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Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
Mov Disord
213
2019
BAG3, FAM47E, GBA, GCH1, INPP5F, MAPT, MCCC1, PD, Parkinson and Movement Disorder, Parkinson's disease, SCARB2, SNCA, TMEM175, genetic loci, protein-coding variant, risk alleles, synuclein
Author NameAffiliation
Lynne KrohnMcGill University
Lynne KrohnMontreal Neurological Institute, McGill University
Alexis BriceInserm U7, Sorbonne Universites, Institut du Cerveau et de la Moelle epiniere
Pentti J TienariHelsinki University Hospital, University of Helsinki
Peter HeutinkHertie Institute for Clinical Brain Research, University of Tubingen
Peter HeutinkGerman Center for Neurodegenerative Diseases (DZNE)
Joshua M ShulmanParkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine
Joshua M ShulmanBaylor College of Medicine
Joshua M ShulmanJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital
Nicholas W WoodUCL Queen Square Institute of Neurology
Nicholas W WoodUCL Queen Square Institute of Neurology
Huw R MorrisUCL Queen Square Institute of Neurology
David A HindsInc.
Peter M VisscherInstitute for Molecular Bioscience, The University of Queensland
Peter M VisscherQueensland Brain Institute, The University of Queensland
Mike A NallsNational Institute on Aging, National Institutes of Health
Mike A Nalls
Mike A NallsNational Institute on Aging, National Institutes of Health
Mike A Nalls
Andrew B SingletonNational Institute on Aging, National Institutes of Health
Andrew B SingletonNational Institute on Aging, National Institutes of Health
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