S Paridhy Vanniya

4PUBLICATIONS
8CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear division
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Publications (4)

|Mar 12, 2025
Clinical Exome Sequencing Identifies, Two Homozygous LOXHD1 Variants in Two Inbred Families With Pre-Lingual Hearing Loss From South India.

Mathuravalli Krishnamoorthy, Chandru Jayasankaran, Sorna Lakshmi

|Aug 10, 2021
PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India.

Paridhy Vanniya S, Jayasankaran Chandru, Justin Margret Jeffrey

|May 18, 2020
Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India.

Jayasankaran Chandru, Justin Margret Jeffrey, Amritkumar Pavithra

|Nov 18, 2017
Recurrence of reported CDH23 mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families - an evaluation.

Paridhy Vanniya S, Jayasankaran Chandru, Amritkumar Pavithra

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Frequent Collaborators

3 joint publications

Jayasankaran Chandru

3 joint publications

C R Srikumari Srisailapathy

2 joint publications

Justin Margret Jeffrey

1 joint publications

Zippora Brownstein