Combining xQTL and genome‐wide association studies from ethnically diverse populations improves druggable gene discovery

Our findings underscore the power and efficiency of gene-based association testing, integrating multi-omic information as a strategic and efficient tool for informed drug target discovery and validation based on human genetic and genomic data for AD and AD-related dementia if broadly applied. These findings additionally highlight the limitations of standard inference based on detecting disease-associated SNPs in GWAS, for which there is generally significantly less power than in gene-based testing.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70859_103217
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00
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article

Combining xQTL and genome‐wide association studies from ethnically diverse populations improves druggable gene discovery

Yuan Hou, Xin Chen, William Robert Martin, Jielin Xu et al.
Alzheimer s & Dementia
Genetic Associations and Epidemiology
article

Combining xQTL and genome‐wide association studies from ethnically diverse populations improves druggable gene discovery

Yuan Hou, Xin Chen, William Robert Martin, Jielin Xu, Andrew A. Pieper, Noah J Lorincz‐Comi, Isabela Rivera Paz, Jonathan L Haines, Chung Mina, Feixiong Cheng, Wenqiang Song, Yadi Zhou
article en

Abstract

Our findings underscore the power and efficiency of gene-based association testing, integrating multi-omic information as a strategic and efficient tool for informed drug target discovery and validation based on human genetic and genomic data for AD and AD-related dementia if broadly applied. These findings additionally highlight the limitations of standard inference based on detecting disease-associated SNPs in GWAS, for which there is generally significantly less power than in gene-based testing.

Alzheimer s & DementiaVol. 21(S5)
Cleveland Clinic (US), Case Western Reserve University (US)
Openalex Percentile: Top 25%
Genetic Associations and Epidemiology
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