Author

Jeffrey G. Meyer

Mayo Clinic

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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Genomics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Assay:ChIP-seq· 1 Research Focus:eQTL / molecular QTL mapping· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1

Frequent Co-Authors

Mine S. CicekiD· 3 shared Aditya Vijay BhagwateiD· 1 shared Adriana Estela Sedeño-CortésiD· 1 shared Alex L. YenkiniD· 1 shared Amber M. McDonaldiD· 1 shared André M. OliveiraiD· 1 shared Andrew B. StergachisiD· 1 shared Andrew R. MardersteiniD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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3 shared papersGenomics

Mine S. CicekORCID

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Author profile →

3 papers

Recent·Most cited

Multi-omics in the All Of Us Research Program expands mapping genetic mechanisms in health and disease

Evin M. Padhi, Elizabeth A. Kiernan, J. Nguyen, Marianne K. DeGorter, Victoria Silva Rosa, Yulia Mostovoy, Alex L. Yenkin, Hang Su, Lee Lichtenstein, Andrew R. Marderstein, Joshua Gillard, Wail Ba-Alawi, Sophie Parsa, Mine S. Cicek, Jeffrey G. Meyer, , Stephen B. Montgomery

The paper reports on the All of Us multi-omics cohort, identifying 182,246 QTLs and demonstrating rare variant effects across proteomic and transcriptomic data.

medRxiv · Nov 1, 2026 · PreprintGenetic & Genomic Medicine

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

Impact of RNA Extraction and Target Capture Methods on RNA Sequencing Using Formalin-Fixed, Paraffin Embedded Tissues

Christopher A. Hilker, Aditya Vijay Bhagwate, Jin Sung Jang, Jeffrey G. Meyer, Asha Nair, Jaime I Davila, Amber M. McDonald, Jennifer L. Winters, Rebecca N. Wehrs, Rory A. Jackson, Joshua A. Gorman, Mine S. Cicek, André M. Oliveira, E. Aubrey Thompson, Bruce W. Eckloff, , Jin Jen

This study evaluates RNA extraction and capture methods for RNA-seq from FFPE tissues, finding high correlation in gene expression profiles with sufficient RNA quality and demonstrating improved fusion detection with TruSeq RNA Access.

bioRxiv · May 31, 2019 · PreprintGenomics