{"meta":{"query_hash":"a3de0b53e150","filters":{"venue":"Hereditary Cancer in Clinical Practice"},"cohort_total":81,"direct_labels_cover":0,"predictions_cover":81,"exported":81,"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/a3de0b53e150","api":"https://metacan.xera.ac/api/v1/cohort?venue=Hereditary+Cancer+in+Clinical+Practice"},"results":[{"id":"W1589453135","doi":"10.1186/1897-4287-10-s2-a33","title":"Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; University of Toronto","funders":"","keywords":"Medicine; MLH1; Penetrance; Proband; Family history; Cancer; MSH2; Colorectal cancer; Population; Oncology; Internal medicine; Mutation; Genetics; Environmental health; DNA mismatch repair; Gene; Biology","score_opus":0.14316540086250323,"score_gpt":0.4829222647890861,"score_spread":0.3397568639265829,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1589453135","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984933,0.0005566282,0.0004132794,0.000025237337,0.000004807076,0.000005812226,0.00025200652,0.000014083232,0.00023489946],"genre_scores_gemma":[0.9994647,0.000088611334,0.00009250088,0.000007939512,0.000004384595,0.0000040754176,0.00024320376,0.000006149057,0.0000883522],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9974202,0.00096604,0.00015720498,0.0009011218,0.0003340118,0.00022144732],"domain_scores_gemma":[0.99528944,0.0023260794,0.0010133359,0.00084405125,0.00018098074,0.0003461141],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0027961058,0.0003174791,0.00074774894,0.0016911003,0.0003046197,0.0006608728,0.0005650333,0.0005059188,0.0013947464],"category_scores_gemma":[0.008703955,0.00028759154,0.0006820091,0.0011729823,0.0005694377,0.0003286698,0.00060475955,0.0002826182,0.00028649112],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00061016256,0.000023776094,0.98778313,0.00002928822,0.0005018694,0.0005037047,0.0004419828,0.00033223163,0.0027434085,0.00021936167,0.00017232021,0.0066388655],"study_design_scores_gemma":[0.000011205121,0.0000741596,0.99834085,0.0000037974692,0.000088145694,0.0004677373,0.00008708579,0.00041729162,0.00015049083,0.0001942501,0.00015705025,0.000007904076],"about_ca_topic_score_codex":0.0062087397,"about_ca_topic_score_gemma":0.0043483377,"teacher_disagreement_score":0.0062087397,"about_ca_system_score_codex":0.00033622378,"about_ca_system_score_gemma":0.000231292,"threshold_uncertainty_score":0.014787376},"labels":[],"label_agreement":null},{"id":"W1978401597","doi":"10.1186/1897-4287-10-s1-a4","title":"Why choose the treatment with cisplatin for BRCA1 breast cancers patients?","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital","funders":"","keywords":"Medicine; Cisplatin; Human genetics; Oncology; Breast cancer; Internal medicine; Bioinformatics; Gynecology; Cancer; Chemotherapy; Gene; Genetics","score_opus":0.036712866719534144,"score_gpt":0.3847710788215182,"score_spread":0.348058212101984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1978401597","genre_codex":"empirical","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92919976,0.0087606795,0.0012560571,0.051680513,0.0007179281,0.00054277293,0.0005489597,0.00003995603,0.007253469],"genre_scores_gemma":[0.9832275,0.0023832072,0.0017705014,0.010915604,0.00041499728,0.00020766721,0.0001775667,0.000007997786,0.0008948498],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.99953234,0.00020972693,0.000057304445,0.00006486785,0.00007281626,0.000062969106],"domain_scores_gemma":[0.99876606,0.0005018036,0.00021851511,0.00004065625,0.00007707574,0.00039603308],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00096378283,0.00010990066,0.0006622192,0.00029517993,0.000823529,0.0005969813,0.0002737731,0.0016336123,0.0033076575],"category_scores_gemma":[0.004121807,0.00019780983,0.000347698,0.00046507845,0.00040689897,0.00062695617,0.00029635042,0.0010934096,0.0008384003],"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":[0.00765455,0.0019150386,0.7233729,0.00068634114,0.00028635986,0.0061576054,0.0011927327,0.0010056996,0.0043768543,0.00122647,0.02283643,0.22928898],"study_design_scores_gemma":[0.00729127,0.014940703,0.77909964,0.0014310536,0.0010101328,0.029297218,0.007212113,0.0060068597,0.008987145,0.014044034,0.13035177,0.0003280865],"about_ca_topic_score_codex":0.0007206162,"about_ca_topic_score_gemma":0.002464779,"teacher_disagreement_score":0.0033076575,"about_ca_system_score_codex":0.00038112546,"about_ca_system_score_gemma":0.0008326259,"threshold_uncertainty_score":0.011065245},"labels":[],"label_agreement":null},{"id":"W1984981380","doi":"10.1186/1897-4287-9-s2-a5","title":"Selenium and the risk of cancer in BRCA1 carriers","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Selenium in Biological Systems","field":"Nursing","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":"Women's College Hospital; University of Toronto","funders":"","keywords":"Breast cancer; Hazard ratio; Medicine; Selenium; Internal medicine; Cancer; Placebo; Ovarian cancer; Incidence (geometry); Oncology; Gynecology; Confidence interval; Pathology; Chemistry","score_opus":0.08437210650244982,"score_gpt":0.40544827887733514,"score_spread":0.32107617237488534,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984981380","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9987937,0.0010855438,0.000014786268,0.000019820378,0.000002759391,0.0000033853512,0.000016773918,0.0000012094002,0.00006208497],"genre_scores_gemma":[0.99945456,0.00031786048,0.000046956236,0.00001648956,0.00000510473,0.0000040125574,0.00003626591,5.317856e-7,0.000118278986],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99975973,0.00011943153,0.000017714621,0.000040986364,0.00003179674,0.000030212428],"domain_scores_gemma":[0.9994661,0.0002095445,0.00018964287,0.000031615284,0.000025896707,0.00007725012],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008287521,0.00025853806,0.00034723556,0.0005568744,0.00024208047,0.00034295328,0.00019701061,0.0006928417,0.000718663],"category_scores_gemma":[0.001918065,0.00032310854,0.00030284288,0.00023534487,0.000340897,0.00013709569,0.00019595811,0.00025602302,0.00007604292],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.02553459,0.00053071394,0.9499901,0.00017652268,0.0006813225,0.00042474733,0.00030010345,0.0002106857,0.009089201,0.00008337601,0.00016240396,0.012816349],"study_design_scores_gemma":[0.0009238752,0.0077518593,0.9865522,0.00003677574,0.0005025367,0.0009928063,0.00013455714,0.00044598742,0.0016313301,0.00017231306,0.0008466232,0.000009139167],"about_ca_topic_score_codex":0.0024625852,"about_ca_topic_score_gemma":0.002339872,"teacher_disagreement_score":0.0024625852,"about_ca_system_score_codex":0.0002495426,"about_ca_system_score_gemma":0.00021144885,"threshold_uncertainty_score":0.004896462},"labels":[],"label_agreement":null},{"id":"W1985970507","doi":"10.1186/1897-4287-8-s1-p1","title":"Colorectal cancer risk in patients with inflammatory bowel disease and Lynch syndrome","year":2010,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Mount Sinai Hospital","funders":"","keywords":"Medicine; Lynch syndrome; Inflammatory bowel disease; Colorectal cancer; Human genetics; Internal medicine; Cancer; Disease; Inflammatory Bowel Diseases; Gastroenterology; Oncology; DNA mismatch repair","score_opus":0.015380145635294978,"score_gpt":0.3406956392089242,"score_spread":0.3253154935736292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985970507","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973712,0.0005945439,0.0000371928,0.0001259967,0.000013101763,0.000009872805,0.00014336716,0.0000039404035,0.0017007639],"genre_scores_gemma":[0.99941635,0.00019227303,0.000048134865,0.00003880932,0.000027061975,0.0000066804905,0.000091018526,8.365419e-7,0.00017888639],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997204,0.000075179814,0.000029164687,0.000047047943,0.000063359694,0.00006480052],"domain_scores_gemma":[0.9993728,0.00014814305,0.00021802983,0.000031999854,0.00005846553,0.00017060024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023602934,0.00018386451,0.00038995908,0.0007963242,0.0005542395,0.0004070629,0.00020015579,0.00061318226,0.0028602444],"category_scores_gemma":[0.0026156302,0.0001651777,0.00024025337,0.0010895261,0.0002668936,0.00040519022,0.00027759446,0.0004927541,0.00029657796],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009698214,0.00002165622,0.9978807,0.0000074398263,0.000013526988,0.00077628903,0.00006700334,0.000014326984,0.000099893645,0.000020552012,0.00011621509,0.0008854848],"study_design_scores_gemma":[0.000009571858,0.0001659127,0.99436104,0.000009934409,0.000032159165,0.0046067066,0.00026173118,0.00010558421,0.000039400165,0.00004646691,0.00035590553,0.000005671879],"about_ca_topic_score_codex":0.005769933,"about_ca_topic_score_gemma":0.006443787,"teacher_disagreement_score":0.005769933,"about_ca_system_score_codex":0.0002274481,"about_ca_system_score_gemma":0.00029963374,"threshold_uncertainty_score":0.011472702},"labels":[],"label_agreement":null},{"id":"W1987304025","doi":"10.1186/1897-4287-9-s1-p40","title":"Risks of cancers for carriers of monoallelic MUTYH mutation with a family history of colorectal cancer","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; Lunenfeld-Tanenbaum Research Institute; Cancer Care Ontario; Mount Sinai Hospital","funders":"National Cancer Institute; National Institutes of Health","keywords":"Medicine; MUTYH; Colorectal cancer; Population; Cancer; Germline mutation; Internal medicine; Oncology; Incidence (geometry); Family history; Lynch syndrome; Endometrial cancer; Gynecology; Mutation; Genetics; DNA mismatch repair; Biology; Gene","score_opus":0.1992363951648351,"score_gpt":0.4344766551320192,"score_spread":0.23524025996718412,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987304025","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977023,0.0008673094,0.00043388305,0.00003810317,0.0000055424644,0.0000077295035,0.00039530432,0.000014950589,0.000534823],"genre_scores_gemma":[0.99916625,0.00022123159,0.00028090345,0.000010410565,0.000007342638,0.0000043401083,0.00019720367,0.0000020995424,0.0001101682],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996549,0.00010729394,0.000026220092,0.000105588806,0.000048488724,0.000057552683],"domain_scores_gemma":[0.99831957,0.00052102323,0.0007557077,0.00014703328,0.00009558098,0.00016111159],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006505997,0.00026832495,0.00022406208,0.0009810181,0.00024284355,0.00029671853,0.00022938529,0.00030046134,0.0025830532],"category_scores_gemma":[0.0023187967,0.00024026755,0.0005627684,0.0007665261,0.0002544806,0.0001886312,0.0003833126,0.00039809142,0.00016264751],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000101229525,0.0000057636694,0.99831355,0.000007970774,0.00008312664,0.00012311099,0.000020521356,0.00011786205,0.0001288735,0.00002104988,0.000048374084,0.001028646],"study_design_scores_gemma":[0.0000066805756,0.00007695879,0.9969236,0.0000068623513,0.00012417944,0.0019131603,0.00006926632,0.0004507822,0.00012587616,0.0000709558,0.00022730968,0.0000042902893],"about_ca_topic_score_codex":0.0039783814,"about_ca_topic_score_gemma":0.003717858,"teacher_disagreement_score":0.0039783814,"about_ca_system_score_codex":0.0001868392,"about_ca_system_score_gemma":0.00017446512,"threshold_uncertainty_score":0.008641183},"labels":[],"label_agreement":null},{"id":"W1996721235","doi":"10.1186/1897-4287-10-s4-a17","title":"Cisplatin in breast cancer treatment in BRCA1 carriers","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital","funders":"","keywords":"Medicine; Cisplatin; Oncology; Breast cancer; Human genetics; Cancer; Internal medicine; Gynecology; Chemotherapy","score_opus":0.04639705013425582,"score_gpt":0.4194264781558468,"score_spread":0.373029428021591,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1996721235","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.83428466,0.12584479,0.00087067357,0.011103396,0.0008050982,0.00029884,0.00076301646,0.00016176653,0.025867686],"genre_scores_gemma":[0.96240103,0.03132139,0.00082903396,0.0013699302,0.0002395798,0.00011532917,0.00047279565,0.00002737861,0.0032236315],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99981207,0.00009100526,0.000017576815,0.000020007092,0.000036616042,0.000022869175],"domain_scores_gemma":[0.99957484,0.00019111224,0.00006560768,0.000018822871,0.00003129787,0.000118274605],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033780985,0.00014185013,0.0006547528,0.0004048333,0.00020966168,0.00032637385,0.00034868554,0.0006261566,0.00339007],"category_scores_gemma":[0.001797882,0.00010226269,0.0002520663,0.0004374806,0.00014983797,0.00028498788,0.0002652351,0.0009203022,0.00047237417],"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":[0.083236985,0.00322932,0.05346125,0.002531611,0.00064977136,0.0027081734,0.00032016344,0.002971904,0.018493209,0.0014382651,0.023346962,0.8076124],"study_design_scores_gemma":[0.037826147,0.11716393,0.5048254,0.0028417748,0.0027763767,0.028541509,0.0011300662,0.007484898,0.034798637,0.008473755,0.25391102,0.00022652205],"about_ca_topic_score_codex":0.0010440507,"about_ca_topic_score_gemma":0.002454354,"teacher_disagreement_score":0.00339007,"about_ca_system_score_codex":0.00047448234,"about_ca_system_score_gemma":0.0006563381,"threshold_uncertainty_score":0.011340916},"labels":[],"label_agreement":null},{"id":"W1997655706","doi":"10.1186/1897-4287-10-s4-a18","title":"Screening with Magnetic Resonance Imaging in women at low and intermediate risk of breast Cancer","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Breast Cancer Treatment Studies","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":"Women's College Hospital","funders":"","keywords":"Medicine; Breast cancer; Mammography; Magnetic resonance imaging; CHEK2; Cancer; Gynecology; Prospective cohort study; Obstetrics; Oncology; Radiology; Internal medicine; Mutation","score_opus":0.015070865253049539,"score_gpt":0.33543488431911694,"score_spread":0.32036401906606743,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997655706","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991505,0.00027062892,0.000032537486,0.00004994115,0.000005370306,0.000008785696,0.000098248885,0.0000020213226,0.00038200626],"genre_scores_gemma":[0.9994128,0.00014559668,0.000063602914,0.000046233596,0.000010127543,0.000010113239,0.0001394086,0.0000010902108,0.00017104416],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99955374,0.00014335747,0.000039613176,0.00007632755,0.00008278991,0.00010422279],"domain_scores_gemma":[0.99933165,0.00015060442,0.00021126632,0.000051194318,0.00006502054,0.0001902909],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00057524926,0.00024384006,0.00041463677,0.0010333463,0.0006534368,0.00054120395,0.00030218673,0.00057918264,0.0011145418],"category_scores_gemma":[0.0032081262,0.0004565785,0.00031037015,0.0009232752,0.0003117744,0.00039100027,0.00043189037,0.0004917676,0.0002960508],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00025310175,0.00007576163,0.9972699,0.000009372087,0.000019543653,0.00036417242,0.00010266074,0.000018205608,0.0002447629,0.000014094014,0.000091560265,0.0015367562],"study_design_scores_gemma":[0.000028575583,0.00032586927,0.997837,0.000010393959,0.000053574266,0.00095467933,0.00018716043,0.000107903,0.00012778968,0.00003459097,0.0003258603,0.0000067566452],"about_ca_topic_score_codex":0.008789567,"about_ca_topic_score_gemma":0.012717876,"teacher_disagreement_score":0.008789567,"about_ca_system_score_codex":0.00030711232,"about_ca_system_score_gemma":0.00026470155,"threshold_uncertainty_score":0.017476797},"labels":[],"label_agreement":null},{"id":"W2001299805","doi":"10.1186/1897-4287-3-2-59","title":"The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs","year":2005,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Helicobacter pylori-related gastroenterology studies","field":"Medicine","cited_by":31,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Coalition for Research in Women's Health; University of Toronto","funders":"Uniwersytet Warszawski; Warszawski Uniwersytet Medyczny","keywords":"Medicine; Colorectal cancer; Allele; NOD2; Cancer; Breast cancer; Internal medicine; Lung cancer; Ovarian cancer; Oncology; Disease; Gastroenterology; Crohn's disease; Gene; Genetics; Biology","score_opus":0.05053155498685956,"score_gpt":0.40567638368073267,"score_spread":0.3551448286938731,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001299805","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992156,0.00034524538,0.00004570058,0.00002784683,0.0000021479561,0.00000484967,0.000047652145,0.0000013937962,0.00030949837],"genre_scores_gemma":[0.99922466,0.00034432762,0.00008456137,0.000018929271,0.0000060605184,0.000003585708,0.000100559984,9.755795e-7,0.00021626784],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99973506,0.00010263067,0.000027892358,0.000051052306,0.00004195309,0.000041410578],"domain_scores_gemma":[0.99919873,0.0001853589,0.0003479901,0.000057994203,0.000058186764,0.00015188316],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004843142,0.00031068394,0.0002967403,0.001036497,0.0003216723,0.00027330287,0.00015121356,0.00026305995,0.002370831],"category_scores_gemma":[0.0016180936,0.00027503385,0.0002139626,0.00082601164,0.00029563165,0.0001518593,0.00043551158,0.00026389668,0.0002160565],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039321114,0.000053487474,0.99283737,0.000028911785,0.00009367062,0.0007615647,0.000115973504,0.000027953933,0.0024799304,0.000053994398,0.000101230136,0.003052695],"study_design_scores_gemma":[0.00002167101,0.00018304815,0.9965454,0.000010938214,0.000049746326,0.002090943,0.000122035235,0.000055253116,0.00027932812,0.000053818672,0.0005850055,0.0000029896426],"about_ca_topic_score_codex":0.002482964,"about_ca_topic_score_gemma":0.0029590519,"teacher_disagreement_score":0.002482964,"about_ca_system_score_codex":0.0001710976,"about_ca_system_score_gemma":0.00018379053,"threshold_uncertainty_score":0.007931232},"labels":[],"label_agreement":null},{"id":"W2001536441","doi":"10.1186/1897-4287-9-s1-o1","title":"Metachronous colorectal cancer risk for mismatch repair gene mutation carriers – the advantage of more extensive surgery","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","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":"University of Toronto; Mount Sinai Hospital","funders":"National Cancer Institute; National Institutes of Health","keywords":"Medicine; Colorectal cancer; Human genetics; DNA mismatch repair; Gene; Mutation; Lynch syndrome; Bioinformatics; Cancer; Oncology; Internal medicine; General surgery; Genetics","score_opus":0.08021747794746385,"score_gpt":0.40948665051217126,"score_spread":0.3292691725647074,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001536441","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99753654,0.00046453346,0.00008127892,0.00031338877,0.000016533268,0.000002058025,0.0000449195,0.0000040073746,0.0015367618],"genre_scores_gemma":[0.9995598,0.00009690125,0.000078360616,0.000034090328,0.00002873172,7.5470285e-7,0.000025623633,0.0000017173953,0.00017394533],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997546,0.00007337527,0.000020138425,0.000054203,0.000036006608,0.00006169007],"domain_scores_gemma":[0.9985018,0.00047087943,0.00045612894,0.000093365365,0.000054846747,0.000422942],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023907748,0.00017703002,0.00028938343,0.0005219379,0.0003628567,0.00042286568,0.00027754655,0.0005554566,0.0075533334],"category_scores_gemma":[0.0032051788,0.00013929403,0.00032838978,0.00047561465,0.00027058672,0.00042936724,0.00029724799,0.00043869144,0.00026390172],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015570989,0.00012755442,0.9756482,0.000023754461,0.00013106324,0.0029603448,0.000092181355,0.00014060698,0.0034517855,0.0002946775,0.00028138148,0.015291257],"study_design_scores_gemma":[0.00004961221,0.00055204245,0.98377603,0.000012602542,0.00016731383,0.013173443,0.00033258004,0.00047027002,0.0003843947,0.0005295366,0.0005390958,0.000013134422],"about_ca_topic_score_codex":0.0014897855,"about_ca_topic_score_gemma":0.00276988,"teacher_disagreement_score":0.0075533334,"about_ca_system_score_codex":0.0001268196,"about_ca_system_score_gemma":0.00032127756,"threshold_uncertainty_score":0.025268435},"labels":[],"label_agreement":null},{"id":"W2003796650","doi":"10.1186/1897-4287-9-s1-p11","title":"Oncologic surveillance for subjects with biallelic mismatch repair gene mutations-10 year follow-up in a kindred","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Human genetics; Genetics; Gene; Mutation; Bioinformatics; Biology","score_opus":0.12719501589697627,"score_gpt":0.40767405160794074,"score_spread":0.28047903571096444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2003796650","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993586,0.0001501815,0.000039191313,0.000048119233,0.0000029345447,0.000003393529,0.000060303373,0.000003947224,0.00033328755],"genre_scores_gemma":[0.9995647,0.00009377144,0.000048091348,0.000026599198,0.0000039445194,0.0000022348213,0.000075515585,0.0000015236524,0.0001836574],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976593,0.000042015527,0.00002484843,0.000045743895,0.00003352317,0.000088025794],"domain_scores_gemma":[0.9993667,0.00013967192,0.00015597376,0.00004737748,0.00011351153,0.00017676031],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033034667,0.00029300695,0.00030612366,0.001127232,0.0011399976,0.00035340237,0.00031644173,0.00054444856,0.0005905252],"category_scores_gemma":[0.0013224706,0.00022295544,0.0004566159,0.0006903099,0.00034307296,0.00026813443,0.00035497488,0.00045413754,0.00016063309],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00027942206,0.00014422176,0.9740562,0.0000108346685,0.000025216501,0.019337546,0.0007102836,0.00010006187,0.0017457402,0.000029245406,0.00016183077,0.00339936],"study_design_scores_gemma":[0.000010998622,0.000509469,0.97952855,0.0000087750905,0.00007130544,0.01796332,0.0007995981,0.00017896786,0.0005450987,0.000037416736,0.00033390065,0.000012613759],"about_ca_topic_score_codex":0.02409623,"about_ca_topic_score_gemma":0.0193994,"teacher_disagreement_score":0.02409623,"about_ca_system_score_codex":0.0006720527,"about_ca_system_score_gemma":0.00055821677,"threshold_uncertainty_score":0.047911942},"labels":[],"label_agreement":null},{"id":"W2006517957","doi":"10.1186/1897-4287-10-s2-a11","title":"Association of tamoxifen use and reduced risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Cancer Care Ontario","funders":"","keywords":"Medicine; Breast cancer; Tamoxifen; Human genetics; Oncology; Mutation; Internal medicine; Bioinformatics; Cancer; Genetics; Gynecology; Gene","score_opus":0.031717171961056605,"score_gpt":0.38101886026497217,"score_spread":0.34930168830391556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2006517957","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984731,0.00082232855,0.000034812343,0.000056821536,0.000006496948,0.0000025756221,0.00022196349,0.0000042779197,0.00037752365],"genre_scores_gemma":[0.99939,0.00021409722,0.000022786846,0.000015080559,0.000009126589,0.0000021771361,0.00014064935,0.0000014691941,0.0002046114],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997718,0.00006871021,0.00002004576,0.00005379688,0.00003408494,0.0000515789],"domain_scores_gemma":[0.9981427,0.0006177839,0.00081665424,0.00012143727,0.000088566405,0.00021287493],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005992874,0.00017696031,0.00021674813,0.0005124227,0.00015640935,0.00032190545,0.00020725866,0.0003769202,0.0026167003],"category_scores_gemma":[0.0030868878,0.00013355825,0.00048952317,0.00038848343,0.00015102797,0.00017947661,0.0001844881,0.00028216103,0.00015511469],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010549112,0.000029835719,0.99514943,0.000013874898,0.00010751615,0.000119384196,0.000031239015,0.000045971392,0.00027924345,0.000018605679,0.000109752626,0.0030402108],"study_design_scores_gemma":[0.00002748076,0.00015886521,0.9986632,0.00000619947,0.00013170866,0.0004637854,0.0000357602,0.00023323898,0.000063956446,0.00002800682,0.00018487376,0.0000030753592],"about_ca_topic_score_codex":0.00555659,"about_ca_topic_score_gemma":0.005480483,"teacher_disagreement_score":0.00555659,"about_ca_system_score_codex":0.0001778711,"about_ca_system_score_gemma":0.00023825462,"threshold_uncertainty_score":0.011048496},"labels":[],"label_agreement":null},{"id":"W2014054572","doi":"10.1186/1897-4287-8-s1-p2","title":"Clinicopathologic and genetic features of young patients with colorectal cancer","year":2010,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Mount Sinai Hospital","funders":"","keywords":"Medicine; Colorectal cancer; Internal medicine; Family history; Lynch syndrome; Gastroenterology; Cancer; DNA mismatch repair","score_opus":0.02646104164699246,"score_gpt":0.381320786250152,"score_spread":0.3548597446031595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2014054572","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981224,0.0003535402,0.000033727207,0.000041988842,0.000006357518,0.000009346266,0.00035218708,0.0000050116582,0.0010754844],"genre_scores_gemma":[0.999218,0.00015661873,0.00004315003,0.000033690376,0.00000979402,0.000005262342,0.00037199995,0.0000011184957,0.0001604067],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998037,0.000018854458,0.000025244228,0.000037817586,0.000058405403,0.000055958557],"domain_scores_gemma":[0.9989158,0.0001606982,0.00035134138,0.000027816448,0.00014947982,0.00039492772],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017389811,0.00020779589,0.00026002995,0.000969898,0.00066325726,0.00041815185,0.00019829515,0.0003103166,0.0020538159],"category_scores_gemma":[0.0015538484,0.00018563382,0.00016790569,0.0009642843,0.0003213664,0.0002692516,0.0002547843,0.00019825224,0.00028187654],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000032915785,0.0000070873375,0.9977537,0.000004995856,0.0000057547154,0.0012577286,0.00007443453,0.000017660657,0.00021640117,0.000007537729,0.00011024467,0.0005114872],"study_design_scores_gemma":[0.0000023232244,0.000036419406,0.99393106,0.0000068186537,0.0000063988223,0.005439378,0.000277048,0.000043432887,0.000035421283,0.000011333204,0.00020698573,0.000003386764],"about_ca_topic_score_codex":0.033311885,"about_ca_topic_score_gemma":0.048901837,"teacher_disagreement_score":0.033311885,"about_ca_system_score_codex":0.00069517345,"about_ca_system_score_gemma":0.0006657623,"threshold_uncertainty_score":0.06623596},"labels":[],"label_agreement":null},{"id":"W2017761747","doi":"10.1186/1897-4287-8-s1-p5","title":"Lynch syndrome-chasing a better ascertainment rate in British Columbia","year":2010,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"BC Cancer Agency","funders":"","keywords":"Lynch syndrome; Medicine; Microsatellite instability; Referral; Population; Genetic testing; Colorectal cancer; Cancer; Family history; Pediatrics; Family medicine; Internal medicine; DNA mismatch repair; Microsatellite; Genetics","score_opus":0.03329477957096011,"score_gpt":0.3838834732757111,"score_spread":0.350588693704751,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017761747","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9602311,0.007057631,0.0006186396,0.0033265336,0.0001432963,0.00017718895,0.009537498,0.0000789893,0.018829169],"genre_scores_gemma":[0.9859218,0.0026038138,0.0007439966,0.0009974431,0.000025770787,0.000066657245,0.002940747,0.000029015828,0.0066707996],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99815804,0.00029888772,0.00019513148,0.00029925563,0.0007500698,0.00029858574],"domain_scores_gemma":[0.9944647,0.000739454,0.00061249273,0.00039463112,0.0030134295,0.00077526603],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014116303,0.00018011831,0.00047003228,0.0020216645,0.0012475793,0.0012649731,0.0009947171,0.00040795116,0.0030468947],"category_scores_gemma":[0.006714912,0.00022583432,0.00021352933,0.004277187,0.0003440016,0.00046315356,0.00064454594,0.0004653823,0.00041475397],"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":[0.00012066266,0.000038834234,0.94420457,0.00021405036,0.00007619161,0.00095336576,0.0017889056,0.00019643808,0.0013377045,0.00048522497,0.014453432,0.036130715],"study_design_scores_gemma":[0.000010710205,0.000016345804,0.9919469,0.00007345081,0.000017792885,0.00036894414,0.00072007574,0.00027707673,0.00009038868,0.0000369658,0.0064292126,0.000012290909],"about_ca_topic_score_codex":0.9755368,"about_ca_topic_score_gemma":0.98720306,"teacher_disagreement_score":0.024463177,"about_ca_system_score_codex":0.010084501,"about_ca_system_score_gemma":0.008464476,"threshold_uncertainty_score":0.07316846},"labels":[],"label_agreement":null},{"id":"W2030459565","doi":"10.1186/1897-4287-10-s1-a14","title":"Identification of patients at high risk of negative psychological consequences associated with BRCA1 mutation","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital; University of Toronto","funders":"","keywords":"Medicine; Anxiety; Breast cancer; Cancer; Genetic predisposition; Genetic testing; Test (biology); Distress; Population; Psychological testing; Clinical psychology; Genetic counseling; Trait; Psychiatry; Internal medicine; Genetics; Disease; Environmental health","score_opus":0.04186750948535035,"score_gpt":0.4015947907953957,"score_spread":0.35972728131004533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2030459565","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99657494,0.00045913097,0.000109180015,0.0005181601,0.000021620024,0.000018793928,0.00015178483,0.000007072581,0.002139293],"genre_scores_gemma":[0.9984504,0.00032604503,0.00026179996,0.0001619835,0.00002750235,0.000011976917,0.00014201208,0.0000023479415,0.0006157753],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998851,0.00003352595,0.000009092927,0.000014881378,0.000024893232,0.000032552158],"domain_scores_gemma":[0.9995246,0.0001367944,0.00013408881,0.0000139069025,0.000040001585,0.00015067933],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018735118,0.0001801537,0.00024973776,0.0008451069,0.0005871528,0.00057705573,0.00017773497,0.0003984105,0.003075918],"category_scores_gemma":[0.0018097984,0.00009623934,0.00015734651,0.0005358439,0.00017283109,0.00030853477,0.00032359746,0.00064454536,0.00035526245],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013821504,0.00012517245,0.9876466,0.000018711595,0.000008862019,0.0012706091,0.0001973089,0.000022850989,0.0006182747,0.000044798093,0.0008097854,0.009098729],"study_design_scores_gemma":[0.000012785213,0.00024021513,0.9875594,0.000026741296,0.000025465524,0.0087378165,0.0014857615,0.00030203263,0.00027941813,0.0002463466,0.0010707057,0.000013377529],"about_ca_topic_score_codex":0.0010827152,"about_ca_topic_score_gemma":0.0017432949,"teacher_disagreement_score":0.003075918,"about_ca_system_score_codex":0.00014399296,"about_ca_system_score_gemma":0.00024443035,"threshold_uncertainty_score":0.010290027},"labels":[],"label_agreement":null},{"id":"W2038939551","doi":"10.1186/1897-4287-4-1-58","title":"A Lowering of Breast and Ovarian Cancer Risk in Women with a BRCA1 Mutation by Selenium Supplementation of Diet","year":2006,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Selenium in Biological Systems","field":"Nursing","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":"Women's College Hospital","funders":"","keywords":"Medicine; Breast cancer; Ovarian cancer; Human genetics; Selenium; Gynecology; Oncology; Internal medicine; Mutation; Physiology; Bioinformatics; Cancer; Genetics; Gene","score_opus":0.022997810975908008,"score_gpt":0.36298927562563105,"score_spread":0.339991464649723,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2038939551","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99641114,0.0025011657,0.00008741906,0.00014128698,0.000019195473,0.00003079351,0.00006257314,0.000007363407,0.0007389375],"genre_scores_gemma":[0.9970168,0.0011709813,0.0002474677,0.00009812036,0.000024427025,0.000026850414,0.00008144337,0.0000018562208,0.0013320807],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99987984,0.000055360437,0.000008295093,0.000016271919,0.000022554468,0.000017640561],"domain_scores_gemma":[0.99974006,0.000098506294,0.000060516835,0.000018731032,0.00002891162,0.00005316155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003787814,0.00019460169,0.0003003087,0.000274162,0.00022589139,0.0001844779,0.00013533664,0.00027203604,0.0022254686],"category_scores_gemma":[0.0010264546,0.00011149839,0.00018748271,0.00020765132,0.00011816953,0.00011196612,0.00017829647,0.00024427284,0.0001467606],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.055652466,0.005473507,0.6548955,0.0010693999,0.0009940605,0.0006647905,0.00044488563,0.00027758974,0.05371085,0.00017462877,0.0017210629,0.22492129],"study_design_scores_gemma":[0.0013302407,0.03227246,0.9556868,0.00007452825,0.000584552,0.00082769134,0.00016340057,0.00017981333,0.004896282,0.00009750536,0.003879894,0.000006744283],"about_ca_topic_score_codex":0.0006370431,"about_ca_topic_score_gemma":0.00092953246,"teacher_disagreement_score":0.0022254686,"about_ca_system_score_codex":0.0000900844,"about_ca_system_score_gemma":0.00018824328,"threshold_uncertainty_score":0.007444918},"labels":[],"label_agreement":null},{"id":"W2045218241","doi":"10.1186/1897-4287-10-s2-a40","title":"Identification of new breast cancer predisposition genes via whole exome sequencing","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cancer Care Ontario; Mount Sinai Hospital","funders":"","keywords":"Exome sequencing; Breast cancer; Penetrance; Massive parallel sequencing; Exome; Genetics; Mendelian inheritance; Phenocopy; Human genetics; Missing heritability problem; Gene; Biology; Medicine; Phenotype; Cancer; Genotype; DNA sequencing; Single-nucleotide polymorphism","score_opus":0.07824366546791871,"score_gpt":0.42622929225953776,"score_spread":0.34798562679161904,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045218241","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8494075,0.013589422,0.10266525,0.003932269,0.00038209299,0.00076046295,0.02154158,0.0011515876,0.00656999],"genre_scores_gemma":[0.78932446,0.016026402,0.16545616,0.0031508917,0.00053729414,0.00056622014,0.019807508,0.00025698452,0.0048741363],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99966466,0.00005939502,0.0000240466,0.00012112425,0.0000943519,0.000036324072],"domain_scores_gemma":[0.99963164,0.00017005698,0.00005374268,0.000053272506,0.00004545996,0.0000458684],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008158751,0.00051214953,0.0005101918,0.0015643456,0.00033069044,0.000632412,0.0005045451,0.0007852745,0.0024498482],"category_scores_gemma":[0.001517372,0.00021972532,0.00054806616,0.0009975196,0.00020226999,0.0005078035,0.0005852058,0.00079748535,0.0008931583],"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":[0.00088643195,0.00033828037,0.10562978,0.00093756634,0.0007740132,0.008611202,0.0005428689,0.001966084,0.67156154,0.003610854,0.011020925,0.1941205],"study_design_scores_gemma":[0.00044901232,0.0011784998,0.5550978,0.0006723364,0.0020892178,0.041981623,0.0004959564,0.029092323,0.19115524,0.015827755,0.16171491,0.00024530067],"about_ca_topic_score_codex":0.00049411366,"about_ca_topic_score_gemma":0.0010821286,"teacher_disagreement_score":0.0024498482,"about_ca_system_score_codex":0.00026913508,"about_ca_system_score_gemma":0.00020504404,"threshold_uncertainty_score":0.008195519},"labels":[],"label_agreement":null},{"id":"W2045346543","doi":"10.1186/1897-4287-8-s1-p17","title":"An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutation","year":2010,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital","funders":"","keywords":"Medicine; Lynch syndrome; MSH6; Family history; Endometrial cancer; Colorectal cancer; Cancer syndrome; Cancer; Internal medicine; Pheochromocytoma; Neurofibromatosis; Oncology; Germline mutation; Gastroenterology; Pathology; DNA mismatch repair; Mutation; Genetics","score_opus":0.03451937262918984,"score_gpt":0.4195818339593144,"score_spread":0.38506246133012456,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045346543","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98186064,0.0024179623,0.003645465,0.00038025904,0.000058880367,0.000102603524,0.0007567714,0.00036693487,0.010410531],"genre_scores_gemma":[0.9958133,0.00062325696,0.0014931571,0.00014254342,0.00007310915,0.00002490587,0.00029969463,0.00004613584,0.0014838838],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997013,0.000029142722,0.000028193615,0.00007781976,0.00005062843,0.00011281395],"domain_scores_gemma":[0.999373,0.000104915314,0.00016844927,0.00006185619,0.000067544635,0.00022425647],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013301466,0.000777333,0.0004966385,0.0018533373,0.0007861051,0.0006842506,0.00044465176,0.0013039998,0.0040585143],"category_scores_gemma":[0.00096699974,0.00044465833,0.0004887275,0.0008577675,0.00045915664,0.00066013756,0.00096209295,0.0006348009,0.0014876917],"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":[0.00016194576,0.000028700317,0.032999944,0.00006598099,0.000022127226,0.9418303,0.0001711433,0.00014496318,0.01954462,0.0003885459,0.0004747986,0.0041669486],"study_design_scores_gemma":[0.000012096203,0.000039793165,0.016407756,0.000009696241,0.000014421436,0.9802343,0.00008963808,0.00020537019,0.0018561977,0.00027049237,0.0008533418,0.000006980332],"about_ca_topic_score_codex":0.0010967671,"about_ca_topic_score_gemma":0.001815598,"teacher_disagreement_score":0.0040585143,"about_ca_system_score_codex":0.00026266646,"about_ca_system_score_gemma":0.00026212557,"threshold_uncertainty_score":0.013577044},"labels":[],"label_agreement":null},{"id":"W2052148215","doi":"10.1186/1897-4287-9-s1-p39","title":"Hereditary non-polyposis colorectal cancer: barriers to and facilitators of screening and disease management","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Memorial University of Newfoundland","funders":"Genome Canada","keywords":"Medicine; Colorectal cancer; Human genetics; Disease; Internal medicine; Disease management; Oncology; Cancer; Family medicine; Bioinformatics; Genetics; Gene","score_opus":0.05012089049675465,"score_gpt":0.3758424172272386,"score_spread":0.32572152673048393,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052148215","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99162674,0.0005699482,0.0005269953,0.0036114107,0.000025124209,0.00013641187,0.000055870725,0.000007979057,0.0034394278],"genre_scores_gemma":[0.9982765,0.00031962636,0.0006330069,0.00018820209,0.0000056262415,0.000066584376,0.000021566644,0.000002890876,0.00048617614],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.99351305,0.003925678,0.00026352284,0.00031011988,0.0008611895,0.0011264667],"domain_scores_gemma":[0.98399055,0.010597306,0.0023221031,0.0002930408,0.0010443218,0.0017526608],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00611432,0.00029499087,0.00044555127,0.0006253029,0.0023929486,0.0013942815,0.00071618974,0.0006564113,0.0018722498],"category_scores_gemma":[0.01632575,0.00030876577,0.00047234423,0.0005341491,0.0015424724,0.0011236747,0.0029579338,0.0012236871,0.00009562068],"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":[0.0002469794,0.0008441578,0.36777604,0.0011445383,0.00015666452,0.0012664903,0.53067744,0.00042795995,0.0013679081,0.0042142794,0.0027959934,0.089081444],"study_design_scores_gemma":[0.000046159,0.00042819942,0.28703168,0.001185555,0.00013825287,0.00090199924,0.6908055,0.0012241992,0.00075786706,0.00262498,0.01478528,0.00007033053],"about_ca_topic_score_codex":0.013803723,"about_ca_topic_score_gemma":0.01781188,"teacher_disagreement_score":0.013803723,"about_ca_system_score_codex":0.0025895047,"about_ca_system_score_gemma":0.006884455,"threshold_uncertainty_score":0.032335997},"labels":[],"label_agreement":null},{"id":"W2056941427","doi":"10.1186/1897-4287-10-s2-a83","title":"Benign serous ovarian tumour: a redefining moment?","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver General Hospital; BC Cancer Agency","funders":"","keywords":"Serous fluid; Serous carcinoma; KRAS; Pathology; Serous Cystadenoma; Medicine; Cystadenocarcinoma; Ovary; Ovarian carcinoma; Ovarian cancer; Cancer research; Biology; Cancer; Internal medicine; Colorectal cancer","score_opus":0.09535101933719978,"score_gpt":0.4364301360810729,"score_spread":0.34107911674387315,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2056941427","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7027567,0.20354761,0.017627344,0.05453525,0.0029901734,0.00009139539,0.00024619215,0.0005518975,0.01765342],"genre_scores_gemma":[0.9318683,0.043367453,0.012947096,0.005938473,0.0020249572,0.000027117383,0.00014637824,0.0000627156,0.003617498],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99974567,0.00004807483,0.00003135006,0.000047643793,0.00007618032,0.000051083043],"domain_scores_gemma":[0.9993685,0.00021816783,0.00013421744,0.00006225799,0.000103105325,0.000113783884],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007680038,0.00027835002,0.0004584617,0.0006479112,0.0005100972,0.001157436,0.0003825936,0.0008817893,0.0013102388],"category_scores_gemma":[0.002012853,0.00020740971,0.00019496644,0.00043365383,0.0014058748,0.0023535576,0.0005775063,0.0011176846,0.00045031303],"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":[0.0009951784,0.00010142482,0.11092405,0.0013445539,0.00007614508,0.18516797,0.0035895673,0.00040507605,0.18536921,0.022360826,0.014808986,0.4748571],"study_design_scores_gemma":[0.000058724603,0.0007029344,0.07228409,0.0008067572,0.00014826363,0.63781637,0.004083585,0.0010822839,0.04040012,0.018881308,0.22359325,0.00014236144],"about_ca_topic_score_codex":0.00041619386,"about_ca_topic_score_gemma":0.0008518805,"teacher_disagreement_score":0.0013102388,"about_ca_system_score_codex":0.00047548502,"about_ca_system_score_gemma":0.0004446287,"threshold_uncertainty_score":0.0043831468},"labels":[],"label_agreement":null},{"id":"W2062689300","doi":"10.1186/1897-4287-9-s1-p38","title":"Late presentation of cancer in compound heterozygote PMS2 mutation carrier","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital","funders":"","keywords":"Medicine; Heterozygote advantage; Human genetics; Presentation (obstetrics); PMS2; Cancer; Mutation; Genetics; Bioinformatics; Internal medicine; Surgery; Gene; Genotype; Biology","score_opus":0.12265892225810518,"score_gpt":0.4534832197053063,"score_spread":0.3308242974472011,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2062689300","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996095,0.0007006594,0.00040155795,0.00024048012,0.00004192478,0.00002183598,0.00018203618,0.00010081431,0.0022156667],"genre_scores_gemma":[0.9982376,0.00023082459,0.00021444158,0.00007426956,0.000036449343,0.0000049666623,0.00011424489,0.000016005617,0.001071242],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998659,0.000010364007,0.000007968504,0.000048237183,0.000023745857,0.000043810604],"domain_scores_gemma":[0.9996861,0.000056439178,0.00008088657,0.000017337326,0.000027733126,0.00013140975],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008091708,0.0008180337,0.00046099484,0.0011290385,0.0007273063,0.00055088906,0.000404699,0.0010947667,0.0041565914],"category_scores_gemma":[0.0007326004,0.00024927175,0.0002717224,0.00049788743,0.00037678622,0.00030415217,0.00029642956,0.00051882985,0.0006000864],"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":[0.00026971224,0.00005229004,0.06509068,0.000047628837,0.000015708974,0.91656446,0.0002738904,0.00009435305,0.013181934,0.0002267865,0.00086032617,0.0033221967],"study_design_scores_gemma":[0.000012137528,0.0002210286,0.05856287,0.000018369308,0.000021875467,0.9372205,0.00019660508,0.00034627732,0.002096844,0.00017682236,0.0011091961,0.00001747844],"about_ca_topic_score_codex":0.002804708,"about_ca_topic_score_gemma":0.002254197,"teacher_disagreement_score":0.0041565914,"about_ca_system_score_codex":0.0003653038,"about_ca_system_score_gemma":0.0002676841,"threshold_uncertainty_score":0.013905168},"labels":[],"label_agreement":null},{"id":"W2069847419","doi":"10.1186/1897-4287-9-s1-o3","title":"Development and testing of the Hereditary Diseases and Genetic Testing (HD-GT) scale","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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; Memorial University of Newfoundland","funders":"Genome Canada","keywords":"Medicine; Human genetics; Genetic testing; Scale (ratio); Genetics; Computational biology; Bioinformatics; Internal medicine; Gene; Biology","score_opus":0.08743992976786646,"score_gpt":0.36327491848395277,"score_spread":0.2758349887160863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069847419","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9712811,0.0003798282,0.006882354,0.0008372853,0.00013245508,0.005086637,0.0034220747,0.00015635509,0.011821807],"genre_scores_gemma":[0.9238598,0.0007034794,0.058341913,0.00036801185,0.00006162324,0.007729936,0.0048633353,0.00004581045,0.004026037],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99694985,0.0009880086,0.0005061374,0.00019992622,0.0011847988,0.00017130318],"domain_scores_gemma":[0.9930916,0.0026069167,0.0016110082,0.000456424,0.0016721061,0.00056201295],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004727151,0.0003210179,0.00048385642,0.0014563258,0.00037267004,0.0007366156,0.00081131136,0.00055118,0.0027631484],"category_scores_gemma":[0.014485095,0.00027905605,0.0009403107,0.000733092,0.00059449044,0.00080775603,0.0018209473,0.0014387901,0.00061632245],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043770057,0.0011410095,0.7827759,0.0005659689,0.0003087458,0.0006868141,0.007922401,0.002398877,0.003757551,0.0048620757,0.015358768,0.17978427],"study_design_scores_gemma":[0.00010377039,0.0008602068,0.96734995,0.00015175865,0.000055874214,0.0009401227,0.0028117315,0.0034396248,0.0010580234,0.002601478,0.020561952,0.000065472384],"about_ca_topic_score_codex":0.0015592767,"about_ca_topic_score_gemma":0.002543199,"teacher_disagreement_score":0.004727151,"about_ca_system_score_codex":0.0008893492,"about_ca_system_score_gemma":0.0012264426,"threshold_uncertainty_score":0.024999857},"labels":[],"label_agreement":null},{"id":"W2073541984","doi":"10.1186/1897-4287-10-s4-a2","title":"Microelements as risk factors for cancer of the lung and larynx","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Selenium in Biological Systems","field":"Nursing","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":"Women's College Hospital","funders":"","keywords":"Medicine; Larynx; Lung cancer; Human genetics; Internal medicine; Oncology; Surgery; Genetics; Gene","score_opus":0.08875314412219437,"score_gpt":0.45520425285709076,"score_spread":0.3664511087348964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073541984","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986492,0.0010011832,0.00007363892,0.000025132227,0.000003772749,0.0000044785206,0.000042163847,0.0000032267694,0.0001971629],"genre_scores_gemma":[0.9994462,0.00025542933,0.00008607107,0.000008109363,0.00000410451,0.0000030665287,0.000037799124,8.5303657e-7,0.00015828418],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99962616,0.00011912484,0.000034324737,0.00009286561,0.00007734845,0.000050115203],"domain_scores_gemma":[0.9994473,0.0001807826,0.00019220765,0.000043720444,0.000046267523,0.00008981416],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041592197,0.00029822247,0.00031176105,0.0010269481,0.00033936827,0.0004567539,0.0002961273,0.00042018213,0.0009565714],"category_scores_gemma":[0.0013149605,0.00027607207,0.000345417,0.0006612281,0.0003631723,0.00017615543,0.00041536667,0.00035034973,0.00009036015],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003934599,0.000020807754,0.9958962,0.00001695239,0.00010811906,0.00025630894,0.00005211535,0.00003279566,0.0012516921,0.000040983432,0.000028638837,0.0019019829],"study_design_scores_gemma":[0.000011795899,0.000096624346,0.99863786,0.000004570385,0.00006855686,0.0005024819,0.00006564107,0.00014986766,0.00026224324,0.00004316852,0.00015473738,0.0000023944674],"about_ca_topic_score_codex":0.006320998,"about_ca_topic_score_gemma":0.006158091,"teacher_disagreement_score":0.006320998,"about_ca_system_score_codex":0.000261614,"about_ca_system_score_gemma":0.00026052154,"threshold_uncertainty_score":0.012568414},"labels":[],"label_agreement":null},{"id":"W2081204032","doi":"10.1186/1897-4287-10-s3-a3","title":"Neoadjuvant chemotherapy with Cisplatin in BRCA1 mutation carriers – results of treatment","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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 College Hospital","funders":"","keywords":"Medicine; Chemotherapy; Breast cancer; Cisplatin; Axilla; Oncology; Stage (stratigraphy); Internal medicine; Mastectomy; Cancer; Surgery","score_opus":0.038950902881454724,"score_gpt":0.39990737972833756,"score_spread":0.3609564768468828,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2081204032","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99826896,0.00065827457,0.00006999305,0.000030280542,0.000007817538,0.00005049181,0.00012796895,0.00000250269,0.00078358117],"genre_scores_gemma":[0.99905103,0.00018560089,0.0001753668,0.0000357672,0.00001033164,0.00004850419,0.00019243218,0.0000018887314,0.000299057],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997503,0.00008210053,0.0000348098,0.000039484563,0.000036660247,0.000056629626],"domain_scores_gemma":[0.9996686,0.00009682966,0.0000966704,0.000019975527,0.000028654094,0.00008934729],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029089514,0.00011377067,0.00041776855,0.00021150387,0.0003004602,0.00022857814,0.00010506175,0.00019695467,0.001559137],"category_scores_gemma":[0.001004459,0.00012656301,0.00016692822,0.00022380802,0.00016208767,0.00016144432,0.00016200564,0.00016399051,0.00027738782],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.022250347,0.0010580325,0.92451894,0.00009178403,0.00006730887,0.0031001454,0.00027681643,0.000577053,0.010071938,0.00011201292,0.0006555235,0.037220046],"study_design_scores_gemma":[0.0007696145,0.013640469,0.96666723,0.0000326489,0.00016688641,0.0060526035,0.00034335937,0.00082351087,0.00590572,0.00014845422,0.0054269754,0.000022391549],"about_ca_topic_score_codex":0.0010682844,"about_ca_topic_score_gemma":0.001607831,"teacher_disagreement_score":0.001559137,"about_ca_system_score_codex":0.0003462833,"about_ca_system_score_gemma":0.00033607648,"threshold_uncertainty_score":0.0052158237},"labels":[],"label_agreement":null},{"id":"W2083459687","doi":"10.1186/1897-4287-10-s3-a4","title":"CHEK2 mutations as markers for high risk of breast cancer","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital","funders":"","keywords":"Medicine; CHEK2; Breast cancer; Human genetics; Oncology; Internal medicine; Cancer; Bioinformatics; Genetics; Mutation; Gene; Germline mutation; Biology","score_opus":0.03316930371569309,"score_gpt":0.41218287956950433,"score_spread":0.37901357585381124,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2083459687","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99407405,0.002737686,0.0004402955,0.00007297874,0.000013403663,0.000022890925,0.0003474203,0.00002165257,0.002269709],"genre_scores_gemma":[0.9989366,0.00034342357,0.00021356602,0.000018302555,0.000010013852,0.0000060299553,0.00015393752,0.0000038822127,0.00031420443],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993374,0.00027459778,0.000054725013,0.00012564585,0.00011677754,0.00009097749],"domain_scores_gemma":[0.99840933,0.00048015223,0.00053975306,0.00014187791,0.00017104803,0.00025784387],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009405925,0.00043931958,0.00043048218,0.0025901983,0.0003088332,0.0006799268,0.00041733586,0.0007122729,0.001275277],"category_scores_gemma":[0.003555831,0.00026668402,0.0004405317,0.0016406048,0.00027021806,0.0003466169,0.00065674423,0.000558911,0.00027854036],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00072830485,0.000023555704,0.99334913,0.000025246192,0.00013036249,0.00067375787,0.000056539433,0.00021312296,0.0014411432,0.00008666532,0.000098018194,0.0031742498],"study_design_scores_gemma":[0.000018020417,0.00013868952,0.9946456,0.000016704063,0.00015903106,0.0023835308,0.0000752923,0.0011617416,0.0005414549,0.00016428373,0.0006852295,0.000010451033],"about_ca_topic_score_codex":0.0034036813,"about_ca_topic_score_gemma":0.0027381333,"teacher_disagreement_score":0.0034036813,"about_ca_system_score_codex":0.00031762928,"about_ca_system_score_gemma":0.00020950461,"threshold_uncertainty_score":0.00676775},"labels":[],"label_agreement":null},{"id":"W2086308222","doi":"10.1186/1897-4287-10-s2-a86","title":"Functional polymorphisms in the TERT promoter are associated with risk of serious ovarian and breast cancer","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Nuclear Structure and Function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Health Services","funders":"","keywords":"Single-nucleotide polymorphism; Breast cancer; Genome-wide association study; Ovarian cancer; Medicine; Oncology; Locus (genetics); SNP; Allele; Genotype; Genetic association; Internal medicine; Cancer; Bioinformatics; Biology; Genetics; Gene","score_opus":0.021497707309898036,"score_gpt":0.3143048693344608,"score_spread":0.29280716202456275,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086308222","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977737,0.00064094656,0.00027798998,0.00018707574,0.000023141707,0.0000030074114,0.00022337271,0.000013326464,0.0008573566],"genre_scores_gemma":[0.9991364,0.00019557081,0.00013831817,0.000025551955,0.000018018314,0.000001623183,0.00012586989,0.0000052993496,0.0003533394],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99979,0.00006619623,0.000030299158,0.000034292803,0.000038918697,0.000040275798],"domain_scores_gemma":[0.9974287,0.00085554615,0.001048557,0.00012270815,0.00012458942,0.00041986178],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026385268,0.00025720155,0.00023911895,0.000571921,0.00026286163,0.00034728373,0.00023532061,0.00044345701,0.0033429973],"category_scores_gemma":[0.0029894488,0.00021330589,0.00035728302,0.00071736326,0.0002444835,0.00014373988,0.00019194708,0.00054898683,0.00024164231],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00085878005,0.000069765774,0.9867269,0.00003175192,0.0001617191,0.0008177553,0.000091674774,0.00015611888,0.0053781974,0.00015920246,0.00025111117,0.0052971523],"study_design_scores_gemma":[0.000028609527,0.00013571755,0.9939912,0.00001678003,0.0001389523,0.0034031824,0.00009595561,0.00049047975,0.0008324938,0.00041970107,0.00043773575,0.000009124136],"about_ca_topic_score_codex":0.0021410212,"about_ca_topic_score_gemma":0.0017697117,"teacher_disagreement_score":0.0033429973,"about_ca_system_score_codex":0.00009140147,"about_ca_system_score_gemma":0.00017530625,"threshold_uncertainty_score":0.011183381},"labels":[],"label_agreement":null},{"id":"W2095341614","doi":"10.1186/1897-4287-10-s4-a19","title":"Impact of BRCA1 mutation on survival after early onset breast cancer","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital","funders":"","keywords":"Medicine; Breast cancer; Christian ministry; Proportional hazards model; Survival analysis; Stage (stratigraphy); Medical record; Oncology; Internal medicine; Mutation; Cancer; Human genetics; Demography; Genetics; Gene","score_opus":0.041006226712933504,"score_gpt":0.43137931775468685,"score_spread":0.39037309104175333,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2095341614","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99891865,0.00049233285,0.00003649147,0.000071923736,0.000009465775,0.0000018451991,0.00023896444,0.0000021964418,0.00022822162],"genre_scores_gemma":[0.9995049,0.00009558794,0.000015044569,0.000020841313,0.000010455393,0.000002061744,0.00019747266,0.000001055167,0.00015255052],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995896,0.00016477866,0.00002664696,0.00006297973,0.00003816582,0.00011779008],"domain_scores_gemma":[0.9983955,0.0006475382,0.00046110462,0.00010324875,0.000075497424,0.00031717986],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008747994,0.0001836194,0.0003048649,0.00026388414,0.00024443245,0.00038814545,0.00024334861,0.00039739814,0.002009624],"category_scores_gemma":[0.0030095552,0.00018004877,0.0005172698,0.00039866564,0.00016258302,0.0003398165,0.00034023484,0.0005539976,0.00018029357],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012376449,0.000049874874,0.9946503,0.000011293462,0.00008734634,0.00017927332,0.000034563793,0.00014331692,0.00017980683,0.000018290848,0.00016636743,0.0032419246],"study_design_scores_gemma":[0.000020532696,0.00028956583,0.99880517,0.000008293554,0.00006455544,0.000226354,0.000041977233,0.0003022816,0.000040608124,0.00004418454,0.0001525637,0.000003822925],"about_ca_topic_score_codex":0.0027543474,"about_ca_topic_score_gemma":0.004149393,"teacher_disagreement_score":0.0027543474,"about_ca_system_score_codex":0.00022906817,"about_ca_system_score_gemma":0.00025724398,"threshold_uncertainty_score":0.0067228675},"labels":[],"label_agreement":null},{"id":"W2095741303","doi":"10.1186/1897-4287-9-8","title":"Lynch syndrome: barriers to and facilitators of screening and disease management","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","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":"University of Toronto; Memorial University of Newfoundland","funders":"University of Toronto; Genome Canada","keywords":"Lynch syndrome; Medicine; Psychosocial; Thematic analysis; Health care; Genetic counseling; Disease management; Nursing; Family medicine; Disease; Genetic testing; Qualitative research; Psychiatry; Colorectal cancer; Cancer; Pathology; Internal medicine; Genetics","score_opus":0.06730824848537992,"score_gpt":0.3896367165858455,"score_spread":0.32232846810046556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2095741303","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9895482,0.0007610938,0.00059695024,0.0053486857,0.00002605843,0.00010782033,0.000044359695,0.0000107188325,0.0035560222],"genre_scores_gemma":[0.99852645,0.00033220247,0.0005311327,0.00018849461,0.0000056398094,0.000047834666,0.00001654811,0.0000021187257,0.00034957315],"study_design_codex":"observational","study_design_gemma":"qualitative","domain_scores_codex":[0.99529946,0.0029320072,0.00016727492,0.00021799498,0.00054241903,0.0008407915],"domain_scores_gemma":[0.99177855,0.0051947087,0.0012061846,0.00012440459,0.00051195396,0.001184224],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0040917774,0.00026479748,0.00029575205,0.00046357696,0.0017462325,0.0010193348,0.00049687026,0.0005674471,0.0018395107],"category_scores_gemma":[0.010872709,0.00020809092,0.00029820655,0.0003224079,0.0013521101,0.00074442255,0.0024743138,0.0009423049,0.00007592097],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00023601388,0.0007577081,0.47760564,0.0012614379,0.00018367743,0.0023704623,0.39610928,0.0006079015,0.0027151268,0.005659301,0.004119095,0.10837438],"study_design_scores_gemma":[0.00005930077,0.00052208896,0.38578418,0.0015887283,0.0001749665,0.0018898561,0.58237606,0.0015785357,0.0010303612,0.0040064417,0.020912835,0.00007658196],"about_ca_topic_score_codex":0.009788376,"about_ca_topic_score_gemma":0.011363032,"teacher_disagreement_score":0.009788376,"about_ca_system_score_codex":0.0017083042,"about_ca_system_score_gemma":0.005820641,"threshold_uncertainty_score":0.021639705},"labels":[],"label_agreement":null},{"id":"W2099902747","doi":"10.1186/1897-4287-12-7","title":"Colorectal cancer and self-reported tooth agenesis","year":2014,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"dental development and anomalies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cancer Care Ontario","funders":"National Cancer Institute","keywords":"Hypodontia; Oligodontia; Medicine; AXIN2; Colorectal cancer; Exact test; Cancer; Anodontia; Internal medicine; Dentistry; Oncology; Genetics; Wnt signaling pathway","score_opus":0.02719669444972208,"score_gpt":0.3685011118746666,"score_spread":0.34130441742494455,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099902747","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992211,0.00021097135,0.000031408432,0.000043123593,0.0000036949407,0.0000037193065,0.00014256465,0.0000023520183,0.00034101613],"genre_scores_gemma":[0.9997688,0.00006085947,0.00003401363,0.000008882172,0.0000045162155,0.0000018572607,0.0000608586,3.7769263e-7,0.000059807808],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99962246,0.00011629222,0.000041622276,0.00008031325,0.000084298896,0.000055127886],"domain_scores_gemma":[0.9958534,0.00096951175,0.002296222,0.00015626979,0.000247344,0.0004772202],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045692158,0.00014178819,0.00018685807,0.0007469595,0.0002774963,0.00029152067,0.00016937006,0.0003376501,0.003407875],"category_scores_gemma":[0.0037077072,0.00014282095,0.00022376685,0.0007482437,0.00029917705,0.00017786026,0.00025013453,0.00031857367,0.0001766284],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000034677847,0.000011349342,0.9992944,0.000007550412,0.000010994537,0.0000838139,0.000018589777,0.0000075302205,0.00006352131,0.0000052167475,0.00002405088,0.0004382197],"study_design_scores_gemma":[0.0000025581028,0.00006592731,0.9988439,0.0000047488843,0.000013722193,0.00086086785,0.00004630936,0.00003871503,0.000041174768,0.000009998658,0.000070703034,0.000001218947],"about_ca_topic_score_codex":0.0038436318,"about_ca_topic_score_gemma":0.004558712,"teacher_disagreement_score":0.0038436318,"about_ca_system_score_codex":0.0001950092,"about_ca_system_score_gemma":0.00028420292,"threshold_uncertainty_score":0.011400461},"labels":[],"label_agreement":null},{"id":"W2101183412","doi":"10.1186/1897-4287-7-16","title":"Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models","year":2009,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Hospital for Sick Children; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Western University; Memorial University of Newfoundland; Cancer Care Ontario; Alberta Health Services","funders":"Canadian Institutes of Health Research","keywords":"Penetrance; Medicine; MSH2; Population; Cohort; Cancer; Colorectal cancer; Oncology; Internal medicine; Genetics; DNA mismatch repair; Biology; Phenotype; Environmental health; Gene","score_opus":0.12137076330534936,"score_gpt":0.4463032201250675,"score_spread":0.32493245681971816,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2101183412","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99947363,0.00005044486,0.0001441731,0.000018704051,8.043158e-7,0.000005911259,0.00020914718,0.0000048783404,0.00009234983],"genre_scores_gemma":[0.9988674,0.000051449504,0.00020533436,0.0000107475735,0.0000016362972,0.000009774192,0.00061766553,0.000005992483,0.00022989494],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99923646,0.00025679637,0.00005028507,0.0002328631,0.00011885455,0.000104783],"domain_scores_gemma":[0.99728215,0.0009354625,0.00067776506,0.00047976247,0.00034208543,0.00028285614],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002269312,0.00057756086,0.00040659442,0.0009836901,0.0008563861,0.00067155715,0.00085226377,0.00036865025,0.001181552],"category_scores_gemma":[0.0036956982,0.00040537742,0.00062429503,0.0007580742,0.0004935664,0.00029124148,0.00066027,0.00042894876,0.00021249676],"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":[0.00015716186,0.000023434508,0.9973074,0.0000038634703,0.00007753641,0.00027084633,0.00020947414,0.00020135095,0.00027745598,0.000018043878,0.000104335246,0.0013489841],"study_design_scores_gemma":[0.000017422446,0.00011058196,0.9966973,0.00000507682,0.00007169239,0.000550733,0.00023852424,0.002019257,0.00008990773,0.000013820352,0.00017784422,0.000007699583],"about_ca_topic_score_codex":0.38005283,"about_ca_topic_score_gemma":0.36119795,"teacher_disagreement_score":0.6199472,"about_ca_system_score_codex":0.002931028,"about_ca_system_score_gemma":0.0012333367,"threshold_uncertainty_score":0.7556814},"labels":[],"label_agreement":null},{"id":"W2105483955","doi":"10.1186/1897-4287-11-14","title":"Experience of BRCA1/2 mutation-negative young women from families with hereditary breast and ovarian cancer: a qualitative study","year":2013,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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; McGill Genome Centre; Jewish General Hospital","funders":"","keywords":"BRCA mutation; Medicine; Genetic testing; Breast cancer; Ovarian cancer; Family history; Mutation; Genetic counseling; Disease; Cancer; Gynecology; Genetics; Internal medicine; Gene","score_opus":0.03033653955999639,"score_gpt":0.4000635456098531,"score_spread":0.3697270060498567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2105483955","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949262,0.0008392936,0.00046400924,0.0011312541,0.00004956902,0.0000899489,0.00015352316,0.000008463188,0.0023376506],"genre_scores_gemma":[0.9957563,0.0012882123,0.00034110973,0.0006264755,0.000022990253,0.00013851865,0.000081262486,0.000016049597,0.0017290105],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.99615604,0.0026246049,0.0001246598,0.0002033763,0.00024385404,0.00064756436],"domain_scores_gemma":[0.9911578,0.0062943203,0.000746309,0.00013203434,0.0005382716,0.0011312193],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0052080434,0.0007438606,0.00093321956,0.0009772163,0.0066209766,0.003219635,0.001306396,0.0017115494,0.0027746852],"category_scores_gemma":[0.010390236,0.0007071694,0.00037876194,0.0009691585,0.005614686,0.0030332622,0.004577324,0.0024051734,0.00035807924],"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":[0.000019546424,0.000013991051,0.002206387,0.000071989234,0.000002377119,0.0010625118,0.9948596,0.00001197387,0.00032063347,0.00019530706,0.00020716742,0.0010285571],"study_design_scores_gemma":[0.0000015450157,0.000030683335,0.0010111157,0.000075810145,0.0000023928942,0.00034625072,0.9962226,0.00001869103,0.00006905812,0.00005021958,0.0021666812,0.0000048921156],"about_ca_topic_score_codex":0.011574941,"about_ca_topic_score_gemma":0.019829292,"teacher_disagreement_score":0.011574941,"about_ca_system_score_codex":0.0032736813,"about_ca_system_score_gemma":0.002965361,"threshold_uncertainty_score":0.027543128},"labels":[],"label_agreement":null},{"id":"W2111916911","doi":"10.1186/1897-4287-10-s2-a21","title":"A study of cancer risks in relatives of patients with serrated polyposis","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Colorectal cancer; Internal medicine; Cancer; Hyperplastic Polyp; Gastroenterology; Oncology; Colonoscopy","score_opus":0.13462104317389118,"score_gpt":0.47959108338335066,"score_spread":0.3449700402094595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111916911","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992803,0.0002961105,0.00008955464,0.000011658321,0.0000027077353,0.000002826619,0.00010176276,0.0000019073966,0.0002132383],"genre_scores_gemma":[0.9995684,0.00012789073,0.00007845791,0.000006000178,0.000004261403,0.0000025225713,0.00009502102,9.462088e-7,0.000116453724],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996463,0.00011102418,0.00003201747,0.00010711757,0.00006084279,0.000042639727],"domain_scores_gemma":[0.99905175,0.00021840945,0.00036695335,0.00012484298,0.00009301622,0.00014508388],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004972341,0.00022644042,0.00036787038,0.0007557772,0.0005571433,0.00032198464,0.00015929315,0.00033183148,0.0009778203],"category_scores_gemma":[0.002565972,0.00025991743,0.000472968,0.00079830113,0.0002016932,0.00028686805,0.0002655552,0.00029910944,0.00021293444],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00020609904,0.000013444447,0.9975363,0.000010814153,0.000044464843,0.00037147323,0.0002018061,0.000031380485,0.00040480008,0.000014946332,0.00003653681,0.0011279443],"study_design_scores_gemma":[0.0000069871094,0.00019242994,0.99697113,0.000005406206,0.00004850519,0.0019928233,0.0002478893,0.00009768582,0.00011552102,0.000022665927,0.00029445023,0.000004360703],"about_ca_topic_score_codex":0.006144393,"about_ca_topic_score_gemma":0.0050970246,"teacher_disagreement_score":0.006144393,"about_ca_system_score_codex":0.00026954338,"about_ca_system_score_gemma":0.00020444588,"threshold_uncertainty_score":0.012217283},"labels":[],"label_agreement":null},{"id":"W2114912392","doi":"10.1186/1897-4287-11-17","title":"Optimizing recruitment to a prostate cancer surveillance program among male BRCA1 mutation carriers: invitation by mail or by telephone","year":2013,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Coalition for Research in Women's Health; University of Toronto","funders":"","keywords":"Medicine; Phone; Family medicine; Public health; Telephone call; Telecommunications; Nursing","score_opus":0.04925684938190949,"score_gpt":0.4094605812287168,"score_spread":0.3602037318468073,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114912392","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9909161,0.000773007,0.0023874491,0.0009705805,0.000039069135,0.0014019505,0.00004373158,0.00004452365,0.0034237038],"genre_scores_gemma":[0.9888581,0.00048387825,0.0076443306,0.0005094558,0.00011231118,0.0011617353,0.000097598866,0.000009134017,0.001123444],"study_design_codex":"design_other","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.9795669,0.018046498,0.00043059175,0.00025248269,0.0008756056,0.00082807196],"domain_scores_gemma":[0.9894399,0.0074735205,0.0015291246,0.00039518563,0.00037733896,0.00078496913],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.013250524,0.00049988774,0.0005485459,0.0007122403,0.00035818576,0.000852708,0.0005328963,0.001421778,0.0037260447],"category_scores_gemma":[0.021713654,0.0001939818,0.0008246063,0.00040772118,0.00028786832,0.0005983813,0.0010625416,0.00045991398,0.0006866522],"study_design_candidate":"nonrandomized_trial","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.047039095,0.018255522,0.23721972,0.0013030051,0.0005757092,0.0005743859,0.0016389046,0.0134000275,0.008674573,0.0006666024,0.0020096735,0.6686429],"study_design_scores_gemma":[0.012739841,0.12314106,0.807856,0.0006633347,0.0017673344,0.0014434595,0.0024553768,0.027805733,0.0110557685,0.0012764516,0.009602129,0.0001934677],"about_ca_topic_score_codex":0.0010141714,"about_ca_topic_score_gemma":0.0020957582,"teacher_disagreement_score":0.013250524,"about_ca_system_score_codex":0.0006638745,"about_ca_system_score_gemma":0.0018821493,"threshold_uncertainty_score":0.07007635},"labels":[],"label_agreement":null},{"id":"W2118803325","doi":"10.1186/1897-4287-4-4-167","title":"Regarding the Use of Tamoxifen Post-Oophorectomy to Prevent Hereditary Breast Cancer","year":2006,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Coalition for Research in Women's Health","funders":"","keywords":"Medicine; Tamoxifen; Oophorectomy; Breast cancer; Gynecology; Human genetics; Oncology; Cancer; General surgery; Bioinformatics; Internal medicine; Hysterectomy; Surgery","score_opus":0.04838948672019777,"score_gpt":0.38456926680010195,"score_spread":0.3361797800799042,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118803325","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.014306127,0.31143597,0.0026830935,0.6132831,0.013477829,0.000115037285,0.0005061901,0.000113691756,0.04407891],"genre_scores_gemma":[0.11749961,0.35823756,0.00604085,0.42235428,0.077197865,0.00020603844,0.00043939945,0.000058647074,0.017965775],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9981364,0.00059881544,0.00026788452,0.00016366849,0.0007319893,0.00010128978],"domain_scores_gemma":[0.9929016,0.0046650134,0.0009727493,0.00017597289,0.00089643314,0.00038813465],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0029126212,0.00030181272,0.0010300988,0.0006729243,0.0007463088,0.000924091,0.0013669495,0.008085726,0.005296348],"category_scores_gemma":[0.0101345,0.00017421761,0.0008428604,0.0006758728,0.000929892,0.0008406935,0.00040801824,0.0042836866,0.0019249473],"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":[0.0023781247,0.00051365804,0.01129061,0.0035732104,0.00070396153,0.006949067,0.00056251435,0.0011045436,0.0043617445,0.010517519,0.19388591,0.7641592],"study_design_scores_gemma":[0.0004639875,0.0013779089,0.015851855,0.00458211,0.0010904421,0.008836178,0.0007024059,0.00049897656,0.0016223213,0.007925493,0.9569494,0.00009901019],"about_ca_topic_score_codex":0.002585332,"about_ca_topic_score_gemma":0.008175814,"teacher_disagreement_score":0.008085726,"about_ca_system_score_codex":0.0006703515,"about_ca_system_score_gemma":0.00129961,"threshold_uncertainty_score":0.017718077},"labels":[],"label_agreement":null},{"id":"W2123694233","doi":"10.1186/1897-4287-10-s2-a74","title":"Metachronous colon cancer risk following surgery for first primary rectal cancer in Lynch syndrome","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Cancer Care Ontario; Mount Sinai Hospital","funders":"","keywords":"Medicine; Colorectal cancer; Lynch syndrome; Stoma (medicine); Abdominoperineal resection; Rectum; Colectomy; Colorectal surgery; Cancer; Primary cancer; General surgery; Internal medicine; Surgery; Oncology; Abdominal surgery; DNA mismatch repair","score_opus":0.07729300608927825,"score_gpt":0.4220719834530834,"score_spread":0.34477897736380514,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2123694233","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992501,0.00033113768,0.000088849614,0.000016084543,0.0000031051159,0.0000036252732,0.000164786,0.0000037902967,0.0001385449],"genre_scores_gemma":[0.999549,0.000144615,0.000071271825,0.000004039372,0.0000063858683,0.0000020752334,0.00012170942,0.000001334593,0.000099447905],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997136,0.00006123902,0.000024267796,0.00009346861,0.000042621785,0.000064657674],"domain_scores_gemma":[0.9985561,0.0002240785,0.00076772546,0.00012522392,0.000073110125,0.00025381736],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039936707,0.00027956683,0.00029051848,0.0009568334,0.00025820083,0.00047725043,0.00028688062,0.000419888,0.0018187732],"category_scores_gemma":[0.002142091,0.0002885005,0.0005250563,0.0006233292,0.00019117647,0.00032348244,0.0004700652,0.0004967206,0.00022900746],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016522125,0.000008854824,0.99847454,0.0000053094427,0.000027627331,0.00017787358,0.00003208726,0.00003923342,0.00022558056,0.000006433298,0.000028663351,0.00080858264],"study_design_scores_gemma":[0.0000029061043,0.00009670026,0.99868697,0.0000032180408,0.000019965317,0.0008694438,0.000042039363,0.00015814614,0.00005285696,0.000011216341,0.000053710228,0.0000028225036],"about_ca_topic_score_codex":0.007033755,"about_ca_topic_score_gemma":0.008511295,"teacher_disagreement_score":0.007033755,"about_ca_system_score_codex":0.00025032373,"about_ca_system_score_gemma":0.00023137384,"threshold_uncertainty_score":0.013985634},"labels":[],"label_agreement":null},{"id":"W2127767332","doi":"10.1186/1897-4287-10-3","title":"The R337H mutation in TP53 and breast cancer in Brazil","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Cancer-related Molecular Pathways","field":"Medicine","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":"Women's College Hospital","funders":"","keywords":"Medicine; Breast cancer; Germline mutation; Li–Fraumeni syndrome; Penetrance; Oncology; Mutation; Cancer; Population; Incidence (geometry); Internal medicine; Family history; Mutation frequency; Genetics; Environmental health; Biology; Gene","score_opus":0.042419182725410225,"score_gpt":0.4333913986520805,"score_spread":0.39097221592667025,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2127767332","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982065,0.0007135209,0.00006884028,0.00011838763,0.0000022646245,0.000011135758,0.00006241447,0.0000033858562,0.00081354176],"genre_scores_gemma":[0.9994936,0.00032408547,0.00007228119,0.000019034558,0.0000017601731,0.0000026339849,0.00003545592,8.960041e-7,0.00005025663],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997806,0.000054279208,0.00002041376,0.00004551376,0.000052984476,0.000046222653],"domain_scores_gemma":[0.9993881,0.00016996465,0.00025491026,0.000037477723,0.0000782686,0.00007123786],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035549013,0.00014631376,0.00016877308,0.001115757,0.00031969725,0.0002722867,0.00022240046,0.0002827583,0.0012121456],"category_scores_gemma":[0.0019320126,0.00021106994,0.00015462235,0.0007057899,0.00040063536,0.00010543249,0.00031623364,0.00018114984,0.00013079187],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006608695,0.00003193124,0.9889052,0.00003820419,0.000020747362,0.0019156999,0.00062507216,0.00003722901,0.0030594135,0.00013400009,0.00010421029,0.0050621745],"study_design_scores_gemma":[0.000022198907,0.0001296621,0.9849886,0.00008604029,0.00005655708,0.011059166,0.0010022267,0.00032462872,0.0009040429,0.0002576156,0.0011610632,0.00000824017],"about_ca_topic_score_codex":0.024859795,"about_ca_topic_score_gemma":0.023521338,"teacher_disagreement_score":0.024859795,"about_ca_system_score_codex":0.00049032614,"about_ca_system_score_gemma":0.00045337304,"threshold_uncertainty_score":0.04943019},"labels":[],"label_agreement":null},{"id":"W2132603400","doi":"10.1186/1897-4287-7-14","title":"Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario","year":2009,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":58,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Public Health Ontario; University of Toronto; Mount Sinai Hospital; Cancer Care Ontario; Lunenfeld-Tanenbaum Research Institute","funders":"Canadian Institutes of Health Research; National Institutes of Health; National Cancer Institute; Cancer Care Ontario","keywords":"MLH1; Lynch syndrome; Medicine; MSH2; Colorectal cancer; Penetrance; Population; Cancer registry; Oncology; Cancer; DNA mismatch repair; Internal medicine; Gynecology; Genetics; Biology; Environmental health; Gene","score_opus":0.0689670318470987,"score_gpt":0.4119250256052817,"score_spread":0.34295799375818303,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2132603400","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976921,0.00009213002,0.00008547378,0.00004308262,0.0000014674774,0.000012128785,0.0014048668,0.0000065084428,0.000662255],"genre_scores_gemma":[0.9987526,0.0000813347,0.00006366342,0.000007817195,0.0000010054794,0.0000072301787,0.0007932658,0.0000024447802,0.00029073627],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994661,0.000058518803,0.000031394808,0.00011623301,0.00018521659,0.00014258834],"domain_scores_gemma":[0.9987827,0.00014090815,0.00049729156,0.00009854099,0.00028826736,0.00019233575],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045743928,0.00018377985,0.00021518196,0.00078536576,0.0008500629,0.000363151,0.0004585926,0.00019035306,0.0018867223],"category_scores_gemma":[0.001744315,0.00025977768,0.0002624064,0.0012629031,0.00031656213,0.00014674284,0.00042123505,0.00015443802,0.00016136568],"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":[0.000027968965,0.0000037847294,0.99824214,0.0000092097725,0.000013388377,0.00011716531,0.0002945019,0.00004147132,0.0002867739,0.000015850175,0.00021754757,0.000730187],"study_design_scores_gemma":[0.0000025142106,0.00000855708,0.9994272,0.000002901377,0.000007720303,0.000095469186,0.00016124296,0.00006435148,0.000035683104,0.000004709247,0.00018808994,0.0000017054266],"about_ca_topic_score_codex":0.915378,"about_ca_topic_score_gemma":0.93327117,"teacher_disagreement_score":0.084622025,"about_ca_system_score_codex":0.0051598675,"about_ca_system_score_gemma":0.0050979485,"threshold_uncertainty_score":0.1702407},"labels":[],"label_agreement":null},{"id":"W2132684917","doi":"10.1186/1897-4287-12-11","title":"Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Medellín, Colombia","year":2014,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital","funders":"National Cancer Institute; NIH Office of the Director; National Institutes of Health","keywords":"Breast cancer; Medicine; Family history; Mutation; Cancer; BRCA mutation; Oncology; Genetic testing; Ovarian cancer; Genetic counseling; Internal medicine; Genetics; Gene; Gynecology; Biology","score_opus":0.019865963021720993,"score_gpt":0.35950848591125373,"score_spread":0.3396425228895327,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2132684917","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976927,0.00045047584,0.000028309794,0.00006032256,0.0000065041772,0.00002517827,0.00087447936,0.000005859985,0.0008560762],"genre_scores_gemma":[0.99840266,0.0003269093,0.000057318724,0.00005937845,0.0000069767784,0.000016312248,0.0008952516,0.0000027921767,0.00023226596],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974793,0.000041557018,0.000029735565,0.0000694662,0.00005957544,0.000051711984],"domain_scores_gemma":[0.9994789,0.00008048556,0.00020566043,0.000028194709,0.00007785002,0.00012903956],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018457415,0.00036886064,0.0003345451,0.0015549554,0.0005955966,0.00052006746,0.00049904006,0.00038964156,0.002408127],"category_scores_gemma":[0.0010646218,0.00024857518,0.00015495386,0.0007805441,0.000277072,0.00022907343,0.00035976237,0.00020821318,0.00028825446],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000051594583,0.00003049142,0.9962442,0.000038166687,0.000013847626,0.0004063274,0.00028074946,0.000017710134,0.0005797315,0.00001002813,0.00036339546,0.001963718],"study_design_scores_gemma":[0.0000059014706,0.000021715443,0.9982821,0.000013284312,0.0000067101,0.0008018541,0.00045305252,0.000031643758,0.00005436853,0.000004261398,0.00032113903,0.0000039607676],"about_ca_topic_score_codex":0.07586461,"about_ca_topic_score_gemma":0.116034575,"teacher_disagreement_score":0.07586461,"about_ca_system_score_codex":0.0012131077,"about_ca_system_score_gemma":0.00041132176,"threshold_uncertainty_score":0.15084606},"labels":[],"label_agreement":null},{"id":"W2137077741","doi":"10.1186/1897-4287-2-2-51","title":"Genetic Screening for Familial Gastric Cancer","year":2004,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Helicobacter pylori-related gastroenterology studies","field":"Medicine","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 Cancer Agency","funders":"","keywords":"CDH1; Cancer; Medicine; Penetrance; Germline mutation; Germline; Missense mutation; Genetics; Cancer research; Mutation; Gene; Biology; Cadherin; Internal medicine; Cell; Phenotype","score_opus":0.09598453469824889,"score_gpt":0.4303219130084784,"score_spread":0.33433737831022947,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2137077741","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93158746,0.028364303,0.0034481063,0.00298557,0.00026379406,0.00018971694,0.0017494161,0.00025334035,0.031158311],"genre_scores_gemma":[0.980327,0.011143254,0.0025489766,0.0005609005,0.00015497221,0.000049288807,0.0012175543,0.00001832628,0.003979767],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976164,0.000053595093,0.000018490975,0.000050405197,0.00006753057,0.00004829277],"domain_scores_gemma":[0.9997588,0.00006642314,0.00004604008,0.000014759551,0.000056148372,0.00005785055],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030675268,0.0004925336,0.00046712157,0.0017124842,0.0008117932,0.00027731963,0.00026588223,0.00071114727,0.0046698255],"category_scores_gemma":[0.001338117,0.00018022912,0.00033165183,0.0011196897,0.00034201393,0.00023759382,0.00032170603,0.00037875702,0.00060380896],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00052329927,0.00012816658,0.78484356,0.00055018015,0.00020031055,0.10844976,0.001136745,0.00034012448,0.010357909,0.0015078912,0.014911406,0.077050686],"study_design_scores_gemma":[0.000047198664,0.00048069505,0.71022254,0.00055131357,0.0003476373,0.25515297,0.0007310617,0.00080810185,0.00411787,0.0017050817,0.025789727,0.00004572719],"about_ca_topic_score_codex":0.004206546,"about_ca_topic_score_gemma":0.0035999136,"teacher_disagreement_score":0.0046698255,"about_ca_system_score_codex":0.0003182801,"about_ca_system_score_gemma":0.0003246967,"threshold_uncertainty_score":0.015622079},"labels":[],"label_agreement":null},{"id":"W2142949382","doi":"10.1186/1897-4287-9-s1-p14","title":"When is a desmoid not a desmoid? Endometrial cancer as an extracolonic manifestation of MYH Associated Polyposis (MAP)","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Soft tissue tumor case studies","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Medicine; MUTYH; Human genetics; Endometrial cancer; Cancer; Oncology; Internal medicine; Mutation; Genetics; Gene; Germline mutation","score_opus":0.18108779340942197,"score_gpt":0.46509228501904215,"score_spread":0.28400449160962016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142949382","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98012805,0.005562619,0.00081691693,0.0018694511,0.00012026908,0.00007788949,0.00011881725,0.000051598792,0.011254431],"genre_scores_gemma":[0.996182,0.0014912796,0.00067516527,0.00045277213,0.00025398398,0.000008950993,0.00005510291,0.000007465879,0.0008732527],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996551,0.000052047264,0.000043927408,0.0000576859,0.000069219444,0.00012196101],"domain_scores_gemma":[0.99943155,0.00018518935,0.00016613536,0.00002804564,0.00003902067,0.00015000266],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003501482,0.00055788754,0.0004449916,0.001582104,0.00084356614,0.0010904699,0.0004416849,0.002027477,0.0026006685],"category_scores_gemma":[0.002477449,0.00048038858,0.00027598522,0.00096333574,0.0010477109,0.0011791195,0.0005566428,0.0007156006,0.0005566796],"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":[0.00022626268,0.00002760619,0.115937546,0.000094551506,0.000015686119,0.8735327,0.00038760834,0.00008626889,0.0019529149,0.00026668957,0.0005642024,0.006907925],"study_design_scores_gemma":[0.000015990707,0.000099810204,0.044307254,0.00006977677,0.000029250572,0.9519999,0.0005852425,0.0002740955,0.00068517216,0.0003808885,0.0015417491,0.000010931809],"about_ca_topic_score_codex":0.00095668255,"about_ca_topic_score_gemma":0.0014744498,"teacher_disagreement_score":0.0026006685,"about_ca_system_score_codex":0.000461172,"about_ca_system_score_gemma":0.000265971,"threshold_uncertainty_score":0.008700132},"labels":[],"label_agreement":null},{"id":"W2145834032","doi":"10.1186/1897-4287-2-1-5","title":"The Prevention of Hereditary Breast and Ovarian Cancer: A Personal View","year":2004,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Coalition for Research in Women's Health","funders":"","keywords":"Medicine; Oophorectomy; Ovarian cancer; Prophylactic Mastectomy; Breast cancer; Tamoxifen; Gynecology; Prophylactic Surgery; Mastectomy; Oncology; Mammography; Obstetrics; Cancer; Internal medicine; Hysterectomy; Surgery","score_opus":0.03536854494760066,"score_gpt":0.3965387940786671,"score_spread":0.36117024913106643,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145834032","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011286933,0.12281737,0.00084186584,0.8054701,0.032183606,0.000013065274,0.00005677272,0.000097034324,0.037391536],"genre_scores_gemma":[0.014919289,0.22212994,0.0025024877,0.5327518,0.116174355,0.000046014313,0.00006050285,0.000054331835,0.111361235],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9988133,0.00029085015,0.0000895659,0.00017023276,0.0005257889,0.000110295456],"domain_scores_gemma":[0.9963702,0.0008050211,0.00014109696,0.00017979683,0.00084630126,0.0016576041],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002108902,0.0007192588,0.0010053086,0.0008599959,0.0017641229,0.003498207,0.00097469415,0.008223577,0.022403657],"category_scores_gemma":[0.0036632386,0.00031546547,0.000529458,0.0006397609,0.0024444342,0.004529014,0.0018221847,0.010991929,0.009510984],"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":[0.00005310738,0.0001702515,0.0021219556,0.00032912713,0.00003026285,0.0007179267,0.0002808226,0.00013350787,0.0006923157,0.0071288487,0.84705436,0.14128754],"study_design_scores_gemma":[0.000020129803,0.00010071354,0.0014550447,0.00044675043,0.000025265386,0.0025989888,0.0002767443,0.00005920028,0.000095372394,0.0053056167,0.9895962,0.000020068235],"about_ca_topic_score_codex":0.0011490717,"about_ca_topic_score_gemma":0.004040011,"teacher_disagreement_score":0.022403657,"about_ca_system_score_codex":0.00082832895,"about_ca_system_score_gemma":0.0015752907,"threshold_uncertainty_score":0.074947715},"labels":[],"label_agreement":null},{"id":"W2147221503","doi":"10.1186/s13053-015-0031-4","title":"Decisions about prophylactic gynecologic surgery: a qualitative study of the experience of female Lynch syndrome mutation carriers","year":2015,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","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":"St. John’s Health Sciences Centre; Memorial University of Newfoundland; Newfoundland and Labrador Centre for Applied Health Research; Health Sciences Centre","funders":"","keywords":"Prophylactic Surgery; Medicine; Lynch syndrome; Worry; Hysterectomy; Psychosocial; Gynecology; BRCA mutation; Gynecologic oncology; Cancer; General surgery; Surgery; Internal medicine; Ovarian cancer; Psychiatry; Anxiety","score_opus":0.20576355215752412,"score_gpt":0.49559034392989537,"score_spread":0.28982679177237125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2147221503","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99481225,0.0005914464,0.00041900112,0.0019816756,0.00004662119,0.00007749584,0.0000733292,0.00000662427,0.0019915225],"genre_scores_gemma":[0.9972191,0.00073153805,0.00026370992,0.000640539,0.000018509747,0.00008194939,0.000034365945,0.000009403893,0.0010009625],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.9943644,0.0042492487,0.00015413313,0.00019414787,0.0003148021,0.00072330324],"domain_scores_gemma":[0.98165774,0.014393251,0.0011782704,0.00018109404,0.0007842913,0.0018053716],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.007829886,0.00053028075,0.00074035925,0.0009787309,0.005587434,0.0026965572,0.0011895598,0.0014478196,0.002980704],"category_scores_gemma":[0.01678099,0.00061393715,0.00028624732,0.0007868103,0.0062014856,0.0025483076,0.0031238014,0.0023371843,0.00024693864],"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":[0.000044108172,0.000041402534,0.00507118,0.00010333192,0.000004398801,0.00083344884,0.99032015,0.000018210523,0.0004923317,0.00024192683,0.00036117653,0.0024683678],"study_design_scores_gemma":[0.0000035649834,0.000052200085,0.0013320767,0.00006967094,0.0000024939936,0.00017707713,0.9960031,0.000030337143,0.00007297999,0.00005384379,0.0021956265,0.000006985599],"about_ca_topic_score_codex":0.012559045,"about_ca_topic_score_gemma":0.0179413,"teacher_disagreement_score":0.012559045,"about_ca_system_score_codex":0.0027131916,"about_ca_system_score_gemma":0.0038032837,"threshold_uncertainty_score":0.041408896},"labels":[],"label_agreement":null},{"id":"W2149983798","doi":"10.1186/1897-4287-3-2-53","title":"Effect of Prior Bilateral Oophorectomy on the Presentation of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers","year":2005,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Health Sciences Centre; BC Cancer Agency; Centre Hospitalier de l’Université de Montréal; McGill University; Coalition for Research in Women's Health; University of Toronto; Sunnybrook Health Science Centre","funders":"","keywords":"Medicine; Oophorectomy; Breast cancer; Ovarian cancer; Gynecology; Cancer; Presentation (obstetrics); Medical record; Family history; Oncology; Internal medicine; Hysterectomy; Obstetrics; Surgery","score_opus":0.019887525505376136,"score_gpt":0.39394378579413536,"score_spread":0.3740562602887592,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149983798","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99897397,0.0006255978,0.0000205771,0.00006743298,0.000010364958,0.0000034807606,0.000034276447,0.0000015418173,0.00026266745],"genre_scores_gemma":[0.99968374,0.0001345628,0.000029207122,0.00001796506,0.000013373564,0.0000023238927,0.000040364605,0.0000014844034,0.00007700859],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993106,0.00026495775,0.000046447305,0.000115785915,0.00014065106,0.000121528356],"domain_scores_gemma":[0.99531084,0.0020094893,0.0013305887,0.00012941372,0.00010463564,0.0011150975],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00067161955,0.00024984492,0.00034376624,0.0006021084,0.00026263765,0.00042980522,0.00023219263,0.00049481494,0.0028583927],"category_scores_gemma":[0.008166022,0.00016985215,0.00049449125,0.00037993796,0.00041880726,0.00033413235,0.00045282664,0.00042915487,0.00018217455],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021249917,0.00011152194,0.99073786,0.000025448737,0.00009389486,0.00037888053,0.00006961197,0.000056688874,0.00080109475,0.0000128196,0.00007746367,0.005509815],"study_design_scores_gemma":[0.000020015646,0.0006092142,0.9979406,0.000011606705,0.000040534258,0.0009626078,0.00013893918,0.00009139189,0.0000676905,0.000015521091,0.00009844843,0.000003315718],"about_ca_topic_score_codex":0.002985136,"about_ca_topic_score_gemma":0.004417552,"teacher_disagreement_score":0.002985136,"about_ca_system_score_codex":0.00033634205,"about_ca_system_score_gemma":0.00039021755,"threshold_uncertainty_score":0.009562314},"labels":[],"label_agreement":null},{"id":"W2153678470","doi":"10.1186/s13053-015-0040-3","title":"The frequency of BRCA1 founder mutation c.5266dupC (5382insC) in breast cancer patients from Ukraine","year":2015,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"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":"Breast cancer; Medicine; Mutation; Founder effect; Genetics; Human genetics; Cancer; Gene; Oncology; Internal medicine; Biology; Genotype; Haplotype","score_opus":0.04803539259013766,"score_gpt":0.3962391227471437,"score_spread":0.348203730157006,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153678470","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996697,0.0000989595,0.000016010354,0.000017092381,0.0000017689619,0.0000010773939,0.000045367793,0.0000018111085,0.00014820317],"genre_scores_gemma":[0.9997689,0.000070806585,0.000010684558,0.000012128594,0.0000022856925,8.695821e-7,0.000051784282,8.105528e-7,0.00008178042],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998517,0.000022523996,0.000019516669,0.000046278077,0.00002951111,0.00003037104],"domain_scores_gemma":[0.9996861,0.000060149767,0.00013277946,0.000024131752,0.000038893944,0.000057954134],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001276917,0.000106824285,0.00022072376,0.00077866536,0.00044259024,0.00030795322,0.00016199483,0.00029232973,0.0011830949],"category_scores_gemma":[0.000648457,0.00018345087,0.00013223602,0.00049467466,0.00026864235,0.000102692764,0.0001809606,0.00024148985,0.0001561203],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000056212746,0.000017584822,0.99335265,0.00001245959,0.000018642622,0.0010416248,0.0005994448,0.00005244843,0.0023898939,0.000022740825,0.0001184478,0.0023179003],"study_design_scores_gemma":[0.000002576308,0.000048364895,0.9954071,0.000006629825,0.000015838596,0.0033054813,0.00041200413,0.00008160779,0.00039853752,0.000021315276,0.0002969614,0.000003538588],"about_ca_topic_score_codex":0.013244467,"about_ca_topic_score_gemma":0.010843849,"teacher_disagreement_score":0.013244467,"about_ca_system_score_codex":0.00029325622,"about_ca_system_score_gemma":0.00024943316,"threshold_uncertainty_score":0.026334763},"labels":[],"label_agreement":null},{"id":"W2155566817","doi":"10.1186/1897-4287-12-19","title":"Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada","year":2014,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":true,"ca_institutions":"Jewish General Hospital; McGill University Health Centre; McGill University; Children's Hospital of Eastern Ontario","funders":"European Commission; Susan G. Komen; Cancer Research Society","keywords":"PALB2; Breast cancer; Proband; Medicine; Ovarian cancer; Penetrance; Genetic counseling; Family history; Missense mutation; Genetics; Oncology; Mutation; Germline mutation; Internal medicine; Cancer; Gynecology; Biology; Gene; Phenotype","score_opus":0.02504093562990263,"score_gpt":0.3491864492446,"score_spread":0.3241455136146974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2155566817","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99672145,0.0002695537,0.00009279555,0.000075217526,0.0000042143156,0.00003227968,0.0005439825,0.0000064359265,0.002254134],"genre_scores_gemma":[0.99809057,0.00021467473,0.0003041199,0.00007185548,0.0000022380002,0.000013564897,0.00043146854,0.0000064129595,0.00086513424],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99955267,0.000020350024,0.000028469914,0.00009222361,0.00018617426,0.00012017014],"domain_scores_gemma":[0.9995832,0.000046239402,0.000070689464,0.000013980685,0.00015571028,0.00013018593],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020132198,0.00048556412,0.00022097454,0.0018121368,0.0030637167,0.00050009246,0.00080281426,0.00038817892,0.0022340456],"category_scores_gemma":[0.0008403059,0.00026289772,0.0002699971,0.002217949,0.00071490224,0.000100645644,0.0006344845,0.0002738501,0.00018106037],"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":[0.00018510592,0.00007402878,0.9454937,0.00007807306,0.0000678013,0.023296269,0.006672446,0.0002663899,0.013300405,0.0002554569,0.0012614656,0.009048869],"study_design_scores_gemma":[0.000021151247,0.000040972587,0.9867339,0.000033867127,0.00005168919,0.007270059,0.0023577623,0.0002767833,0.00094720884,0.00003958834,0.0022136054,0.000013309464],"about_ca_topic_score_codex":0.9576897,"about_ca_topic_score_gemma":0.9747702,"teacher_disagreement_score":0.042310297,"about_ca_system_score_codex":0.009679002,"about_ca_system_score_gemma":0.009006203,"threshold_uncertainty_score":0.08511889},"labels":[],"label_agreement":null},{"id":"W2159930556","doi":"10.1186/1897-4287-9-10","title":"Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Greece","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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 College Hospital","funders":"","keywords":"Breast cancer; Family history; Medicine; Ovarian cancer; BRCA mutation; Mutation; BRCA2 Protein; Exon; Genetic counseling; Oncology; Cancer; Genetic testing; Internal medicine; Germline mutation; Genetics; Gene; Biology","score_opus":0.03838164162584651,"score_gpt":0.3633994320891377,"score_spread":0.3250177904632912,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2159930556","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995802,0.00007231993,0.000015405909,0.000012471208,0.0000015642719,0.000007133828,0.00009831074,0.0000017661285,0.00021096629],"genre_scores_gemma":[0.99946374,0.00009060048,0.00003756666,0.00003364873,0.000003898226,0.00000915069,0.00025651473,0.0000016237351,0.00010328217],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99958795,0.0000798511,0.000060759165,0.00012323371,0.00009096881,0.000057302386],"domain_scores_gemma":[0.99948406,0.00012261953,0.00017106076,0.000039241564,0.00006188195,0.00012116486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002626384,0.00027376632,0.00035697897,0.0012710934,0.00026649135,0.00039521276,0.00039226233,0.00059927994,0.0012134925],"category_scores_gemma":[0.0012089618,0.00023847257,0.0001991928,0.00056929037,0.0003097597,0.00022465957,0.00036942444,0.00018966912,0.0003161206],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00004390035,0.000037451246,0.9964948,0.000015258323,0.000029139868,0.00073010207,0.00020040658,0.000039564926,0.00075336994,0.000009983965,0.00009084287,0.0015550544],"study_design_scores_gemma":[0.000012753672,0.00012256324,0.994989,0.00000950779,0.00001729272,0.003808637,0.0004517359,0.00009740109,0.00019145687,0.000025135672,0.00026881995,0.00000576598],"about_ca_topic_score_codex":0.0034290792,"about_ca_topic_score_gemma":0.0028540837,"teacher_disagreement_score":0.0034290792,"about_ca_system_score_codex":0.00042518627,"about_ca_system_score_gemma":0.0002842048,"threshold_uncertainty_score":0.006818235},"labels":[],"label_agreement":null},{"id":"W2166679122","doi":"10.1186/1897-4287-9-s2-a4","title":"Neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients","year":2011,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital; University of Toronto; Sunnybrook Health Science Centre","funders":"","keywords":"Medicine; Breast cancer; Oncology; Neoadjuvant therapy; Cisplatin; Chemotherapy; Internal medicine; Pathological; Complete response; Disease; Induction chemotherapy; Adjuvant; Cancer","score_opus":0.04110243064764945,"score_gpt":0.37083522708149586,"score_spread":0.3297327964338464,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2166679122","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99823606,0.0012721651,0.00007002105,0.00007876043,0.000008230249,0.000022465267,0.000022842034,0.0000030787292,0.0002864551],"genre_scores_gemma":[0.999106,0.00048212594,0.00013472715,0.000059653983,0.000011273939,0.000026201298,0.000053223983,8.661518e-7,0.00012588345],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997831,0.00012157097,0.000020507121,0.000017796805,0.000034868426,0.000022104994],"domain_scores_gemma":[0.99962986,0.00012451845,0.0001123,0.000016178517,0.000021969758,0.0000952735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002738394,0.000095008436,0.00034211972,0.00018108507,0.00020844619,0.00018607489,0.00008613295,0.000216787,0.00043383637],"category_scores_gemma":[0.0014684693,0.00014497542,0.00014214801,0.00017373504,0.00013241949,0.00015286349,0.00012059271,0.00020563965,0.000099982164],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.016331496,0.0009897518,0.868845,0.000171416,0.0001408629,0.0028505241,0.0004668232,0.0012575453,0.021232845,0.000086786014,0.0008260124,0.08680101],"study_design_scores_gemma":[0.00066990004,0.03289949,0.943811,0.00007942357,0.00016105828,0.007660004,0.00035452377,0.002150438,0.006741501,0.00013932135,0.0053057726,0.000027586533],"about_ca_topic_score_codex":0.00033169074,"about_ca_topic_score_gemma":0.0008014334,"teacher_disagreement_score":0.00043383637,"about_ca_system_score_codex":0.00020255716,"about_ca_system_score_gemma":0.00023968867,"threshold_uncertainty_score":0.0014696121},"labels":[],"label_agreement":null},{"id":"W2260334960","doi":"10.1186/s13053-016-0046-5","title":"Recurrent mutations of BRCA1, BRCA2 and PALB2 in the population of breast and ovarian cancer patients in Southern Poland","year":2016,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":44,"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 College Hospital","funders":"","keywords":"PALB2; Ovarian cancer; Breast cancer; Founder effect; Mutation; Medicine; Genetics; Population; BRCA2 Protein; Mutation frequency; Cancer; Oncology; Germline mutation; Gene; Internal medicine; Biology; Genotype; Haplotype","score_opus":0.02810701771477897,"score_gpt":0.3734757585455711,"score_spread":0.3453687408307921,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2260334960","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997645,0.0000658671,0.000023886054,0.000011702253,9.473515e-7,0.000004190408,0.000034513847,0.0000011638297,0.00009321165],"genre_scores_gemma":[0.9997154,0.00008904218,0.000030772477,0.000016547745,0.0000028105972,0.000004766805,0.00007659076,0.000001075464,0.0000629679],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997663,0.000029705216,0.000028647655,0.000088947236,0.000042058677,0.00004439478],"domain_scores_gemma":[0.9997204,0.00002975239,0.00012300204,0.000021231424,0.000034520686,0.00007108508],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023527014,0.00024604087,0.0003409999,0.0008901928,0.000577292,0.00046102057,0.00022024634,0.0002986615,0.0010057497],"category_scores_gemma":[0.0008640066,0.000303337,0.00019954336,0.00067859195,0.0004396801,0.00023516832,0.0005241775,0.0002517255,0.00016871147],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010178906,0.000021936683,0.9952915,0.000012601347,0.000031388317,0.0007379861,0.00046136277,0.000029840803,0.0015630268,0.000015156065,0.000080825834,0.0016526536],"study_design_scores_gemma":[0.000024086936,0.000115346586,0.9946601,0.000008927419,0.000042366795,0.0036940752,0.00082000386,0.00008445933,0.00014937553,0.000033179418,0.0003624799,0.0000055875316],"about_ca_topic_score_codex":0.0071993372,"about_ca_topic_score_gemma":0.005600572,"teacher_disagreement_score":0.0071993372,"about_ca_system_score_codex":0.00030652087,"about_ca_system_score_gemma":0.00033938896,"threshold_uncertainty_score":0.01431489},"labels":[],"label_agreement":null},{"id":"W2282807596","doi":"10.1186/1897-4287-13-s2-a8","title":"Pathological complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients","year":2015,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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 College Hospital; Sunnybrook Health Science Centre","funders":"","keywords":"Medicine; Pathological; Breast cancer; Cisplatin; Oncology; Complete response; Human genetics; Internal medicine; Neoadjuvant therapy; Cancer; Chemotherapy; Bioinformatics; Gene","score_opus":0.06436959264548699,"score_gpt":0.4151363659360734,"score_spread":0.3507667732905864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2282807596","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986339,0.00065344886,0.0000695153,0.000026299944,0.0000045326124,0.000023315597,0.00021688352,0.0000023883592,0.00036960767],"genre_scores_gemma":[0.99904686,0.00024533845,0.00009597646,0.00004246333,0.000008911933,0.000038285816,0.00043806768,0.0000016437144,0.000082384606],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995258,0.00021284772,0.000060560033,0.00005009402,0.000080814614,0.0000700083],"domain_scores_gemma":[0.99930155,0.0003312141,0.00018544694,0.00004188678,0.000038076345,0.000101765305],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053753227,0.00015044499,0.00069684495,0.00029319865,0.00021567103,0.00027643132,0.00015108386,0.0003027066,0.00073828606],"category_scores_gemma":[0.0017128021,0.00020469516,0.00029065146,0.0003697937,0.00027032217,0.0001736885,0.00026100138,0.00026326015,0.00019168173],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0077068047,0.00034852765,0.96106637,0.00015456253,0.00011686435,0.0019945153,0.00021020822,0.0009886742,0.0042029903,0.000058559952,0.00046466792,0.022687264],"study_design_scores_gemma":[0.00024992498,0.00369374,0.989253,0.000023112263,0.000080808866,0.0037522423,0.00013117073,0.00048231438,0.0013056967,0.00006772263,0.0009493607,0.00001091468],"about_ca_topic_score_codex":0.0005506738,"about_ca_topic_score_gemma":0.0010368965,"teacher_disagreement_score":0.00073828606,"about_ca_system_score_codex":0.00036338877,"about_ca_system_score_gemma":0.0004280662,"threshold_uncertainty_score":0.002842784},"labels":[],"label_agreement":null},{"id":"W2594637960","doi":"10.1186/s13053-017-0064-y","title":"Screening with magnetic resonance imaging, mammography and ultrasound in women at average and intermediate risk of breast cancer","year":2017,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"MRI in cancer diagnosis","field":"Medicine","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women's College Hospital; University of Toronto","funders":"Ministerstwo Edukacji i Nauki","keywords":"Medicine; Mammography; Breast cancer; Ultrasound; Magnetic resonance imaging; Cancer; Radiology; Gynecology; Obstetrics; Internal medicine","score_opus":0.022981617738435274,"score_gpt":0.3663224555859947,"score_spread":0.3433408378475594,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2594637960","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99798167,0.0012498269,0.000052070907,0.0001301061,0.00001078335,0.0000142664485,0.000066710054,0.0000054217026,0.00048903475],"genre_scores_gemma":[0.9990189,0.00043291,0.00021398772,0.00007389669,0.00002918611,0.000017688533,0.00013180383,0.0000010137671,0.000080539714],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99867696,0.0005425423,0.00014740186,0.00015187683,0.0002576281,0.00022356426],"domain_scores_gemma":[0.99837047,0.00042531046,0.00046381378,0.00006931606,0.00012556439,0.0005455769],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016550055,0.00033566167,0.0006811344,0.0016102316,0.0006306301,0.0005892734,0.0004913564,0.0009108259,0.0006654026],"category_scores_gemma":[0.006568044,0.00063086365,0.0004896991,0.0012903499,0.0003838875,0.00076664117,0.0007562803,0.00064364355,0.00015464536],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00078092347,0.00011972818,0.9942585,0.000018751369,0.000044262182,0.00022964724,0.00011676231,0.00004775137,0.00014920704,0.0000147163355,0.00010611608,0.0041136276],"study_design_scores_gemma":[0.000042599306,0.00065896503,0.99791986,0.000019326302,0.00006307494,0.0006069964,0.00022409082,0.00019386824,0.00005882512,0.000047161502,0.00015395354,0.0000112325715],"about_ca_topic_score_codex":0.005293334,"about_ca_topic_score_gemma":0.01028168,"teacher_disagreement_score":0.005293334,"about_ca_system_score_codex":0.0004207154,"about_ca_system_score_gemma":0.00049246324,"threshold_uncertainty_score":0.010525048},"labels":[],"label_agreement":null},{"id":"W2761551051","doi":"10.1186/s13053-017-0074-9","title":"Meeting abstracts from the Annual Conference on Hereditary Cancers 2015","year":2017,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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 Cancer Agency","funders":"Ministerstwo Edukacji i Nauki","keywords":"Medicine; Human genetics; Family medicine; Library science; Genetics; Gene","score_opus":0.07501333567325744,"score_gpt":0.42984896510826665,"score_spread":0.35483562943500924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2761551051","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.007445897,0.21645789,0.003686114,0.13065192,0.34784976,0.0011232608,0.010523508,0.0006809956,0.28158057],"genre_scores_gemma":[0.022591809,0.12644637,0.0019800954,0.015650533,0.14108348,0.0006563735,0.011521741,0.00027024833,0.6797994],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99934095,0.00010687612,0.0000749616,0.00011403211,0.0002413816,0.00012181402],"domain_scores_gemma":[0.9979153,0.00017557251,0.00016589092,0.00006840182,0.001037572,0.0006371597],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017712235,0.0014796081,0.0008322832,0.0024249465,0.000756004,0.0019473481,0.001209547,0.0025085611,0.19537722],"category_scores_gemma":[0.0026007353,0.000327653,0.000802183,0.0011304698,0.00028671985,0.0009261205,0.0018946924,0.0016318215,0.075700246],"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":[0.00016184831,0.000048906015,0.0007565222,0.00039291408,0.000017487135,0.00011547555,0.000017263686,0.000054658958,0.00041968608,0.00032878033,0.9007702,0.09691622],"study_design_scores_gemma":[0.000040292824,0.00007615749,0.005020668,0.0007199388,0.000026488893,0.000274096,0.000052804546,0.000066912384,0.00022468218,0.00043827973,0.9930482,0.0000115539015],"about_ca_topic_score_codex":0.002163349,"about_ca_topic_score_gemma":0.006111249,"teacher_disagreement_score":0.19537722,"about_ca_system_score_codex":0.0011847899,"about_ca_system_score_gemma":0.0015830465,"threshold_uncertainty_score":0.6536019},"labels":[],"label_agreement":null},{"id":"W2799877715","doi":"10.1186/s13053-018-0088-y","title":"CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome","year":2018,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Cancer Genomics and Diagnostics","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":"Canadian Centre for Applied Research in Cancer Control; Vancouver General Hospital; Canada's Michael Smith Genome Sciences Centre; Genome British Columbia; University of British Columbia; Surrey Memorial Hospital; Pancreas Centre (Canada); Spinal Cord Injury BC; BC Cancer Agency","funders":"Canadian Institutes of Health Research; Victoria General Hospital Foundation; BC Cancer Foundation; Michael Smith Health Research BC","keywords":"Medicine; CDKN2A; Pancreatic ductal adenocarcinoma; Human genetics; Adenocarcinoma; Melanoma; Internal medicine; Oncology; Pathology; Cancer research; Pancreatic cancer; Cancer; Genetics; Gene; Biology","score_opus":0.022055499595211747,"score_gpt":0.33933743245530074,"score_spread":0.317281932860089,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2799877715","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982646,0.00025541874,0.00009804586,0.000121270394,0.000011691541,0.000010936226,0.000046673485,0.000008844692,0.0011825359],"genre_scores_gemma":[0.9994591,0.00012682608,0.00013536394,0.00005596109,0.000015276648,0.0000021595806,0.000025036587,0.0000031296463,0.00017718544],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99973863,0.00003207024,0.000050388368,0.00008210984,0.000052134925,0.00004471934],"domain_scores_gemma":[0.99942315,0.00016640608,0.00015959665,0.000031905052,0.000058663016,0.00016027935],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021306078,0.000445905,0.00039011173,0.0010271829,0.0009428913,0.00054230745,0.0002618059,0.0007710022,0.0020038595],"category_scores_gemma":[0.0018879207,0.0003088547,0.00029861226,0.00044650177,0.00046704456,0.0005371857,0.00044675826,0.00043375755,0.00026316004],"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":[0.00016917358,0.000077959456,0.40766695,0.000032271488,0.000024038485,0.5786366,0.0013705844,0.000110002744,0.0075774277,0.0001623148,0.00032108754,0.00385157],"study_design_scores_gemma":[0.000015897915,0.00016907844,0.20529625,0.000025480547,0.000041002022,0.79117644,0.00074718177,0.00032337825,0.0013997019,0.0001156519,0.0006727821,0.000017123282],"about_ca_topic_score_codex":0.0030097282,"about_ca_topic_score_gemma":0.003337584,"teacher_disagreement_score":0.0030097282,"about_ca_system_score_codex":0.00035774295,"about_ca_system_score_gemma":0.00035286695,"threshold_uncertainty_score":0.0067035556},"labels":[],"label_agreement":null},{"id":"W2803644870","doi":"10.1186/s13053-018-0089-x","title":"Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland","year":2018,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital","funders":"Breast Cancer Campaign","keywords":"Founder effect; Ovarian cancer; Medicine; Mutation; Cancer; Genetics; Internal medicine; Oncology; Biology; Gene; Haplotype; Genotype","score_opus":0.042973811094034836,"score_gpt":0.38868209627555944,"score_spread":0.34570828518152463,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2803644870","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996867,0.00010502424,0.000016569535,0.000011213488,9.541404e-7,0.0000037560549,0.00003664603,0.000001237273,0.0001378815],"genre_scores_gemma":[0.9996561,0.00012868685,0.000033548586,0.000016971466,0.0000025108275,0.0000043795244,0.00007914508,0.000001383269,0.00007720749],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974555,0.00003186942,0.000039413724,0.000089818,0.00005067797,0.000042669675],"domain_scores_gemma":[0.9995559,0.0000687644,0.00020625394,0.00003841789,0.00004046971,0.00009011599],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022023437,0.00017516506,0.00035243842,0.0010585553,0.0003777245,0.00037986462,0.00016405697,0.00030070636,0.0011898351],"category_scores_gemma":[0.0011683766,0.0003482862,0.00019531476,0.00087512494,0.0004093366,0.00026395635,0.00043631773,0.0002391178,0.0001470046],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009097974,0.00001901752,0.9962608,0.000012006514,0.00002315917,0.0007025289,0.00021810256,0.000020454956,0.001071549,0.000015167411,0.000062489635,0.0015037379],"study_design_scores_gemma":[0.000017475457,0.000049800088,0.9964205,0.00000624908,0.000024149389,0.002680682,0.00030891882,0.00005989516,0.0001625567,0.000026813123,0.00023882647,0.0000040105483],"about_ca_topic_score_codex":0.0034274322,"about_ca_topic_score_gemma":0.00348965,"teacher_disagreement_score":0.0034274322,"about_ca_system_score_codex":0.00023230667,"about_ca_system_score_gemma":0.0002478952,"threshold_uncertainty_score":0.0068150163},"labels":[],"label_agreement":null},{"id":"W2915905957","doi":"10.1186/s13053-017-0081-x","title":"Meeting abstracts from the Annual Conference on Hereditary Cancers 2016","year":2017,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital","funders":"","keywords":"Medicine; Human genetics; Family medicine; General surgery; Genetics; Gene","score_opus":0.06925084681675492,"score_gpt":0.41581265170353054,"score_spread":0.3465618048867756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2915905957","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.011495114,0.23903811,0.0043203384,0.10420177,0.29879254,0.0011409621,0.012721216,0.00095217786,0.32733774],"genre_scores_gemma":[0.023257956,0.13740191,0.0024570813,0.011419584,0.1135755,0.00070217304,0.012480945,0.00051072997,0.6981941],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992518,0.00014430436,0.00008804785,0.0001522265,0.00024258633,0.00012113647],"domain_scores_gemma":[0.99833316,0.00013992736,0.00015075902,0.00009003443,0.00070907304,0.0005770344],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015776677,0.001513638,0.0008008303,0.0024179858,0.00072519336,0.0019908785,0.0010549959,0.0019228808,0.22378041],"category_scores_gemma":[0.0024304944,0.00040588438,0.0007594769,0.0011331107,0.00033317425,0.00093978,0.0024774368,0.0016633319,0.106257856],"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":[0.000190095,0.00005282349,0.001500945,0.00049205945,0.000025993279,0.00022457527,0.000033502314,0.00005969888,0.0007969619,0.00045373183,0.8564832,0.13968638],"study_design_scores_gemma":[0.000025131701,0.000043151515,0.0032333187,0.0005199641,0.000015385296,0.00042692426,0.00004109723,0.00004173228,0.00018320957,0.00028620628,0.9951762,0.000007645105],"about_ca_topic_score_codex":0.0015524863,"about_ca_topic_score_gemma":0.0040372782,"teacher_disagreement_score":0.22378041,"about_ca_system_score_codex":0.0010748703,"about_ca_system_score_gemma":0.001256177,"threshold_uncertainty_score":0.74862003},"labels":[],"label_agreement":null},{"id":"W2956051026","doi":"10.1186/s13053-019-0114-8","title":"Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study","year":2019,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Colorectal Cancer Screening and Detection","field":"Medicine","cited_by":27,"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 Toronto; Sinai Health System; Toronto Metropolitan University; Toronto General Hospital; University of Victoria","funders":"","keywords":"Colonoscopy; Medicine; Proband; Colorectal cancer; Psychological intervention; Transtheoretical model; Family medicine; Cancer; Internal medicine; Nursing","score_opus":0.10026862717239039,"score_gpt":0.4810025563720725,"score_spread":0.38073392919968213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2956051026","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9945263,0.00034196602,0.0005301022,0.00095229666,0.000023657009,0.0001814698,0.0002381584,0.000008664964,0.0031972332],"genre_scores_gemma":[0.9963954,0.000528126,0.0005235306,0.00040846705,0.000007860212,0.00022261192,0.00009119523,0.000010661919,0.0018121718],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.9941911,0.0035081683,0.00017814164,0.00038415016,0.00051763543,0.0012207626],"domain_scores_gemma":[0.9833908,0.011432047,0.0013605377,0.00032625961,0.001867147,0.001623213],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00887447,0.00046508116,0.00051538553,0.001686521,0.010985886,0.0025809582,0.0016608499,0.0011009848,0.0037576908],"category_scores_gemma":[0.015211676,0.00052264286,0.00034629373,0.0017205292,0.0053949915,0.0018726554,0.0036707316,0.001719234,0.000290718],"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":[0.000021625077,0.000028547443,0.006013816,0.00009887627,0.0000025451607,0.000456547,0.9906658,0.000014828223,0.00032199448,0.00018268403,0.00023832943,0.0019545082],"study_design_scores_gemma":[0.0000017886163,0.00001790597,0.004056935,0.00008878602,0.0000022722847,0.000090408525,0.9939659,0.00002548366,0.000085954875,0.00003979381,0.0016178555,0.0000068382606],"about_ca_topic_score_codex":0.2548184,"about_ca_topic_score_gemma":0.36178297,"teacher_disagreement_score":0.2548184,"about_ca_system_score_codex":0.015577147,"about_ca_system_score_gemma":0.017492192,"threshold_uncertainty_score":0.5066704},"labels":[],"label_agreement":null},{"id":"W2967729168","doi":"10.1186/s13053-019-0123-7","title":"Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome","year":2019,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","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 Toronto; Princess Margaret Cancer Centre; Sinai Health System; Toronto Metropolitan University; University of Victoria","funders":"Canadian Institutes of Health Research","keywords":"Lynch syndrome; Medicine; Endometrial cancer; Psychosocial; Gynecology; Ovarian cancer; Cancer; Cancer screening; Family medicine; Obstetrics; Colorectal cancer; Internal medicine; Psychiatry","score_opus":0.048173868991235776,"score_gpt":0.371975688980215,"score_spread":0.3238018199889792,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2967729168","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99894565,0.00019887689,0.000018972485,0.0001604035,0.0000035264597,0.000011085154,0.00005655249,0.0000012746681,0.00060364255],"genre_scores_gemma":[0.9996879,0.00009730958,0.000030313171,0.000033533277,0.0000035462392,0.000007781964,0.000037544745,3.1742462e-7,0.00010180407],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99944645,0.00024240463,0.000051449046,0.000036924044,0.00014311438,0.00007967984],"domain_scores_gemma":[0.99586076,0.0016016312,0.0016076039,0.00008704351,0.00026063432,0.00058238796],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011136985,0.00013947066,0.00017898546,0.00061100186,0.0004802329,0.0006210671,0.00017452553,0.00040414365,0.0030423845],"category_scores_gemma":[0.0086605465,0.00014256012,0.00025604208,0.00043996266,0.00031143008,0.0003919932,0.00043682838,0.00062369404,0.0001415607],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000040345218,0.00019457635,0.9963983,0.00001773855,0.000028317996,0.000050966708,0.00085184927,0.000022826287,0.000063500935,0.000015671245,0.00007823638,0.0022375183],"study_design_scores_gemma":[0.000005331465,0.00019975996,0.99746597,0.000016426802,0.000015866348,0.00015421421,0.00184219,0.00008380189,0.000025676938,0.000018472652,0.00016950515,0.0000027486517],"about_ca_topic_score_codex":0.0027176489,"about_ca_topic_score_gemma":0.0041190833,"teacher_disagreement_score":0.0030423845,"about_ca_system_score_codex":0.00027602076,"about_ca_system_score_gemma":0.00045031257,"threshold_uncertainty_score":0.0101777315},"labels":[],"label_agreement":null},{"id":"W2997615781","doi":"10.1186/s13053-019-0131-7","title":"Serum selenium level and cancer risk: a nested case-control study","year":2019,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Selenium in Biological Systems","field":"Nursing","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":"Public Health Ontario; Women's College Hospital; University of Toronto","funders":"Narodowe Centrum Badań i Rozwoju","keywords":"Medicine; Nested case-control study; Selenium; Case-control study; Cancer; Human genetics; Oncology; Environmental health; Internal medicine; Genetics","score_opus":0.09653594519607833,"score_gpt":0.42592329502821596,"score_spread":0.32938734983213763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2997615781","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978108,0.00052272464,0.001103655,0.000039112554,0.000010922324,0.00006946165,0.00022496197,0.0000062052763,0.00021213102],"genre_scores_gemma":[0.9987142,0.00013968858,0.0007010091,0.000034881872,0.000008435546,0.000039702427,0.00024112649,0.0000025123163,0.00011846141],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986274,0.00049622,0.000114976145,0.00045457884,0.00022155323,0.000085216954],"domain_scores_gemma":[0.99856514,0.00039019485,0.0003107492,0.00034696687,0.00022611645,0.00016086301],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021548716,0.00045160195,0.00065289024,0.00054912944,0.0006702585,0.0006792733,0.0006577674,0.0004583384,0.0008907121],"category_scores_gemma":[0.0029806811,0.000645084,0.00072534365,0.0006155115,0.0005378202,0.00028676193,0.00049903535,0.0005139271,0.0001787421],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011625652,0.0003331798,0.9913947,0.00007563229,0.00089254696,0.0005155823,0.00039681862,0.000075564734,0.0033236295,0.00008445127,0.00017395485,0.0015712708],"study_design_scores_gemma":[0.00040942564,0.001224171,0.98989886,0.00005007843,0.001200928,0.002761185,0.0004095332,0.0013278561,0.0010519137,0.00022438697,0.0014209466,0.00002079316],"about_ca_topic_score_codex":0.0060774935,"about_ca_topic_score_gemma":0.006388772,"teacher_disagreement_score":0.0060774935,"about_ca_system_score_codex":0.00040470788,"about_ca_system_score_gemma":0.0005376972,"threshold_uncertainty_score":0.012084246},"labels":[],"label_agreement":null},{"id":"W3009341808","doi":"10.1186/s13053-020-0134-4","title":"On the road with Henry Lynch","year":2020,"lang":"en","type":"editorial","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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; Women's College Hospital; Public Health Ontario","funders":"","keywords":"Medicine; Human genetics; General surgery; Genetics","score_opus":0.03396448844212369,"score_gpt":0.3948101661481399,"score_spread":0.3608456777060162,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3009341808","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000024583911,0.008140851,0.00009938166,0.099460796,0.890359,0.000010957195,0.000024285082,0.0000384087,0.001841798],"genre_scores_gemma":[0.00038164752,0.005030894,0.00010443254,0.07023043,0.9140149,0.000025817923,0.000015496478,0.00003596709,0.010160452],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9957385,0.00124826,0.0003905629,0.000506992,0.0018385778,0.00027718733],"domain_scores_gemma":[0.978953,0.011003839,0.0010460009,0.0004106757,0.004609632,0.00397683],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.007411046,0.002881629,0.002796587,0.002698403,0.0029592363,0.00751753,0.0024984623,0.015795944,0.014174598],"category_scores_gemma":[0.030831547,0.001076691,0.0015688355,0.0010208985,0.0022779657,0.0056850016,0.0019294259,0.026645817,0.009964016],"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":[0.000016547225,0.000004542184,0.00001176656,0.0000635939,0.000005577149,0.000060959264,0.000008521014,0.000009827644,0.0000115364655,0.00025035877,0.99707127,0.0024854983],"study_design_scores_gemma":[0.00005765842,0.00002281876,0.00016311294,0.00037127396,0.00002479988,0.00020527154,0.00006227534,0.00007105654,0.000037619513,0.0011224513,0.9978411,0.000020544885],"about_ca_topic_score_codex":0.0024546797,"about_ca_topic_score_gemma":0.008406663,"teacher_disagreement_score":0.015795944,"about_ca_system_score_codex":0.0023603702,"about_ca_system_score_gemma":0.0033596235,"threshold_uncertainty_score":0.047418773},"labels":[],"label_agreement":null},{"id":"W3012648599","doi":"10.1186/s13053-020-0136-2","title":"Group plus “mini” individual pre-test genetic counselling sessions for hereditary cancer shorten provider time and improve patient satisfaction","year":2020,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"St. John’s Health Sciences Centre; Memorial University of Newfoundland","funders":"","keywords":"Medicine; Genetic counseling; Session (web analytics); Family medicine; Genetic testing; Likert scale; Test (biology); Cancer; Patient satisfaction; Nursing; Internal medicine; Psychology; Genetics","score_opus":0.0378496976598535,"score_gpt":0.36756219552091096,"score_spread":0.32971249786105744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3012648599","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9912555,0.00019225132,0.0011397529,0.0010770642,0.000053558782,0.000360926,0.00015058064,0.00020997327,0.0055602924],"genre_scores_gemma":[0.9901002,0.00021604417,0.0050633615,0.00077289925,0.00007282307,0.00051223626,0.00015960418,0.000020245603,0.0030827262],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9993259,0.0003625393,0.000035909117,0.000053487598,0.0000891582,0.00013318822],"domain_scores_gemma":[0.99730384,0.0010624977,0.00037915807,0.0001389972,0.00011316979,0.0010022975],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013616068,0.00020147848,0.00026420233,0.00017783516,0.00043582954,0.00028299782,0.0004760464,0.00055435544,0.030681638],"category_scores_gemma":[0.004080098,0.00010274095,0.00031664726,0.00015532634,0.00015047369,0.00036336642,0.00074905274,0.0005691618,0.0015091189],"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":[0.0066408804,0.022894153,0.10153868,0.0011720129,0.00014916809,0.00044326822,0.0055452487,0.0016186091,0.0077449037,0.000504352,0.037086938,0.81466174],"study_design_scores_gemma":[0.004381854,0.05347793,0.8573709,0.0006596055,0.00040674995,0.0028002495,0.012263696,0.007474727,0.0057141753,0.0016494974,0.053659316,0.00014141707],"about_ca_topic_score_codex":0.0010183452,"about_ca_topic_score_gemma":0.0022074224,"teacher_disagreement_score":0.030681638,"about_ca_system_score_codex":0.0003209417,"about_ca_system_score_gemma":0.00090842776,"threshold_uncertainty_score":0.10264033},"labels":[],"label_agreement":null},{"id":"W3090337911","doi":"10.1186/s13053-020-00152-z","title":"Preferences for breast cancer prevention among women with a BRCA1 or BRCA2 mutation","year":2020,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Women's College Hospital; University of Toronto","funders":"Medical Research Council; National Institute for Health and Care Research; Manchester Biomedical Research Centre; Creighton University; National Health and Medical Research Council; Amgen","keywords":"Medicine; Breast cancer; Tamoxifen; Family medicine; BRCA mutation; Genetic testing; Gynecology; Mastectomy; Cancer; Oophorectomy; Oncology; Demography; Internal medicine; Hysterectomy; Surgery","score_opus":0.06348420012984277,"score_gpt":0.40833641000836407,"score_spread":0.3448522098785213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3090337911","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982645,0.00013106853,0.00008768061,0.00028295928,0.0000065760582,0.000014414699,0.00010536887,0.0000015965015,0.0011058998],"genre_scores_gemma":[0.999027,0.00013809097,0.00021523157,0.00018829401,0.0000072245066,0.000016970269,0.000076284065,8.257104e-7,0.00032998697],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99938285,0.00033445467,0.00004995253,0.000051442436,0.000111418085,0.00006996518],"domain_scores_gemma":[0.99804986,0.0010347507,0.00049420237,0.00004883995,0.000116921874,0.0002553638],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011877036,0.00013197678,0.00015992382,0.0004245862,0.00041089556,0.0006811584,0.00012829217,0.00044483787,0.005634498],"category_scores_gemma":[0.0041541955,0.00011914191,0.00034859544,0.00033216728,0.000261742,0.00041667896,0.00036578052,0.00037194244,0.00036509038],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005583997,0.0003470123,0.9608015,0.0001374583,0.00010454753,0.00037144902,0.006928399,0.0002513738,0.0012403983,0.00023735291,0.0014056118,0.02761642],"study_design_scores_gemma":[0.000111899775,0.0011477993,0.93997157,0.00017799661,0.00009858287,0.0012781805,0.04346189,0.0016412915,0.00068396376,0.000999029,0.010363695,0.00006408568],"about_ca_topic_score_codex":0.003119384,"about_ca_topic_score_gemma":0.0039694994,"teacher_disagreement_score":0.005634498,"about_ca_system_score_codex":0.00029520076,"about_ca_system_score_gemma":0.00022920492,"threshold_uncertainty_score":0.018849254},"labels":[],"label_agreement":null},{"id":"W3204480707","doi":"10.1186/s13053-021-00196-9","title":"Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline","year":2021,"lang":"en","type":"review","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Hospital for Sick Children; Princess Margaret Cancer Centre; Juravinski Cancer Centre; Cancer Care Ontario; McMaster University; Women's College Hospital; University Health Network; University of Toronto","funders":"Cancer Care Ontario","keywords":"Medicine; Guideline; Breast cancer; Ovarian cancer; Cancer; Gynecology; Oncology; Intensive care medicine; Internal medicine; Pathology","score_opus":0.13217463245639902,"score_gpt":0.5145659086664909,"score_spread":0.38239127621009183,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3204480707","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.003456529,0.54267097,0.030435266,0.34102497,0.017823076,0.01328617,0.009759091,0.0013966825,0.040147226],"genre_scores_gemma":[0.02392311,0.56598204,0.23163454,0.12258355,0.005714694,0.021873772,0.012101211,0.00029608392,0.01589098],"study_design_codex":"not_applicable","study_design_gemma":"systematic_review","domain_scores_codex":[0.9867923,0.005676894,0.0037330703,0.0006464321,0.0025982186,0.0005531835],"domain_scores_gemma":[0.9681258,0.0136909755,0.0035795656,0.0006302277,0.012818923,0.0011545841],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.014874951,0.002362173,0.004090058,0.005920219,0.0013292466,0.002935679,0.0076579787,0.011181452,0.0074853543],"category_scores_gemma":[0.05353278,0.0012971096,0.009763003,0.0034096052,0.0010387949,0.0029841382,0.0028065545,0.008224507,0.0042993715],"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":[0.00026993357,0.0002862888,0.0011884035,0.088859804,0.0015689394,0.00068129884,0.0010875321,0.002282911,0.00076842745,0.0066561527,0.5178146,0.3785357],"study_design_scores_gemma":[0.0009920554,0.00023928928,0.0033990524,0.37559363,0.004051738,0.00079498667,0.0005191204,0.0015319268,0.00047837527,0.01303547,0.59921455,0.00014994519],"about_ca_topic_score_codex":0.02073027,"about_ca_topic_score_gemma":0.025851022,"teacher_disagreement_score":0.02073027,"about_ca_system_score_codex":0.0053896545,"about_ca_system_score_gemma":0.019779107,"threshold_uncertainty_score":0.07866722},"labels":[],"label_agreement":null},{"id":"W41280559","doi":"10.1186/1897-4287-10-s3-a7","title":"Selenium and the risk of cancer of the lung and larynx. A case-control study from a region with low selenium","year":2012,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Selenium in Biological Systems","field":"Nursing","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":"Women's College Hospital","funders":"","keywords":"Medicine; Lung cancer; Selenium; Case-control study; Odds ratio; Selenoprotein; Internal medicine; GPX1; Cancer; Oncology; Gastroenterology; Glutathione peroxidase; Oxidative stress","score_opus":0.03555176334568002,"score_gpt":0.3691562455495878,"score_spread":0.3336044822039078,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W41280559","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99939597,0.0002812632,0.00010076012,0.00001689223,0.0000027962399,0.000010979768,0.00004741978,0.0000019439233,0.00014203398],"genre_scores_gemma":[0.9994135,0.00014270324,0.000117085976,0.000016789305,0.000004651954,0.000010633601,0.00009579236,0.0000010998212,0.00019771425],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992878,0.00024328317,0.00006814172,0.0001993138,0.00013201141,0.00006955763],"domain_scores_gemma":[0.99925476,0.00020496217,0.00020347869,0.00011396618,0.00009437431,0.00012845424],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010492437,0.00041435857,0.00049232075,0.0011635243,0.0008057649,0.00060531835,0.0004496893,0.00063335296,0.0009333027],"category_scores_gemma":[0.0020127965,0.0005957752,0.0004650415,0.00078945514,0.0004407518,0.00022189593,0.0005509103,0.00046264436,0.00015020117],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00072800997,0.00017353207,0.99452114,0.000024740477,0.00028996568,0.00049901934,0.00032682155,0.000037615944,0.0017785111,0.00004614647,0.00007589801,0.001498508],"study_design_scores_gemma":[0.00008264258,0.00042076252,0.99716717,0.0000065897616,0.00016532923,0.0012107708,0.00018781018,0.00017262163,0.0002689269,0.000024608518,0.00028839815,0.0000044179837],"about_ca_topic_score_codex":0.014502768,"about_ca_topic_score_gemma":0.0124032665,"teacher_disagreement_score":0.014502768,"about_ca_system_score_codex":0.00043124636,"about_ca_system_score_gemma":0.00035304896,"threshold_uncertainty_score":0.028836668},"labels":[],"label_agreement":null},{"id":"W4213438283","doi":"10.1186/s13053-022-00214-4","title":"Women’s perceptions of PERSPECTIVE: a breast cancer risk stratification e-platform","year":2022,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Université Laval; McGill University; McGill University Health Centre; Centre Intégré Universitaire de Santé et de Services Sociaux du Centre-Sud-de-l'Île-de-Montréal; Jewish General Hospital","funders":"Government of Canada; Fondation du cancer du sein du Québec; Ministère de l'Économie, de l’Innovation et des Exportations du Québec; Canada Excellence Research Chairs, Government of Canada; Génome Québec; Canadian Institutes of Health Research; Genome Canada","keywords":"Medicine; Breast cancer; Stratification (seeds); Risk stratification; Perspective (graphical); Human genetics; Perception; Risk perception; Oncology; Gynecology; Internal medicine; Cancer; Epistemology; Artificial intelligence; Genetics","score_opus":0.034316004104080394,"score_gpt":0.4029026587449529,"score_spread":0.3685866546408725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4213438283","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956116,0.00007359923,0.00061261957,0.00064186426,0.00002379212,0.00022275822,0.00006841869,0.000017762552,0.0027276943],"genre_scores_gemma":[0.99483335,0.00021247611,0.0031237565,0.00037079467,0.000015575899,0.00023988503,0.0000759671,0.0000052386213,0.0011230042],"study_design_codex":"design_other","study_design_gemma":"qualitative","domain_scores_codex":[0.99892056,0.00073105824,0.000046505087,0.00004862141,0.00015443233,0.000098728255],"domain_scores_gemma":[0.9965012,0.0023992886,0.00027339632,0.00012824647,0.00023998308,0.00045796225],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00290273,0.00024557312,0.0001919674,0.00020718419,0.00056211546,0.0011599268,0.0002360478,0.00048454574,0.003295544],"category_scores_gemma":[0.007297087,0.00015411747,0.00030889534,0.00017672998,0.0003648277,0.0010714971,0.0015357777,0.0005728391,0.00036820068],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003399448,0.0071817604,0.32564542,0.0019471705,0.000107013824,0.0022527587,0.20432119,0.00068116747,0.0222648,0.0017346157,0.008810625,0.421654],"study_design_scores_gemma":[0.0013151193,0.04439324,0.51500064,0.0013439038,0.0005665895,0.0026554542,0.3099459,0.003897339,0.01566457,0.0023722502,0.10254769,0.00029725608],"about_ca_topic_score_codex":0.0007714193,"about_ca_topic_score_gemma":0.0011234665,"teacher_disagreement_score":0.003295544,"about_ca_system_score_codex":0.0004196275,"about_ca_system_score_gemma":0.00070876745,"threshold_uncertainty_score":0.0153512955},"labels":[],"label_agreement":null},{"id":"W4220660697","doi":"10.1186/s13053-022-00215-3","title":"Genetic susceptibility to hereditary non-medullary thyroid cancer","year":2022,"lang":"en","type":"review","venue":"Hereditary Cancer in Clinical Practice","topic":"Thyroid Cancer Diagnosis and Treatment","field":"Medicine","cited_by":31,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; Women's College Hospital; University of Toronto","funders":"","keywords":"Medullary thyroid cancer; Medicine; Thyroid cancer; Genetic predisposition; Multifactorial Inheritance; Medullary cavity; Disease; Penetrance; Cancer; Thyroid; Genetics; Bioinformatics; Gene; Pathology; Internal medicine; Biology; Single-nucleotide polymorphism; Phenotype; Genotype","score_opus":0.12755371161215875,"score_gpt":0.48529112609866343,"score_spread":0.35773741448650465,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4220660697","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004392487,0.99689555,0.00015711239,0.00024312145,0.000084357904,0.000003992844,0.00004924947,0.000010521498,0.0021168033],"genre_scores_gemma":[0.0022444604,0.9968796,0.00013461716,0.00010298487,0.00006891748,0.0000036778688,0.00007195869,0.0000015711961,0.00049224857],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99989235,0.00001948934,0.000014711492,0.00002355423,0.00003863997,0.000011287226],"domain_scores_gemma":[0.9998479,0.00008615922,0.000021670168,0.0000037434315,0.00003099653,0.000009469468],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022142653,0.00038112584,0.0006705943,0.001266661,0.00016970711,0.00044192557,0.0003490978,0.00038952142,0.0034368052],"category_scores_gemma":[0.0005977457,0.000104616585,0.0003410012,0.0011537606,0.00020288692,0.00029201581,0.00029709868,0.0005643424,0.0009749997],"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":[0.000053388707,0.000034425393,0.0013818814,0.015245123,0.00017661366,0.0007184527,0.000076752265,0.0002719192,0.0014224157,0.0018786276,0.02487388,0.9538667],"study_design_scores_gemma":[0.000018085742,0.000077439734,0.007070156,0.0100000715,0.00048242765,0.01224516,0.00010731519,0.00010876632,0.0007343901,0.0021228427,0.9670115,0.000021809014],"about_ca_topic_score_codex":0.0016272113,"about_ca_topic_score_gemma":0.0020236608,"teacher_disagreement_score":0.0034368052,"about_ca_system_score_codex":0.00033388843,"about_ca_system_score_gemma":0.0006657426,"threshold_uncertainty_score":0.011497259},"labels":[],"label_agreement":null},{"id":"W4223599799","doi":"10.1186/s13053-022-00220-6","title":"Germline BRCA1 and BRCA2 mutations and the risk of bladder or kidney cancer in Poland","year":2022,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Public Health Ontario; Women's College Hospital; University of Toronto","funders":"Pomorski Uniwersytet Medyczny W Szczecinie","keywords":"Medicine; Germline; Human genetics; Germline mutation; Bladder cancer; Kidney cancer; Oncology; Gynecology; Internal medicine; Cancer; Mutation; Cancer research; Genetics; Gene; Biology","score_opus":0.029249761061793528,"score_gpt":0.3909781609123933,"score_spread":0.3617283998505998,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4223599799","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99929667,0.00042971503,0.000040785835,0.000022826323,0.0000015144196,0.0000028712336,0.00008194871,0.0000019981726,0.000121587516],"genre_scores_gemma":[0.99946195,0.00028084326,0.000074817115,0.000012116685,0.0000029764492,0.0000028062452,0.00007576122,0.000001021842,0.00008772805],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976903,0.000040920855,0.000028271077,0.000078120014,0.00004444557,0.000039189013],"domain_scores_gemma":[0.9995641,0.00005874676,0.00024085918,0.000019667083,0.00003444541,0.00008226863],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035963993,0.00019364677,0.00030556967,0.00094477384,0.0002750716,0.00043804268,0.00025277724,0.00028458683,0.00114296],"category_scores_gemma":[0.0009405414,0.00026883068,0.00023511991,0.00071061484,0.00023543104,0.00018653696,0.00044702727,0.00024366993,0.00011477381],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009821811,0.000010607101,0.99775785,0.000020273692,0.000039451486,0.00017656716,0.00006505549,0.000025868523,0.00044536774,0.000015086458,0.000037509733,0.0013082466],"study_design_scores_gemma":[0.000014134764,0.00006580379,0.9982494,0.000014178911,0.0000410327,0.0010768422,0.000099507175,0.00008519916,0.00013224036,0.000035705627,0.000183645,0.0000023724915],"about_ca_topic_score_codex":0.0051418743,"about_ca_topic_score_gemma":0.0035115615,"teacher_disagreement_score":0.0051418743,"about_ca_system_score_codex":0.00022586556,"about_ca_system_score_gemma":0.0003303306,"threshold_uncertainty_score":0.010223925},"labels":[],"label_agreement":null},{"id":"W4223888919","doi":"10.1186/s13053-022-00221-5","title":"Reflex BRCA1 and BRCA2 tumour genetic testing for high-grade serous ovarian cancer: streamlined for clinicians but what do patients think?","year":2022,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Women's College Hospital; Ontario Institute for Cancer Research; Health Sciences Centre; University Health Network; University of Toronto; Hospital for Sick Children; St. Lawrence College; Sunnybrook Health Science Centre; Sinai Health System; Canada Research Chairs; Princess Margaret Cancer Centre","funders":"Canadian Institutes of Health Research","keywords":"Medicine; Serous ovarian cancer; Ovarian cancer; Reflex; Genetic testing; Human genetics; Oncology; Internal medicine; Serous fluid; Reproductive medicine; Gynecology; Pathology; Cancer; Genetics; Pregnancy; Gene","score_opus":0.05766587701275982,"score_gpt":0.39846509805624447,"score_spread":0.34079922104348465,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4223888919","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.90096515,0.012542908,0.0005874018,0.07619857,0.00046749713,0.00015202544,0.00025215614,0.00007415816,0.008760182],"genre_scores_gemma":[0.9883583,0.005055027,0.001113791,0.004333235,0.0002445067,0.000033690623,0.0001247649,0.0000088424795,0.0007278548],"study_design_codex":"observational","study_design_gemma":"qualitative","domain_scores_codex":[0.99859077,0.0005039466,0.00010469111,0.00008752511,0.0005132797,0.00019985481],"domain_scores_gemma":[0.9927263,0.0013487904,0.0023108479,0.0002117664,0.001138595,0.0022636293],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021704414,0.0001487403,0.00029171025,0.00019434911,0.0009781953,0.0013758797,0.00056792784,0.00081500673,0.0029111996],"category_scores_gemma":[0.013321638,0.00014492469,0.00024067018,0.00040699187,0.0015467058,0.0009034648,0.0007247992,0.0010088072,0.00036516873],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044861416,0.00032937614,0.7498784,0.0012247697,0.00011343283,0.0013724255,0.012201076,0.00023805027,0.0017308966,0.00029930196,0.037582513,0.19458115],"study_design_scores_gemma":[0.00016074168,0.0010618404,0.9179047,0.0018330704,0.00015754113,0.0036450624,0.04335111,0.00038847158,0.00062907644,0.0009754326,0.029798195,0.000094742856],"about_ca_topic_score_codex":0.029518321,"about_ca_topic_score_gemma":0.08220312,"teacher_disagreement_score":0.029518321,"about_ca_system_score_codex":0.002451107,"about_ca_system_score_gemma":0.0059150183,"threshold_uncertainty_score":0.05869299},"labels":[],"label_agreement":null},{"id":"W4223889552","doi":"10.1186/s13053-022-00223-3","title":"Delineating the role of osteoprotegerin as a marker of breast cancer risk among women with a BRCA1 mutation","year":2022,"lang":"en","type":"review","venue":"Hereditary Cancer in Clinical Practice","topic":"Bone Metabolism and Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; Women's College Hospital; University of Toronto","funders":"Canadian Institutes of Health Research; Peter Gilgan Foundation; Department of Family and Community Medicine, University of Toronto; University of Toronto","keywords":"Medicine; Breast cancer; Osteoprotegerin; RANKL; Oncology; Cancer; Bioinformatics; Internal medicine; Biomarker; Germline mutation; Cancer research; Estrogen receptor; Mutation; Receptor; Gene; Genetics; Activator (genetics); Biology","score_opus":0.02516032702234747,"score_gpt":0.3806828576709828,"score_spread":0.3555225306486353,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4223889552","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.06958384,0.92381585,0.0020516564,0.0021198862,0.0001440456,0.000026783433,0.00026817442,0.00001949605,0.0019704055],"genre_scores_gemma":[0.3312659,0.65866494,0.0063691973,0.0011824379,0.0007744942,0.000052268915,0.0004618907,0.000009863332,0.0012189258],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9996208,0.00014288348,0.000053080537,0.000056721514,0.00010523196,0.000021358323],"domain_scores_gemma":[0.9990969,0.00047972833,0.0002374576,0.000014535349,0.00013364546,0.000037772006],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009837258,0.0002930572,0.0006143739,0.0014501668,0.00012992795,0.00076563214,0.0002530162,0.000391711,0.00039447861],"category_scores_gemma":[0.0017971839,0.00011900712,0.00038277253,0.0009797614,0.00023177103,0.0004093838,0.00020696226,0.00048751823,0.0001380595],"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":[0.0011443276,0.00014615967,0.38209826,0.0064538266,0.0009782494,0.0011417703,0.0004377351,0.00051814766,0.011422816,0.0015130738,0.0038109056,0.5903348],"study_design_scores_gemma":[0.00007769465,0.0023346595,0.83270067,0.006611478,0.003746988,0.011863787,0.0012024079,0.0019386437,0.007344234,0.0038638886,0.12821841,0.00009720069],"about_ca_topic_score_codex":0.0011606474,"about_ca_topic_score_gemma":0.001914643,"teacher_disagreement_score":0.0014501668,"about_ca_system_score_codex":0.00023947122,"about_ca_system_score_gemma":0.00043594066,"threshold_uncertainty_score":0.005202532},"labels":[],"label_agreement":null},{"id":"W4281632563","doi":"10.1186/s13053-022-00227-z","title":"Beyond the pill: contraception and the prevention of hereditary ovarian cancer","year":2022,"lang":"en","type":"review","venue":"Hereditary Cancer in Clinical Practice","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; Women's College Hospital; University of Toronto","funders":"Peter Gilgan Foundation; Canada Research Chairs","keywords":"Medicine; Ovarian cancer; Pill; Gynecology; Population; Family planning; Cancer; Hormonal contraception; Obstetrics; Oncology; Internal medicine; Environmental health; Pharmacology; Research methodology","score_opus":0.12658735088645365,"score_gpt":0.47452507511653685,"score_spread":0.3479377242300832,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4281632563","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00004679614,0.9994467,0.000016755264,0.00012519368,0.00007194913,0.0000021384467,0.0000065607055,0.0000014746806,0.00028245538],"genre_scores_gemma":[0.00046665012,0.9991032,0.000058743535,0.00013313416,0.00007639421,0.0000032291045,0.000011383589,5.411439e-7,0.0001467924],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995565,0.00014259496,0.0000711196,0.000052043964,0.00014928341,0.000028448554],"domain_scores_gemma":[0.99937755,0.0004300899,0.0000832165,0.00001104923,0.000079556885,0.000018449055],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00063151726,0.0006244968,0.0014708395,0.0026530721,0.00028206123,0.0008249316,0.00068324053,0.001201081,0.003802646],"category_scores_gemma":[0.0014719934,0.00021941737,0.00085262966,0.0023241674,0.00040475168,0.0009475969,0.00046598085,0.0014182526,0.00082756253],"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":[0.00007558588,0.000064270826,0.00030695953,0.06981033,0.00032473495,0.0001856674,0.000093653354,0.0002474601,0.00042441848,0.0029764606,0.021257933,0.90423244],"study_design_scores_gemma":[0.000048715923,0.00016093704,0.0030021684,0.05382597,0.0006357397,0.0024140452,0.00015653408,0.00012234153,0.00026599347,0.002369349,0.9369703,0.000028021446],"about_ca_topic_score_codex":0.0025327634,"about_ca_topic_score_gemma":0.003944436,"teacher_disagreement_score":0.003802646,"about_ca_system_score_codex":0.0005585792,"about_ca_system_score_gemma":0.0011548756,"threshold_uncertainty_score":0.012721181},"labels":[],"label_agreement":null},{"id":"W4283375173","doi":"10.1186/s13053-022-00229-x","title":"Psychological and health behaviour outcomes following multi-gene panel testing for hereditary breast and ovarian cancer risk: a mini-review of the literature","year":2022,"lang":"en","type":"review","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Princess Margaret Cancer Centre; Women's College Hospital; University of Toronto","funders":"","keywords":"Medicine; Ovarian cancer; Breast cancer; Human genetics; Genetic testing; Oncology; Hereditary Cancer; Bioinformatics; Gene; Cancer; Gynecology; Internal medicine; Genetics","score_opus":0.21115643196130168,"score_gpt":0.507392173409288,"score_spread":0.2962357414479863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283375173","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00081543496,0.99858475,0.000022827862,0.00019240107,0.00005643262,0.000019338515,0.00014711639,0.0000015600517,0.00016021899],"genre_scores_gemma":[0.006087372,0.99327445,0.00008910482,0.00021374667,0.00009035304,0.00005873394,0.00013565551,0.0000012271395,0.000049326663],"study_design_codex":"systematic_review","study_design_gemma":"not_applicable","domain_scores_codex":[0.9982438,0.0005372148,0.0006059231,0.0002170806,0.00031911215,0.00007678254],"domain_scores_gemma":[0.9862255,0.01102296,0.0017885717,0.000088094275,0.0007612812,0.000113652706],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023913477,0.00084476353,0.003832083,0.0056480593,0.00032061417,0.0019227043,0.001202181,0.001381318,0.003886359],"category_scores_gemma":[0.01233273,0.0004748699,0.0029379968,0.0066331434,0.0005691571,0.0014589049,0.0008143321,0.00097483944,0.0003217404],"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":[0.000284756,0.00009397916,0.0050891484,0.66393185,0.0031252878,0.00026395745,0.0006977334,0.00017942952,0.00016801887,0.00042559276,0.0066991705,0.31904104],"study_design_scores_gemma":[0.00010290324,0.00057606905,0.07532518,0.8220972,0.019994667,0.0027908054,0.0019689407,0.000206798,0.0002250595,0.0008614111,0.07573898,0.00011196769],"about_ca_topic_score_codex":0.0052542263,"about_ca_topic_score_gemma":0.009043342,"teacher_disagreement_score":0.0056480593,"about_ca_system_score_codex":0.0015315528,"about_ca_system_score_gemma":0.0028672584,"threshold_uncertainty_score":0.013001204},"labels":[],"label_agreement":null},{"id":"W4298394297","doi":"10.1186/s13053-022-00241-1","title":"Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium","year":2022,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Genetic factors in colorectal cancer","field":"Medicine","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":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Mount Sinai Hospital; Sinai Health System","funders":"National Cancer Institute; Centro de Investigación Biomédica en Red de Cáncer; Manchester Biomedical Research Centre; Support Program for Longyuan Youth and Fundamental Research Funds for the Universities of Gansu Province; Sigrid Juséliuksen Säätiö; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Fundação de Amparo à Pesquisa do Estado de São Paulo; Emil Aaltosen Säätiö; Deutsche Krebshilfe; Kreftforeningen; Conselho Nacional de Desenvolvimento Científico e Tecnológico; Ministerio de Economía y Competitividad; Third Health Programme; Cancer Council NSW; Cancer Research UK; Suomen Lääketieteen Säätiö; Academy of Finland; European Commission; Relander Foundation; Centres de Recerca de Catalunya; Parc Geneteg Cymru; Health and Care Research Wales; Jane ja Aatos Erkon Säätiö; Generalitat de Catalunya; National Institute for Health and Care Research","keywords":"Lynch syndrome; Medicine; DNA mismatch repair; Colorectal cancer; Internal medicine; Cancer; Oncology; Database; General surgery","score_opus":0.05809978887824663,"score_gpt":0.41165231410334663,"score_spread":0.3535525252251,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4298394297","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956001,0.00055862207,0.00014192508,0.000049645518,0.000007161165,0.000013621682,0.0031772086,0.000010203277,0.0004414888],"genre_scores_gemma":[0.99353373,0.00022934943,0.00010689537,0.000016866657,0.00000850989,0.000018039902,0.0060039805,0.0000041931207,0.00007836879],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9978606,0.00069593656,0.00031559364,0.0005183308,0.0004335868,0.00017596569],"domain_scores_gemma":[0.99561536,0.0009511753,0.0018609544,0.00045802662,0.0007404074,0.00037402424],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020643147,0.00028103075,0.0004594618,0.0031213895,0.00020529523,0.00074515824,0.0005091745,0.0004906661,0.00058248267],"category_scores_gemma":[0.005576249,0.00025837764,0.00059385557,0.0028569459,0.00018534182,0.0005566568,0.0010281081,0.00031486514,0.00015382706],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001714078,0.0000065277977,0.99861324,0.000013138087,0.00011682687,0.00002279036,0.000041130217,0.00006410633,0.000068063586,0.000019614841,0.00009736474,0.00076575775],"study_design_scores_gemma":[0.000008538217,0.000040271087,0.9994586,0.0000048274474,0.00003598438,0.00009874696,0.0000801882,0.000109886656,0.000034544377,0.000006336966,0.00011931917,0.0000027487479],"about_ca_topic_score_codex":0.010215556,"about_ca_topic_score_gemma":0.009916797,"teacher_disagreement_score":0.010215556,"about_ca_system_score_codex":0.00044838592,"about_ca_system_score_gemma":0.00035732012,"threshold_uncertainty_score":0.02031219},"labels":[],"label_agreement":null},{"id":"W4380538153","doi":"10.1186/s13053-023-00252-6","title":"Genetic testing for hereditary breast cancer in Poland: 1998–2022","year":2023,"lang":"en","type":"letter","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Public Health Ontario; Women's College Hospital; University of Toronto","funders":"","keywords":"Medicine; Genetic testing; Breast cancer; Ovarian cancer; Cancer; Mutation; Family history; Genetic counseling; Gynecology; Oncology; Human genetics; Internal medicine; Genetics; Gene; Biology","score_opus":0.06430251631606665,"score_gpt":0.405457494591815,"score_spread":0.34115497827574837,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4380538153","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00999054,0.0034824284,0.00026493522,0.95564175,0.016758906,0.00012762299,0.00015520323,0.000044873734,0.0135337245],"genre_scores_gemma":[0.032562386,0.0053704525,0.0006369678,0.91553044,0.018372593,0.00015458262,0.000102601625,0.00003201644,0.02723806],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.998995,0.00020292183,0.00017871124,0.00015834706,0.00027218237,0.00019268252],"domain_scores_gemma":[0.9984315,0.0005339768,0.00020245643,0.00004493828,0.00041830595,0.00036878162],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012789572,0.0006376137,0.00037886517,0.0006384149,0.0030300885,0.0014226388,0.0010753409,0.019275876,0.0020997769],"category_scores_gemma":[0.0074208495,0.00048383986,0.0004637153,0.00068029366,0.0010669586,0.0012742887,0.0010590991,0.010480266,0.0013008087],"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":[0.00023793046,0.00021175218,0.013648847,0.0002138243,0.000032247746,0.05381305,0.0013913215,0.000219806,0.0020884417,0.0035195656,0.88830173,0.03632154],"study_design_scores_gemma":[0.00026218468,0.00026390934,0.026493052,0.0010931235,0.00006310599,0.041486938,0.00169489,0.0014851154,0.00077317486,0.0033039153,0.9230051,0.00007551646],"about_ca_topic_score_codex":0.022358235,"about_ca_topic_score_gemma":0.043065608,"teacher_disagreement_score":0.022358235,"about_ca_system_score_codex":0.005370446,"about_ca_system_score_gemma":0.002648942,"threshold_uncertainty_score":0.044456184},"labels":[],"label_agreement":null},{"id":"W4383873822","doi":"10.1186/s13053-023-00253-5","title":"Meeting abstracts from the Annual Conference “Clinical Genetics of Cancer 2022”","year":2023,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Cancer Genomics and Diagnostics","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; Women's College Hospital; BC Cancer Agency","funders":"HORIZON EUROPE Excellent Science; Narodowe Centrum Badań i Rozwoju","keywords":"Medicine; Human genetics; Cancer genetics; Family medicine; Computational biology; Cancer; Genetics; Internal medicine; Biology; Gene","score_opus":0.0708493497935563,"score_gpt":0.4281884487877879,"score_spread":0.3573390989942316,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4383873822","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.006582204,0.13123976,0.004470116,0.09468759,0.48891288,0.0014546427,0.0064035454,0.0006709261,0.26557833],"genre_scores_gemma":[0.0114118885,0.05707716,0.0019148352,0.015503851,0.24655125,0.0010732998,0.008760193,0.00036002728,0.65734744],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99906343,0.00024357629,0.00009433086,0.00019684873,0.00026117073,0.00014062699],"domain_scores_gemma":[0.9977755,0.00031096188,0.00013881078,0.000086018204,0.00093808194,0.0007505879],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019783804,0.0022168106,0.0011891758,0.0019479545,0.00057856494,0.0021356277,0.0013258702,0.0032533912,0.20866038],"category_scores_gemma":[0.0023645216,0.0003392777,0.00094031385,0.00087273173,0.00036154682,0.0010364368,0.0015817177,0.0022618284,0.10079186],"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":[0.00033087085,0.000060712493,0.00045340462,0.00039112841,0.000026591557,0.00021329345,0.000017133534,0.00005931809,0.0009598686,0.00039675809,0.9299708,0.06712002],"study_design_scores_gemma":[0.00005853534,0.0000850921,0.002021401,0.00035673263,0.000017065455,0.00024374103,0.00002220317,0.000085256186,0.00019239365,0.00032104756,0.9965863,0.000010176962],"about_ca_topic_score_codex":0.00089904154,"about_ca_topic_score_gemma":0.0021309948,"teacher_disagreement_score":0.20866038,"about_ca_system_score_codex":0.0011204168,"about_ca_system_score_gemma":0.0010073641,"threshold_uncertainty_score":0.6980385},"labels":[],"label_agreement":null},{"id":"W4389140174","doi":"10.1186/s13053-023-00271-3","title":"Choices for cancer prevention for women with a BRCA1 mutation? a personal view","year":2023,"lang":"en","type":"letter","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Public Health Ontario; Women's College Hospital; University of Toronto","funders":"","keywords":"Medicine; Breast cancer; Ovarian cancer; Context (archaeology); BRCA mutation; Genetic testing; Cancer prevention; Cancer; Psychological intervention; Gynecology; Mutation; Genetic counseling; Oncology; Family medicine; Bioinformatics; Internal medicine; Gene; Genetics; Psychiatry","score_opus":0.06993272549130715,"score_gpt":0.43911896984108795,"score_spread":0.3691862443497808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389140174","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000090532,0.0016089252,0.000033898516,0.98904335,0.008303716,0.0000028928962,0.0000058762753,0.0000069786824,0.00090383197],"genre_scores_gemma":[0.0012506112,0.0017827201,0.00014178325,0.97665316,0.017541872,0.000012616507,0.000004527636,0.0000072661064,0.0026055023],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99675447,0.0013316388,0.00027351532,0.00042844834,0.00087400625,0.00033782722],"domain_scores_gemma":[0.9909375,0.004612692,0.0005323692,0.00022223615,0.0018157935,0.0018794242],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004135001,0.0007477782,0.001073064,0.000723728,0.004859319,0.003964932,0.002419141,0.040834222,0.008561042],"category_scores_gemma":[0.024027646,0.0005801141,0.0011177614,0.00073481473,0.0047139935,0.0072126794,0.002219357,0.048904378,0.0059577525],"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":[0.000018439216,0.000028045157,0.00030308738,0.000052644988,0.000006467837,0.0011939859,0.00035611595,0.000043894674,0.00007593736,0.0019930124,0.98889905,0.0070293904],"study_design_scores_gemma":[0.0000623607,0.00006124086,0.0006640656,0.00071389385,0.000019725634,0.0060653295,0.0019585267,0.00021003447,0.00009493513,0.010354862,0.97971606,0.000078990706],"about_ca_topic_score_codex":0.0076412046,"about_ca_topic_score_gemma":0.012297038,"teacher_disagreement_score":0.040834222,"about_ca_system_score_codex":0.0050599026,"about_ca_system_score_gemma":0.0052628564,"threshold_uncertainty_score":0.03671229},"labels":[],"label_agreement":null},{"id":"W4396581478","doi":"10.1186/s13053-024-00278-4","title":"Information needs of Lynch syndrome and BRCA 1/2 mutation carriers considering risk-reducing gynecological surgery: a qualitative study of the decision-making process","year":2024,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Juravinski Hospital; Juravinski Cancer Centre; McMaster University","funders":"","keywords":"Medicine; Human genetics; Lynch syndrome; BRCA mutation; Gynecology; Cancer; Internal medicine; Genetics; Breast cancer; Gene; DNA mismatch repair","score_opus":0.038501030879887786,"score_gpt":0.431280714465684,"score_spread":0.39277968358579624,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396581478","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99160516,0.00046123966,0.0013524763,0.0028597948,0.00005433609,0.00022751962,0.00018411312,0.000010044572,0.0032453192],"genre_scores_gemma":[0.9948285,0.000765428,0.0011198363,0.000858233,0.00001892383,0.00027498414,0.00008663239,0.00001547815,0.0020319102],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.9922536,0.005731791,0.00022021493,0.00028180538,0.00047588072,0.0010367327],"domain_scores_gemma":[0.9732944,0.022510963,0.001034492,0.00022627586,0.0012020407,0.0017318806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.012109771,0.00051528064,0.000676544,0.0013985484,0.0067316433,0.0031893025,0.0013133003,0.0016491746,0.0035940977],"category_scores_gemma":[0.020296022,0.00061730744,0.0004328604,0.0014244812,0.0057617733,0.0033837124,0.0036052368,0.002704936,0.00028185613],"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":[0.00003788095,0.000035521676,0.0017253988,0.00010759761,0.000003130921,0.0005495897,0.9941214,0.000029250281,0.0004467342,0.00048041556,0.00027004155,0.0021930148],"study_design_scores_gemma":[0.0000040072055,0.00003642954,0.00052346196,0.000086907385,0.0000024938556,0.00010023442,0.9962225,0.000054907854,0.00011297099,0.0001298402,0.0027201627,0.000006002794],"about_ca_topic_score_codex":0.010556186,"about_ca_topic_score_gemma":0.013096404,"teacher_disagreement_score":0.012109771,"about_ca_system_score_codex":0.0051617334,"about_ca_system_score_gemma":0.0062901997,"threshold_uncertainty_score":0.06404334},"labels":[],"label_agreement":null},{"id":"W4396865901","doi":"10.1186/s13053-024-00277-5","title":"The risk of skin cancer in women who carry BRCA1 or BRCA2 mutations","year":2024,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Cutaneous Melanoma Detection and Management","field":"Medicine","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; Princess Margaret Cancer Centre; University Health Network; University of Toronto; Public Health Ontario; McMaster University; Women's College Hospital","funders":"Canadian Institutes of Health Research; Peter Gilgan Foundation; Women's College Hospital; Canadian Cancer Society; Cleveland Clinic","keywords":"Medicine; Skin cancer; Cancer; Melanoma; Population; Cohort; Germline mutation; Risk factor; Breast cancer; Referral; Dermatology; Prospective cohort study; Oncology; Internal medicine; Gynecology; Mutation; Family medicine; Cancer research; Genetics; Environmental health","score_opus":0.043316628975653436,"score_gpt":0.42073732594227425,"score_spread":0.37742069696662084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396865901","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989152,0.0005155394,0.000029645844,0.000055716675,0.000005785393,0.0000041245485,0.00015244918,0.0000021420701,0.0003193301],"genre_scores_gemma":[0.9992981,0.00029329097,0.000057090085,0.00002504012,0.000009497435,0.0000041441476,0.00013001445,9.732424e-7,0.00018175959],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998429,0.000037548565,0.000009847749,0.000040167488,0.000030039278,0.000039482537],"domain_scores_gemma":[0.99936885,0.00013483713,0.00031957997,0.00003611426,0.000042813146,0.00009785448],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029945667,0.00017822898,0.00016249591,0.0004830695,0.000277604,0.00031444908,0.00019082117,0.0004035562,0.0018134761],"category_scores_gemma":[0.0013625239,0.00020355154,0.00027753942,0.0004596822,0.00014941453,0.00022034947,0.00019218774,0.00033942476,0.00021428578],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008318366,0.000016759206,0.99795,0.000006628897,0.000021887558,0.00012837438,0.000032375985,0.000016775419,0.00017415595,0.0000056694935,0.00006810815,0.0014960014],"study_design_scores_gemma":[0.000006214057,0.00009322352,0.99849486,0.00000758938,0.000026318008,0.00095994945,0.00007474024,0.00005781997,0.000069989466,0.000024172283,0.00018319472,0.0000019768572],"about_ca_topic_score_codex":0.0035033287,"about_ca_topic_score_gemma":0.0038462162,"teacher_disagreement_score":0.0035033287,"about_ca_system_score_codex":0.00013699324,"about_ca_system_score_gemma":0.00016988892,"threshold_uncertainty_score":0.0069658756},"labels":[],"label_agreement":null},{"id":"W4401905534","doi":"10.1186/s13053-024-00285-5","title":"Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional study","year":2024,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Cancer survivorship and care","field":"Medicine","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":"Université Laval; Centre Intégré de Santé et Services Sociaux de Chaudière-Appalache; Hôpital de l'Enfant-Jésus","funders":"Centre Hospitalier Universitaire de Québec; Université Laval","keywords":"Medicine; Breast cancer; Cancer; Anxiety; Quality of life (healthcare); Prophylactic Mastectomy; Internal medicine; Regret; Mastectomy; Population; Cancer prevention; Oncology; Psychiatry","score_opus":0.08787053162047231,"score_gpt":0.48100817835571325,"score_spread":0.39313764673524093,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401905534","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996166,0.000080206,0.000024741013,0.00002338274,0.0000026219823,0.000013966281,0.0000811965,8.868153e-7,0.00015639562],"genre_scores_gemma":[0.9995801,0.00009122725,0.00005790136,0.000043805936,0.000005856788,0.00001680146,0.00011150609,5.467658e-7,0.00009226054],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963033,0.00014009942,0.000042370946,0.00005355883,0.00008187036,0.000051675877],"domain_scores_gemma":[0.9986198,0.0003117279,0.00060806464,0.000079232566,0.00015270378,0.00022848343],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011059933,0.0001756628,0.00028825225,0.00056913326,0.00048095625,0.00046959225,0.00023419989,0.0004534662,0.0012717606],"category_scores_gemma":[0.0022928994,0.00030566612,0.00041403875,0.00045736908,0.00019574953,0.00039582112,0.0003943624,0.0006060009,0.00020413696],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000047632693,0.00012747911,0.99860954,0.000009935334,0.000035432706,0.000041788528,0.00026314944,0.00000963422,0.00007785214,0.000005824617,0.000060386523,0.00071122625],"study_design_scores_gemma":[0.0000067492615,0.0003962007,0.99824584,0.000008049724,0.000029911262,0.00029385797,0.00078187895,0.00006656684,0.000025886335,0.0000074563022,0.00013353021,0.0000041111693],"about_ca_topic_score_codex":0.004139671,"about_ca_topic_score_gemma":0.004431791,"teacher_disagreement_score":0.004139671,"about_ca_system_score_codex":0.0002224365,"about_ca_system_score_gemma":0.00023905648,"threshold_uncertainty_score":0.008231103},"labels":[],"label_agreement":null},{"id":"W4402655020","doi":"10.1186/s13053-024-00291-7","title":"Blood molybdenum level as a marker of cancer risk on BRCA1 carriers","year":2024,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"Metalloenzymes and iron-sulfur proteins","field":"Energy","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":"Women's College Hospital","funders":"","keywords":"Medicine; Ovarian cancer; Internal medicine; Cancer; Confounding; Prospective cohort study; Molybdenum; Population; Breast cancer; Oncology; Incidence (geometry); Gynecology; Environmental health","score_opus":0.0679198805482929,"score_gpt":0.4106302604572704,"score_spread":0.3427103799089775,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402655020","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990778,0.0004878246,0.00005730325,0.000032007196,0.000002896841,0.0000026056493,0.00016729948,0.0000036351923,0.00016862064],"genre_scores_gemma":[0.99937564,0.00017704937,0.0001103544,0.00001030892,0.000005569626,0.000002757783,0.0001427056,0.0000016926178,0.00017396719],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99984455,0.000043215154,0.0000085946995,0.000041898584,0.00003308722,0.000028576549],"domain_scores_gemma":[0.9988626,0.00023394793,0.00066872785,0.000049174192,0.00007024993,0.00011535725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004051883,0.00029361824,0.00025716575,0.000632462,0.0002469045,0.00033878916,0.00026164917,0.00037827983,0.0015480195],"category_scores_gemma":[0.001815732,0.000161798,0.00024834066,0.00055669,0.00014817054,0.00018346171,0.00020169395,0.00037026196,0.00017553389],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00034843976,0.000025000687,0.9966973,0.000012391107,0.000045281755,0.0000716194,0.000031472722,0.000048452897,0.0010497564,0.0000125047145,0.000055774315,0.0016020634],"study_design_scores_gemma":[0.000008240024,0.0001946506,0.9987986,0.0000068475524,0.000059857903,0.000248419,0.000033052227,0.00014411724,0.00034210214,0.000020031292,0.00014186585,0.0000022416048],"about_ca_topic_score_codex":0.0028615734,"about_ca_topic_score_gemma":0.0019543709,"teacher_disagreement_score":0.0028615734,"about_ca_system_score_codex":0.00018078092,"about_ca_system_score_gemma":0.0001883668,"threshold_uncertainty_score":0.0056898},"labels":[],"label_agreement":null},{"id":"W4404379065","doi":"10.1186/s13053-024-00300-9","title":"Breast cancer and ATM mutations: treatment implications","year":2024,"lang":"en","type":"review","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; Women's College Hospital","funders":"","keywords":"Medicine; Breast cancer; Cancer; Genetic testing; Mutation; Oncology; Ovarian cancer; Genetic counseling; BRCA mutation; Germline mutation; Human genetics; Internal medicine; Gynecology; Bioinformatics; Gene; Genetics; Biology","score_opus":0.10916908036121592,"score_gpt":0.501773816522757,"score_spread":0.39260473616154107,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404379065","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000052515825,0.9979145,0.00006005657,0.0006323334,0.000387654,0.0000023753444,0.000012730835,0.000005839055,0.00093189604],"genre_scores_gemma":[0.00037466505,0.9980804,0.00010861793,0.0004736077,0.00030171077,0.000004432332,0.000028708766,0.0000015494064,0.0006262957],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99976605,0.000048678714,0.000030240986,0.000039433107,0.00008889235,0.000026691952],"domain_scores_gemma":[0.99946576,0.00027953903,0.000050100567,0.000016755026,0.00014285329,0.00004504033],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007020808,0.0008679963,0.0014448845,0.002063856,0.00034932882,0.0008892709,0.0012305352,0.0012649406,0.0054091187],"category_scores_gemma":[0.0012648471,0.00023083178,0.0007733333,0.0017983005,0.00050379324,0.0013802141,0.00062753516,0.0028280201,0.002148346],"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":[0.000060034665,0.000057821668,0.00011829775,0.0081336815,0.00006035994,0.00019949302,0.000029207737,0.0003695984,0.0004165118,0.002429778,0.06027332,0.9278519],"study_design_scores_gemma":[0.00001948837,0.0000612432,0.0006303195,0.0056800595,0.00009174143,0.001730443,0.000037577753,0.00006791893,0.00012777574,0.002420067,0.9891201,0.000013150248],"about_ca_topic_score_codex":0.0011973822,"about_ca_topic_score_gemma":0.0026705335,"teacher_disagreement_score":0.0054091187,"about_ca_system_score_codex":0.00082133425,"about_ca_system_score_gemma":0.0010264721,"threshold_uncertainty_score":0.018095315},"labels":[],"label_agreement":null},{"id":"W4409775561","doi":"10.1186/s13053-025-00314-x","title":"Chemotherapy receipt in affected BRCA1/2 and PALB2 carriers with operable breast cancer: the impact of early detection and pre-diagnostic awareness on clinical outcomes and treatment","year":2025,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"McGill University Health Centre; McGill University; Jewish General Hospital","funders":"Fonds de Recherche du Québec - Santé","keywords":"Medicine; PALB2; Breast cancer; Oncology; Internal medicine; Chemotherapy; Stage (stratigraphy); Cancer; Disease; Germline mutation; Mutation","score_opus":0.025525359648531226,"score_gpt":0.41863128959592905,"score_spread":0.3931059299473978,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409775561","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99969494,0.00013808449,0.000009101859,0.0000093162025,9.731016e-7,0.0000017270078,0.000064692176,4.810651e-7,0.00008080394],"genre_scores_gemma":[0.9997874,0.00005125788,0.000013321179,0.0000059444787,0.0000021305248,0.0000017987862,0.00010594578,4.1519314e-7,0.000031725438],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99971205,0.00006934265,0.00004001661,0.00007210399,0.00004881103,0.000057559926],"domain_scores_gemma":[0.9988034,0.00029850478,0.00067797146,0.000034856188,0.000047311147,0.00013796885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003559113,0.000105663064,0.00022141237,0.0004785759,0.00019028265,0.00027948123,0.00019878717,0.00023680454,0.00086108525],"category_scores_gemma":[0.0018027665,0.00012960649,0.00020006401,0.00050982746,0.00015509606,0.00024853108,0.00021961892,0.00022725604,0.00009169454],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015341124,0.000014064781,0.99867743,0.0000040699133,0.0000104969695,0.00009794395,0.000025053892,0.00002216722,0.000096487194,0.0000028001784,0.00002061225,0.0008755905],"study_design_scores_gemma":[0.0000037400582,0.00007082215,0.9993518,0.0000034563302,0.000010922794,0.00032960004,0.000052486543,0.000060108207,0.00006272453,0.000004661565,0.000048550217,9.715809e-7],"about_ca_topic_score_codex":0.003993268,"about_ca_topic_score_gemma":0.005393083,"teacher_disagreement_score":0.003993268,"about_ca_system_score_codex":0.00037732307,"about_ca_system_score_gemma":0.00021957769,"threshold_uncertainty_score":0.007940054},"labels":[],"label_agreement":null},{"id":"W4410507717","doi":"10.1186/s13053-025-00315-w","title":"Knowledge and perceptions of genetic testing for patients with breast cancer in Nigeria: a survey of healthcare providers","year":2025,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Princess Margaret Cancer Centre; University Health Network; University of Toronto; Public Health Ontario","funders":"Princess Margaret Cancer Foundation","keywords":"Medicine; Breast cancer; Genetic testing; Genetic counseling; Family medicine; Health care; Human genetics; Cancer; Nursing; Gynecology; Internal medicine","score_opus":0.04137667275703745,"score_gpt":0.4148555396466104,"score_spread":0.373478866889573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410507717","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99811894,0.00027252838,0.000026069834,0.00067568436,0.000007803993,0.0000136004655,0.00008106148,8.582104e-7,0.0008033333],"genre_scores_gemma":[0.998995,0.00046429914,0.000061089806,0.00029319752,0.000004579892,0.000010936934,0.00003633285,7.143055e-7,0.00013384943],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991918,0.00028534714,0.00009915519,0.00007407905,0.00016479242,0.00018495362],"domain_scores_gemma":[0.9968111,0.0011198327,0.0010354083,0.00005759819,0.0003674314,0.00060870836],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014239989,0.00011553079,0.0002611689,0.00040600647,0.00089599885,0.00071685883,0.00022517961,0.0004552018,0.002147413],"category_scores_gemma":[0.005892261,0.00026117064,0.00017616367,0.00060475204,0.0005518189,0.0005926896,0.00065221486,0.00072445255,0.00016822458],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003495052,0.00011852668,0.9638709,0.00012238363,0.000013255744,0.00044417806,0.026028804,0.00004160781,0.00026425841,0.00008276769,0.0009535397,0.008024769],"study_design_scores_gemma":[0.00001301088,0.00031873348,0.8298952,0.00047656428,0.000026610625,0.0010976754,0.16464189,0.000305952,0.00013173171,0.000090200905,0.0029819862,0.000020397587],"about_ca_topic_score_codex":0.02457059,"about_ca_topic_score_gemma":0.024504198,"teacher_disagreement_score":0.02457059,"about_ca_system_score_codex":0.00086476025,"about_ca_system_score_gemma":0.0015930717,"threshold_uncertainty_score":0.048855126},"labels":[],"label_agreement":null},{"id":"W4413871486","doi":"10.1186/s13053-025-00321-y","title":"Medullary breast cancer and germline BRCA1 mutations: a possible criterion for genetic testing","year":2025,"lang":"en","type":"review","venue":"Hereditary Cancer in Clinical Practice","topic":"BRCA gene mutations in cancer","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":"Public Health Ontario; Women's College Hospital","funders":"","keywords":"Breast cancer; Medicine; Medullary cavity; Oncology; Genetic testing; Cancer; Germline mutation; Medullary carcinoma; Internal medicine; Mutation; Genetic counseling; Male breast cancer; Genetics; Biology; Gene","score_opus":0.08774496049105565,"score_gpt":0.4740090845263608,"score_spread":0.3862641240353052,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413871486","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00015967304,0.99826556,0.00014219014,0.0004344575,0.00021708924,0.000002596556,0.00001540726,0.000005676594,0.00075727026],"genre_scores_gemma":[0.0017829876,0.99661225,0.00030704692,0.0005466126,0.0002543271,0.0000046315813,0.00005283929,0.0000021066528,0.00043718188],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99970776,0.00007211282,0.00005044297,0.000046439978,0.00009851682,0.000024745488],"domain_scores_gemma":[0.99937195,0.00041637273,0.000065020686,0.0000127981075,0.00010761389,0.000026294794],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006086926,0.00054826157,0.0012745344,0.0025631727,0.0002163313,0.00076599926,0.0007601311,0.000980316,0.0020974092],"category_scores_gemma":[0.0015395978,0.00021154321,0.0004970391,0.0016621683,0.0005567969,0.000874117,0.0005234069,0.001455241,0.00092428207],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000076448276,0.000030771345,0.0010772096,0.017825538,0.00016347785,0.0013639684,0.00007383901,0.00023531135,0.0010443835,0.0038054078,0.036608275,0.9376954],"study_design_scores_gemma":[0.000023117802,0.00006813686,0.003008882,0.010235235,0.0003246272,0.019333707,0.00012905234,0.000105658524,0.0006122454,0.0030067926,0.9631207,0.00003180969],"about_ca_topic_score_codex":0.0012815063,"about_ca_topic_score_gemma":0.0022393228,"teacher_disagreement_score":0.0025631727,"about_ca_system_score_codex":0.00054199505,"about_ca_system_score_gemma":0.0011061508,"threshold_uncertainty_score":0.00701648},"labels":[],"label_agreement":null},{"id":"W4416918846","doi":"10.1186/s13053-025-00326-7","title":"Skin cancer risk in hereditary mixed cancer syndromes","year":2025,"lang":"en","type":"article","venue":"Hereditary Cancer in Clinical Practice","topic":"DNA Repair Mechanisms","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; BC Cancer Agency","funders":"","keywords":"Skin cancer; Cancer; Cancer syndrome; Basal cell carcinoma; Li–Fraumeni syndrome; Melanoma; Basal cell; Ovarian cancer; Breast cancer","score_opus":0.03068870075451181,"score_gpt":0.39970959390465366,"score_spread":0.36902089315014186,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416918846","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.027232207,0.96664953,0.00090528623,0.00063551706,0.0001383162,0.000014287942,0.00044095266,0.000018330114,0.003965582],"genre_scores_gemma":[0.22130013,0.7742285,0.0016527371,0.00042233136,0.00021537604,0.00002747849,0.00057247846,0.000007961868,0.0015729555],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997826,0.00006181507,0.000035524128,0.00004809537,0.000055821725,0.000016200524],"domain_scores_gemma":[0.99962807,0.00019654137,0.000105497704,0.00000825209,0.000046420202,0.000015210159],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003036023,0.0002537547,0.00034955653,0.00084253633,0.00013419153,0.00042691705,0.00018447859,0.0002717048,0.0022490998],"category_scores_gemma":[0.0011443851,0.00009216634,0.00050624856,0.00084349466,0.0001307142,0.0002815086,0.00026935665,0.00029123563,0.00018876306],"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":[0.0005266167,0.000055446588,0.093293145,0.026279943,0.0020955359,0.004905182,0.0005784343,0.000690538,0.006352613,0.004016999,0.010617654,0.85058784],"study_design_scores_gemma":[0.00009634063,0.0006775492,0.35665014,0.023323294,0.008855983,0.07879186,0.0014074523,0.00081925775,0.009187405,0.0075063156,0.5125761,0.00010830619],"about_ca_topic_score_codex":0.001071345,"about_ca_topic_score_gemma":0.0018835337,"teacher_disagreement_score":0.0022490998,"about_ca_system_score_codex":0.00020420429,"about_ca_system_score_gemma":0.00035545387,"threshold_uncertainty_score":0.007523954},"labels":[],"label_agreement":null}]}