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Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2020
Differences in the Presentation and Progression of Parkinson's Disease by SexHirotaka Iwaki, Cornelis Blauwendraat, Hampton L Leonard, et al.
Nature Communications|September 9, 2024
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genesKurt Farrell, Jack Humphrey, Timothy Chang, et al.
Sleep Advances : a Journal of the Sleep Research Society|February 23, 2026
The North American Prodromal Synucleinopathy study: protocol for a multi-site, longitudinal, observational study of idiopathic/isolated rapid eye movement sleep behavior disorderMiranda M Lim, Lee E Neilson, Jonathan E Elliott, et al.
Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.
Acta Neuropathologica Communications|January 31, 2020
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodiesTatiana Orme, Dena Hernandez, Owen A Ross, et al.
Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.
JAMA Neurology|January 4, 2022
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysisCalwing Liao, Charles-Etienne Castonguay, Karl Heilbron, et al.
The Lancet. Neurology|October 15, 2017
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysisBarbara Schormair, Chen Zhao, Steven Bell, et al.
Neurology|October 19, 2014
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseJessie Theuns, Aline Verstraeten, Kristel Sleegers, et al.
The Journal of Clinical Investigation|June 11, 2026
Biallelic inactivating variants in the chromatin remodeler DMAP1 cause a syndromic neurodevelopmental disorderQin Wang, Andrew K Sobering, Christian Tirrito, et al.
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