Author

Marja G. Brolinson

National Institutes of HealthORCID 0000-0002-8815-3364Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Alan H. DeCherneyiD· 1 shared Alexandra M. PochiD· 1 shared Briana YoungiD· 1 shared Dawn E. Watkins‐ChowiD· 1 shared Donald F. ConradiD· 1 shared Francesco John DeMayoiD· 1 shared Kenneth Ivan AstoniD· 1 shared M. Blake EvansiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenomics

Alan H. DeCherneyORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintSep 15, 2026

PRDM9-mediated meiotic hotspot specification is constrained in humans despite extensive sequence diversity

Rachel L. Cosby, Marja G. Brolinson, Alexandra M. Poch…·Todd S. Macfarlan

The paper functionally characterizes human PRDM9 alleles to show that despite sequence diversity, most alleles function similarly, while rare variants show extreme DNA binding effects.

DOI 10.64898/2026.09.10.750150

humanDNA methylation

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GenomicsEndocrinologyPeer-reviewedJul 27, 2022

The estrogen receptor α cistrome in human endometrium and epithelial organoids

Sylvia C. Hewitt, San‐Pin Wu, Tianyuan Wang…·Francesco John DeMayo

The paper integrates ESR1 cistrome and transcriptome data from endometrial biopsies and organoids to identify estrogen-regulated genes and their functional roles in endometrial health.

26 citations

humanChIP-seq

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