Publications by authors named "Mahalingam Subathra"

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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, Subathra Mahalingam

Ann Hum Genet· May 2025

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Gene Mutation in Type 1 Familial Triglyceridemia Presenting as Recurrent Pancreatitis and Complicated by COVID19.
Dhanasekhar Kesavelu, Soundaram Valliyappan, Sarah Nalliannan, Priyadarshini Pande, Subathra Mahalingam

J Pediatr Genet· December 2024

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Low incidence of variants among the prelingual hearing impaired from southern India.
Murugesan Kalaimathi, Mahalingam Subathra, Justin Margret Jeffrey, Mathiyalagan Selvakumari, Jayasankaran Chandru

J Genet· July 2021

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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, Subathra Mahalingam

Eur Arch Otorhinolaryngol· November 2020

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Infantile spasms: Etiology, lead time and treatment response in a resource limited setting.
Priyanka Surana, Joseph D Symonds, Prabhar Srivastava, Thenral S Geetha, Romit Jain, Subathra Mahalingam

Epilepsy Behav Rep· October 2020

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Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.
Mahalingam Subathra, Arabandi Ramesh, Mathiyalagan Selvakumari, N P Karthikeyen, C R Srikumari Srisailapathy

Ann Hum Genet· September 2016

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Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.
Mahalingam Subathra, Mathiyalagan Selvakumari, Arabandi Ramesh, Rajagopalan Ramakrishnan, Kalpita Rashmi Karan

Ann Hum Genet· May 2014

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