Author

Ashmita Kc

Brigham and Women's HospitalORCID 0000-0002-8831-5124Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:zebrafish· 2 Assay:DNA methylation· 1 Assay:electrophysiology· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Calum A. MacRaeiD· 2 shared Aernout LuttuniD· 1 shared Alex Williams· 1 shared Chris FinckiD· 1 shared Christian MülleriD· 1 shared Dajun QuaniD· 1 shared Daniela PanákováiD· 1 shared Emily PaniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersPhysiology

Calum A. MacRaeORCID

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2 papers

Recent·Most cited

PhysiologybioRxivPreprintApr 23, 2026

Beyond Glycogen Storage: AMPKγ2 Regulates Cardiac Hypertrophy and Electrophysiology via Myosin Interaction

Qianyun Ge, Kusumika Saha, Micah L. Burch…·Wandi Zhu

This study shows PRKAG2 variants cause cardiac hypertrophy and electrical changes in zebrafish, independent of glycogen storage, through AMPKγ2-myosin interactions.

DOI 10.64898/2026.04.20.719766

zebrafishimaging

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Developmental BiologyArteriosclerosis Thrombosis and Vascular BiologyPeer-reviewedFeb 19, 2026

Prdm16 amplifies Notch signaling and suppresses venous lineage specification to prevent arteriovenous malformations during vascular development

Jore Van Wauwe, Pavithra Janarthanan, Sander Craps…·Manu Beerens

This study shows Prdm16 enhances Notch signaling in arterial endothelial cells and suppresses venous fate to prevent arteriovenous malformations in zebrafish and human cells.

DOI 10.1161/atvbaha.125.323552

zebrafishhuman

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