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Plos Genetics|March 23, 2012
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene databaseChristina M Lill, Johannes T Roehr, Matthew B McQueen, et al.
JAMA Neurology|April 17, 2013
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodiesMichael A Nalls, Raquel Duran, Grisel Lopez, et al.
The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.
Annals of Neurology|May 3, 2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's DiseaseDongbing Lai, Babak Alipanahi, Pierre Fontanillas, et al.
Annals of Clinical and Translational Neurology|April 25, 2015
Variants associated with Gaucher disease in multiple system atrophyJun Mitsui, Takashi Matsukawa, Hidenao Sasaki, et al.
The Lancet. Neurology|September 3, 2011
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control studyOwen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
American Journal of Human Genetics|June 10, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxiasPaulina Cunha, Emilien Petit, Marie Coutelier, et al.
Brain : a Journal of Neurology|November 23, 2019
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementiaCornelis Blauwendraat, Xylena Reed, Lynne Krohn, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
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