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Analysis of common and rare variants in late-onset Parkinson disease. Neurol Genet. 2020;6(1):385..
Common and rare GCH1 variants are associated with Parkinson's disease. Neurobiol Aging. 2019;73:231.e1-231.e6..
SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease. Mov Disord. 2019;34(4):526-535..
Association study of essential tremor genetic loci in Parkinson's disease. Neurobiol Aging. 2018;66:178.e13-178.e15..
Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Mov Disord. 2018;33(6):1016-1020..
Sequencing of the GBA coactivator, Saposin C, in Parkinson disease. Neurobiol Aging. 2018;..
TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects. J Mol Neurosci. 2018;64(3):341-345..
The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder. Neurobiol Aging. 2017;49:218.e13-218.e15..
Measurement of narcolepsy symptoms: The Narcolepsy Severity Scale. Neurology. 2017;88(14):1358-1365..
RIC3 variants are not associated with Parkinson's disease in French-Canadians and French. Neurobiol Aging. 2017;53:194.e9-194.e11..
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease. Neurobiol Aging. 2016;45:212.e13-212.e17..
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder. Neurobiol Aging. 2016;43:180.e7-180.e13..