Multi‐omics integration highlights transposable elements as latent regulatory factors involved in the preclinical processes of Alzheimer's disease and related dementias‐ADRD

By integrating genomic and methylation data, we offer novel insights into the role of TEs in AD pathogenesis and their contribution to increased disease risk. Our ongoing work, leveraging ChIP-seq data on DNA accessibility (chromatin state), aims to further characterize these latent regulatory elements and their impact on gene regulation in a context-specific manner.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70855_106069
Primary Topic
Chromosomal and Genetic Variations
Type
article
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article

Multi‐omics integration highlights transposable elements as latent regulatory factors involved in the preclinical processes of Alzheimer's disease and related dementias‐ADRD

Yinan Zheng, Sudha S. Seshadri, Xueqiu Jian, Chakkarai Sathyaseelan et al.
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Chromosomal and Genetic Variations
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Multi‐omics integration highlights transposable elements as latent regulatory factors involved in the preclinical processes of Alzheimer's disease and related dementias‐ADRD

Yinan Zheng, Sudha S. Seshadri, Xueqiu Jian, Chakkarai Sathyaseelan, Habil Zare, Jayandra J. Himali, Qiong Yang, Muralidharan Sargurupremraj
article en

Abstract

By integrating genomic and methylation data, we offer novel insights into the role of TEs in AD pathogenesis and their contribution to increased disease risk. Our ongoing work, leveraging ChIP-seq data on DNA accessibility (chromatin state), aims to further characterize these latent regulatory elements and their impact on gene regulation in a context-specific manner.

Alzheimer s & DementiaVol. 21(S1)
Boston University (US), Northwestern University (US), The University of Texas at San Antonio Health Science Center (US), Institute for Neurodegenerative Disorders (US), Framingham Heart Study (US), The University of Texas at San Antonio (US)
Partnerships for the goals
Openalex Percentile: Top 24%
Chromosomal and Genetic Variations
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