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NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Neurology|August 12, 2004
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodiesJ Johnson, S M Hague, M Hanson, et al.
Plos Genetics|March 17, 2012
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americansRehan Qayyum, Beverly M Snively, Elad Ziv, et al.
Brain : a Journal of Neurology|December 2, 2025
Long-read sequencing identifies FGF14 repeat expansions in Parkinson's diseaseFulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
LRRK2-Associated Parkinsonism With and Without <i>In Vivo</i> Evidence of Alpha-Synuclein AggregatesLana M Chahine, David-Erick Lafontant, Seung Ho Choi, et al.
NPJ Parkinson'S Disease|October 17, 2024
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's diseaseClodagh Towns, Zih-Hua Fang, Manuela M X Tan, et al.
NPJ Dementia|June 22, 2026
Haplotype-resolved DNA methylation at the <i>APOE</i> locus identifies allele-specific epigenetic signatures relevant to Alzheimer's disease riskRylee M Genner, Melissa Meredith, Kensuke Daida, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|September 1, 2020
The Parkinson's Disease Genome-Wide Association Study Locus BrowserFrancis P Grenn, Jonggeol J Kim, Mary B Makarious, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
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