C R Srikumari Srisailapathy

6PUBLICATIONS
9CO-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 (6)

|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 GNPTAB, GNPTG, and NAGPA variants associated with stuttering.

Nandhini Devi Gunasekaran, Chandru Jayasankaran, Jeffrey Justin Margret

|Jan 09, 2023
FMR1 gene CGG repeat distribution among the three individual cohorts with intellectual disability, autism, and primary ovarian insufficiency from Tamil Nadu, Southern India.

Indhumathi Nagarathinam, Samuel S Chong, Thelma B K

|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

Jayasankaran Chandru

5 joint publications

Justin Margret Jeffrey

3 joint publications

S Paridhy Vanniya

2 joint publications

Pavithra Amritkumar