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Acta Neuropathologica|November 1, 2015
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bankKevin F Bieniek, Owen A Ross, Kerry A Cormier, et al.
Archives of Neurology|August 11, 2010
Association of alpha-, beta-, and gamma-Synuclein with diffuse lewy body diseaseKenya Nishioka, Christian Wider, Carles Vilariño-Güell, et al.
Cell Reports|June 21, 2016
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and HumansYubin Wang, Joshua Hersheson, Dulce Lopez, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Neuro-Degenerative Diseases|July 12, 2007
Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutationJanel Johnson, Coro Paisán-Ruíz, Grisel Lopez, et al.
Neurobiology of Disease|June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodiesJoshua T Geiger, Jinhui Ding, Barbara Crain, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Parkinsonism & Related Disorders|June 2, 2007
Lrrk2-associated parkinsonism is a major cause of disease in Northern SpainMaría C González-Fernández, Elena Lezcano, Owen A Ross, et al.
American Journal of Neurodegenerative Disease|December 10, 2013
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16Alexandra I Soto-Ortolaza, Michael G Heckman, Catherine Labbé, et al.
Parkinsonism & Related Disorders|August 24, 2020
Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's diseaseAlexandra I Soto-Beasley, Ronald L Walton, Rebecca R Valentino, et al.
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