Author

An T. Hoang

Whitehead Institute for Biomedical Research

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Assay:ChIP-seq· 3 Research Focus:gene regulatory network inference· 3 Organism:human· 3 Approach:machine learning (classical)· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Research Focus:benchmarking· 1 Approach:experimental assay· 1

Frequent Co-Authors

Deborah C. MashiD· 3 shared Olivia CorradiniD· 3 shared Bibi S. Kassim· 2 shared Bryan C. QuachiD· 2 shared Chesna Apere· 2 shared Chidera OkekeiD· 2 shared Eric Otto JohnsoniD· 2 shared Hannah K. Ramcharan· 2 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Deborah C. MashORCID

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Author profile →

3 papers

Recent·Most cited

Variation in enhancer activity across brain regions defines neurological disease risk and shapes cellular pathology

Hannah K. Ramcharan, Yasmine N. Sami, Kathryn Hazel, Chidera Okeke, Zia Barnard, An T. Hoang, Scott McCallum, Chesna Apere, Wenjuan Du, Megan Madden, Yike Huang, Xochitl Luna, Gesmira Molla, Deborah C. Mash, Olivia Corradin

The paper identifies brain region-specific enhancers linked to neurological disease risk and shows their role in cellular pathology using enhancer activity data and GWAS integration.

bioRxiv · Sep 22, 2026 · PreprintGenetics

Heterogeneous epigenetic variation converges on splicing dysregulation in opioid addiction

Fatir A. Qureshi, Chesna Apere, Chidera Okeke, Bibi S. Kassim, Marina Iskhakova, Richard C. Sallari, Maharshi Chakraborty, Laura Morgan, Zia Barnard, Xochitl Luna, Megan Madden, Pavanna G. Rotti, An T. Hoang, Hannah K. Ramcharan, Bryan C. Quach, , Olivia Corradin

This study identifies epigenetic variation linked to opioid overdose using H3K27ac profiling and machine learning, revealing splicing dysregulation and CELF5 as a key factor.

medRxiv · Dec 29, 2025 · PreprintGenetic & Genomic Medicine

Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid dependence

Olivia Corradin, Richard C. Sallari, An T. Hoang, Bibi S. Kassim, Gabriella Ben Hutta, Lizette Cuoto, Bryan C. Quach, Katreya Lovrenert, Cameron Hays, Berkley E. Gryder, Marina Iskhakova, Hannah M. Cates, Yanwei Song, Cynthia F. Bartels, Dana B. Hancock, , Peter C. Scacheri

The paper identifies case-specific epigenetic alterations in opioid dependence using ChIP-seq and Hi-C, revealing convergent regulatory loci associated with genetic and environmental risk factors.

bioRxiv · Jun 15, 2021 · PreprintGenomics