Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Year: 2011
Type: review
Source: The Lancet
Author: ‡
Language: English
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Funders: U.S. Department of Defense, U.S. Department of Health and Human Services, Massachusetts General Hospital, American Parkinson Disease Association, University of Dundee, Queen Mary University of London, Wellcome Trust, National Institute for Health and Care Research, Parkinson's UK, University College London, European Commission, University of Bristol, Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Universiteit van Amsterdam, Radboud Universiteit, Vrije Universiteit Amsterdam, Eberhard Karls Universität Tübingen, Bundesministerium für Bildung und Forschung, Eisai, Landspítali Háskólasjúkrahús, Centre National de la Recherche Scientifique, Deutsches Zentrum für Neurodegenerative Erkrankungen, Université Pierre et Marie Curie, Hersenstichting, National Institutes of Health, Medical Research Council, National Institute on Aging, National Institute of Neurological Disorders and Stroke, National Institute of Environmental Health Sciences, National Center for Research Resources, Congressionally Directed Medical Research Programs
Awards: G226565915, Verbundprojekt: Nationales Genomforschungsnetz 2: Systematisch-Methodische Plattform GEM: Standort Kiel: PopGen: Populationsrepräsentative Biobank Schleswig-Holstein, G2845388095, Prospective studies on Parkinson's disease, A systematic investigation into the pathogenesis and course of Parkinson's syndrome, G3327757157, Washington University Center for Translational Neuroscience, G3945394334, G4119534169, G4265316335, Verbundprojekt Funktionelle Genomik der Parkinson-Erkrankung : Genomik, funktionelle Analyse und Bioinformatik (Teilprojekt 1, TP2, TP8, TP9, TP10, TP12, TP16), NEURON-Verbund: Identifikation von Genen, die familiäre Formen der Parkinson Erkrankung verursachen, Teilprojekt 1, G4653495942, G4721042799, Dissecting Molecular Genetic Risk Factors in Parkinson's Disease: collaborations with approved protocols with the laboratory of neurogenetics, WTCCC Part Two., ERANET 1 NEURON 3: Identification of copy number variants in familial and pathologically proven PD, G5850682332, Structural MRI marker(s) of Parkinson's Disease's Progression, G6804723138, MECHANISMS OF DEEP BRAIN STIMULATION, Investigations of Dementia in Parkinson Disease, Mentorship Program Patient-Oriented Research on Aging, G7310981802, NIHR Senior Investigator Award, Washington University Institute of Clinical and Translational Sciences (UL1), IAPP on novel genetic and phenotypic markers of Parkinson's disease and Essential Tremor, G8083352728, G8098035348, Identification of copy number variants in familial and pathologically proven PD, REFUND CHECK AND WAS DE-OBLIGATED IN THE AMOUNT OF $28,044., Genome wide SNP analysis in Parkinson's disease, A systematic investigation into the pathogenesis and course of Parkinson's syndrome., G9000060582, G992107779
OpenAlex ID: W2165465283