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Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.Biorxiv : the Preprint Server for Biology|November 19, 2025
Random forest model improves annotation and discovery of variants of uncertain significance in Alzheimer's and other neurological disordersCaroline Jonson, Mary B Makarious, Mathew J Koretsky, et al.G3 (Bethesda, Md.)|November 20, 2024
GenoTools: an open-source Python package for efficient genotype data quality control and analysisDan Vitale, Mathew J Koretsky, Nicole Kuznetsov, et al.Human Molecular Genetics|July 30, 2011
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of associationAndrew R Wood, Dena G Hernandez, Michael A Nalls, et al.Cell Reports Methods|September 20, 2023
A fully automated FAIMS-DIA mass spectrometry-based proteomic pipelineLuke Reilly, Erika Lara, Daniel Ramos, et al.Patterns (New York, N.Y.)|July 6, 2023
Application of Aligned-UMAP to longitudinal biomedical studiesAnant Dadu, Vipul K Satone, Rachneet Kaur, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.Lancet (London, England)|February 5, 2011
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies, Michael A Nalls, Vincent Plagnol, et al.Pageof 48