Author

Kyunghee Choi

Washington University in St. LouisORCID 0000-0002-9634-9375Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:gene regulatory network inference· 2 Organism:mouse· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Andrew Daniel HoffmanniD· 1 shared Brian L. BlackiD· 1 shared Chul KimiD· 1 shared Erika Hanson· 1 shared Haiyong Zhao· 1 shared Ivan P. G. MoskowitziD· 1 shared Jeffrey D. SteimleiD· 1 shared John M. CunninghamiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperDevelopmental Biology

Andrew Daniel HoffmannORCID

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2 papers

Recent·Most cited

ETV2 primes hematoendothelial gene enhancers prior to hematoendothelial fate commitment

Jeffrey D. Steimle, Chul Kim, Megan Rowton, Rangarajan D. Nadadur, Zhezhen Wang, Matthew Stocker, Andrew Daniel Hoffmann, Erika Hanson, Junghun Kweon, Tanvi Sinha, Kyunghee Choi, Brian L. Black, John M. Cunningham, Ivan P. G. Moskowitz, Kohta Ikegami

This paper identifies sequential phases of ETV2-dependent gene expression that drive hematoendothelial fate commitment from mesoderm progenitors.

Cell Reports · Jun 1, 2023Peer-reviewedDevelopmental Biology

Continuous single cell transcriptome dynamics reveal a default vascular smooth muscle fate of FLK1 mesoderm

Haiyong Zhao, Kyunghee Choi

The paper uses scRNA-seq to study FLK1 mesoderm development, finding that vascular smooth muscle is the default fate and hemangiogenic progenitors share a close transcriptional program.

bioRxiv · Jun 3, 2019 · PreprintDevelopmental Biology