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Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.Cell Genomics|March 23, 2023
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanismElisangela Bressan, Xylena Reed, Vikas Bansal, et al.Nature Genetics|June 21, 2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsyGünter U Höglinger, Nadine M Melhem, Dennis W Dickson, et al.Nature Genetics|November 17, 2009
Genome-wide association study reveals genetic risk underlying Parkinson's diseaseJavier Simón-Sánchez, Claudia Schulte, Jose M Bras, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 30, 2019
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightSara Bandres-Ciga, Sarah Ahmed, Marya S Sabir, et al.Cell Stem Cell|December 2, 2022
A reference human induced pluripotent stem cell line for large-scale collaborative studiesCaroline B Pantazis, Andrian Yang, Erika Lara, et al.JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.Nature|January 22, 2015
Common genetic variants influence human subcortical brain structuresDerrek P Hibar, Jason L Stein, Miguel E Renteria, et al.Nature Neuroscience|November 8, 2016
Novel genetic loci underlying human intracranial volume identified through genome-wide associationHieab H H Adams, Derrek P Hibar, Vincent Chouraki, et al.Nature Communications|January 19, 2017
Novel genetic loci associated with hippocampal volumeDerrek P Hibar, Hieab H H Adams, Neda Jahanshad, et al.Pageof 32