Sripriya Sarangapani

Chennai, TN, India

Last Updated: 09/26/2026

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Found 10 publications

Genetic analysis of congenital stationary night blindness and Oguchi disease in an Indian cohort.

Genetic analysis of congenital stationary night blindness and Oguchi disease in an Indian cohort.

Journal: Acta ophthalmologica

Published: February 05, 2024

Genetic testing in four Indian families with suspected Stickler syndrome.

Genetic testing in four Indian families with suspected Stickler syndrome.

Journal: Indian journal of ophthalmology

Published: July 06, 2022

Association of HERPUD1 genetic variant rs2217332 with age-related macular degeneration and polypoidal choroidal vasculopathy in an Indian cohort.

Association of HERPUD1 genetic variant rs2217332 with age-related macular degeneration and polypoidal choroidal vasculopathy in an Indian cohort.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: April 09, 2022

Leber hereditary optic neuropathy-new insights and old challenges.

Leber hereditary optic neuropathy-new insights and old challenges.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: June 09, 2020

Screening for mutation hotspots in Bardet-Biedl syndrome patients from India.

Screening for mutation hotspots in Bardet-Biedl syndrome patients from India.

Journal: The Indian journal of medical research

Published: May 29, 2018

IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis.

IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis.

Journal: Human genetics

Published: February 27, 2018

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Journal: Nature genetics

Published: September 30, 2016

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.

Journal: Nature genetics

Published: November 07, 2015

Genetic association of SNPs near ATOH7, CARD10, CDKN2B, CDC7 and SIX1/SIX6 with the endophenotypes of primary open angle glaucoma in Indian population.

Genetic association of SNPs near ATOH7, CARD10, CDKN2B, CDC7 and SIX1/SIX6 with the endophenotypes of primary open angle glaucoma in Indian population.

Journal: PloS one

Published: June 04, 2014

Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma.

Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma.

Journal: Nature genetics

Published: March 24, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026