Author

Vrisha Madhuri

Christian Medical College, VelloreORCID 0000-0003-4494-222XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Organism:zebrafish· 1

Frequent Co-Authors

Aarti SevilimeduiD· 1 shared Agnes SelinaiD· 1 shared Alka V. Ekbote· 1 shared Ashis KumariD· 1 shared Gandham SriLakshmi BhavaniiD· 1 shared Hitesh Hasmukhlal ShahiD· 1 shared Katta M. GirishaiD· 1 shared Mir Tariq AltafiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aarti SevilimeduORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJun 11, 2025

An iPSC-based iMSC Model for Osteogenesis Imperfecta: A Platform for Disease Modeling and Drug Screening

Ashis Kumar, Vignesh Kumar, Agnes Selina…·Vasanth Thamodaran

This paper develops an iPSC-derived iMSC model of Osteogenesis Imperfecta that recapitulates disease phenotypes and enables drug screening.

DOI 10.1101/2025.06.11.659155

humanexperimental assay

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Genetic & Genomic MedicinemedRxivPreprintApr 5, 2024

Biallelic Variants in CCN2 Underlie an Autosomal Recessive Kyphomelic Dysplasia

Swati Singh, Sumita Danda, Neetu Sharma…·Katta M. Girisha

This study identifies biallelic CCN2 variants as the cause of autosomal recessive kyphomelic dysplasia through clinical, genetic, and zebrafish model analyses.

2 citations

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