Publications by authors named "Amritkumar Pavithra"

Claim this Profile
C
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, Chodisetty Sarvani, Jeffrey Justin Margret, Pavithra Amritkumar

Ann Hum Genet· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
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, Hela Azaiez, C R Srikumari Srisailapathy

Adv Genet (Hoboken)· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
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, S Paridhy Vanniya, G Nandhini Devi

Eur Arch Otorhinolaryngol· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India.
Pavithra Amritkumar, Justin Margret Jeffrey, Jayasankaran Chandru, Paridhy Vanniya S, M Kalaimathi

BMC Med Genet· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
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, Justin Margret Jeffrey, Murugesan Kalaimathi

Ann Hum Genet· March 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare compound heterozygosity involving dominant and recessive mutations of GJB2 gene in an assortative mating hearing impaired Indian family.
Amritkumar Pavithra, Jayasankaran Chandru, Justin Margret Jeffrey, N P Karthikeyen, C R Srikumari Srisailapathy

Eur Arch Otorhinolaryngol· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Autosomal dominant hearing loss resulting from p.R75Q mutation in the GJB2 gene: nonsyndromic presentation in a South Indian family.
Amritkumar Pavithra, Mathiyalagan Selvakumari, Venkatesan Nityaa, Narasimhan Sharanya, Rajagopalan Ramakrishnan

Ann Hum Genet· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
High incidence of GJB2 gene mutations among assortatively mating hearing impaired families in Kerala: future implications.
Amritkumar Pavithra, Justin Margret Jeffrey, Jayasankaran Chandru, Arabandi Ramesh, C R Srikumari Srisailapathy

J Genet· April 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis