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Journal Articles (3)
Meeting Abstract (3)

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Investigative Ophthalmology & Visual Science (6)

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ARVO Annual Meeting Abstract (3)
Genetics (2)
Letters to the Editor (1)

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Eye Anatomy and Disorders (3)
Genetics (3)
Visual Neuroscience (1)

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mutation (3)
optic atrophy, hereditary, leber (3)
dna, mitochondrial (2)
india (2)
carrying (1)
haplotypes (1)
heterogeneity (1)
heteroplasmy (1)
mitochondria (1)
penetrance, genetic (1)

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ARVO Annual Meeting Abstract June 2020

Next-generation sequencing of the complete mitochondrial genome in individuals with Leber hereditary optic neuropathy negative for the common pathogenic mitochondrial DNA mutations

Srilekha Sundaramurthy; Ambika Selvakumar; Vidhya Dharani; Mathavan Sinnakaruppan; Sripriya Sarangapani; Patrick Yu-Wai-Man

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):5183. doi:

ARVO Annual Meeting Abstract July 2019

Brain and Optic Nerve Study with Artificial Intelligence (BONSAI)

Dan Milea; Zhubo Jiang; Caroline Vasseneix; Clare Fraser; Philippe Goher; Raymond Najjar; Shweta SInghal; Daniel Ting; Ambika Selvakumar; Jost B Jonas; Nancy Newman; Neil Miller; Yong Liu; Valerie Biousse; Tien Yin Wong

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1476. doi:

ARVO Annual Meeting Abstract July 2018

Genetic Survey of the Primary Mitochondrial Mutations along with Clinical Correlation in suspected Leber Hereditary Optic Neuropathy (LHON) patients from an Indian Cohort

Srilekha Sundaramurthy; Jayaprakash Mani; Vidhya Dharani; Soumittra Nagasamy; Sripriya Sarangapani; Mathavan Sinnakaruppan; Ambika SelvaKumar

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3355. doi:

Letters to the Editor January 2018

Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate

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Nahid Akhtar Khan; Periyasamy Govindaraj; Nagasamy Soumittra; Sonika Sharma; Sundaramoorthy Srilekha; Selvakumar Ambika; Ayyasamy Vanniarajan; Angamuthu Kanikannan Meena; Megha S. Uppin; Challa Sundaram; Parayil Sankaran Bindu; Narayanappa Gayathri; Arun B. Taly; Kumarasamy Thangaraj
TAGS: haplotypes, heteroplasmy, mutation, optic atrophy, hereditary, leber, penetrance, genetic
Invest. Ophthalmol. Vis. Sci.. 2018; 59(1):382. doi: https://doi.org/10.1167/iovs.17-23468

Genetics August 2017

Leber's Hereditary Optic Neuropathy–Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India

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Nahid Akhtar Khan; Periyasamy Govindaraj; Nagasamy Soumittra; Sonika Sharma; Sundaramoorthy Srilekha; Selvakumar Ambika; Ayyasamy Vanniarajan; Angamuthu Kanikannan Meena; Megha S. Uppin; Challa Sundaram; Parayil Sankaran Bindu; Narayanappa Gayathri; Arun B. Taly; Kumarasamy Thangaraj
TAGS: dna, mitochondrial, mitochondria, mutation, optic atrophy, hereditary, leber, india
Invest. Ophthalmol. Vis. Sci.. 2017; 58(10):3923-3930. doi: https://doi.org/10.1167/iovs.16-20695

Includes: Supplemental Content

Genetics June 2013

Haplogroup Heterogeneity of LHON Patients Carrying the m.14484T>C Mutation in India

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Nahid Akhtar Khan; Periyasamy Govindaraj; Nagasamy Soumittra; Sundaramoorthy Srilekha; Selvakumar Ambika; Ayyasamy Vanniarajan; Angamuthu K. Meena; Megha S. Uppin; Challa Sundaram; Arun B. Taly; Parayil Sankaran Bindu; Narayanappa Gayathri; Kumarasamy Thangaraj
TAGS: heterogeneity, india, mutation, optic atrophy, hereditary, leber, carrying, dna, mitochondrial
Invest. Ophthalmol. Vis. Sci.. 2013; 54(6):3999-4005. doi: https://doi.org/10.1167/iovs.13-11925

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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