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Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.Parkinsonism & Related Disorders|November 15, 2020
Association of mitochondrial genomic background with risk of Multiple System AtrophyRebecca R Valentino, Michael G Heckman, Patrick W Johnson, et al.Annals of Neurology|January 27, 2006
Lrrk2 and Lewy body diseaseOwen A Ross, Mathias Toft, Andrew J Whittle, et al.Acta Neuropathologica|May 2, 2025
Widespread distribution of α-synuclein oligomers in LRRK2-related Parkinson's diseaseHiroaki Sekiya, Lukas Franke, Yuki Hashimoto, et al.Biorxiv : the Preprint Server for Biology|January 7, 2025
Widespread Distribution of α-Synuclein Oligomers in LRRK2-related Parkinson's DiseaseHiroaki Sekiya, Lukas Franke, Yuki Hashimoto, et al.Parkinsonism & Related Disorders|April 3, 2007
Identification of potential protein interactors of Lrrk2Justus C Dächsel, Julie P Taylor, Su San Mok, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 2, 2017
Establishing diagnostic criteria for Perry syndromeTakayasu Mishima, Shinsuke Fujioka, Hiroyuki Tomiyama, et al.Neurologia I Neurochirurgia Polska|July 21, 2020
Spinocerebellar ataxia type 6 family with phenotypic overlap with Multiple System AtrophyRana Hanna Al-Shaikh, Anna I Wernick, Audrey J Strongosky, et al.Journal of Alzheimer'S Disease & Parkinsonism|July 21, 2025
A Blood Screening Test for Dementia with Lewy Bodies for Primary CareMelissa Petersen, Tanis J Ferman, Fan Zhang, et al.The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|October 2, 2019
CLEC3B p.S106G Mutant in a Caucasian Population of Successful Neurological AgingAna Kolicheski, Ronald L Walton, Alexandra I Soto-Beasley, et al.Pageof 77