Author

C. R. Srikumari Srisailapathy

University of MadrasORCID 0000-0002-1315-5090Unclaimed 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:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Jayasankaran ChandruiD· 1 shared Jeffrey Justin MargretiD· 1 shared Karen B. AvrahamiD· 1 shared Le ChengiD· 1 shared Mathuravalli KrishnamoorthyiD· 1 shared Noam ShomroniD· 1 shared Paridhy Vanniya SubramanyamiD· 1 shared Tom RabinowitziD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Jayasankaran ChandruORCID

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1 paper

Recent·Most cited

GeneticsAnnals of Human GeneticsPeer-reviewedAug 9, 2021

Genetic and phenotypic heterogeneity in PNPT1, MYO15A, PTPRQ and SLC12A2 variants detected among hearing impaired assortative mating families in Southern India

Paridhy Vanniya Subramanyam, Jayasankaran Chandru, Jeffrey Justin Margret…·C. R. Srikumari Srisailapathy

The paper identifies six variants in four genes associated with hearing loss in four South Indian families, highlighting genetic and phenotypic heterogeneity.

13 citations

humanwhole-exome sequencing

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