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Scientific Reports|February 7, 2023
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementiaDouglas P Wightman, Jeanne E Savage, Christiaan A de Leeuw, et al.Neurobiology of Aging|April 12, 2023
The genetic overlap between Alzheimer's disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson's diseaseDouglas P Wightman, Jeanne E Savage, Elleke Tissink, et al.American Journal of Human Genetics|February 13, 2026
Rare-variant aggregation highlights disease-linked genes associated with brain volume variationDouglas P Wightman, Bernardo A P C Maciel, Rachel M Brouwer, et al.Nature Genetics|February 10, 2025
Prioritizing effector genes at trait-associated loci using multimodal evidenceMarijn Schipper, Christiaan A de Leeuw, Bernardo A P C Maciel, et al.Communications Biology|July 16, 2022
Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental healthElleke Tissink, Siemon C de Lange, Jeanne E Savage, et al.Neurobiology of Disease|June 7, 2023
Shared genetic loci between Alzheimer's disease and multiple sclerosis: Crossroads between neurodegeneration and immune systemVera Fominykh, Alexey A Shadrin, Piotr P Jaholkowski, et al.Nature Genetics|September 8, 2021
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's diseaseDouglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genomic analyses reveal new insights into Alzheimer's diseaseEmil Uffelmann, Douglas P Wightman, Shahram Bahrami, et al.Acta Neuropathologica|September 6, 2022
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkersIris E Jansen, Sven J van der Lee, Duber Gomez-Fonseca, et al.Pageof 1