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Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2)Sarah Furtado, Haydeh Payami, Paul J Lockhart, et al.The Lancet. Neurology|October 21, 2006
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of dataHon-Chung Fung, Sonja Scholz, Mar Matarin, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2015
The NINDS Parkinson's disease biomarkers programLiana S Rosenthal, Daniel Drake, Roy N Alcalay, et al.Plos One|December 7, 2007
Amyotrophic lateral sclerosis: an emerging era of collaborative gene discoveryKatrina Gwinn, Roderick A Corriveau, Hiroshi Mitsumoto, et al.Plos Genetics|June 26, 2007
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humansJoyce van de Leemput, Jayanth Chandran, Melanie A Knight, et al.Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|June 25, 2003
Hereditary dysautonomias: current knowledge and collaborations for the futureMath P Cuajungco, Yukio Ando, Felicia B Axelrod, et al.Archives of Neurology|December 15, 2004
Analysis of the PINK1 gene in a large cohort of cases with Parkinson diseaseEkaterina Rogaeva, Janel Johnson, Anthony E Lang, et al.Parkinsonism & Related Disorders|October 23, 2016
Knowledge gaps and research recommendations for essential tremorFranziska Hopfner, Dietrich Haubenberger, Wendy R Galpern, et al.Biomarkers in Medicine|June 24, 2017
Parkinson's disease biomarkers: perspective from the NINDS Parkinson's Disease Biomarkers ProgramKatrina Gwinn, Karen K David, Christine Swanson-Fischer, et al.Science Translational Medicine|August 17, 2018
Finding useful biomarkers for Parkinson's diseaseAlice S Chen-Plotkin, Roger Albin, Roy Alcalay, et al.Pageof 7