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Stroke|January 31, 2013
Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhageChristopher D Anderson, Alessandro Biffi, Michael A Nalls, et al.Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.Annals of Neurology|May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophySonja W Scholz, Henry Houlden, Claudia Schulte, et al.Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.Annals of Neurology|April 26, 2021
Investigation of Autosomal Genetic Sex Differences in Parkinson's DiseaseCornelis Blauwendraat, Hirotaka Iwaki, Mary B Makarious, et al.Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
PD GENEration: An International Parkinson's Disease Genetic Research StudyKamalini Ghosh Galvelis, Allison A Dilliott, Megan Dini, et al.Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in <i>GBA1</i>Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.Human Molecular Genetics|March 1, 2013
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT NetworkZhao Chen, Hua Tang, Rehan Qayyum, et al.JAMA Neurology|June 8, 2026
Pathology and Genetics in a Global Cohort of Parkinsonian DisordersLesley Y Wu, Tessa du Toit, Tatiana Georgiades, et al.Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.Pageof 48