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Human Molecular Genetics|May 6, 2014
Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associationsRita Guerreiro, José Brás, John Hardy, et al.Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|February 18, 2015
Multiple system atrophy: the application of genetics in understanding etiologyMonica Federoff, Lucia V Schottlaender, Henry Houlden, et al.Medical Education|October 1, 2008
Learning not to take it seriously: junior doctors' accounts of errorLeanda Kroll, Andrew Singleton, Joe Collier, et al.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.The FEBS Journal|November 22, 2008
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body diseaseJose Bras, Andrew Singleton, Mark R Cookson, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 31, 2012
DYT16: the original casesSarah Camargos, Andrew J Lees, Andrew Singleton, et al.Human Mutation|December 19, 2009
A thorough assessment of benign genetic variability in GRN and MAPTRita J Guerreiro, Nicole Washecka, John Hardy, et al.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.Neuroscience Letters|August 28, 2004
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish populationJordi Clarimon, Johanna Eerola, Olli Hellström, 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.Pageof 27