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JAMA Neurology|July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson DiseaseCornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Brain : a Journal of Neurology|September 8, 2022
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 lociMarc P M Soutar, Daniela Melandri, Benjamin O'Callaghan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.
JAMA Neurology|August 8, 2013
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic riskValentina Moskvina, Denise Harold, GianCarlo Russo, et al.
Neurobiology of Aging|December 3, 2014
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesMike A Nalls, Jose Bras, Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 28, 2020
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's DiseaseManuela M X Tan, Michael A Lawton, Edwin Jabbari, et al.
Human Molecular Genetics|June 11, 2010
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individualsJason J Corneveaux, Amanda J Myers, April N Allen, et al.
Biorxiv : the Preprint Server for Biology|April 29, 2026
The complete genome of the KOLF2.1J reference iPSC linePilar Alvarez Jerez, Arang Rhie, Juhyun Kim, et al.
Neurobiology of Aging|June 13, 2016
ABCA7 p.G215S as potential protective factor for Alzheimer's diseaseCeleste Sassi, Michael A Nalls, Perry G Ridge, et al.
Human Molecular Genetics|February 4, 2017
A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smokingTianxiao Huan, Roby Joehanes, Claudia Schurmann, et al.
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