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Sripriya Sarangapani

Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma
2012 · Eranga N Vithana, Chiea-Chuen Khor, et al. · Nature Genetics · 243
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
2016 · Chiea Chuen Khor, Tan Do, et al. · Nature Genetics · 187
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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
2017 · Tin Aung, Mineo Ozaki, et al. · Nature Genetics · 156
Leber hereditary optic neuropathy—new insights and old challenges
2020 · Srilekha Sundaramurthy, Ambika SelvaKumar, et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 52
Genetic Association of SNPs near ATOH7, CARD10, CDKN2B, CDC7 and SIX1/SIX6 with the Endophenotypes of Primary Open Angle Glaucoma in Indian Population
2015 · Ferdinamarie Sharmila Philomenadin, Rashima Asokan, et al. · PLoS ONE · 34
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Screening for mutation hotspots in Bardet–Biedl syndrome patients from India
2018 · Sathya Priya Chandrasekar, Sheela Namboothiri, et al. · The Indian Journal of Medical Research · 23
IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis
2018 · Anil Chekuri, Aditya A. Guru, et al. · Human Genetics · 22
Genetic testing in four Indian families with suspected Stickler syndrome
2022 · Suganya Kandeeban, Kaustubh Kandale, et al. · Indian Journal of Ophthalmology · 4
Genetic analysis of congenital stationary night blindness and Oguchi disease in an Indian cohort
2025 · Srilekha Sundaramurthy, Sivasankar Malaichamy, et al. · Acta Ophthalmologica · 3
Association of HERPUD1 genetic variant rs2217332 with age-related macular degeneration and polypoidal choroidal vasculopathy in an Indian cohort
2022 · Lakshmi Priyankka Alagappan, Yazhini Ramaswamy, et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2
Risk Factors for Proliferative Diabetic Retinopathy and Diabetic Macular Edema in the South Indian Population
2020 · Alessandra Rizza, Gayatri Susarla, et al. · Investigative Ophthalmology & Visual Science · 1
Next Generation Sequencing in presumptive diagnosis of syndromes in childhood retinal dystrophies - case series from India
2024 · Harshavardhini Gnanasekaran, Srikrupa N. Natarajan, et al. · Human Gene
Complete mitochondrial genome sequencing in individuals with Leber hereditary optic neuropathy negative for the common pathogenic mitochondrial DNA mutations
2021 · Srilekha Sundaramurthy, Ambika Selvakumar, et al. · Investigative Ophthalmology & Visual Science
Whole Genome Sequencing of Large Consanguineous Pedigrees from South India Identifies New Candidate Genes for Lens Thickness
2021 · Bao Jian Fan, P Ferdina Marie Sharmila, et al. · Investigative Ophthalmology & Visual Science
Next-generation sequencing of the complete mitochondrial genome in individuals with Leber hereditary optic neuropathy negative for the common pathogenic mitochondrial DNA mutations
2020 · Srilekha Sundaramurthy, Ambika Selvakumar, et al. · Investigative Ophthalmology & Visual Science
Genetic Correlation between Corneal Hysteresis and Vertical Cup-disc Ratio in South Indian Consanguineous Pedigrees
2020 · Bao Jian Fan, P Ferdina Marie Sharmila, et al. · Investigative Ophthalmology & Visual Science
Genetic Survey of the Primary Mitochondrial Mutations along with Clinical Correlation in suspected Leber Hereditary Optic Neuropathy (LHON) patients from an Indian Cohort
2018 · Srilekha Sundaramurthy, Jayaprakash Mani, et al. · Investigative Ophthalmology & Visual Science
High-throughput genetic analysis in a cohort of patients with Ocular Developmental Anomalies
2017 · Suganya Kandeeban, Sudha Karthikeyan, et al. · Canadian Journal of Biotechnology
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Works count: 18
Citation count: 727
H-index: 7
I10-index: 7
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