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Neuroscience Letters|December 1, 2009
Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North AfricaKenya Nishioka, Carles Vilariño-Güell, Stephanie A Cobb, et al.
Human Mutation|May 7, 2014
Genetic screening and functional characterization of PDGFRB mutations associated with basal ganglia calcification of unknown etiologyMonica Sanchez-Contreras, Matthew C Baker, NiCole A Finch, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 13, 2012
Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorderThomas G Schulze, Nirmala Akula, René Breuer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndromeJanel O Johnson, Giovanni Stevanin, Joyce van de Leemput, et al.
Neurology. Genetics|January 31, 2018
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)Mira Mäkelä, Karri Kaivola, Miko Valori, et al.
Biological Psychiatry|July 17, 2012
Alzheimer risk variant CLU and brain function during agingMadhav Thambisetty, Lori L Beason-Held, Yang An, et al.
Neurobiology of Aging|April 7, 2020
Comprehensive assessment of PINK1 variants in Parkinson's diseaseLynne Krohn, Francis P Grenn, Mary B Makarious, et al.
Annals of Neurology|March 17, 2015
Polygenic risk of Parkinson disease is correlated with disease age at onsetValentina Escott-Price, , Mike A Nalls, et al.
Frontiers in Neurology|July 28, 2020
Association Between Glucocerebrosidase Mutations and Parkinson's Disease in IrelandDiana A Olszewska, Allan McCarthy, Alexandra I Soto-Beasley, et al.
Genome Medicine|June 12, 2016
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobeCornelis Blauwendraat, Margherita Francescatto, J Raphael Gibbs, et al.
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