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Plos One|September 7, 2012
Creation of an open-access, mutation-defined fibroblast resource for neurological disease researchSelina Wray, Matthew Self, , et al.Brain : a Journal of Neurology|November 23, 2019
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementiaCornelis Blauwendraat, Xylena Reed, Lynne Krohn, 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.Medrxiv : the Preprint Server for Health Sciences|August 16, 2024
PSMF1 variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathwaysFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.Nature Communications|April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethalityFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.Neurology|September 18, 2020
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, 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 39