{"id":"W2986932567","doi":"10.1016/s1474-4422(19)30320-5","title":"Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies","year":2019,"lang":"en","type":"review","venue":"The Lancet Neurology","topic":"Parkinson's Disease Mechanisms and Treatments","field":"Medicine","cited_by":2541,"is_retracted":false,"has_abstract":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"Division of Human Resource Management; National Institute on Aging; Medical Research Council; School of Public Health, University of California Berkeley; Fédération pour la Recherche sur le Cerveau; Norges Forskningsråd; Agence Nationale de la Recherche; Chung Hua University; Obstetric Anaesthetists' Association; Biogen; London Mathematical Society; Parkinson's UK; Novartis; PSP Association; Adrienne Helis Malvin Medical Research Foundation; GE Healthcare; North Carolina GlaxoSmithKline Foundation; National Institutes of Health; Rosetrees Trust; Association France Parkinson; European Commission; Sanofi; Barts Charity; Boehringer Ingelheim; Michael J. Fox Foundation for Parkinson's Research; Roche; Institut de France; Fondation Roger de Spoelberch; H. Lundbeck A/S; Burroughs Wellcome Fund","keywords":"Genome-wide association study; Disease; LRRK2; Genetic association; Single-nucleotide polymorphism; Mendelian randomization; Genetics; Biology; Meta-analysis; Mendelian inheritance; Heritability; Missing heritability problem; Parkinson's disease; Bioinformatics; Medicine; Genotype; Gene; Genetic variants; Internal medicine","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null}