{"id":"W2340656051","doi":"10.1126/science.aap8757","title":"Analysis of shared heritability in common disorders of the brain","year":2018,"lang":"en","type":"article","venue":"Science","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2028,"is_retracted":false,"has_abstract":true,"ca_institutions":"Sunnybrook Health Science Centre; University of Calgary; BC Mental Health & Substance Use Services; Montreal Neurological Institute and Hospital; Dalhousie University; University of Toronto; SickKids Foundation; Douglas Mental Health University Institute; McGill University; Centre Hospitalier de l’Université de Montréal; University of British Columbia; Hospital for Sick Children; University Health Network; Occupational Cancer Research Centre","funders":"National Institute of Mental Health; Institute of Zoology, Chinese Academy of Sciences; Menzies Centre for Australian Studies, King's College London, University of London; NIHR Maudsley Biomedical Research Centre; State University of New York Upstate Medical University; National Institutes of Health; Novo Nordisk Fonden; Universitätsklinikum Jena; Lee Kong Chian School of Medicine, Nanyang Technological University; State University of New York; Lundbeckfonden; Chinese University of Hong Kong; Virginia Commonwealth University; Vetenskapsrådet; Agence Nationale de la Recherche; Universiteit Maastricht; National Center for Advancing Translational Sciences; Medical Research Council; University of Wollongong; Oxford Health NHS Foundation Trust; Nanyang Technological University; Uniklinikum Giessen und Marburg; King's College London; National Institute of Neurological Disorders and Stroke; Syracuse University; Kunming Institute of Zoology, Chinese Academy of Sciences; NSW Health Pathology; National University of Singapore; Wellcome Trust; University College London; University of California, Santa Barbara; Royal College of Surgeons in Ireland; Chinese Academy of Sciences; University of Oxford; Lawrence Berkeley National Laboratory; Motor Neurone Disease Association; University of North Carolina at Chapel Hill; Parkinson's UK; NorthShore University HealthSystem; National Institute on Aging; National Institute for Health and Care Research","keywords":"Heritability; Genome-wide association study; Missing heritability problem; Etiology; Genetic association; Comorbidity; Twin study; Epidemiology; Psychiatry; Phenotype; Medicine; Clinical psychology; Psychology; Biology; Genetics; Genetic variants; Single-nucleotide polymorphism; Internal medicine; Genotype","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.01036892081720274,"score_gpt":0.2946172120931,"score_spread":0.2842482912758972,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}