Association of whole genome sequencing variants with time to Alzheimer's disease
Our preliminary findings highlight the critical role of APOE in the timing of AD onset, while also identifying potential novel loci associated with the disease. Except for APOE, there was limited overlap between our Cox GWAS results and those from case-control GWAS, suggesting distinct genetic factors influencing AD risk over time. Meta-analysis of the results from the two datasets, along with assessment of rarer variants, are underway. We will also perform multi-ancestral analysis and seek to expand the sample size for black and Hispanic populations.
Authors
- Xueqiu Jian (ORCID: https://orcid.org/0000-0002-0313-6494)
- Habil Zare (ORCID: https://orcid.org/0000-0001-5902-6238)
- Dongyu Wang (ORCID: https://orcid.org/0000-0002-1317-2739)
- Mohsen Sharifi Tabar
- Gina M. Peloso
- Josh C. Bis
- Anita L. DeStefano
- Sudha Seshadri
- Bruce M. Psaty
Institutions
- The University of Texas at San Antonio Health Science Center (US)
- University of Washington (US)
Publication Details
- Journal
- Alzheimer s & Dementia
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1002/alz70855_107062
- Primary Topic
- Genetic Associations and Epidemiology
- Type
- article
- Field-Weighted Citation Impact
- 0.00