Author

Emily King

Broad Institute

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 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 3 Organism:human· 3 Research Focus:differential expression· 2 Assay:scRNA-seq· 2 Research Focus:variant effect prediction· 2 Assay:ATAC-seq· 1 Approach:deep learning· 1 Approach:experimental assay· 1

Frequent Co-Authors

Vijay G. SankaraniD· 3 shared Alexis CaulieriD· 2 shared Lara WahlsteriD· 2 shared Adam J. de SmithiD· 1 shared Alexandra K. TurveyiD· 1 shared Allison Zhang· 1 shared Anders S. HanseniD· 1 shared Andrew LeeiD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 28 mutual co-author links

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3 shared papersGenomics

Vijay G. SankaranORCID

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Author profile →

3 papers

Recent·Most cited

Single-cell multiomic mapping of genetic predisposition to childhood B-cell acute lymphoblastic leukemia

Andrew Lee, Anna‐Lena Neehus, Lara Wahlster, Gaurav Agarwal, Chen Weng, Allison Zhang, Tanxin Liu, Spencer D. Shelton, Tianyi Ye, Lucrezia della Volpe, Ofir Cohn, Michael Poeschla, Emily King, Samuel A Ha, Alexandra K. Turvey, , Vijay G. Sankaran

The paper uses single-cell multiomic analysis to identify genetic variants and regulatory disruptions linked to childhood B-cell acute lymphoblastic leukemia.

bioRxiv · Aug 7, 2026 · PreprintCancer Biology

Cohesin loading at regulatory elements shapes 3D genome folding during erythropoiesis

V. D. Ramanathan, C. Guo, Masahiro Nagano, Viraat Y. Goel, Clarice KY Hong, Ariel D. Swett, Alexis Caulier, Emily King, Zuzana Tóthová, Vijay G. Sankaran, Anders S. Hansen

The paper identifies 'matchmaker' cis-regulatory elements in erythropoiesis that strengthen loops between neighboring elements and are linked to gene expression and cohesin loading.

bioRxiv · Aug 6, 2026 · PreprintGenomics

Transcription factor networks disproportionately enrich for heritability of blood cell phenotypes

Jorge Diego Martin-Rufino, Alexis Caulier, Seayoung Lee, Nicole Castano, Emily King, Samantha R. Joubran, Marcus Kenneth Jones, Seth Raphael Goldman, Uma P. Arora, Lara Wahlster, Eric S. Lander, Vijay G. Sankaran

The paper identifies TF-sensitive chromatin regions as highly enriched for heritability of blood cell phenotypes, using a novel single-cell multi-omics approach.

Science · Apr 4, 2025Peer-reviewedGenomics