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Movement Disorders : Official Journal of the Movement Disorder Society|September 3, 2011
Parkinson's disease and α-synuclein expressionMichael J Devine, Katrina Gwinn, Andrew Singleton, et al.Annals of Neurology|October 28, 2006
Genetics of Parkinson's disease and parkinsonismJohn Hardy, Huaiban Cai, Mark R Cookson, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 9, 2002
X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?Virgilio Gerald H Evidente, Katrina Gwinn-Hardy, John Hardy, et al.Journal of Neurology|December 14, 2004
Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity featuresMelissa Hanson, Melissa Honour, Amanda Singleton, et al.Neuron|June 17, 2016
The Evolution of Genetics: Alzheimer's and Parkinson's DiseasesAndrew Singleton, John HardyHuman Molecular Genetics|August 31, 2011
A generalizable hypothesis for the genetic architecture of disease: pleomorphic risk lociAndrew Singleton, John HardyHuman Molecular Genetics|September 14, 2019
Progress in the genetic analysis of Parkinson's diseaseAndrew Singleton, John HardyArchives of Neurology|March 12, 2008
The HapMap: charting a course for genetic discovery in neurological diseasesJohn Hardy, Andrew SingletonMovement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletionOkan Dogu, Janel Johnson, Dena Hernandez, et al.Pageof 94