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Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.Science Translational Medicine|August 17, 2018
Finding useful biomarkers for Parkinson's diseaseAlice S Chen-Plotkin, Roger Albin, Roy Alcalay, et al.Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.Biorxiv : the Preprint Server for Biology|January 7, 2025
Long-read sequencing of hundreds of diverse brains provides insight into the impact of structural variation on gene expression and DNA methylationKimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.Biorxiv : the Preprint Server for Biology|October 1, 2025
A Common PD-Risk GBA1 Variant Disrupts LIMP2 Interaction, Impairs Glucocerebrosidase Function, and Drives Lysosomal and Mitochondrial DysfunctionOliver B Davis, Jennifer E Kung, Sonnet S Davis, et al.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.Cell Reports|June 9, 2021
An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of α-synucleinEleanna Kara, Alessandro Crimi, Anne Wiedmer, 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.Pageof 39