Gene; DNA methylation","score_opus":0.036202625280582,"score_gpt":0.2978246800680739,"score_spread":0.2616220547874919,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4285188752","genre_codex":"protocol","genre_gemma":"protocol","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"protocol","genre_consensus":"protocol","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011754023,0.0003770426,0.0032843074,0.00008674606,0.00016267775,0.9015226,0.00023354837,0.0003287359,0.09282898],"genre_scores_gemma":[0.0004156408,0.000060389255,0.020075016,0.00023614462,0.0010689507,0.8979349,0.00010774486,0.0005364897,0.0795647],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9945908,0.00007848336,0.0014055816,0.0021973401,0.00056553795,0.0011622373],"domain_scores_gemma":[0.99640954,0.000072693605,0.0010953834,0.0017962839,0.00028744407,0.00033863087],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.001361014,0.0012745373,0.0011760775,0.00030654707,0.00057545997,0.0005350942,0.0011398157,0.0009157646,0.00052344456],"category_scores_gemma":[0.00017228305,0.0013884652,0.00066496554,0.000050503135,0.00026676993,0.000030829273,0.0025667157,0.00084484665,0.00003068844],"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":[0.0005513675,0.00019506652,0.001916349,0.0042481264,0.0008017702,0.0000232776,0.00019206027,0.000015259262,0.7315206,0.013878288,0.0011488285,0.24550903],"study_design_scores_gemma":[0.001566322,0.0015277028,0.00039329007,0.0011360396,0.00007037956,0.00007698284,0.000010303424,0.0000125437955,0.124361515,0.0014668948,0.8679154,0.0014626319],"about_ca_topic_score_codex":0.000012669138,"about_ca_topic_score_gemma":0.000008320711,"teacher_disagreement_score":0.8667666,"about_ca_system_score_codex":0.00016582926,"about_ca_system_score_gemma":0.00044022253,"threshold_uncertainty_score":0.99948615},"labels":[],"label_agreement":null},{"id":"W4295876078","doi":"10.1101/2022.09.09.507324","title":"The imprinted <i>Mir483</i> is a growth suppressor and metabolic regulator functioning through IGF1","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Clinical Research Institute","funders":"Japan Society for the Promotion of Science; Cambridge Institute for Medical Research, University of Cambridge; Biotechnology and Biological Sciences Research Council; Medical Research Council; Directorate for Biological Sciences; Cancer Research UK; Anatomical Society; Francis Crick Institute; Uehara Memorial Foundation","keywords":"Genomic imprinting; Psychological repression; Biology; Transgene; microRNA; Imprinting (psychology); Regulator; Suppressor; Endocrinology; Growth factor; Gene expression; Gene; Cell biology; Phenotype; Promoter; Internal medicine; Genetics; Receptor; DNA methylation; Medicine","score_opus":0.009018086399011983,"score_gpt":0.21248517553880977,"score_spread":0.2034670891397978,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4295876078","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98224616,0.01351404,0.0010635845,0.0006006941,0.0015424755,0.00071057706,0.00016561334,0.00010884025,0.00004802011],"genre_scores_gemma":[0.9923025,0.0034044837,0.0024600527,0.00062977057,0.0005561334,0.0003831092,0.0000019314996,0.0001739046,0.00008813892],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9966529,0.00021402806,0.00059798884,0.0013808194,0.00040746515,0.0007467901],"domain_scores_gemma":[0.99724275,0.000046601614,0.00046523678,0.0016823175,0.0003572919,0.00020578268],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006643034,0.0006341826,0.0005063884,0.000080288584,0.0008282444,0.0003809453,0.0007802741,0.0004615371,0.00007816883],"category_scores_gemma":[0.00029252493,0.00058013195,0.00026736685,0.00028654854,0.00023605532,0.000013526355,0.0025591035,0.0007234777,0.000011100833],"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":[0.000028836255,0.00005306131,0.0061794133,0.0001303004,0.0004441468,0.0000050582794,0.000024727866,0.000018696554,0.99119973,0.00060072955,0.0013055555,0.000009734093],"study_design_scores_gemma":[0.00063623587,0.00011670167,0.078624465,0.00006639419,0.00019202406,4.2190618e-7,0.000029581339,0.00013450318,0.75236696,0.000013746986,0.16698313,0.00083582505],"about_ca_topic_score_codex":0.00011404411,"about_ca_topic_score_gemma":0.0000028142883,"teacher_disagreement_score":0.23883276,"about_ca_system_score_codex":0.000051246345,"about_ca_system_score_gemma":0.0003450975,"threshold_uncertainty_score":0.999665},"labels":[],"label_agreement":null},{"id":"W4296588680","doi":"10.3390/ijms231810580","title":"Preserved Sleep for the Same Level of Respiratory Disturbance in Children with Prader-Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Stollery Children's Hospital; Women and Children’s Health Research Institute; University of Alberta","funders":"","keywords":"Respiratory disturbance index; Polysomnography; Medicine; Respiratory system; Body mass index; Sleep disorder; Apnea; Internal medicine; Oxygen saturation; Obstructive sleep apnea; Sleep apnea; Pediatrics; Insomnia; Oxygen","score_opus":0.035198408290163324,"score_gpt":0.28358443421939183,"score_spread":0.2483860259292285,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4296588680","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9916355,0.001857697,0.005410865,0.0007268427,0.00017635906,0.00014020444,0.000022457469,6.794167e-7,0.000029365137],"genre_scores_gemma":[0.9978885,0.000021928496,0.0017741289,0.00022152113,0.000038184575,0.000014310191,0.0000025410827,0.000006180321,0.000032724613],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99890155,0.000058996684,0.00026907495,0.00014582345,0.00050645805,0.000118109274],"domain_scores_gemma":[0.99936944,0.000027965712,0.000314331,0.00011154302,0.00015305786,0.000023664472],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000691939,0.000069265414,0.00009900494,0.00008344844,0.00007777702,0.000026151327,0.0009178864,0.000018621224,0.000010070215],"category_scores_gemma":[0.000102802405,0.000047334805,0.00008420972,0.000121947,0.0001476365,0.000008699419,0.00018225108,0.00008597186,8.4250935e-8],"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":[0.000035575333,0.00022191455,0.7254764,0.000008602326,0.0005337733,0.000009890468,0.00019688149,0.06812247,0.19916825,0.0004048035,0.00024075047,0.0055806856],"study_design_scores_gemma":[0.0011268763,0.0016422041,0.96795344,0.000026390739,0.00002181577,0.0008113127,0.00036848758,0.00039459192,0.024581159,0.00021286627,0.0027328178,0.00012802807],"about_ca_topic_score_codex":0.000028263667,"about_ca_topic_score_gemma":0.000009511995,"teacher_disagreement_score":0.24247704,"about_ca_system_score_codex":0.000016344298,"about_ca_system_score_gemma":0.00013712168,"threshold_uncertainty_score":0.19302572},"labels":[],"label_agreement":null},{"id":"W4297199830","doi":"10.1016/j.omtm.2022.09.012","title":"Hypothalamic AAV-BDNF gene therapy improves metabolic function and behavior in the Magel2-null mouse model of Prader-Willi syndrome","year":2022,"lang":"en","type":"article","venue":"Molecular Therapy — Methods & Clinical Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Institute of Neurological Disorders and Stroke; National Cancer Institute","keywords":"Endocrinology; Internal medicine; Adipokine; Energy homeostasis; Leptin; Transgene; Neurotrophic factors; Genetic enhancement; Medicine; Adeno-associated virus; Obesity; Biology; Gene; Receptor; Vector (molecular biology)","score_opus":0.06070591502524848,"score_gpt":0.35561151785137285,"score_spread":0.2949056028261244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4297199830","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9562891,0.006284447,0.036176965,0.00016628714,0.00019592993,0.0008423451,0.000009364406,0.00001277778,0.000022795979],"genre_scores_gemma":[0.83563393,0.0023947502,0.16006817,0.0011564058,0.000026947047,0.00046492423,0.00004582744,0.000056361252,0.00015269774],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9959653,0.001524642,0.00098803,0.00073729444,0.0003786935,0.00040606616],"domain_scores_gemma":[0.9987636,0.000103271916,0.0003124508,0.0006674756,0.0000643659,0.00008883334],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.003718286,0.00032133833,0.000507346,0.000111637775,0.00017423909,0.000034787055,0.0005137055,0.00018111513,0.000025071979],"category_scores_gemma":[0.000097975295,0.00026457795,0.00024294047,0.00021845971,0.00013321762,0.000006800463,0.00033810228,0.00037040983,0.0000012195042],"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":[0.000031693715,0.0004052637,0.005616732,0.000007501147,0.00016047039,0.0000024415147,0.0001926291,0.00020022012,0.7975551,0.000026968773,0.0000041180774,0.1957969],"study_design_scores_gemma":[0.0031914823,0.0015884092,0.5108097,0.000006199959,0.000075126714,0.00010368409,0.00030453925,0.0005740004,0.47396797,0.0005861471,0.0082008,0.0005919008],"about_ca_topic_score_codex":0.000014465378,"about_ca_topic_score_gemma":0.000001882368,"teacher_disagreement_score":0.505193,"about_ca_system_score_codex":0.000017902235,"about_ca_system_score_gemma":0.00019330268,"threshold_uncertainty_score":0.9999806},"labels":[],"label_agreement":null},{"id":"W4308636364","doi":"10.1186/s13148-022-01358-9","title":"First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders","year":2022,"lang":"en","type":"article","venue":"Clinical Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"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; Det Sundhedsvidenskabelige Fakultet, Københavns Universitet; Istituto Auxologico Italiano; Ministero dell'Università e della Ricerca; RWTH Aachen University; Gentofte Hospital; Instituto de Salud Carlos III; Rigshospitalet; University of Exeter; Faculty of Health and Medical Sciences, University of Western Australia; Universität Hamburg; University Hospital Southampton NHS Foundation Trust; Diabetes UK; National Institute for Health and Care Research; Wellcome Trust; Japan Agency for Medical Research and Development","keywords":"Imprinting (psychology); Locus (genetics); Human genetics; Genomic imprinting; Diagnostic test; Medicine; Genetics; Biology; Pediatrics; Gene","score_opus":0.0947107233993399,"score_gpt":0.3618741946444731,"score_spread":0.26716347124513323,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4308636364","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97322124,0.001119464,0.023929648,0.00012390297,0.0005657412,0.0006631243,0.000095714626,0.000018450259,0.000262726],"genre_scores_gemma":[0.94418865,0.0002277735,0.054961096,0.000096268304,0.00017387551,0.00011208658,0.000031762982,0.0000518916,0.00015657122],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99763775,0.00015316755,0.0010063429,0.00056870957,0.00018399188,0.0004500672],"domain_scores_gemma":[0.99792194,0.00085921696,0.0004180799,0.0004843756,0.00017434386,0.00014203033],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009443836,0.00021781035,0.00037059558,0.000040160212,0.00027551607,0.000019100871,0.00039365908,0.00014982131,0.000029326411],"category_scores_gemma":[0.006497549,0.00023708842,0.00029324472,0.00015523564,0.00020635089,9.853094e-7,0.0008304908,0.00021836025,0.0000019702545],"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":[0.00007446772,0.0011314006,0.41709045,0.0002992481,0.00029468053,0.0000048345723,0.00008195424,0.05112894,0.01993252,0.00008704537,0.0006648794,0.5092096],"study_design_scores_gemma":[0.011467369,0.014401812,0.7085917,0.00013797046,0.00045419604,0.00009150589,0.0020200897,0.14723454,0.021003356,0.0014245501,0.09105189,0.0021210427],"about_ca_topic_score_codex":0.00008767374,"about_ca_topic_score_gemma":0.00011891677,"teacher_disagreement_score":0.50708854,"about_ca_system_score_codex":0.000013802468,"about_ca_system_score_gemma":0.00023041718,"threshold_uncertainty_score":0.9668185},"labels":[],"label_agreement":null},{"id":"W4309899484","doi":"10.3389/fgene.2022.1041943","title":"Do the diverse phenotypes of Prader-Willi syndrome reflect extremes of covariation in typical populations?","year":2022,"lang":"en","type":"article","venue":"Frontiers in Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Common Fund; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Institute of Mental Health; Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada; NIH Office of the Director; Natural Sciences and Engineering Research Council of Canada; National Cancer Institute; National Institutes of Health; National Institute on Drug Abuse; Simon Fraser University; University of Alberta","keywords":"Phenotype; Biology; Autism; Autism spectrum disorder; Mood; Cognition; Phenotypic trait; Genetics; Genomic imprinting; Psychology; Gene; Developmental psychology; Neuroscience; Clinical psychology; DNA methylation","score_opus":0.02794259510006615,"score_gpt":0.2690863082636271,"score_spread":0.24114371316356098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4309899484","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9926155,0.0025123612,0.0040460527,0.00010162547,0.00040167762,0.00021139688,0.000016577129,0.0000020361917,0.00009277931],"genre_scores_gemma":[0.98451847,0.00017015655,0.0151499,0.000024510953,0.000019291207,0.00001752782,0.000031432777,0.000011987288,0.000056737616],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989953,0.0001405751,0.00033669913,0.00019734568,0.00017467186,0.00015540818],"domain_scores_gemma":[0.99949974,0.000009925359,0.00014879671,0.0002899822,0.0000327094,0.000018842204],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026717834,0.00008921707,0.00016203991,0.00010030557,0.000053037875,0.0000054008656,0.00023535354,0.00006388051,0.000028929973],"category_scores_gemma":[0.00006551985,0.000083413644,0.000053926928,0.00025355112,0.000065105574,0.0000019938464,0.00021353188,0.00010115811,2.856015e-7],"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":[0.000022336333,0.0001902554,0.9308374,0.000033972578,0.00004640628,0.0000010984221,0.00055929495,0.02381828,0.034105793,0.00030267984,0.0007912525,0.009291237],"study_design_scores_gemma":[0.0006285788,0.00047947303,0.98536265,0.000015922065,0.000028279746,0.000021117785,0.0021509556,0.0025195833,0.0042473436,0.0018912354,0.0024830855,0.00017176589],"about_ca_topic_score_codex":0.000034392437,"about_ca_topic_score_gemma":0.000021618684,"teacher_disagreement_score":0.054525267,"about_ca_system_score_codex":0.000026779486,"about_ca_system_score_gemma":0.000053717027,"threshold_uncertainty_score":0.34015098},"labels":[],"label_agreement":null},{"id":"W4310262032","doi":"10.1177/00220345221132268","title":"Novel Genetic Determinants of Dental Maturation in Children","year":2022,"lang":"en","type":"review","venue":"Journal of Dental Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; Medical Research Council; University of Bristol; Erasmus Medisch Centrum; ZonMw; National Institutes of Health; Foundation for the National Institutes of Health; Cancer Research UK; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; Erasmus Universiteit Rotterdam; National Institute for Health and Care Research","keywords":"Genome-wide association study; Population stratification; Craniofacial; Population; Genetics; Allele; Genetic association; Medicine; Biology; Genotype; Gene; Single-nucleotide polymorphism","score_opus":0.07988921791753534,"score_gpt":0.41610109155240066,"score_spread":0.3362118736348653,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4310262032","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.38989383,0.6096894,0.000007948801,7.383191e-7,0.00012128286,0.00023171422,0.000015120689,3.7418317e-7,0.000039563554],"genre_scores_gemma":[0.04707675,0.9520635,0.00046308927,0.0000025319343,0.0002096643,0.000011821139,0.00002960615,0.000035328656,0.00010771759],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9975192,0.00027554532,0.0009218394,0.00023408169,0.0007350968,0.00031425396],"domain_scores_gemma":[0.998974,0.00004590825,0.0005558564,0.00024054406,0.00009322688,0.00009045695],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010655529,0.00017574978,0.00064421,0.00044726863,0.00005823969,0.000033139568,0.0006340695,0.00019030826,0.00010287332],"category_scores_gemma":[0.0002277302,0.0001511744,0.0003770222,0.00030990806,0.000073617266,0.0000049074974,0.00055116945,0.0005988481,0.0000046418336],"study_design_candidate":"design_other","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":[0.00002407734,0.0001916523,0.013551201,0.00088707946,0.000106929154,0.000025678975,0.000012152202,0.0000045618185,0.0041512726,3.4763866e-7,0.00006126292,0.9809838],"study_design_scores_gemma":[0.0038044793,0.005678743,0.3608895,0.0100811,0.00050580373,0.052889694,0.00089212094,0.00004292817,0.006495998,0.000026604066,0.5574041,0.0012889354],"about_ca_topic_score_codex":0.00005710843,"about_ca_topic_score_gemma":0.00003740638,"teacher_disagreement_score":0.97969484,"about_ca_system_score_codex":0.000092131755,"about_ca_system_score_gemma":0.0004027603,"threshold_uncertainty_score":0.6164713},"labels":[],"label_agreement":null},{"id":"W4311093575","doi":"10.3390/ijms232315115","title":"Comparison of Body Composition, Muscle Strength and Cardiometabolic Profile in Children with Prader-Willi Syndrome and Non-Alcoholic Fatty Liver Disease: A Pilot Study","year":2022,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Medicine; Internal medicine; Lean body mass; Endocrinology; Fatty liver; Anthropometry; Blood pressure; Body mass index; Lipid profile; Obesity; Disease; Diabetes mellitus; Body weight","score_opus":0.013275722476765062,"score_gpt":0.28248746350098497,"score_spread":0.2692117410242199,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311093575","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99757594,0.0018148493,0.00024663584,0.00007880501,0.000060044196,0.0001902034,0.000015862026,0.0000010788157,0.000016600146],"genre_scores_gemma":[0.9991652,0.00006535741,0.00069625804,0.000028719785,0.000020216516,0.000008949811,0.000006623939,0.000005929717,0.000002738238],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99881834,0.00009468664,0.0002682966,0.00019939544,0.0005094646,0.00010984493],"domain_scores_gemma":[0.9994912,0.000008536676,0.00024038264,0.000081166225,0.00011378001,0.00006494831],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033110302,0.000089677706,0.00017642141,0.00019057859,0.00007990506,0.000041916046,0.0002978583,0.000010386896,0.0000074517266],"category_scores_gemma":[0.000018854123,0.00007615818,0.000030910393,0.0001543923,0.00014421274,0.000013358475,0.00023921326,0.000089820234,8.934633e-8],"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":[0.0000110975725,0.00051057624,0.9306488,0.000003860116,0.00014232822,0.000011940653,0.00015885923,0.0012029997,0.06616645,0.000011590641,0.0000037635157,0.0011277413],"study_design_scores_gemma":[0.0008649875,0.0028060537,0.9921604,0.000018345605,0.00003421054,0.00047382357,0.00048419018,0.00036881582,0.0026704248,0.000009242124,0.000021062488,0.00008849227],"about_ca_topic_score_codex":0.00006712684,"about_ca_topic_score_gemma":0.0000047633885,"teacher_disagreement_score":0.06349602,"about_ca_system_score_codex":0.000010709838,"about_ca_system_score_gemma":0.00008698718,"threshold_uncertainty_score":0.31056407},"labels":[],"label_agreement":null},{"id":"W4313214635","doi":"10.1016/j.xgen.2022.100233","title":"Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq","year":2022,"lang":"en","type":"article","venue":"Cell Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Terry Fox Research Institute; Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"","keywords":"Autosome; Biology; Genetics; Haplotype; DNA methylation; Indel; DNA sequencing; Human genome; Allele; Chromosome; Genome; DNA; Gene; Genotype; Single-nucleotide polymorphism","score_opus":0.022737167996274805,"score_gpt":0.24062852284335023,"score_spread":0.21789135484707542,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4313214635","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9890325,0.001561348,0.009013537,0.000004777066,0.00014200651,0.00013537848,0.000008156979,0.0000058145656,0.000096502634],"genre_scores_gemma":[0.996984,0.00022762424,0.0026238197,0.00001592014,0.00006155982,0.0000053244607,0.000019771473,0.000020426989,0.000041534677],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992916,0.000043599408,0.00018660507,0.0002583171,0.00006666383,0.00015319395],"domain_scores_gemma":[0.9996686,0.000008054795,0.000116294854,0.00013731065,0.000022712606,0.000047000613],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018661772,0.000102997044,0.00011903179,0.00004346182,0.0001797237,0.000019925874,0.000058492486,0.000055378696,0.00001496834],"category_scores_gemma":[0.0000070998894,0.000122061996,0.00003468964,0.000057789926,0.000037858932,0.000004027853,0.00015515924,0.000072989504,2.427543e-7],"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":[0.000008061656,0.000008137835,0.0069000428,0.000039257913,0.000013938901,5.017517e-7,0.00020646016,0.0024867372,0.9799573,0.0000010780948,5.2665285e-7,0.010377985],"study_design_scores_gemma":[0.0007786574,0.0003092062,0.018740792,0.000012990655,0.00007299919,0.00016965409,0.0012029145,0.014947579,0.96177876,0.000069506976,0.001598135,0.0003188265],"about_ca_topic_score_codex":0.0000447199,"about_ca_topic_score_gemma":0.000014061405,"teacher_disagreement_score":0.018178532,"about_ca_system_score_codex":0.00004726816,"about_ca_system_score_gemma":0.00005175663,"threshold_uncertainty_score":0.49775437},"labels":[],"label_agreement":null},{"id":"W4315753440","doi":"10.1210/clinem/dgad015","title":"Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial","year":2023,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of British Columbia; University of Alberta; Hospital for Sick Children; University of Toronto; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Placebo; Medicine; Anxiety; Clinical endpoint; Context (archaeology); Distress; Randomized controlled trial; Internal medicine; Clinical trial; Psychiatry; Clinical psychology","score_opus":0.03399671080429532,"score_gpt":0.37521815995375923,"score_spread":0.3412214491494639,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4315753440","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9871194,0.009298094,0.00003356498,0.0015637447,0.0016057149,0.0002871289,0.000013024885,0.000010042851,0.000069329275],"genre_scores_gemma":[0.98734385,0.011191624,0.00016728189,0.00017907175,0.0009843963,0.000009569346,0.00001331193,0.000026825035,0.000084088926],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.996878,0.0007180195,0.0013599881,0.00030608408,0.00023190741,0.00050596555],"domain_scores_gemma":[0.9985392,0.00027367924,0.00055473024,0.00034929204,0.00012792097,0.00015518516],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013170562,0.00022548,0.0008034813,0.00013377809,0.00009725241,0.000028985445,0.000506501,0.0002251782,0.000013906289],"category_scores_gemma":[0.00087666255,0.0001560558,0.00024776862,0.00021745454,0.0004470665,0.000011076169,0.00024236881,0.0006157193,0.000005414066],"study_design_candidate":"design_other","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":[0.00953471,0.0022901732,0.057776295,0.00020480459,0.0025937858,0.0006650679,0.0033329993,0.00074936275,0.1686244,0.0005150122,0.005326179,0.7483872],"study_design_scores_gemma":[0.17282963,0.007577716,0.65855616,0.00014509924,0.0011182653,0.005912409,0.0060026553,0.00013883672,0.018260047,0.000707612,0.12772034,0.001031259],"about_ca_topic_score_codex":0.000044628236,"about_ca_topic_score_gemma":0.00002130894,"teacher_disagreement_score":0.74735594,"about_ca_system_score_codex":0.000006496469,"about_ca_system_score_gemma":0.0001605489,"threshold_uncertainty_score":0.6363771},"labels":[],"label_agreement":null},{"id":"W4319163406","doi":"10.1038/s41598-023-29248-x","title":"Noncanonical regulation of imprinted gene Igf2 by amyloid-beta 1–42 in Alzheimer’s disease","year":2023,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"Dalhousie University; Natural Sciences and Engineering Research Council of Canada; Fondation Brain Canada","keywords":"Epigenetics; DNA methylation; Genomic imprinting; MECP2; Histone; Biology; Epigenomics; Insulin-like growth factor 2; Methylation; Gene expression; Endocrinology; Regulation of gene expression; Internal medicine; Gene; Genetics; Medicine; Phenotype","score_opus":0.015123925852903532,"score_gpt":0.2634072047206951,"score_spread":0.24828327886779158,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4319163406","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99755794,0.00052764337,0.00013481698,0.00010332075,0.0011598185,0.00020159943,0.000007953836,0.000016657097,0.0002902728],"genre_scores_gemma":[0.9978499,0.000020528783,0.00022246066,0.000011180714,0.000040284263,0.000015697484,0.00045777738,0.000016168378,0.0013660388],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982971,0.00003948668,0.00048299364,0.00062906544,0.0002690056,0.00028232732],"domain_scores_gemma":[0.99883413,0.0000069781036,0.000200521,0.0007385507,0.00009392621,0.00012588609],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00078161235,0.00011267183,0.00014288044,0.00010862825,0.000066031535,0.000041423016,0.00013234175,0.000080526836,0.000038875864],"category_scores_gemma":[0.00011988786,0.0001121245,0.000096043055,0.00042957597,0.00014318047,0.0000046860173,0.00018872667,0.000049685947,0.000013001226],"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":[0.00000571238,0.000038776627,0.03638388,0.00000930453,0.00001699572,0.000016763408,0.000021280714,0.00021174533,0.9565146,0.0000052216656,0.0045966418,0.0021790853],"study_design_scores_gemma":[0.00019559992,0.000037589787,0.23951961,0.000021622793,0.00002296554,0.00003527182,0.00002588152,0.00060300913,0.74196583,0.00029581625,0.01710714,0.00016966318],"about_ca_topic_score_codex":0.000035554243,"about_ca_topic_score_gemma":0.000014407878,"teacher_disagreement_score":0.21454877,"about_ca_system_score_codex":0.000009696787,"about_ca_system_score_gemma":0.00016238858,"threshold_uncertainty_score":0.45723045},"labels":[],"label_agreement":null},{"id":"W4319321105","doi":"10.3389/fnins.2023.1126970","title":"Prader–Willi syndrome: Symptoms and topiramate response in light of genetics","year":2023,"lang":"en","type":"article","venue":"Frontiers in Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Topiramate; Impulsivity; Medicine; Psychiatry; Pharmacogenetics; Uniparental disomy; Pediatrics; Psychology; Epilepsy; Genetics; Chromosome; Genotype; Biology; Karyotype","score_opus":0.008980407679292904,"score_gpt":0.23955489099761398,"score_spread":0.2305744833183211,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4319321105","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981928,0.00050515356,0.0003211761,0.0002448347,0.0005145809,0.00013585394,0.0000034058298,0.0000076308725,0.0000745501],"genre_scores_gemma":[0.9980166,0.0005749561,0.00093152816,0.00010342006,0.000008118658,0.000009142282,0.0000014171314,0.0000109283,0.000343875],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989054,0.00008418698,0.0002231667,0.00037544162,0.00012735662,0.00028444553],"domain_scores_gemma":[0.99961495,0.000011265949,0.000057985406,0.0002510074,0.000013686196,0.000051127037],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038978795,0.000098861994,0.00014325186,0.00018674857,0.000030320469,0.000017088598,0.00023029269,0.000074024465,7.617504e-7],"category_scores_gemma":[0.00023001194,0.00010084597,0.000024471,0.00051038404,0.00014020967,0.0000046455384,0.000209742,0.000067086694,8.246555e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000012595114,0.000023974642,0.4528757,0.000028924766,0.0000016104697,0.000011978732,0.0001246821,0.00042183214,0.54375064,0.000008738988,0.00026585127,0.0024734973],"study_design_scores_gemma":[0.00032269093,0.00045222972,0.9722926,0.000030046995,0.0000019989818,0.00005590552,0.0001032557,0.002378057,0.017960316,0.000060577724,0.0062145987,0.0001276946],"about_ca_topic_score_codex":0.0000041609565,"about_ca_topic_score_gemma":0.0000019573579,"teacher_disagreement_score":0.52579033,"about_ca_system_score_codex":0.000007639004,"about_ca_system_score_gemma":0.000042622083,"threshold_uncertainty_score":0.41123796},"labels":[],"label_agreement":null},{"id":"W4319736580","doi":"10.3920/978-90-8686-940-4_750","title":"750. Genome-wide association study for ectopic ureter in three dog breeds","year":2022,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Labrador Retriever; Breed; Bonferroni correction; Veterinary medicine; Felis catus; Ectopic ureter; Biology; Medicine; Urinary system; Genetics; CATS; Anatomy; Internal medicine; Pathology","score_opus":0.011485576845644734,"score_gpt":0.2430181393045681,"score_spread":0.23153256245892334,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4319736580","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969691,0.00009244617,0.0010337908,0.00023387851,0.00016006752,0.0005159756,0.000006341361,0.000007087869,0.0009812964],"genre_scores_gemma":[0.995642,0.000003735785,0.00044601128,0.00040767464,0.000076883756,0.00018647964,0.0000406858,0.000014277803,0.0031822305],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991853,0.000042646498,0.00017906354,0.00025053674,0.00012254564,0.00021986374],"domain_scores_gemma":[0.9996639,0.000025720492,0.000062911706,0.00019175104,0.000030641582,0.000025090078],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003762291,0.000085032996,0.00010592661,0.000040406863,0.000092077695,0.000018123217,0.0001496798,0.000045224107,0.00014351116],"category_scores_gemma":[0.000089551875,0.00008629965,0.00006372348,0.00007749986,0.0000042566667,0.0000012628172,0.00021407042,0.000065696244,0.0000031136024],"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":[0.000005027131,0.00010082321,0.9761962,0.000004107724,0.000039109684,5.314132e-7,0.00008340265,0.00014672804,0.02253144,0.0000071735235,0.0003726171,0.00051282346],"study_design_scores_gemma":[0.0010917034,0.0007682808,0.9769832,6.889969e-7,0.0000128092925,0.0000019386134,0.0004875644,0.00012568008,0.001398603,0.00013182344,0.018854601,0.00014314547],"about_ca_topic_score_codex":0.000073189665,"about_ca_topic_score_gemma":0.00021351464,"teacher_disagreement_score":0.021132838,"about_ca_system_score_codex":0.000055010074,"about_ca_system_score_gemma":0.000028400902,"threshold_uncertainty_score":0.35191977},"labels":[],"label_agreement":null},{"id":"W4320001616","doi":"10.1016/b978-0-12-821785-6.00011-6","title":"Genomic imprinting and developmental physiology: intrauterine growth and postnatal period","year":2023,"lang":"en","type":"book-chapter","venue":"Elsevier eBooks","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"Medical Research Council","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Offspring; Period (music); Phenotype; In utero; Gene; Epigenetics; Gene expression; Placenta; Fetus; Genetics; Physiology; DNA methylation; Pregnancy","score_opus":0.00891226907335172,"score_gpt":0.20934734329443333,"score_spread":0.20043507422108162,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4320001616","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7189839,0.0008857332,0.0000020254843,0.00003592616,0.0002017497,0.00028231405,0.000031610605,0.000029349594,0.27954736],"genre_scores_gemma":[0.4727835,0.0042579956,0.0028763663,0.00028272567,0.00064886827,0.000037503516,0.00020807036,0.00025103803,0.5186539],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9986343,0.000013070617,0.00030409347,0.00065393717,0.00008777999,0.00030683994],"domain_scores_gemma":[0.9995126,0.00000988856,0.00012781759,0.00020393248,0.00003469815,0.000111027395],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000108270244,0.00037355864,0.00033535744,0.00007085347,0.00012800925,0.00004972672,0.00015136076,0.00031135735,0.000021524227],"category_scores_gemma":[0.000023764009,0.0003776919,0.00008308686,0.000006642492,0.0001815577,0.0000017905203,0.0009575102,0.00020458216,0.00003293894],"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":[0.000009284862,0.0000031494246,0.00023573315,0.00018040474,0.00020604375,0.000018956047,0.00015850084,8.8792504e-8,0.46782956,0.00041467333,0.000013995424,0.5309296],"study_design_scores_gemma":[0.0033875478,0.0012003816,0.14621252,0.00090798293,0.00040370406,0.0060917237,0.00048271634,0.000042334814,0.043218352,0.006289692,0.78696674,0.0047962824],"about_ca_topic_score_codex":0.0000012585189,"about_ca_topic_score_gemma":0.000005627657,"teacher_disagreement_score":0.7869528,"about_ca_system_score_codex":0.000012287091,"about_ca_system_score_gemma":0.000069160764,"threshold_uncertainty_score":0.9998675},"labels":[],"label_agreement":null},{"id":"W4320484851","doi":"10.31542/r.2726","title":"It’s a burden but… having a sibling with Prader Willi syndrome: stress, growth, and perceived burden","year":2022,"lang":"en","type":"dissertation","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"MacEwan University","funders":"MacEwan University","keywords":"Neurotypical; Sibling; Feeling; Psychology; Clinical psychology; Population; Sibling relationship; Developmental psychology; Medicine; Environmental health; Autism spectrum disorder; Social psychology","score_opus":0.007328141478877899,"score_gpt":0.23978635506320425,"score_spread":0.23245821358432636,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4320484851","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99153304,0.0014608674,0.000053061845,0.0004236871,0.00022770134,0.00047163514,0.000033335946,0.000031865107,0.005764788],"genre_scores_gemma":[0.9762703,0.0010765573,0.0014126947,0.00016933875,0.00021916014,0.00012262768,0.0018995412,0.00012493524,0.018704822],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.997776,0.00006469219,0.00037023425,0.000948827,0.00036970922,0.0004705725],"domain_scores_gemma":[0.9990497,0.000020081246,0.00023587726,0.00043102054,0.000116080366,0.0001471959],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00011746337,0.00048122063,0.00041237767,0.00015441971,0.0002981474,0.000152512,0.00032904977,0.00035957884,0.00042755227],"category_scores_gemma":[0.00007564973,0.0004391285,0.00011820182,0.00015768965,0.000056125667,0.0000074558548,0.00020901146,0.0003572037,0.0000039975243],"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":[0.00012842022,0.0002784486,0.04317015,0.003280213,0.002552812,0.00014089195,0.0117290905,0.00089326146,0.9240667,0.00012242404,0.0024508783,0.011186695],"study_design_scores_gemma":[0.009620313,0.009085269,0.6477646,0.0028481453,0.0023295786,0.0062324656,0.21414255,0.0012825354,0.029935846,0.00013864535,0.06721528,0.009404734],"about_ca_topic_score_codex":0.0008387738,"about_ca_topic_score_gemma":0.0003793041,"teacher_disagreement_score":0.8941309,"about_ca_system_score_codex":0.000020120568,"about_ca_system_score_gemma":0.00019607862,"threshold_uncertainty_score":0.99980605},"labels":[],"label_agreement":null},{"id":"W4321499146","doi":"10.1111/ijpo.13006","title":"Incorporation of patient and family values and preferences for health‐related outcomes in paediatric obesity management: A systematic review","year":2023,"lang":"en","type":"review","venue":"Pediatric Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lakehead University; University of Calgary; University of Alberta; Trillium Health Centre","funders":"Obesity Canada; Canadian Institutes of Health Research; Alberta Innovates","keywords":"Medicine; Psychological intervention; CINAHL; MEDLINE; Scopus; PsycINFO; Overweight; Systematic review; Obesity; Family medicine; Clinical psychology; Psychiatry","score_opus":0.022933263316062918,"score_gpt":0.2934605941422216,"score_spread":0.27052733082615865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4321499146","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.048393298,0.94756573,0.000021616543,0.000009117902,0.00010306114,0.0038231618,0.000059611928,0.000012104191,0.000012288109],"genre_scores_gemma":[0.0032468028,0.9957832,0.0003581784,0.000024743349,0.0000336582,0.00031112964,0.00014156282,0.000027249245,0.00007345197],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.9974414,0.0003143735,0.0013153101,0.0005134115,0.00017421198,0.00024127439],"domain_scores_gemma":[0.9982849,0.00011136025,0.0011565583,0.00031332223,0.000056827543,0.00007704207],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0009851053,0.00031822058,0.0018409977,0.00022450813,0.00006394482,0.00001812771,0.00016451017,0.00021080195,6.4461244e-7],"category_scores_gemma":[0.00026045943,0.00025436614,0.00020916013,0.0003896871,0.00002606724,0.0000048973775,0.0003117598,0.00010593659,0.000002443209],"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":[7.839692e-7,0.000072959716,0.0095062535,0.9741801,0.000120133096,8.576085e-7,0.000030545896,4.3004755e-7,1.1982564e-7,0.000008560015,0.00008386278,0.015995376],"study_design_scores_gemma":[0.004915535,0.0050636916,0.21507755,0.7194307,0.03457883,0.00018583388,0.00089902815,0.00012774522,0.000005863218,0.0049887183,0.008725028,0.006001473],"about_ca_topic_score_codex":0.000032505566,"about_ca_topic_score_gemma":0.000009159311,"teacher_disagreement_score":0.25474942,"about_ca_system_score_codex":0.000024026147,"about_ca_system_score_gemma":0.00010044683,"threshold_uncertainty_score":0.9999909},"labels":[],"label_agreement":null},{"id":"W4321748330","doi":"10.1002/jbmr.4795","title":"Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism","year":2020,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Care Foundation","funders":"National Health and Medical Research Council; Seventh Framework Programme; Elizabeth Blackwell Institute for Health Research, University of Bristol; Menzies Institute for Medical Research; Medical Research Council; International Seafood Sustainability Foundation; Versus Arthritis; Australian Cancer Research Foundation; Medical Research Council Canada; University of Tasmania; University of Bristol; University of New South Wales; Wellcome Trust","keywords":"Osteoporosis; Femoral neck; Genetics; Exome sequencing; Biology; Bone mineral; Endocrinology; Internal medicine; Medicine; Gene; Phenotype","score_opus":0.036031992470024955,"score_gpt":0.3250637518560142,"score_spread":0.28903175938598924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4321748330","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98842734,0.010341858,0.000030718194,0.00083008676,0.00003739851,0.00009381413,0.000004667534,6.440182e-7,0.00023349063],"genre_scores_gemma":[0.99634445,0.0026180034,0.00062375324,0.0000754442,0.000116940566,0.0000013662321,0.000002410544,0.000010751641,0.00020687838],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9987849,0.00015033026,0.00037171438,0.00015750037,0.00029757663,0.00023797502],"domain_scores_gemma":[0.99942255,0.00003121756,0.00013616515,0.00009475406,0.00014911755,0.00016619684],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001074072,0.00009043108,0.0003221946,0.000116737174,0.000032864653,0.00003037135,0.000088014305,0.0000927047,0.000014391417],"category_scores_gemma":[0.0002483621,0.00007417942,0.000058535785,0.00014157296,0.00007383069,0.00000941569,0.00017237867,0.00027550478,5.9324503e-7],"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":[0.00015928096,0.000035837333,0.03498815,0.00007497179,0.000037532227,0.00007619613,0.00014482053,0.000009347159,0.95786476,0.000022518838,0.0004765704,0.0061100037],"study_design_scores_gemma":[0.004847091,0.002184237,0.66550756,0.00018225615,0.000042697226,0.0006467584,0.00071729533,0.00026303454,0.3182665,0.0002404816,0.0068526897,0.00024942422],"about_ca_topic_score_codex":0.00007474499,"about_ca_topic_score_gemma":0.000020425505,"teacher_disagreement_score":0.63959825,"about_ca_system_score_codex":0.000004697548,"about_ca_system_score_gemma":0.00006991532,"threshold_uncertainty_score":0.3024949},"labels":[],"label_agreement":null},{"id":"W4324156277","doi":"10.1186/s13059-023-02869-1","title":"Conservation and divergence of canonical and non-canonical imprinting in murids","year":2023,"lang":"en","type":"review","venue":"Genome biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"BC Children's Hospital; University of British Columbia","funders":"Institute of Genetics; National Institute for Physiological Sciences; Japan Society for the Promotion of Science; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Fondation ARC pour la Recherche sur le Cancer; Provincial Health Services Authority; Fondation pour la Recherche Médicale; European Research Council; BC Children's Hospital; Tokyo University of Agriculture; NODAI Genome Research Center, Tokyo University of Agriculture; Sumitomo Foundation; Children's Hospital Foundation","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Gene; DNA methylation; Promoter; Genome; Gene expression","score_opus":0.03974186645115925,"score_gpt":0.3235652243091437,"score_spread":0.28382335785798446,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4324156277","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.19801389,0.8013768,0.000055668832,0.0000170696,0.00012516583,0.00030257524,0.000034382618,0.0000047471294,0.00006966714],"genre_scores_gemma":[0.026178163,0.9730591,0.00037576602,0.000022459732,0.00009382863,0.000034402394,0.00012697406,0.000026874759,0.0000824385],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9984282,0.000109734945,0.00058297825,0.00053868245,0.00004181668,0.00029857623],"domain_scores_gemma":[0.9993473,0.00006276509,0.00023426591,0.00025420386,0.0000340795,0.00006732808],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037576628,0.00023004423,0.0007907847,0.00010557366,0.000033395,0.000008422072,0.00017976828,0.0004848855,0.000007614795],"category_scores_gemma":[0.00015015331,0.00020605844,0.00010042956,0.00013911455,0.00019835918,0.0000012602234,0.0006677301,0.00015993499,0.000004585747],"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":[0.000013652062,0.00006845863,0.056432083,0.01229446,0.00044234406,0.000011812289,0.000095669086,0.0000028294928,0.05086889,0.00030866478,0.00004626499,0.87941486],"study_design_scores_gemma":[0.00071850576,0.00069889013,0.07677842,0.0015890568,0.00022569775,0.00020974713,0.000056660894,0.000031796608,0.00016988676,0.0001098666,0.91858155,0.00082994264],"about_ca_topic_score_codex":0.00021308521,"about_ca_topic_score_gemma":0.00010058856,"teacher_disagreement_score":0.91853523,"about_ca_system_score_codex":0.000013701005,"about_ca_system_score_gemma":0.0002341667,"threshold_uncertainty_score":0.84028196},"labels":[],"label_agreement":null},{"id":"W4361266110","doi":"10.1158/0008-5472.c.6494585","title":"Data from The c-Myc Oncogene Directly Induces the H19 Noncoding RNA by Allele-Specific Binding to Potentiate Tumorigenesis","year":2023,"lang":"en","type":"preprint","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Toronto; Ontario Institute for Cancer Research","funders":"Canadian Institutes of Health Research; University of Pennsylvania; U.S. Department of Defense","keywords":"Gene knockdown; Biology; Chromatin immunoprecipitation; Genomic imprinting; Cancer research; Carcinogenesis; Transcription factor; Oncogene; Long non-coding RNA; Gene; Molecular biology; N-Myc; Gene expression; Promoter; DNA methylation; Genetics; RNA; Cell cycle; Cell culture","score_opus":0.08365703510303053,"score_gpt":0.29795378096500286,"score_spread":0.21429674586197234,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361266110","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98336923,0.0044702566,0.0037420043,0.003074462,0.001963451,0.00074668095,0.0016443997,0.000076200515,0.000913304],"genre_scores_gemma":[0.9770284,0.0064033424,0.0027563998,0.0007626746,0.0017503296,0.000121748184,0.00597909,0.00017601505,0.0050219977],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99630815,0.0002176968,0.0006404818,0.0017040606,0.00045737988,0.00067224546],"domain_scores_gemma":[0.9959189,0.00013950493,0.0003175761,0.0033531967,0.000103190076,0.00016762572],"candidate_categories":["metaepi_narrow","open_science"],"consensus_categories":[],"category_scores_codex":[0.0010494579,0.0005552903,0.00043465267,0.00006163468,0.0004777908,0.0004562127,0.0037852621,0.00039452515,0.00014247153],"category_scores_gemma":[0.00019771434,0.00035419757,0.00023280412,0.0002353637,0.000083065504,0.0000055649302,0.009205531,0.00047222452,0.00027081656],"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":[0.000010233998,0.000031030457,0.00066445477,0.000015151468,0.0004027238,0.0000045595266,0.00011382687,0.0002566816,0.87447315,0.0000039983415,0.11360358,0.010420623],"study_design_scores_gemma":[0.00047617298,0.00012156631,0.009792404,0.00020684897,0.00024254431,0.0000211226,0.0017541414,0.00040262385,0.5116743,0.00012963866,0.47378233,0.0013962827],"about_ca_topic_score_codex":0.0015054686,"about_ca_topic_score_gemma":0.00042694947,"teacher_disagreement_score":0.3627988,"about_ca_system_score_codex":0.000038740556,"about_ca_system_score_gemma":0.00015600545,"threshold_uncertainty_score":0.999891},"labels":[],"label_agreement":null},{"id":"W4361271943","doi":"10.1016/j.stemcr.2023.03.004","title":"Differentiation of uniparental human embryonic stem cells into granulosa cells reveals a paternal contribution to gonadal development","year":2023,"lang":"en","type":"article","venue":"Stem Cell Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Azrieli Foundation; Israel Science Foundation; Rosetrees Trust","keywords":"Biology; Genomic imprinting; Parthenogenesis; Sexual differentiation; Induced pluripotent stem cell; Embryonic stem cell; Imprinting (psychology); Genetics; Gonad; Genome; Gene; Stem cell; Cellular differentiation; Embryo; Gene expression; DNA methylation; Endocrinology","score_opus":0.009669179166216433,"score_gpt":0.2306244832353495,"score_spread":0.22095530406913308,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361271943","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99811655,0.00009467519,0.0006906968,0.000010660077,0.0005452018,0.00040414114,0.0000113349515,0.000023214972,0.00010353222],"genre_scores_gemma":[0.99667346,0.000019244439,0.00015990874,0.000017148071,0.000061801766,0.000032488948,0.0002181569,0.000025748695,0.0027920143],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99820006,0.00005962295,0.000649122,0.0004597063,0.00028725702,0.00034421092],"domain_scores_gemma":[0.9989813,0.0000072530793,0.000382121,0.0003613069,0.00013440533,0.00013360895],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036708705,0.00019555501,0.00024706518,0.000091475544,0.00012556596,0.000027800937,0.00012306968,0.00012496942,0.000013437414],"category_scores_gemma":[0.0000035715982,0.00019387086,0.00010635365,0.00015480482,0.000021879729,0.0000037487682,0.0002315868,0.00005972315,0.00002163411],"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":[0.000006727386,0.000047080273,0.020915458,0.000099279336,0.000032606964,0.000019837818,0.00021524561,0.00009624649,0.9764205,0.0000031431096,0.00030294067,0.001840921],"study_design_scores_gemma":[0.00026171192,0.00018050695,0.053713802,0.00005632856,0.000018424274,0.000024079156,0.00017310742,0.000014662734,0.94223183,0.00001918576,0.0030985803,0.00020776023],"about_ca_topic_score_codex":0.000037184374,"about_ca_topic_score_gemma":0.000027341324,"teacher_disagreement_score":0.034188665,"about_ca_system_score_codex":0.000050050854,"about_ca_system_score_gemma":0.0000861312,"threshold_uncertainty_score":0.7905824},"labels":[],"label_agreement":null},{"id":"W4361298710","doi":"10.1038/s41380-022-01909-9","title":"Focal adhesion is associated with lithium response in bipolar disorder: evidence from a network-based multi-omics analysis","year":2023,"lang":"en","type":"article","venue":"Molecular Psychiatry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Institute of Mental Health; National Institutes of Health; University of California, San Diego; Genome Atlantic; Dalhousie University; Research Nova Scotia; U.S. Department of Veterans Affairs; Paul G. Allen Frontiers Group; National Center for Advancing Translational Sciences; Agence Nationale de la Recherche; Georgia Clinical and Translational Science Alliance; Dalhousie Medical Research Foundation; JPB Foundation; Canadian Institutes of Health Research; American Heart Association","keywords":"Genome-wide association study; Transcriptome; Bipolar disorder; Biology; Computational biology; Gene expression profiling; Candidate gene; Gene regulatory network; Gene; Genetics; Lithium (medication); Bioinformatics; Single-nucleotide polymorphism; Gene expression; Endocrinology","score_opus":0.011765825665352742,"score_gpt":0.25582661969630155,"score_spread":0.2440607940309488,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361298710","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96881413,0.0050828042,0.024613874,0.0009786059,0.00018370742,0.0002382241,0.000039658134,0.00004473916,0.000004242605],"genre_scores_gemma":[0.989289,0.00015762408,0.009206689,0.0007888603,0.00005589652,0.000037511196,0.00030188,0.000057239136,0.00010531709],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9977062,0.00038610402,0.0003645399,0.0007402366,0.00027510882,0.0005278575],"domain_scores_gemma":[0.9988736,0.00006890511,0.00016049348,0.00070611766,0.000072565694,0.00011833025],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006734569,0.00027880818,0.00032729263,0.00021636728,0.00010196458,0.000049715974,0.00031925153,0.0002531947,0.00002226882],"category_scores_gemma":[0.00026717162,0.00026972278,0.00026819756,0.0014975598,0.000058445534,0.0000050665994,0.00014540573,0.00019218374,0.000021772124],"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":[0.0004255735,0.00015805737,0.82791054,0.000012513494,0.00052146416,0.00003499445,0.00007148165,0.037152372,0.13269979,0.000001528465,0.00039058767,0.0006210828],"study_design_scores_gemma":[0.0018354635,0.00066111085,0.9299213,0.00020843712,0.00035573766,0.0000039356783,0.00010498388,0.05532939,0.009791096,0.000038864062,0.0011829403,0.00056673924],"about_ca_topic_score_codex":0.0002445656,"about_ca_topic_score_gemma":0.00063177926,"teacher_disagreement_score":0.1229087,"about_ca_system_score_codex":0.000027670258,"about_ca_system_score_gemma":0.00022892216,"threshold_uncertainty_score":0.9999755},"labels":[],"label_agreement":null},{"id":"W4361859041","doi":"10.1177/27528464231166828","title":"Multi-suture craniosynostosis in Sotos Syndrome: A case Report","year":2023,"lang":"en","type":"article","venue":"Craniomaxillofacial Research & Innovation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Craniosynostosis; Sotos syndrome; Medicine; Apert syndrome; Craniofacial; Craniosynostoses; Fibrous joint; Presentation (obstetrics); Surgery; Pediatrics; Psychiatry","score_opus":0.08185742521882457,"score_gpt":0.38844126206859964,"score_spread":0.3065838368497751,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361859041","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974907,0.00005935311,0.00054296514,0.0004619524,0.00028042606,0.0006259199,0.000022410848,0.000053572625,0.0004627088],"genre_scores_gemma":[0.9967445,0.000054031512,0.00078640244,0.00006457959,0.00010359444,0.0001478677,0.00028304718,0.000046937577,0.0017690122],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9972903,0.00013418816,0.0006004935,0.0006769162,0.0005455772,0.0007524954],"domain_scores_gemma":[0.99855435,0.000025462272,0.000106226544,0.00055487256,0.00067190034,0.00008716696],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0025659013,0.00019773125,0.00020508395,0.0009586151,0.00030507037,0.00009463902,0.00025759696,0.00032016492,0.000058499925],"category_scores_gemma":[0.0023687915,0.00020730883,0.00007256288,0.0043127215,0.00013445769,0.000014443082,0.00033822173,0.00037150757,0.000100392],"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":[0.00002735279,0.00012184959,0.030820215,0.000055479544,0.00004046211,0.018496739,0.00023307904,0.00004547461,0.93298453,0.000115676106,0.0013426698,0.015716463],"study_design_scores_gemma":[0.004473358,0.0011393243,0.7574667,0.00017499174,0.000019032715,0.07830615,0.0028281752,0.0021780122,0.09123373,0.0007666151,0.060062144,0.001351801],"about_ca_topic_score_codex":0.00028202328,"about_ca_topic_score_gemma":0.00015549632,"teacher_disagreement_score":0.8417508,"about_ca_system_score_codex":0.00005696482,"about_ca_system_score_gemma":0.00021676208,"threshold_uncertainty_score":0.8453809},"labels":[],"label_agreement":null},{"id":"W4362467524","doi":"10.3389/fnins.2023.1189154","title":"Corrigendum: Prader-Willi syndrome: Symptoms and topiramate response in light of genetics","year":2023,"lang":"en","type":"erratum","venue":"Frontiers in Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Topiramate; Response inhibition; Genetics; Psychology; Medicine; Neuroscience; Biology; Cognition; Epilepsy","score_opus":0.01347448799535661,"score_gpt":0.2436208831035782,"score_spread":0.2301463951082216,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4362467524","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9539538,0.005839913,0.00040906647,0.00027619852,0.0382592,0.00051351276,0.000050677045,0.000018607496,0.0006790507],"genre_scores_gemma":[0.76678544,0.023646014,0.00359387,0.0007557355,0.0003989998,0.00013108776,0.000117205236,0.0002922452,0.2042794],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9975483,0.0001829694,0.0005211104,0.00091056863,0.00030281759,0.00053426274],"domain_scores_gemma":[0.9990152,0.000012862833,0.00024120318,0.0005907742,0.00003766183,0.00010227313],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005275498,0.00030703534,0.00045627408,0.00039038106,0.000052116968,0.00004334311,0.00061544054,0.00045290776,0.0000018221757],"category_scores_gemma":[0.00046347437,0.00032301716,0.00007422987,0.00057730963,0.00028902988,0.00000560776,0.0004968173,0.00038721916,0.0000014106981],"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":[0.00009007805,0.00025125445,0.30970216,0.00091711996,0.00003846526,0.00019061052,0.0005901076,0.00041733886,0.21193025,0.000017251703,0.4677771,0.008078274],"study_design_scores_gemma":[0.00058439735,0.0013625155,0.6658242,0.0003720328,0.00001849397,0.00018673993,0.00014093149,0.0017560873,0.0023288417,0.00007036362,0.3267483,0.0006071006],"about_ca_topic_score_codex":0.00001772108,"about_ca_topic_score_gemma":0.000014342772,"teacher_disagreement_score":0.35612205,"about_ca_system_score_codex":0.000029653516,"about_ca_system_score_gemma":0.00025225684,"threshold_uncertainty_score":0.9999222},"labels":[],"label_agreement":null},{"id":"W4366601899","doi":"10.1111/pcmr.13089","title":"<scp>BORIS</scp> / <scp>CTCFL</scp> ‐mediated chromatin accessibility alterations promote a pro‐invasive transcriptional signature in melanoma cells","year":2023,"lang":"en","type":"article","venue":"Pigment Cell & Melanoma Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Health Centre; McGill University; Jewish General Hospital","funders":"Canadian Institutes of Health Research; Israel Science Foundation; Israel Cancer Research Fund","keywords":"Chromatin; Melanoma; Ectopic expression; Biology; Reprogramming; Transcription factor; Bivalent chromatin; Promoter; Cancer research; Chromatin immunoprecipitation; Transcriptional regulation; Cell biology; Regulation of gene expression; Gene; Gene expression; Chromatin remodeling; Genetics","score_opus":0.0338307159432611,"score_gpt":0.30853544248746506,"score_spread":0.27470472654420397,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4366601899","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99236816,0.0012118461,0.00012637673,0.00019314348,0.0003106637,0.0018188038,0.00015510853,0.000064787855,0.0037511224],"genre_scores_gemma":[0.98864293,0.0005913337,0.0006766387,0.000056436813,0.00033548876,0.00058742485,0.0010854099,0.000078650446,0.007945668],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99488604,0.0006430093,0.0007314879,0.0012470734,0.0010709995,0.0014214005],"domain_scores_gemma":[0.9977598,0.0005439488,0.00016383598,0.00078665215,0.0003894525,0.0003562732],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.001985123,0.0004242325,0.00040160472,0.00045774016,0.00036288786,0.00022894728,0.00080389244,0.00048697845,0.00008401386],"category_scores_gemma":[0.0009708246,0.0004090255,0.00020477202,0.0012057265,0.0001956495,0.000028644361,0.0004737963,0.00076452375,0.00035610647],"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":[0.000006089492,0.00040167297,0.01137085,0.00026282683,0.00006103731,0.00004434015,0.0011757987,0.00016807909,0.97919816,0.000018195387,0.0068814573,0.0004114781],"study_design_scores_gemma":[0.0016220297,0.00082895136,0.10965777,0.00009237402,0.000021342761,0.000013944219,0.0016691837,0.0012945598,0.8645132,0.00023352774,0.019910945,0.00014216152],"about_ca_topic_score_codex":0.000079517115,"about_ca_topic_score_gemma":0.00013070166,"teacher_disagreement_score":0.11468496,"about_ca_system_score_codex":0.00012956426,"about_ca_system_score_gemma":0.0005865555,"threshold_uncertainty_score":0.99983615},"labels":[],"label_agreement":null},{"id":"W4367055664","doi":"10.1111/age.13326","title":"Association between TH/MAOB gene single nucleotide polymorphisms and excitability in Labrador Retrievers","year":2023,"lang":"en","type":"article","venue":"Animal Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Key Research and Development Program of China","keywords":"Biology; Genetics; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.017531844249562497,"score_gpt":0.24093426038299606,"score_spread":0.22340241613343356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367055664","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99851793,0.00060607865,0.000039979175,0.00029662868,0.00012307148,0.00016098266,0.000028787885,0.000026570178,0.00019998108],"genre_scores_gemma":[0.9977302,0.00049420336,0.00086214225,0.00008321118,0.00024092976,0.0000058464398,0.00006706102,0.000031204356,0.00048517666],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986533,0.00006526386,0.00028466666,0.00041587098,0.00017903288,0.00040184965],"domain_scores_gemma":[0.99946094,0.000037286507,0.00010133398,0.00025008025,0.000054578828,0.000095761716],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000372094,0.00015807232,0.00018079595,0.00006911025,0.000065564695,0.00004005651,0.0001400366,0.00020985914,0.0000130742665],"category_scores_gemma":[0.00015413763,0.00017712102,0.000057256366,0.00028925162,0.00004637391,0.0000040458076,0.00023183641,0.00009798166,0.000025210655],"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":[0.0000061511664,0.000019148065,0.48461872,0.000008331272,0.000027342248,0.0000016737953,0.000055476954,0.000007937464,0.51156414,0.0000017070746,0.00018856765,0.003500795],"study_design_scores_gemma":[0.00038060243,0.0004044039,0.8962874,0.000007062336,0.00002252411,0.0000037889697,0.00009942644,0.00011375737,0.097822845,0.00007813176,0.0045848372,0.00019522673],"about_ca_topic_score_codex":0.000062419684,"about_ca_topic_score_gemma":0.00007723584,"teacher_disagreement_score":0.41374132,"about_ca_system_score_codex":0.000042440235,"about_ca_system_score_gemma":0.000036034082,"threshold_uncertainty_score":0.7222786},"labels":[],"label_agreement":null},{"id":"W4367311515","doi":"10.3390/ijms24098013","title":"Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader–Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Sudomotor; Medicine; Internal medicine; Autonomic nervous system; Heart rate; Body mass index; Heart rate variability; Blood pressure; Valsalva maneuver; Endocrinology; Baroreflex; Obesity; Sympathetic nervous system; Cardiology; SWEAT; Cardiac function curve; Heart failure","score_opus":0.0158908415102191,"score_gpt":0.2718626255902935,"score_spread":0.2559717840800744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367311515","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998035,0.0006065324,0.00048911455,0.00016427274,0.00044608294,0.000075012766,0.0000018105854,0.0000027815845,0.00017935464],"genre_scores_gemma":[0.99946517,0.0000770654,0.00038611612,0.000018105695,0.000038416994,0.000001986442,0.0000026351818,0.0000042264564,0.0000062511504],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9987068,0.00010219219,0.00030646045,0.00014556025,0.00064049155,0.00009848156],"domain_scores_gemma":[0.9993315,0.000010517816,0.00025774914,0.00006610159,0.00030262934,0.00003153465],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020499905,0.00006391544,0.00010511976,0.00022647849,0.00002830525,0.000031019143,0.00024531782,0.000044476285,0.0000037925981],"category_scores_gemma":[0.00016233111,0.000057217323,0.00005481061,0.00015485729,0.000070263784,0.000012821124,0.00008716831,0.00004854249,0.0000015695333],"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":[0.000007715259,0.00024393461,0.15629128,0.000040284584,0.00039571148,0.00004626729,0.00053853384,0.07833812,0.6860269,0.0005679515,0.00006289222,0.07744044],"study_design_scores_gemma":[0.000722655,0.00032125536,0.9724634,0.00010942395,0.000033601442,0.00094063894,0.00058728614,0.007385467,0.017030595,0.000276182,0.000046270718,0.00008316924],"about_ca_topic_score_codex":0.000020954401,"about_ca_topic_score_gemma":0.00000527656,"teacher_disagreement_score":0.8161722,"about_ca_system_score_codex":0.0000365093,"about_ca_system_score_gemma":0.00019743654,"threshold_uncertainty_score":0.23332548},"labels":[],"label_agreement":null},{"id":"W4367839824","doi":"10.1002/ajmg.a.63224","title":"Uniparental disomy of multiple chromosomes in two cases with a complex phenotype","year":2023,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women's Health Research Institute","funders":"","keywords":"Uniparental disomy; Biology; Genetics; Imprinting (psychology); Aneuploidy; Genomic imprinting; Phenotype; Chromosome; Trisomy; Karyotype; DNA methylation; Gene","score_opus":0.023218995591417393,"score_gpt":0.3083044668812433,"score_spread":0.2850854712898259,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367839824","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988439,0.0003914681,0.00028238748,0.00025047618,0.0001022244,0.000068239795,0.000010112076,0.0000034484676,0.000047726342],"genre_scores_gemma":[0.9975241,0.0007656237,0.0013814883,0.00010098589,0.00016252461,0.000002827641,0.000022373708,0.00002061467,0.000019491501],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9984307,0.00008996389,0.00048527843,0.00016776094,0.0005511941,0.00027505783],"domain_scores_gemma":[0.99910456,0.0000746881,0.00032532148,0.00018879396,0.000094534385,0.00021208882],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036127862,0.00013251478,0.00034475015,0.00010475047,0.000024417375,0.000008604,0.00032545545,0.000039290142,0.000056667395],"category_scores_gemma":[0.00022800057,0.000103811406,0.00008562078,0.0003680489,0.000401606,0.000002106363,0.00014490668,0.00013685155,0.0000036073227],"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":[0.00021691422,0.00039571646,0.76334596,0.000051778625,0.000293175,0.00029581756,0.00056948443,0.0021810138,0.11869022,0.000013532994,0.0015660247,0.11238036],"study_design_scores_gemma":[0.0072215,0.008920644,0.9185741,0.0005227173,0.00010996528,0.0021944193,0.0055527003,0.0036796085,0.027564643,0.000040738127,0.024958625,0.0006603431],"about_ca_topic_score_codex":0.000102335296,"about_ca_topic_score_gemma":0.00023665295,"teacher_disagreement_score":0.15522814,"about_ca_system_score_codex":0.0000090084895,"about_ca_system_score_gemma":0.0002150077,"threshold_uncertainty_score":0.4233306},"labels":[],"label_agreement":null},{"id":"W4381839637","doi":"10.1002/ajmg.a.63337","title":"Five siblings expand the spectrum of <i>GPC6</i>‐related skeletal dysplasia","year":2023,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Sunnybrook Health Science Centre","funders":"","keywords":"Phenotype; Missense mutation; Short stature; Dysplasia; Biology; Proband; Genetics; Endocrinology; Medicine; Internal medicine; Gene; Mutation","score_opus":0.00747837789242804,"score_gpt":0.2644649982211528,"score_spread":0.25698662032872477,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4381839637","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99538964,0.00095704605,0.00033281147,0.0025853042,0.00043192576,0.00007624664,0.000004563795,0.0000054804727,0.00021700752],"genre_scores_gemma":[0.99498075,0.0038106753,0.00034726792,0.00023072155,0.0003300155,0.0000024029994,0.000007756966,0.0000248764,0.0002655445],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99785995,0.00012967165,0.00068423885,0.0001899015,0.00079130713,0.00034495065],"domain_scores_gemma":[0.99870884,0.0000830558,0.00055347045,0.000289339,0.00011750344,0.00024776632],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010352453,0.00015443642,0.00033368228,0.00009687652,0.00006193087,0.000017529179,0.000616159,0.000110692796,0.000092616785],"category_scores_gemma":[0.00035372988,0.00010761772,0.00021994133,0.00049036613,0.00058650144,0.0000022116901,0.0002281232,0.00028156236,0.000016169766],"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":[0.00020427685,0.00064849603,0.065900005,0.00015327345,0.002793827,0.00025500104,0.0040943045,0.0037860244,0.42465034,0.00026627528,0.044085085,0.4531631],"study_design_scores_gemma":[0.009232509,0.021889301,0.30094033,0.00094052585,0.00080843386,0.006878731,0.016521484,0.006563115,0.262145,0.001656748,0.37049684,0.0019269751],"about_ca_topic_score_codex":0.000013470783,"about_ca_topic_score_gemma":0.0000064612914,"teacher_disagreement_score":0.4512361,"about_ca_system_score_codex":0.0000063890056,"about_ca_system_score_gemma":0.00024214052,"threshold_uncertainty_score":0.43885234},"labels":[],"label_agreement":null},{"id":"W4382560327","doi":"10.1038/s41572-023-00443-4","title":"Imprinting disorders","year":2023,"lang":"en","type":"review","venue":"Nature Reviews Disease Primers","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"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","funders":"Biotechnology and Biological Sciences Research Council","keywords":"Psychology; Medicine","score_opus":0.030277463018884242,"score_gpt":0.3558298068552445,"score_spread":0.3255523438363603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4382560327","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000012478513,0.99676174,0.00004093462,0.000027860475,0.0007425424,0.0017305509,0.0000433449,0.000056577184,0.00058395416],"genre_scores_gemma":[0.000008426712,0.9963123,0.0005193685,0.0001264834,0.00056806643,0.00032182114,0.0006995222,0.00019537665,0.0012485874],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99688154,0.00028888648,0.00088893616,0.0010883274,0.00024873458,0.0006035494],"domain_scores_gemma":[0.9977864,0.000034481254,0.00059533544,0.0011547517,0.000042897154,0.00038615524],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00058105757,0.00073127437,0.0015252642,0.00015329421,0.00012455965,0.000061106184,0.0007339033,0.00082300033,0.000042546035],"category_scores_gemma":[0.0008460457,0.0005888409,0.0017914526,0.00045913228,0.000069322945,0.0000032218059,0.00056633307,0.0008073074,0.00051740214],"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":[0.0000010817497,0.000024187691,0.00002115913,0.017810093,0.00019335942,0.0000020837986,0.000002108589,4.1518402e-7,0.000008409805,0.00002065967,0.0030608214,0.9788556],"study_design_scores_gemma":[0.00009652792,0.000022875269,0.000065940425,0.007284692,0.00093719835,0.000008096417,0.0000037923107,0.0000014521501,0.0000018678021,0.000021003141,0.9909258,0.0006307645],"about_ca_topic_score_codex":0.0000037613052,"about_ca_topic_score_gemma":0.0000037759794,"teacher_disagreement_score":0.987865,"about_ca_system_score_codex":0.00003898355,"about_ca_system_score_gemma":0.00038551906,"threshold_uncertainty_score":0.9996563},"labels":[],"label_agreement":null},{"id":"W4384563092","doi":"10.1016/j.bonr.2023.101700","title":"Bone mineral density and its relationship with ground reaction force characteristics during gait in young adults with Prader-Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"Bone Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"California State University","keywords":"Ground reaction force; Bone mineral; Gait; Medicine; Physical medicine and rehabilitation; Internal medicine; Physics; Osteoporosis","score_opus":0.00916072216521198,"score_gpt":0.21182089288813408,"score_spread":0.20266017072292208,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4384563092","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992913,0.000119056946,0.000028026177,0.00006302424,0.00007261814,0.00028369116,0.0000021569924,0.000030853982,0.0001092424],"genre_scores_gemma":[0.9977909,0.000085379805,0.0002086512,0.0000079922465,0.000052806266,0.000029170928,0.00013171448,0.000032328004,0.0016610599],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987502,0.000025018146,0.00032889706,0.0004491674,0.00016800401,0.00027872797],"domain_scores_gemma":[0.9993376,0.000009547445,0.00024058718,0.0002641476,0.00006884685,0.0000792531],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020811774,0.0001658126,0.00020041352,0.0000894244,0.00010502553,0.000031815063,0.00002675849,0.000118844706,0.0000012371813],"category_scores_gemma":[0.00010712925,0.00014874362,0.000026291797,0.00019135168,0.000030434916,0.000013838966,0.000068307876,0.00011553318,0.0000020899663],"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":[0.000017446322,0.000025678437,0.8691512,0.0001012108,0.000022157621,0.00048472756,0.00011426283,0.000017791572,0.12994683,0.0000043386945,0.000007984847,0.000106406704],"study_design_scores_gemma":[0.0004749073,0.00018750272,0.97093093,0.00013449756,0.000022130887,0.02565841,0.00011449884,0.00007090831,0.0021439423,0.000011013747,0.000040710354,0.00021053554],"about_ca_topic_score_codex":0.00007881396,"about_ca_topic_score_gemma":0.00020662566,"teacher_disagreement_score":0.12780288,"about_ca_system_score_codex":0.000021742098,"about_ca_system_score_gemma":0.000041430772,"threshold_uncertainty_score":0.6065589},"labels":[],"label_agreement":null},{"id":"W4385258318","doi":"10.7202/1101833ar","title":"Vers une éthique de la relation de communication avec les personnes atteintes du syndrome d’Angelman","year":2023,"lang":"fr","type":"article","venue":"Nouvelles perspectives en sciences sociales","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Humanities; Political science; Sociology; Philosophy","score_opus":0.01971266041107919,"score_gpt":0.30066621482164135,"score_spread":0.28095355441056213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385258318","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97045517,0.011421371,0.00080998393,0.010196264,0.00019657113,0.00019167554,0.000021025366,0.00006197951,0.006645973],"genre_scores_gemma":[0.9789226,0.013438484,0.005184305,0.000083740386,0.0003393767,0.000023565448,0.000028247012,0.00003338434,0.0019463091],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.9970107,0.0013110163,0.00027191298,0.00055836677,0.00026321574,0.0005847913],"domain_scores_gemma":[0.9987043,0.00058029225,0.00019565162,0.00027930658,0.00013382972,0.00010662834],"candidate_categories":["metaepi_narrow","sts"],"consensus_categories":[],"category_scores_codex":[0.002547972,0.00026152932,0.00023937157,0.000151223,0.0011210049,0.0001907545,0.0006014057,0.0005211758,0.00007083694],"category_scores_gemma":[0.0010750862,0.0002860164,0.00020308552,0.00068612536,0.003281924,0.000032005617,0.00030269407,0.00031035623,0.000046252724],"study_design_candidate":"qualitative","study_design_consensus":"qualitative","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000028382512,0.0004392747,0.13771932,0.0002572036,0.00045155227,0.000038146278,0.5863683,0.0037971875,0.16756943,0.086913124,0.0046566324,0.011761455],"study_design_scores_gemma":[0.00050626934,0.0004402305,0.35845497,0.00025758502,0.00009087741,0.00037720194,0.61794513,0.002994223,0.003911501,0.0042145816,0.010191965,0.0006154466],"about_ca_topic_score_codex":0.002657372,"about_ca_topic_score_gemma":0.00060582825,"teacher_disagreement_score":0.22073567,"about_ca_system_score_codex":0.00045513394,"about_ca_system_score_gemma":0.00094591366,"threshold_uncertainty_score":0.9999592},"labels":[],"label_agreement":null},{"id":"W4385293731","doi":"10.1016/j.humov.2023.103125","title":"Contributing factors to postural stability in Prader-Willi syndrome","year":2023,"lang":"en","type":"article","venue":"Human Movement Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"California State University, Sacramento; California State University","keywords":"Gait; Balance (ability); Medicine; Physical medicine and rehabilitation; Dynamic balance; Physical therapy; Vestibular system; Proprioception; Sensory system; Somatosensory system; Psychology; Audiology","score_opus":0.030043446840477196,"score_gpt":0.29442643094762094,"score_spread":0.2643829841071437,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385293731","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990659,0.000017431817,0.00004705741,0.00018546457,0.00014135992,0.00029251786,0.0000066279513,0.000021436555,0.0002222068],"genre_scores_gemma":[0.99946004,0.0000029696405,0.00010387808,0.00019533573,0.00001902357,0.000014858489,0.000019271642,0.000007966597,0.00017667843],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9983216,0.000024336428,0.00023430413,0.00050756487,0.0002953322,0.0006168443],"domain_scores_gemma":[0.9994289,0.000010050716,0.00005132072,0.0003264868,0.000058062997,0.00012512274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00089996186,0.00012098026,0.000118685035,0.0001242168,0.0002592388,0.00006414818,0.0003696613,0.000037982583,0.000028814464],"category_scores_gemma":[0.0002279767,0.00011133605,0.00003842836,0.000581385,0.00012960157,0.000007801685,0.0005117694,0.000059890695,0.000022787766],"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":[1.7634463e-7,0.000014568625,0.41036382,0.00000436583,0.0000019305946,6.134654e-7,0.00014333062,0.00004673925,0.58925635,0.000045113447,0.000025938725,0.00009702762],"study_design_scores_gemma":[0.00017873944,0.00019151786,0.9271044,0.000012695181,0.0000012758345,0.0000018146411,0.0006717733,0.00005551984,0.07137392,0.00010416155,0.00016562306,0.00013854878],"about_ca_topic_score_codex":0.00009014955,"about_ca_topic_score_gemma":0.000056657296,"teacher_disagreement_score":0.51788247,"about_ca_system_score_codex":0.000051508963,"about_ca_system_score_gemma":0.00005746154,"threshold_uncertainty_score":0.45401523},"labels":[],"label_agreement":null},{"id":"W4386163647","doi":"10.5114/ada.2023.130520","title":"Micronutrient deficiency with skin and systemic symptoms: a case report of acrodermatitis enteropathica","year":2023,"lang":"en","type":"article","venue":"Advances in Dermatology and Allergology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"Uniwersytet Łódzki","keywords":"Acrodermatitis enteropathica; Medicine; Micronutrient; Dermatology; Micronutrient deficiency; Nutritional deficiency; Internal medicine; Pathology; Zinc deficiency (plant disorder); Malnutrition","score_opus":0.0038063530549514385,"score_gpt":0.23452844538153617,"score_spread":0.23072209232658472,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386163647","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9879878,0.010959076,0.00051835825,0.00014596387,0.00007728273,0.00013096545,0.0000040774844,0.000010066929,0.00016642133],"genre_scores_gemma":[0.9945655,0.00481316,0.00046464446,0.00006384246,0.0000084561725,0.000029417779,0.000016992723,0.000009979952,0.000028017905],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.99894214,0.0000806372,0.0003309454,0.00034468377,0.000042185446,0.00025938998],"domain_scores_gemma":[0.99955016,0.000038164748,0.00014171844,0.00019433071,0.00003474766,0.000040851242],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011825678,0.00012757696,0.00025527674,0.000094314724,0.0000572286,0.0000043623254,0.000075105105,0.00014228404,0.0000021653245],"category_scores_gemma":[0.000037405825,0.00011167356,0.000020876516,0.00011068729,0.0002711452,0.000007052987,0.00016014432,0.00007783305,0.000001253986],"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":[0.0001128148,0.00014043359,0.8930842,0.0011184525,0.00012646292,0.040586665,0.0015422904,0.00035957652,0.040496595,0.0011082236,0.00013292028,0.021191318],"study_design_scores_gemma":[0.0013062318,0.00035547212,0.03742701,0.00011238261,0.00001901685,0.94650453,0.0012036161,0.00018665906,0.008192527,0.0002712259,0.0041724886,0.0002488098],"about_ca_topic_score_codex":0.000020562338,"about_ca_topic_score_gemma":0.00018973321,"teacher_disagreement_score":0.9059179,"about_ca_system_score_codex":0.000003224707,"about_ca_system_score_gemma":0.00002571798,"threshold_uncertainty_score":0.45539156},"labels":[],"label_agreement":null},{"id":"W4386474232","doi":"10.1126/sciadv.adi2050","title":"Establishment of paternal methylation imprint at the<i>H19/Igf2</i>imprinting control region","year":2023,"lang":"en","type":"article","venue":"Science Advances","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cegep de Saint Hyacinthe","funders":"National Institute of General Medical Sciences; Österreichischen Akademie der Wissenschaften","keywords":"CTCF; Imprinting (psychology); Genomic imprinting; Germline; Biology; Allele; DNA methylation; Genetics; Methylation; Epigenetics; Transcription factor; Enhancer; Gene; Gene expression","score_opus":0.011732794425499926,"score_gpt":0.27135333768446734,"score_spread":0.25962054325896744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386474232","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954332,0.00045771,0.0029515314,0.00023386322,0.00027203924,0.00014549772,0.000002147949,0.000013101945,0.0004909069],"genre_scores_gemma":[0.99889773,0.00016312492,0.00035510183,0.000058725214,0.0000656914,0.0000139851345,0.0000036181457,0.000006662957,0.0004353646],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988375,0.000030075847,0.00021587574,0.00032873792,0.00028538957,0.0003024714],"domain_scores_gemma":[0.9993519,0.000023818064,0.00017242963,0.00028929595,0.00011310251,0.000049431423],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007899726,0.000090411275,0.00009661025,0.000060718183,0.00023122106,0.000033593606,0.00034007657,0.000029622908,0.0000069760595],"category_scores_gemma":[0.00019637168,0.00006473598,0.00005679677,0.0003740889,0.00033850878,0.000017674858,0.00028607377,0.000042842184,0.000011311094],"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":[0.0000047425265,0.000006045324,0.026365928,0.000009484682,0.0000046616155,3.764712e-7,0.00005752717,0.0016660154,0.91954094,0.000024874758,0.000020338348,0.052299093],"study_design_scores_gemma":[0.000258393,0.00012214437,0.09378149,0.000016138229,0.0000062398167,0.000013904757,0.00027830407,0.00058654207,0.8992063,0.00020454235,0.0054258406,0.000100165875],"about_ca_topic_score_codex":0.000026759175,"about_ca_topic_score_gemma":0.000014840082,"teacher_disagreement_score":0.067415565,"about_ca_system_score_codex":0.000017756727,"about_ca_system_score_gemma":0.000057473924,"threshold_uncertainty_score":0.26398563},"labels":[],"label_agreement":null},{"id":"W4386979591","doi":"10.1093/hmg/ddad160","title":"Higher incidence of embryonic defects in mouse offspring conceived with assisted reproduction from fathers with sperm epimutations","year":2023,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Health Canada; McGill University; McGill University Health Centre","funders":"Health Canada; Canadian Institutes of Health Research; Genome Canada; Alliance de recherche numérique du Canada; Génome Québec; McGill University","keywords":"Biology; Offspring; Haploinsufficiency; Reproductive technology; DNA methylation; Epigenetics; Andrology; Genomic imprinting; Embryo; Sperm; Infertility; Genetics; Epigenome; Fertilisation; Assisted reproductive technology; Embryo culture; Pregnancy; Embryogenesis; Phenotype; Gene","score_opus":0.0183436499955824,"score_gpt":0.2577326108397527,"score_spread":0.23938896084417027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386979591","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978513,0.00045703657,0.0010765049,0.000034843426,0.000045599423,0.00026971483,0.0000080594655,0.000026014839,0.00023093633],"genre_scores_gemma":[0.9963255,0.00006873313,0.002933579,0.000031866417,0.000042233827,0.000027440834,0.00011632726,0.000054092878,0.00040025328],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985944,0.00007598861,0.00026143924,0.0005612153,0.00022386348,0.00028310597],"domain_scores_gemma":[0.99900967,0.0000106809075,0.00016614296,0.00063244725,0.00011773801,0.00006330464],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012679747,0.00019371051,0.00020524183,0.00010676973,0.00006520847,0.000023866685,0.00019028841,0.00010651158,0.00001312268],"category_scores_gemma":[0.00003208877,0.00018357245,0.00005632746,0.00032336498,0.00013457342,0.000004033019,0.00009952276,0.00010246295,0.000006950293],"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":[0.000016335685,0.00003996391,0.035886753,0.000018866398,0.00006816705,0.000019675155,0.00014065873,0.011190704,0.9521993,0.000034824683,0.000012259862,0.00037250877],"study_design_scores_gemma":[0.0008182538,0.0004010092,0.4540074,0.00005702642,0.000038362752,0.000012217839,0.00021269087,0.00015026655,0.54385006,0.000055497665,0.00016677231,0.00023046222],"about_ca_topic_score_codex":0.000122967,"about_ca_topic_score_gemma":0.00022522904,"teacher_disagreement_score":0.41812065,"about_ca_system_score_codex":0.000021066535,"about_ca_system_score_gemma":0.00007632077,"threshold_uncertainty_score":0.7485867},"labels":[],"label_agreement":null},{"id":"W4387007789","doi":"10.1016/j.humimm.2023.08.026","title":"P124 Like mother, not like daughter? Discovery of a novel DPA1 allele due to discrepant HLA typing between a patient and her daughter","year":2023,"lang":"en","type":"article","venue":"Human Immunology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Calgary Laboratory Services; Alberta Biodiversity Monitoring Institute; Alberta Hospital Edmonton; University of Alberta","funders":"","keywords":"Daughter; Typing; Human leukocyte antigen; Allele; Biology; Genetics; Evolutionary biology; Gene; Antigen","score_opus":0.02087135998219418,"score_gpt":0.2581338103177378,"score_spread":0.2372624503355436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387007789","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978254,0.00040885637,0.00083451765,0.0002114523,0.00014109872,0.00024550434,0.00005149989,0.000022264501,0.00025943868],"genre_scores_gemma":[0.99685323,0.00007693481,0.0009236474,0.00026214545,0.0000740066,0.00003671114,0.00014390281,0.000046325982,0.0015830944],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99858207,0.000050182425,0.00037650645,0.00048821824,0.00008999002,0.00041304348],"domain_scores_gemma":[0.99925417,0.000020730828,0.0001277384,0.0004961918,0.0000444758,0.000056681925],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013201499,0.00021256607,0.0003270092,0.000115524555,0.000109184984,0.00003420797,0.0002270529,0.00017552318,0.000027292526],"category_scores_gemma":[0.000022777363,0.0001970179,0.00009732302,0.00011583496,0.00012664965,0.000007532757,0.0007153544,0.00010669132,0.000019013652],"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":[0.000031542524,0.00007412816,0.0044603115,0.00003377595,0.0002293574,0.0000042450774,0.0005993341,0.00001628075,0.9882385,0.000110860405,0.00050488906,0.0056967656],"study_design_scores_gemma":[0.0032415064,0.0029847184,0.6379329,0.00019585481,0.00012566986,0.0002078803,0.0017282449,0.00010724721,0.20672163,0.00021580294,0.14534694,0.0011916017],"about_ca_topic_score_codex":0.00013565163,"about_ca_topic_score_gemma":0.000047378144,"teacher_disagreement_score":0.78151685,"about_ca_system_score_codex":0.000011461293,"about_ca_system_score_gemma":0.000026813419,"threshold_uncertainty_score":0.80341566},"labels":[],"label_agreement":null},{"id":"W4387107787","doi":"10.1016/j.gtc.2023.08.005","title":"Management of Monogenic and Syndromic Obesity","year":2023,"lang":"en","type":"review","venue":"Gastroenterology Clinics of North America","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"","keywords":"Medicine; Ciliopathies; Leptin receptor; Bardet–Biedl syndrome; Leptin; Proopiomelanocortin; Obesity; Proprotein convertase; Population; Genetics; Internal medicine; Bioinformatics; Endocrinology; Gene; Receptor; Biology; LDL receptor; Phenotype","score_opus":0.025486957283478273,"score_gpt":0.3056754722720263,"score_spread":0.280188514988548,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387107787","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3146091,0.6843837,0.00023226079,0.0000057641028,0.00019651522,0.00042085032,0.00012194329,0.000009493147,0.000020365696],"genre_scores_gemma":[0.0053834585,0.99232984,0.0018052288,0.000025467261,0.000036436857,0.00003303821,0.00024063955,0.00004929765,0.000096606105],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9978563,0.00013289916,0.0010023294,0.000553611,0.00010529385,0.00034955153],"domain_scores_gemma":[0.9982666,0.000032471606,0.00095266977,0.0006118522,0.000048868256,0.00008758415],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00018230674,0.00031812492,0.0013957862,0.00011042726,0.000027300723,0.0000036757697,0.00041375868,0.00018808186,0.000005707528],"category_scores_gemma":[0.000027951919,0.00030417,0.00047335858,0.00012671365,0.0002814979,0.0000013258475,0.00073508103,0.00016655616,0.0000131577635],"study_design_candidate":"design_other","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":[0.000024269766,0.00014332011,0.040655036,0.010075814,0.0018129905,0.000014531995,0.000007327603,0.000013618049,0.0000032265868,0.0000014588408,0.00012256019,0.94712585],"study_design_scores_gemma":[0.0022424457,0.007354011,0.17339066,0.006378281,0.0051182136,0.0005377195,0.00009362513,0.000037739817,0.000007279386,0.000033728855,0.80384076,0.0009655374],"about_ca_topic_score_codex":0.000009201177,"about_ca_topic_score_gemma":0.000011103737,"teacher_disagreement_score":0.9461603,"about_ca_system_score_codex":0.0000064975184,"about_ca_system_score_gemma":0.000044558932,"threshold_uncertainty_score":0.99994105},"labels":[],"label_agreement":null},{"id":"W4387126575","doi":"10.25011/cim.v46i3.41654","title":"<i>H19</i> Promoter DNA Methylation is Lower Among Early Abortion Patients Undergoing IVF Embryo Transfer","year":2023,"lang":"en","type":"article","venue":"Clinical and investigative medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Binzhou Medical University; Health Commission of Guizhou Province","keywords":"DNA methylation; CpG site; Methylation; Biology; Epigenetics; Bisulfite sequencing; Andrology; Genomic imprinting; Molecular biology; DNMT1; Embryo; Chorionic villi; Gene expression; Placenta; Genetics; Gene; Pregnancy; Fetus; Medicine","score_opus":0.058576794826459784,"score_gpt":0.3041478477299784,"score_spread":0.2455710529035186,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387126575","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.995932,0.000092517424,0.00039479035,0.0024823465,0.0004505464,0.000249809,0.000005360896,0.000023257007,0.0003693905],"genre_scores_gemma":[0.9970433,0.00027641634,0.00011094776,0.0012609076,0.00036356738,0.000013610015,0.000109868495,0.000021062167,0.0008003008],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985083,0.000118898606,0.00051625544,0.0004506079,0.00017953239,0.00022640209],"domain_scores_gemma":[0.999358,0.000045860932,0.00008272156,0.00018881782,0.00012422299,0.00020036077],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050169,0.00016751623,0.0002469387,0.000047017977,0.00009329586,0.000013802155,0.00008607608,0.00017580923,0.00003667977],"category_scores_gemma":[0.00065882085,0.0001272841,0.00006988652,0.00019090624,0.0015211519,0.000012688369,0.000070618386,0.0001506894,0.000019904757],"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":[0.000020058727,0.00007152405,0.88618183,0.00006261054,0.00010764662,0.0000020382538,0.0006735547,0.0000024672386,0.09571259,0.0001302154,0.0034427484,0.013592722],"study_design_scores_gemma":[0.0014561714,0.0016544806,0.97439295,0.000131831,0.000044079847,8.155587e-7,0.00008170207,0.00008795814,0.01767402,0.0025530695,0.0017543919,0.00016853638],"about_ca_topic_score_codex":0.000019794139,"about_ca_topic_score_gemma":0.000012628627,"teacher_disagreement_score":0.08821111,"about_ca_system_score_codex":0.000003981057,"about_ca_system_score_gemma":0.000033090455,"threshold_uncertainty_score":0.56047475},"labels":[],"label_agreement":null},{"id":"W4387380018","doi":"10.1210/jendso/bvad114.535","title":"SAT239 Deceased Donor Parathyroid Allotransplant For Sever Refractory Iatrogenic Hypoparathyroidism","year":2023,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Medicine; Hypoparathyroidism; Surgery; Transplantation; Refractory (planetary science); Thyroidectomy; Parathyroid hormone; Calcium; Urology; Internal medicine; Thyroid","score_opus":0.013135653093870554,"score_gpt":0.25808794207897645,"score_spread":0.2449522889851059,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387380018","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9947124,0.0029216122,0.000674968,0.0008768383,0.00055351056,0.00018688203,0.000026520296,0.000009606019,0.000037654834],"genre_scores_gemma":[0.9934939,0.0018260942,0.0020625978,0.00050405023,0.00080692035,0.000011290389,0.000015592506,0.00003277818,0.0012467649],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9988313,0.00005026405,0.00038852406,0.0001802013,0.00020325181,0.00034647284],"domain_scores_gemma":[0.9991577,0.000039338942,0.0002874601,0.00029119334,0.00012954941,0.00009473511],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035793963,0.00015919896,0.00019862983,0.000020493777,0.00015313785,0.000025440648,0.00039796313,0.00007163477,0.000004854427],"category_scores_gemma":[0.00008675904,0.00011019794,0.0011868626,0.00012473855,0.000048251444,0.0000060147413,0.00011121591,0.00016834999,0.0000067521305],"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":[0.00003674895,0.000046958277,0.002779249,0.000017560124,0.00033931597,0.0000032135288,0.00011482378,0.00039536302,0.82042617,0.000012245684,0.17557727,0.00025108358],"study_design_scores_gemma":[0.005765714,0.0010896676,0.07808634,0.00004316656,0.0004640039,0.001556075,0.00065302727,0.0004984227,0.3616585,0.00049175945,0.54909307,0.0006002773],"about_ca_topic_score_codex":0.000002870843,"about_ca_topic_score_gemma":0.000003297897,"teacher_disagreement_score":0.45876765,"about_ca_system_score_codex":0.00002298782,"about_ca_system_score_gemma":0.00013726387,"threshold_uncertainty_score":0.44937417},"labels":[],"label_agreement":null},{"id":"W4387405660","doi":"10.1210/jendso/bvad114.1504","title":"FRI597 Impact Of Theophylline On BMI In Pseudohypoparathyroidism Type 1a - Results Of An Open Label Extension Trial","year":2023,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Medicine; Theophylline; Internal medicine; Placebo; Endocrinology; Randomized controlled trial; Pediatrics; Biology; Genetics; Pathology","score_opus":0.0470399291479838,"score_gpt":0.36809215505548765,"score_spread":0.3210522259075038,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387405660","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99894786,0.00017002573,0.0000040497316,0.0002761321,0.00027885038,0.00018504584,0.000017610415,0.0000013957923,0.000119010336],"genre_scores_gemma":[0.9982622,0.00031006194,0.00066320924,0.000046555317,0.00022044043,9.982261e-7,0.000008529857,0.0000134365955,0.00047451435],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988451,0.000115739516,0.00053555996,0.00014132804,0.00019313172,0.00016911926],"domain_scores_gemma":[0.99887854,0.00003466349,0.000509029,0.00036727134,0.00016307182,0.00004743768],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007364896,0.00010775143,0.0002695953,0.000031438212,0.000034177123,0.000011368356,0.00051689235,0.000056514615,0.0000049240048],"category_scores_gemma":[0.00028183608,0.00006616976,0.00025690018,0.0002557408,0.000044495162,0.0000071523236,0.0003018352,0.00016116371,0.0000013080003],"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":[0.004585486,0.00030380508,0.0003474036,0.000009582681,0.00010866895,0.0000037879363,0.00018995856,0.0018392026,0.98270345,0.0000081481085,0.008855743,0.001044739],"study_design_scores_gemma":[0.13365299,0.037932783,0.15986654,0.00030726046,0.00014893508,0.00036505525,0.001492523,0.0024353026,0.6586852,0.0019020613,0.002661213,0.0005501067],"about_ca_topic_score_codex":0.00010890373,"about_ca_topic_score_gemma":0.000006269155,"teacher_disagreement_score":0.32401824,"about_ca_system_score_codex":0.0000169289,"about_ca_system_score_gemma":0.000120354096,"threshold_uncertainty_score":0.26983246},"labels":[],"label_agreement":null},{"id":"W4387934009","doi":"10.1016/j.jcjd.2023.10.245","title":"CASE REPORT: UNCONTROLLED HYPERTHYROIDISM IN PREGNANCY ASSOCIATED WITH FETAL HEART MALFORMATION","year":2023,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Fetus; Fetal heart; Pregnancy; Obstetrics","score_opus":0.00930572246304908,"score_gpt":0.20480487173414708,"score_spread":0.195499149271098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387934009","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99853987,0.0008320447,0.000006247313,0.00023267968,0.00012908147,0.00008777106,0.0000076033,0.0000026532866,0.00016206648],"genre_scores_gemma":[0.9995883,0.0000054139987,0.000083527324,0.000050987386,0.000048150887,0.000004018651,0.000027055903,0.0000128851925,0.00017965618],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99919975,0.000041560193,0.00029630613,0.000096511576,0.00007622376,0.0002896631],"domain_scores_gemma":[0.99939984,0.000015204947,0.00017045549,0.00011145201,0.000108140455,0.00019493168],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029981256,0.00008532783,0.00016577335,0.00016518823,0.000060829574,0.000030054898,0.0000704974,0.00007298049,0.000009306229],"category_scores_gemma":[0.00036483604,0.00007266161,0.00006335462,0.00019006846,0.00002920651,0.000008189235,0.000009692536,0.0000850996,0.0000031454185],"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":[0.0000022096467,0.000018538387,0.97271216,0.000017399854,0.0001456594,0.0048121875,0.00018559437,0.00084642676,0.017247152,0.0000036403828,0.0012858706,0.002723175],"study_design_scores_gemma":[0.0037055155,0.000977353,0.9738945,0.00044889172,0.000060456514,0.0096721165,0.0005713699,0.0007118667,0.007872249,0.00008464258,0.0016074507,0.00039358705],"about_ca_topic_score_codex":0.00016669548,"about_ca_topic_score_gemma":0.006970511,"teacher_disagreement_score":0.009374902,"about_ca_system_score_codex":0.000028601127,"about_ca_system_score_gemma":0.00038043218,"threshold_uncertainty_score":0.38897085},"labels":[],"label_agreement":null},{"id":"W4388125647","doi":"10.1038/s41596-023-00898-5","title":"EpiTyping: analysis of epigenetic aberrations in parental imprinting and X-chromosome inactivation using RNA-seq","year":2023,"lang":"en","type":"review","venue":"Nature Protocols","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"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":"Horizon 2020 Framework Programme; Azrieli Foundation; Israel Science Foundation; United States-Israel Binational Science Foundation; Rosetrees Trust; European Commission","keywords":"Epigenetics; Biology; Genomic imprinting; Imprinting (psychology); Genetics; Computational biology; Induced pluripotent stem cell; Bacterial artificial chromosome; X-inactivation; Gene; DNA methylation; Genome; Embryonic stem cell; X chromosome; Gene expression","score_opus":0.06462302765635829,"score_gpt":0.4095442324961036,"score_spread":0.3449212048397453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388125647","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.018927976,0.93818593,0.0004283046,0.000008886847,0.00011209459,0.04212366,0.00006502895,0.000022152943,0.00012595896],"genre_scores_gemma":[0.023580233,0.9508834,0.0031610196,0.000021603713,0.00031656865,0.02112265,0.0006178656,0.00015506515,0.0001415955],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99808526,0.0001432594,0.00075809704,0.00057627365,0.00016931152,0.00026779654],"domain_scores_gemma":[0.9988061,0.00004534041,0.00059708994,0.0004088759,0.00008716591,0.000055406334],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00038624174,0.00030550023,0.0010254976,0.00054518745,0.000064996864,0.000041569558,0.00021858342,0.0008159339,0.000007997417],"category_scores_gemma":[0.00029302028,0.00029033172,0.0004147306,0.0012074786,0.000048832822,0.000005226735,0.00027750374,0.00045340986,0.0000012404623],"study_design_candidate":"design_other","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":[0.00001330552,0.00019737265,0.009386983,0.02466464,0.004533981,0.0000079716165,0.00017951474,0.00084839016,0.03731401,0.0001376503,0.00002612359,0.92269003],"study_design_scores_gemma":[0.0041242186,0.0015561202,0.06963102,0.076573454,0.018471582,0.00023729897,0.0005942657,0.01008786,0.021597004,0.00059232506,0.789786,0.0067488593],"about_ca_topic_score_codex":0.000054369724,"about_ca_topic_score_gemma":0.000066225184,"teacher_disagreement_score":0.9159412,"about_ca_system_score_codex":0.000052150794,"about_ca_system_score_gemma":0.00019463508,"threshold_uncertainty_score":0.9999549},"labels":[],"label_agreement":null},{"id":"W4388214035","doi":"10.1101/2023.10.30.564869","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of <i>ZDBF2</i>","year":2023,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"NODAI Genome Research Center, Tokyo University of Agriculture; Japan Society for the Promotion of Science; Tokyo University of Agriculture; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Retrotransposon; Biology; Genomic imprinting; Genetics; DNA methylation; Epigenetics; Gene; Long terminal repeat; Exon; Genome; Transposable element; Gene expression","score_opus":0.023161678223940645,"score_gpt":0.2361491103900183,"score_spread":0.21298743216607766,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388214035","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.993304,0.00077713677,0.0041920627,0.000046713736,0.00078704336,0.00064483634,0.00016228078,0.0000827616,0.0000031208754],"genre_scores_gemma":[0.9939922,0.00095075613,0.004366125,0.000042970434,0.00039936285,0.00008010298,0.000021892036,0.00014332013,0.0000032785642],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9968362,0.00022018145,0.0010550803,0.0011096903,0.0002877191,0.00049113453],"domain_scores_gemma":[0.99779546,0.000015867618,0.00058057427,0.0009972947,0.00047749354,0.00013333587],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00069911993,0.0004609721,0.0005089688,0.00030813445,0.00008113551,0.00010849104,0.00050046307,0.000670609,0.000012602285],"category_scores_gemma":[0.000107242784,0.00055199524,0.00020721133,0.0003409932,0.00008991021,0.000028353148,0.00017233021,0.00042781123,0.00000854845],"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":[0.000037428395,0.00009278215,0.06669538,0.00027561683,0.000035936682,0.0000038550033,0.00004379134,0.0014386948,0.9313317,0.000026226893,0.0000042396136,0.000014386363],"study_design_scores_gemma":[0.0003601098,0.00013972902,0.49349603,0.00016258018,0.000023061446,2.54004e-8,0.000015212544,0.0005453457,0.5048422,0.0000010077321,0.0000940452,0.00032062206],"about_ca_topic_score_codex":0.000060825394,"about_ca_topic_score_gemma":0.00003011226,"teacher_disagreement_score":0.42680064,"about_ca_system_score_codex":0.00007880111,"about_ca_system_score_gemma":0.00025634948,"threshold_uncertainty_score":0.99969316},"labels":[],"label_agreement":null},{"id":"W4388302377","doi":"10.1002/oby.23928","title":"Diazoxide choline extended‐release tablet in people with <scp>Prader‐Willi</scp> syndrome: results from long‐term open‐label study","year":2023,"lang":"en","type":"article","venue":"Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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 Heart, Lung, and Blood Institute; National Institute of Child Health and Human Development; School of Medicine, Indiana University; University of California, Irvine; York University; Queen Mary University of London; National Institutes of Health; Barts Health NHS Trust; Alder Hey Children's NHS Foundation Trust; Children's Hospital Colorado","keywords":"Diazoxide; Open label; Choline; Pharmacology; Chemistry; Medicine; Endocrinology; Insulin","score_opus":0.018834351259318843,"score_gpt":0.2702023846741543,"score_spread":0.2513680334148355,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388302377","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980106,0.00020940803,0.00009334081,0.00008947083,0.00014849375,0.0008147184,0.00017668078,0.000043266336,0.0004140362],"genre_scores_gemma":[0.99533486,0.00017271553,0.00045558324,0.000108974324,0.000087832246,0.00006491626,0.00066740613,0.00005304598,0.0030546745],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.997564,0.0001418402,0.00043413677,0.0009668062,0.00028006232,0.00061313633],"domain_scores_gemma":[0.9985271,0.000076126096,0.00016971455,0.0009513208,0.000072775925,0.00020294957],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005323576,0.00031849096,0.00041364177,0.00009758164,0.00015329359,0.00013289708,0.0006951689,0.00017026946,0.000018192075],"category_scores_gemma":[0.00036912647,0.00029190717,0.00005078536,0.00054519414,0.000049168404,0.00001684744,0.00093753514,0.0002224016,0.000106816355],"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":[0.00002682478,0.0015560244,0.97208625,0.000023889015,0.00013360595,0.0001688251,0.00049081055,0.00014334526,0.022401512,0.000001941678,0.0012911523,0.0016758223],"study_design_scores_gemma":[0.00563764,0.00074271427,0.98790234,0.000053454034,0.000042965792,0.000058939284,0.0005032802,0.0001269224,0.0041765803,0.000021121838,0.0005415978,0.0001924519],"about_ca_topic_score_codex":0.0016335024,"about_ca_topic_score_gemma":0.0024348625,"teacher_disagreement_score":0.01822493,"about_ca_system_score_codex":0.000030503857,"about_ca_system_score_gemma":0.00011404516,"threshold_uncertainty_score":0.9999533},"labels":[],"label_agreement":null},{"id":"W4388461661","doi":"10.1016/j.gim.2023.101023","title":"Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections","year":2023,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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. Thomas Hospital; Hospital for Sick Children","funders":"Yale Center for Clinical Investigation, Yale School of Medicine; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Eye Institute; National Heart, Lung, and Blood Institute; Perelman School of Medicine, University of Pennsylvania; Intellectual and Developmental Disabilities Research Center; Horizon 2020; National Human Genome Research Institute; Epilepsy Society; Deutsche Forschungsgemeinschaft; European Commission; Broad Institute; National Institute for Health and Care Research; Institute for Translational Medicine and Therapeutics; HORIZON EUROPE Framework Programme; Yale New Haven Hospital; Cancer Research UK; Wellcome Trust; University of Pennsylvania; National Center for Advancing Translational Sciences; Medical Research Council; Hartwell Foundation; Health Research Institute, University of Limerick; Horizon 2020 Framework Programme; Children's Hospital of Philadelphia; Yale University; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Missense mutation; Phenotype; Frameshift mutation; Gene knockdown; Biology; Exome sequencing; Neurodevelopmental disorder; Allele; Genetics; Gene","score_opus":0.03252461494893546,"score_gpt":0.29081579455699774,"score_spread":0.2582911796080623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388461661","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99541974,0.002222236,0.00030083116,0.000272261,0.00095003884,0.00034199358,0.000011363445,0.000036172696,0.00044535263],"genre_scores_gemma":[0.9940357,0.0042015305,0.0008668907,0.00014069786,0.00025314954,0.000047296366,0.00008019415,0.000042461284,0.00033208],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99831784,0.00010092262,0.00042657513,0.00051485165,0.00022237931,0.000417419],"domain_scores_gemma":[0.99931514,0.000039514045,0.00008831298,0.0003635443,0.000052021085,0.0001414624],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00049488933,0.00022583405,0.00031222115,0.00021902294,0.00013734562,0.000019682971,0.00014228345,0.00015580548,0.0000197806],"category_scores_gemma":[0.00023381574,0.00021872077,0.000039599454,0.00041302224,0.0001056256,0.0000032331907,0.0003748383,0.00015348906,0.000021146328],"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":[0.000016890228,0.00010823104,0.36558777,0.00029632173,0.00035533123,0.00026194393,0.0016016392,0.0012150636,0.5980447,0.00011771878,0.0031378476,0.029256545],"study_design_scores_gemma":[0.00166422,0.0005991501,0.9786985,0.00023073229,0.000062451436,0.0005613045,0.0006460524,0.0009788878,0.0030194141,0.00010133728,0.0129863,0.00045165012],"about_ca_topic_score_codex":0.00016182906,"about_ca_topic_score_gemma":0.00009234368,"teacher_disagreement_score":0.6131107,"about_ca_system_score_codex":0.000032867392,"about_ca_system_score_gemma":0.000067924535,"threshold_uncertainty_score":0.8919174},"labels":[],"label_agreement":null},{"id":"W4389024517","doi":"10.1096/fasebj.30.1_supplement.802.8","title":"Human growth gene family chromosomal architecture is affected by maternal obesity, gestational diabetes and insulin treatment","year":2016,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Manitoba","funders":"Canadian Institutes of Health Research","keywords":"Endocrinology; Internal medicine; Biology; Insulin resistance; Locus (genetics); Chromatin; Gestational diabetes; Chromatin immunoprecipitation; Gene; Gene expression; Insulin; Promoter; Pregnancy; Genetics; Gestation; Medicine","score_opus":0.00672912589708902,"score_gpt":0.21356819966136048,"score_spread":0.20683907376427146,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389024517","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99768686,0.0011222078,0.000413424,0.00048398983,0.000071675,0.000088899775,0.000068243244,0.0000058406927,0.00005887674],"genre_scores_gemma":[0.9982151,0.0004551281,0.00039589047,0.00021106684,0.00029409,0.000005759617,0.00001575052,0.000017620152,0.00038959345],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991717,0.000083287676,0.0001645473,0.00018693754,0.00013848142,0.00025506873],"domain_scores_gemma":[0.99959236,0.000012609104,0.000101927886,0.00013589124,0.000050258725,0.000106963875],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011875535,0.00015811449,0.00011684001,0.000027943219,0.00024432578,0.000065475775,0.00015697393,0.00006817479,0.000055900622],"category_scores_gemma":[0.000013400945,0.00008394547,0.00007094909,0.000028860244,0.00009411842,0.000003820041,0.00008486961,0.0000731239,0.0000066412917],"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":[0.0000058142746,0.00004060512,0.032282125,0.0000036537967,0.00009310461,0.0000028230477,0.000055107164,0.0000017860906,0.95979387,0.0000044997714,0.00036157016,0.00735503],"study_design_scores_gemma":[0.0008391804,0.00044198867,0.26820418,0.00001903899,0.000023891345,0.00024241593,0.000013724732,0.0000046037576,0.72960156,0.00023032575,0.00027210865,0.00010694884],"about_ca_topic_score_codex":0.0000126091345,"about_ca_topic_score_gemma":0.0000023856226,"teacher_disagreement_score":0.23592207,"about_ca_system_score_codex":0.000019455389,"about_ca_system_score_gemma":0.00003431944,"threshold_uncertainty_score":0.3423197},"labels":[],"label_agreement":null},{"id":"W4389341139","doi":"10.5772/intechopen.113912","title":"Founder Effect: Breeding a Dog for the Elderly Gentleman Reveals an Animal Model of a Human Genetic Disorder","year":2023,"lang":"en","type":"book-chapter","venue":"Genetics.","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Breed; Biology; Population; Genetics; Population bottleneck; Allele; Genotyping; Founder effect; Mutation; Gene; Genotype; Demography; Microsatellite; Haplotype","score_opus":0.03272385351567018,"score_gpt":0.283637738525617,"score_spread":0.2509138850099468,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389341139","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9710346,0.005073463,0.012063716,0.00012911584,0.0004966849,0.0028938258,0.0002986932,0.00006195061,0.007947954],"genre_scores_gemma":[0.89660436,0.0010661008,0.0043108882,0.00009386515,0.0009745286,0.00022983502,0.00031931512,0.00045221954,0.095948875],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9975112,0.000032868014,0.000684876,0.0008698628,0.00033879312,0.0005624119],"domain_scores_gemma":[0.9980756,0.00006067053,0.00040329644,0.0011075175,0.0002113893,0.00014152876],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00037569884,0.00056999805,0.0005539011,0.000111988964,0.00026930784,0.000067969486,0.0007210087,0.0005751717,0.000036823305],"category_scores_gemma":[0.00004061061,0.0004843807,0.00046448765,0.000041435367,0.00019819039,0.0000028245909,0.00041382684,0.00020704065,0.000013777286],"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":[0.000051632538,0.00007515186,0.0010769527,0.0006860955,0.0008966897,0.0000027446185,0.00020337699,0.0049608066,0.95724106,0.0024942812,0.0022637993,0.030047392],"study_design_scores_gemma":[0.029278915,0.18054564,0.057746086,0.0034988264,0.014168779,0.00076795736,0.0012375173,0.16028641,0.17532349,0.1685705,0.18695952,0.021616338],"about_ca_topic_score_codex":0.000021389815,"about_ca_topic_score_gemma":0.0001229148,"teacher_disagreement_score":0.7819176,"about_ca_system_score_codex":0.000018551571,"about_ca_system_score_gemma":0.000092982154,"threshold_uncertainty_score":0.9997608},"labels":[],"label_agreement":null},{"id":"W4390222174","doi":"10.1016/j.nsa.2023.103880","title":"Using eye-tracking to measure hyperphagia in Prader-Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"Neuroscience Applied","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto","funders":"","keywords":"Measure (data warehouse); Tracking (education); Psychology; Artificial intelligence; Computer science; Data mining","score_opus":0.05030297828866744,"score_gpt":0.3089278877563804,"score_spread":0.258624909467713,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390222174","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977556,0.000020390988,0.0009917289,0.00015090479,0.0002833686,0.00028321258,0.0000019478912,0.000034901168,0.00047797267],"genre_scores_gemma":[0.99828416,0.00001109278,0.0008577207,0.0006202404,0.000043360935,0.000024454375,0.0000034871236,0.000026511409,0.00012896853],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9983982,0.000023715762,0.00020327696,0.00061294396,0.0002588891,0.00050299853],"domain_scores_gemma":[0.99947226,0.0000071445547,0.000047769096,0.0003340258,0.00002364776,0.000115146395],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031593812,0.00015120168,0.00014265795,0.00014357119,0.00012020359,0.000063007596,0.00034296917,0.00008488902,0.0000045864417],"category_scores_gemma":[0.00013067517,0.00015622606,0.000040176277,0.00086741446,0.000060439797,0.000005196485,0.00025954255,0.00010037704,0.000045494267],"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":[7.4821077e-7,0.000015349964,0.015275448,0.0000066550538,0.0000010190467,0.0000044865687,0.000055752564,0.0037859397,0.9790546,0.000017188926,0.000048004815,0.0017348438],"study_design_scores_gemma":[0.00040615632,0.00014207493,0.8840539,0.000028518582,0.000006073973,0.00011481082,0.00019798914,0.002068759,0.10779922,0.000043740827,0.004752517,0.00038625643],"about_ca_topic_score_codex":0.0000138512305,"about_ca_topic_score_gemma":0.0000060183916,"teacher_disagreement_score":0.87125534,"about_ca_system_score_codex":0.000014019949,"about_ca_system_score_gemma":0.000058428646,"threshold_uncertainty_score":0.6370714},"labels":[],"label_agreement":null},{"id":"W4390223190","doi":"10.1016/j.nsa.2023.103883","title":"Exploring the role of social cognition in autism behaviours within Prader-Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"Neuroscience Applied","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto","funders":"","keywords":"Autism; Psychology; Cognition; Social cognition; Developmental psychology; Cognitive psychology; Neuroscience","score_opus":0.041965605319048575,"score_gpt":0.2557095995503657,"score_spread":0.21374399423131712,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390223190","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99894524,0.000009250747,0.000024480043,0.00013391778,0.00017777308,0.00017715992,0.0000046436635,0.000015558804,0.00051199313],"genre_scores_gemma":[0.99971306,0.000017763907,0.000035239336,0.00007850894,0.00001880077,0.00007111336,0.000009779727,0.000012082798,0.00004363676],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9991016,0.000023516763,0.00017774447,0.00028003697,0.00017975668,0.0002373544],"domain_scores_gemma":[0.9997242,0.000008494424,0.00007782544,0.00015220616,0.000009844664,0.00002742209],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023859649,0.000086227454,0.00009100995,0.000060101014,0.000120454846,0.000020019812,0.00022764043,0.00004062923,0.0000022440645],"category_scores_gemma":[0.000029908422,0.00007379042,0.000034961406,0.00037175385,0.00014105631,0.0000054063235,0.00014515503,0.00008614997,0.000006033654],"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":[7.9209997e-7,0.000020803578,0.0030611784,0.0000037293948,0.0000010782825,7.702259e-7,0.00030656884,0.00013977267,0.9934745,0.00041807193,0.000009229475,0.0025635045],"study_design_scores_gemma":[0.00019788115,0.00007692982,0.85937107,0.000005979605,0.000006326555,0.000024065326,0.00074793916,0.00019604425,0.13852341,0.00027445744,0.00047246774,0.00010344654],"about_ca_topic_score_codex":0.000013176924,"about_ca_topic_score_gemma":0.000006562234,"teacher_disagreement_score":0.8563099,"about_ca_system_score_codex":0.0000041214666,"about_ca_system_score_gemma":0.000031041836,"threshold_uncertainty_score":0.3009086},"labels":[],"label_agreement":null},{"id":"W4390267137","doi":"10.7554/elife.92942.1.sa1","title":"Reviewer #1 (Public Review): BMP signalling facilitates transit amplification in the developing chick and human cerebellum","year":2023,"lang":"en","type":"peer-review","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Institute of Genetics; Menzies Centre for Australian Studies, King's College London, University of London; University of East Anglia; King's College London; Queen Mary University of London","keywords":"Cell biology; Granule cell; Cerebellum; Biology; Bone morphogenetic protein; Sonic hedgehog; Cerebellar cortex; Granule (geology); Signalling; Neurogenesis; BMPR2; Progenitor cell; Neuroscience; Dentate gyrus; Signal transduction; Stem cell; Genetics; Central nervous system","score_opus":0.060833655691213434,"score_gpt":0.3158129804725798,"score_spread":0.2549793247813663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390267137","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0033119319,0.92782736,0.0024818212,0.061328493,0.0006850601,0.0026331758,0.000069841284,0.000039830553,0.0016224621],"genre_scores_gemma":[0.0040549487,0.9409266,0.00082226086,0.011670783,0.00039714464,0.00037107422,0.0029475442,0.000082650586,0.038726978],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9973775,0.00028913238,0.0008676045,0.00076112413,0.00030140346,0.00040322164],"domain_scores_gemma":[0.9985929,0.000050673327,0.00025029536,0.0006361191,0.000408763,0.00006126006],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0021188431,0.00039770588,0.0006539509,0.00007694502,0.00014808554,0.00006565382,0.0005365806,0.0002499062,0.00009876771],"category_scores_gemma":[0.0008315857,0.00028743673,0.00020709579,0.0003218647,0.00006836001,0.0000040959235,0.00015590039,0.0003256046,0.000034012628],"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":[7.8217516e-7,0.00004236466,0.00029951945,0.048975497,0.00015123896,0.000002563973,0.00012022009,0.0000024273488,0.005709283,0.0001232859,0.901977,0.042595793],"study_design_scores_gemma":[0.00011601095,0.00005972701,0.0020271565,0.013242876,0.00009349119,0.000021261318,0.00004892841,0.000003086494,0.00010554644,0.000044546217,0.98382884,0.00040854147],"about_ca_topic_score_codex":0.00012252135,"about_ca_topic_score_gemma":0.00032719946,"teacher_disagreement_score":0.0818518,"about_ca_system_score_codex":0.000018730525,"about_ca_system_score_gemma":0.000120210025,"threshold_uncertainty_score":0.9999578},"labels":[],"label_agreement":null},{"id":"W4391069390","doi":"10.1016/b978-0-12-816478-5.00056-x","title":"Endocrinologic and Growth Cases: Short Stature","year":2024,"lang":"en","type":"book-chapter","venue":"Elsevier eBooks","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Short stature; Uniparental disomy; Small for gestational age; Pediatrics; Biology; Medicine; Chromosome; Genetics; Gestational age; Pregnancy; Karyotype","score_opus":0.012741959985496066,"score_gpt":0.23816888732993757,"score_spread":0.2254269273444415,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391069390","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.009519035,0.016372854,0.000002186156,0.000046672496,0.00034434703,0.00030099403,0.000062613784,0.000029487672,0.9733218],"genre_scores_gemma":[0.073054634,0.001867459,0.00025694183,0.000221385,0.00039413964,0.000020320089,0.00008381925,0.00009131365,0.92401],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9986256,0.000009754184,0.0002579878,0.00066627807,0.00013313901,0.00030725205],"domain_scores_gemma":[0.99936837,0.0000105463705,0.000055956825,0.00039234085,0.00006134561,0.00011143782],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000068857546,0.0003940295,0.00030670126,0.00006876404,0.00006257102,0.00006243202,0.00017106888,0.0004080684,0.000048603604],"category_scores_gemma":[0.000018798526,0.00034494582,0.00016817106,0.000006526853,0.0001288211,8.9519466e-7,0.00041901832,0.0003372146,0.000061205865],"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":[0.000007659027,0.0000056162244,0.00014891723,0.0003201387,0.0003446272,0.0002533944,0.000047443853,2.2475565e-7,0.0067640976,0.004724866,0.00059665786,0.98678637],"study_design_scores_gemma":[0.000102234764,0.00025707218,0.00013510334,0.00015741824,0.0001410027,0.0010902554,0.000014170311,0.0000012208237,0.0017292759,0.004324462,0.991596,0.00045182763],"about_ca_topic_score_codex":7.245996e-7,"about_ca_topic_score_gemma":0.000010754086,"teacher_disagreement_score":0.9909993,"about_ca_system_score_codex":0.000012849796,"about_ca_system_score_gemma":0.000058073372,"threshold_uncertainty_score":0.9999003},"labels":[],"label_agreement":null},{"id":"W4391321767","doi":"10.1177/10497323231225412","title":"Mothering a Child With Complexity and Rarity: A Narrative Inquiry Exploring Prader-Willi Syndrome","year":2024,"lang":"en","type":"article","venue":"Qualitative Health Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Victoria; University of Calgary; Mount Royal University","funders":"Mount Royal University","keywords":"Narrative; Narrative inquiry; Normative; Psychology; Mental health; Developmental psychology; Quality of life (healthcare); Everyday life; Psychotherapist","score_opus":0.5099474836932916,"score_gpt":0.5163274933563686,"score_spread":0.0063800096630770575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391321767","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98507816,0.0060934997,0.002494284,0.0052247406,0.000098042525,0.0005603885,0.00001323555,0.00003255141,0.00040509854],"genre_scores_gemma":[0.9946022,0.00075631274,0.003827033,0.00015618681,0.00012735894,0.00019344864,0.000024924768,0.0000463099,0.0002662494],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.99675107,0.0011979918,0.00028626987,0.00065675465,0.00043072575,0.0006771656],"domain_scores_gemma":[0.9990777,0.00019909823,0.00004760447,0.00027356474,0.00015026175,0.00025181918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0032580958,0.00018355512,0.00025780604,0.00017436063,0.00051500107,0.00013063077,0.00014356928,0.000074970005,0.000024858695],"category_scores_gemma":[0.0002243932,0.0001533196,0.00004006397,0.00039496104,0.0005831168,0.000017550388,0.00022523644,0.0004980135,0.000011959621],"study_design_candidate":"qualitative","study_design_consensus":"qualitative","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000053854736,0.0002177084,0.00209711,0.0038174947,0.0005956168,0.000046241672,0.9338012,0.00003369704,0.0068468023,0.0108440695,0.0014733584,0.040172886],"study_design_scores_gemma":[0.0018014436,0.00984794,0.07353084,0.0027563763,0.00001537526,0.0015438495,0.8577283,0.000946782,0.0021857372,0.0038964956,0.04473232,0.0010145293],"about_ca_topic_score_codex":0.00033977613,"about_ca_topic_score_gemma":0.00009426618,"teacher_disagreement_score":0.07607285,"about_ca_system_score_codex":0.000062505555,"about_ca_system_score_gemma":0.00029215854,"threshold_uncertainty_score":0.6252192},"labels":[],"label_agreement":null},{"id":"W4391771437","doi":"10.1101/2024.02.12.24302716","title":"Fine-mapping genomic loci refines bipolar disorder risk genes","year":2024,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 British Columbia; Centre for Addiction and Mental Health; Dalhousie University","funders":"National Health and Medical Research Council; Canadian Institutes of Health Research; NIHR Maudsley Biomedical Research Centre; Stanley Center for Psychiatric Research, Broad Institute; National Institutes of Health; Vetenskapsrådet; National Institute of Mental Health; Stockholms Läns Landsting; Instituto de Salud Carlos III; Universitat de Barcelona; National Research Foundation; Medical Research Council; Università di Bologna; Department of Health and Social Care; National Research Foundation of Korea; King's College London; Departament d'Innovació, Universitats i Empresa, Generalitat de Catalunya; Victoria General Hospital Foundation; Generalitat de Catalunya; European Regional Development Fund; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Karl-Franzens-Universität Graz; Japan Agency for Medical Research and Development; Deutsche Forschungsgemeinschaft; Japan Society for the Promotion of Science; Medizinische Universität Graz; Amt der Steiermärkischen Landesregierung; GlaxoSmithKline; Centres de Recerca de Catalunya; Michael Smith Health Research BC; Maudsley Charity; Wellcome Trust; Ministerio de Ciencia e Innovación; European Commission; University of California, Irvine; Broad Institute; Ministerio de Economía y Competitividad; University of Pittsburgh; Centro de Investigación Biomédica en Red de Salud Mental; National Alliance for Research on Schizophrenia and Depression; U.S. Department of Health and Human Services","keywords":"Biology; Genetics; Single-nucleotide polymorphism; Computational biology; Exome sequencing; Gene; Epigenomics; Genome; Genome-wide association study; Phenotype; DNA methylation","score_opus":0.012729237597689158,"score_gpt":0.24100159496176624,"score_spread":0.22827235736407708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391771437","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.90716,0.08961822,0.0011190873,0.00029336775,0.0011096484,0.0002629658,0.000108910855,0.00005220526,0.00027561354],"genre_scores_gemma":[0.98519444,0.0074457857,0.00267854,0.00007929052,0.0012392566,0.00008434542,0.00029477358,0.00013984377,0.002843721],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9977179,0.00010676297,0.0004814979,0.0010541981,0.00017737078,0.00046226906],"domain_scores_gemma":[0.99854887,0.000013945474,0.0002261377,0.001011672,0.000086144784,0.00011320913],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00039318105,0.00046963937,0.00038216935,0.00013403087,0.00012098281,0.00011455018,0.00055803615,0.00050442974,0.000068097266],"category_scores_gemma":[0.00013040483,0.0004376392,0.00036234685,0.00011793603,0.00008161387,0.0000010610263,0.0027292396,0.0005592184,0.000171553],"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":[0.0000074756076,0.00006386557,0.33106187,0.0007948744,0.0006632105,0.000016068594,0.00019119676,0.0019095878,0.5652935,0.000024698196,0.0025399872,0.09743368],"study_design_scores_gemma":[0.00033156262,0.00011032678,0.1273515,0.00018467037,0.00021437129,0.000059222744,0.000071559916,0.0010868526,0.031726453,0.000999027,0.83678293,0.0010815207],"about_ca_topic_score_codex":0.00031817376,"about_ca_topic_score_gemma":0.00016490028,"teacher_disagreement_score":0.83424294,"about_ca_system_score_codex":0.000020645353,"about_ca_system_score_gemma":0.000148903,"threshold_uncertainty_score":0.99980754},"labels":[],"label_agreement":null},{"id":"W4392049994","doi":"10.7554/elife.94502","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2024,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"NODAI Genome Research Center, Tokyo University of Agriculture; Canadian Institutes of Health Research; Mitsubishi Foundation; Japan Society for the Promotion of Science; Ministry of Education, Culture, Sports, Science and Technology; Tokyo University of Agriculture; Takeda Science Foundation","keywords":"Retrotransposon; Genomic imprinting; Imprinting (psychology); Biology; Genetics; Lineage (genetic); Gene; Computational biology; Genome; Transposable element; DNA methylation; Gene expression","score_opus":0.0193719705543862,"score_gpt":0.2651506837435218,"score_spread":0.2457787131891356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392049994","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99309266,0.0019852929,0.004338251,0.000041668187,0.0002570248,0.00015148491,0.0000125311535,0.000020501699,0.000100588004],"genre_scores_gemma":[0.99766684,0.00056703103,0.0012832256,0.000034245255,0.00020272828,0.000008492777,0.00018667085,0.000023281547,0.000027486865],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99903303,0.000050034414,0.00033092272,0.00030334937,0.0001102688,0.00017241584],"domain_scores_gemma":[0.99966204,0.0000057521584,0.000052415315,0.00016751284,0.000073092495,0.0000392027],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018129105,0.00011221864,0.00011406216,0.00009396547,0.000028632476,0.000036952122,0.000102105376,0.00011757593,0.000021101854],"category_scores_gemma":[0.000018460585,0.00011903519,0.000068248824,0.00012553064,0.000028906756,0.00001676524,0.00001496308,0.00008685854,0.0000041465664],"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":[0.000016210657,0.000027597725,0.017577764,0.00006258951,0.0000081774215,0.0000010910749,0.00048592512,0.0004776163,0.974612,0.00005200905,0.0000041412322,0.0066748927],"study_design_scores_gemma":[0.00023689293,0.00025305952,0.39934134,0.000067305744,0.000008161182,0.0000063830657,0.00021980956,0.0023378255,0.5967784,0.0000103217135,0.00061544316,0.00012505092],"about_ca_topic_score_codex":0.000019217969,"about_ca_topic_score_gemma":0.000043606182,"teacher_disagreement_score":0.38176358,"about_ca_system_score_codex":0.000015337366,"about_ca_system_score_gemma":0.000045517074,"threshold_uncertainty_score":0.4854114},"labels":[],"label_agreement":null},{"id":"W4392080976","doi":"10.7554/elife.94502.1","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2024,"lang":"en","type":"preprint","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Genomic imprinting; Biology; Retrotransposon; DNA methylation; Genetics; Imprinting (psychology); Gene; Genome; Transposable element; Gene expression","score_opus":0.024138101324923143,"score_gpt":0.27022452178437434,"score_spread":0.2460864204594512,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392080976","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9923512,0.0019567623,0.0040730536,0.000060513332,0.0005918833,0.00047800285,0.000050168957,0.000033642802,0.00040480285],"genre_scores_gemma":[0.99388564,0.0009517838,0.0037238144,0.000031054366,0.0002796004,0.00003241062,0.0009563464,0.000058327332,0.000081022714],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9979071,0.000101899306,0.0007546815,0.0007785045,0.00016620789,0.00029161602],"domain_scores_gemma":[0.9990792,0.000006536439,0.00021013537,0.00046800752,0.00017125177,0.000064828855],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00027756757,0.00031090147,0.0003201055,0.000215223,0.000033201042,0.000076792625,0.00028067586,0.0005214383,0.000044429464],"category_scores_gemma":[0.00002161577,0.00033057164,0.00019597386,0.00012484852,0.000054981338,0.000008686248,0.0001891023,0.00037616084,0.0000046596624],"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":[0.00003303941,0.00006527972,0.009676701,0.00038332178,0.000027956303,0.0000013809733,0.00053740595,0.0029277657,0.9809551,0.00007812808,0.0000037623377,0.00531013],"study_design_scores_gemma":[0.0005076533,0.00044957068,0.32098714,0.00032659326,0.000050603696,0.000010373299,0.00052062096,0.004856668,0.67129296,0.0003601055,0.00014203507,0.0004957195],"about_ca_topic_score_codex":0.000098614975,"about_ca_topic_score_gemma":0.0002021883,"teacher_disagreement_score":0.3113104,"about_ca_system_score_codex":0.000039309445,"about_ca_system_score_gemma":0.00013029465,"threshold_uncertainty_score":0.99991465},"labels":[],"label_agreement":null},{"id":"W4392131917","doi":"10.1002/mgg3.2402","title":"A homozygous stop codon in <i>HORMAD2</i> in a patient with recurrent digynic triploid miscarriage","year":2024,"lang":"en","type":"article","venue":"Molecular Genetics & Genomic Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children; McGill University; McGill University Health Centre","funders":"Canadian Institutes of Health Research; McGill University Health Centre; Génome Québec; McGill University","keywords":"Biology; Genetics; Sanger sequencing; Meiosis; SNP array; Exome sequencing; Aneuploidy; Single-nucleotide polymorphism; Gene; Genotype; Chromosome; Phenotype; Mutation","score_opus":0.006433787523581298,"score_gpt":0.23030253521634822,"score_spread":0.22386874769276693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392131917","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9470256,0.048672628,0.0018191431,0.000425426,0.00040314195,0.00065178936,0.000010644275,0.000020550526,0.00097107585],"genre_scores_gemma":[0.99549544,0.0025895084,0.0009281643,0.00040044074,0.00015252532,0.00008800848,0.00009704649,0.0000881677,0.00016071551],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9974578,0.00013370582,0.00065048365,0.00082856405,0.0003217966,0.0006076561],"domain_scores_gemma":[0.99903375,0.00002007619,0.00009189766,0.00062393554,0.000050146067,0.00018021115],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00036811872,0.0003862827,0.0004083129,0.00028806762,0.000030144109,0.000038008147,0.0003032755,0.00017885838,0.0000423168],"category_scores_gemma":[0.000053847434,0.00032854648,0.00009203552,0.00042137716,0.0001302322,0.000003051067,0.00020125206,0.00028515235,0.000017546612],"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":[0.000078118646,0.00010786466,0.00091540616,0.00013991262,0.00008145522,0.001165093,0.001210758,0.0014708932,0.944583,0.00003726278,0.00030111027,0.04990912],"study_design_scores_gemma":[0.020668318,0.022388672,0.048475537,0.0051385886,0.00064473605,0.009088321,0.0042082686,0.013815359,0.3639224,0.0009627297,0.5057127,0.004974397],"about_ca_topic_score_codex":0.00010460896,"about_ca_topic_score_gemma":0.00018264509,"teacher_disagreement_score":0.5806606,"about_ca_system_score_codex":0.00009258319,"about_ca_system_score_gemma":0.00019934932,"threshold_uncertainty_score":0.9999167},"labels":[],"label_agreement":null},{"id":"W4392361808","doi":"10.5664/jcsm.11078","title":"14 and 6 Hz like spike wave activity is a common finding in young patients with Prader–Willi syndrome","year":2024,"lang":"en","type":"article","venue":"Journal of Clinical Sleep Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Spike (software development); Audiology; Electroencephalography; Internal medicine; Psychiatry; Pediatrics","score_opus":0.028019368282374633,"score_gpt":0.33454208332579044,"score_spread":0.3065227150434158,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392361808","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958335,0.0012324768,0.00033633236,0.0015252031,0.000756307,0.00011714092,0.0000026023324,0.0000032041498,0.00019324158],"genre_scores_gemma":[0.99825406,0.0005748311,0.0004009328,0.00029744755,0.00034946884,0.0000013037502,0.0000039323836,0.000018897243,0.00009910131],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983538,0.00009737472,0.00077269244,0.00025926658,0.00030481548,0.00021207947],"domain_scores_gemma":[0.99912405,0.00013716418,0.00030659948,0.0001651295,0.000087735476,0.00017933242],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011039857,0.00015227203,0.0005003199,0.000093532835,0.000031859334,0.000022063647,0.00011160457,0.00017193324,0.00003514705],"category_scores_gemma":[0.000377688,0.0000982526,0.0000971385,0.00013063151,0.00013616854,0.000011579273,0.000088282766,0.0004610288,0.0000014310788],"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":[0.00003759521,0.00016230244,0.92722076,0.00008166633,0.00018867438,0.00005513918,0.0001508296,0.0000051915636,0.0011479296,0.0000027390686,0.00057970884,0.07036747],"study_design_scores_gemma":[0.0023756432,0.003641742,0.9881562,0.0006140305,0.000092264796,0.00054676307,0.00006096985,0.0002674926,0.00011619542,0.000038869715,0.0039699282,0.00011990662],"about_ca_topic_score_codex":0.000021674226,"about_ca_topic_score_gemma":0.000028266932,"teacher_disagreement_score":0.07024757,"about_ca_system_score_codex":0.000013917928,"about_ca_system_score_gemma":0.00005083784,"threshold_uncertainty_score":0.40066248},"labels":[],"label_agreement":null},{"id":"W4392466924","doi":"10.3389/fcell.2024.1369751","title":"Roles of endogenous retroviral elements in the establishment and maintenance of imprinted gene expression","year":2024,"lang":"en","type":"article","venue":"Frontiers in Cell and Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Epigenetics; Genetics; Gene silencing; DNA methylation; Histone; Imprinting (psychology); Endogenous retrovirus; Gene; Germline; Regulation of gene expression; Gene expression; Genome","score_opus":0.007685880341422367,"score_gpt":0.2102407274092707,"score_spread":0.20255484706784832,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392466924","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9923321,0.005962206,0.00086788164,0.000019284482,0.00014317293,0.00012952118,0.000011280788,0.000001539581,0.00053298625],"genre_scores_gemma":[0.9832467,0.0015608864,0.015067606,0.0000314312,0.000009698094,0.0000107926235,0.000030167703,0.0000050664967,0.000037695372],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992655,0.000046413217,0.00026187112,0.00022415718,0.000042573418,0.00015946937],"domain_scores_gemma":[0.99984133,0.000010319809,0.00004647592,0.00007383049,0.000010135554,0.000017907305],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023843082,0.000089578716,0.0001402065,0.00007110861,0.000016217688,0.0000067425326,0.00009910447,0.00007700991,0.0000031788527],"category_scores_gemma":[0.000016147278,0.00006354705,0.000019442145,0.00007139183,0.00009562248,0.000002736442,0.00014777157,0.000057083173,1.7215906e-7],"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":[0.00001639128,0.0000231606,0.18721558,0.000047611167,0.000009531662,0.000002287078,0.00039680974,7.261909e-7,0.80210847,0.000007303475,0.00015241973,0.010019707],"study_design_scores_gemma":[0.0005498809,0.0002400571,0.029334141,0.00005752807,0.0000047222525,0.00004253478,0.0024451443,0.00005922633,0.9644246,0.00019508306,0.002538482,0.00010860695],"about_ca_topic_score_codex":0.00002674471,"about_ca_topic_score_gemma":0.000011407053,"teacher_disagreement_score":0.16231611,"about_ca_system_score_codex":0.0000108177055,"about_ca_system_score_gemma":0.000034218167,"threshold_uncertainty_score":0.25913736},"labels":[],"label_agreement":null},{"id":"W4392564506","doi":"10.1101/gad.351238.123","title":"A maternal-effect<i>Padi6</i>variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos","year":2024,"lang":"en","type":"article","venue":"Genes & Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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":"Biotechnology and Biological Sciences Research Council; Directorate for Biological Sciences; Medical Research Council; Associazione Italiana per la Ricerca sul Cancro; Medical Research Council Canada; Wellcome Trust","keywords":"Biology; Maternal to zygotic transition; Reprogramming; Genomic imprinting; Epigenetics; Zygote; DNA methylation; Genetics; Embryo; Oocyte; Imprinting (psychology); Gene; XIST; Cell biology; X-inactivation; Embryogenesis; Gene expression; X chromosome","score_opus":0.004728806393827955,"score_gpt":0.21467845354063803,"score_spread":0.20994964714681008,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392564506","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9955985,0.003754149,0.000085545566,0.000053572836,0.00007116041,0.0003107545,0.0000013824972,0.000012170089,0.000112763715],"genre_scores_gemma":[0.995559,0.0010041812,0.0030206684,0.000048816604,0.000028818293,0.00003916163,0.00001747553,0.000030174968,0.00025173472],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987218,0.00005615941,0.00037399118,0.0004396247,0.00012149823,0.00028693507],"domain_scores_gemma":[0.99966574,0.000022239805,0.00006605088,0.00016257972,0.000022709164,0.000060669296],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002991595,0.00019663837,0.00021340595,0.00015249857,0.000045363267,0.00007188399,0.000089598,0.000118856835,0.000021958578],"category_scores_gemma":[0.000028854101,0.0001897856,0.000027546124,0.00012135624,0.000050379454,0.000009300465,0.00019335558,0.000079675425,0.000017867083],"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":[0.000044591667,0.000034342487,0.043303125,0.00080616365,0.00009855849,0.00006147985,0.0020485218,0.00013840589,0.91434664,0.000073791314,0.000008762325,0.03903561],"study_design_scores_gemma":[0.0007137743,0.00037592388,0.28611633,0.000448212,0.000031299503,0.0004946058,0.0010847921,0.00015330728,0.67282945,0.00011508594,0.03719271,0.0004445169],"about_ca_topic_score_codex":0.00032266602,"about_ca_topic_score_gemma":0.00016448378,"teacher_disagreement_score":0.2428132,"about_ca_system_score_codex":0.000033173925,"about_ca_system_score_gemma":0.00011830071,"threshold_uncertainty_score":0.7739232},"labels":[],"label_agreement":null},{"id":"W4392588876","doi":"10.1016/j.gimo.2024.101191","title":"P295: Expanding the prenatal phenotype of a rare syndrome due to variants in DPH1","year":2024,"lang":"en","type":"article","venue":"Genetics in Medicine Open","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; University of British Columbia","funders":"","keywords":"Phenotype; Genetics; Medicine; Biology; Gene","score_opus":0.021632580676808268,"score_gpt":0.3134563342496481,"score_spread":0.2918237535728398,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392588876","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98864776,0.0056144022,0.0010608111,0.0008379323,0.00045259195,0.0006708113,0.000009642749,0.0000043048663,0.002701768],"genre_scores_gemma":[0.9974536,0.00019733753,0.0014823303,0.00017290577,0.00015484441,0.00005355278,0.00002162659,0.000028031407,0.00043578216],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986388,0.000078461235,0.00040699652,0.00040656814,0.00018139319,0.00028778773],"domain_scores_gemma":[0.99934083,0.000040161856,0.000047689242,0.00046793526,0.000034010514,0.00006937975],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007286631,0.00015494363,0.0002778889,0.00012744509,0.00003126488,0.00003924562,0.0007488539,0.00009682261,0.000104883075],"category_scores_gemma":[0.00017263906,0.000112579735,0.000032558888,0.00039451403,0.00007290617,0.000004023756,0.00076076493,0.00014329697,0.000011081251],"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":[0.00010324726,0.00016198926,0.024677325,0.00077894144,0.00022798749,0.0007296129,0.0061201714,0.0033394927,0.80236006,0.0006218547,0.004129773,0.15674956],"study_design_scores_gemma":[0.0055724564,0.0052550556,0.75960666,0.007052505,0.00014835622,0.0025366151,0.005260369,0.004196958,0.16733506,0.0029531033,0.03864465,0.0014382019],"about_ca_topic_score_codex":0.00024239691,"about_ca_topic_score_gemma":0.00020990492,"teacher_disagreement_score":0.7349293,"about_ca_system_score_codex":0.000023764676,"about_ca_system_score_gemma":0.00011574304,"threshold_uncertainty_score":0.45908684},"labels":[],"label_agreement":null},{"id":"W4392606465","doi":"10.1016/j.gimo.2024.101206","title":"P311: Use of a DNA methylation signature for the diagnosis of TET3-related Beck-Fahrner syndrome and expansion of its related phenotype","year":2024,"lang":"en","type":"article","venue":"Genetics in Medicine Open","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Sunnybrook Health Science Centre; McMaster Children's Hospital; London Health Sciences Centre; McMaster University","funders":"","keywords":"DNA methylation; Phenotype; Signature (topology); Genetics; Methylation; Biology; Epigenetics; Computational biology; DNA; Mathematics; Gene","score_opus":0.033605987518793345,"score_gpt":0.30864572344937263,"score_spread":0.2750397359305793,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392606465","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9652869,0.03303382,0.00026149477,0.00040026434,0.00018961557,0.0006749658,0.000024683572,0.0000027333097,0.00012550472],"genre_scores_gemma":[0.99218005,0.00597346,0.0013300744,0.000028901599,0.000019923154,0.000042673917,0.000056412544,0.000025565185,0.0003429488],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988146,0.000058460013,0.00054431753,0.0002872909,0.00015338766,0.00014193986],"domain_scores_gemma":[0.99911994,0.00022028288,0.00017441325,0.00031673408,0.0001330443,0.000035582907],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00058268954,0.00013472594,0.00030897063,0.00008966105,0.00002746062,0.000011543394,0.00025334177,0.0002022252,0.000072435134],"category_scores_gemma":[0.00040484275,0.000093128605,0.000053499236,0.00024438507,0.00014545547,0.0000065538297,0.0002623519,0.00011136335,3.418235e-7],"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":[0.00003779181,0.00004412346,0.004748653,0.00044800932,0.00023875319,0.0000022345612,0.0007713677,0.0013164249,0.93967223,0.00017107381,0.00045531822,0.052093998],"study_design_scores_gemma":[0.0034226128,0.0029150501,0.12604359,0.0026911858,0.00064898486,0.000069617454,0.0010381765,0.012573428,0.8350865,0.0013147803,0.013736913,0.0004591699],"about_ca_topic_score_codex":0.000085645246,"about_ca_topic_score_gemma":0.000023144083,"teacher_disagreement_score":0.12129493,"about_ca_system_score_codex":0.0000062953286,"about_ca_system_score_gemma":0.000062507585,"threshold_uncertainty_score":0.37976745},"labels":[],"label_agreement":null},{"id":"W4392963254","doi":"10.1186/s42269-024-01184-4","title":"Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities","year":2024,"lang":"en","type":"article","venue":"Bulletin of the National Research Centre/Bulletin of the National Research Center","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Polytechnique Montréal","funders":"National Research Centre","keywords":"Craniofacial; Anthropometry; Cohort; Medicine; Pediatrics; Demography; Internal medicine; Psychiatry; Sociology","score_opus":0.055547979690193,"score_gpt":0.34230058108356926,"score_spread":0.28675260139337627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392963254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98862785,0.0008896939,0.000008422506,0.0043346486,0.00015184062,0.00092337205,0.00035494813,0.0000020143507,0.0047072307],"genre_scores_gemma":[0.99809974,0.0002645998,0.00007287969,0.000026047659,0.000077779325,0.000016847327,0.000008755485,0.000016512015,0.0014168388],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9924931,0.0013473391,0.0006689522,0.00036110176,0.004741686,0.00038784547],"domain_scores_gemma":[0.9941237,0.0005432101,0.00021744019,0.00030030616,0.0047492553,0.00006608738],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.011238961,0.00014446172,0.00023374608,0.0004237669,0.00017995953,0.000024204295,0.0009553848,0.00014464482,0.00071460597],"category_scores_gemma":[0.013800387,0.00008902406,0.0002510061,0.00086084276,0.0012642274,0.000004789673,0.0011639596,0.00049170095,0.0000050729504],"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":[0.0004860072,0.0012354112,0.60336953,0.00090839434,0.0006615987,2.0900563e-7,0.00030069952,0.0002205297,0.34812924,0.00055305136,0.041024726,0.0031106032],"study_design_scores_gemma":[0.0006694701,0.0001190655,0.7120784,0.00037197568,0.00000729632,0.000011321843,0.00015693341,0.00007972742,0.27232593,0.00041942563,0.013684342,0.000076139586],"about_ca_topic_score_codex":0.000870287,"about_ca_topic_score_gemma":0.000059634312,"teacher_disagreement_score":0.10870884,"about_ca_system_score_codex":0.00019512109,"about_ca_system_score_gemma":0.00064768386,"threshold_uncertainty_score":0.9945068},"labels":[],"label_agreement":null},{"id":"W4393313966","doi":"10.1177/23333936241242929","title":"<i>“Unable to Feed My Hungry Child”</i> : Experiences of Mothers Caring for Children With Prader-Willi Syndrome","year":2024,"lang":"en","type":"article","venue":"Global Qualitative Nursing Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Victoria; University of Calgary; Mount Royal University","funders":"Mount Royal University","keywords":"Narrative; Harm; Narrative inquiry; Psychological intervention; Psychology; Health care; Nursing; Care work; Social work; Developmental psychology; Work (physics); Medicine; Social psychology","score_opus":0.040380520247156694,"score_gpt":0.41724506398624933,"score_spread":0.3768645437390926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4393313966","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9900492,0.0021350866,0.0039306227,0.00060731434,0.00014460272,0.0007569883,0.0000607931,0.000019663301,0.0022957593],"genre_scores_gemma":[0.99424547,0.0000152314815,0.0051097004,0.000033084587,0.00007364554,0.00014440737,0.00003578686,0.000029336188,0.00031336478],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.99782324,0.00023808361,0.00024828332,0.00061385694,0.00045763946,0.0006189232],"domain_scores_gemma":[0.9991942,0.0000812811,0.000041670002,0.0002875244,0.0002434478,0.00015185872],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010793847,0.00017416745,0.0002192902,0.000101697864,0.0002063308,0.00010121721,0.00030769163,0.000099279794,0.000009387149],"category_scores_gemma":[0.00023669944,0.000148954,0.0000893418,0.00058242097,0.00038817196,0.000010253198,0.00008933742,0.00012829556,0.0000063978355],"study_design_candidate":"qualitative","study_design_consensus":"qualitative","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002744827,0.0010655421,0.017259099,0.0014291873,0.0022237343,0.0000116520405,0.65064955,0.0014400807,0.18332049,0.010376656,0.025155088,0.10679444],"study_design_scores_gemma":[0.0022452506,0.012731044,0.09462249,0.0044671455,0.00011322564,0.000818904,0.7942507,0.00029328384,0.080079086,0.004721192,0.0041899546,0.0014677192],"about_ca_topic_score_codex":0.00012522933,"about_ca_topic_score_gemma":0.0000065456834,"teacher_disagreement_score":0.14360115,"about_ca_system_score_codex":0.00009175754,"about_ca_system_score_gemma":0.00017220534,"threshold_uncertainty_score":0.6074168},"labels":[],"label_agreement":null},{"id":"W4393979228","doi":"10.1172/jci.insight.169425","title":"Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome","year":2024,"lang":"en","type":"article","venue":"JCI Insight","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"Natural Sciences and Engineering Research Council of Canada; Medical Research Council; Children's Hospital Research Institute of Manitoba; National Institute for Health and Care Research; Barts Charity","keywords":"Missense mutation; HMGA2; Phenotype; Biology; Frameshift mutation; Nonsense; Exome sequencing; Genetics; Gene","score_opus":0.008349228860406082,"score_gpt":0.22047653144521603,"score_spread":0.21212730258480994,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4393979228","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957946,0.000580878,0.0010440447,0.0001830223,0.00037315517,0.000117088166,0.000017113369,0.000008127269,0.0018819775],"genre_scores_gemma":[0.99854517,0.00024171248,0.00007266036,0.000041236563,0.00009208973,0.0000057208917,0.00004361939,0.00001720237,0.000940563],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992963,0.00002900505,0.0002366986,0.00019590568,0.0001096311,0.0001324742],"domain_scores_gemma":[0.9995667,0.000010259368,0.00007619679,0.000290643,0.000030221589,0.000025976591],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011026861,0.000097706215,0.00013038397,0.00004310835,0.000028458246,0.00001863448,0.00015663973,0.00008495758,0.000085492866],"category_scores_gemma":[0.000018176786,0.00006904995,0.0000843182,0.000145621,0.000048542675,0.0000041637522,0.00008878011,0.00005486601,0.000010606637],"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":[0.0000036118095,0.000029688237,0.00062246923,0.000057191828,0.00005500897,0.000003264015,0.00016523222,0.0000044271583,0.99742407,0.00025823698,0.00005982047,0.0013169848],"study_design_scores_gemma":[0.00014257591,0.00026847457,0.0744233,0.000065724,0.00002989283,0.00009201593,0.000036469693,0.00020226324,0.9075437,0.00008410392,0.017003438,0.00010801708],"about_ca_topic_score_codex":0.000013117647,"about_ca_topic_score_gemma":0.0000018404759,"teacher_disagreement_score":0.08988034,"about_ca_system_score_codex":0.000004374296,"about_ca_system_score_gemma":0.000048474456,"threshold_uncertainty_score":0.28157753},"labels":[],"label_agreement":null},{"id":"W4394533346","doi":"10.6084/m9.figshare.20064356","title":"Additional file 2 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"dataset","venue":"Open MIND","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Imprinting (psychology); Loss function; Variation (astronomy); Function (biology); Biology; Genetics; Phenotype; Gene; Physics","score_opus":0.015247790909407094,"score_gpt":0.24014230705323636,"score_spread":0.22489451614382927,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394533346","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.020776143,0.00010289715,0.00004324389,0.000008962436,0.000060715563,0.00027372604,0.9787001,3.287154e-7,0.000033876364],"genre_scores_gemma":[0.008159707,0.000044650318,0.00052277866,0.000009867389,0.00003573997,0.000077157834,0.990663,0.000013421015,0.00047369214],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99893844,0.0000419728,0.00032696003,0.00040788949,0.00015323814,0.00013147965],"domain_scores_gemma":[0.9990835,0.00006898717,0.00050098775,0.00022434883,0.00007821976,0.000043958153],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00018397406,0.00016079006,0.00023048339,0.00006237533,0.00007959328,0.0000321233,0.0001644434,0.00019617639,0.31345308],"category_scores_gemma":[0.00023032753,0.00018138588,0.000036425845,0.00007537608,0.000037480873,0.000010001416,0.0005676337,0.00009855374,0.000004158235],"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":[0.000014534835,0.000060008384,0.0000032475557,0.000069435206,0.00009334524,6.046339e-7,0.000011750613,0.00001985209,0.025749646,3.875712e-7,0.97300094,0.00097622414],"study_design_scores_gemma":[0.00046206778,0.00037090923,0.0048579457,0.00011495531,0.00008399017,0.00014609285,0.00005350336,0.00017219382,0.0015689563,0.00000941134,0.9919263,0.0002336855],"about_ca_topic_score_codex":0.00005635029,"about_ca_topic_score_gemma":0.000012912328,"teacher_disagreement_score":0.3134489,"about_ca_system_score_codex":0.000010216258,"about_ca_system_score_gemma":0.000076928736,"threshold_uncertainty_score":0.73967016},"labels":[],"label_agreement":null},{"id":"W4394820316","doi":"10.1002/brb3.3437","title":"Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region","year":2024,"lang":"en","type":"article","venue":"Brain and Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Genome Canada","funders":"","keywords":"Imprinting (psychology); Phenotype; Biology; Genetics; Genomic imprinting; Gene; DNA methylation; Gene expression","score_opus":0.011160155900873575,"score_gpt":0.2493671151816012,"score_spread":0.23820695928072763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394820316","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99357635,0.0006362856,0.00507786,0.00016243038,0.00020999459,0.00019513581,0.0000055453193,0.000048579048,0.00008781173],"genre_scores_gemma":[0.99853545,0.000027011949,0.00074307655,0.00007444473,0.00019519152,0.00002580457,0.00006210319,0.00003282906,0.00030407507],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99890876,0.000045347777,0.00019469227,0.00042368966,0.00011123749,0.00031629394],"domain_scores_gemma":[0.99962586,0.00003163718,0.00005779366,0.00017532549,0.00002548344,0.000083879466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013768591,0.00017463729,0.00014106861,0.00005737379,0.00018488042,0.00014122154,0.000087569155,0.00013911125,0.00002474247],"category_scores_gemma":[0.00008177369,0.00015034014,0.00007464285,0.00013665309,0.000050567123,0.000009066739,0.00010811386,0.0001391412,0.0000029303453],"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":[0.000017822977,0.000053520132,0.09358935,0.000054003904,0.00012692786,0.000047976635,0.00039974067,0.000020131974,0.8619635,0.00066210557,0.000095130024,0.042969797],"study_design_scores_gemma":[0.00059144606,0.00026328294,0.9898456,0.00012976147,0.00016327912,0.00039273422,0.00022462111,0.0015130457,0.0058903038,0.00014585909,0.00044811555,0.00039195435],"about_ca_topic_score_codex":0.000013094129,"about_ca_topic_score_gemma":0.00003435836,"teacher_disagreement_score":0.89625627,"about_ca_system_score_codex":0.000024367178,"about_ca_system_score_gemma":0.000043509674,"threshold_uncertainty_score":0.6130693},"labels":[],"label_agreement":null},{"id":"W4394903714","doi":"10.1016/j.lingua.2024.103724","title":"The linguistic and metalinguistic abilities of monolingual and bilingual speakers with Prader–Willi syndrome","year":2024,"lang":"en","type":"article","venue":"Lingua","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Wilfrid Laurier University; University of Ottawa","funders":"","keywords":"Grammaticality; Neuroscience of multilingualism; Psychology; Linguistics; Metalinguistic awareness; Catalan; Semantics (computer science); Multilingualism; Grammar; Computer science","score_opus":0.006109767730625988,"score_gpt":0.2346713497487275,"score_spread":0.2285615820181015,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394903714","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97475827,0.024047947,0.00014720821,0.00006383814,0.00032854342,0.00016574528,0.0000075635126,0.000031715437,0.0004491591],"genre_scores_gemma":[0.99720526,0.00066341466,0.0013865988,0.000021753049,0.00023702194,0.0000065984864,0.000005355536,0.000044069428,0.0004299218],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99887335,0.000036701887,0.00028134848,0.0004026741,0.00013906654,0.0002668271],"domain_scores_gemma":[0.9993531,0.00014273584,0.00006592159,0.00027727478,0.00008339499,0.000077541634],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031212618,0.00019083591,0.00019751572,0.00004759973,0.00013052336,0.00010660633,0.00011508664,0.00008608108,0.0000031115235],"category_scores_gemma":[0.00078441505,0.00012827691,0.00005231592,0.0000927456,0.00038095273,0.0000020243535,0.00012385548,0.00012301166,0.0000013930799],"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":[0.00023246731,0.0006433371,0.2122866,0.011439086,0.008548566,0.00059459824,0.06534042,0.0014882291,0.35140973,0.045233417,0.00035844278,0.3024251],"study_design_scores_gemma":[0.0066404315,0.016455159,0.26696408,0.0041109654,0.0031112107,0.018882366,0.02840186,0.016929125,0.14599061,0.020516597,0.46572223,0.0062753744],"about_ca_topic_score_codex":0.00007708741,"about_ca_topic_score_gemma":0.000046500747,"teacher_disagreement_score":0.4653638,"about_ca_system_score_codex":0.0000057746734,"about_ca_system_score_gemma":0.00014199506,"threshold_uncertainty_score":0.52309805},"labels":[],"label_agreement":null},{"id":"W4396541254","doi":"10.1016/j.parkreldis.2024.106782","title":"Intronic GAA-FGF14 Expansion in an italian patient presenting with early-onset cerebellar ataxia","year":2024,"lang":"en","type":"article","venue":"Parkinsonism & Related Disorders","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre de réadaptation Lethbridge-Layton-Mackay; McGill University; Montreal Neurological Institute and Hospital","funders":"","keywords":"Ataxia; Cerebellar ataxia; Medicine; Trinucleotide repeat expansion; Neuroscience; Psychology; Pediatrics; Genetics; Biology; Allele; Gene","score_opus":0.004506469812084299,"score_gpt":0.21869580084253476,"score_spread":0.21418933103045046,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396541254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99381053,0.0042998325,0.00016874849,0.00019586702,0.00022809127,0.0003343552,0.000008004583,0.00005437247,0.000900223],"genre_scores_gemma":[0.99842906,0.00063825236,0.00033861876,0.00004671995,0.000034406054,0.000041060608,0.00012773229,0.00006938902,0.00027476874],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.99813116,0.0001144792,0.0003486371,0.00068595534,0.00019963448,0.00052011973],"domain_scores_gemma":[0.99933404,0.000014456255,0.0000746193,0.00042854509,0.000028573682,0.000119767355],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016569134,0.0002631695,0.00017565073,0.000119149074,0.000109409324,0.00011921853,0.00019479015,0.00022820706,0.0000503929],"category_scores_gemma":[0.000027658436,0.00023841838,0.00008686551,0.00026624315,0.00008531957,0.000017068862,0.00013567507,0.00026266684,0.000037227983],"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":[0.00020034668,0.00084018946,0.43983284,0.00038092566,0.000713628,0.00013168555,0.010146018,0.009367943,0.09900534,0.00015028678,0.0014566767,0.43777412],"study_design_scores_gemma":[0.0054833535,0.005804616,0.23334743,0.00083907414,0.00027069286,0.00040611904,0.0056902524,0.023920862,0.036583707,0.0027325328,0.6814844,0.003436959],"about_ca_topic_score_codex":0.00023783802,"about_ca_topic_score_gemma":0.00028587124,"teacher_disagreement_score":0.6800277,"about_ca_system_score_codex":0.000027227792,"about_ca_system_score_gemma":0.000095021845,"threshold_uncertainty_score":0.97224194},"labels":[],"label_agreement":null},{"id":"W4396577216","doi":"10.1101/2024.05.01.591988","title":"Atlas of imprinted and allele-specific DNA methylation in the human body","year":2024,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Cancer Research","funders":"","keywords":"Atlas (anatomy); DNA methylation; Allele; Genomic imprinting; Genetics; Methylation; Biology; DNA; Gene; Anatomy; Gene expression","score_opus":0.012893020779266278,"score_gpt":0.23550915114002885,"score_spread":0.22261613036076258,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396577216","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9943504,0.004430638,0.00026426863,0.00012847349,0.00026289918,0.0004678123,0.000035584428,0.000025548456,0.000034379485],"genre_scores_gemma":[0.9981109,0.00064553437,0.00081934006,0.000040809075,0.00023917323,0.00007109235,0.0000018126212,0.0000649011,0.000006463893],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9980589,0.00014530242,0.0005126283,0.00075804704,0.00021493009,0.00031014808],"domain_scores_gemma":[0.99860954,0.000020699235,0.0002342729,0.000913227,0.00015236772,0.00006989795],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0007504915,0.00034232705,0.0003360087,0.00016016136,0.00006479549,0.00010985725,0.00042863257,0.00041924312,0.000011681399],"category_scores_gemma":[0.00007104311,0.00030020162,0.00012699018,0.00022140949,0.00011471961,0.000003274895,0.0008170022,0.00046339314,0.0000069515445],"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":[0.000004184459,0.000047290323,0.0033632892,0.00023291267,0.00007724461,0.0000055275123,0.00002184691,0.000014037111,0.99564755,0.00045384176,0.00012388715,0.0000083720815],"study_design_scores_gemma":[0.00032602,0.000103492755,0.25655997,0.00017428816,0.00005585575,1.0261449e-7,0.000017397788,0.0001029442,0.73600525,0.00002089768,0.006243724,0.0003900436],"about_ca_topic_score_codex":0.000046013647,"about_ca_topic_score_gemma":0.0000053609506,"teacher_disagreement_score":0.2596423,"about_ca_system_score_codex":0.000031616753,"about_ca_system_score_gemma":0.0001220935,"threshold_uncertainty_score":0.999945},"labels":[],"label_agreement":null},{"id":"W4396900582","doi":"10.1002/ajmg.a.63625","title":"Adults with paternal <scp>UPD14</scp> causing <scp>Kagami–Ogata</scp> syndrome: Case report and review of the literature","year":2024,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University; Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Neurocognitive; Uniparental disomy; Natural history; Medicine; Pediatrics; Genetics; Biology; Chromosome; Internal medicine; Psychiatry; Gene; Karyotype","score_opus":0.011795043137920696,"score_gpt":0.2921715514607239,"score_spread":0.2803765083228032,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396900582","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.12290936,0.87584895,0.0000878941,0.00008384974,0.0005774477,0.00038793669,0.000057108573,0.0000047932504,0.000042670832],"genre_scores_gemma":[0.004683985,0.9930899,0.0009246224,0.00029088228,0.0005368954,0.00001630575,0.000050244085,0.00010459747,0.00030255303],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.9951073,0.00046990387,0.0019154703,0.00065034546,0.0013207204,0.00053624716],"domain_scores_gemma":[0.9953971,0.00018782142,0.0025535822,0.0008384242,0.000419457,0.0006036439],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0016090636,0.00065041473,0.0020522391,0.00014575168,0.000095685624,0.00009324226,0.00069414737,0.00040744618,0.000008435202],"category_scores_gemma":[0.0016899295,0.00037365462,0.000747514,0.0006789205,0.0007298205,0.000006062005,0.00063597295,0.0012095328,0.0000026402627],"study_design_candidate":"design_other","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":[0.000003947063,0.00015952523,0.000310468,0.0726812,0.002279775,0.069826245,0.00053766585,0.0000035994276,0.00003938746,0.0000024874578,0.01046239,0.8436933],"study_design_scores_gemma":[0.0001940413,0.00074260274,0.00004545551,0.121058375,0.0013727675,0.44675764,0.00018907772,0.0000041330945,0.000028527227,0.000002752682,0.42952204,0.00008258579],"about_ca_topic_score_codex":0.000018794588,"about_ca_topic_score_gemma":0.000008228453,"teacher_disagreement_score":0.8436107,"about_ca_system_score_codex":0.000031605403,"about_ca_system_score_gemma":0.0012390998,"threshold_uncertainty_score":0.99987155},"labels":[],"label_agreement":null},{"id":"W4397048300","doi":"10.1681/asn.20233411s1809b","title":"A Case of Primary Pseudohypoparathyroidism Presenting with Normal Serum Phosphorus","year":2023,"lang":"en","type":"article","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Wilfrid Laurier University","funders":"","keywords":"Pseudohypoparathyroidism; Phosphorus; Endocrinology; Internal medicine; Medicine; Primary (astronomy); Parathyroid hormone; Chemistry; Calcium","score_opus":0.011535097335196963,"score_gpt":0.24277431809430894,"score_spread":0.23123922075911196,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4397048300","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985943,0.00033564118,0.00016969963,0.00069143326,0.000058068632,0.00007006853,0.000006480949,0.000002754595,0.000071548624],"genre_scores_gemma":[0.9946109,0.00040355365,0.0039631627,0.0007458413,0.00012763249,0.000001362426,0.0000011774417,0.00001578027,0.00013056815],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99901694,0.00008274034,0.00038101492,0.00012547578,0.00015309884,0.00024070116],"domain_scores_gemma":[0.99843615,0.00003678457,0.0010612495,0.0002607016,0.00015634578,0.000048741993],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034526963,0.00010950554,0.00034579434,0.000026756681,0.000066023546,0.0000046398004,0.00028944912,0.00005557421,0.0000028899499],"category_scores_gemma":[0.000026340633,0.00007466971,0.00034145138,0.00028636827,0.00048796498,0.0000043432165,0.00025846608,0.00015086649,5.8821036e-7],"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":[0.000083551684,0.000053694395,0.033066507,0.000028853938,0.00039114116,0.00003727763,0.00039730596,0.00066803524,0.95047325,0.0000027290725,0.0125168925,0.0022807473],"study_design_scores_gemma":[0.0018052458,0.0030283413,0.8264145,0.000028692613,0.0002227146,0.020611504,0.0037216758,0.00050575676,0.13180901,0.00006552272,0.011517693,0.0002693001],"about_ca_topic_score_codex":0.00006357338,"about_ca_topic_score_gemma":0.0000036873464,"teacher_disagreement_score":0.81866425,"about_ca_system_score_codex":0.0000092348455,"about_ca_system_score_gemma":0.00013164464,"threshold_uncertainty_score":0.30449426},"labels":[],"label_agreement":null},{"id":"W4399868159","doi":"10.3389/fendo.2024.1403470","title":"Puberty in girls with Prader-Willi syndrome: cohort evaluation and clinical recommendations in a Latin American tertiary center","year":2024,"lang":"en","type":"article","venue":"Frontiers in Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Western Ontario; London Health Sciences Centre; Western University","funders":"","keywords":"Adrenarche; Medicine; Menarche; Precocious puberty; Breast development; Bone age; Body mass index; Pediatrics; Cohort; Pubic hair; Gynecology; Endocrinology; Internal medicine; Hormone","score_opus":0.01361965296480214,"score_gpt":0.30474418857863667,"score_spread":0.2911245356138345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399868159","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99508566,0.0011420243,0.0009296338,0.0015807806,0.00050384854,0.0004428787,0.0000069661614,0.00001021903,0.00029801924],"genre_scores_gemma":[0.99186033,0.0011963283,0.006404715,0.00017846421,0.000031652904,0.00011222488,0.00008898457,0.000019640365,0.00010767398],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983421,0.00026147114,0.00041397818,0.0005309122,0.000087712855,0.00036380536],"domain_scores_gemma":[0.9996318,0.000030794155,0.00005972506,0.00021071768,0.000021214868,0.000045730143],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036462213,0.00014153976,0.00025886105,0.00024446766,0.000019055069,0.000021675942,0.000105651125,0.00009414507,0.00001607611],"category_scores_gemma":[0.00010456975,0.0001295592,0.000035447647,0.00023131527,0.00017926053,0.000008602575,0.00010368819,0.00025282605,0.0000022699044],"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":[0.0000044267267,0.000070805065,0.9084147,0.000012481896,0.000050296247,0.000013606762,0.000052079147,0.00002768791,0.00009817036,0.0000067634573,0.00083016994,0.0904188],"study_design_scores_gemma":[0.0009658505,0.00025974517,0.98844165,0.00006020411,0.000019332909,0.00018035498,0.00024465047,0.0028094118,0.00004907269,0.00007412812,0.006744845,0.0001507625],"about_ca_topic_score_codex":0.00019113497,"about_ca_topic_score_gemma":0.00084355177,"teacher_disagreement_score":0.09026804,"about_ca_system_score_codex":0.00005324512,"about_ca_system_score_gemma":0.00008340861,"threshold_uncertainty_score":0.52832705},"labels":[],"label_agreement":null},{"id":"W4400680892","doi":"10.1075/bpa.18.11gar","title":"The narrative abilities of Spanish monolinguals and Spanish–Catalan bilinguals with Prader–Willi syndrome","year":2024,"lang":"en","type":"book-chapter","venue":"Bilingual processing and acquisition","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Catalan; Narrative; Psychology; Linguistics; Philosophy","score_opus":0.008256167356345505,"score_gpt":0.23601341544831253,"score_spread":0.227757248091967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400680892","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9468552,0.04483047,0.000052194613,0.00016188045,0.00017057722,0.00043059562,0.000056943063,0.000038736205,0.007403402],"genre_scores_gemma":[0.95965284,0.0018277349,0.0004671386,0.00004295535,0.00033964877,0.000012703035,0.00010328574,0.000091530695,0.03746214],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99823934,0.000023903624,0.0004803551,0.0007239864,0.00024617516,0.000286218],"domain_scores_gemma":[0.9989635,0.00005985952,0.00034674566,0.0003091768,0.00023305308,0.000087695174],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00031770865,0.00041614624,0.00040971246,0.000077620585,0.0003436608,0.00022610826,0.00013907168,0.00034147233,0.000008082305],"category_scores_gemma":[0.00005761107,0.00029056065,0.00008278706,0.000043361415,0.00061089377,0.000010489557,0.00018301758,0.0002328317,0.0000018155652],"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":[0.0004679996,0.0006111844,0.005578683,0.031664457,0.0057611475,0.00023361816,0.08148364,0.0004724967,0.3472468,0.028938062,0.0009024973,0.4966394],"study_design_scores_gemma":[0.010413878,0.033566434,0.019355854,0.04880068,0.006015404,0.028791223,0.11788273,0.0026334377,0.16867153,0.25127143,0.29583263,0.016764775],"about_ca_topic_score_codex":0.00001566122,"about_ca_topic_score_gemma":0.000020418576,"teacher_disagreement_score":0.47987464,"about_ca_system_score_codex":0.000014439984,"about_ca_system_score_gemma":0.00027044775,"threshold_uncertainty_score":0.99995464},"labels":[],"label_agreement":null},{"id":"W4401041830","doi":"","title":"D’une myopathie centronucléaire du Labrador aux rôles des acides gras à très longue chaîne chez les mammifères : Étude des gènes Hacd","year":2013,"lang":"fr","type":"dissertation","venue":"HAL (Le Centre pour la Communication Scientifique Directe)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Humanities; Art","score_opus":0.010689998265768257,"score_gpt":0.2175778906622948,"score_spread":0.20688789239652655,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401041830","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9620283,0.02114445,0.008766935,0.0025707653,0.00038439507,0.000669192,0.000077958386,0.00010196892,0.004255983],"genre_scores_gemma":[0.94059277,0.010356337,0.024572128,0.000061421284,0.00014883943,0.00014332125,0.002499532,0.00016533557,0.021460306],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99342054,0.002785288,0.0009890961,0.0013119199,0.00047003897,0.001023138],"domain_scores_gemma":[0.9936807,0.00038746223,0.00081655406,0.0016501921,0.0030433582,0.00042169922],"candidate_categories":["metaepi_narrow","sts"],"consensus_categories":[],"category_scores_codex":[0.0021237426,0.00088477985,0.00071818044,0.00019770485,0.00156069,0.0006150922,0.0014617695,0.00082848663,0.0004858712],"category_scores_gemma":[0.0021386866,0.0009315383,0.00051299884,0.00050543295,0.0013038127,0.00006039286,0.00062687317,0.0004947686,0.000121767785],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000038151607,0.0011879173,0.10215215,0.0013880533,0.0004939526,0.00001364171,0.028509773,0.00008131288,0.44525036,0.007591589,0.00061553746,0.41267756],"study_design_scores_gemma":[0.0011364801,0.00001146331,0.39472675,0.0031029873,0.0002441078,0.00010897114,0.0065489807,0.0020990781,0.5762636,0.00091304566,0.013580232,0.0012642806],"about_ca_topic_score_codex":0.016828252,"about_ca_topic_score_gemma":0.046201482,"teacher_disagreement_score":0.41141328,"about_ca_system_score_codex":0.00010685641,"about_ca_system_score_gemma":0.0003723846,"threshold_uncertainty_score":0.99973917},"labels":[],"label_agreement":null},{"id":"W4401745747","doi":"10.36557/pbpc.v3i2.148","title":"SÍNDROME DE PERLMAN: CORRELAÇÕES ENTRE MUTAÇÃO GENÉTICA, MANIFESTAÇÕES CLÍNICAS E PROGNÓSTICO DE SOBREVIVÊNCIA: UMA REVISÃO SISTEMÁTICA.","year":2024,"lang":"pt","type":"article","venue":"Periódicos Brasil Pesquisa Científica","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Intégré de Santé et de Services Sociaux des Laurentides","funders":"","keywords":"Medicine","score_opus":0.015175228881172101,"score_gpt":0.27333768476774833,"score_spread":0.2581624558865762,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401745747","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93694305,0.04660837,0.004949432,0.002168993,0.0024747727,0.0014973942,0.00024439272,0.00030435834,0.004809212],"genre_scores_gemma":[0.9811603,0.0025196068,0.0025493875,0.00077230023,0.0015061101,0.00020945293,0.00023081792,0.00031349063,0.010738548],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9918436,0.00058769557,0.0015029815,0.0025014298,0.0009061703,0.0026581506],"domain_scores_gemma":[0.996337,0.00022440981,0.00034880533,0.0016532887,0.00029846778,0.0011380565],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0014927746,0.0012706236,0.0011039049,0.00034740046,0.0007139913,0.00102816,0.0013822975,0.0010585788,0.0021089055],"category_scores_gemma":[0.0009936433,0.0013026146,0.0010915218,0.0007794759,0.0005439042,0.000041027793,0.0010246602,0.0010189443,0.0010242723],"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":[0.0003473721,0.004641027,0.100447826,0.020113414,0.004577274,0.0039539034,0.019660868,0.0004189085,0.5643457,0.008288265,0.04602942,0.227176],"study_design_scores_gemma":[0.0052409046,0.006937591,0.13833337,0.008447705,0.00576192,0.02665372,0.019908577,0.081667386,0.040045798,0.0005154557,0.65717447,0.009313136],"about_ca_topic_score_codex":0.00003327699,"about_ca_topic_score_gemma":0.000049755567,"teacher_disagreement_score":0.611145,"about_ca_system_score_codex":0.00046405543,"about_ca_system_score_gemma":0.0015333443,"threshold_uncertainty_score":0.99975353},"labels":[],"label_agreement":null},{"id":"W4402900588","doi":"10.1002/ajmg.a.63864","title":"Diagnosis of <i>TET3</i>‐Related Beck–Fahrner Syndrome in an Individual With Chorioretinal and Iris Colobomata Using a <scp>DNA</scp> Methylation Signature","year":2024,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; McMaster Children's Hospital; Western University; London Health Sciences Centre; McMaster University","funders":"Government of Canada; Ontario Genomics; Genome Canada","keywords":"Epigenetics; Genetics; DNA methylation; Phenotype; Biology; Mendelian inheritance; Gene","score_opus":0.012154073577251978,"score_gpt":0.27700099732080485,"score_spread":0.2648469237435529,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402900588","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9904699,0.008647766,0.0004099132,0.00020423501,0.00013697999,0.00009265001,0.00001652131,0.0000045359475,0.000017531494],"genre_scores_gemma":[0.9935257,0.0020628811,0.004145325,0.00008735221,0.000109016226,0.0000049921127,0.000019625555,0.000034017983,0.000011131336],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99786156,0.00016228762,0.0006343636,0.00030649724,0.00073783525,0.00029744193],"domain_scores_gemma":[0.9989117,0.00012045101,0.0003578154,0.00018263928,0.00011725911,0.0003101277],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086086965,0.00020198268,0.00041697614,0.00017954702,0.00003549834,0.000051387105,0.00030944776,0.00020810946,0.000029322167],"category_scores_gemma":[0.00023146675,0.0001619906,0.00008520364,0.00038855834,0.0004389434,0.000011257949,0.00013472246,0.00039138945,4.612579e-7],"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":[0.00009905643,0.0007572349,0.5083145,0.0004182413,0.0016205161,0.0010838709,0.004103219,0.0023610718,0.2352552,0.00006508626,0.0010074083,0.24491462],"study_design_scores_gemma":[0.008264962,0.036031436,0.71765643,0.006246516,0.00226371,0.02653022,0.012699266,0.018033616,0.12112959,0.0005046806,0.04916196,0.0014776043],"about_ca_topic_score_codex":0.00003202187,"about_ca_topic_score_gemma":0.000016037638,"teacher_disagreement_score":0.243437,"about_ca_system_score_codex":0.000015377147,"about_ca_system_score_gemma":0.00032284265,"threshold_uncertainty_score":0.6605785},"labels":[],"label_agreement":null},{"id":"W4402953928","doi":"","title":"[Angelman syndrome: current approach and the future of therapies].","year":2024,"lang":"en","type":"review","venue":"PubMed","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Angelman syndrome; Current (fluid); Psychology; Computer science; Medicine; Biology; Genetics; Engineering; Electrical engineering","score_opus":0.024940484383216083,"score_gpt":0.2648798148217039,"score_spread":0.23993933043848784,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402953928","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00023767698,0.99730116,0.000020297151,0.000040312032,0.0006123199,0.0012183135,0.000026526188,0.0000073024826,0.00053608115],"genre_scores_gemma":[0.0011110218,0.9963765,0.00006957076,0.000011648286,0.00040752397,0.0014474384,0.00007613807,0.00004418205,0.00045596345],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9987602,0.00012262151,0.00034149096,0.00039933663,0.00012023577,0.0002560736],"domain_scores_gemma":[0.9992893,0.000013038885,0.0001744905,0.00044145487,0.00002303329,0.00005873242],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004330214,0.0002826553,0.000717445,0.000053104483,0.000036611276,0.000041081654,0.00030707385,0.00020766952,0.0000020331406],"category_scores_gemma":[0.000018111723,0.00015078082,0.00037510187,0.00013081229,0.00015698747,9.175192e-7,0.00030883704,0.00022362328,0.0000024004778],"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":[0.0000013965079,0.000014199693,0.000003409741,0.006485656,0.0002661513,4.483948e-7,0.000019401827,3.9273267e-8,2.506977e-7,0.00015989052,0.000565783,0.9924834],"study_design_scores_gemma":[0.00019835678,0.000013983313,0.00020300908,0.00033532432,0.0006190125,0.0002740414,0.000031858748,0.0000013172147,0.0000010891324,0.00004089308,0.99811065,0.00017044866],"about_ca_topic_score_codex":0.000002136966,"about_ca_topic_score_gemma":6.563096e-7,"teacher_disagreement_score":0.9975449,"about_ca_system_score_codex":0.0000071578916,"about_ca_system_score_gemma":0.000042008807,"threshold_uncertainty_score":0.6148663},"labels":[],"label_agreement":null},{"id":"W4403025409","doi":"10.1101/2024.09.30.615881","title":"Quorum sensing and DNA methylation play active roles in clinical <i>Burkholderia</i> phase variation","year":2024,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut National de la Recherche Scientifique","funders":"","keywords":"Quorum sensing; Phase variation; DNA methylation; Variation (astronomy); DNA; Burkholderia; Methylation; Phase (matter); Biofilm; Biology; Computational biology; Genetics; Chemistry; Bacteria; Physics; Gene; Phenotype","score_opus":0.014557304331403976,"score_gpt":0.2720955192083499,"score_spread":0.25753821487694595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403025409","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942296,0.0017321599,0.0021169442,0.0001937172,0.0010748984,0.0004903003,0.00008623409,0.00005974858,0.000016369591],"genre_scores_gemma":[0.9950977,0.00050525786,0.003518178,0.00011995459,0.00062755984,0.000027560776,0.0000023957336,0.0000962925,0.0000051003044],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9972678,0.0002449376,0.0007233354,0.001170309,0.00019084479,0.0004028082],"domain_scores_gemma":[0.9986416,0.000045580666,0.000336533,0.0006605956,0.00015611076,0.00015956686],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0010153162,0.00042215563,0.000462373,0.00018126969,0.00007727807,0.00018478026,0.0001820708,0.0007785218,0.000005604839],"category_scores_gemma":[0.00035056172,0.00046445912,0.00014601552,0.00020078286,0.00008473337,0.000007603484,0.0008185486,0.00062811066,0.000011078353],"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":[0.00002962731,0.000089327565,0.0009037052,0.00012880092,0.00014402343,0.000013319791,0.00002220295,0.00005196601,0.9982795,0.000042613803,0.000051194856,0.00024368131],"study_design_scores_gemma":[0.00164267,0.00023464668,0.14384723,0.00045834135,0.00019139427,2.1458371e-7,0.000015560614,0.0033401647,0.84644014,0.000024654062,0.0029202327,0.00088477606],"about_ca_topic_score_codex":0.00005035835,"about_ca_topic_score_gemma":0.000013328938,"teacher_disagreement_score":0.1518394,"about_ca_system_score_codex":0.00006501943,"about_ca_system_score_gemma":0.00037402642,"threshold_uncertainty_score":0.9997807},"labels":[],"label_agreement":null},{"id":"W4403053527","doi":"10.1101/gr.279273.124","title":"High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation","year":2024,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":77,"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 Bulletin of Medical History","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute on Drug Abuse; National Institute on Aging; Fonds Wetenschappelijk Onderzoek; National Institute of Standards and Technology; Lustgarten Foundation; National Cancer Institute; National Institutes of Health; National Science Foundation","keywords":"Biology; Indel; 1000 Genomes Project; Structural variation; Genome; Computational biology; Genetics; Concordance; Human genome; Whole genome sequencing; Personal genomics; DNA sequencing; Nanopore sequencing; Copy-number variation; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.06116980272795516,"score_gpt":0.3402952870025182,"score_spread":0.2791254842745631,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403053527","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9912265,0.006544724,0.001047158,0.00013535483,0.00008134527,0.0005730255,0.00022782676,0.000008301711,0.00015579164],"genre_scores_gemma":[0.9962531,0.00046485115,0.0025293864,0.0000288903,0.00023546001,0.000042174994,0.0002411149,0.000031685333,0.00017338173],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9982191,0.00020506841,0.000356458,0.00045754344,0.00039343827,0.00036841613],"domain_scores_gemma":[0.99882245,0.00011792979,0.00006319318,0.0005798153,0.00035967148,0.000056935714],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050558796,0.0001409048,0.0002143637,0.00015208914,0.00013922216,0.000058163285,0.00044311705,0.00010487917,0.000056804813],"category_scores_gemma":[0.00007873564,0.00011063173,0.00008540128,0.00045832185,0.00012678688,0.000003650378,0.0004734621,0.00015963992,0.000013507595],"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":[0.000009423416,0.000016016187,0.001079885,0.0001180744,0.00012444894,0.0000036337888,0.0014256709,0.00038090904,0.99357647,0.00015379346,0.00017084148,0.0029408277],"study_design_scores_gemma":[0.0005319716,0.0015355895,0.3484671,0.00022142554,0.000063426705,0.000035354216,0.002180136,0.00012744656,0.62297255,0.0014732606,0.021962008,0.00042971916],"about_ca_topic_score_codex":0.0048905876,"about_ca_topic_score_gemma":0.00012308812,"teacher_disagreement_score":0.37060395,"about_ca_system_score_codex":0.0000542886,"about_ca_system_score_gemma":0.0003956972,"threshold_uncertainty_score":0.73931384},"labels":[],"label_agreement":null},{"id":"W4403463613","doi":"10.1210/clinem/dgae730","title":"Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver–Russell Syndrome and Focus on the <i>IGF1R</i> Gene","year":2024,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Hospital Foundation","funders":"Ministero della Salute","keywords":"Macrocephaly; Genetics; Genetic heterogeneity; Context (archaeology); Genetic testing; Biology; Genotype; Allele; Medicine; Gene; Phenotype","score_opus":0.03834019508968787,"score_gpt":0.3381296966635877,"score_spread":0.29978950157389983,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403463613","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98208106,0.010019088,0.0004581297,0.0054444,0.0014702476,0.000144324,0.0000063864854,0.000006812751,0.0003695479],"genre_scores_gemma":[0.9942622,0.0035808904,0.0009417947,0.00045751862,0.00063161633,0.000006765147,0.000002573997,0.000021705508,0.00009488904],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99782324,0.0005275,0.0009280621,0.0002364589,0.00016887364,0.00031589437],"domain_scores_gemma":[0.99814975,0.0011033711,0.00024831644,0.0003266605,0.00008476987,0.000087120716],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00111504,0.00016854385,0.0003525683,0.0000809185,0.00014574695,0.00006488702,0.00038258,0.0001083553,0.000020253216],"category_scores_gemma":[0.0013983282,0.00009879279,0.00019432412,0.00014786943,0.00027150047,0.000008415997,0.0001543395,0.00062505837,0.000010503112],"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":[0.0022673022,0.0019431689,0.037281703,0.00022924862,0.007063531,0.0024575833,0.004776557,0.018107248,0.3618208,0.04336273,0.010233484,0.5104567],"study_design_scores_gemma":[0.008212727,0.003900064,0.7798402,0.00031905438,0.0017933497,0.012631862,0.001291032,0.0027005998,0.025703706,0.015924364,0.14666556,0.0010174938],"about_ca_topic_score_codex":0.000027874981,"about_ca_topic_score_gemma":0.00003285406,"teacher_disagreement_score":0.7425585,"about_ca_system_score_codex":0.000006804655,"about_ca_system_score_gemma":0.00012295265,"threshold_uncertainty_score":0.40286532},"labels":[],"label_agreement":null},{"id":"W4403513920","doi":"10.1093/omcr/omae114","title":"Rhythmic high-amplitude delta with superimposed spikes (RHADS): a treatment dilemma","year":2024,"lang":"en","type":"article","venue":"Oxford Medical Case Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Pathognomonic; Electroencephalography; Rhythm; Medicine; Subclinical infection; Ictal; Neuroscience; Delta Rhythm; Audiology; Psychology; Psychiatry; Internal medicine; Alpha rhythm","score_opus":0.009904330234463906,"score_gpt":0.25748594776313666,"score_spread":0.24758161752867275,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403513920","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9947795,0.0019056696,0.00169498,0.00039396217,0.00038487968,0.00027454513,0.000010198781,0.000056400917,0.0004998537],"genre_scores_gemma":[0.99678475,0.00034180682,0.0014690174,0.00010714914,0.00043107034,0.00008093763,0.00014055254,0.000047456935,0.0005972639],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99814665,0.000031994576,0.00039372485,0.0006632516,0.00036022844,0.0004041485],"domain_scores_gemma":[0.99897087,0.000022985869,0.00006151829,0.0005251485,0.0000503306,0.00036916064],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025576376,0.00025807123,0.00024821004,0.000047728092,0.00008565912,0.00007554149,0.00005351344,0.00020571868,0.00024262855],"category_scores_gemma":[0.00013067643,0.0001773574,0.00013102536,0.00011239352,0.00010346612,0.000004525256,0.000097462,0.000111165136,0.0000048774677],"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":[0.00009126304,0.00045053553,0.013410079,0.00038007012,0.0007425061,0.71403563,0.0002316203,0.00004910683,0.08390144,0.0006579697,0.0012846104,0.18476519],"study_design_scores_gemma":[0.00060352666,0.0016154598,0.0018767215,0.0001647336,0.00012557674,0.5566172,0.00006304604,0.00019553138,0.013787408,0.00007955218,0.4244594,0.00041185817],"about_ca_topic_score_codex":0.0004656099,"about_ca_topic_score_gemma":0.000193891,"teacher_disagreement_score":0.4231748,"about_ca_system_score_codex":0.000042188283,"about_ca_system_score_gemma":0.0004161132,"threshold_uncertainty_score":0.72324246},"labels":[],"label_agreement":null},{"id":"W4404090810","doi":"10.1183/13993003.congress-2024.pa1356","title":"Oxygenation and ventilation parameters in children with Prader-Willi syndrome without or with growth hormone treatment.","year":2024,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Oxygenation; Ventilation (architecture); Medicine; Growth hormone; Internal medicine; Cardiology; Hormone","score_opus":0.008769696045770952,"score_gpt":0.2270032696700938,"score_spread":0.21823357362432283,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404090810","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970188,0.0005882249,0.0016802554,0.000093003786,0.000018675559,0.00033007452,0.0000034354337,0.000020394982,0.00024714397],"genre_scores_gemma":[0.9944126,0.00029721324,0.0041553187,0.000023571043,0.000019901157,0.000035482957,0.000053283566,0.00002391219,0.0009787156],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992807,0.000017460297,0.00011495063,0.00034003647,0.000085564985,0.00016127632],"domain_scores_gemma":[0.9997829,0.0000052880587,0.00002876289,0.00012042287,0.00001788616,0.000044690747],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000054454547,0.0001450619,0.00011228501,0.00007135454,0.000031498792,0.00006460011,0.00003946548,0.000064908134,0.000009171657],"category_scores_gemma":[0.00000595771,0.000087652414,0.000018954828,0.00013371662,0.000039230716,0.0000089700125,0.00002062785,0.000037455462,0.000002247478],"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":[0.000040265208,0.000117635595,0.96862,0.00004106101,0.00048030287,0.000008570036,0.0001875227,0.00015916902,0.021583267,0.000058068756,0.00010513599,0.008598989],"study_design_scores_gemma":[0.0009659167,0.0024055138,0.98818046,0.00004240342,0.000054008327,0.0010768825,0.00007165442,0.0005670208,0.0061644088,0.000014441604,0.00025966775,0.00019761719],"about_ca_topic_score_codex":0.00011127701,"about_ca_topic_score_gemma":0.00010205674,"teacher_disagreement_score":0.019560453,"about_ca_system_score_codex":0.000017610011,"about_ca_system_score_gemma":0.000044838904,"threshold_uncertainty_score":0.35743618},"labels":[],"label_agreement":null},{"id":"W4404318525","doi":"10.1136/jmg-2024-110115","title":"Long-read sequencing for detection and subtyping of Prader-Willi and Angelman syndromes","year":2024,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; BC Children's Hospital; Hospital for Sick Children; Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"Canadian Institutes of Health Research; Canada Research Chairs; BC Cancer Agency; Simons Foundation Autism Research Initiative; BC Children's Hospital","keywords":"Subtyping; Angelman syndrome; Proband; Genetics; Genomic imprinting; Biology; Uniparental disomy; Multiplex ligation-dependent probe amplification; Computational biology; DNA methylation; Mutation; Computer science; Gene; Exon; Karyotype; Chromosome","score_opus":0.022827214892635048,"score_gpt":0.2930482432374433,"score_spread":0.2702210283448082,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404318525","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94779575,0.02419968,0.0272648,0.0003341272,0.00030340638,0.00007936031,0.0000028013646,0.0000026135945,0.000017460816],"genre_scores_gemma":[0.99132013,0.00549512,0.0027695845,0.00004309521,0.0003109516,0.0000016095671,0.0000016606111,0.000015855183,0.000041974206],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990707,0.000028724888,0.00035377804,0.00014439686,0.000259873,0.000142507],"domain_scores_gemma":[0.99951714,0.00004969038,0.00012502067,0.00008053317,0.00008763258,0.00013999491],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005875427,0.000093275135,0.00017521804,0.00007051985,0.000034229986,0.000030494173,0.00009716278,0.00016768498,0.000009428212],"category_scores_gemma":[0.00027172134,0.00007708165,0.00007099134,0.000055609067,0.00009290135,0.0000038722737,0.00007346875,0.0001263008,1.4775885e-7],"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":[0.000012225781,0.000038659662,0.011110044,0.0010404229,0.0003225913,0.000019469333,0.0003325368,0.000053795688,0.53539014,0.00004314816,0.00021007098,0.4514269],"study_design_scores_gemma":[0.0051237545,0.011822906,0.19038005,0.0039295834,0.0010219066,0.023875937,0.0025485035,0.036831323,0.6363414,0.0017912381,0.085096985,0.00123644],"about_ca_topic_score_codex":0.0000043370715,"about_ca_topic_score_gemma":0.000009426024,"teacher_disagreement_score":0.45019045,"about_ca_system_score_codex":0.0000097956445,"about_ca_system_score_gemma":0.0001284551,"threshold_uncertainty_score":0.31432986},"labels":[],"label_agreement":null},{"id":"W4404867725","doi":"10.1515/med-2024-1058","title":"A bibliometric analysis of Prader-Willi syndrome from 2002 to 2022","year":2024,"lang":"en","type":"article","venue":"Open Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Web of science; Citation; Library science; Pathology; Meta-analysis","score_opus":0.023543982914768582,"score_gpt":0.32062748842251615,"score_spread":0.2970835055077476,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404867725","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9818978,0.009108232,0.002128157,0.0013015403,0.00030907005,0.0002650006,0.00006287833,0.000007544087,0.004919784],"genre_scores_gemma":[0.990151,0.0005762568,0.0013121067,0.00034899783,0.00011421965,0.000021524693,0.0001509103,0.000019960591,0.007305054],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99872345,0.000038497525,0.00033453124,0.0004512141,0.00025316613,0.00019916556],"domain_scores_gemma":[0.9992162,0.00004252539,0.000060337712,0.0004741659,0.00006705018,0.00013970974],"candidate_categories":["bibliometrics","insufficient_payload"],"consensus_categories":["bibliometrics"],"category_scores_codex":[0.00042300715,0.00013208484,0.00038129106,0.012816849,0.000029886167,0.000046072793,0.00049101777,0.00007983963,0.003268678],"category_scores_gemma":[0.00024266564,0.00010436232,0.00009622054,0.05736905,0.000044849516,0.0000043655523,0.00041241598,0.000069011396,0.000056603843],"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":[0.000006709755,0.00011256418,0.03781963,0.000097723234,0.004515684,0.000028111843,0.00038974333,0.0002259281,0.7107811,0.00005418736,0.07491272,0.17105593],"study_design_scores_gemma":[0.00052006234,0.0010670654,0.6437887,0.00018082975,0.0010669694,0.00004144365,0.00028953652,0.0007995315,0.0064818864,0.000036476245,0.34545553,0.0002719581],"about_ca_topic_score_codex":0.001136865,"about_ca_topic_score_gemma":0.000056321358,"teacher_disagreement_score":0.7042992,"about_ca_system_score_codex":0.000009266384,"about_ca_system_score_gemma":0.000046954538,"threshold_uncertainty_score":0.998372},"labels":[],"label_agreement":null},{"id":"W4405422020","doi":"10.1002/ajmg.a.63961","title":"Community‐Sourced Reporting of Mortalities in Angelman Syndrome (1979–2022)","year":2024,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pierre Elliott Trudeau Foundation","funders":"National Center for Research Resources; Ionis Pharmaceuticals; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Ultragenyx Pharmaceutical","keywords":"Medicine; Epilepsy; Population; Life expectancy; Incidence (geometry); Epidemiology; Angelman syndrome; Psychiatry; Pediatrics; Sudden infant death syndrome; Public health; Demography; Gerontology; Environmental health; Pathology","score_opus":0.024672327748454365,"score_gpt":0.31726265589703473,"score_spread":0.2925903281485804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405422020","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99391854,0.004476601,0.00050239154,0.00043052604,0.0003740953,0.00005882437,0.0000042762726,0.000004998538,0.00022973306],"genre_scores_gemma":[0.9972193,0.0012516002,0.0010667035,0.00013500007,0.00016470056,0.0000029043463,0.000007701937,0.00002803596,0.00012405225],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99691606,0.000269336,0.0016926125,0.0001658585,0.0006713488,0.00028480202],"domain_scores_gemma":[0.99828,0.00006972632,0.0010067712,0.0003207816,0.000108812725,0.00021391475],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0028302646,0.00015448395,0.00050374895,0.00016393971,0.000038465387,0.000025608644,0.00045914453,0.00010993913,0.00006662662],"category_scores_gemma":[0.0010254394,0.00013521429,0.00020369301,0.00030664413,0.0003803243,0.0000034387672,0.00022365653,0.0005213579,0.0000018651019],"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":[0.00010300986,0.000821011,0.30283457,0.0009585542,0.0015769161,0.0021264718,0.00683192,0.0013256001,0.23773998,0.00013140174,0.004527395,0.44102317],"study_design_scores_gemma":[0.0037335518,0.019631967,0.63756233,0.0066101095,0.00055362313,0.036798343,0.040785264,0.004054022,0.07778948,0.00080031535,0.16964932,0.002031659],"about_ca_topic_score_codex":0.00012482174,"about_ca_topic_score_gemma":0.000042850934,"teacher_disagreement_score":0.4389915,"about_ca_system_score_codex":0.000015443002,"about_ca_system_score_gemma":0.00031836657,"threshold_uncertainty_score":0.55138785},"labels":[],"label_agreement":null},{"id":"W4405422616","doi":"10.1186/s12916-024-03804-2","title":"Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"BMC Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Economic and Social Research Council; Biotechnology and Biological Sciences Research Council; Directorate for Biological Sciences; Linköpings Universitet","keywords":"DNA methylation; Methylation; Epigenetics; Genetics; Biology; Pyrosequencing; Genomic imprinting; Differentially methylated regions; Methyltransferase; Quantitative trait locus; Gene; Gene expression","score_opus":0.0224369532210712,"score_gpt":0.28216838151881024,"score_spread":0.25973142829773904,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405422616","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98984504,0.008658921,0.00070713577,0.00013430289,0.00011852082,0.00033435997,0.000024070589,0.000016675021,0.0001609628],"genre_scores_gemma":[0.99757224,0.00066836603,0.000702932,0.000022203654,0.00026072492,0.00004991328,0.00018629536,0.00003271212,0.0005046359],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99893004,0.00003584371,0.0002254,0.00040249777,0.00018237568,0.00022386087],"domain_scores_gemma":[0.9994862,0.00001427178,0.000081113925,0.0002449656,0.00007923838,0.000094215284],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000097361095,0.00016153451,0.0001789321,0.00006937478,0.000049070426,0.000008329961,0.00009427589,0.00006931762,0.00014422179],"category_scores_gemma":[0.000038810693,0.0001234621,0.000034266042,0.00010572494,0.00008836335,0.000003804867,0.000076623684,0.000044249864,0.0000036800764],"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":[0.00005027183,0.000031527517,0.016290672,0.00048893626,0.000077564364,0.0000036274582,0.0007033194,0.00002754776,0.9636291,0.000029560671,0.00002188335,0.01864599],"study_design_scores_gemma":[0.0011065397,0.0014827648,0.21639398,0.0010667356,0.000094001756,0.00011548286,0.00054847344,0.00006842839,0.77883536,0.000009979863,0.00013245537,0.00014582361],"about_ca_topic_score_codex":0.000027516375,"about_ca_topic_score_gemma":0.00036502496,"teacher_disagreement_score":0.2001033,"about_ca_system_score_codex":0.000014527658,"about_ca_system_score_gemma":0.000040886374,"threshold_uncertainty_score":0.50346386},"labels":[],"label_agreement":null},{"id":"W4406139981","doi":"10.1136/ebnurs-2024-104171","title":"Evaluating psychiatric care for people with Prader-Willi syndrome","year":2025,"lang":"en","type":"article","venue":"Evidence-Based Nursing","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Athabasca University; University of Alberta","funders":"","keywords":"Psychiatry; Psychology; Medicine","score_opus":0.02627206680414197,"score_gpt":0.33837608166813,"score_spread":0.31210401486398803,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406139981","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9259635,0.0108683705,0.05988996,0.0016814938,0.0004991159,0.00077165576,0.000005325636,0.00002930093,0.00029123813],"genre_scores_gemma":[0.9627135,0.00003955912,0.036445424,0.00028226705,0.00011930234,0.00011497165,0.000037339523,0.000030418949,0.00021722325],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9985058,0.00009097043,0.00025838395,0.0005505562,0.00019921116,0.00039508485],"domain_scores_gemma":[0.99906635,0.00008837123,0.00012278945,0.00043663013,0.0002174287,0.00006841691],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033772434,0.00021082924,0.00022845906,0.000121629,0.0003127377,0.000072169925,0.000229248,0.00012431541,0.00001027848],"category_scores_gemma":[0.0002663983,0.00019356603,0.00012632081,0.00035214188,0.000060959286,0.000009156589,0.000029908306,0.000090085916,0.0000027402414],"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":[0.00012757932,0.00039010274,0.37711143,0.002824687,0.00029272446,0.0000020164998,0.0013045088,0.02087497,0.17589173,0.0002295898,0.003046905,0.41790375],"study_design_scores_gemma":[0.008233236,0.012398764,0.8446576,0.01486355,0.0011669731,0.00026203177,0.006770879,0.013463518,0.087461166,0.00062053726,0.0078823455,0.0022194253],"about_ca_topic_score_codex":0.000020682257,"about_ca_topic_score_gemma":0.000019458399,"teacher_disagreement_score":0.46754614,"about_ca_system_score_codex":0.000065748885,"about_ca_system_score_gemma":0.00046148716,"threshold_uncertainty_score":0.78933936},"labels":[],"label_agreement":null},{"id":"W4406169200","doi":"10.1097/scs.0000000000011045","title":"Outcomes of Tongue Reduction Surgery in Beckwith-Wiedemann Syndrome: A Systematic Review","year":2025,"lang":"en","type":"review","venue":"Journal of Craniofacial Surgery","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Izaak Walton Killam Health Centre; Dalhousie University","funders":"","keywords":"Macroglossia; Medicine; Beckwith–Wiedemann syndrome; Glossectomy; Tongue; Surgery; Drooling","score_opus":0.024410323628179156,"score_gpt":0.3075404588100349,"score_spread":0.28313013518185576,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406169200","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0036467677,0.99385464,0.000030238478,0.000047125013,0.0015652501,0.0007781028,0.000019202942,0.0000037652264,0.000054912707],"genre_scores_gemma":[0.0019780223,0.99737626,0.00005052661,0.000047545607,0.00013483092,0.000043137523,0.000034562145,0.00004240159,0.00029271713],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.99424857,0.0006407265,0.0039802953,0.00033181984,0.00045047482,0.00034810326],"domain_scores_gemma":[0.99508864,0.00047169384,0.0035117497,0.0005109725,0.00030667518,0.000110287634],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0031954036,0.00048191898,0.006526633,0.0007088681,0.00003870211,0.000024200303,0.00035766335,0.0004519711,0.000026366975],"category_scores_gemma":[0.0034288166,0.00037074048,0.002876651,0.0006133707,0.000061388324,0.000011723339,0.00011751843,0.00033888264,0.0000038864277],"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":[0.000005049864,0.00011977952,0.0012924342,0.96153706,0.00078968785,0.00006477532,0.000009628122,0.0000013163616,0.000022227574,0.0000023654893,0.0015632019,0.034592457],"study_design_scores_gemma":[0.00013426534,0.00006861064,0.001772471,0.95343083,0.0028106377,0.0033234155,0.000034613142,1.3251251e-7,0.000014258743,0.0000115613675,0.037867658,0.0005315365],"about_ca_topic_score_codex":0.00001709651,"about_ca_topic_score_gemma":0.0000025063598,"teacher_disagreement_score":0.036304455,"about_ca_system_score_codex":0.00006545628,"about_ca_system_score_gemma":0.0012506045,"threshold_uncertainty_score":0.9998745},"labels":[],"label_agreement":null},{"id":"W4406465014","doi":"10.1016/j.ajhg.2024.12.020","title":"Discovery of a DNA methylation profile in individuals with Sifrim-Hitz-Weiss syndrome","year":2025,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; Université de Montréal; London Health Sciences Centre","funders":"Ministerie van Onderwijs, Cultuur en Wetenschap; Government of Canada; Ontario Genomics; Ontario Genomics Institute; Genome Canada","keywords":"DNA methylation; Genetics; Methylation; Computational biology; Biology; DNA; Psychology; Gene; Gene expression","score_opus":0.00852832446146463,"score_gpt":0.26459059037541943,"score_spread":0.2560622659139548,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406465014","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975518,0.00075374474,0.0011464349,0.00012214518,0.000045168454,0.00013732839,0.000005277211,0.0000013937866,0.0002366842],"genre_scores_gemma":[0.99739313,0.00012320235,0.0021550541,0.000072698575,0.0000376974,0.000003693573,0.000004439883,0.000014916979,0.00019517707],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9988624,0.00013836956,0.00048030843,0.00014221644,0.00019191948,0.00018477897],"domain_scores_gemma":[0.998881,0.00002901464,0.00064345537,0.00030375583,0.000113092436,0.000029671928],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043052278,0.00013081654,0.0003202125,0.00014478837,0.000048945276,0.000026009347,0.0003646954,0.00003431317,0.0000046588484],"category_scores_gemma":[0.000034596676,0.00008929094,0.000087929795,0.00028787556,0.00026463473,0.0000052888468,0.00011712061,0.00012933926,4.6440516e-7],"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":[0.00005587368,0.00016554665,0.14494088,0.000039957395,0.000314704,0.0000062809045,0.0003919022,0.0011139774,0.84174633,0.0000818527,0.00011223214,0.011030449],"study_design_scores_gemma":[0.0009067771,0.0039669313,0.7378773,0.00016838757,0.00011809904,0.00021506056,0.0014938952,0.000030671214,0.25424838,0.00044780714,0.00033711796,0.00018958503],"about_ca_topic_score_codex":0.000016223132,"about_ca_topic_score_gemma":0.000011142669,"teacher_disagreement_score":0.5929364,"about_ca_system_score_codex":0.000014375774,"about_ca_system_score_gemma":0.00013761401,"threshold_uncertainty_score":0.3641179},"labels":[],"label_agreement":null},{"id":"W4406547971","doi":"10.1016/j.yobg.2013.05.021","title":"10.1016/j.yobg.2013.05.021","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Intracytoplasmic sperm injection; Medicine; In vitro fertilisation; Imprinting (psychology); Andrology; Human fertilization; Sperm; Embryo; Cell biology; Anatomy; Genetics; Biology; Gene","score_opus":0.004542760661689865,"score_gpt":0.1786053454299288,"score_spread":0.17406258476823894,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406547971","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.056403756,0.00021353953,0.000005922692,0.00022798515,0.0000035760813,0.0001319497,0.000007748949,0.000021722319,0.9429838],"genre_scores_gemma":[0.0045189206,0.000002487514,0.0004243269,0.000082700186,0.00019788336,0.00001242635,0.000037857626,0.00002628503,0.9946971],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999168,0.000023104732,0.00014673911,0.0002909483,0.00009345743,0.00027775936],"domain_scores_gemma":[0.99945587,0.0000044704916,0.000023926792,0.00035684003,0.00003552647,0.00012334196],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00008572188,0.00013333793,0.00011502354,0.000024761886,0.000056774257,0.000028449263,0.00019446897,0.00009042842,0.9641408],"category_scores_gemma":[0.000022173419,0.00013272105,0.000072578456,0.00007353399,0.000023975474,0.0000017334137,0.00008413619,0.0000490321,0.9296196],"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":[0.000016183349,0.000036436068,0.0000015038797,0.000005097159,0.00002868439,0.0000017004947,0.000006134887,0.00009876311,0.028963959,1.8998884e-7,0.26051104,0.7103303],"study_design_scores_gemma":[0.00020595906,0.00026246553,0.00021688653,0.0000074811783,0.000009581666,0.00003844906,0.0000013791135,0.00004878299,0.007793755,0.0000019858737,0.9912305,0.00018276238],"about_ca_topic_score_codex":0.000019389894,"about_ca_topic_score_gemma":2.924469e-7,"teacher_disagreement_score":0.73071945,"about_ca_system_score_codex":0.0000057530924,"about_ca_system_score_gemma":0.000022761986,"threshold_uncertainty_score":0.5412207},"labels":[],"label_agreement":null},{"id":"W4406644320","doi":"10.1007/s12519-024-00865-4","title":"Sex dimorphic associations of Prader–Willi imprinted gene expressions in umbilical cord with prenatal and postnatal growth in healthy infants","year":2025,"lang":"en","type":"article","venue":"World Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas; Instituto de Salud Carlos III; Ministerio de Ciencia e Innovación; European Regional Development Fund; Generalitat Valenciana; Asociación Española de Pediatría","keywords":"Umbilical cord; Sexual dimorphism; Medicine; Birth weight; Fetus; Gene expression; Genomic imprinting; Gene; Endocrinology; Physiology; Internal medicine; Pregnancy; Biology; Genetics; Immunology; DNA methylation","score_opus":0.008866216166149948,"score_gpt":0.26644502545546084,"score_spread":0.2575788092893109,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406644320","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974199,0.001565262,0.000383154,0.00030862816,0.00009270977,0.00011780886,0.000018984763,0.0000015405506,0.000092039525],"genre_scores_gemma":[0.99673843,0.0008094923,0.0022307076,0.00006751801,0.00007866517,0.0000026836785,0.000010188167,0.000008834176,0.000053462656],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988689,0.00007699475,0.0005326305,0.00016366312,0.0001607788,0.00019702583],"domain_scores_gemma":[0.9992664,0.00007385634,0.00032754795,0.000114898874,0.00013962391,0.00007769275],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035250233,0.000106362175,0.00025068686,0.00036626423,0.000032525568,0.000012664706,0.00014178874,0.000089020345,0.0000035042362],"category_scores_gemma":[0.00034323236,0.00009258686,0.000047705165,0.00047329906,0.000044021577,0.000008307819,0.00013209431,0.00025585774,1.145604e-7],"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":[0.000059338436,0.00014121407,0.98631305,0.000059382848,0.000020114676,0.00000755962,0.000075045624,0.00005059047,0.012248088,0.000026035614,0.00008271211,0.0009168463],"study_design_scores_gemma":[0.0017824544,0.0005040534,0.9895956,0.00006804616,0.00002974229,0.00008288566,0.00012215815,0.00004199067,0.0075560524,0.000049320326,0.000061422936,0.000106286],"about_ca_topic_score_codex":0.00005761723,"about_ca_topic_score_gemma":0.00019424334,"teacher_disagreement_score":0.004692035,"about_ca_system_score_codex":0.000028728233,"about_ca_system_score_gemma":0.00026395606,"threshold_uncertainty_score":0.37755826},"labels":[],"label_agreement":null},{"id":"W4406645055","doi":"10.1016/b978-84-8086-959-1.00566-6","title":"10.1016/b978-84-8086-959-1.00566-6","year":2000,"lang":"en","type":"book-chapter","venue":"Time to knit","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Dermatology","score_opus":0.0064289515322694495,"score_gpt":0.17671278670579396,"score_spread":0.17028383517352452,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406645055","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000071095266,0.00090487715,0.0000040311215,0.00007512473,0.000009469834,0.0003103392,0.00007223327,0.000036504563,0.9985163],"genre_scores_gemma":[0.000034604414,0.000009042124,0.00024885396,0.00008646006,0.000620491,0.000016834147,0.00034589818,0.00014059323,0.99849725],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9982568,0.000016749833,0.00036918765,0.0007089671,0.00021927724,0.00042903688],"domain_scores_gemma":[0.99875194,0.000009822864,0.00012662119,0.00079679,0.00008520765,0.00022962678],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.000113414106,0.00047150787,0.00038820406,0.000099466735,0.000081160455,0.00005186938,0.0004336369,0.0005513358,0.97116023],"category_scores_gemma":[0.000026226176,0.0004984994,0.00026385742,0.000027635979,0.000064564054,0.0000018472083,0.0002893613,0.00021220792,0.94950366],"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":[0.000038134232,0.000025831012,9.9164716e-8,0.00003087774,0.00019688014,0.0000102660415,0.000005110485,0.00003447427,0.0044110464,0.000013656509,0.19199733,0.8032363],"study_design_scores_gemma":[0.00023251258,0.0003878772,0.000007660811,0.00007182689,0.000064285894,0.00007000124,3.9522618e-7,0.0000071914687,0.0010173811,0.00005281849,0.9974885,0.00059957895],"about_ca_topic_score_codex":0.000007518404,"about_ca_topic_score_gemma":3.6963368e-7,"teacher_disagreement_score":0.80549115,"about_ca_system_score_codex":0.000022157335,"about_ca_system_score_gemma":0.00008922351,"threshold_uncertainty_score":0.9997467},"labels":[],"label_agreement":null},{"id":"W4408007158","doi":"10.1101/2025.02.25.25322869","title":"Neurophysiological dysconnectivity across multiple resting state brain networks and cognitive impairment in children with Prader-Willi Syndrome","year":2025,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Holland Bloorview Kids Rehabilitation Hospital; Western University; Mental Health Research Canada; Hospital for Sick Children; Toronto Rehabilitation Institute; University of Toronto","funders":"","keywords":"Neurophysiology; Cognitive impairment; Neuroscience; Cognition; Resting state fMRI; Psychology; Functional connectivity","score_opus":0.010606764872508511,"score_gpt":0.2566367630351931,"score_spread":0.24602999816268462,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408007158","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9960731,0.00056648784,0.0019968625,0.00010495059,0.00011837587,0.0009871796,0.00009616183,0.00002747396,0.000029403283],"genre_scores_gemma":[0.99877894,0.00016895599,0.00037694085,0.00019738883,0.00006861607,0.00012311841,0.00015568719,0.000033564207,0.00009678824],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9973898,0.0003071841,0.00036395056,0.0011958812,0.0001406321,0.00060253625],"domain_scores_gemma":[0.99902916,0.00013754026,0.00022107098,0.00042411787,0.0000703851,0.00011770408],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004470277,0.00043720246,0.00047751117,0.000055999408,0.00012670692,0.00007779869,0.00025582445,0.00033021093,0.0000026425917],"category_scores_gemma":[0.00043071897,0.00037570548,0.00008972469,0.0001360565,0.00018991441,0.0000037769637,0.0016638242,0.00064149307,7.3392056e-7],"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":[0.000016583213,0.00010651166,0.9859372,0.0000691179,0.00016274648,0.000009896228,0.000085438296,0.007865594,0.003019603,7.0283454e-7,0.0000068302365,0.0027197988],"study_design_scores_gemma":[0.0012380506,0.0006281406,0.9935934,0.0003325409,0.000029987254,0.00016543969,0.00006024107,0.0027707324,0.0007106213,0.00003169523,0.000018130997,0.0004210416],"about_ca_topic_score_codex":0.00017246413,"about_ca_topic_score_gemma":0.00012572923,"teacher_disagreement_score":0.007656201,"about_ca_system_score_codex":0.000018083108,"about_ca_system_score_gemma":0.00008894744,"threshold_uncertainty_score":0.99986947},"labels":[],"label_agreement":null},{"id":"W4408128735","doi":"10.1210/clinem/dgaf142","title":"Fiber Intervention Study in Prader-Willi Syndrome: Insights into Metabolic and Microbiota Shifts","year":2025,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; University of Alberta","funders":"Chinese University of Hong Kong; Weston Family Foundation","keywords":"Crossover study; Randomized controlled trial; Fiber; Intervention (counseling); Crossover; Medicine; Biology; Internal medicine; Computer science; Materials science; Alternative medicine; Nursing; Composite material; Pathology; Artificial intelligence","score_opus":0.01961927069978049,"score_gpt":0.3457885065733603,"score_spread":0.3261692358735798,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408128735","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96978885,0.02781356,0.00013553808,0.0010709281,0.0008027984,0.0002670167,5.7499545e-7,0.00000370424,0.00011701755],"genre_scores_gemma":[0.9936256,0.0048843743,0.0004530558,0.00040486632,0.000176998,0.000005757028,0.0000014554029,0.000013876545,0.00043404583],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9967487,0.001074303,0.0014692107,0.00028309805,0.00012686562,0.00029782293],"domain_scores_gemma":[0.9986886,0.00017783417,0.00053081656,0.0003951737,0.00013074405,0.00007682607],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014391522,0.00020141536,0.0007300924,0.00020152559,0.00008141151,0.000023832215,0.00048708223,0.00016834488,0.000022840426],"category_scores_gemma":[0.00067180936,0.00013543361,0.00024280985,0.00020295847,0.00025354032,0.000011692501,0.00043583862,0.000567434,0.000006339138],"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":[0.00038404396,0.004887449,0.51017034,0.00014565377,0.004641176,0.00010642958,0.0023778253,0.00017979044,0.08268855,0.001465816,0.0019051755,0.39104778],"study_design_scores_gemma":[0.003373621,0.0005316767,0.93270934,0.000043658714,0.0003013516,0.0003124213,0.000534147,0.000007150918,0.0015039166,0.00068494614,0.059876066,0.00012172493],"about_ca_topic_score_codex":0.000069540256,"about_ca_topic_score_gemma":0.00008986668,"teacher_disagreement_score":0.422539,"about_ca_system_score_codex":0.0000051960105,"about_ca_system_score_gemma":0.00009138079,"threshold_uncertainty_score":0.5522822},"labels":[],"label_agreement":null},{"id":"W4408717504","doi":"10.5664/jcsm.11664","title":"Personalized endpoints in Prader-Willi syndrome: a case study with goal attainment scaling","year":2025,"lang":"en","type":"article","venue":"Journal of Clinical Sleep Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Nova Scotia Health Authority; Dalhousie University","funders":"","keywords":"Medicine; Goal Attainment Scaling; Physical medicine and rehabilitation; Physical therapy","score_opus":0.02838142673211102,"score_gpt":0.380721298490769,"score_spread":0.352339871758658,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408717504","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99452883,0.0011031046,0.001584965,0.0018377141,0.00045073967,0.00028535142,5.9457983e-7,0.0000025920126,0.00020610145],"genre_scores_gemma":[0.99776363,0.00016868117,0.001015313,0.0005213551,0.00030079638,0.000005385452,0.0000015239075,0.000013412305,0.00020991886],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99736685,0.00028555322,0.0014587451,0.00029080268,0.00035040604,0.0002476354],"domain_scores_gemma":[0.9987302,0.0001777522,0.0005021034,0.00025207398,0.00016045771,0.00017744843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002740299,0.00017487226,0.0006904452,0.00012561104,0.00005032675,0.000011951379,0.00020791659,0.0001319859,0.00004970225],"category_scores_gemma":[0.001096176,0.00011401336,0.00014309594,0.00020467844,0.00017882715,0.000004781376,0.00010150196,0.00040341972,0.0000010860441],"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":[0.00019676644,0.0013888942,0.9447022,0.00006268891,0.00076372543,0.0035268248,0.00047467995,0.00018209036,0.0013934739,0.000010018827,0.00044575369,0.046852864],"study_design_scores_gemma":[0.03553086,0.022167055,0.8729006,0.0012845447,0.00068075286,0.031263072,0.023015402,0.00045949256,0.00026066115,0.00007002595,0.011925346,0.00044217383],"about_ca_topic_score_codex":0.000047684945,"about_ca_topic_score_gemma":0.000044707434,"teacher_disagreement_score":0.0718016,"about_ca_system_score_codex":0.000024166731,"about_ca_system_score_gemma":0.00014218564,"threshold_uncertainty_score":0.464933},"labels":[],"label_agreement":null},{"id":"W4409058591","doi":"10.1101/2025.03.27.645693","title":"Identification of genetic and non-genetic modifiers of genomic imprinting through whole genome screening in humans","year":2025,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Genomic imprinting; Identification (biology); Genetics; Biology; Genome; Computational biology; Gene; DNA methylation","score_opus":0.010503323862083018,"score_gpt":0.2263524698867477,"score_spread":0.21584914602466468,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409058591","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9739172,0.003163156,0.02184889,0.000019705922,0.00023336502,0.0006388267,0.00015266635,0.000016260905,0.000009961742],"genre_scores_gemma":[0.97929156,0.0008705167,0.019558936,0.000026059628,0.00010521461,0.00007249911,0.0000016570857,0.000063181236,0.000010405028],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9970572,0.00009806689,0.0011833097,0.001011285,0.00020852563,0.00044161818],"domain_scores_gemma":[0.9976226,0.000019019966,0.0008218552,0.0011643006,0.00028492193,0.000087306544],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004695519,0.0004246529,0.00060762,0.00027010852,0.00007670642,0.000056344776,0.00056110206,0.00049520284,0.000004728526],"category_scores_gemma":[0.00010811342,0.00052511186,0.00016276853,0.00024943915,0.00018217215,0.000008395938,0.001001365,0.0003108485,0.0000018948834],"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":[0.000008283397,0.00005026528,0.07704968,0.0006786353,0.00011764567,0.0000019281476,0.000038380393,0.0033659355,0.91865635,0.000010976276,0.000002822483,0.000019110406],"study_design_scores_gemma":[0.00039946524,0.000047763966,0.66840506,0.00021724211,0.00007052076,3.277674e-8,0.00001835903,0.00082903804,0.32956102,0.0000034658412,0.00011922296,0.00032882846],"about_ca_topic_score_codex":0.00016906374,"about_ca_topic_score_gemma":0.000006336394,"teacher_disagreement_score":0.5913554,"about_ca_system_score_codex":0.00003860602,"about_ca_system_score_gemma":0.00030071853,"threshold_uncertainty_score":0.99972004},"labels":[],"label_agreement":null},{"id":"W4409986288","doi":"10.1038/s41467-025-59109-2","title":"Allelic effects on KLHL17 expression underlie a pancreatic cancer genome-wide association signal at chr1p36.33","year":2025,"lang":"en","type":"article","venue":"Nature Communications","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Sinai Health System; Lunenfeld-Tanenbaum Research Institute; University of Toronto","funders":"Division of Cancer Epidemiology and Genetics, National Cancer Institute; National Heart, Lung, and Blood Institute; Medical Research Council; Centers for Disease Control and Prevention; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; Cancer Research UK; Centre International de Recherche sur le Cancer; World Health Organization","keywords":"Pancreatic cancer; Allele; Genetics; Association (psychology); Biology; Genome; Cancer; Computational biology; Gene; Bioinformatics; Psychology","score_opus":0.008902243679664534,"score_gpt":0.28194286931593504,"score_spread":0.2730406256362705,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409986288","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9652033,0.019691942,0.00038015962,0.0062640584,0.00025044128,0.00047237676,0.000023489254,0.00003653518,0.00767774],"genre_scores_gemma":[0.98903054,0.0028899126,0.0011447894,0.0024376174,0.00007600642,0.00015348785,0.00023216341,0.000017829576,0.004017638],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99900866,0.00016847435,0.00018775063,0.00026998826,0.00014240625,0.00022274737],"domain_scores_gemma":[0.998272,0.00029785724,0.00013617829,0.0011296312,0.00011310829,0.000051234816],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017403912,0.00015107296,0.0001542958,0.000062641106,0.00035612265,0.00003186265,0.00058881706,0.00040031673,0.00002538954],"category_scores_gemma":[0.00039497335,0.00014413362,0.000097675525,0.00015356034,0.000029785342,0.0000031078512,0.00053551607,0.0003748059,0.00001821695],"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":[0.000021277967,0.00014490905,0.14641021,0.00006468736,0.00024526447,3.9807554e-7,0.00008668021,0.00015953172,0.82699513,0.00023852143,0.021467466,0.0041658953],"study_design_scores_gemma":[0.0008260993,0.000121346566,0.52036315,0.00019974887,0.000102725564,0.0000015165506,0.000043618693,0.00017772368,0.14164793,0.00017217158,0.33605987,0.00028405662],"about_ca_topic_score_codex":0.000020334997,"about_ca_topic_score_gemma":0.00019807153,"teacher_disagreement_score":0.6853472,"about_ca_system_score_codex":0.0001868324,"about_ca_system_score_gemma":0.00009213907,"threshold_uncertainty_score":0.58775985},"labels":[],"label_agreement":null},{"id":"W4410400129","doi":"10.7554/elife.94502.2","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2025,"lang":"en","type":"preprint","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Retrotransposon; Genomic imprinting; Imprinting (psychology); Biology; Lineage (genetic); Genetics; Evolutionary biology; Genome; Gene; Transposable element; DNA methylation; Gene expression","score_opus":0.023738000150062555,"score_gpt":0.27654331456724995,"score_spread":0.2528053144171874,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410400129","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9909949,0.0015508109,0.006162165,0.000042226315,0.0005102873,0.0004368245,0.00008065222,0.000019812042,0.00020236487],"genre_scores_gemma":[0.9936153,0.0014549815,0.0034191832,0.000061603234,0.00025429137,0.000031595373,0.0010774804,0.000027156364,0.00005839584],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9981116,0.00012996832,0.00069243996,0.0006234429,0.0001791305,0.0002634285],"domain_scores_gemma":[0.99894005,0.000008529244,0.0002825136,0.00047666425,0.00023585162,0.00005638591],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0002806366,0.0002640319,0.00031911477,0.00018388663,0.000045162036,0.000040763807,0.0003056295,0.0004665784,0.000016761385],"category_scores_gemma":[0.00004844977,0.00030881938,0.00015899369,0.00011514094,0.00004750849,0.000009923163,0.00012605921,0.00028829332,0.000001391521],"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":[0.000044604058,0.000075084994,0.038719807,0.0002323217,0.00002303396,6.3603386e-7,0.00051326957,0.004915292,0.9511567,0.000024006924,0.0000048385195,0.004290437],"study_design_scores_gemma":[0.0005212972,0.00021369386,0.5113246,0.00024072056,0.000025669759,0.0000022717236,0.00022407358,0.0016627886,0.485203,0.000025086374,0.00027347077,0.00028336412],"about_ca_topic_score_codex":0.00007337188,"about_ca_topic_score_gemma":0.00012390023,"teacher_disagreement_score":0.47260475,"about_ca_system_score_codex":0.000036968242,"about_ca_system_score_gemma":0.00017129975,"threshold_uncertainty_score":0.9999364},"labels":[],"label_agreement":null},{"id":"W4410513017","doi":"10.3899/jrheum.2025-0390.pv145a","title":"RHUPUS SYNDROME: DESCRIPTION OF CLINICAL MANIFESTATIONS, ANALYTICAL FINDINGS, AND THERAPEUTIC APPROACH IN A SERIES OF 10 CASES","year":2025,"lang":"en","type":"article","venue":"The Journal of Rheumatology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Series (stratigraphy); Intensive care medicine; Dermatology","score_opus":0.033455077217247484,"score_gpt":0.30994438929590884,"score_spread":0.27648931207866134,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410513017","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99694836,0.0016898968,0.0009464458,0.00016804348,0.00009029233,0.00006041542,0.00000161103,6.808479e-7,0.00009426133],"genre_scores_gemma":[0.9973873,0.0015926993,0.0008895429,0.000018299314,0.000002107647,8.150718e-7,0.0000015123046,0.00000412337,0.00010358305],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99882597,0.00021656413,0.00071177253,0.00008100194,0.00006495508,0.00009972573],"domain_scores_gemma":[0.99933875,0.00012780831,0.0002900041,0.00012656848,0.00009481008,0.000022035762],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00083307305,0.00006954175,0.00032890242,0.00009651554,0.000023175813,0.0000042108322,0.00013292725,0.00010221228,0.0000074042605],"category_scores_gemma":[0.00029771755,0.000048822014,0.000068175825,0.000097296004,0.00021819734,0.000003802029,0.00006425855,0.000106597276,1.8440197e-7],"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":[0.00021457946,0.00012335558,0.98944646,0.00013394408,0.0001900067,0.000004304336,0.00014017471,0.00009682548,0.007107261,0.00068327755,0.00012213408,0.0017376906],"study_design_scores_gemma":[0.0013689102,0.0012647937,0.96578604,0.00017963159,0.0001582378,0.025643582,0.0020414845,0.00059482706,0.0017557647,0.0008094965,0.0002955333,0.00010168273],"about_ca_topic_score_codex":0.000036978727,"about_ca_topic_score_gemma":0.000017755796,"teacher_disagreement_score":0.025639279,"about_ca_system_score_codex":0.0000037066452,"about_ca_system_score_gemma":0.000091032656,"threshold_uncertainty_score":0.1990904},"labels":[],"label_agreement":null},{"id":"W4410708037","doi":"10.1016/j.ssmqr.2025.100574","title":"Dietary care and familialisation of children with Prader-Willi syndrome","year":2025,"lang":"en","type":"article","venue":"SSM - Qualitative Research in Health","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Fondation Maladies Rares; Taylor’s University; Rare Disease Foundation","keywords":"Pediatrics; Medicine; Psychology; Gerontology","score_opus":0.09358133874853918,"score_gpt":0.4812231762503912,"score_spread":0.387641837501852,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410708037","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9923203,0.0057566212,0.00017107958,0.0007087857,0.00002301817,0.0005421762,0.000028272007,0.0000032808928,0.00044645352],"genre_scores_gemma":[0.9965375,0.0011271383,0.002028821,0.00006631929,0.000013673447,0.000035115485,0.00007974292,0.000010019448,0.00010169275],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9976869,0.0010828289,0.00029929925,0.00033764198,0.00024312762,0.00035015357],"domain_scores_gemma":[0.99932724,0.00012257633,0.00007405821,0.0002241993,0.00017678396,0.00007511021],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001849847,0.000096916214,0.00019848811,0.00018843982,0.00010166829,0.000011511098,0.00011166962,0.00007131514,0.0000023092755],"category_scores_gemma":[0.00019977108,0.00008437691,0.000023699502,0.0003357135,0.00026733926,0.000004388016,0.00012027269,0.00018185414,6.731355e-7],"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":[0.000064376814,0.00037013055,0.7225256,0.005449136,0.00044057702,0.0000022701036,0.10457748,0.00016636432,0.02260491,0.0036487696,0.00072431826,0.1394261],"study_design_scores_gemma":[0.0009829855,0.0029176155,0.9252912,0.0004747947,0.0000037046127,0.000014258495,0.0671302,0.000024404326,0.0017446893,0.0009728696,0.000299385,0.0001439435],"about_ca_topic_score_codex":0.0013938,"about_ca_topic_score_gemma":0.00018283592,"teacher_disagreement_score":0.20276558,"about_ca_system_score_codex":0.000046441302,"about_ca_system_score_gemma":0.00043925093,"threshold_uncertainty_score":0.34407905},"labels":[],"label_agreement":null},{"id":"W4410901524","doi":"10.1136/jmg-2024-110262","title":"Using long-read sequencing to detect and subtype a case with Temple syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Toronto; BC Children's Hospital; University of British Columbia; Hospital for Sick Children; B.C. Women's Hospital & Health Centre; Canada's Michael Smith Genome Sciences Centre","funders":"Canadian Institutes of Health Research; Canada Research Chairs; BC Cancer Agency; BC Children's Hospital","keywords":"Genomic imprinting; Methylation; DNA methylation; Uniparental disomy; Biology; Multiplex; Genetics; Imprinting (psychology); Nanopore sequencing; Computational biology; Epigenomics; Differentially methylated regions; DNA sequencing; Chromosome; Gene; Karyotype","score_opus":0.029574987797891677,"score_gpt":0.31418456008569773,"score_spread":0.28460957228780603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410901524","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9489957,0.0023117573,0.048086353,0.00029201552,0.00016087237,0.00008796898,0.0000013390406,0.0000022535291,0.0000617479],"genre_scores_gemma":[0.968589,0.00026833132,0.03057393,0.00036805368,0.00010886831,0.000001007007,5.997575e-7,0.000014778038,0.00007540039],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.9988165,0.00005148917,0.00036062,0.00018004121,0.000352982,0.00023837808],"domain_scores_gemma":[0.9992178,0.000024822264,0.00013454453,0.0001811397,0.00015098954,0.00029069593],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005334757,0.0001303181,0.00022228519,0.000103531376,0.00007901089,0.000036187193,0.00018944872,0.00015784304,0.00002386735],"category_scores_gemma":[0.00028006185,0.000101307625,0.000052539417,0.00016314661,0.000069848866,0.0000023147875,0.0001771873,0.00017367277,6.989032e-7],"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":[0.00024984285,0.00015216367,0.10082847,0.0005574212,0.0012223031,0.017785193,0.00052517233,0.00383821,0.60655075,0.000050834617,0.0009759302,0.2672637],"study_design_scores_gemma":[0.0070892842,0.010361601,0.060132846,0.0025252819,0.00086514174,0.7047761,0.0023177622,0.0048673754,0.18369886,0.00045658907,0.021520158,0.0013889963],"about_ca_topic_score_codex":0.000034246405,"about_ca_topic_score_gemma":0.000055695557,"teacher_disagreement_score":0.6869909,"about_ca_system_score_codex":0.000026192154,"about_ca_system_score_gemma":0.00047058583,"threshold_uncertainty_score":0.4131205},"labels":[],"label_agreement":null},{"id":"W4410954163","doi":"10.7554/elife.94502.3.sa4","title":"Author response: Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2025,"lang":"en","type":"peer-review","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Retrotransposon; Genomic imprinting; Imprinting (psychology); Biology; Lineage (genetic); Genetics; Evolutionary biology; Gene; Genome; Transposable element; DNA methylation; Gene expression","score_opus":0.039182077467243795,"score_gpt":0.3219329710292623,"score_spread":0.28275089356201855,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410954163","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9728725,0.018153684,0.0038628543,0.0025452178,0.0009947816,0.0009629556,0.0001888379,0.000027642678,0.00039153604],"genre_scores_gemma":[0.9661079,0.0075604604,0.0034958394,0.00041155054,0.00030434068,0.00006989839,0.004602569,0.00006935863,0.017378062],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.997133,0.00039199667,0.0010792355,0.00078474847,0.00025021864,0.00036076203],"domain_scores_gemma":[0.9984813,0.000028848239,0.00039177458,0.0006045958,0.00041887653,0.00007461357],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0008547438,0.00038508433,0.00057029014,0.00028493057,0.00006052099,0.000039508723,0.0003792547,0.0006036018,0.00012302384],"category_scores_gemma":[0.00019908888,0.00040707437,0.00024797226,0.00029558063,0.00006059969,0.000014363328,0.00006100173,0.00030297713,0.0000026684477],"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":[0.00018529616,0.000086795524,0.0013003133,0.0016457629,0.000033250315,0.0000013143704,0.00013152517,0.00013442902,0.984133,0.000015355377,0.0023157306,0.010017226],"study_design_scores_gemma":[0.0019472054,0.0019932871,0.4140977,0.006113557,0.00026185391,0.000027660262,0.00041376217,0.00070330704,0.34592387,0.000028467734,0.22706391,0.0014254329],"about_ca_topic_score_codex":0.00007223418,"about_ca_topic_score_gemma":0.00021710899,"teacher_disagreement_score":0.63820916,"about_ca_system_score_codex":0.00005507578,"about_ca_system_score_gemma":0.00032233386,"threshold_uncertainty_score":0.9998381},"labels":[],"label_agreement":null},{"id":"W4410954493","doi":"10.7554/elife.94502.3","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2025,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Japan Society for the Promotion of Science; Canadian Institutes of Health Research; Mitsubishi Foundation; Takeda Science Foundation","keywords":"Retrotransposon; Genomic imprinting; Biology; Imprinting (psychology); Genetics; Lineage (genetic); Evolutionary biology; Genome; Gene; Transposable element; DNA methylation; Gene expression","score_opus":0.015134527507421214,"score_gpt":0.2638693933611692,"score_spread":0.248734865853748,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410954493","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.992692,0.00070868694,0.005966142,0.00004811245,0.00017568539,0.00017493861,0.000007403971,0.000010670492,0.0002163566],"genre_scores_gemma":[0.9977371,0.00035630114,0.0015405521,0.000078884514,0.00008069072,0.000009076066,0.00014265414,0.000012233865,0.000042504464],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990631,0.00005840392,0.0003540858,0.00026951212,0.00008761429,0.00016729393],"domain_scores_gemma":[0.99956685,0.000005380471,0.00008643498,0.00020052373,0.00011125432,0.000029530443],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016544011,0.00010707542,0.00013004756,0.00010191193,0.000038812963,0.000018620689,0.00012325753,0.00012335253,0.000011320794],"category_scores_gemma":[0.00003124822,0.00011929323,0.000059062462,0.00013815779,0.00003145403,0.000011367928,0.000019346458,0.00007331661,0.0000012838367],"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":[0.000027983127,0.00004288604,0.0810019,0.000034898483,0.0000073341103,2.4397968e-7,0.0002132257,0.00051592704,0.91362673,0.000060044364,0.00000368566,0.0044651483],"study_design_scores_gemma":[0.00034897847,0.00012378032,0.5195243,0.000033297234,0.0000054571183,9.754164e-7,0.00017607506,0.0005050782,0.47896188,0.000009095217,0.00023781827,0.00007325647],"about_ca_topic_score_codex":0.00002450808,"about_ca_topic_score_gemma":0.00006750954,"teacher_disagreement_score":0.4385224,"about_ca_system_score_codex":0.00001536214,"about_ca_system_score_gemma":0.000051109037,"threshold_uncertainty_score":0.48646367},"labels":[],"label_agreement":null},{"id":"W4411210085","doi":"10.1093/brain/awaf227","title":"Deciphering <i>DST</i> -associated disorders: biallelic variants affecting DST-b cause a congenital myopathy","year":2025,"lang":"en","type":"article","venue":"Brain","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Else Kröner-Fresenius-Stiftung; Austrian Science Fund; Deutsche Forschungsgemeinschaft; Technische Universität München; Bundesministerium für Bildung und Forschung; Institute for Advanced Study","keywords":"Myopathy; Medicine; Genetics; Pathology; Biology","score_opus":0.00739109569379996,"score_gpt":0.24457897087131977,"score_spread":0.23718787517751982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411210085","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99182713,0.0005964155,0.002601571,0.00038403555,0.00039480068,0.00024225256,0.0000086662185,0.000039862218,0.0039052814],"genre_scores_gemma":[0.9967878,0.00006769914,0.00046912985,0.0006371316,0.00009928124,0.000021599006,0.00003438336,0.00002837575,0.0018546244],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9987463,0.000094400755,0.00024070841,0.00041589147,0.000102082195,0.00040061492],"domain_scores_gemma":[0.9994404,0.000059057224,0.00008327907,0.00030396844,0.000045245466,0.00006809624],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003233857,0.00018961761,0.00017769939,0.0000522065,0.00015893561,0.00006639019,0.00021074635,0.00016750106,0.000023239518],"category_scores_gemma":[0.0008485132,0.0002030273,0.00011615261,0.00021244884,0.000041088693,0.0000044082713,0.00026067722,0.00010553508,0.000013107212],"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":[0.000019535113,0.00018352813,0.047820188,0.000042373205,0.0003992699,0.000008246995,0.00026371074,0.00010846467,0.9103586,0.000089510584,0.0033386557,0.037367932],"study_design_scores_gemma":[0.008452111,0.0011009031,0.81729937,0.0003941616,0.00026894888,0.000099902856,0.0020230587,0.0023686297,0.09536718,0.0009960819,0.06956662,0.0020630532],"about_ca_topic_score_codex":0.00011354871,"about_ca_topic_score_gemma":0.00048198982,"teacher_disagreement_score":0.8149914,"about_ca_system_score_codex":0.000021853411,"about_ca_system_score_gemma":0.00008581222,"threshold_uncertainty_score":0.82792133},"labels":[],"label_agreement":null},{"id":"W4411696543","doi":"10.1080/15592294.2025.2523191","title":"<i>PIK3R1</i> and <i>G0S2</i> are human placenta-specific imprinted genes associated with germline-inherited maternal DNA methylation","year":2025,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Hospital Foundation","funders":"Biotechnology and Biological Sciences Research Council; Fondation ARC pour la Recherche sur le Cancer; Medical Research Council; Ministerio de Economía y Competitividad; European Commission; Wellcome Trust","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Differentially methylated regions; DNA methylation; Reprogramming; Epigenetics; Methylation; Genetics; Placenta; Germline; Gene; Gene expression; Fetus; Pregnancy","score_opus":0.010777392000606172,"score_gpt":0.24372743590884283,"score_spread":0.23295004390823665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411696543","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9918984,0.0032833945,0.0035016146,0.00012234524,0.00019269896,0.0002707348,0.000026948483,0.00003818207,0.000665654],"genre_scores_gemma":[0.99584705,0.0009864587,0.0012553221,0.00020820592,0.0001064365,0.000020705138,0.00013651483,0.000043997803,0.0013953074],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9984439,0.00009814278,0.00037770608,0.000529211,0.00017590361,0.00037514762],"domain_scores_gemma":[0.9990882,0.000021529893,0.00021227682,0.00040475326,0.00017406086,0.0000991316],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00020814511,0.0002844413,0.00026735265,0.00008503978,0.00020704481,0.00009497358,0.00020410428,0.00022206764,0.000023321729],"category_scores_gemma":[0.00004158467,0.0002695579,0.000070324866,0.00020104149,0.000116381074,0.000003890337,0.00026955525,0.00012675971,0.000003697017],"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":[0.000021413765,0.00006288065,0.1279022,0.000033556633,0.00015014058,0.0000040072596,0.000030127389,0.00009440242,0.86562985,0.000030441679,0.00029982548,0.005741183],"study_design_scores_gemma":[0.0010996916,0.00020436951,0.4541444,0.00010270275,0.000053862805,0.000014103245,0.00008240247,0.000116282,0.53395486,0.00008104628,0.009838913,0.0003073439],"about_ca_topic_score_codex":0.000019725581,"about_ca_topic_score_gemma":0.000091505935,"teacher_disagreement_score":0.33167493,"about_ca_system_score_codex":0.000026181755,"about_ca_system_score_gemma":0.000042587322,"threshold_uncertainty_score":0.9999757},"labels":[],"label_agreement":null},{"id":"W4412430336","doi":"10.1172/jci168962","title":"Organ-specific features of human kidney lymphatics are disrupted in chronic transplant rejection","year":2025,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Infection and Immunity","funders":"Foulkes Foundation; Rosetrees Trust; Kidney Research UK; National Institute for Health and Care Research; Wellcome Trust","keywords":"Lymphatic system; Kidney; Kidney transplantation; Pathology; Medicine; Organ transplantation; Graft rejection; Transplant rejection; Immunology; Transplantation; Biology; Immune system; Internal medicine","score_opus":0.03431954953857322,"score_gpt":0.3447410962103921,"score_spread":0.31042154667181887,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412430336","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99745303,0.00070449995,0.000688097,0.00050463126,0.0003882623,0.00007343191,0.0000027362323,0.0000019637243,0.00018333823],"genre_scores_gemma":[0.99791026,0.00075694383,0.0007254174,0.00019528976,0.00026169245,9.492082e-7,0.00001759629,0.000007197909,0.00012467567],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99843925,0.00014002284,0.0010583961,0.00013379277,0.00012824727,0.000100284844],"domain_scores_gemma":[0.9988988,0.00004298626,0.00066598534,0.00014431533,0.00016268209,0.000085238],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00074109685,0.00008469723,0.00027309236,0.000098542005,0.00003070722,0.000012913883,0.00013027393,0.00018517493,0.000007221238],"category_scores_gemma":[0.00051649066,0.00007410171,0.00013542228,0.00016726484,0.00010344417,0.000006238306,0.000022162401,0.00016256426,4.432424e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00004113839,0.00008181755,0.24715324,0.00010344398,0.000071001596,0.000002897933,0.00006533541,0.00017586756,0.7455932,0.00016091079,0.0018189676,0.004732207],"study_design_scores_gemma":[0.0013988126,0.00049037713,0.80202323,0.00049928785,0.000035964225,0.000021691876,0.00007476743,0.00007018454,0.19264916,0.00080286135,0.0018538968,0.00007976212],"about_ca_topic_score_codex":0.000009714931,"about_ca_topic_score_gemma":0.00002303448,"teacher_disagreement_score":0.55487,"about_ca_system_score_codex":0.000030222101,"about_ca_system_score_gemma":0.00030014454,"threshold_uncertainty_score":0.30217797},"labels":[],"label_agreement":null},{"id":"W4412647599","doi":"10.1186/s13072-025-00612-7","title":"Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans","year":2025,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"Associazione Italiana per la Ricerca sul Cancro; Fondazione Telethon; Government of Canada; Ministero dell’Istruzione, dell’Università e della Ricerca; Genome Canada; Ontario Genomics; Ontario Genomics Institute","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Identification (biology); Human genetics; Methylation; DNA methylation; Computational biology; Evolutionary biology; Gene; Gene expression; Ecology","score_opus":0.009737937297583843,"score_gpt":0.26503081419409186,"score_spread":0.25529287689650804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412647599","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.898701,0.0016483639,0.0989565,0.000016294984,0.00008217882,0.00037465038,0.000010930343,0.000004647929,0.00020541697],"genre_scores_gemma":[0.96367836,0.00049919257,0.035675004,0.000010664272,0.000022290751,0.000017465536,0.000015847785,0.000025696034,0.00005549605],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9977526,0.00009764483,0.001292435,0.00042942294,0.00016714673,0.00026073348],"domain_scores_gemma":[0.99855447,0.000043762968,0.00066203164,0.00053208676,0.00017113042,0.000036513633],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003969345,0.00020848202,0.00040355435,0.0002058671,0.000047570407,0.000013288243,0.0002760476,0.00018327117,0.00000790156],"category_scores_gemma":[0.00015043304,0.00023991552,0.000109674715,0.0002732836,0.00017976487,0.0000056073623,0.0002624271,0.00009266349,6.5195724e-7],"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":[0.000009054631,0.000048624614,0.09784201,0.00028174062,0.00006636017,2.2655693e-7,0.00036703562,0.0041746194,0.8891202,0.00003469687,0.0000027687524,0.0080526145],"study_design_scores_gemma":[0.00040976785,0.000086634784,0.49921015,0.00008157846,0.00003252976,0.0000011808747,0.00020716542,0.0037787845,0.49590868,0.00017165049,0.0000122929005,0.000099596225],"about_ca_topic_score_codex":0.00023660531,"about_ca_topic_score_gemma":0.00003630533,"teacher_disagreement_score":0.40136814,"about_ca_system_score_codex":0.00001679679,"about_ca_system_score_gemma":0.000090689966,"threshold_uncertainty_score":0.9783471},"labels":[],"label_agreement":null},{"id":"W4413043874","doi":"10.1016/j.jpag.2025.07.011","title":"Sex Hormone Replacement Therapy and Bleeding Patterns among Adolescents and Young Adult Females with Prader–Willi Syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Pediatric and Adolescent Gynecology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Medicine; Discontinuation; Hypogonadotropic hypogonadism; Pediatrics; Cohort; Retrospective cohort study; Hormone replacement therapy (female-to-male); Young adult; Amenorrhea; Medical record; Gynecology; Internal medicine; Hormone; Testosterone (patch); Pregnancy","score_opus":0.00877229070462568,"score_gpt":0.22905813423431554,"score_spread":0.22028584352968986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413043874","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9910285,0.007637331,0.0006711602,0.00022316781,0.00019722595,0.00020902211,0.0000025455276,0.0000041258095,0.000026958214],"genre_scores_gemma":[0.9684,0.030713838,0.0002895691,0.00022960716,0.00018413934,0.000003813079,0.0000023882349,0.000015233951,0.00016139212],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988094,0.00006689061,0.00040194998,0.00030632163,0.00013022726,0.00028518803],"domain_scores_gemma":[0.9992642,0.00002322523,0.00033124414,0.00012529524,0.00011838411,0.0001376834],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025886192,0.00020769001,0.00032353107,0.00014607586,0.000118311335,0.000048665588,0.00010224729,0.00015657007,0.0000032117969],"category_scores_gemma":[0.00006326236,0.00016228382,0.000047227546,0.000084147825,0.000095705276,0.000012223922,0.00014204059,0.0002021786,1.7617076e-7],"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":[0.000031722317,0.0001019155,0.9939642,0.00014475909,0.00010269255,0.00000999981,0.000060691385,0.0000032848432,0.0021048712,0.000005975078,0.00025380167,0.0032161179],"study_design_scores_gemma":[0.0029373849,0.0014221075,0.99372464,0.00010149455,0.00011726471,0.0005925294,0.0004846791,0.000031604308,0.00022884602,0.000012058083,0.00017415432,0.00017324877],"about_ca_topic_score_codex":0.000009114023,"about_ca_topic_score_gemma":0.000011224921,"teacher_disagreement_score":0.023076508,"about_ca_system_score_codex":0.000015714444,"about_ca_system_score_gemma":0.00006437108,"threshold_uncertainty_score":0.6617742},"labels":[],"label_agreement":null},{"id":"W4413051636","doi":"10.1177/19160216251364759","title":"Outcomes After Tonsillectomy in Children With Angelman Syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Otolaryngology - Head and Neck Surgery","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto; Children's Hospital of Eastern Ontario; University of Ottawa; Hospital for Sick Children","funders":"","keywords":"Angelman syndrome; Tonsillectomy; Medicine; Pediatrics; Psychology; Audiology; Surgery; Genetics; Biology","score_opus":0.006749925338824258,"score_gpt":0.23728858320458346,"score_spread":0.2305386578657592,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413051636","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965424,0.002718467,0.0000348106,0.00034170374,0.00014175003,0.00009842597,0.0000015947413,0.0000027936708,0.000118033386],"genre_scores_gemma":[0.9985809,0.00032967635,0.00034995927,0.0005191075,0.000033005253,0.0000070570563,0.0000038669864,0.00001152099,0.00016491461],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990082,0.00007299337,0.0003927555,0.00019488815,0.0000793539,0.0002518335],"domain_scores_gemma":[0.9995181,0.00004773603,0.00014415171,0.00016285476,0.000056880068,0.0000702749],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028299223,0.00015218976,0.00043378197,0.00026619103,0.00003909557,0.000016125332,0.00009173563,0.00014650662,0.000017265666],"category_scores_gemma":[0.000072817566,0.000114491595,0.000116951676,0.00014729213,0.000078278485,0.000008730587,0.000073478186,0.00017128976,0.0000011504909],"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":[0.000067341076,0.00006571837,0.9973307,0.000018032839,0.00016738525,0.00007913371,0.000014286666,0.0000027731655,0.0015351777,0.00000352515,0.0001868117,0.00052910275],"study_design_scores_gemma":[0.00076612557,0.00022483806,0.9941638,0.00011430385,0.000029782617,0.003039716,0.000010529197,0.0000017331588,0.0007155093,0.000023965089,0.00078757387,0.00012211641],"about_ca_topic_score_codex":0.000020173335,"about_ca_topic_score_gemma":0.00003918359,"teacher_disagreement_score":0.0031669047,"about_ca_system_score_codex":0.000009026348,"about_ca_system_score_gemma":0.00012555922,"threshold_uncertainty_score":0.46688318},"labels":[],"label_agreement":null},{"id":"W4413470125","doi":"10.1101/2025.08.19.670946","title":"PHLDA2 promotes breast cancer metastasis by co-opting a developmental program for placental vascular remodeling","year":2025,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Canadian Institutes of Health Research; Mark Foundation For Cancer Research; Alexander von Humboldt-Stiftung; California Institute for Regenerative Medicine","keywords":"Metastasis; Breast cancer; Extracellular matrix; Cancer research; Cancer; Biology; Downregulation and upregulation; Ectopic expression; Medicine; Internal medicine; Cell biology; Gene; Genetics","score_opus":0.01170163615709603,"score_gpt":0.25379344334756443,"score_spread":0.2420918071904684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413470125","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9839518,0.0041403826,0.005922536,0.00013360546,0.0006115431,0.0025058126,0.0025366617,0.00018381352,0.000013849689],"genre_scores_gemma":[0.9100058,0.00065612496,0.0869128,0.00015685664,0.00040476632,0.0016607039,0.00002232347,0.00015205712,0.000028565692],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99657166,0.00009122578,0.0006667459,0.0014952663,0.00032137518,0.0008537208],"domain_scores_gemma":[0.99823374,0.000020183332,0.00038683074,0.0006763973,0.00044404998,0.00023877763],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000601711,0.00072273536,0.00061429053,0.00013642234,0.0002990282,0.00024264958,0.00061839435,0.0006160634,0.000023907562],"category_scores_gemma":[0.00012745633,0.000794178,0.00038087065,0.00020734654,0.000090958645,0.000011151338,0.00076194433,0.0003830616,0.0000043820414],"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":[0.000029079878,0.00023117293,0.004693034,0.0007624997,0.00081321935,0.000001663668,0.000008892343,0.00013611697,0.991878,0.0000059931103,0.00094581814,0.0004945478],"study_design_scores_gemma":[0.001601968,0.0001409353,0.009718296,0.0008654783,0.00043271715,3.564621e-7,0.000027806032,0.0032999415,0.94579303,6.646835e-7,0.03649376,0.0016250679],"about_ca_topic_score_codex":0.00010158097,"about_ca_topic_score_gemma":0.0000041619205,"teacher_disagreement_score":0.08099027,"about_ca_system_score_codex":0.00020333224,"about_ca_system_score_gemma":0.0010254716,"threshold_uncertainty_score":0.9994509},"labels":[],"label_agreement":null},{"id":"W4413865128","doi":"10.1080/23772484.2025.2551371","title":"Tongue reduction surgery in Beckwith-Wiedemann syndrome, effects on eating and swallowing function: A case report","year":2025,"lang":"en","type":"article","venue":"Acta Oto-Laryngologica Case Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's & Women's Health Centre of British Columbia","funders":"","keywords":"Beckwith–Wiedemann syndrome; Swallowing; Medicine; Tongue; Reduction (mathematics); Surgery; Biology; Pathology; Mathematics; Genetics","score_opus":0.009042725035187077,"score_gpt":0.2413880340848116,"score_spread":0.23234530904962453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413865128","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99636894,0.00067579845,0.00007449949,0.00015736753,0.00078866404,0.0005677699,0.0000013078811,0.000046476278,0.001319167],"genre_scores_gemma":[0.99859595,0.00006759109,0.0002802229,0.00019221361,0.00011944873,0.00014377563,0.00006325242,0.000025916755,0.0005116376],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99746305,0.00015453126,0.0007898755,0.0010157508,0.00014926794,0.00042752863],"domain_scores_gemma":[0.9985929,0.00014864371,0.0003606489,0.0007127555,0.00007094805,0.000114091694],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.001047155,0.0003152288,0.00044125924,0.00022560218,0.00026431613,0.00006223081,0.000042648604,0.0003372522,0.00001439029],"category_scores_gemma":[0.0012940113,0.00029535184,0.00016056882,0.00031564044,0.000054427866,0.00001490866,0.00021347534,0.00022925618,0.0000013421421],"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":[0.000026335701,0.00011261997,0.09627176,0.00016173847,0.00012193102,0.8379818,0.00003504313,0.00003247036,0.06093215,0.000006727412,0.00052142114,0.0037959605],"study_design_scores_gemma":[0.00020098634,0.0002932891,0.093016155,0.00024642167,0.000062604,0.89651895,0.00019673537,0.000031503423,0.0076412987,0.000052421517,0.0014486619,0.00029098583],"about_ca_topic_score_codex":0.00031892577,"about_ca_topic_score_gemma":0.000046007015,"teacher_disagreement_score":0.058537092,"about_ca_system_score_codex":0.00004290781,"about_ca_system_score_gemma":0.00010861465,"threshold_uncertainty_score":0.9999499},"labels":[],"label_agreement":null},{"id":"W4414189985","doi":"10.7759/cureus.92316","title":"Peripheral Precocious Puberty Due to Autonomous Gonadal Activation: A Multicenter Experience","year":2025,"lang":"en","type":"article","venue":"Cureus","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child, Adolescent and Family Mental Health","funders":"","keywords":"Precocious puberty; Peripheral; Intervention (counseling); Delayed puberty","score_opus":0.008811375058414252,"score_gpt":0.2654567955905583,"score_spread":0.25664542053214406,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414189985","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98464084,0.0002306542,0.00832621,0.00042121508,0.000429126,0.000223298,0.0000037247657,0.000017974347,0.005706966],"genre_scores_gemma":[0.9918509,0.000010584567,0.0028772282,0.0011123475,0.0001212998,0.00007302909,0.000016173086,0.000011518429,0.0039268984],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9991889,0.00002069342,0.00015512247,0.00032937012,0.000067505236,0.00023841295],"domain_scores_gemma":[0.999512,0.0000059727477,0.000032182972,0.00031693184,0.000058969163,0.00007390281],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000047775702,0.00012345795,0.00010632066,0.000018573735,0.00008970502,0.000041609692,0.00020724047,0.00009160954,0.000111444235],"category_scores_gemma":[0.000091483096,0.000118730306,0.000056602366,0.00007204485,0.000029259356,0.0000043354266,0.00018725921,0.000051995597,0.0000109753955],"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":[0.000043891996,0.00018045897,0.018974734,0.000034222838,0.00011641841,0.000004880472,0.001581084,0.0002761769,0.92043006,0.00014871336,0.0074259555,0.050783385],"study_design_scores_gemma":[0.0010489183,0.00031253137,0.1933805,0.000054009815,0.00001894928,0.000043823395,0.0010274516,0.00072315685,0.3121764,0.00006223702,0.49064055,0.0005114754],"about_ca_topic_score_codex":0.000088391535,"about_ca_topic_score_gemma":0.000053909927,"teacher_disagreement_score":0.60825366,"about_ca_system_score_codex":0.00003959576,"about_ca_system_score_gemma":0.00007038811,"threshold_uncertainty_score":0.48416814},"labels":[],"label_agreement":null},{"id":"W4414526620","doi":"10.1210/jcemcr/luaf221","title":"Late Diagnosis of Prader-Willi Syndrome in an Adolescent With Significant Complications of Type 2 Diabetes","year":2025,"lang":"en","type":"article","venue":"JCEM Case Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Type 2 diabetes; Glycated hemoglobin; Diabetes mellitus; Socioeconomic status; Nephrotic syndrome; Type 1 diabetes","score_opus":0.013891197457164158,"score_gpt":0.2597249773187525,"score_spread":0.24583377986158833,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414526620","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991078,0.00034667042,0.000057359623,0.000068994246,0.00004843781,0.00022395988,0.000008425667,0.0000043982395,0.00013397493],"genre_scores_gemma":[0.9993425,0.00005822294,0.00044813444,0.000030146733,0.000005998052,0.00003065683,0.00003207288,0.000009783971,0.000042488646],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991427,0.000029479237,0.00036145104,0.00025662317,0.00007190171,0.00013785367],"domain_scores_gemma":[0.9991871,0.000011266305,0.00020028625,0.00044456992,0.00011542444,0.000041351905],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012293975,0.00009321122,0.00018176499,0.00006650089,0.000021950214,0.000006020822,0.000043638658,0.00006416709,0.0000054381585],"category_scores_gemma":[0.00003532896,0.00008212383,0.000037057245,0.0001840752,0.000059152582,0.0000026072732,0.000054542277,0.00004501802,2.2415865e-7],"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":[0.0000014805495,0.00023547586,0.9335716,0.00012445603,0.00004219415,0.00023998212,0.000021877826,0.00031827332,0.064107105,0.00001293879,0.000039454997,0.001285162],"study_design_scores_gemma":[0.00018132191,0.00033753022,0.9305982,0.00019522985,0.000039039853,0.0026084427,0.00006841367,0.00010348618,0.06534172,0.000040235118,0.00036386136,0.00012252272],"about_ca_topic_score_codex":0.000055106826,"about_ca_topic_score_gemma":0.00003424269,"teacher_disagreement_score":0.0029733966,"about_ca_system_score_codex":0.0000079929405,"about_ca_system_score_gemma":0.00008309407,"threshold_uncertainty_score":0.33489126},"labels":[],"label_agreement":null},{"id":"W4414830981","doi":"10.1093/jas/skaf300.473","title":"PSVI-11 Role of differentially expressed and imprinted genes in high and low fertility produced cattle pregnancies.","year":2025,"lang":"en","type":"article","venue":"Journal of Animal Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Conceptus; Genomic imprinting; Sire; Gene; Transcriptome; Embryo; Candidate gene; Estrous cycle","score_opus":0.0061400961333712934,"score_gpt":0.23700934132095217,"score_spread":0.23086924518758087,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414830981","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984131,0.0012519154,0.00008929927,0.000084963904,0.000059419457,0.00006556597,0.0000013104116,8.7393937e-7,0.00003358969],"genre_scores_gemma":[0.99922025,0.00014077369,0.00059146347,0.000011794386,0.000015324686,9.0119113e-7,2.0722072e-7,0.0000023875361,0.000016918166],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999266,0.00002021014,0.00025246394,0.00019049924,0.00012423426,0.00014658918],"domain_scores_gemma":[0.99953663,0.000007718482,0.00013482512,0.00011657533,0.00015125479,0.00005299397],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032964186,0.00006928407,0.00014362678,0.00007418558,0.000041177384,0.000027565615,0.00018385203,0.000038142505,0.0000025430745],"category_scores_gemma":[0.00017133872,0.00005544458,0.00002536303,0.00014697906,0.00021879972,0.000010481673,0.00020001657,0.0000502124,4.286298e-8],"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":[0.00003397597,0.000036844336,0.114949346,0.000025429319,0.000004490525,3.0802838e-7,0.000044006505,0.0000038723883,0.8811051,0.000016072781,0.000001912744,0.003778603],"study_design_scores_gemma":[0.00017993558,0.00015137643,0.49663883,0.00004251064,0.000003628068,0.000006492884,0.00005021743,0.000055039854,0.5027822,0.00004614572,0.000015840471,0.000027766895],"about_ca_topic_score_codex":0.00004910419,"about_ca_topic_score_gemma":0.000021062235,"teacher_disagreement_score":0.3816895,"about_ca_system_score_codex":0.000008559985,"about_ca_system_score_gemma":0.00015959685,"threshold_uncertainty_score":0.22609644},"labels":[],"label_agreement":null},{"id":"W4415352898","doi":"10.1101/2025.10.19.25338239","title":"Geography, Ancestry, Age and Sex Shape Somatic Autosomal Mosaic Chromosomal Alterations in Blood","year":2025,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Concordia University; Wilfrid Laurier University; Vector Institute; Ontario Institute for Cancer Research; Amgen (Canada); University of Toronto","funders":"National Institute of Environmental Health Sciences; National Human Genome Research Institute; National Cancer Institute; National Institutes of Health; Partenariat Canadien Contre Le Cancer; Health Canada; Government of Ontario","keywords":"Germline; Germline mutation; Somatic cell; Heritability; Genetic variation; Mosaic; Population; Missing heritability problem","score_opus":0.015384877325018871,"score_gpt":0.26030946620960743,"score_spread":0.24492458888458857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415352898","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99550056,0.0024189362,0.00013557998,0.00011424672,0.00031823505,0.00039162816,0.00006991388,0.00002605174,0.0010248361],"genre_scores_gemma":[0.99569243,0.0007381305,0.002278893,0.00010550337,0.00019242766,0.00012424137,0.0002758199,0.000024436602,0.0005681066],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99812484,0.00009965044,0.0004522708,0.0007921951,0.00014769795,0.00038332545],"domain_scores_gemma":[0.9990984,0.000018237923,0.00013669246,0.00061425945,0.000033533626,0.000098852615],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00018513217,0.00034777436,0.0003717836,0.0001559471,0.00009062649,0.00010844477,0.00035653976,0.00039739764,0.000031325664],"category_scores_gemma":[0.00006602097,0.00036775976,0.00014217806,0.00012752878,0.000106723244,0.0000030924832,0.00096279336,0.000337035,0.0000022276815],"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":[0.0000046894966,0.00022352261,0.8645471,0.00065444,0.00024791947,0.00007437195,0.00020867168,0.0004772705,0.12812962,0.000038053673,0.00007175484,0.00532264],"study_design_scores_gemma":[0.0012521031,0.00024870073,0.9505795,0.0005873344,0.00017260389,0.0001179566,0.00009086084,0.0045355875,0.038997266,0.000662917,0.0018975468,0.00085757865],"about_ca_topic_score_codex":0.00010798598,"about_ca_topic_score_gemma":0.00010481429,"teacher_disagreement_score":0.08913235,"about_ca_system_score_codex":0.00000765144,"about_ca_system_score_gemma":0.00015109059,"threshold_uncertainty_score":0.99987745},"labels":[],"label_agreement":null},{"id":"W4415388695","doi":"10.1111/jir.70053","title":"Codesigning a Neurocognitive Assessment Protocol for Hyperphagia: Perspectives From Stakeholders in Prader–Willi Syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Intellectual Disability Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health; SickKids Foundation; Hospital for Sick Children; Mental Health Research Canada","funders":"","keywords":"Neurocognitive; Protocol (science); Cognition; Stakeholder; Clinical trial; MEDLINE","score_opus":0.16058149419635448,"score_gpt":0.45914981158828366,"score_spread":0.2985683173919292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415388695","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.965465,0.00010746105,0.0076519125,0.0006859404,0.000068152025,0.025231663,0.000015051681,0.0000037498921,0.00077103515],"genre_scores_gemma":[0.9861638,0.000018573288,0.0028740559,0.000039201626,0.00008214453,0.010629334,0.000004748253,0.00001931386,0.00016883778],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.997419,0.0006378063,0.00063579314,0.00044268198,0.00041863546,0.0004460912],"domain_scores_gemma":[0.99744123,0.0012101841,0.00013207253,0.00027006003,0.00084491563,0.00010153544],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022054506,0.00017247035,0.00033802455,0.0001951943,0.00013866696,0.00009425911,0.00039907795,0.00014561438,0.00011600478],"category_scores_gemma":[0.0068277908,0.00014845535,0.00020225246,0.00039617205,0.00042376702,0.00001366604,0.00021936468,0.0006229504,0.0000019742652],"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":[0.0015114357,0.0067199157,0.25517806,0.00096604606,0.0012805078,0.000028243807,0.01098972,0.0006171869,0.65838814,0.00025568757,0.011135649,0.052929416],"study_design_scores_gemma":[0.014904555,0.016068472,0.70963734,0.0017088107,0.00009777861,0.0002840452,0.13457805,0.0028270402,0.09078187,0.0068323263,0.021279188,0.0010005235],"about_ca_topic_score_codex":0.000059023823,"about_ca_topic_score_gemma":0.00003803594,"teacher_disagreement_score":0.5676063,"about_ca_system_score_codex":0.00021069232,"about_ca_system_score_gemma":0.00064926,"threshold_uncertainty_score":0.8173996},"labels":[],"label_agreement":null},{"id":"W4415450113","doi":"10.1210/jendso/bvaf149.1774","title":"SAT-206 Development of a Minimum Dataset (MDS) for the Monitoring of Growth Hormone Therapy in Children with Prader Willi Syndrome (PWS) - A GloBE-Reg Initiative","year":2025,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Trinity College","funders":"","keywords":"Consistency (knowledge bases); Data collection; Growth hormone; Human growth hormone; Clinical trial; Quality (philosophy); Data quality","score_opus":0.013573048782031773,"score_gpt":0.26830445786840357,"score_spread":0.2547314090863718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415450113","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99566203,0.0024165348,0.0009327162,0.000495965,0.0000902303,0.00032542998,0.0000676247,9.3921875e-7,0.000008544826],"genre_scores_gemma":[0.99158144,0.0007673633,0.0074234433,0.00009333356,0.000062552404,0.000013803308,0.000018397668,0.000011136485,0.000028558557],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999005,0.00004413493,0.00045077078,0.00013011793,0.00018447258,0.00018546787],"domain_scores_gemma":[0.99909675,0.00005072396,0.00044659007,0.0002309801,0.00015046827,0.000024465737],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031990034,0.00013481137,0.00024191946,0.000026386264,0.00008115271,0.000010596391,0.00041449044,0.000042738935,0.0000013578621],"category_scores_gemma":[0.00006672716,0.00007401814,0.00019078502,0.00017528521,0.000093093084,0.000007672779,0.00017061194,0.00014245842,5.9417996e-8],"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":[0.0000971782,0.00044628643,0.7558758,0.00012337766,0.003810601,7.991351e-7,0.0016921211,0.0002780598,0.2260427,0.000021408225,0.006129427,0.0054822206],"study_design_scores_gemma":[0.0024314518,0.00044637045,0.8759554,0.00013801172,0.000074589036,0.00015135083,0.0010783238,0.000016263883,0.117837936,0.000043030755,0.0017248868,0.000102381426],"about_ca_topic_score_codex":0.000017162567,"about_ca_topic_score_gemma":0.0000030598383,"teacher_disagreement_score":0.120079584,"about_ca_system_score_codex":0.000024710258,"about_ca_system_score_gemma":0.00022592464,"threshold_uncertainty_score":0.30183724},"labels":[],"label_agreement":null},{"id":"W4415988284","doi":"10.4244/eij-e-25-00046","title":"HALT &amp;ndash; an evolving understanding of the mechanisms of formation and clinical relevance","year":2025,"lang":"en","type":"article","venue":"EuroIntervention","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"St. Paul's Hospital; University of British Columbia","funders":"","keywords":"Clinical significance; Relevance (law); MEDLINE; Mechanism (biology)","score_opus":0.04608982617497265,"score_gpt":0.32808199130562643,"score_spread":0.2819921651306538,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415988284","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.71662873,0.00015936143,0.28263825,0.000055227778,0.00015943166,0.00006997791,0.000001590102,0.0000022749734,0.00028517185],"genre_scores_gemma":[0.99787706,0.000040661194,0.0017732995,0.000018927609,0.000010282335,3.7929405e-7,0.000006768113,0.0000042618594,0.00026838575],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993718,0.00009051472,0.00030172386,0.00011811323,0.000055671593,0.00006214894],"domain_scores_gemma":[0.9995685,0.000011484077,0.00017299344,0.00018627447,0.000047739042,0.000012981853],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036588713,0.000047050995,0.00007822868,0.000023885274,0.000039931852,0.00000946752,0.00008374751,0.00004144591,0.0000050040458],"category_scores_gemma":[0.0001974012,0.00003936538,0.00010153299,0.000052461015,0.0000408978,0.0000067869814,0.00010858315,0.00003973795,2.5148782e-7],"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":[0.000016401335,0.00008096736,0.019055033,0.00023588372,0.000044042925,6.633222e-8,0.000052574687,0.000018182682,0.9688932,0.005790582,0.00019610561,0.0056169606],"study_design_scores_gemma":[0.001378538,0.0009781258,0.4722832,0.0010999857,0.000104624414,0.00002871972,0.00075947796,0.0032205693,0.49527955,0.023603303,0.0010681648,0.00019574264],"about_ca_topic_score_codex":0.000007099369,"about_ca_topic_score_gemma":0.000032485343,"teacher_disagreement_score":0.47361365,"about_ca_system_score_codex":0.000007112544,"about_ca_system_score_gemma":0.000011195278,"threshold_uncertainty_score":0.16052735},"labels":[],"label_agreement":null},{"id":"W4416343701","doi":"10.1016/j.placenta.2025.08.110","title":"Loss of maternally imprinted Sfmbt2 microRNA cluster results in placental junctional zone abnormalities and FGR in mice","year":2025,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"microRNA; Genomic imprinting; Cluster (spacecraft); Placenta","score_opus":0.005163278851479605,"score_gpt":0.22752422390185265,"score_spread":0.22236094505037304,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416343701","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977729,0.00038634875,0.0001262559,0.0002793722,0.0001849191,0.00013936736,0.000041781754,0.0000032698802,0.0010658343],"genre_scores_gemma":[0.9970836,0.00016430813,0.00044970188,0.00014221793,0.00002306958,0.000006211787,0.000062826504,0.000007730821,0.0020603142],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99905723,0.000045586174,0.00035343322,0.0002636981,0.000074643816,0.0002054115],"domain_scores_gemma":[0.9997143,0.000020427704,0.00007360415,0.0001325565,0.000029064473,0.000030015744],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022209657,0.00011688842,0.00014695247,0.00009990785,0.000018968107,0.0000152713,0.00011406682,0.00009749115,0.000011764873],"category_scores_gemma":[0.000043241347,0.00012004156,0.000033348148,0.000084741,0.000064441694,0.0000043066993,0.00022879239,0.000084846346,0.0000021388914],"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":[0.00073117955,0.00013705538,0.39299336,0.00014853507,0.000051160918,0.0000062092795,0.00029332857,0.00010506233,0.60410553,0.00004829273,0.0005703969,0.0008099009],"study_design_scores_gemma":[0.005635397,0.000118699754,0.6537027,0.00021733716,0.000011619685,0.0000952264,0.0008912299,0.00037706763,0.33369046,0.00003217064,0.005011788,0.00021634741],"about_ca_topic_score_codex":0.00046020435,"about_ca_topic_score_gemma":0.00060486083,"teacher_disagreement_score":0.27041504,"about_ca_system_score_codex":0.000024208159,"about_ca_system_score_gemma":0.000047105932,"threshold_uncertainty_score":0.48951524},"labels":[],"label_agreement":null},{"id":"W4416902275","doi":"10.1111/cpr.70150","title":"Analysis of Human Uniparental Embryonic Stem Cells Reveals New Putative Imprinted Loci","year":2025,"lang":"en","type":"article","venue":"Cell Proliferation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"HORIZON EUROPE Health; Azrieli Foundation; Israel Science Foundation; United States-Israel Binational Science Foundation; HORIZON EUROPE Framework Programme; Rosetrees Trust; European Commission","keywords":"Genomic imprinting; Epigenetics; Imprinting (psychology); Embryonic stem cell; DNA methylation; Induced pluripotent stem cell; Gene; Transcriptome","score_opus":0.011090431045441662,"score_gpt":0.26579381092282833,"score_spread":0.25470337987738667,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416902275","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98102736,0.00024494622,0.017158004,0.000036655456,0.00007372844,0.0002281134,0.00000803419,0.000007773644,0.0012153611],"genre_scores_gemma":[0.9908757,0.00002147532,0.000272377,0.00006782434,0.000035927686,0.000008727422,0.00019905655,0.000008615976,0.00851026],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99912333,0.00006395677,0.00029021318,0.00028585695,0.000088260436,0.00014836417],"domain_scores_gemma":[0.99943084,0.000007142999,0.00014810212,0.0002582136,0.00010850393,0.00004719349],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013696548,0.00011805657,0.00020537726,0.00015003039,0.00006764555,0.000025275309,0.00012480807,0.00010358469,0.000027768887],"category_scores_gemma":[0.000008944061,0.00011996439,0.0001353119,0.00036997115,0.000028267788,0.0000032930523,0.00008749479,0.00005519202,0.0000038544695],"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":[0.0000065993863,0.00004123114,0.015416915,0.000033594824,0.00026316315,1.5882075e-7,0.00011610601,0.00083548785,0.9814879,0.00006150905,0.0003896436,0.0013477439],"study_design_scores_gemma":[0.0003793667,0.00014842936,0.019424653,0.000009675096,0.00028661065,4.4029753e-7,0.00021144847,0.0016410601,0.97748363,0.00006534322,0.00023892643,0.00011039849],"about_ca_topic_score_codex":0.000032742853,"about_ca_topic_score_gemma":0.000023651477,"teacher_disagreement_score":0.016885625,"about_ca_system_score_codex":0.000019584213,"about_ca_system_score_gemma":0.000091536065,"threshold_uncertainty_score":0.4892006},"labels":[],"label_agreement":null},{"id":"W6888996397","doi":"10.25384/sage.19307754","title":"sj-pdf-1-jcn-10.1177_08830738221081244 - Supplemental material for Further Characterization of <i>SMC1A</i> Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome","year":2022,"lang":"en","type":"article","venue":"Sage Journals Data","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Sherbrooke","funders":"","keywords":"Cornelia de Lange Syndrome; Epilepsy; Loss function; Neurology; Function (biology)","score_opus":0.020017718384738037,"score_gpt":0.2576234164026141,"score_spread":0.23760569801787607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6888996397","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9551636,0.0004044643,0.0048845573,0.00009193146,0.00045202335,0.00024720083,0.03872454,0.000004661535,0.000027000797],"genre_scores_gemma":[0.97042644,0.00018476819,0.00062132947,0.00006874642,0.00024927946,0.000027789269,0.028115943,0.000030074463,0.00027560405],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986892,0.00010540749,0.00046577633,0.0003096576,0.00019548445,0.0002344969],"domain_scores_gemma":[0.99886745,0.000016304348,0.00044251373,0.0005584822,0.00005525584,0.000059994825],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000492209,0.0001390373,0.0002361077,0.00004261164,0.00010015028,0.000027688302,0.00047979745,0.000067731125,0.01596249],"category_scores_gemma":[0.000045144345,0.00014263559,0.00008535839,0.000071665505,0.000037860773,0.00001577932,0.0006040666,0.000077166216,0.000005115031],"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":[0.0001383424,0.00010360664,0.029074732,0.000034691944,0.00012628117,0.0000035230528,0.000048539037,0.0000064366245,0.96496123,6.272873e-7,0.00144833,0.004053636],"study_design_scores_gemma":[0.0036608577,0.0018820899,0.59233063,0.00018367932,0.0003569342,0.00043420095,0.000678174,0.00043331707,0.32240856,0.00020183076,0.07688715,0.0005425981],"about_ca_topic_score_codex":0.00007961958,"about_ca_topic_score_gemma":0.000013924363,"teacher_disagreement_score":0.64255273,"about_ca_system_score_codex":0.000018875751,"about_ca_system_score_gemma":0.000062868436,"threshold_uncertainty_score":0.9849371},"labels":[],"label_agreement":null},{"id":"W6889108574","doi":"10.25384/sage.19307754.v1","title":"sj-pdf-1-jcn-10.1177_08830738221081244 - Supplemental material for Further Characterization of <i>SMC1A</i> Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Sherbrooke","funders":"","keywords":"Cornelia de Lange Syndrome; Epilepsy; Loss function; Neurology; Function (biology)","score_opus":0.012900142201018398,"score_gpt":0.21949446814310822,"score_spread":0.20659432594208982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6889108574","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.68334436,0.000026483196,0.00004229578,0.00001575693,0.00012868724,0.00022521969,0.31615707,0.00000596312,0.00005415322],"genre_scores_gemma":[0.6529099,0.0000010998667,0.00007308869,0.000035202578,0.00009717689,0.00017136124,0.34640515,0.0000205759,0.00028649005],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99910223,0.000046047007,0.00027319454,0.00025361142,0.00012641399,0.0001985254],"domain_scores_gemma":[0.99941444,0.000013613887,0.0002427416,0.00022060894,0.00006773947,0.00004085627],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0000636539,0.00012891463,0.00017598318,0.000027700513,0.00006606529,0.000012754178,0.00017817022,0.00007408384,0.19980869],"category_scores_gemma":[0.00005483793,0.00014127002,0.00010771837,0.00005748608,0.000010299323,0.0000050867948,0.00022263543,0.000042948323,0.000036601872],"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":[0.00012226791,0.00008776587,0.006405959,0.000138951,0.00007284459,0.0000020110986,0.00007228465,0.000012267917,0.97438174,0.0000013775308,0.01809984,0.0006027119],"study_design_scores_gemma":[0.001868937,0.0016051106,0.31985044,0.0001483109,0.00007951351,0.00007230107,0.0002588248,0.00017711124,0.4751272,0.00003862203,0.20037001,0.0004036399],"about_ca_topic_score_codex":0.00002646906,"about_ca_topic_score_gemma":0.000005826737,"teacher_disagreement_score":0.49925452,"about_ca_system_score_codex":0.000019391742,"about_ca_system_score_gemma":0.000047934544,"threshold_uncertainty_score":0.8009228},"labels":[],"label_agreement":null},{"id":"W6901816567","doi":"10.6084/m9.figshare.20064365","title":"Additional file 7 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Function (biology); Channel (broadcasting); HEK 293 cells; Gene; Loss function; Variation (astronomy); Cell","score_opus":0.013486072645029401,"score_gpt":0.20281614346042673,"score_spread":0.18933007081539732,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6901816567","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10513295,0.00012742022,0.000027784077,0.000010839493,0.000016661183,0.000110411966,0.89451677,0.0000039760102,0.000053212003],"genre_scores_gemma":[0.6000251,0.0000013286176,0.000079825775,0.000013715806,0.000017161568,0.000106213774,0.39958686,0.000007381625,0.00016242085],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994309,0.00002080302,0.00015745721,0.00019022453,0.00010795447,0.000092669994],"domain_scores_gemma":[0.99956703,0.000052480795,0.00019054048,0.00008848306,0.00007368238,0.00002775532],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000041111296,0.000073379066,0.00008654573,0.000033426666,0.000076434524,0.0000069505672,0.000046316563,0.00005371396,0.37976465],"category_scores_gemma":[0.00038510296,0.00008578964,0.000025733198,0.00006656122,0.0000058362803,0.000005739018,0.00018960718,0.000046499124,0.000003737069],"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":[0.000013251308,0.000068740475,0.000044509652,0.00021424379,0.00006792904,5.8777835e-7,0.0000632468,0.0002874524,0.26222044,0.0000069825282,0.7361942,0.0008184351],"study_design_scores_gemma":[0.0023562717,0.0019546852,0.6297923,0.0012164568,0.000082957195,0.0008736113,0.00052191457,0.022066524,0.039458442,0.00017709176,0.3005413,0.0009584205],"about_ca_topic_score_codex":0.000003502345,"about_ca_topic_score_gemma":6.960411e-7,"teacher_disagreement_score":0.6297478,"about_ca_system_score_codex":0.0000065973645,"about_ca_system_score_gemma":0.000026579633,"threshold_uncertainty_score":0.62080234},"labels":[],"label_agreement":null},{"id":"W6902075749","doi":"10.6084/m9.figshare.28040116","title":"Additional file 4 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Regulator; Track (disk drive); Epigenetics; Pregnancy; Folic acid; Folic acid supplementation","score_opus":0.0175098936779545,"score_gpt":0.24244197318072602,"score_spread":0.22493207950277153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902075749","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.24811302,0.0006115622,7.586236e-7,0.0000061389514,0.00000877496,0.00016476584,0.7509608,0.0000073794863,0.00012675655],"genre_scores_gemma":[0.4964413,0.000010088662,0.00020408159,0.0000040301425,0.000049399543,0.00031047166,0.5027069,0.00001626293,0.00025747638],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99927557,0.000016647748,0.00015035346,0.0002755353,0.00012701785,0.0001549005],"domain_scores_gemma":[0.9995388,0.000048226248,0.00009911307,0.00014615359,0.00011798583,0.00004972818],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000008628007,0.000116732626,0.00010709123,0.000043328484,0.00003640228,0.000011855471,0.00008384955,0.000068127614,0.7440098],"category_scores_gemma":[0.00014593873,0.00010900429,0.000050304152,0.000077646204,0.000013172532,0.0000052356886,0.00009935431,0.000034258737,0.00004290284],"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":[0.00008210883,0.00021338437,0.00024093238,0.0027804603,0.0004339426,0.000013008607,0.00085219456,0.00010305303,0.3995543,0.0000045674146,0.5292454,0.06647665],"study_design_scores_gemma":[0.00032166849,0.0007232623,0.090608425,0.008277287,0.00002322651,0.00006714543,0.00016354951,0.00005120843,0.8877105,0.0000031936777,0.011854301,0.00019619378],"about_ca_topic_score_codex":0.0000020335292,"about_ca_topic_score_gemma":0.000059536993,"teacher_disagreement_score":0.7439669,"about_ca_system_score_codex":0.000009811486,"about_ca_system_score_gemma":0.00005229185,"threshold_uncertainty_score":0.44450662},"labels":[],"label_agreement":null},{"id":"W6902109544","doi":"10.6084/m9.figshare.20064371","title":"Additional file 9 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Function (biology); Loss function; Channel (broadcasting); Gene; HEK 293 cells; Variation (astronomy); Mutation","score_opus":0.013477445620077237,"score_gpt":0.20279957040024266,"score_spread":0.1893221247801654,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902109544","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10514284,0.00012755053,0.000027842496,0.000010856189,0.00001666583,0.000110438,0.8945065,0.0000039774136,0.00005332749],"genre_scores_gemma":[0.60110945,0.0000013288151,0.00007990192,0.000013738798,0.000017184886,0.00010578896,0.39850208,0.000007388228,0.00016314028],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99943095,0.000020807183,0.00015745375,0.00019018205,0.000107946085,0.00009265814],"domain_scores_gemma":[0.9995671,0.000052516036,0.00019052908,0.00008845573,0.00007368346,0.000027750137],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00004110495,0.00007336928,0.00008653284,0.00003342509,0.000076434575,0.000006948466,0.0000462813,0.00005370534,0.38196295],"category_scores_gemma":[0.00038880017,0.00008577678,0.000025732445,0.00006655805,0.0000058356773,0.0000057388215,0.00018951968,0.000046482957,0.0000037434042],"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":[0.000013155206,0.00006822963,0.000044242366,0.00021100414,0.0000674207,5.833733e-7,0.000062770414,0.00028540383,0.25960398,0.00000682358,0.7388358,0.0008005799],"study_design_scores_gemma":[0.0023433233,0.0019421015,0.6321219,0.0012001023,0.000082531886,0.0008694151,0.0005195403,0.02197183,0.03912941,0.0001762858,0.29869014,0.00095341314],"about_ca_topic_score_codex":0.0000034366208,"about_ca_topic_score_gemma":6.9435333e-7,"teacher_disagreement_score":0.6320777,"about_ca_system_score_codex":0.00000659585,"about_ca_system_score_gemma":0.000026568634,"threshold_uncertainty_score":0.61860204},"labels":[],"label_agreement":null},{"id":"W6902126386","doi":"10.6084/m9.figshare.28040104.v1","title":"Additional file 1 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Regulator; Epigenetics; EPIC; CpG site; Table (database); Offspring; Pregnancy; Folic acid; DNA methylation","score_opus":0.017674961586394373,"score_gpt":0.24242228909963967,"score_spread":0.2247473275132453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902126386","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.24758174,0.0006063353,7.49971e-7,0.000006172738,0.000008766323,0.00016455568,0.751498,0.0000073752612,0.00012631134],"genre_scores_gemma":[0.4935008,0.000009981703,0.0002065814,0.000004038512,0.000049454535,0.00031658798,0.5056344,0.000016306118,0.00026185703],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99927557,0.00001666443,0.00015024285,0.00027561997,0.00012700146,0.00015489524],"domain_scores_gemma":[0.9995373,0.000048534395,0.00009908315,0.0001462832,0.0001190709,0.00004972954],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000008625234,0.000116740215,0.00010705803,0.000043323238,0.000036388537,0.000011827449,0.000083841274,0.00006812763,0.7512339],"category_scores_gemma":[0.00014787163,0.00010901073,0.00005030352,0.00007768168,0.000013169504,0.0000052313026,0.00009938532,0.000034266122,0.00004328919],"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":[0.00007866812,0.00020752123,0.00023354866,0.0026818642,0.0004223438,0.000012473641,0.00082799443,0.00010149402,0.39301506,0.00000432336,0.53857046,0.06384425],"study_design_scores_gemma":[0.00031882818,0.0007131119,0.09071309,0.008275939,0.000023260689,0.000067091256,0.00016381982,0.000050975763,0.88737136,0.0000031560385,0.012103217,0.00019615094],"about_ca_topic_score_codex":0.0000020291595,"about_ca_topic_score_gemma":0.000058947335,"teacher_disagreement_score":0.7511906,"about_ca_system_score_codex":0.000009810622,"about_ca_system_score_gemma":0.000052445706,"threshold_uncertainty_score":0.44453287},"labels":[],"label_agreement":null},{"id":"W6902230824","doi":"10.6084/m9.figshare.28040116.v1","title":"Additional file 4 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Regulator; Track (disk drive); Epigenetics; Pregnancy; Folic acid; Folic acid supplementation","score_opus":0.0175098936779545,"score_gpt":0.24244197318072602,"score_spread":0.22493207950277153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902230824","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.24811302,0.0006115622,7.586236e-7,0.0000061389514,0.00000877496,0.00016476584,0.7509608,0.0000073794863,0.00012675655],"genre_scores_gemma":[0.4964413,0.000010088662,0.00020408159,0.0000040301425,0.000049399543,0.00031047166,0.5027069,0.00001626293,0.00025747638],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99927557,0.000016647748,0.00015035346,0.0002755353,0.00012701785,0.0001549005],"domain_scores_gemma":[0.9995388,0.000048226248,0.00009911307,0.00014615359,0.00011798583,0.00004972818],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000008628007,0.000116732626,0.00010709123,0.000043328484,0.00003640228,0.000011855471,0.00008384955,0.000068127614,0.7440098],"category_scores_gemma":[0.00014593873,0.00010900429,0.000050304152,0.000077646204,0.000013172532,0.0000052356886,0.00009935431,0.000034258737,0.00004290284],"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":[0.00008210883,0.00021338437,0.00024093238,0.0027804603,0.0004339426,0.000013008607,0.00085219456,0.00010305303,0.3995543,0.0000045674146,0.5292454,0.06647665],"study_design_scores_gemma":[0.00032166849,0.0007232623,0.090608425,0.008277287,0.00002322651,0.00006714543,0.00016354951,0.00005120843,0.8877105,0.0000031936777,0.011854301,0.00019619378],"about_ca_topic_score_codex":0.0000020335292,"about_ca_topic_score_gemma":0.000059536993,"teacher_disagreement_score":0.7439669,"about_ca_system_score_codex":0.000009811486,"about_ca_system_score_gemma":0.00005229185,"threshold_uncertainty_score":0.44450662},"labels":[],"label_agreement":null},{"id":"W6902261421","doi":"10.6084/m9.figshare.26558375","title":"Additional file 1 of Genome-wide placental DNA methylations in fetal overgrowth and associations with leptin, adiponectin and fetal growth factors","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Adiponectin; Fetus; Fetal growth; DNA; Mutation","score_opus":0.010948731234723045,"score_gpt":0.21346683007641326,"score_spread":0.20251809884169023,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902261421","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.22140858,0.00021361887,0.000002767999,0.000013894198,0.000008098484,0.00008682093,0.7776585,0.0000075767484,0.0006001323],"genre_scores_gemma":[0.5698584,0.0000032847734,0.00025583466,0.000010523914,0.000027248614,0.000056459867,0.42960495,0.000011494998,0.00017185698],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994103,0.000020043846,0.00012554973,0.00022422933,0.00008720554,0.00013270914],"domain_scores_gemma":[0.999549,0.00023412015,0.0000635484,0.00006277253,0.00004217731,0.00004838714],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000019227671,0.0001042954,0.00010035546,0.000059849397,0.000050399147,0.000032936845,0.00004412882,0.00007777654,0.2828255],"category_scores_gemma":[0.00088501483,0.0000960407,0.000036422418,0.00010767491,0.000014670683,0.0000088504985,0.000083778126,0.00007599035,0.000016096621],"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":[0.000011060131,0.00008167807,0.0198671,0.00024891787,0.00026617103,0.000009115476,0.000327187,0.000028296085,0.010257106,0.000010206683,0.96763,0.0012631544],"study_design_scores_gemma":[0.0002368424,0.00019637318,0.9309309,0.0004310291,0.00001472878,0.000033389035,0.0002115988,0.00020622964,0.0028093266,0.00001833704,0.06469709,0.00021417023],"about_ca_topic_score_codex":0.000011198777,"about_ca_topic_score_gemma":0.000068604866,"teacher_disagreement_score":0.9110638,"about_ca_system_score_codex":0.0000152389075,"about_ca_system_score_gemma":0.00007473957,"threshold_uncertainty_score":0.7178301},"labels":[],"label_agreement":null},{"id":"W6902356380","doi":"10.6084/m9.figshare.26558375.v1","title":"Additional file 1 of Genome-wide placental DNA methylations in fetal overgrowth and associations with leptin, adiponectin and fetal growth factors","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Adiponectin; Fetus; Fetal growth; DNA; Mutation","score_opus":0.010948731234723045,"score_gpt":0.21346683007641326,"score_spread":0.20251809884169023,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902356380","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.22140858,0.00021361887,0.000002767999,0.000013894198,0.000008098484,0.00008682093,0.7776585,0.0000075767484,0.0006001323],"genre_scores_gemma":[0.5698584,0.0000032847734,0.00025583466,0.000010523914,0.000027248614,0.000056459867,0.42960495,0.000011494998,0.00017185698],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994103,0.000020043846,0.00012554973,0.00022422933,0.00008720554,0.00013270914],"domain_scores_gemma":[0.999549,0.00023412015,0.0000635484,0.00006277253,0.00004217731,0.00004838714],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000019227671,0.0001042954,0.00010035546,0.000059849397,0.000050399147,0.000032936845,0.00004412882,0.00007777654,0.2828255],"category_scores_gemma":[0.00088501483,0.0000960407,0.000036422418,0.00010767491,0.000014670683,0.0000088504985,0.000083778126,0.00007599035,0.000016096621],"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":[0.000011060131,0.00008167807,0.0198671,0.00024891787,0.00026617103,0.000009115476,0.000327187,0.000028296085,0.010257106,0.000010206683,0.96763,0.0012631544],"study_design_scores_gemma":[0.0002368424,0.00019637318,0.9309309,0.0004310291,0.00001472878,0.000033389035,0.0002115988,0.00020622964,0.0028093266,0.00001833704,0.06469709,0.00021417023],"about_ca_topic_score_codex":0.000011198777,"about_ca_topic_score_gemma":0.000068604866,"teacher_disagreement_score":0.9110638,"about_ca_system_score_codex":0.0000152389075,"about_ca_system_score_gemma":0.00007473957,"threshold_uncertainty_score":0.7178301},"labels":[],"label_agreement":null},{"id":"W6906496455","doi":"10.17605/osf.io/9r4wf","title":"Sex-dependent placental mQTL provide insight into the prenatal origins of childhood-onset traits and conditions","year":2022,"lang":"en","type":"article","venue":"OSF Preprints (OSF Preprints)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Pregnancy; Offspring; Fetus; Placenta","score_opus":0.006172744144943737,"score_gpt":0.22861543610749452,"score_spread":0.2224426919625508,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6906496455","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9786868,0.00002404965,0.0001713836,0.0001986752,0.00012805572,0.000748947,0.000118078344,0.000019107947,0.019904874],"genre_scores_gemma":[0.98204875,0.000084357904,0.0003021818,0.000109705325,0.000057987505,0.00025879996,0.000089301655,0.000029918448,0.017019024],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9974967,0.00038417775,0.000408664,0.0011005538,0.00031255808,0.0002973427],"domain_scores_gemma":[0.99845946,0.00007769463,0.00021072147,0.0010774457,0.000052505467,0.00012214777],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0011759009,0.00022140772,0.00022754497,0.00006618397,0.0005792917,0.00003915,0.00069068157,0.00009757389,0.022468848],"category_scores_gemma":[0.00035011518,0.000210372,0.00012812078,0.00010485189,0.00021067291,0.000011687728,0.003140619,0.00030827257,0.0024049357],"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":[0.00011143156,0.000931127,0.06866714,0.00018064807,0.0006459228,0.000015888769,0.016240552,0.0036540003,0.8773136,0.0011018105,0.002449952,0.028687906],"study_design_scores_gemma":[0.0022105852,0.000046275884,0.17179005,0.000048577873,0.00013280832,0.00096007093,0.0027169464,0.00038276013,0.6075173,0.0008472948,0.21265204,0.00069527136],"about_ca_topic_score_codex":0.00021846849,"about_ca_topic_score_gemma":0.000066078595,"teacher_disagreement_score":0.2697963,"about_ca_system_score_codex":0.00010260765,"about_ca_system_score_gemma":0.00022064499,"threshold_uncertainty_score":0.9983718},"labels":[],"label_agreement":null},{"id":"W6920790104","doi":"10.6084/m9.figshare.20064368.v1","title":"Additional file 8 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Function (biology); Extracellular; Channel (broadcasting); Loss function; HEK 293 cells; Gene; Variation (astronomy)","score_opus":0.013470722356893429,"score_gpt":0.2027671882946675,"score_spread":0.18929646593777408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6920790104","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.105474524,0.00012751453,0.000027807944,0.000010851535,0.000016658574,0.00011042204,0.8941747,0.0000039518823,0.000053574116],"genre_scores_gemma":[0.6012159,0.0000013142712,0.000079978556,0.000013736131,0.000017178647,0.00010644644,0.39839387,0.000007381771,0.00016418195],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99943095,0.000020807911,0.00015745455,0.00019020162,0.000107933396,0.00009266535],"domain_scores_gemma":[0.99956703,0.000052523377,0.00019055056,0.00008847907,0.000073687435,0.000027753444],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0000411125,0.00007337712,0.000086545144,0.000033418066,0.00007643078,0.000006949708,0.00004631117,0.000053713236,0.38291934],"category_scores_gemma":[0.00038881792,0.00008578584,0.000025732998,0.00006652562,0.0000058357964,0.000005738154,0.00018956579,0.00004649786,0.0000037574166],"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":[0.000013183248,0.000068371155,0.000044029905,0.00021146843,0.00006757528,5.8471727e-7,0.000062905056,0.0002860498,0.25849804,0.0000069236585,0.73992014,0.0008207247],"study_design_scores_gemma":[0.0023537902,0.0019533683,0.6305425,0.0012050711,0.000082879305,0.0008730373,0.000521565,0.022061806,0.03976006,0.00017697838,0.29951143,0.00095748884],"about_ca_topic_score_codex":0.0000034963866,"about_ca_topic_score_gemma":6.9531296e-7,"teacher_disagreement_score":0.63049847,"about_ca_system_score_codex":0.0000065970667,"about_ca_system_score_gemma":0.000026582187,"threshold_uncertainty_score":0.6176448},"labels":[],"label_agreement":null},{"id":"W6920793839","doi":"10.6084/m9.figshare.28040107","title":"Additional file 2 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Methylation; DNA methylation; Epigenetics; Cord blood; Genotype; Table (database); Regulator","score_opus":0.01710101841153143,"score_gpt":0.24193957841293662,"score_spread":0.22483856000140517,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6920793839","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.2469692,0.0006161637,7.36603e-7,0.000006154299,0.000008827748,0.00016457109,0.75209785,0.000007386259,0.00012913845],"genre_scores_gemma":[0.49234524,0.000010233768,0.00020272649,0.000004044009,0.00005018427,0.00031148674,0.5067968,0.000016306783,0.00026298495],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992758,0.000016659302,0.00015030394,0.0002754325,0.00012697263,0.00015484345],"domain_scores_gemma":[0.9995383,0.00004791172,0.00009920898,0.00014602848,0.000118830765,0.000049722963],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000008582504,0.00011670654,0.00010708181,0.000043297507,0.000036390957,0.000011850734,0.00008379894,0.000068127985,0.74799496],"category_scores_gemma":[0.0001462518,0.000108978405,0.00005029469,0.0000776269,0.00001316934,0.0000052345545,0.000099372635,0.000034258963,0.00004287002],"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":[0.000079699,0.00021122194,0.00023093341,0.0027529318,0.0004300063,0.00001301475,0.0008436547,0.000103784965,0.38812578,0.0000044719727,0.5405688,0.066635676],"study_design_scores_gemma":[0.0003220401,0.00071595924,0.08979991,0.008215113,0.000023273304,0.00006748446,0.00016292566,0.000050861156,0.8878739,0.0000031910333,0.012568836,0.00019652935],"about_ca_topic_score_codex":0.0000020477014,"about_ca_topic_score_gemma":0.000059263726,"teacher_disagreement_score":0.7479521,"about_ca_system_score_codex":0.000009813171,"about_ca_system_score_gemma":0.000052233936,"threshold_uncertainty_score":0.44440106},"labels":[],"label_agreement":null},{"id":"W6920795910","doi":"10.6084/m9.figshare.26986429","title":"Additional file 10 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.013896958573758356,"score_gpt":0.2409133182193833,"score_spread":0.22701635964562494,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6920795910","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.43123087,0.00040525355,0.0000019922622,0.000027731281,0.000015086006,0.00007600817,0.5675754,0.0000030205015,0.0006646389],"genre_scores_gemma":[0.9016872,0.000011447722,0.00043477857,0.000019179324,0.00003330521,0.00004257505,0.09755169,0.0000063956336,0.000213421],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9995362,0.0000102614895,0.00015068905,0.00016403824,0.000055262713,0.00008355643],"domain_scores_gemma":[0.9997204,0.000100078316,0.00003828085,0.00007126952,0.000042457945,0.000027496682],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00002849856,0.00005553768,0.0000810907,0.000023997247,0.0000124705575,0.0000086712635,0.000046440866,0.00006911536,0.32148138],"category_scores_gemma":[0.0006003199,0.000055470387,0.00002474614,0.000054962853,0.000018822948,0.0000029164019,0.00016008399,0.00004498913,0.0000105121135],"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":[0.0000056245913,0.000020856703,0.0020862815,0.00047723245,0.00002437109,0.0000033523527,0.000035484594,0.0000056102185,0.043478917,0.000007368408,0.94743276,0.0064221164],"study_design_scores_gemma":[0.00032342164,0.0002642072,0.60325617,0.0029779263,0.000009208348,0.00005656363,0.00007380067,0.0034677272,0.026885,0.0000334175,0.36241743,0.00023515969],"about_ca_topic_score_codex":0.000019079827,"about_ca_topic_score_gemma":0.000025765,"teacher_disagreement_score":0.6011699,"about_ca_system_score_codex":0.0000030905765,"about_ca_system_score_gemma":0.00010993078,"threshold_uncertainty_score":0.6791389},"labels":[],"label_agreement":null},{"id":"W6921018293","doi":"10.6084/m9.figshare.28040110","title":"Additional file 3 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Cognition; Regulator; Pregnancy; Epigenetics; Folic acid; Track (disk drive); Folic acid supplementation","score_opus":0.01738066982375489,"score_gpt":0.24208178526760682,"score_spread":0.22470111544385193,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6921018293","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.2485809,0.00060888357,7.534618e-7,0.0000061428377,0.000008838255,0.00016446452,0.75049573,0.000007362684,0.00012692713],"genre_scores_gemma":[0.4950478,0.000010115967,0.00020443159,0.0000040370214,0.00004999278,0.00031129026,0.50408936,0.000016310642,0.00026663663],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992756,0.00001664974,0.00015030405,0.0002755099,0.00012702512,0.00015488431],"domain_scores_gemma":[0.99953693,0.000048141028,0.0000990974,0.00014608231,0.000120031735,0.000049725644],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000008621657,0.000116725176,0.000107068045,0.000043310003,0.000036385674,0.000011849686,0.000083793006,0.000068122325,0.7469474],"category_scores_gemma":[0.0001478353,0.0001089853,0.00005030058,0.000077655306,0.000013170362,0.000005234987,0.00009931957,0.000034259712,0.00004372225],"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":[0.000080506994,0.00021111913,0.00023799721,0.0027721403,0.0004295275,0.000012835522,0.0008427576,0.00010332882,0.40088966,0.0000043750433,0.5285674,0.06584833],"study_design_scores_gemma":[0.00032055716,0.0007071024,0.08959679,0.008200855,0.000022904127,0.000066041786,0.000161941,0.000050684856,0.8884454,0.000003141837,0.012229822,0.00019476682],"about_ca_topic_score_codex":0.0000020502314,"about_ca_topic_score_gemma":0.000059313847,"teacher_disagreement_score":0.7469037,"about_ca_system_score_codex":0.000009846242,"about_ca_system_score_gemma":0.00005247225,"threshold_uncertainty_score":0.44442916},"labels":[],"label_agreement":null},{"id":"W6921028860","doi":"10.6084/m9.figshare.26986399","title":"Additional file 1 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.012503434411400817,"score_gpt":0.23530005347426144,"score_spread":0.22279661906286063,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6921028860","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.23480166,0.0002697112,0.0000015222105,0.000019712204,0.000011483482,0.000058064856,0.7644159,0.0000022780334,0.00041964644],"genre_scores_gemma":[0.8352612,0.000010802365,0.00053070387,0.000021197826,0.000031369735,0.000052738433,0.16398032,0.0000060677567,0.00010557911],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99955714,0.000009629035,0.00014378155,0.00015695281,0.00005237335,0.000080115955],"domain_scores_gemma":[0.9997077,0.00012518687,0.000036933332,0.000067368754,0.000036592923,0.000026191627],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000024101848,0.000052819447,0.00007746948,0.00002323183,0.000011781935,0.000008049095,0.00004384282,0.000064916894,0.3810009],"category_scores_gemma":[0.0006690168,0.00005272602,0.00002349173,0.0000537763,0.000018013723,0.000002738034,0.00015385404,0.000046121047,0.000007705209],"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":[0.000002977645,0.000014099837,0.0016855975,0.00033906024,0.00001706759,0.0000024395029,0.000026890706,0.000004106614,0.029668067,0.0000046752266,0.9633866,0.0048484467],"study_design_scores_gemma":[0.00023379292,0.00019465038,0.6325032,0.0030870484,0.000006875721,0.0000527395,0.00006921372,0.0028279268,0.01840979,0.000024954426,0.3423949,0.00019489504],"about_ca_topic_score_codex":0.000018763723,"about_ca_topic_score_gemma":0.000024974584,"teacher_disagreement_score":0.6308176,"about_ca_system_score_codex":0.000002896908,"about_ca_system_score_gemma":0.000108603934,"threshold_uncertainty_score":0.61956495},"labels":[],"label_agreement":null},{"id":"W6921174781","doi":"10.6084/m9.figshare.28040110.v1","title":"Additional file 3 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Cognition; Regulator; Pregnancy; Epigenetics; Folic acid; Track (disk drive); Folic acid supplementation","score_opus":0.01738066982375489,"score_gpt":0.24208178526760682,"score_spread":0.22470111544385193,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6921174781","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.2485809,0.00060888357,7.534618e-7,0.0000061428377,0.000008838255,0.00016446452,0.75049573,0.000007362684,0.00012692713],"genre_scores_gemma":[0.4950478,0.000010115967,0.00020443159,0.0000040370214,0.00004999278,0.00031129026,0.50408936,0.000016310642,0.00026663663],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992756,0.00001664974,0.00015030405,0.0002755099,0.00012702512,0.00015488431],"domain_scores_gemma":[0.99953693,0.000048141028,0.0000990974,0.00014608231,0.000120031735,0.000049725644],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000008621657,0.000116725176,0.000107068045,0.000043310003,0.000036385674,0.000011849686,0.000083793006,0.000068122325,0.7469474],"category_scores_gemma":[0.0001478353,0.0001089853,0.00005030058,0.000077655306,0.000013170362,0.000005234987,0.00009931957,0.000034259712,0.00004372225],"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":[0.000080506994,0.00021111913,0.00023799721,0.0027721403,0.0004295275,0.000012835522,0.0008427576,0.00010332882,0.40088966,0.0000043750433,0.5285674,0.06584833],"study_design_scores_gemma":[0.00032055716,0.0007071024,0.08959679,0.008200855,0.000022904127,0.000066041786,0.000161941,0.000050684856,0.8884454,0.000003141837,0.012229822,0.00019476682],"about_ca_topic_score_codex":0.0000020502314,"about_ca_topic_score_gemma":0.000059313847,"teacher_disagreement_score":0.7469037,"about_ca_system_score_codex":0.000009846242,"about_ca_system_score_gemma":0.00005247225,"threshold_uncertainty_score":0.44442916},"labels":[],"label_agreement":null},{"id":"W6924816004","doi":"10.15468/dl.xt8vn7","title":"Occurrence Download","year":2022,"lang":"en","type":"dataset","venue":"Global Biodiversity Information Facility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Download; Matching (statistics); Range (aeronautics); Alien; The Internet","score_opus":0.010486658535468119,"score_gpt":0.21445995961899314,"score_spread":0.20397330108352502,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6924816004","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.006994305,0.000060027887,0.0000048666434,0.000046607474,0.00052924437,0.00020758795,0.9920532,0.000015852647,0.00008827443],"genre_scores_gemma":[0.000074227675,0.00014172879,0.0000021538974,0.00041480715,0.0000023164528,0.0000064129567,0.9993579,2.1435914e-8,4.263183e-7],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99883926,0.00005730386,0.00027975684,0.000258972,0.00030633647,0.00025836442],"domain_scores_gemma":[0.9990345,0.000003141771,0.00021855439,0.00053088693,0.00010777749,0.00010512968],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00019620766,0.00022232409,0.00017097138,0.000040553292,0.00027211034,0.00006795089,0.0004916233,0.00024151789,0.014364592],"category_scores_gemma":[0.00010337198,0.00024856048,0.00015453594,0.00013365019,0.00008112789,0.000014450419,0.00087669294,0.00017723642,0.012174533],"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":[0.000013150091,0.000023296345,0.0012579903,0.00006018923,0.000034578028,5.287155e-7,0.000008024992,0.000023634388,0.0000039755487,1.1482908e-8,0.99730384,0.0012707779],"study_design_scores_gemma":[0.00026158165,0.00010571514,0.0002442945,6.082194e-7,0.000028591541,0.000017545253,0.00011711736,4.5349992e-8,0.000027473168,1.5844647e-7,0.9989373,0.00025956891],"about_ca_topic_score_codex":0.00019312596,"about_ca_topic_score_gemma":0.0000061623255,"teacher_disagreement_score":0.0073046717,"about_ca_system_score_codex":0.00007915782,"about_ca_system_score_gemma":0.00013731333,"threshold_uncertainty_score":0.99999666},"labels":[],"label_agreement":null},{"id":"W6929020360","doi":"10.4224/23001184","title":"Winter solstice, 2016","year":2016,"lang":"en","type":"article","venue":"NPARC","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Herzberg Institute of Astrophysics","funders":"","keywords":"","score_opus":0.008009952740876309,"score_gpt":0.2285688314137787,"score_spread":0.2205588786729024,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929020360","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92992455,0.000089585235,0.0098331375,0.0008672631,0.00024846473,0.00006773832,0.0000063682714,0.000012887421,0.058950022],"genre_scores_gemma":[0.98365414,0.00007386517,0.0020051876,0.00022109314,0.00020836569,0.0000064623705,0.0000025633049,0.000012953672,0.013815362],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99946344,0.000013957242,0.000094102186,0.00018768694,0.0000572868,0.0001835232],"domain_scores_gemma":[0.99964714,0.0000067654623,0.000026736809,0.00023461536,0.00003106197,0.000053661002],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006641937,0.000072704715,0.00005863389,0.000013503412,0.000026695687,0.000009129465,0.000116626456,0.000056111243,0.00049606705],"category_scores_gemma":[0.00005962951,0.00004612406,0.00004926384,0.000018214267,0.00003632235,0.0000012231538,0.000096163,0.000018555205,0.00022380715],"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":[0.0000031013049,0.00000905985,0.003258625,0.00000236128,0.000012286025,5.026925e-7,0.000004758064,1.3334648e-7,0.94210976,0.000053623495,0.01405208,0.0404937],"study_design_scores_gemma":[0.0006840398,0.00021520305,0.023373306,0.000042295163,0.000011177669,0.00004386745,0.000020072519,0.0000053628482,0.57017434,0.0010988455,0.40410852,0.00022299569],"about_ca_topic_score_codex":6.7008176e-7,"about_ca_topic_score_gemma":0.0000011994539,"teacher_disagreement_score":0.39005643,"about_ca_system_score_codex":0.0000037325353,"about_ca_system_score_gemma":0.00002249637,"threshold_uncertainty_score":0.54315865},"labels":[],"label_agreement":null},{"id":"W6929956472","doi":"10.5281/zenodo.10445082","title":"Counting is not Enough. Modelling Relevance in Art Exhibition Ecosystems","year":2020,"lang":"en","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Relevance (law); Exhibition; Leverage (statistics); Interpretation (philosophy); Institution; Data collection; Value (mathematics)","score_opus":0.03607981117598916,"score_gpt":0.22888931049986377,"score_spread":0.19280949932387462,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929956472","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.89439124,0.00028433136,0.05640359,0.0025649024,0.000112445676,0.00053837016,0.00013040057,0.00020817491,0.045366533],"genre_scores_gemma":[0.9972109,0.00018199194,0.0006078099,0.000514383,0.00017863781,4.6201315e-8,0.00060737773,0.00043711843,0.00026170572],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99883705,0.00009759774,0.00023402926,0.00039658434,0.00017489197,0.00025983417],"domain_scores_gemma":[0.99942666,0.0000060004877,0.00008161445,0.00021770176,0.00017331779,0.000094692616],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00031038493,0.0001036033,0.00010537647,0.00004819879,0.00040440547,0.00020513723,0.00033608216,0.00006677955,0.0008508474],"category_scores_gemma":[0.00027728933,0.00012079946,0.00003936204,0.00019959715,0.00003144847,0.000013134679,0.00043844353,0.00013159231,0.0018042695],"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":[0.000087929875,0.0001128785,0.00006628727,0.00027515434,0.00005220415,0.00001164986,0.0021099371,0.010794784,0.851067,0.0006048872,0.09171238,0.043104913],"study_design_scores_gemma":[0.00038851003,0.0001698465,0.00009339828,0.000035683664,0.0000038997964,0.00004010712,0.000202888,0.023766167,0.015421418,0.00001692331,0.9597052,0.0001560028],"about_ca_topic_score_codex":0.000008616669,"about_ca_topic_score_gemma":3.6291536e-7,"teacher_disagreement_score":0.86799276,"about_ca_system_score_codex":0.000027059968,"about_ca_system_score_gemma":0.0000033318024,"threshold_uncertainty_score":0.99897295},"labels":[],"label_agreement":null},{"id":"W6929982221","doi":"10.5281/zenodo.10943409","title":"Neognathus terrestris","year":2023,"lang":"en","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Lumbricus terrestris; Litter; Bombus terrestris; Distribution (mathematics)","score_opus":0.027199308787913417,"score_gpt":0.2471511671842255,"score_spread":0.2199518583963121,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929982221","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9191678,0.00011681006,0.0016345901,0.0005836245,0.00017351449,0.0002570064,0.00006838918,0.00047622478,0.07752203],"genre_scores_gemma":[0.99509585,0.00014672533,0.00016343925,0.00009318023,0.0001743109,2.9944605e-8,0.0014573688,0.00061540847,0.0022536842],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990678,0.00008513632,0.00012757098,0.00029337427,0.00014442806,0.00028169053],"domain_scores_gemma":[0.999401,0.000003645999,0.000039910046,0.000326935,0.00013236159,0.00009616177],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00028925115,0.00008462736,0.0000662755,0.000094010014,0.0007410131,0.00020670812,0.00047664417,0.00005749844,0.0014030262],"category_scores_gemma":[0.0003024902,0.0000905257,0.000044278946,0.00030516557,0.000058417314,0.000004742292,0.00091435405,0.00008135013,0.005064277],"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":[0.000015427142,0.00005433909,0.000058930415,0.00003318898,0.000053113225,0.000010340393,0.000283505,0.00013989743,0.35317698,0.00030665958,0.36261192,0.2832557],"study_design_scores_gemma":[0.00024938543,0.00017324772,0.0056667505,0.0000071919353,0.0000043622636,0.000088489614,0.00016553543,0.00017997241,0.0060407273,0.000043505337,0.9872662,0.00011465978],"about_ca_topic_score_codex":0.000005742661,"about_ca_topic_score_gemma":1.00929185e-7,"teacher_disagreement_score":0.62465423,"about_ca_system_score_codex":0.000012919441,"about_ca_system_score_gemma":0.0000023233958,"threshold_uncertainty_score":0.9995098},"labels":[],"label_agreement":null},{"id":"W6930041778","doi":"10.5281/zenodo.12129107","title":"Walter benjamin flaneur pdf","year":2024,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Modernity; Capital (architecture); Architecture; Publishing; Diversity (politics); Key (lock); Modernism (music); Product (mathematics); Late modernity","score_opus":0.016527927299610664,"score_gpt":0.2351124061943877,"score_spread":0.21858447889477703,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930041778","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0008460752,0.0010271003,0.00044883447,0.00014968759,0.0002826481,0.00027428422,0.00016593606,0.00021673518,0.9965887],"genre_scores_gemma":[0.00923571,0.0004290404,0.00024306531,0.00013948779,0.0007884093,5.2092105e-8,0.0031880094,0.007921983,0.9780542],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9986837,0.00010229791,0.00016805813,0.0005552935,0.00018089029,0.00030975376],"domain_scores_gemma":[0.9991919,0.0000019915828,0.00007794348,0.00052627135,0.00008717987,0.00011473068],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00018125397,0.00019741859,0.00014341912,0.00016518471,0.0002435432,0.00035362903,0.0006395718,0.00019406597,0.06608598],"category_scores_gemma":[0.00013776697,0.00020310076,0.00008006791,0.00014276736,0.00007941718,0.0000021712463,0.001216919,0.00019131317,0.07914103],"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":[0.000003091159,0.000023810546,7.457813e-7,0.00012422325,0.00007201043,0.000006136679,0.000036431284,0.0000015439667,0.014344273,0.000071220726,0.9691688,0.016147736],"study_design_scores_gemma":[0.00016710503,0.00017167714,0.000036484333,0.00007316049,0.000021889839,0.00017149484,0.000036938887,0.000013828715,0.00088446855,0.000018957186,0.99818087,0.00022312079],"about_ca_topic_score_codex":0.00001369652,"about_ca_topic_score_gemma":7.144738e-7,"teacher_disagreement_score":0.029012097,"about_ca_system_score_codex":0.000019269355,"about_ca_system_score_gemma":0.000003164651,"threshold_uncertainty_score":0.9347677},"labels":[],"label_agreement":null},{"id":"W6930168875","doi":"10.5281/zenodo.11670281","title":"[+[!LIVE!]+] 24 Hours of Le Mans 2024 Live Streams FREE On TV Channel 15-16 June 2024","year":2024,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Channel (broadcasting); Test (biology); STREAMS; Time lag; Daylight","score_opus":0.018156951389832744,"score_gpt":0.2304228953282263,"score_spread":0.21226594393839354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930168875","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0027617244,0.0028089134,0.00044803423,0.00043301866,0.0011939205,0.0006161249,0.0013409685,0.00024843603,0.99014884],"genre_scores_gemma":[0.033185385,0.0013283831,0.0001915646,0.00009223321,0.00076165795,2.1590938e-7,0.0020944043,0.006847368,0.9554988],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99817836,0.000137632,0.00027142366,0.00071360776,0.0003160716,0.00038288723],"domain_scores_gemma":[0.99863005,0.000005115318,0.00016989352,0.0008812074,0.0001688556,0.00014488075],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00024590487,0.0002947392,0.00026046386,0.00027287684,0.00022462758,0.0002036812,0.0010209267,0.00027349807,0.023552647],"category_scores_gemma":[0.00020518024,0.000301001,0.00014682708,0.00023137238,0.00016171212,0.0000042257784,0.0016857417,0.00031226847,0.009325186],"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":[0.000015777921,0.000105110994,0.0000013621805,0.00023441721,0.00021192484,0.000008832962,0.00017789712,0.000013825597,0.004759394,0.00016441381,0.986316,0.007990991],"study_design_scores_gemma":[0.0004028501,0.00053071126,0.000032540764,0.00033271342,0.000049706305,0.000061217244,0.00062300864,0.000021376476,0.002182312,0.000108840824,0.9953537,0.00030103154],"about_ca_topic_score_codex":0.00013843118,"about_ca_topic_score_gemma":0.000008251406,"teacher_disagreement_score":0.034650072,"about_ca_system_score_codex":0.000039695104,"about_ca_system_score_gemma":0.000013130488,"threshold_uncertainty_score":0.9999442},"labels":[],"label_agreement":null},{"id":"W6930601871","doi":"10.5281/zenodo.13356387","title":"Certainement ! Voici dix titres captivants pour VeeloBooster Avis","year":2024,"lang":"fr","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Nucleofection; Gloom; Limiting; Laziness","score_opus":0.022631854584985532,"score_gpt":0.2446868193546193,"score_spread":0.22205496476963377,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930601871","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.018497456,0.0049474067,0.0017940761,0.0020815865,0.0008673536,0.0008546308,0.0005584301,0.0002609725,0.9701381],"genre_scores_gemma":[0.23572902,0.00090901315,0.0006876289,0.00030019635,0.0013306793,1.7564278e-7,0.0027670434,0.007535805,0.7507404],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9974679,0.00027666666,0.000377391,0.0009175435,0.00032471423,0.00063582003],"domain_scores_gemma":[0.998556,0.0000074681375,0.00016009943,0.0007127591,0.0003188216,0.000244843],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00033511355,0.00039486957,0.0002765575,0.00020958966,0.000636812,0.00072988454,0.00096068974,0.00030565955,0.09381882],"category_scores_gemma":[0.0003012828,0.00040793334,0.00016836653,0.00022406902,0.0001882619,0.000007712061,0.0024298597,0.0003355245,0.06103911],"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":[0.000019989251,0.00017179357,0.00001114351,0.0004931839,0.00040145265,0.00003284811,0.0006698762,0.000028450624,0.07494699,0.00070049893,0.74992347,0.1726003],"study_design_scores_gemma":[0.0004482626,0.00038730772,0.00047689932,0.00027976793,0.00008316952,0.00022189491,0.00040283738,0.00011684621,0.0026012266,0.0000699264,0.9944759,0.00043597465],"about_ca_topic_score_codex":0.00005090621,"about_ca_topic_score_gemma":0.0000025322954,"teacher_disagreement_score":0.2445524,"about_ca_system_score_codex":0.00012414658,"about_ca_system_score_gemma":0.000013770217,"threshold_uncertainty_score":0.9998373},"labels":[],"label_agreement":null},{"id":"W6930757390","doi":"10.5281/zenodo.16794414","title":"CanPests V1","year":2025,"lang":"en","type":"dataset","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Guelph","funders":"Genome Canada","keywords":"Barcode; DNA barcoding; Identifier; Host (biology); Identification (biology)","score_opus":0.01664895475827676,"score_gpt":0.24944338761015736,"score_spread":0.2327944328518806,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930757390","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011091203,0.00038693886,0.00024114383,0.00029825186,0.00030765694,0.0003788739,0.9851316,0.00009949842,0.012046883],"genre_scores_gemma":[0.0009906951,0.00050869666,0.00008399148,0.00026759738,0.00026747157,4.7110575e-8,0.995327,0.0004142343,0.0021402708],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99848956,0.00015666957,0.00023272996,0.0005497658,0.00022034699,0.00035093466],"domain_scores_gemma":[0.998583,0.00000521334,0.0001124668,0.0008549651,0.00031972714,0.00012463288],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0002737482,0.00020488452,0.00016971416,0.00015142407,0.00090193364,0.00036402547,0.0012218532,0.00022298026,0.0031526927],"category_scores_gemma":[0.00055710593,0.00022546387,0.00008378056,0.00021624115,0.00009993346,0.000003553025,0.0022731652,0.00025167095,0.00091104466],"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":[0.000007187793,0.00004619019,4.026609e-7,0.000103184655,0.00006105066,0.0000037687914,0.000014874888,0.000009112927,0.0026190083,0.000009679492,0.9837709,0.013354658],"study_design_scores_gemma":[0.0002440274,0.00017298033,0.000092679205,0.00004619128,0.00002772347,0.00009550548,0.00003847057,0.00000516946,0.00055095996,0.0000053697786,0.99849826,0.00022266542],"about_ca_topic_score_codex":0.000049987975,"about_ca_topic_score_gemma":0.00000125094,"teacher_disagreement_score":0.014727376,"about_ca_system_score_codex":0.00004232834,"about_ca_system_score_gemma":0.000012931499,"threshold_uncertainty_score":0.99986684},"labels":[],"label_agreement":null},{"id":"W6931064577","doi":"10.5281/zenodo.5116165","title":"D1.6 International Cooperation Strategy","year":2016,"lang":"en","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"European Commission","keywords":"Alliance; European commission; Declaration; Commission; The arctic; White paper; Launched","score_opus":0.02369546661939615,"score_gpt":0.24508168185509804,"score_spread":0.2213862152357019,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931064577","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.792081,0.000116789895,0.04402672,0.0019131949,0.00035569692,0.00035387735,0.00015202594,0.00023882804,0.16076186],"genre_scores_gemma":[0.99610674,0.000116048475,0.00020286615,0.00008202812,0.0002059762,2.7398205e-8,0.0005541298,0.00030947386,0.0024226985],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99923134,0.00007623441,0.00013217439,0.00025960023,0.00012787401,0.00017278975],"domain_scores_gemma":[0.9993567,0.00000314024,0.000045105746,0.00022931685,0.00029560138,0.00007014496],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0002157598,0.00007462321,0.000050729308,0.000050982842,0.00044109233,0.00021185847,0.00042403335,0.000049552313,0.0046625035],"category_scores_gemma":[0.00025469298,0.00006197328,0.000030024867,0.00007538533,0.000058986534,0.000011528211,0.00046094856,0.000042855892,0.0016040613],"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":[0.00001363666,0.000038620146,0.000025196097,0.0000049533674,0.000030328032,0.0000010802809,0.000039670547,0.000028219683,0.6965903,0.0010222965,0.038032416,0.26417327],"study_design_scores_gemma":[0.0004352394,0.00020961098,0.002036057,0.000010786878,0.0000032954738,0.000091061,0.00005088091,0.00005620125,0.021921787,0.000044051823,0.9750344,0.00010658645],"about_ca_topic_score_codex":0.000002671403,"about_ca_topic_score_gemma":1.8303793e-7,"teacher_disagreement_score":0.937002,"about_ca_system_score_codex":0.000024380179,"about_ca_system_score_gemma":0.0000030438057,"threshold_uncertainty_score":0.9991733},"labels":[],"label_agreement":null},{"id":"W6931358202","doi":"10.5281/zenodo.439971","title":"ga4gh/dockstore: 1.2.0-alpha.6","year":2017,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Orthopaedic Innovation Centre","funders":"","keywords":"Component (thermodynamics); Relation (database); Work (physics); Set (abstract data type); Process (computing)","score_opus":0.022769126339747703,"score_gpt":0.24991136867366276,"score_spread":0.22714224233391506,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931358202","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005532148,0.0009703534,0.0012157689,0.00010433834,0.00026719624,0.0003241127,0.00019135798,0.000282475,0.9960912],"genre_scores_gemma":[0.03884006,0.001412971,0.00067819044,0.0001550606,0.0014958801,8.926748e-8,0.0055597723,0.012886651,0.93897134],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9986123,0.00011714727,0.00014752499,0.00054881175,0.00021806336,0.00035614293],"domain_scores_gemma":[0.9984774,0.0000020025302,0.00020765694,0.0010188009,0.00014887322,0.00014528244],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00025335362,0.00021649289,0.0001791942,0.000134681,0.0009587518,0.00041228323,0.0012587283,0.00023470112,0.01315371],"category_scores_gemma":[0.00034190333,0.00023298798,0.00009063323,0.00006761579,0.0001537359,0.0000037033726,0.0014300821,0.00017708175,0.0044459226],"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":[0.000004526326,0.000030818293,0.0000025837505,0.000051657185,0.00006996786,0.0000040787254,0.000025390234,0.0000013597357,0.009820642,0.000090190064,0.9239948,0.065904],"study_design_scores_gemma":[0.000318125,0.000174135,0.00016570494,0.000070447706,0.000017760527,0.00012492205,0.000021771328,0.000007956652,0.00077679195,0.000013805941,0.99804765,0.00026093828],"about_ca_topic_score_codex":0.000032318265,"about_ca_topic_score_gemma":9.699422e-7,"teacher_disagreement_score":0.074052855,"about_ca_system_score_codex":0.000026108992,"about_ca_system_score_gemma":0.0000056979534,"threshold_uncertainty_score":0.99632925},"labels":[],"label_agreement":null},{"id":"W6931713377","doi":"10.5683/sp2/ofslnc","title":"Data from: Haploids adapt faster than diploids across a range of environments","year":2021,"lang":"en","type":"dataset","venue":"Borealis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Ploidy; Range (aeronautics); Selection (genetic algorithm); Population; Adaptation (eye); Doubled haploidy","score_opus":0.032682732112443595,"score_gpt":0.2854356545845056,"score_spread":0.252752922472062,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931713377","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.013257187,0.0022857147,0.000115507835,0.00003203329,0.0001693056,0.00016306108,0.98390275,0.0000035608216,0.00007088604],"genre_scores_gemma":[0.0019899341,0.001967648,0.00037546802,0.00012964828,0.00040465733,0.000018588975,0.99475884,0.00004406965,0.00031114477],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9979281,0.000085018786,0.00043419207,0.000864213,0.00031130135,0.00037720794],"domain_scores_gemma":[0.9964605,0.000015640691,0.0002710501,0.0031131392,0.000029058572,0.000110609406],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00018073399,0.00034625563,0.00044367788,0.000025322362,0.000055734876,0.00004693642,0.0012411522,0.00048237885,0.00014119237],"category_scores_gemma":[0.00010295554,0.000337275,0.00014900391,0.00004875037,0.000115675306,0.000004534489,0.0023305705,0.00017176107,0.000014770487],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0000116401525,0.00009463032,0.00063830084,0.000052176572,0.00027681582,0.000010294898,0.000019307727,0.0000014825266,0.013179622,8.317067e-8,0.98475647,0.00095917605],"study_design_scores_gemma":[0.0005058631,0.00010057131,0.012014921,0.00007859737,0.00013497243,0.000013562123,0.00010852913,0.0000066050684,0.0039394903,0.000002775468,0.98276114,0.0003329654],"about_ca_topic_score_codex":0.010736943,"about_ca_topic_score_gemma":0.006156691,"teacher_disagreement_score":0.01137662,"about_ca_system_score_codex":0.00001078005,"about_ca_system_score_gemma":0.00007470668,"threshold_uncertainty_score":0.9999079},"labels":[],"label_agreement":null},{"id":"W6931780144","doi":"10.5683/sp2/4wynm9","title":"Using Light Detection and Ranging (LiDAR) and Google Earth imagery to identify whether ponds are connected to stable ground water inputs","year":2021,"lang":"en","type":"dataset","venue":"Borealis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of British Columbia","funders":"","keywords":"Threatened species; Groundwater; Hydrology (agriculture); Terrain; Water table; Topographic Wetness Index; Resilience (materials science); Vegetation (pathology); Surface water","score_opus":0.014771187722420072,"score_gpt":0.2660982649202878,"score_spread":0.25132707719786773,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931780144","genre_codex":"empirical","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5849425,0.0005631242,0.00066703325,0.00019622699,0.00020221718,0.00029755634,0.41308635,0.000011227672,0.00003374841],"genre_scores_gemma":[0.06576208,0.0003017183,0.0011437627,0.0012886026,0.00060355535,0.00004724966,0.93037176,0.000099877056,0.0003813616],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9985647,0.00007615672,0.0002237363,0.00061057694,0.0001395859,0.0003852222],"domain_scores_gemma":[0.9991614,0.000008458027,0.000080799306,0.00045376006,0.00012170648,0.00017385912],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00020248212,0.00027647705,0.0003033622,0.00013765457,0.00015467557,0.00026685433,0.00011335119,0.00027415797,0.00002799786],"category_scores_gemma":[0.00009083395,0.0002499468,0.000051541287,0.00010123335,0.000023452552,0.0000064420988,0.0004667695,0.00012041572,0.0000031732461],"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":[0.000014358283,0.000012824382,0.00006661326,0.00010133474,0.000068926674,0.000016435812,0.000050498842,0.000008471273,0.8386463,8.235127e-8,0.16042294,0.00059121987],"study_design_scores_gemma":[0.0002495559,0.000087234796,0.0027531215,0.000118705015,0.000069952555,0.00013575367,0.000097488686,0.000008785855,0.24024232,0.0000029446999,0.75589454,0.00033959764],"about_ca_topic_score_codex":0.0029033641,"about_ca_topic_score_gemma":0.004885131,"teacher_disagreement_score":0.598404,"about_ca_system_score_codex":0.000015685588,"about_ca_system_score_gemma":0.000030282183,"threshold_uncertainty_score":0.9999953},"labels":[],"label_agreement":null},{"id":"W6931862107","doi":"10.5683/sp2/jojyop","title":"Coexpression Analysis of Human Genes Across Many Microarray Data Sets","year":2019,"lang":"en","type":"dataset","venue":"Borealis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Columbia College; Genome British Columbia","funders":"","keywords":"Microarray analysis techniques; Gene; Microarray; Gene expression profiling; Gene expression; Gene regulatory network; Expression (computer science); DNA microarray","score_opus":0.036466880075834616,"score_gpt":0.34118089168534155,"score_spread":0.30471401160950695,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931862107","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.050281253,0.0011474628,0.000035896574,0.000010860308,0.00010859254,0.00016243347,0.9482032,0.0000038904996,0.00004643293],"genre_scores_gemma":[0.0040572947,0.00096335605,0.00018831328,0.00006933899,0.0001310586,0.000007094777,0.99439347,0.000026990287,0.00016308286],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9980783,0.000071677605,0.00046618955,0.0008111007,0.00023335329,0.00033939682],"domain_scores_gemma":[0.99584275,0.000011477328,0.0004334167,0.0035343408,0.00009976747,0.00007822659],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0002955016,0.0003019502,0.0005810184,0.000091256676,0.00008486405,0.000042929096,0.0014363327,0.0004764825,0.000074672906],"category_scores_gemma":[0.000052069085,0.00027702143,0.00023624262,0.00017357447,0.00008547277,0.000003026217,0.0015539202,0.00012236515,0.000005295938],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000004905662,0.000045466117,0.0007586958,0.00010220519,0.0009435232,0.0000016833592,0.0000116645815,0.000022439397,0.123515844,1.7912865e-7,0.8739767,0.0006166638],"study_design_scores_gemma":[0.00023272833,0.00009852213,0.010866555,0.000046190005,0.0009303099,0.0000061790615,0.000054602944,0.000035420187,0.014355329,9.319724e-7,0.97305715,0.00031607182],"about_ca_topic_score_codex":0.007952329,"about_ca_topic_score_gemma":0.0037292382,"teacher_disagreement_score":0.10916052,"about_ca_system_score_codex":0.000008013783,"about_ca_system_score_gemma":0.000054747514,"threshold_uncertainty_score":0.9999682},"labels":[],"label_agreement":null},{"id":"W6939420541","doi":"10.6084/m9.figshare.20064362","title":"Additional file 6 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Channel (broadcasting); Selectivity; Gene; Function (biology); HEK 293 cells; Cell; Genomic imprinting; Filter (signal processing); Mutation","score_opus":0.013462243930767316,"score_gpt":0.2027190654999588,"score_spread":0.1892568215691915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6939420541","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10468476,0.00012780887,0.000027835791,0.000010854621,0.000016675627,0.00011066759,0.89496356,0.000003979296,0.00005387753],"genre_scores_gemma":[0.6012328,0.0000013266039,0.00007994092,0.000013736342,0.000017186452,0.00010657706,0.39837742,0.000007392087,0.00016357529],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994309,0.000020808307,0.00015745792,0.00019020941,0.000107953536,0.000092663264],"domain_scores_gemma":[0.99956703,0.00005252015,0.00019055017,0.00008848035,0.00007368666,0.00002775412],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00004111334,0.00007337505,0.00008654396,0.000033423974,0.00007642095,0.000006950364,0.00004631561,0.000053712745,0.3810167],"category_scores_gemma":[0.00038879778,0.00008578553,0.000025732748,0.00006656413,0.000005835811,0.0000057388265,0.00018960166,0.00004649868,0.0000037373927],"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":[0.000013239476,0.00006865476,0.0000442016,0.00021139935,0.00006755338,5.8428833e-7,0.00006299358,0.00028182942,0.2599124,0.0000070155356,0.73852074,0.00080934726],"study_design_scores_gemma":[0.0023376117,0.001935434,0.63182837,0.001195109,0.00008226091,0.00086584117,0.0005185924,0.021630552,0.038728233,0.00017567059,0.29975197,0.0009503458],"about_ca_topic_score_codex":0.0000035331673,"about_ca_topic_score_gemma":7.0672814e-7,"teacher_disagreement_score":0.6317842,"about_ca_system_score_codex":0.000006588656,"about_ca_system_score_gemma":0.000026575915,"threshold_uncertainty_score":0.6195491},"labels":[],"label_agreement":null},{"id":"W6939728741","doi":"10.6084/m9.figshare.20064371.v1","title":"Additional file 9 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Function (biology); Loss function; Channel (broadcasting); Gene; HEK 293 cells; Variation (astronomy); Mutation","score_opus":0.013477445620077237,"score_gpt":0.20279957040024266,"score_spread":0.1893221247801654,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6939728741","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10514284,0.00012755053,0.000027842496,0.000010856189,0.00001666583,0.000110438,0.8945065,0.0000039774136,0.00005332749],"genre_scores_gemma":[0.60110945,0.0000013288151,0.00007990192,0.000013738798,0.000017184886,0.00010578896,0.39850208,0.000007388228,0.00016314028],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99943095,0.000020807183,0.00015745375,0.00019018205,0.000107946085,0.00009265814],"domain_scores_gemma":[0.9995671,0.000052516036,0.00019052908,0.00008845573,0.00007368346,0.000027750137],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00004110495,0.00007336928,0.00008653284,0.00003342509,0.000076434575,0.000006948466,0.0000462813,0.00005370534,0.38196295],"category_scores_gemma":[0.00038880017,0.00008577678,0.000025732445,0.00006655805,0.0000058356773,0.0000057388215,0.00018951968,0.000046482957,0.0000037434042],"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":[0.000013155206,0.00006822963,0.000044242366,0.00021100414,0.0000674207,5.833733e-7,0.000062770414,0.00028540383,0.25960398,0.00000682358,0.7388358,0.0008005799],"study_design_scores_gemma":[0.0023433233,0.0019421015,0.6321219,0.0012001023,0.000082531886,0.0008694151,0.0005195403,0.02197183,0.03912941,0.0001762858,0.29869014,0.00095341314],"about_ca_topic_score_codex":0.0000034366208,"about_ca_topic_score_gemma":6.9435333e-7,"teacher_disagreement_score":0.6320777,"about_ca_system_score_codex":0.00000659585,"about_ca_system_score_gemma":0.000026568634,"threshold_uncertainty_score":0.61860204},"labels":[],"label_agreement":null},{"id":"W6939841432","doi":"10.6084/m9.figshare.26986399.v1","title":"Additional file 1 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.012503434411400817,"score_gpt":0.23530005347426144,"score_spread":0.22279661906286063,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6939841432","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.23480166,0.0002697112,0.0000015222105,0.000019712204,0.000011483482,0.000058064856,0.7644159,0.0000022780334,0.00041964644],"genre_scores_gemma":[0.8352612,0.000010802365,0.00053070387,0.000021197826,0.000031369735,0.000052738433,0.16398032,0.0000060677567,0.00010557911],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99955714,0.000009629035,0.00014378155,0.00015695281,0.00005237335,0.000080115955],"domain_scores_gemma":[0.9997077,0.00012518687,0.000036933332,0.000067368754,0.000036592923,0.000026191627],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000024101848,0.000052819447,0.00007746948,0.00002323183,0.000011781935,0.000008049095,0.00004384282,0.000064916894,0.3810009],"category_scores_gemma":[0.0006690168,0.00005272602,0.00002349173,0.0000537763,0.000018013723,0.000002738034,0.00015385404,0.000046121047,0.000007705209],"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":[0.000002977645,0.000014099837,0.0016855975,0.00033906024,0.00001706759,0.0000024395029,0.000026890706,0.000004106614,0.029668067,0.0000046752266,0.9633866,0.0048484467],"study_design_scores_gemma":[0.00023379292,0.00019465038,0.6325032,0.0030870484,0.000006875721,0.0000527395,0.00006921372,0.0028279268,0.01840979,0.000024954426,0.3423949,0.00019489504],"about_ca_topic_score_codex":0.000018763723,"about_ca_topic_score_gemma":0.000024974584,"teacher_disagreement_score":0.6308176,"about_ca_system_score_codex":0.000002896908,"about_ca_system_score_gemma":0.000108603934,"threshold_uncertainty_score":0.61956495},"labels":[],"label_agreement":null},{"id":"W6957852115","doi":"10.6084/m9.figshare.20064368","title":"Additional file 8 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Function (biology); Extracellular; Channel (broadcasting); Loss function; HEK 293 cells; Gene; Variation (astronomy)","score_opus":0.013470722356893429,"score_gpt":0.2027671882946675,"score_spread":0.18929646593777408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6957852115","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.105474524,0.00012751453,0.000027807944,0.000010851535,0.000016658574,0.00011042204,0.8941747,0.0000039518823,0.000053574116],"genre_scores_gemma":[0.6012159,0.0000013142712,0.000079978556,0.000013736131,0.000017178647,0.00010644644,0.39839387,0.000007381771,0.00016418195],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99943095,0.000020807911,0.00015745455,0.00019020162,0.000107933396,0.00009266535],"domain_scores_gemma":[0.99956703,0.000052523377,0.00019055056,0.00008847907,0.000073687435,0.000027753444],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0000411125,0.00007337712,0.000086545144,0.000033418066,0.00007643078,0.000006949708,0.00004631117,0.000053713236,0.38291934],"category_scores_gemma":[0.00038881792,0.00008578584,0.000025732998,0.00006652562,0.0000058357964,0.000005738154,0.00018956579,0.00004649786,0.0000037574166],"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":[0.000013183248,0.000068371155,0.000044029905,0.00021146843,0.00006757528,5.8471727e-7,0.000062905056,0.0002860498,0.25849804,0.0000069236585,0.73992014,0.0008207247],"study_design_scores_gemma":[0.0023537902,0.0019533683,0.6305425,0.0012050711,0.000082879305,0.0008730373,0.000521565,0.022061806,0.03976006,0.00017697838,0.29951143,0.00095748884],"about_ca_topic_score_codex":0.0000034963866,"about_ca_topic_score_gemma":6.9531296e-7,"teacher_disagreement_score":0.63049847,"about_ca_system_score_codex":0.0000065970667,"about_ca_system_score_gemma":0.000026582187,"threshold_uncertainty_score":0.6176448},"labels":[],"label_agreement":null},{"id":"W6957913438","doi":"10.60692/zzd1c-pvz77","title":"Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities","year":2024,"lang":"en","type":"article","venue":"Greater South Information System","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Polytechnique Montréal","funders":"","keywords":"Craniofacial; Anthropometry; Cohort; Craniofacial abnormality; Nose; Body height; Epidemiology","score_opus":0.017783148243118496,"score_gpt":0.20723936109702287,"score_spread":0.18945621285390438,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6957913438","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99753857,0.000054172113,0.001662044,0.0000018953451,0.00012949479,0.00023035187,0.00005932778,0.0000041168996,0.00032000968],"genre_scores_gemma":[0.99993235,0.0000015293649,0.000024794319,0.0000024336352,0.000012917615,0.000005940221,0.0000049054893,0.000003248738,0.000011909805],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99928355,0.000043010336,0.00039845778,0.00007829709,0.00011854425,0.000078152545],"domain_scores_gemma":[0.9995884,0.0000015048934,0.00014262756,0.00016529298,0.00008438208,0.000017804614],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003463256,0.00007267175,0.00012696657,0.00012914481,0.000023306442,0.0000146623615,0.000076583594,0.00006560606,0.0000063214184],"category_scores_gemma":[0.000024757497,0.00004943429,0.00005311196,0.00019983256,0.00005153444,0.000013652698,0.00006023117,0.000034036788,0.0000012610569],"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":[0.0000068035533,0.000001753485,0.99261314,0.00036434722,0.000044990655,1.300917e-8,0.0021064545,0.000012188855,0.0037773508,0.0000011632627,0.000001031948,0.001070795],"study_design_scores_gemma":[0.00017829225,0.000041383686,0.83384794,0.000100240875,0.000009192085,0.000019405845,0.0017680507,0.0001811157,0.16381131,2.6882796e-7,0.0000040626705,0.000038744045],"about_ca_topic_score_codex":0.000087792105,"about_ca_topic_score_gemma":0.0000016371002,"teacher_disagreement_score":0.16003397,"about_ca_system_score_codex":0.000010788135,"about_ca_system_score_gemma":0.000027667482,"threshold_uncertainty_score":0.20158719},"labels":[],"label_agreement":null},{"id":"W6958412846","doi":"10.6084/m9.figshare.20064359.v1","title":"Additional file 5 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Loss function; Function (biology); Channel (broadcasting); Variation (astronomy); Gene; Imprinting (psychology)","score_opus":0.013466912802269063,"score_gpt":0.20276054185243894,"score_spread":0.1892936290501699,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958412846","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10516379,0.00012733403,0.000027750795,0.00001083634,0.000016659089,0.00011042777,0.894486,0.0000039760566,0.000053212123],"genre_scores_gemma":[0.6007552,0.000001327436,0.00007990738,0.000013726838,0.000017173605,0.00010638831,0.3988563,0.000007386708,0.00016252558],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994309,0.00002080748,0.00015745476,0.00019020631,0.00010795313,0.00009265467],"domain_scores_gemma":[0.99956703,0.000052512663,0.00019054652,0.00008847936,0.00007367215,0.00002775283],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000041112005,0.000073374285,0.000086544824,0.000033424578,0.000076432894,0.0000069473017,0.000046311943,0.000053715194,0.38280165],"category_scores_gemma":[0.000388782,0.00008578202,0.000025734484,0.00006656076,0.0000058354913,0.000005738372,0.00018959386,0.000046495472,0.0000037299624],"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":[0.0000131240295,0.000068068584,0.000044111544,0.00021048133,0.000067258654,5.819945e-7,0.00006255355,0.00028423945,0.25912017,0.000006930763,0.7393161,0.00080640183],"study_design_scores_gemma":[0.0023362034,0.0019352135,0.63551867,0.0011955557,0.0000822509,0.000866354,0.00051779824,0.02174734,0.038973924,0.00017481661,0.2957017,0.00095013634],"about_ca_topic_score_codex":0.0000035003823,"about_ca_topic_score_gemma":6.957566e-7,"teacher_disagreement_score":0.63547456,"about_ca_system_score_codex":0.0000065963295,"about_ca_system_score_gemma":0.000026571883,"threshold_uncertainty_score":0.61776257},"labels":[],"label_agreement":null},{"id":"W6958421332","doi":"10.6084/m9.figshare.20064359","title":"Additional file 5 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Loss function; Function (biology); Channel (broadcasting); Variation (astronomy); Gene; Imprinting (psychology)","score_opus":0.013466912802269063,"score_gpt":0.20276054185243894,"score_spread":0.1892936290501699,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958421332","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10516379,0.00012733403,0.000027750795,0.00001083634,0.000016659089,0.00011042777,0.894486,0.0000039760566,0.000053212123],"genre_scores_gemma":[0.6007552,0.000001327436,0.00007990738,0.000013726838,0.000017173605,0.00010638831,0.3988563,0.000007386708,0.00016252558],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994309,0.00002080748,0.00015745476,0.00019020631,0.00010795313,0.00009265467],"domain_scores_gemma":[0.99956703,0.000052512663,0.00019054652,0.00008847936,0.00007367215,0.00002775283],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000041112005,0.000073374285,0.000086544824,0.000033424578,0.000076432894,0.0000069473017,0.000046311943,0.000053715194,0.38280165],"category_scores_gemma":[0.000388782,0.00008578202,0.000025734484,0.00006656076,0.0000058354913,0.000005738372,0.00018959386,0.000046495472,0.0000037299624],"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":[0.0000131240295,0.000068068584,0.000044111544,0.00021048133,0.000067258654,5.819945e-7,0.00006255355,0.00028423945,0.25912017,0.000006930763,0.7393161,0.00080640183],"study_design_scores_gemma":[0.0023362034,0.0019352135,0.63551867,0.0011955557,0.0000822509,0.000866354,0.00051779824,0.02174734,0.038973924,0.00017481661,0.2957017,0.00095013634],"about_ca_topic_score_codex":0.0000035003823,"about_ca_topic_score_gemma":6.957566e-7,"teacher_disagreement_score":0.63547456,"about_ca_system_score_codex":0.0000065963295,"about_ca_system_score_gemma":0.000026571883,"threshold_uncertainty_score":0.61776257},"labels":[],"label_agreement":null},{"id":"W6958549180","doi":"10.6084/m9.figshare.26630146.v1","title":"Additional file 1 of Safety and efficacy of pegunigalsidase alfa in patients with Fabry disease who were previously treated with agalsidase alfa: results from BRIDGE, a phase 3 open-label study","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Fabry disease; Selection (genetic algorithm); Enzyme replacement therapy; Clinical trial; Disease","score_opus":0.017343677665007842,"score_gpt":0.2640277896681375,"score_spread":0.24668411200312967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958549180","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.42165363,0.00012893735,3.8023336e-7,0.000006064277,0.0000027204035,0.00053648796,0.5775677,0.0000046229734,0.00009949481],"genre_scores_gemma":[0.5247413,0.0000026694847,0.00006662445,0.0000103909115,0.000015170837,0.00012286348,0.47483742,0.00001820993,0.00018535134],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9986623,0.0000671724,0.00035892538,0.0005339876,0.00018946131,0.00018818019],"domain_scores_gemma":[0.9989662,0.00020925196,0.00016669912,0.0003686262,0.0001508011,0.00013841802],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00003635164,0.00020731661,0.00027955478,0.000054695145,0.000039646005,0.000049503833,0.00020105898,0.00006274216,0.13034016],"category_scores_gemma":[0.00081728515,0.0001625746,0.0000316382,0.00016191027,0.000026347863,0.000014707035,0.00025228807,0.00008547921,0.000013552368],"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":[0.004373082,0.0050073983,0.0027676162,0.00033643673,0.00042486642,0.00009975236,0.00031295695,0.000033632485,0.00022120823,2.580702e-7,0.9630951,0.023327684],"study_design_scores_gemma":[0.022564242,0.0038008012,0.9326538,0.007955466,0.00008621733,0.000004495711,0.000094125186,0.0002898662,0.0004380568,0.0000014909635,0.031700194,0.00041124513],"about_ca_topic_score_codex":0.00006165942,"about_ca_topic_score_gemma":0.00006203679,"teacher_disagreement_score":0.93139493,"about_ca_system_score_codex":0.000011100321,"about_ca_system_score_gemma":0.00019033033,"threshold_uncertainty_score":0.87045485},"labels":[],"label_agreement":null},{"id":"W6968859774","doi":"10.5281/zenodo.4651578","title":"Supplementary Figures","year":2021,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Guelph","funders":"","keywords":"Venn diagram; Intersection (aeronautics); Diagram; Network analysis; Social network analysis; Gene","score_opus":0.020402151944611393,"score_gpt":0.24610364579427374,"score_spread":0.22570149384966234,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6968859774","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0014493301,0.0015500083,0.00075147406,0.00021188203,0.00021118126,0.00033330935,0.0011297616,0.00014397173,0.99421906],"genre_scores_gemma":[0.02016302,0.0024936395,0.0021305985,0.00055672723,0.0016766983,1.2248832e-7,0.10159553,0.015795812,0.85558784],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99882156,0.00013201094,0.0001471436,0.0004479498,0.00017666121,0.00027469496],"domain_scores_gemma":[0.9991998,0.00000189568,0.000087859524,0.00050098664,0.000111214234,0.00009823312],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00015431589,0.00016002114,0.0001310416,0.00010201774,0.00039931998,0.00021917553,0.0005808947,0.00014202477,0.15554096],"category_scores_gemma":[0.00012019831,0.00017775517,0.00007087425,0.000116259456,0.00006590717,0.0000011259672,0.0012168235,0.00012682467,0.00078033947],"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":[0.0000026645384,0.000035893478,0.0000035258954,0.00008084503,0.00008096105,0.000004720412,0.00002591756,0.0000020847708,0.022068772,0.00005277942,0.9577864,0.019855449],"study_design_scores_gemma":[0.00025069457,0.00012811413,0.00009745446,0.00005938132,0.000013616936,0.00010461839,0.00008816066,0.0000043718087,0.0020242697,0.000006332602,0.9970306,0.00019234496],"about_ca_topic_score_codex":0.0000453673,"about_ca_topic_score_gemma":0.0000023586745,"teacher_disagreement_score":0.15476061,"about_ca_system_score_codex":0.000018475903,"about_ca_system_score_gemma":0.000004388183,"threshold_uncertainty_score":0.9999977},"labels":[],"label_agreement":null},{"id":"W6977119697","doi":"10.6084/m9.figshare.26986429.v1","title":"Additional file 10 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.013896958573758356,"score_gpt":0.2409133182193833,"score_spread":0.22701635964562494,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977119697","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.43123087,0.00040525355,0.0000019922622,0.000027731281,0.000015086006,0.00007600817,0.5675754,0.0000030205015,0.0006646389],"genre_scores_gemma":[0.9016872,0.000011447722,0.00043477857,0.000019179324,0.00003330521,0.00004257505,0.09755169,0.0000063956336,0.000213421],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9995362,0.0000102614895,0.00015068905,0.00016403824,0.000055262713,0.00008355643],"domain_scores_gemma":[0.9997204,0.000100078316,0.00003828085,0.00007126952,0.000042457945,0.000027496682],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00002849856,0.00005553768,0.0000810907,0.000023997247,0.0000124705575,0.0000086712635,0.000046440866,0.00006911536,0.32148138],"category_scores_gemma":[0.0006003199,0.000055470387,0.00002474614,0.000054962853,0.000018822948,0.0000029164019,0.00016008399,0.00004498913,0.0000105121135],"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":[0.0000056245913,0.000020856703,0.0020862815,0.00047723245,0.00002437109,0.0000033523527,0.000035484594,0.0000056102185,0.043478917,0.000007368408,0.94743276,0.0064221164],"study_design_scores_gemma":[0.00032342164,0.0002642072,0.60325617,0.0029779263,0.000009208348,0.00005656363,0.00007380067,0.0034677272,0.026885,0.0000334175,0.36241743,0.00023515969],"about_ca_topic_score_codex":0.000019079827,"about_ca_topic_score_gemma":0.000025765,"teacher_disagreement_score":0.6011699,"about_ca_system_score_codex":0.0000030905765,"about_ca_system_score_gemma":0.00010993078,"threshold_uncertainty_score":0.6791389},"labels":[],"label_agreement":null},{"id":"W6977166992","doi":"10.6084/m9.figshare.28040104","title":"Additional file 1 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Regulator; Epigenetics; EPIC; CpG site; Table (database); Offspring; Pregnancy; Folic acid; DNA methylation","score_opus":0.017674961586394373,"score_gpt":0.24242228909963967,"score_spread":0.2247473275132453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977166992","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.24758174,0.0006063353,7.49971e-7,0.000006172738,0.000008766323,0.00016455568,0.751498,0.0000073752612,0.00012631134],"genre_scores_gemma":[0.4935008,0.000009981703,0.0002065814,0.000004038512,0.000049454535,0.00031658798,0.5056344,0.000016306118,0.00026185703],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99927557,0.00001666443,0.00015024285,0.00027561997,0.00012700146,0.00015489524],"domain_scores_gemma":[0.9995373,0.000048534395,0.00009908315,0.0001462832,0.0001190709,0.00004972954],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000008625234,0.000116740215,0.00010705803,0.000043323238,0.000036388537,0.000011827449,0.000083841274,0.00006812763,0.7512339],"category_scores_gemma":[0.00014787163,0.00010901073,0.00005030352,0.00007768168,0.000013169504,0.0000052313026,0.00009938532,0.000034266122,0.00004328919],"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":[0.00007866812,0.00020752123,0.00023354866,0.0026818642,0.0004223438,0.000012473641,0.00082799443,0.00010149402,0.39301506,0.00000432336,0.53857046,0.06384425],"study_design_scores_gemma":[0.00031882818,0.0007131119,0.09071309,0.008275939,0.000023260689,0.000067091256,0.00016381982,0.000050975763,0.88737136,0.0000031560385,0.012103217,0.00019615094],"about_ca_topic_score_codex":0.0000020291595,"about_ca_topic_score_gemma":0.000058947335,"teacher_disagreement_score":0.7511906,"about_ca_system_score_codex":0.000009810622,"about_ca_system_score_gemma":0.000052445706,"threshold_uncertainty_score":0.44453287},"labels":[],"label_agreement":null},{"id":"W6977240968","doi":"10.6084/m9.figshare.20064362.v1","title":"Additional file 6 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"","keywords":"Channel (broadcasting); Selectivity; Gene; Function (biology); HEK 293 cells; Cell; Genomic imprinting; Filter (signal processing); Mutation","score_opus":0.013462243930767316,"score_gpt":0.2027190654999588,"score_spread":0.1892568215691915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977240968","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10468476,0.00012780887,0.000027835791,0.000010854621,0.000016675627,0.00011066759,0.89496356,0.000003979296,0.00005387753],"genre_scores_gemma":[0.6012328,0.0000013266039,0.00007994092,0.000013736342,0.000017186452,0.00010657706,0.39837742,0.000007392087,0.00016357529],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994309,0.000020808307,0.00015745792,0.00019020941,0.000107953536,0.000092663264],"domain_scores_gemma":[0.99956703,0.00005252015,0.00019055017,0.00008848035,0.00007368666,0.00002775412],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00004111334,0.00007337505,0.00008654396,0.000033423974,0.00007642095,0.000006950364,0.00004631561,0.000053712745,0.3810167],"category_scores_gemma":[0.00038879778,0.00008578553,0.000025732748,0.00006656413,0.000005835811,0.0000057388265,0.00018960166,0.00004649868,0.0000037373927],"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":[0.000013239476,0.00006865476,0.0000442016,0.00021139935,0.00006755338,5.8428833e-7,0.00006299358,0.00028182942,0.2599124,0.0000070155356,0.73852074,0.00080934726],"study_design_scores_gemma":[0.0023376117,0.001935434,0.63182837,0.001195109,0.00008226091,0.00086584117,0.0005185924,0.021630552,0.038728233,0.00017567059,0.29975197,0.0009503458],"about_ca_topic_score_codex":0.0000035331673,"about_ca_topic_score_gemma":7.0672814e-7,"teacher_disagreement_score":0.6317842,"about_ca_system_score_codex":0.000006588656,"about_ca_system_score_gemma":0.000026575915,"threshold_uncertainty_score":0.6195491},"labels":[],"label_agreement":null},{"id":"W6977277581","doi":"10.6084/m9.figshare.12875880","title":"Additional file 4 of The testosterone-dependent and independent transcriptional networks in the hypothalamus of Gpr54 and Kiss1 knockout male mice are not fully equivalent","year":2020,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver Coastal Health Research Institute; University of British Columbia; BC Cancer Agency","funders":"Biotechnology and Biological Sciences Research Council","keywords":"Transcription (linguistics); Hypothalamus; Transcription factor; Knockout mouse; Set (abstract data type); Gene","score_opus":0.026509787740033253,"score_gpt":0.20900716677144707,"score_spread":0.1824973790314138,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977277581","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.14733939,0.0005324969,0.0000024486164,0.00030859213,0.00001724651,0.00022642149,0.8512721,0.000002141555,0.00029915647],"genre_scores_gemma":[0.9426054,0.000010105586,0.00006701795,0.0004030249,0.00007812063,0.00010519376,0.05660747,0.000009448335,0.00011423334],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9992539,0.000049707996,0.00018848249,0.00020871311,0.00017101136,0.00012818167],"domain_scores_gemma":[0.9995438,0.0001032006,0.00013162731,0.00013303597,0.00004841147,0.000039942934],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000033688542,0.00010234257,0.000111433,0.000011991288,0.000038267048,0.000014365222,0.00019533728,0.00008638801,0.20984936],"category_scores_gemma":[0.00032620222,0.000073443385,0.000055263507,0.000052726442,0.000025547479,0.0000034867876,0.00017860191,0.00010771013,0.0000061186292],"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":[0.00004283681,0.00011304035,0.0015208661,0.0003458923,0.0000632444,0.0000066997636,0.0003757063,0.00043248414,0.06349487,0.00000419063,0.9300118,0.0035883863],"study_design_scores_gemma":[0.0007339407,0.0003009995,0.8686633,0.0008951923,0.000019160703,0.00022108293,0.00071268296,0.000648719,0.00793981,0.000007436969,0.11962755,0.00023008621],"about_ca_topic_score_codex":0.0000031559211,"about_ca_topic_score_gemma":0.000019944533,"teacher_disagreement_score":0.8671425,"about_ca_system_score_codex":0.000003548867,"about_ca_system_score_gemma":0.00003616122,"threshold_uncertainty_score":0.79087293},"labels":[],"label_agreement":null},{"id":"W6977385879","doi":"10.6084/m9.figshare.12875880.v1","title":"Additional file 4 of The testosterone-dependent and independent transcriptional networks in the hypothalamus of Gpr54 and Kiss1 knockout male mice are not fully equivalent","year":2020,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver Coastal Health Research Institute; University of British Columbia; BC Cancer Agency","funders":"","keywords":"Transcription (linguistics); Hypothalamus; Transcription factor; Knockout mouse; Set (abstract data type); Gene","score_opus":0.026509787740033253,"score_gpt":0.20900716677144707,"score_spread":0.1824973790314138,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977385879","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.14733939,0.0005324969,0.0000024486164,0.00030859213,0.00001724651,0.00022642149,0.8512721,0.000002141555,0.00029915647],"genre_scores_gemma":[0.9426054,0.000010105586,0.00006701795,0.0004030249,0.00007812063,0.00010519376,0.05660747,0.000009448335,0.00011423334],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9992539,0.000049707996,0.00018848249,0.00020871311,0.00017101136,0.00012818167],"domain_scores_gemma":[0.9995438,0.0001032006,0.00013162731,0.00013303597,0.00004841147,0.000039942934],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000033688542,0.00010234257,0.000111433,0.000011991288,0.000038267048,0.000014365222,0.00019533728,0.00008638801,0.20984936],"category_scores_gemma":[0.00032620222,0.000073443385,0.000055263507,0.000052726442,0.000025547479,0.0000034867876,0.00017860191,0.00010771013,0.0000061186292],"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":[0.00004283681,0.00011304035,0.0015208661,0.0003458923,0.0000632444,0.0000066997636,0.0003757063,0.00043248414,0.06349487,0.00000419063,0.9300118,0.0035883863],"study_design_scores_gemma":[0.0007339407,0.0003009995,0.8686633,0.0008951923,0.000019160703,0.00022108293,0.00071268296,0.000648719,0.00793981,0.000007436969,0.11962755,0.00023008621],"about_ca_topic_score_codex":0.0000031559211,"about_ca_topic_score_gemma":0.000019944533,"teacher_disagreement_score":0.8671425,"about_ca_system_score_codex":0.000003548867,"about_ca_system_score_gemma":0.00003616122,"threshold_uncertainty_score":0.79087293},"labels":[],"label_agreement":null},{"id":"W6981561337","doi":"","title":"Equipment of the Canadian Infantrymen, 1939â1982: A Material/Historical Assessment","year":2012,"lang":"en","type":"article","venue":"Scholars Commons (Wilfrid Laurier University)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Nucleofection; TSG101; Gestational period; Hyporeflexia; Diafiltration; Pretext; Demotion; Fusible alloy","score_opus":0.01137819886418987,"score_gpt":0.21724751768928485,"score_spread":0.205869318825095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6981561337","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98077476,0.00013736404,0.00006191196,0.00044496055,0.0006743213,0.00016991931,0.000046489276,0.000007288858,0.017683012],"genre_scores_gemma":[0.99618936,0.000016743512,0.00080075883,0.00010874613,0.000076597506,0.0000012056572,0.000027493144,0.000014881049,0.0027642013],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.9989191,0.00013985163,0.00015842731,0.00018872292,0.00018115122,0.00041270835],"domain_scores_gemma":[0.9990358,0.000007149339,0.000101285215,0.00052186014,0.000070221926,0.00026372148],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025889816,0.00014054947,0.00014719272,0.000113222384,0.00033977983,0.000030146248,0.00046880258,0.00013755132,0.000084563406],"category_scores_gemma":[0.00003083895,0.00012789786,0.000116837284,0.00023395814,0.000077734636,0.000015007814,0.00040428428,0.00017261112,0.0000046386044],"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":[0.000021652271,0.00019271235,0.81527704,0.000030311012,0.00021271351,0.0000067899864,0.00018404257,0.00003303379,0.17130804,0.004088469,0.0071482314,0.0014969578],"study_design_scores_gemma":[0.00034897914,0.000072248156,0.20701261,0.000017291035,0.0000494876,0.000018321383,0.00013916728,0.000003854808,0.028272158,0.000014268917,0.76385564,0.00019596617],"about_ca_topic_score_codex":0.009745152,"about_ca_topic_score_gemma":0.019461483,"teacher_disagreement_score":0.75670743,"about_ca_system_score_codex":0.00032747752,"about_ca_system_score_gemma":0.00037137305,"threshold_uncertainty_score":0.9984308},"labels":[],"label_agreement":null},{"id":"W6986523904","doi":"","title":"Preferential maternal LOH in the IGF2R gene in breast cancer","year":2004,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Loss of heterozygosity; Gene silencing; Tumor suppressor gene; Allele; Breast cancer; Suppressor; Genomic imprinting; Gene; Oncogene","score_opus":0.010007778219956463,"score_gpt":0.24256093424842365,"score_spread":0.23255315602846718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6986523904","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99217266,0.0006505372,1.4933465e-7,0.000028483208,0.0008106522,0.0004953692,0.00060273893,0.000015042045,0.0052243564],"genre_scores_gemma":[0.9960391,0.0009987485,0.00013138384,0.00020319772,0.00013324645,0.0001993246,0.00090216973,0.00010856923,0.0012842377],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99707246,0.0002368513,0.0006793013,0.00089797186,0.0004372142,0.0006761809],"domain_scores_gemma":[0.99885684,0.000015119313,0.00029682854,0.00059866626,0.00012275703,0.00010981258],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005020686,0.00054131274,0.00041582892,0.00019621945,0.0002171828,0.00007969196,0.0008038542,0.00071535853,0.00017019294],"category_scores_gemma":[0.00006054933,0.0004772624,0.00022220981,0.00026729732,0.00003631056,0.00001658543,0.00015001505,0.00080105895,0.00003877784],"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":[0.00020734925,0.00030523515,0.005458923,0.0003046258,0.00016042731,0.000047511738,0.000023032952,0.00038460636,0.9265861,0.00090238213,0.0000054347624,0.0656144],"study_design_scores_gemma":[0.0024940055,0.00017771717,0.5445847,0.00067556405,0.0001146771,0.00030417676,0.00034669417,0.000009193666,0.43982044,0.0018768092,0.008377929,0.0012181336],"about_ca_topic_score_codex":0.0025391784,"about_ca_topic_score_gemma":0.009120999,"teacher_disagreement_score":0.53912574,"about_ca_system_score_codex":0.00021017555,"about_ca_system_score_gemma":0.00011511478,"threshold_uncertainty_score":0.9997679},"labels":[],"label_agreement":null},{"id":"W6990818766","doi":"","title":"Epigenetic rRgulation in the Placenta and its Role in Fetal Growth","year":2011,"lang":"en","type":"dissertation","venue":"Library and Archives Canada (Government of Canada)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Epigenetics; Fetus; Gene expression; DNA methylation; Gene","score_opus":0.0029103864237724516,"score_gpt":0.14994564764007634,"score_spread":0.1470352612163039,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6990818766","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95816284,0.0018923428,0.0000020445234,0.00012451388,0.000081996885,0.0001747235,0.000026447182,6.7994955e-7,0.03953441],"genre_scores_gemma":[0.9963188,0.00070639077,0.000070599875,0.00014762147,0.000027932421,0.000010618701,0.00008975499,0.0000148317995,0.0026134062],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989308,0.000057333567,0.00021588863,0.00022729363,0.0003908292,0.00017784664],"domain_scores_gemma":[0.99967664,0.000025373787,0.0001324571,0.00010913123,5.228712e-7,0.00005586109],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000015334519,0.00014971005,0.00014675001,0.000021758782,0.000044415312,0.000011063784,0.00014957528,0.000058055197,0.000007182363],"category_scores_gemma":[0.0000050320787,0.00013268365,0.000016185304,0.00003936688,0.000015038098,0.000008232354,0.000054279277,0.00009871716,1.0872692e-9],"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":[0.00065900997,0.00011254698,0.4060207,0.00092951744,0.00013035773,0.00005027338,0.0013184069,0.00007164672,0.54467034,0.009483163,0.00013638535,0.03641764],"study_design_scores_gemma":[0.00031842888,0.00007981662,0.8481343,0.00009564406,0.000012665591,0.000007870594,0.004084574,0.00029193863,0.14530626,0.0004148086,0.0010533939,0.00020029795],"about_ca_topic_score_codex":0.0031297305,"about_ca_topic_score_gemma":0.115466096,"teacher_disagreement_score":0.4421136,"about_ca_system_score_codex":0.000001733047,"about_ca_system_score_gemma":0.00044155325,"threshold_uncertainty_score":0.90067434},"labels":[],"label_agreement":null},{"id":"W6996532089","doi":"","title":"Spontaneous errors of imprinting in mouse embryos","year":2003,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Embryonic stem cell; Allele; Gene; Embryo","score_opus":0.009657258820101017,"score_gpt":0.2337788373484205,"score_spread":0.2241215785283195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6996532089","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96631116,0.00044183162,2.5553317e-7,0.0000021468866,0.0006368178,0.00048454874,0.0001867037,0.000026064281,0.031910446],"genre_scores_gemma":[0.9808159,0.0003293138,0.0010755056,0.00006892562,0.00002988477,0.00005292221,0.00058277114,0.0001877265,0.01685705],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99645805,0.00023130227,0.0010870489,0.0010693271,0.0004157072,0.0007385887],"domain_scores_gemma":[0.99799025,0.00003518,0.0006691462,0.0008586763,0.00025682012,0.00018990555],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.000667921,0.0006477175,0.00071182504,0.00030437374,0.00022195734,0.00002814853,0.00059009035,0.0009900074,0.00010591268],"category_scores_gemma":[0.0007470666,0.0007445804,0.00038446448,0.00029866476,0.000047245707,0.0000129777545,0.0001715242,0.00075476547,0.00003703825],"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":[0.000058718197,0.00014216738,0.00024640554,0.000297003,0.000113072194,0.000080307334,0.0000053705294,0.00008829165,0.9707969,0.00075738446,0.0000017551749,0.027412625],"study_design_scores_gemma":[0.0009787023,0.00030403532,0.0030876824,0.00025769984,0.00007594335,0.00044263154,0.0005268634,0.00001245319,0.9823826,0.00045956462,0.010486256,0.0009855843],"about_ca_topic_score_codex":0.00028278102,"about_ca_topic_score_gemma":0.0013437334,"teacher_disagreement_score":0.02642704,"about_ca_system_score_codex":0.00012420591,"about_ca_system_score_gemma":0.00008643533,"threshold_uncertainty_score":0.9995005},"labels":[],"label_agreement":null},{"id":"W7002531279","doi":"","title":"\\n Gene Boy Came Home\\n . \\n Gene Boy revient chez lui Canada [Québec] 2007, 25 minutes","year":2008,"lang":"fr","type":"article","venue":"Érudit (Université de Montréal)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Gene; Sequence (biology); Mutation; Period (music)","score_opus":0.00490611341446776,"score_gpt":0.14933979929379043,"score_spread":0.14443368587932268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7002531279","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.61647487,0.3615604,0.00018716615,0.019767271,0.0008673819,0.00026229967,0.00014453547,0.000017872955,0.0007181996],"genre_scores_gemma":[0.55035317,0.11888551,0.0034673698,0.0013744558,0.0008676325,0.0000134238035,0.00028543515,0.0001146963,0.3246383],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9970181,0.00013824261,0.0004343563,0.0008888416,0.0003916073,0.001128839],"domain_scores_gemma":[0.9979493,0.000021777327,0.00031221547,0.0008980918,0.00022213081,0.0005964683],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00019435839,0.00055609574,0.0005657078,0.000088537345,0.000718582,0.000020746224,0.000609452,0.0004209743,0.00028665963],"category_scores_gemma":[0.00006966252,0.0006731839,0.00033670067,0.00027356434,0.00015340054,0.000014517803,0.00070816075,0.00026485496,0.00009979943],"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":[0.00004562169,0.00016837915,0.010789039,0.00016078434,0.0005534898,0.002664665,0.00023381099,0.0004455089,0.09990078,0.00003812307,0.8650262,0.019973602],"study_design_scores_gemma":[0.0011144998,0.00025195396,0.014620209,0.00007070584,0.00021743112,0.0043613873,0.00044841095,0.00023655387,0.03142259,0.0000068756876,0.9464911,0.0007582387],"about_ca_topic_score_codex":0.81572115,"about_ca_topic_score_gemma":0.92412466,"teacher_disagreement_score":0.3239201,"about_ca_system_score_codex":0.0037922773,"about_ca_system_score_gemma":0.0013256884,"threshold_uncertainty_score":0.9995719},"labels":[],"label_agreement":null},{"id":"W7009757408","doi":"","title":"Étiologie du biais de l'inactivation du chromosome X (ICX) dans les cellules sanguines des femmes vieillissantes : sélection hémizygote et acquisition de mutations somatiques","year":2022,"lang":"fr","type":"dissertation","venue":"Papyrus : Institutional Repository (Université de Montréal)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Y chromosome; Mutation; Genetic inheritance","score_opus":0.010375550707803358,"score_gpt":0.21131897041939962,"score_spread":0.20094341971159627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7009757408","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9726652,0.014415203,0.007850052,0.0005595258,0.0006162295,0.0003930592,0.00012703457,0.000095013624,0.003278712],"genre_scores_gemma":[0.98353624,0.0052099247,0.0032137225,0.00008879764,0.00037167632,0.00011057639,0.003380438,0.000057388243,0.004031216],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9973523,0.00053237344,0.0004967257,0.0007170026,0.0003453737,0.0005562359],"domain_scores_gemma":[0.9984157,0.00012734553,0.00056906434,0.00031647508,0.00036852944,0.00020290089],"candidate_categories":["metaepi_narrow","sts"],"consensus_categories":[],"category_scores_codex":[0.00037978886,0.00051687355,0.00036622773,0.00027308997,0.007109479,0.00011765418,0.00036394663,0.00058695005,0.000118757394],"category_scores_gemma":[0.00027955143,0.0006282467,0.00038464827,0.00031333353,0.00037523537,0.00008584133,0.0002177762,0.00034729554,0.000006608294],"study_design_candidate":"bench_or_experimental","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":[0.00015124767,0.0002579294,0.11772207,0.00024290926,0.00033773694,0.00014841452,0.027949,0.013127045,0.8346476,0.0017965356,0.00019841421,0.003421125],"study_design_scores_gemma":[0.0008108104,0.00048306579,0.46696904,0.00026796953,0.00039348422,0.0018781568,0.081471495,0.004216889,0.43541917,0.0006229945,0.006721015,0.0007458955],"about_ca_topic_score_codex":0.031088237,"about_ca_topic_score_gemma":0.007470683,"teacher_disagreement_score":0.3992284,"about_ca_system_score_codex":0.0037301055,"about_ca_system_score_gemma":0.0015356267,"threshold_uncertainty_score":0.99961686},"labels":[],"label_agreement":null},{"id":"W7014341601","doi":"","title":"Placental phenotypes associated with abnormal genomic imprinting on distal mouse chromosome 7","year":2011,"lang":"en","type":"other","venue":"cIRcle (University of British Columbia)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Cancer Institute; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Genomic imprinting; Imprinting (psychology); Phenotype; Gene; Gene silencing; Allele; X-inactivation; Chromosome; Chromosome 15","score_opus":0.005143948671483187,"score_gpt":0.1556041518590389,"score_spread":0.1504602031875557,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7014341601","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95091724,0.00017521232,0.00006582661,0.0000024503536,0.00009484867,0.00022161481,0.00038074885,0.00004208622,0.04809996],"genre_scores_gemma":[0.8835975,0.0001777636,0.0002642992,0.000015015301,0.00007844856,5.7988166e-7,0.00027479892,0.00016526772,0.11542631],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99889594,0.000036671696,0.00010615923,0.00051078567,0.00013513543,0.00031532953],"domain_scores_gemma":[0.99924904,0.0000048913525,0.00027884572,0.00032072753,0.00004747233,0.00009903631],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00007055974,0.000108657834,0.000296735,0.000041240208,0.00010403863,0.000040969662,0.00032672862,0.00031705532,0.00044629633],"category_scores_gemma":[0.000014150809,0.00031308745,0.00012898094,0.00006484568,0.00019667877,0.000004250815,0.00023674718,0.00013729132,0.000025872072],"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":[0.00021126782,0.0026021404,0.11570182,0.00095726445,0.005114484,0.0005329757,0.0005964812,0.0000798077,0.16111499,0.0000070099627,0.14861327,0.5644685],"study_design_scores_gemma":[0.001897434,0.00064796745,0.9873579,0.00044743667,0.00011036668,0.00008899862,0.0003841964,0.000012383476,0.0001220422,0.000003710474,0.008258162,0.00066940946],"about_ca_topic_score_codex":0.026696319,"about_ca_topic_score_gemma":0.10755954,"teacher_disagreement_score":0.87165606,"about_ca_system_score_codex":0.000034874178,"about_ca_system_score_gemma":0.00007872892,"threshold_uncertainty_score":0.9999321},"labels":[],"label_agreement":null},{"id":"W7025249809","doi":"","title":"Visitor Statistics (Second Quarter 2017)","year":2017,"lang":"en","type":"article","venue":"eVols (University of Hawaii)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Quarter (Canadian coin); Visitor pattern; Statistical analysis; Descriptive statistics; Official statistics","score_opus":0.0093110109981566,"score_gpt":0.22116217715698588,"score_spread":0.2118511661588293,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7025249809","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.968916,0.00009052363,0.009304138,0.00017660884,0.0002289538,0.000081281636,0.000070830974,0.000005249947,0.0211264],"genre_scores_gemma":[0.98535484,0.00003467476,0.007345203,0.000017833474,0.000078827135,9.426109e-8,0.000024220262,0.0000070556257,0.00713725],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994824,0.000016042739,0.000068436515,0.00019752605,0.00008319834,0.00015237782],"domain_scores_gemma":[0.99918205,0.0000052006844,0.0001454576,0.0005270936,0.00007534818,0.000064840126],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000072323535,0.000081001745,0.00011592245,0.000023317007,0.0002746453,0.000025090254,0.00038818677,0.00008139264,0.0003253744],"category_scores_gemma":[0.000021794349,0.00009901972,0.00006329642,0.000011450952,0.0001245645,0.000007332923,0.00020396155,0.00004699799,0.00005121907],"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":[0.00007813856,0.000183777,0.08039265,0.00015314734,0.00034327968,0.000049765305,0.0007600881,0.000016797221,0.62774384,0.0019808852,0.26012084,0.028176766],"study_design_scores_gemma":[0.0012812368,0.00042071124,0.8467966,0.000025390724,0.00004357378,0.00002725584,0.0019744535,0.00016111606,0.009794173,0.00023610995,0.13890977,0.00032961767],"about_ca_topic_score_codex":0.000081062775,"about_ca_topic_score_gemma":0.0001901227,"teacher_disagreement_score":0.7664039,"about_ca_system_score_codex":0.0000053398653,"about_ca_system_score_gemma":0.000035499306,"threshold_uncertainty_score":0.4037907},"labels":[],"label_agreement":null},{"id":"W7027120210","doi":"","title":"Characterization of molecular mechanisms underlying the neurogenic effect of the bHLH protein Hes6","year":2004,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"HEK 293 cells; Central nervous system; Context (archaeology); Signal transduction; Component (thermodynamics)","score_opus":0.008477156222236971,"score_gpt":0.2248475464572891,"score_spread":0.21637039023505214,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7027120210","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967093,0.00017354866,0.00000784086,0.00001288264,0.00048178787,0.0014444946,0.00015004222,0.000016176178,0.0010039365],"genre_scores_gemma":[0.9984235,0.000062342784,0.0001208798,0.00006558903,0.000011572415,0.00013311832,0.00038928914,0.00012539039,0.0006682917],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9972969,0.00048885937,0.000685554,0.00063325657,0.0005129092,0.00038246988],"domain_scores_gemma":[0.997798,0.000028014545,0.0009073669,0.0009707296,0.00022064612,0.000075231845],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006079547,0.0004912071,0.0004709392,0.00008366983,0.00037753876,0.000027550423,0.0008266894,0.00053589337,0.00001980276],"category_scores_gemma":[0.00037812692,0.00034785655,0.00053600053,0.0003098336,0.000068858426,0.000011719971,0.00022516606,0.0004831377,0.000006064021],"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":[0.000042026717,0.000041256102,0.000009934182,0.0003412863,0.00018090692,0.0000020215634,0.0000033247,0.000042203705,0.98646134,0.0026489603,4.629688e-8,0.010226672],"study_design_scores_gemma":[0.0005362612,0.00046741808,0.0041985535,0.00031947356,0.00020642702,0.000028947077,0.000029980558,0.00000579754,0.9918153,0.0016244872,0.00044960872,0.00031768813],"about_ca_topic_score_codex":0.000065204316,"about_ca_topic_score_gemma":0.000057684923,"teacher_disagreement_score":0.0099089835,"about_ca_system_score_codex":0.000059468155,"about_ca_system_score_gemma":0.000084688356,"threshold_uncertainty_score":0.99989736},"labels":[],"label_agreement":null},{"id":"W7027226843","doi":"","title":"Conflict And Solidarity Between Anti-Colonial Environmentalism, Indigenous Anti-Pipeline Resistance, And The Labour","year":2025,"lang":"en","type":"other","venue":"York University Digital Library (York University)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Solidarity; Indigenous; Resistance (ecology); Colonialism; Dilemma; Witness; Investment (military); Government (linguistics)","score_opus":0.005045456279234641,"score_gpt":0.16410674898363098,"score_spread":0.15906129270439634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7027226843","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3875327,0.00327434,0.00027110623,0.00043686206,0.00015488098,0.0008379053,0.004296146,0.00014701755,0.60304904],"genre_scores_gemma":[0.2708369,0.0027535236,0.00020059294,0.000097232034,0.0001472606,1.0560287e-7,0.0005828205,0.000078146644,0.7253034],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99864465,0.00010318308,0.00013740468,0.0006366561,0.0001351809,0.00034290832],"domain_scores_gemma":[0.9991848,0.00004043069,0.00019954694,0.0004050154,0.000010670127,0.00015952057],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00004250611,0.00035815552,0.00044826683,0.00025931373,0.0003156474,0.00017457374,0.00055894826,0.00045515457,0.00008278422],"category_scores_gemma":[0.000009933049,0.00036741118,0.00014052137,0.00027286593,0.00073497265,0.000036263707,0.0011570966,0.00023261178,0.000009725067],"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":[0.0007376484,0.00044383848,0.35042816,0.0008833355,0.0030883083,0.00053235644,0.0010611867,0.000013243103,0.00052752445,0.014077446,0.6196086,0.008598349],"study_design_scores_gemma":[0.0019966315,0.00005274513,0.01142728,0.00008599118,0.00014731238,0.000008287682,0.0005689734,0.0000011204314,0.0001308327,0.00002585818,0.9851638,0.0003911394],"about_ca_topic_score_codex":0.00014107116,"about_ca_topic_score_gemma":0.000032688386,"teacher_disagreement_score":0.36555523,"about_ca_system_score_codex":0.000021227113,"about_ca_system_score_gemma":0.00016317272,"threshold_uncertainty_score":0.9998778},"labels":[],"label_agreement":null},{"id":"W7035931548","doi":"","title":"Alberta's Response to the Criticism of the Oil Sands","year":2011,"lang":"en","type":"other","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Criticism; Oil sands; Petroleum; Oil exploration","score_opus":0.008224423501912994,"score_gpt":0.2288817281846325,"score_spread":0.22065730468271952,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7035931548","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.015466486,0.0008643389,0.00014046693,0.0010500257,0.00051232905,0.00014633033,0.00002266845,0.0000071520194,0.9817902],"genre_scores_gemma":[0.044887487,0.0000857328,0.00042281728,0.00080565584,0.00016865267,0.000015225661,0.0000043523105,0.0001242805,0.9534858],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992599,0.000090738446,0.00014593471,0.00022826904,0.00009924655,0.00017593164],"domain_scores_gemma":[0.99901164,0.000018136836,0.000075109485,0.00082495285,0.000028269178,0.00004188993],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00017198661,0.00015158296,0.00013558923,0.000028834324,0.000033702832,0.000008185695,0.00049447996,0.00019492887,0.0016509177],"category_scores_gemma":[0.0001704327,0.00007880212,0.00012865159,0.000059496328,0.00006567273,1.7658239e-7,0.0003150924,0.000064372995,0.00009011545],"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":[0.000040610572,0.0000277589,0.00018880525,0.000035968795,0.00009181844,2.4989384e-7,0.000101636906,9.936296e-7,0.08583234,0.00006406127,0.9085341,0.005081655],"study_design_scores_gemma":[0.000112516864,0.00010358264,0.0011691768,0.00005780639,0.000019297795,0.000011723772,0.00003980056,5.733381e-7,0.028319092,0.0000052859523,0.9700425,0.00011859349],"about_ca_topic_score_codex":0.00078736915,"about_ca_topic_score_gemma":0.0012659068,"teacher_disagreement_score":0.061508454,"about_ca_system_score_codex":0.0000024335336,"about_ca_system_score_gemma":0.000054958702,"threshold_uncertainty_score":0.99926174},"labels":[],"label_agreement":null},{"id":"W7038500911","doi":"","title":"JFE Shoji Power Canada 5-part series: Part 1","year":2022,"lang":"en","type":"other","venue":"Bulletin of Miscellaneous Information (Royal Gardens Kew)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Power (physics); Market power; Hydro power; Competition (biology)","score_opus":0.003719003126380845,"score_gpt":0.16499147767262493,"score_spread":0.16127247454624408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7038500911","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00054871343,0.00060878927,1.1827366e-7,0.00013347954,0.00073371554,0.00026138427,0.000286201,0.000029262219,0.9973983],"genre_scores_gemma":[0.000896335,0.0003417517,0.00024781292,0.0005437462,0.00021526283,0.000024515084,0.0007111209,0.00012366482,0.9968958],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99853706,0.00005308735,0.00047726196,0.00025792746,0.00034947993,0.00032520454],"domain_scores_gemma":[0.9989147,0.0000115928315,0.00038906006,0.0004960728,0.00007472101,0.00011381509],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00013174968,0.00029811432,0.0002934775,0.000027770868,0.00007728208,0.000025394778,0.00033460156,0.00025019798,0.5947165],"category_scores_gemma":[0.000084851024,0.0003178978,0.00012422197,0.000006177622,0.00006376195,1.3678069e-8,0.00024631133,0.00016821912,0.00064252183],"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":[0.000014992942,0.00001580106,0.000014306995,0.00012102201,0.00008346541,0.0000071996196,0.0000163988,0.000116427975,0.0000050526637,0.0000038121075,0.99926454,0.00033699983],"study_design_scores_gemma":[0.00026119757,0.0002006135,0.00001671673,0.000046084304,0.000025421177,0.00013741336,0.00020343933,8.481285e-7,0.00006470632,6.665252e-7,0.9986983,0.00034457914],"about_ca_topic_score_codex":0.106423564,"about_ca_topic_score_gemma":0.15156932,"teacher_disagreement_score":0.594074,"about_ca_system_score_codex":0.000040205545,"about_ca_system_score_gemma":0.00018647985,"threshold_uncertainty_score":0.9999273},"labels":[],"label_agreement":null},{"id":"W7084600370","doi":"10.1007/978-3-031-95288-3_32","title":"Predicting the Thermal Performance of Concrete Floor Slabs Connected to Balconies Through Thermal Breaks","year":2025,"lang":"en","type":"book-chapter","venue":"Lecture notes in civil engineering","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Inro Consultants (Canada); Western University","funders":"","keywords":"Thermal transmittance; Thermal; Slab; Envelope (radar); Classification of discontinuities; Energy consumption; Building envelope; Heat flow","score_opus":0.005516717204196268,"score_gpt":0.19740018646219423,"score_spread":0.19188346925799796,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7084600370","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96243036,0.0042187995,0.006051692,0.00019110942,0.0006299167,0.00057585665,0.00004449353,0.00004609813,0.025811695],"genre_scores_gemma":[0.9967367,0.00015793611,0.0011510595,0.00018707084,0.00032883318,0.000023102313,0.0000375579,0.00006798866,0.0013097309],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9986638,0.000015130507,0.00040069452,0.00040281157,0.00016292918,0.00035465477],"domain_scores_gemma":[0.99916345,0.0001017585,0.00012538258,0.0004871756,0.00008463863,0.00003760992],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00015903021,0.00038948652,0.0003804838,0.00007807119,0.000055707,0.000022831773,0.00038024454,0.0004124541,0.00006362566],"category_scores_gemma":[0.0002361521,0.0003176104,0.00014167445,0.00007574888,0.00005410263,0.0000040724503,0.00028986068,0.00041071797,0.0000029197645],"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":[0.000059840928,0.0000041651547,0.0025902828,0.00071016455,0.00048729105,0.000005565427,0.0011197954,0.21281639,0.76752114,0.0003570859,0.000039717983,0.014288537],"study_design_scores_gemma":[0.001991719,0.0012567334,0.015670491,0.0042952774,0.00033565698,0.00012013884,0.000052193525,0.045580227,0.8892524,0.000093023686,0.038917042,0.0024350905],"about_ca_topic_score_codex":0.000043655178,"about_ca_topic_score_gemma":0.000053283202,"teacher_disagreement_score":0.16723616,"about_ca_system_score_codex":0.000022425142,"about_ca_system_score_gemma":0.000080967395,"threshold_uncertainty_score":0.9999276},"labels":[],"label_agreement":null},{"id":"W7087864474","doi":"","title":"MJM MedTalks (S02E11): Global Surgery in our “Backyard”; A Discussion with Dr. Evan Wong","year":2025,"lang":"en","type":"article","venue":"DOAJ (DOAJ: Directory of Open Access Journals)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Montreal General Hospital; McGill University Health Centre","funders":"","keywords":"Conversation; Glossary; Medical journal; Alternative medicine; Medical advice; Space (punctuation); Health care","score_opus":0.10068166216111152,"score_gpt":0.5066879391136836,"score_spread":0.4060062769525721,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7087864474","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9871659,0.0072688493,0.00054764334,0.0007205879,0.0004797522,0.00036237587,0.000020815925,0.0000114772265,0.0034225741],"genre_scores_gemma":[0.9959543,0.0024984484,0.00023993923,0.00025005336,0.00010913805,0.00003157147,0.000028498678,0.000031013817,0.0008570616],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99755675,0.00021792405,0.0007435126,0.0005961018,0.00039150615,0.00049421034],"domain_scores_gemma":[0.99859184,0.000037949212,0.00043793593,0.00056630746,0.00017791547,0.00018808023],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00097364624,0.00033521265,0.00065631483,0.00034800533,0.00014183138,0.0004986451,0.0013375975,0.00018914035,0.00030520943],"category_scores_gemma":[0.00028703146,0.00023780337,0.00021109483,0.00088433555,0.00007199021,0.00006836299,0.0011775248,0.00023000882,0.000004996684],"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":[0.0001290094,0.00015151469,0.8213439,0.000077419994,0.00015015261,0.000022386086,0.000020866728,0.00014451913,0.13992634,0.0000083475215,0.014739163,0.023286402],"study_design_scores_gemma":[0.00066817587,0.000021507733,0.93393934,0.00079730514,0.000053389802,0.000041293773,0.00026190677,0.000032608514,0.055884957,0.00062464346,0.0072732293,0.0004016295],"about_ca_topic_score_codex":0.0003818972,"about_ca_topic_score_gemma":0.00022184581,"teacher_disagreement_score":0.112595476,"about_ca_system_score_codex":0.0000687685,"about_ca_system_score_gemma":0.00034641946,"threshold_uncertainty_score":0.969734},"labels":[],"label_agreement":null},{"id":"W7093955905","doi":"","title":"Marley's Journey","year":2018,"lang":"","type":"article","venue":"Scholarship at UWindsor (University of Windsor)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Angelman syndrome; Girl; Storytelling; Schedule; Documentary film; Character (mathematics)","score_opus":0.018462896464875325,"score_gpt":0.2310371623334759,"score_spread":0.21257426586860056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7093955905","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97787243,0.0015996862,0.0004639233,0.00083414087,0.0009382676,0.0003464282,0.00008607245,0.000022843114,0.017836234],"genre_scores_gemma":[0.97767836,0.00064754643,0.0026998813,0.00021033878,0.0007105746,2.962179e-7,0.00006221126,0.00007182288,0.017918954],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99632794,0.0003549058,0.00048531953,0.0011810781,0.00060794933,0.0010428319],"domain_scores_gemma":[0.9967214,0.000034292872,0.0006247292,0.0013399933,0.00069738785,0.00058221404],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0010088662,0.00055350875,0.00062217825,0.00028161053,0.0011241824,0.000085798965,0.0014471444,0.00092138484,0.0035237246],"category_scores_gemma":[0.00022991293,0.0007401827,0.00061427656,0.0005267023,0.0012289665,0.000055351837,0.0017566857,0.0005467678,0.00085346436],"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":[0.0005600997,0.00044756866,0.32933262,0.00024348382,0.00093427947,0.00004887687,0.0021032193,0.000014642654,0.64013994,0.00011433511,0.0041532833,0.021907674],"study_design_scores_gemma":[0.004465675,0.002505648,0.63176906,0.00035794245,0.00048661363,0.0003043359,0.0035454617,0.00010960964,0.11386422,0.00022840699,0.24087337,0.0014896622],"about_ca_topic_score_codex":0.00009579782,"about_ca_topic_score_gemma":0.00027414484,"teacher_disagreement_score":0.5262757,"about_ca_system_score_codex":0.00011084527,"about_ca_system_score_gemma":0.00038431247,"threshold_uncertainty_score":0.9999245},"labels":[],"label_agreement":null},{"id":"W7095003899","doi":"10.5281/zenodo.17442667","title":"Cheilosia (Cheilosia) pseudogrossa Stackelberg 1968","year":2025,"lang":"","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Apex (geometry); Stackelberg competition; Cluster (spacecraft); Face (sociological concept); Differential (mechanical device)","score_opus":0.019091397514554513,"score_gpt":0.2523788569098605,"score_spread":0.23328745939530598,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7095003899","genre_codex":"other","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.42396992,0.0049456805,0.013979788,0.0040219766,0.0012358908,0.0017816812,0.00059557386,0.00050204375,0.5489674],"genre_scores_gemma":[0.98625857,0.0013408149,0.00050322287,0.0004775551,0.00037495972,1.2500395e-7,0.0019109673,0.0014700611,0.007663719],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9962784,0.00050015294,0.0006604828,0.001194644,0.00041178384,0.0009545196],"domain_scores_gemma":[0.9972533,0.00001682829,0.00023492808,0.0012785614,0.0008926582,0.00032370407],"candidate_categories":["metaepi_narrow","sts","scholarly_communication","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0009146532,0.00043482284,0.00036048226,0.0002957041,0.0029706873,0.0013259421,0.0018265318,0.0003612545,0.006751411],"category_scores_gemma":[0.00081487425,0.0005112043,0.00023191345,0.00086887245,0.0004235669,0.000025229521,0.003919006,0.00047718018,0.003344802],"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":[0.00015619416,0.00072153757,0.00015193861,0.000575279,0.0007218133,0.000015555515,0.00069805054,0.00010084647,0.37726185,0.004271309,0.26812857,0.34719706],"study_design_scores_gemma":[0.0012039825,0.0005474411,0.0022413682,0.00012964998,0.00008594813,0.00014117673,0.0004774143,0.00035101137,0.022159833,0.00015351654,0.9720259,0.0004828166],"about_ca_topic_score_codex":0.000021467398,"about_ca_topic_score_gemma":5.275312e-7,"teacher_disagreement_score":0.7038973,"about_ca_system_score_codex":0.00014697728,"about_ca_system_score_gemma":0.00003294284,"threshold_uncertainty_score":0.999734},"labels":[],"label_agreement":null},{"id":"W7097295217","doi":"","title":"MICHAELA MÜLLER CHARACTERIZATION OF A NEW LARGE FAMILY OF EXTINCT SHORT RETROPOSONS IN THE PROTOZOAN PARASITE LEISHMANIA AND THEIR ROLE IN POST-TRANSCRIPTIONAL REGULATION OF GENE EXPRESSION","year":2015,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Retroposon; Gene; Leishmania; Protozoan parasite; Gene expression; Parasite hosting; Expression (computer science)","score_opus":0.014579935964184743,"score_gpt":0.23551275708582398,"score_spread":0.22093282112163923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7097295217","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99726695,0.00021546984,0.0018594527,0.000046267443,0.00001727856,0.00039630954,0.000017801447,0.0000014165887,0.00017904886],"genre_scores_gemma":[0.9986898,0.00004011821,0.0010058082,0.000028045879,0.000021494643,0.000013175071,0.00014420618,0.0000073654082,0.000050011724],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992756,0.000067202214,0.00029341737,0.00015433403,0.0001077322,0.00010170565],"domain_scores_gemma":[0.9996214,0.0000043716595,0.00009409494,0.00016557315,0.00008777724,0.000026784503],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028958736,0.00008390102,0.0001365178,0.000053938234,0.000010233147,0.0000042719857,0.00008884347,0.00008707809,0.0000075647895],"category_scores_gemma":[0.000022500957,0.00005940182,0.000033297776,0.00008443366,0.000027466645,0.000007201086,0.000034488763,0.000038633916,1.1324029e-7],"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":[0.00004297913,0.00006461372,0.09555417,0.000014026913,0.0000058970813,7.1860896e-8,0.0009978517,0.000008477823,0.9022606,0.000025799143,0.0000041138496,0.0010213956],"study_design_scores_gemma":[0.0003231426,0.00012910568,0.54396045,0.00002072129,0.000002378054,0.0000041196527,0.000696747,0.00014501385,0.4544944,0.000024439776,0.0001609674,0.00003855283],"about_ca_topic_score_codex":0.00008602229,"about_ca_topic_score_gemma":0.000068891386,"teacher_disagreement_score":0.44840625,"about_ca_system_score_codex":0.000004127722,"about_ca_system_score_gemma":0.000055007346,"threshold_uncertainty_score":0.24223359},"labels":[],"label_agreement":null},{"id":"W7099903259","doi":"","title":"DOI: 10.1007/s00268-001-0279-x WORLD Journal of SURGERY","year":2002,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Sigmoidoscopy; Hematocrit; Aspirin; Orthostatic vital signs; Blood loss; Phlebotomy; Disease","score_opus":0.026740635851965542,"score_gpt":0.22990150805316908,"score_spread":0.20316087220120355,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7099903259","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9383018,0.0025558793,0.0005200377,0.00036684438,0.00040848128,0.000063623804,0.0000022637587,0.000008863118,0.05777218],"genre_scores_gemma":[0.92793024,0.00035489877,0.001580205,0.00028315958,0.00039517222,0.0000014442301,0.000006922019,0.000018554243,0.06942943],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99902636,0.000036922836,0.00037448038,0.00016385941,0.00015097467,0.00024739117],"domain_scores_gemma":[0.99932384,0.000028436141,0.00016477403,0.00024333053,0.00013532165,0.00010428981],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00025617066,0.00012154792,0.00019313926,0.00009961926,0.00004257139,0.000028937442,0.00016641535,0.0000749726,0.007967374],"category_scores_gemma":[0.00011163273,0.00010137047,0.0001737564,0.00011322123,0.00003978004,0.0000030494118,0.000080061545,0.000079824524,0.00017343258],"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":[0.000016264627,0.00033427298,0.026069079,0.00004010448,0.00019645944,0.000020287123,0.000036796708,0.000047582118,0.32076305,0.000042988973,0.5767562,0.075676925],"study_design_scores_gemma":[0.0006552706,0.00019361403,0.012530552,0.0000287363,0.00003081935,0.0003638259,0.00006150638,0.00010306872,0.10081984,0.000041079304,0.8848731,0.00029861103],"about_ca_topic_score_codex":0.00000780403,"about_ca_topic_score_gemma":0.000007559643,"teacher_disagreement_score":0.30811688,"about_ca_system_score_codex":0.0000063861494,"about_ca_system_score_gemma":0.000022574937,"threshold_uncertainty_score":0.9929395},"labels":[],"label_agreement":null},{"id":"W7100321571","doi":"","title":"Does Distance Still Matter in the Age of the Internet?","year":2011,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Social distance; Interpersonal communication; Distance education; Interpersonal relationship; Phone; Geographical distance","score_opus":0.01056121854065204,"score_gpt":0.21263784390657206,"score_spread":0.20207662536592003,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7100321571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9820817,0.000043513373,0.00085660577,0.00013085933,0.0000994509,0.00007637275,0.000001193803,9.777234e-7,0.016709326],"genre_scores_gemma":[0.996336,0.000006988724,0.00030927334,0.0005204123,0.000016923637,0.000005037856,0.0000015563566,0.0000043523937,0.0027994637],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996238,0.000030849416,0.00010511106,0.00010353741,0.00004656976,0.00009017577],"domain_scores_gemma":[0.9996672,0.0000036204467,0.000031060365,0.00028132697,0.00001011349,0.000006673072],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008773752,0.00005070963,0.00004853764,0.000005715251,0.000007842847,0.0000053935655,0.00028041625,0.0000302239,0.00013872469],"category_scores_gemma":[0.000011120694,0.000018652616,0.000042300922,0.00003147693,0.000054493546,6.5252436e-7,0.00010416666,0.000034434557,0.000006084432],"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":[0.00000883216,0.00008230758,0.86084425,0.000025577197,0.000021963691,0.0000022815216,0.0017905663,0.0000013144626,0.13310426,0.0005226231,0.0016986653,0.0018973398],"study_design_scores_gemma":[0.0001033503,0.00003170089,0.85765743,0.000011045064,0.0000036419297,0.000007097999,0.000312667,0.0000055491614,0.12610604,0.00022877738,0.015477892,0.0000548057],"about_ca_topic_score_codex":0.00012889,"about_ca_topic_score_gemma":0.0002124974,"teacher_disagreement_score":0.014254291,"about_ca_system_score_codex":0.000001300049,"about_ca_system_score_gemma":0.000004826302,"threshold_uncertainty_score":0.15189381},"labels":[],"label_agreement":null},{"id":"W7100427132","doi":"","title":"© 2003 Canadian Medical Association or its licensors","year":2003,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Association (psychology); MEDLINE; Disease; Epidemiology","score_opus":0.008659148788515756,"score_gpt":0.23585082484500236,"score_spread":0.2271916760564866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7100427132","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5510106,0.00032653098,0.00017486486,0.0008076615,0.00053204247,0.00016710632,0.000005274133,0.000013524037,0.4469624],"genre_scores_gemma":[0.73674417,0.00019950485,0.00097171805,0.0027533518,0.00013888328,0.000008616562,0.0000037328507,0.00001742317,0.2591626],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99916667,0.00004597817,0.00012502048,0.00017331976,0.00019732272,0.00029166514],"domain_scores_gemma":[0.99938023,0.0000058929395,0.00003053816,0.00012640822,0.00015447894,0.0003024441],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00031769267,0.00007595293,0.00006945802,0.000024689944,0.000057558573,0.000017376418,0.00008949178,0.000258098,0.036480848],"category_scores_gemma":[0.0019648818,0.00006247865,0.00002669094,0.00011401448,0.0000069538273,9.978633e-7,0.000016083786,0.00006785327,0.0009379872],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00000961946,0.00011387073,0.036255773,0.000029266426,0.00027328564,0.0000357991,0.0001088023,0.000033285,0.070758455,0.0023450109,0.8719083,0.018128546],"study_design_scores_gemma":[0.00024775384,0.000060621507,0.0072026188,0.0000034698583,0.0000048496167,0.000049654183,0.000068519636,0.000042557116,0.031365607,6.2991955e-7,0.96083593,0.00011778734],"about_ca_topic_score_codex":0.00097450777,"about_ca_topic_score_gemma":0.020642826,"teacher_disagreement_score":0.18779978,"about_ca_system_score_codex":0.00003032691,"about_ca_system_score_gemma":0.0007425796,"threshold_uncertainty_score":0.9998399},"labels":[],"label_agreement":null},{"id":"W7105111214","doi":"10.71781/29692","title":"Étiologie du biais de l'inactivation du chromosome X (ICX) dans les cellules sanguines des femmes vieillissantes : sélection hémizygote et acquisition de mutations somatiques","year":2022,"lang":"fr","type":"dissertation","venue":"Papyrus : Institutional Repository (Université de Montréal)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Mutation; Population; Y chromosome; Chromosome","score_opus":0.010375550707803358,"score_gpt":0.21131897041939962,"score_spread":0.20094341971159627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7105111214","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9726652,0.014415203,0.007850052,0.0005595258,0.0006162295,0.0003930592,0.00012703457,0.000095013624,0.003278712],"genre_scores_gemma":[0.98353624,0.0052099247,0.0032137225,0.00008879764,0.00037167632,0.00011057639,0.003380438,0.000057388243,0.004031216],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9973523,0.00053237344,0.0004967257,0.0007170026,0.0003453737,0.0005562359],"domain_scores_gemma":[0.9984157,0.00012734553,0.00056906434,0.00031647508,0.00036852944,0.00020290089],"candidate_categories":["metaepi_narrow","sts"],"consensus_categories":[],"category_scores_codex":[0.00037978886,0.00051687355,0.00036622773,0.00027308997,0.007109479,0.00011765418,0.00036394663,0.00058695005,0.000118757394],"category_scores_gemma":[0.00027955143,0.0006282467,0.00038464827,0.00031333353,0.00037523537,0.00008584133,0.0002177762,0.00034729554,0.000006608294],"study_design_candidate":"bench_or_experimental","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":[0.00015124767,0.0002579294,0.11772207,0.00024290926,0.00033773694,0.00014841452,0.027949,0.013127045,0.8346476,0.0017965356,0.00019841421,0.003421125],"study_design_scores_gemma":[0.0008108104,0.00048306579,0.46696904,0.00026796953,0.00039348422,0.0018781568,0.081471495,0.004216889,0.43541917,0.0006229945,0.006721015,0.0007458955],"about_ca_topic_score_codex":0.031088237,"about_ca_topic_score_gemma":0.007470683,"teacher_disagreement_score":0.3992284,"about_ca_system_score_codex":0.0037301055,"about_ca_system_score_gemma":0.0015356267,"threshold_uncertainty_score":0.99961686},"labels":[],"label_agreement":null},{"id":"W7149233415","doi":"","title":"Abstracts from the 2008 TOS Fall Symposium","year":2009,"lang":"","type":"article","venue":"Digital Commons - University of South Florida (University of South Florida)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"National park; Biodiversity; Spring (device); Taxon; Biodiversity conservation","score_opus":0.011010728880447023,"score_gpt":0.17576765909810563,"score_spread":0.1647569302176586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7149233415","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9754115,0.0006568209,0.0021297445,0.0011521316,0.00058785966,0.00050456077,0.002625649,0.0000422801,0.016889483],"genre_scores_gemma":[0.9965753,0.00032856612,0.00055256486,0.000074860945,0.00027829438,4.971688e-8,0.00040359222,0.000037530594,0.0017492454],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9966993,0.00011673258,0.00051836274,0.0010795608,0.0007128578,0.0008732345],"domain_scores_gemma":[0.9964348,0.000107056425,0.0009642814,0.0015213022,0.0004877067,0.00048483358],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00025729783,0.0006802273,0.0009081998,0.00016765416,0.00093723834,0.00012338425,0.0022964806,0.00065734173,0.00015213275],"category_scores_gemma":[0.000075142205,0.00083496154,0.0009539606,0.0005277951,0.00115579,0.00012916792,0.0011756461,0.00059803325,0.00010183468],"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":[0.004338561,0.0026202938,0.7225227,0.00067807635,0.0073961243,0.00072658254,0.14949447,0.0077615897,0.044658747,0.00090427365,0.015345598,0.04355304],"study_design_scores_gemma":[0.008541682,0.0026026876,0.70510733,0.0006771907,0.0015956294,0.0000464857,0.18987975,0.00076773495,0.0028806012,0.00026290133,0.08493575,0.002702287],"about_ca_topic_score_codex":0.00083793246,"about_ca_topic_score_gemma":0.00020352202,"teacher_disagreement_score":0.069590144,"about_ca_system_score_codex":0.00008541257,"about_ca_system_score_gemma":0.0003927938,"threshold_uncertainty_score":0.9994101},"labels":[],"label_agreement":null},{"id":"W75734716","doi":"10.1023/a:1026592318341","title":"Parental Imprinting in Drosophila","year":2000,"lang":"en","type":"review","venue":"Genetica","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Heterochromatin; Genetics; Epigenetics; Drosophila melanogaster; Chromatin; Gene silencing; DNA methylation; Gene; Evolutionary biology; Gene expression","score_opus":0.0219007618739802,"score_gpt":0.29581888315751415,"score_spread":0.27391812128353393,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W75734716","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0029476308,0.99154055,0.000010146732,0.000006790662,0.00020809138,0.00044621454,0.000018363891,0.000012482399,0.0048097414],"genre_scores_gemma":[0.002032402,0.99579704,0.0007089476,0.000034646517,0.0004239476,0.00008934628,0.00020177668,0.00009224632,0.0006196354],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99775225,0.0001091465,0.00065429945,0.000786994,0.00014605593,0.0005512505],"domain_scores_gemma":[0.99902296,0.000012969885,0.00015800032,0.00067468046,0.000016658978,0.00011472451],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00016909356,0.00044328687,0.00081042305,0.00012953558,0.000052107018,0.000046104633,0.00045604503,0.0004678565,0.00016780713],"category_scores_gemma":[0.0000348294,0.00042588174,0.0004104382,0.00018522945,0.000069803864,9.898854e-7,0.0003192575,0.00024823847,0.00017618098],"study_design_candidate":"design_other","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":[9.3903054e-7,0.000033219843,0.00011280182,0.0008994609,0.00004267061,0.0000056950935,0.000007540897,0.000005313941,0.00016600333,0.0000060812195,0.000119353455,0.9986009],"study_design_scores_gemma":[0.000174854,0.00008501208,0.0003259961,0.0012147499,0.00008892827,0.00016554538,0.000007501616,0.000004690467,0.00006904041,0.000021409602,0.9973779,0.0004643936],"about_ca_topic_score_codex":0.000010917631,"about_ca_topic_score_gemma":0.000007371469,"teacher_disagreement_score":0.9981365,"about_ca_system_score_codex":0.000024176488,"about_ca_system_score_gemma":0.00017621092,"threshold_uncertainty_score":0.9998193},"labels":[],"label_agreement":null},{"id":"W769689815","doi":"10.1096/fasebj.29.1_supplement.lb34","title":"TMED2 is Sufficient for Trophoblast Fusion","year":2015,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill Genome Centre","funders":"","keywords":"Syncytiotrophoblast; Cell fusion; Cell biology; Syncytium; Cytotrophoblast; Gene knockdown; Trophoblast; Chemistry; Biology; Molecular biology; Cell culture; Placenta; Fetus; Genetics","score_opus":0.023448337501254173,"score_gpt":0.2570063313903431,"score_spread":0.23355799388908896,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W769689815","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99029464,0.0005451948,0.007632461,0.000590308,0.00041436925,0.0001009668,0.0000060965394,0.0000027877245,0.00041316974],"genre_scores_gemma":[0.9969274,0.00006651614,0.0009188036,0.00040990554,0.0005064195,0.000004106159,0.000005504014,0.000012362898,0.001148998],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99937874,0.000031840085,0.00014439705,0.00011179957,0.0001285751,0.00020466959],"domain_scores_gemma":[0.9994999,0.0000072128737,0.00008165283,0.00017631118,0.000117650205,0.00011725842],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000410385,0.00007967211,0.00007088356,0.000018055662,0.00014926285,0.000046294554,0.00019153564,0.00004708117,0.000027223165],"category_scores_gemma":[0.000072500865,0.000050453888,0.000096193035,0.000035431618,0.00003324098,0.0000012996545,0.000078851095,0.000076521465,0.00001529981],"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":[0.000033588683,0.000028875484,0.0009533542,0.0000033704746,0.000028386561,0.0000011386088,0.00037343468,0.00019877756,0.97929204,0.000013208777,0.015012663,0.0040611443],"study_design_scores_gemma":[0.0017069593,0.0012209788,0.0027632476,0.000019760471,0.00004026241,0.0009779115,0.0019895828,0.0009977878,0.88942176,0.0002544618,0.10039879,0.00020850716],"about_ca_topic_score_codex":0.0000035226828,"about_ca_topic_score_gemma":0.0000014120119,"teacher_disagreement_score":0.089870304,"about_ca_system_score_codex":0.00001177315,"about_ca_system_score_gemma":0.000081683975,"threshold_uncertainty_score":0.20574498},"labels":[],"label_agreement":null},{"id":"W85551801","doi":"10.1007/978-0-387-73693-8_24","title":"Neurodevelopmental Abnormalities in the Brainstem of Prenatal Mice Lacking the Prader-Willi Syndrome Gene Necdin","year":2007,"lang":"en","type":"article","venue":"Advances in experimental medicine and biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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","funders":"Alberta Heritage Foundation for Medical Research","keywords":"Brainstem; Failure to thrive; Neurodevelopmental disorder; Hypotonia; Medicine; Endocrinology; Internal medicine; Pediatrics; Autism; Psychiatry","score_opus":0.020183711785846745,"score_gpt":0.3135054386557513,"score_spread":0.29332172686990454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W85551801","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9759577,0.022496011,0.000073911106,0.00027848216,0.00020397032,0.00020955557,0.0000023154441,0.0000025651868,0.0007754838],"genre_scores_gemma":[0.99774253,0.0011638486,0.0003052374,0.0006444683,0.000077865996,0.000016405495,0.000024952882,0.000007365743,0.000017307146],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99898887,0.00009059347,0.00034449776,0.00024089751,0.00007505926,0.0002601063],"domain_scores_gemma":[0.9996261,0.00009298939,0.00009807956,0.0001471014,0.000011350628,0.000024392652],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00052393693,0.00013504866,0.00017638192,0.000057182362,0.000052458458,0.0000038656262,0.0002220883,0.00007186933,0.0000070072597],"category_scores_gemma":[0.000050996532,0.00007688818,0.000024105331,0.00011294953,0.0004105408,0.0000093961635,0.00013216074,0.00010070416,3.1135485e-7],"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":[0.000024637744,0.00012446877,0.22160444,0.000054619122,0.000024810106,0.000012633504,0.0056317733,0.00001622296,0.7546864,0.000556804,0.00002542838,0.017237777],"study_design_scores_gemma":[0.0032859033,0.0031069089,0.47967842,0.0002020834,0.000013028636,0.0025444732,0.07424586,0.000036733385,0.4162378,0.000229471,0.019954648,0.00046469152],"about_ca_topic_score_codex":0.00008371181,"about_ca_topic_score_gemma":0.000078659934,"teacher_disagreement_score":0.3384486,"about_ca_system_score_codex":0.0000094203915,"about_ca_system_score_gemma":0.00001366783,"threshold_uncertainty_score":0.3135409},"labels":[],"label_agreement":null}]}