Author

Jayaprakash Shenthar

Sri Jayadeva Institute of Cardiovascular Sciences and ResearchORCID 0000-0003-4509-7515Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:database / resource· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Perundurai Subramaniam DhandapanyiD· 3 shared Vinay Jaya RaoiD· 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

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Perundurai Subramaniam DhandapanyORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 19, 2025

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.

1 citation

humanwhole-exome sequencing

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GenomicsbioRxivPreprintJan 30, 2025

Indian Wellderly exomes underscore NRAP roles in elderly hypertrophic cardiomyopathy

Prasanth Chimata, Ankit Sharma, Radhika Agrawal…·Perundurai Subramaniam Dhandapany

The paper identifies NRAP as a gene associated with elderly hypertrophic cardiomyopathy using an Indian Wellderly exome dataset and functional analysis.

DOI 10.1101/789065

humanwhole-exome sequencing

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Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedMar 14, 2022

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

Robert Lesurf, Abdelrahman Said, Oyediran Akinrinade…·R. Sultana

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

46 citationstop 2%

humanwhole-genome sequencing

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