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Human Molecular Genetics|July 13, 2016
Identification of genetic modifiers of age-at-onset for familial Parkinson's diseaseErin M Hill-Burns, Owen A Ross, William T Wissemann, et al.Brain : a Journal of Neurology|May 29, 2023
Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body diseaseJon-Anders Tunold, Manuela M X Tan, Shunsuke Koga, et al.Clinical Epigenetics|December 28, 2018
Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarctionCavin K Ward-Caviness, Golareh Agha, Brian H Chen, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseKenya Nishioka, Mounir Kefi, Barbara Jasinska-Myga, et al.Brain Communications|January 11, 2021
Variants in PPP2R2B and IGF2BP3 are associated with higher tau depositionVijay K Ramanan, Xuewei Wang, Scott A Przybelski, et al.Plos One|October 3, 2013
NOTCH3 variants and risk of ischemic strokeOwen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, et al.Acta Neuropathologica Communications|June 1, 2023
Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degenerationShunsuke Koga, Michael A Metrick, Lawrence I Golbe, et al.Molecular Neurodegeneration Advances|June 22, 2026
miRNA family miR-29 inhibits PINK1-PRKN signaling via ATG9ABriana N Markham, Chloe Ramnarine, Songeun Kim, et al.Brain Communications|August 5, 2026
Evaluating MAPT p.A152T as a risk factor for the 3R tauopathy Pick's diseaseNicole Tamvaka, William Scotton, Meredith T Lilley, et al.Neurology. Genetics|May 14, 2021
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor SubtypesIsabel Alfradique-Dunham, Rami Al-Ouran, Rainer von Coelln, et al.Pageof 77