Author

Vinay Jaya Rao

Institute for Stem Cell Biology and Regenerative MedicineORCID 0000-0002-2188-7670Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Developmental Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Approach:statistical model· 3 Organism:human· 2 Research Focus:cell type annotation· 1 Organism:mouse· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Perundurai Subramaniam DhandapanyiD· 3 shared Jayaprakash ShenthariD· 2 shared A. Orioli· 1 shared Abdelrahman SaidiD· 1 shared Adam P GiessiD· 1 shared Afshan SiddiqiD· 1 shared Alex Stuckey· 1 shared Alexander SieghartiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Perundurai Subramaniam DhandapanyORCID

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Author profile →

3 papers

Recent·Most cited

Cell-autonomous Wnt activity promotes transient re-programming and cell cycle re-entry of coronary artery endothelial cells

Bhavnesh Bishnoi, Alfia Nirguni Saini, Vinay Jaya Rao, Omkar Golatkar, Ravindra Kailasrao Zirmire, Shruthi Viswanath, Perundurai Subramaniam Dhandapany, Soumyashree Das

The paper identifies Wnt signaling as essential for coronary artery endothelial cell reprogramming and collateral artery formation in mice, with implications for cardiovascular disease.

bioRxiv · Feb 23, 2026 · PreprintDevelopmental Biology

Clonal hematopoiesis gene variants in South Asian Indians with premature coronary artery disease

Vinay Jaya Rao, Jayaprakash Shenthar, Pradeep Natarajan, Perundurai Subramaniam Dhandapany

The paper investigates the association between clonal hematopoiesis gene variants and premature coronary artery disease in South Asian Indians, finding high prevalence and specific gene variant associations.

medRxiv · Jul 19, 2025 · PreprintGenetic & Genomic Medicine

Whole genome sequencing delineates regulatory and novel genic variants in childhood cardiomyopathy

Robert Lesurf, Abdelrahman Said, Oyediran Akinrinade, Jeroen Breckpot, Kathleen Delfosse, Ting Liu, Roderick Yao, Gabrielle Persad, Fintan McKenna, Ramil R. Noche, Winona Oliveros, Kaia Mattioli, Shreya Shah, Anastasia Miron, Qian Yang, , R. Sultana

This study uses whole-genome sequencing to identify regulatory and novel genic variants contributing to childhood cardiomyopathy.

npj Genomic Medicine · Mar 14, 2022Peer-reviewedGenetic & Genomic Medicine