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ARVO Annual Meeting Abstract July 2019

Whole Exome Sequencing identifies rare gene variants and pathways in a large south Indian family with Primary Open Angle Glaucoma

Periasamy Sundaresan; Mohd Hussain Shah; Manojkumar K; Bharanidharan D; Mohideen Abdul Kader; Krishnadas S R; Ramakrishnan R

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1611. doi:

ARVO Annual Meeting Abstract July 2018

Targeted sequencing to identify the candidate gene in two south Indian POAG families

Periasamy Sundaresan; MOHD HUSSAIN SHAH; Krishnadas S R; Bharanidharan D; Manoj Kumar, K; Mohideen Abdul Kader

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5139. doi:

ARVO Annual Meeting Abstract June 2017

Identification and characterization of variants and a novel 4bp deletion in the regulatory region of SIX6 , a risk factor for Primary Open Angle Glaucoma

MOHD HUSSAIN SHAH; Noemi Tabanera; Subbiah R Krishnadas; Manju Pillai; Paola Bovolenta; Periasamy Sundaresan

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4900. doi:

ARVO Annual Meeting Abstract September 2016

World-wide genome-wide association study for exfoliation syndrome identifies 4 novel genetic loci.

Tin Aung; Mineo Ozaki; Francesca Pasutto; Rand R Allingham; Unnur Thorsteinsdottir; Jamie E Craig; Fotis Topouzis; Yuri Astakhov; Periasamy Sundaresan; Chiea-Chuen Khor

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12) doi:

ARVO Annual Meeting Abstract September 2016

Identification of SIX6 gene variants in Indian Primary Open Angle Glaucoma patients

Periasamy Sundaresan; Mohd. Hussain Shah; Krishnadas subbiah Ramasamy; Manju Pillai

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):823. doi:

ARVO Annual Meeting Abstract June 2015

Heritability of anterior segment optical coherence tomography parameters in the Indian Family Angle Closure Evaluation

Robert Wojciechowski; Pradeep Y Ramulu; Sabyasachi Sengupta; Palaniswamy Krishnamurthy; Srinivasan Kavitha; Periasamy Sundaresan; Rengaraj Venkatesh

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):5818. doi:

ARVO Annual Meeting Abstract June 2015

TSPAN12 mutation spectrum of a cohort of Familial Exudative Vitreoretinopathy patients

Xianjun Zhu; Periasamy Sundaresan; Yu Zhou; Xiong Zhu

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2900. doi:

ARVO Annual Meeting Abstract June 2015

Cytokines and chemokines profile in aqueous humor of PACG eyes

Roopam Duvesh; Krishnadas SR; George Puthuran; Sharmila Rajendrababu; Rengaraj Venkatesh; Srinivasan Kavitha; Pradeep Y Ramulu; Robert Wojciechowski; Periasamy Sundaresan; Primary Angle Closure Glaucoma

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):3482. doi:

ARVO Annual Meeting Abstract June 2015

Establishment of Retinal Mitoscriptome Gene Expression Signature for Diabetic Retinopathy Using Human Cadaver Eye

Periasamy Sundaresan; Gowthaman Govindarajan; Karthick Srinivasan; Kim Ramasamy

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4295. doi:

ARVO Annual Meeting Abstract April 2014

Ascorbate concentrations and polymorphisms in sodium transporter vitamin C genes in human plasma, aqueous humor and lens in an ascorbate depleted setting

Srinivasan Senthilkumari; Badri Talwar; Kuppamuthu Dharmalingam; Ravilla D Ravindran; R. Jayanthi; Periasamy Sundaresan; Charu Saravanan; Ian S Young; Alan D Dangour; Astrid E Fletcher; Lens Ascorbate study group

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1565. doi:

ARVO Annual Meeting Abstract April 2014

Genetic variation near GRB2 and KCNB2 identified by a genome-wide association study are reproducibly associated with Diabetic Retinopathy.

Georgia Kaidonis; Jamie E Craig; Rhys Fogarty; Mark C Gillies; Weiyong Shen; Shiwani Sharma; Binoy Appukuttan; Bishwanath Pal; Periasamy Sundaresan; Kathryn P Burdon

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):2237. doi:

ARVO Annual Meeting Abstract April 2014

Involvement of collagen - related genes and its influence on keratoconus and primary open angle glaucoma patients in India

Periasamy Sundaresan; Namburi Prasanthi; Govindarajan Gowthaman; Subbaiah R Krishnadas; Manoranjan Das; Colin E Willoughby

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3822. doi:

ARVO Annual Meeting Abstract April 2014

LONG PCR BASED ANALYSIS OF WHOLE MITOCHONDRIAL GENOME OF LEBER’S HEREDITARY OPTIC NEUROPATHY (LHON) PATIENTS

Bibhuti Ballav Saikia; Jayashree Charmakani; Mahesh k Shanmugam; Periasamy Sundaresan; Molecular Genetics

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6207. doi:

Glaucoma August 2013

Association Study in a South Indian Population Supports rs1015213 as a Risk Factor for Primary Angle Closure

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Roopam Duvesh; Anshuman Verma; Rengaraj Venkatesh; Srinivasan Kavitha; Pradeep Y. Ramulu; Robert Wojciechowski; Periasamy Sundaresan
TAGS: primary angle closure suspect, risk factors, single nucleotide polymorphism, genotype determination, glaucoma
Invest. Ophthalmol. Vis. Sci.. 2013; 54(8):5624-5628. doi: https://doi.org/10.1167/iovs.13-12186

Genetics August 2013

Mutational Analysis of MIR184 in Sporadic Keratoconus and Myopia

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Judith Lechner; Ha Ae Bae; Jasenka Guduric-Fuchs; Aine Rice; Gowthaman Govindarajan; Salina Siddiqui; Layal Abi Farraj; Shea Ping Yip; Maurice Yap; Manoranjan Das; Emmanuelle Souzeau; Doug Coster; Richard A. Mills; Richard Lindsay; Tony Phillips; Paul Mitchell; Manir Ali; Chris F. Inglehearn; Periasamy Sundaresan; Jamie E. Craig; David A. Simpson; Kathryn P. Burdon; Colin E. Willoughby
TAGS: keratoconus, mutation, mutation analysis, myopia
Invest. Ophthalmol. Vis. Sci.. 2013; 54(8):5266-5272. doi: https://doi.org/10.1167/iovs.13-12035

ARVO Annual Meeting Abstract June 2013

A Variant in the SLC35D1 gene is associated with Age-Related Cataract in India

Periasamy Sundaresan; Ravilla Ravidran; Praveen Vashist; Saravanan Vijayan; Dorothea Nitsch; Giovanni Maraini; Monica Camparini; Chakravarthy Usha; James Hejtmancik; Astrid Fletcher

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):2970. doi:

ARVO Annual Meeting Abstract June 2013

Identification of Mutations in Candidate Genes in Patients with Globe Anomalies: A Targeted Next-Generation Sequencing Approach

Sushil Dubey; Perumalsamy Vijayalakshmi; Sharwan Kedia; Periasamy Sundaresan

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):3366. doi:

ARVO Annual Meeting Abstract June 2013

Clinical Profile Of A Large Family With Primary Open Angle Glaucoma (POAG) In South Indian Population

MOHIDEEN KADER; Rengappa Ramakrishnan; Subbiah Ramaswami Krishnadas; Prasanthi Namburi; Periasamy Sundaresan; Alan Robin; Pradeep Ramulu; John Fingert

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):6237. doi:

Genetics November 2012

Polymorphisms in ARMS2/HTRA1 and Complement Genes and Age-Related Macular Degeneration in India: Findings from the INDEYE Study

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Periasamy Sundaresan; Praveen Vashist; Ravilla D. Ravindran; Ashwini Shanker; Dorothea Nitsch; Bareng A. S. Nonyane; Liam Smeeth; Usha Chakravarthy; Astrid E. Fletcher
TAGS: age-related macular degeneration, complement system proteins, genes, htra1 gene, india, polymorphism, single nucleotide polymorphism
Invest. Ophthalmol. Vis. Sci.. 2012; 53(12):7492-7497. doi: https://doi.org/10.1167/iovs.12-10073

Includes: Supplemental Content

Genetics April 2012

Evaluation of SNPs on Chromosome 2p with Primary Open Angle Glaucoma in the South Indian Cohort

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Suganthalakshmi Balasubbu; Subbaiah R. Krishnadas; Xiaodong Jiao; J. Fielding Hejtmancik; Periasamy Sundaresan
TAGS: chromosomes, cohort studies, glaucoma, open-angle glaucoma, single nucleotide polymorphism
Invest. Ophthalmol. Vis. Sci.. 2012; 53(4):1861-1864. doi: https://doi.org/10.1167/iovs.11-8602

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Whole Exome Sequencing identifies rare gene variants and pathways in a large south Indian family with Primary Open Angle Glaucoma

Targeted sequencing to identify the candidate gene in two south Indian POAG families

Identification and characterization of variants and a novel 4bp deletion in the regulatory region of SIX6 , a risk factor for Primary Open Angle Glaucoma

World-wide genome-wide association study for exfoliation syndrome identifies 4 novel genetic loci.

Identification of SIX6 gene variants in Indian Primary Open Angle Glaucoma patients

Heritability of anterior segment optical coherence tomography parameters in the Indian Family Angle Closure Evaluation

TSPAN12 mutation spectrum of a cohort of Familial Exudative Vitreoretinopathy patients

Cytokines and chemokines profile in aqueous humor of PACG eyes

Establishment of Retinal Mitoscriptome Gene Expression Signature for Diabetic Retinopathy Using Human Cadaver Eye

Ascorbate concentrations and polymorphisms in sodium transporter vitamin C genes in human plasma, aqueous humor and lens in an ascorbate depleted setting

Genetic variation near GRB2 and KCNB2 identified by a genome-wide association study are reproducibly associated with Diabetic Retinopathy.

Involvement of collagen - related genes and its influence on keratoconus and primary open angle glaucoma patients in India

LONG PCR BASED ANALYSIS OF WHOLE MITOCHONDRIAL GENOME OF LEBER’S HEREDITARY OPTIC NEUROPATHY (LHON) PATIENTS

Association Study in a South Indian Population Supports rs1015213 as a Risk Factor for Primary Angle Closure

Mutational Analysis of MIR184 in Sporadic Keratoconus and Myopia

A Variant in the SLC35D1 gene is associated with Age-Related Cataract in India

Identification of Mutations in Candidate Genes in Patients with Globe Anomalies: A Targeted Next-Generation Sequencing Approach

Clinical Profile Of A Large Family With Primary Open Angle Glaucoma (POAG) In South Indian Population

Polymorphisms in ARMS2/HTRA1 and Complement Genes and Age-Related Macular Degeneration in India: Findings from the INDEYE Study

Evaluation of SNPs on Chromosome 2p with Primary Open Angle Glaucoma in the South Indian Cohort

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