Author

Maxwell A. Dippel

Benaroya Research Institute

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

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Genetics· 1 Genomics· 1

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Ching‐Huang HoiD· 2 shared John P. RayiD· 2 shared Adriana Estela Sedeño-CortésiD· 1 shared Andrew B. StergachisiD· 1 shared Arpit Mishra· 1 shared Benjamin J. MalloryiD· 1 shared Carl G. de BoeriD· 1 shared Daniela WitteniD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Ching‐Huang HoORCID

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2 papers

Recent·Most cited

Linking candidate causal autoimmune variants to T cell networks using genetic and epigenetic screens in primary human T cells.

Ching‐Huang Ho, Maxwell A. Dippel, Meghan S. McQuade, LeAnn P. Nguyen, Arpit Mishra, Stephan Pribitzer, Samantha R. Hardy, Harshpreet Chandok, Florence M. Chardon, Troy A. McDiarmid, Hannah A. DeBerg, Jane Hoyt Buckner, Jay Shendure, Carl G. de Boer, Michael H. Guo, , John P. Ray

The paper identifies 545 expression-modulating variants in CD4+ T cells linked to autoimmune diseases and shows they regulate genes in a lymphocyte activation network.

Nature Genetics · Sep 18, 2025Peer-reviewedGenetics

Somatic epimutations cap genetic determinism in the human diploid chromatin epigenome

Mitchell Robert Vollger, Elliott G. Swanson, Shane J. Neph, Benjamin J. Mallory, Danilo Dubocanin, Ching‐Huang Ho, Y. H. Hank Cheng, Jane E. Ranchalis, Katherine M. Munson, Adriana Estela Sedeño-Cortés, Devaraja G. Mudeppa, William E. Fondrie, Stephanie C. Bohaczuk, Maxwell A. Dippel, Yizi Mao, , Andrew B. Stergachis

The paper introduces FIRE to comprehensively map haplotype-selective chromatin accessibility in diploid human genomes, revealing somatic epimutations that contribute to non-genetic chromatin alterations.

bioRxiv · Jun 14, 2024 · PreprintGenomics