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Acta Neuropathologica Communications|July 14, 2022
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measuresRebecca R Valentino, Chloe Ramnarine, Michael G Heckman, et al.
Acta Neuropathologica|March 9, 2017
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementiaJennifer S Yokoyama, Celeste M Karch, Chun C Fan, et al.
Parkinsonism & Related Disorders|August 14, 2016
LRRK2 variation and dementia with Lewy bodiesMichael G Heckman, Alexandra I Soto-Ortolaza, Monica Y Sanchez Contreras, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
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.
Nature Communications|June 9, 2021
A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speechKeith A Josephs, Joseph R Duffy, Heather M Clark, et al.
JAMA Neurology|August 30, 2016
Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson DiseaseMarie Y Davis, Catherine O Johnson, James B Leverenz, et al.
NPJ Parkinson'S Disease|June 7, 2024
Genome-wide determinants of mortality and motor progression in Parkinson's diseaseManuela M X Tan, Michael A Lawton, Miriam I Pollard, et al.
Neurobiology of Aging|December 29, 2009
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's diseaseRejko Krüger, Manu Sharma, Olaf Riess, et al.
Molecular Neurodegeneration|April 13, 2012
Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implicationsMariet Allen, Fanggeng Zou, High Seng Chai, et al.
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