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The Lancet. Neurology|May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association studyCyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.Molecular Psychiatry|December 5, 2024
X-chromosome-wide association study for Alzheimer's diseaseJulie Le Borgne, Lissette Gomez, Sami Heikkinen, et al.The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.Nature Genetics|June 18, 2025
Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populationsAude Nicolas, Richard Sherva, Benjamin Grenier-Boley, et al.Nature Communications|June 8, 2021
Common variants in Alzheimer's disease and risk stratification by polygenic risk scoresItziar de Rojas, Sonia Moreno-Grau, Niccolo Tesi, et al.Nature Genetics|April 5, 2022
New insights into the genetic etiology of Alzheimer's disease and related dementiasCéline Bellenguez, Fahri Küçükali, Iris E Jansen, et al.Pageof 9