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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.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, 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.
Nature Structural & Molecular Biology|December 12, 2024
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1Pilar Álvarez Jerez, Peter Wild Crea, Daniel M Ramos, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Pathology and genetics in a global cohort of Parkinsonian DisordersLesley Y Wu, Tessa du Toit, Tatiana Georgiades, et al.
American Journal of Human Genetics|April 16, 2019
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain MalformationLong Guo, Débora Romeo Bertola, Asako Takanohashi, et al.
NPJ Parkinson'S Disease|June 7, 2024
Genome-wide determinants of mortality and motor progression in Parkinson's diseaseManuela M X Tan, Michael A Lawton, Miriam I Pollard, et al.
The Lancet. Neurology|March 28, 2016
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association dataKin Y Mok, Una Sheerin, Javier Simón-Sánchez, et al.
The Lancet. Neurology|August 15, 2015
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling studyMike A Nalls, Cory Y McLean, Jacqueline Rick, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohortLara M Lange, Catalina Cerquera-Cleves, Ai Huey Tan, et al.
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