Author

Sunil Kumar Singh

University of Wisconsin–MadisonORCID 0000-0001-7639-9212Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Organism:mouse· 1 Assay:scATAC-seq· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Elizabeth J. LeslieiD· 3 shared Robert A. CornelliD· 3 shared Azeez ButaliiD· 2 shared Eric Chien-Wei LiaoiD· 2 shared Kaylia Mekelda DuncaniD· 2 shared Kelsey R. Robinson· 2 shared Lord Jephthah Joojo GowansiD· 2 shared Sarah W. CurtisiD· 2 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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3 shared papersDevelopmental Biology

Elizabeth J. LeslieORCID

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3 papers

Recent·Most cited

Developmental BiologybioRxivPreprintApr 30, 2026

Conservation of transcriptional regulatory networks in zebrafish and human periderm facilitates identification of GRHL1 as an orofacial cleft risk gene

Sunil Kumar Singh, Annika Helverson, Colin Kenny…·Robert A. Cornell

The paper identifies GRHL1 as an orofacial cleft risk gene by analyzing conserved transcriptional regulatory networks between zebrafish and human periderm using single-cell multiome sequencing and functional validation.

DOI 10.64898/2026.04.27.720742

zebrafishhuman

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GeneticsbioRxivPreprintFeb 14, 2026

Zfp750 prevents oral adhesions and promotes temporary epithelial fusions

Sunil Kumar Singh, Emily Adelizzi, Caleb S. Heffner…·Robert A. Cornell

The paper investigates the role of Zfp750 in periderm development and orofacial cleft risk by analyzing genetic variants and mouse models.

1 citation

mousestatistical model

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Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedSep 2, 2025

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

Kelsey R. Robinson, Sunil Kumar Singh, Rachel B Walkup…·Elizabeth J. Leslie

The paper identifies rare variants in PRKCI as a novel cause of Van der Woude syndrome and other peridermopathy features through clinical and functional analyses.

4 citations

humanexperimental assay

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