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Jayasankaran Chandru

5PUBLICATIONS

8CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Translation and interpretation studiesEpigenetics (incl. genome methylation and epigenomics)

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Publications (5)

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|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

|Jun 17, 2024

Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High-Throughput Sequencing in a Unique Cohort from South India.

Jeffrey Justin Margret, Chandru Jayasankaran, Pavithra Amritkumar

|Jan 09, 2023

Evaluation of recurrent <i>GNPTAB</i>, <i>GNPTG</i>, and <i>NAGPA</i> variants associated with stuttering.

Nandhini Devi Gunasekaran, Chandru Jayasankaran, Jeffrey Justin Margret

|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

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Frequent Collaborators

5 joint publications

C R Srikumari Srisailapathy

4 joint publications

Justin Margret Jeffrey

3 joint publications

S Paridhy Vanniya

2 joint publications

Pavithra Amritkumar

1 joint publications

Mathuravalli Krishnamoorthy

1 joint publications

Zippora Brownstein

1 joint publications

Karen B Avraham

1 joint publications

Noam Shomron

Frequent Collaborators

5 joint publications

C R Srikumari Srisailapathy

4 joint publications

Justin Margret Jeffrey

3 joint publications

S Paridhy Vanniya

2 joint publications

Pavithra Amritkumar

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