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Meeting Abstract (12)
Journal Articles (2)

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Investigative Ophthalmology & Visual Science (14)

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ARVO Annual Meeting Abstract (12)
Biochemistry and Molecular Biology (1)
Retina (1)

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Eye Anatomy and Disorders (2)
Genetics (2)
Biochemistry and Molecular Biology (1)
Cornea (1)
Lens (1)
Retina (1)

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mutation (2)
asian indians (1)
autosomal recessive inheritance (1)
cataract (1)
diagnostic imaging (1)
electroretinography (1)
family (1)
genes (1)
genetic linkage analysis (1)
heterogeneity (1)

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ARVO Annual Meeting Abstract June 2017

Retinoblastoma and Next-Gen-Sequencing Era: Challenges and Opportunities at Clinics and Counseling in India

Govindasamy Kumaramanickavel; Sivasankar Malaichamy; Rohit Shetty; Arkasubhra Ghosh; Somasekar Seshagiri; Vedam L Ramprasad

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):854. doi:

ARVO Annual Meeting Abstract June 2013

Keratoconus Gene Mapping: Candidate Genes in the 14q11.2 homozygous region

Govindasamy Kumaramanickavel; Venkata Ramana Anandula; Vedam Ramprasad; Nalla Thambi Jeyabalan; Arkasubhra Ghosh; Rohit Shetty

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5303. doi:

ARVO Annual Meeting Abstract June 2013

Homozygosity Mapping of Keratoconus to 12p13.1 region: The Ideal Candidate Genes

Venkata Ramana Anandula; Venkata Ramana Anandula; Vedam Ramprasad; Nalla Thambi Jeyabalan; Rohit Shetty; Arkasubhra Ghosh; Govindasamy Kumaramanickavel; Basic Science research

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5304. doi:

ARVO Annual Meeting Abstract April 2011

Homozygosity Mapping of a Consanguineous South Indian Keratoconus Family to the Cytogenetic Region 14q11.2

Govindasamy Kumaramanickavel; Anandula Venkataramana; Vedam Ramprasad; Rohit Shetty

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):69. doi:

ARVO Annual Meeting Abstract April 2011

Gene Mapping in a Highly Inbred Consanguineous Foveal Hypoplasia Family to cytonenetic region 16q24.1

Venkata Ramana Anandula; Vedam Ramprasad; Rohit Shetty; Govindasamy Kumaramanickavel

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3290. doi:

Retina December 2009

CERKL Mutations Cause an Autosomal Recessive Cone-Rod Dystrophy with Inner Retinopathy

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Tomas S. Aleman; Nagasamy Soumittra; Artur V. Cideciyan; Alexander M. Sumaroka; Vedam Lakshmi Ramprasad; Waldo Herrera; Elizabeth A. M. Windsor; Sharon B. Schwartz; Robert C. Russell; Alejandro J. Roman; Chris F. Inglehearn; Govindasamy Kumaramanickavel; Edwin M. Stone; Gerald A. Fishman; Samuel G. Jacobson
TAGS: autosomal recessive inheritance, mutation, progressive cone-rod dystrophy, retina, retinal diseases, retinitis pigmentosa, retinal cone, rod photoreceptors, photoreceptors, electroretinography
Invest. Ophthalmol. Vis. Sci.. 2009; 50(12):5944-5954. doi: https://doi.org/10.1167/iovs.09-3982

ARVO Annual Meeting Abstract May 2008

Pseudoexfoliation Syndrome in India: Association of G135D Polymorphism in LOXL1 Gene

V. Ramprasad; R. George; N. Soumittra; F. Sharmila; L. Vijaya; G. Kumaramanickavel

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):1722. doi:

ARVO Annual Meeting Abstract May 2008

Homozygosity Mapping in Consanguineous Retinal Dystrophy Families: Identification of a Novel c.955G>A Splice Site Mutation in the Lebercilin Gene in Leber Congential Amaurosis

G. Kumaramanickavel; V. L. Ramprasad; N. Soumittra; D. Nancarrow; P. Sen; M. McKibbin; G. A. Williams; T. Arokiasamy; L. Praveena; C. F. Inglehearn

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):2979. doi:

ARVO Annual Meeting Abstract May 2007

Identification and Characterization of SLC4A11 Mutations in Fuchs Endothelial Corneal Dystrophy (FECD)

E. N. Vithana; V. H. K. Yong; P. Morgan; V. Ramprasad; S. Nagasamy; G. Kumaramanickevel; J. R. Casey; D. T. H. Tan; C. P. Pang; T. Aung

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):1329. doi:

ARVO Annual Meeting Abstract May 2007

Characterization of Novel SLC4A11 Mutations Identified in Recessive Congenital Hereditary Endothelial Dystrophy (CHED2)

P. E. Morgan; M. Saincher; E. N. Vithana; V. Ramprasad; G. Kumaramanickevel; T. Aung; J. R. Casey

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):5863. doi:

ARVO Annual Meeting Abstract May 2006

Linkage Analysis and Molecular Genetic Study of Inherited Congenital Microcoria in an Indian Pedigree – Refining the MCOR Locus At 13q31–q32

V. Ramprasad; S. Sarangapani; R. George; D. Nancarrow; S. Sandeep; H. Arvind; D. Kumar; L. Vijaya; G. Kumaramanickavel

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):3278. doi:

Biochemistry and Molecular Biology January 2005

Truncating Mutation in the NHS Gene: Phenotypic Heterogeneity of Nance-Horan Syndrome in an Asian Indian Family

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Vedam Lakshmi Ramprasad; Alka Thool; Sakthivel Murugan; Derek Nancarrow; Prateep Vyas; Srinivas Kamalakar Rao; Authiappan Vidhya; Krishnamoorthy Ravishankar; Govindasamy Kumaramanickavel
TAGS: asian indians, family, genes, heterogeneity, mutation, nance-horan syndrome, phenotype, reverse transcriptase polymerase chain reaction, cataract, genetic linkage analysis
Invest. Ophthalmol. Vis. Sci.. 2005; 46(1):17-23. doi: https://doi.org/10.1167/iovs.04-0477

ARVO Annual Meeting Abstract May 2004

Congenital microcoria gene:Linkage homogeneity to locus 13q31–32

G. Kumaramanickavel; S. Sripriya; V.L. Ramprasad; G.J. Ronnie; A. Hemamalini; S. Saxena; L. Vijaya

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):4757. doi:

ARVO Annual Meeting Abstract December 2002

Polymorphic Variations in iNOS, ALR2, IGF-1 Genes and Susceptibility to Diabetic Retinopathy in Asian Indian Patients

G Kumaramanickavel; S Sripriya; VL Ramprasad; RN Vellanki; NK Upadyay; B Sukumar; T Sharma

Invest. Ophthalmol. Vis. Sci.. 2002; 43(13):1343. doi:

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Online ISSN: 1552-5783

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

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