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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 16, 2005
Prion genotypes in Central America suggest selection for the V129 alleleJohn Hardy, Sonja Scholz, Whitney Evans, et al.Alzheimer Disease and Associated Disorders|July 3, 2009
A case of dementia with PRNP D178Ncis-129M and no insomniaRita J Guerreiro, Tina Vaskov, Cynthia Crews, et al.Trends in Neurosciences|March 16, 2010
Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signalingStephanie Schorge, Joyce van de Leemput, 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.Annals of Neurology|April 27, 2005
Torsin A haplotype predisposes to idiopathic dystoniaJordi Clarimon, Hilmir Asgeirsson, Andrew Singleton, et al.Molecular Systems Biology|September 17, 2009
A simple and efficient algorithm for genome-wide homozygosity analysis in diseaseWei Liu, Jinhui Ding, Jesse Raphael Gibbs, et al.Plos One|October 18, 2008
Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3Njideka Okubadejo, Angela Britton, Cynthia Crews, 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.Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2006
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's diseaseHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.Pageof 94