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Nature|February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populationsMattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.Brain : a Journal of Neurology|May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegiaEleanna Kara, Arianna Tucci, Claudia Manzoni, et al.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.Molecular Neurobiology|November 24, 2016
Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-AmericansJing Dong, Annah Wyss, Jingyun Yang, et al.Science Signaling|February 24, 2026
Temporal proteomic and phosphoproteomic dynamics during neuronal differentiation in the reference iPSC line KOLF2.1JYing Hao, Ziyi Li, Erika Lara, et al.NPJ Parkinson'S Disease|April 2, 2022
Multi-modality machine learning predicting Parkinson's diseaseMary B Makarious, Hampton L Leonard, Dan Vitale, et al.Brain : a Journal of Neurology|October 21, 2017
Clinical, pathological and functional characterization of riboflavin-responsive neuropathyAndreea Manole, Zane Jaunmuktane, Iain Hargreaves, et al.Neurobiology of Aging|March 17, 2018
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3Celeste Sassi, Michael A Nalls, Perry G Ridge, et al.Neurobiology of Aging|September 6, 2016
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositisQiang Gang, Conceição Bettencourt, Pedro M Machado, et al.Acta Neuropathologica|July 1, 2020
Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson diseaseS Bandres-Ciga, S Saez-Atienzar, J J Kim, et al.Pageof 48