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Meeting Abstract (6)
Journal Articles (2)

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Investigative Ophthalmology & Visual Science (8)

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ARVO Annual Meeting Abstract (6)
Genetics (1)
Retina (1)

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Eye Anatomy and Disorders (2)
Genetics (2)
Retina (2)

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family (2)
mutation (2)
retinitis pigmentosa (2)
carrying (1)
chromosomes (1)
dominant autosomal hereditary disorder with incomplete penetrance (1)
genes (1)
ligation (1)
medical history (1)
single nucleotide polymorphism (1)

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ARVO Annual Meeting Abstract June 2013

A Longitudinal Study of Stargardt Disease: Quantitative Assessment of Fundus Autofluorescence, Progression and Genotype Correlations

Kaoru Fujinami; Noemi Lois; Rajarshi Mukhopadhyay; Vikki McBain; Kazushige Tsunoda; Kazuo Tsubota; Fred Fitzke; Anthony Moore; Andrew Webster; Michel Michaelides

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):666. doi:

Retina December 2011

Autosomal Dominant Retinitis Pigmentosa with Intrafamilial Variability and Incomplete Penetrance in Two Families Carrying Mutations in PRPF8

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Cécilia G. Maubaret; Veronika Vaclavik; Rajarshi Mukhopadhyay; Naushin H. Waseem; Amanda Churchill; Graham E. Holder; Anthony T. Moore; Shomi S. Bhattacharya; Andrew R. Webster
TAGS: dominant autosomal hereditary disorder with incomplete penetrance, family, mutation, retinitis pigmentosa, carrying
Invest. Ophthalmol. Vis. Sci.. 2011; 52(13):9304-9309. doi: https://doi.org/10.1167/iovs.11-8372

Genetics August 2011

A 112 kb Deletion in Chromosome 19q13.42 Leads to Retinitis Pigmentosa

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Anna M. Rose; Rajarshi Mukhopadhyay; Andrew R. Webster; Shomi S. Bhattacharya; Naushin H. Waseem
TAGS: chromosomes, retinitis pigmentosa, family, medical history, genes, ligation, mutation, single nucleotide polymorphism
Invest. Ophthalmol. Vis. Sci.. 2011; 52(9):6597-6603. doi: https://doi.org/10.1167/iovs.11-7861

ARVO Annual Meeting Abstract April 2011

de Novo Mutation In The Chm Gene In A Family With Choroideraemia

Rajarshi Mukhopadhyay; Louise Ocaka; Donna S. Mackay; Andrew R. Webster

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5387. doi:

ARVO Annual Meeting Abstract April 2010

Phenotypic Survey of Patients and Families With Retinitis Pigmentosa Due to Mutations in the RP1 Gene

R. Mukhopadhyay; Z. Li; D. Mackay; S. Devery; G. Wright; A. G. Robson; G. E. Holder; A. T. Moore; A. R. Webster

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):1355. doi:

ARVO Annual Meeting Abstract April 2010

Identification of Large Deletions in PRPF31 in Autosomal Dominant Retinitis Pigmentosa

A. M. Rose; A. R. Webster; R. Mukhopadhyay; S. S. Bhattacharya; N. H. Waseem

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):4093. doi:

ARVO Annual Meeting Abstract April 2009

A Survey of Molecular Pathology of 175 Families With Dominant Retinitis Pigmentosa

R. Mukhopadhyay; Z. Li; S. Devery; G. Wright; T. Colclough; J. O'Sullivan; G. Black; S. Bhattacharya; A. Webster; A. Moore

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):2297. doi:

ARVO Annual Meeting Abstract April 2009

Comparison of Orbscan IIz, Pentacam and Ultrasound Pachymetry in Centre and Mid-periphery

D. R. Mukhopadhyay; R. V. North; K. E. Hamilton

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):2852. doi:

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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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