Showing results (281-290 of 761) with videos related to

Sort By:
Pageof 77
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Neurology. Genetics|January 22, 2024
Machine Learning Models of Polygenic Risk for Enhanced Prediction of Alzheimer Disease EndophenotypesNathaniel B Gunter, Robel K Gebre, Jonathan Graff-Radford, et al.
Parkinsonism & Related Disorders|December 10, 2023
Genetics of Parkinson's disease heterogeneity: A genome-wide association study of clinical subtypesJarosław Dulski, Ryan J Uitti, Alexandra Beasley, et al.
Acta Neuropathologica Communications|September 18, 2020
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measuresRebecca R Valentino, Nikoleta Tamvaka, Michael G Heckman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutationsCoro Paisán-Ruiz, Rocio Guevara, Monica Federoff, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 20, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literatureCaroline Jonson, Kristin S Levine, Julie Lake, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literatureCaroline Jonson, Kristin S Levine, Julie Lake, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Parkinsonism & Related Disorders|April 13, 2011
Human leukocyte antigen variation and Parkinson's diseaseAndreas Puschmann, Christophe Verbeeck, Michael G Heckman, et al.
Brain : a Journal of Neurology|June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron diseaseJanel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
Pageof 77