Author

Wenjuan Du

Whitehead Institute for Biomedical ResearchPrimary ORCID profile (0000-0002-0790-9546 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Wenjuan DuiD1 paper · Utrecht University

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1

Frequent Co-Authors

Olivia CorradiniD· 2 shared Xochitl Luna· 2 shared An T. Hoang· 1 shared Bingbing YuaniD· 1 shared Chesna Apere· 1 shared Chidera OkekeiD· 1 shared Deborah C. MashiD· 1 shared Dheeraj MalhotraiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetics

Olivia CorradinORCID

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2 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

Functional genomic dissection of MS risk loci reveals convergence of cis and trans gene regulatory mechanisms in microglia

Michael D. Gallagher, Xochitl Luna, Wenjuan Du, Kathryn E.A. Hazel, Moritz List, Zeynep Aydin, Orian Stapleton, Yiran Cheng, Bingbing Yuan, Keya Viswanathan, Heather R. Keys, George W. Bell, Dheeraj Malhotra, Richard A. Young, Rudolf Jaenisch, Olivia Corradin

The paper identifies cis and trans gene regulatory mechanisms in microglia linked to multiple sclerosis risk SNPs using computational and CRISPR perturbation approaches.

medRxiv · Jun 16, 2025 · PreprintGenetic & Genomic Medicine