Associated Papers
Association of LRRK2 p.A419V with Parkinson's Disease in East Asians and analysis of age at onset.
Lim KS et al.
Npj Parkinson's Disease, 2026
41629305 (PubMed )
Supplement: 41531_2026_1265_MOESM2_ESM.xlsx › Supplementary_Table_9
Understanding monogenic Parkinson's disease at a global scale.
Junker J et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.
Li Y et al.
Journal of Human Genetics, 2020
Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.
Benitez BA et al.
Molecular Neurodegeneration, 2016
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.
Foo JN et al.
Human Molecular Genetics, 2014
A case of α-synuclein gene duplication presenting with head-shaking movements.
Itokawa K et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2013
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.
Ross OA et al.
The Lancet. Neurology, 2011
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.
Nuytemans K et al.
Human Mutation, 2010
20506312 (PubMed )
Supplement: humu0031-0763-SD1.pdf
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
Zabetian CP et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2009
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