Ellen M. Wijsman
Affiliations: | Biostatistics - Public Health | University of Washington, Seattle, Seattle, WA |
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Biostatistics BiologyGoogle:
"Ellen Wijsman"
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Publications
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| Magalhães Borges V, Horimoto ARVR, Wijsman EM, et al. (2024) Genomic Exploration of Essential Hypertension in African-Brazilian Quilombo Populations: A Comprehensive Approach with Pedigree Analysis and Family-Based Association Studies. Medrxiv : the Preprint Server For Health Sciences |
| Rajabli F, Benchek P, Tosto G, et al. (2023) Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences |
| Horimoto ARVR, Boyken LA, Blue EE, et al. (2023) Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations. Hgg Advances. 4: 100207 |
| Braggin JE, Bucks SA, Course MM, et al. (2019) Alternative splicing in a presenilin 2 variant associated with Alzheimer disease. Annals of Clinical and Translational Neurology. 6: 762-777 |
| Saad M, Wijsman EM. (2019) Association score testing for rare variants and binary traits in family data with shared controls. Briefings in Bioinformatics. 20: 245-253 |
| Beecham GW, Vardarajan B, Blue E, et al. (2018) Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease. Neurology. Genetics. 4: e286 |
| Ullah E, Mall R, Abbas MM, et al. (2018) Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees. Genome Research |
| Chapman NH, Bernier RA, Webb SJ, et al. (2018) Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder. Human Genetics |
| Bis JC, Jian X, Kunkle BW, et al. (2018) Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry |
| Anttila V, Bulik-Sullivan B, et al. (2018) Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360 |