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Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2009
Expanding the clinical phenotype of SNCA duplication carriersKenya Nishioka, Owen A Ross, Kenji Ishii, et al.Neurologia I Neurochirurgia Polska|February 27, 2025
Screening for PRKN and PINK1 mutations in Ecuadorian patients with early-onset Parkinson's DiseaseTobias M Franz, Rohitha K Punathil, Alexandra I Soto-Beasley, et al.Parkinsonism & Related Disorders|October 28, 2008
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonismOwen A Ross, Cleanthe Spanaki, Alida Griffith, et al.Brain Pathology (Zurich, Switzerland)|April 2, 2020
Clinicopathologic and genetic features of multiple system atrophy with Lewy body diseaseShunsuke Koga, Fuyao Li, Na Zhao, et al.Parkinsonism & Related Disorders|December 14, 2011
First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutationAndreas Puschmann, Elisabet Englund, Owen A Ross, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
LRRK2 variation and Parkinson's disease in African AmericansOwen A Ross, Greggory J Wilhoite, Justin A Bacon, et al.Journal of Alzheimer'S Disease : JAD|July 11, 2022
Polygenic Scores of Alzheimer's Disease Risk Genes Add Only Modestly to APOE in Explaining Variation in Amyloid PET BurdenVijay K Ramanan, Michael G Heckman, Scott A Przybelski, et al.Parkinsonism & Related Disorders|September 18, 2014
Early-onset Parkinson's disease due to PINK1 p.Q456X mutation--clinical and functional studyJoanna Siuda, Barbara Jasinska-Myga, Magdalena Boczarska-Jedynak, et al.Parkinsonism & Related Disorders|April 4, 2016
Tremor in progressive supranuclear palsyShinsuke Fujioka, Avi A Algom, Melissa E Murray, et al.BMC Medical Genetics|December 7, 2016
A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor ticsPatrick R Blackburn, Michael T Zimmermann, Jennifer M Gass, et al.Pageof 49