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Nature Genetics|November 21, 2022
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's diseaseHenne Holstege, Marc Hulsman, Camille Charbonnier, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
APOE stratified genome-wide association studies provide novel insights into the genetic etiology of Alzheimers's diseaseJesper Qvist Thomassen, Leonard Hampton, Brittany Ulms, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 29, 2023
Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypesYann Le Guen, Guo Luo, Aditya Ambati, et al.
Science Translational Medicine|June 3, 2016
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart diseaseRobert A Scott, Daniel F Freitag, Li Li, et al.
Nature Communications|April 21, 2026
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagyJigyasha Timsina, Chenyang Jiang, Daniel L McCartney, et al.
Nature Genetics|April 5, 2011
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's diseasePaul Hollingworth, Denise Harold, Rebecca Sims, et al.
Molecular Psychiatry|December 5, 2024
X-chromosome-wide association study for Alzheimer's diseaseJulie Le Borgne, Lissette Gomez, Sami Heikkinen, et al.
Plos One|June 13, 2014
Gene-wide analysis detects two new susceptibility genes for Alzheimer's diseaseValentina Escott-Price, Céline Bellenguez, Li-San Wang, 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.
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