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Journal Articles (4)
Meeting Abstract (4)

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Investigative Ophthalmology & Visual Science (8)

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ARVO Annual Meeting Abstract (4)
Genetics (3)
Retina (1)

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Genetics (4)
Eye Anatomy and Disorders (3)
Retina (3)
Low Vision (1)
Visual Psychophysics and Physiological Optics (1)

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mutation (3)
retinal dystrophies (3)
alleles (1)
autosomal recessive inheritance (1)
child (1)
dideoxy chain termination dna sequencing (1)
dna (1)
exons (1)
family (1)
high-resolution melt curve analysis (1)

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ARVO Annual Meeting Abstract July 2018

Novel management of pediatric iris stromal cysts

Arundhati Dev Borman; Cecilia Fenerty; Susmito Biswas

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5212. doi:

Genetics September 2016

Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1

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Gavin Arno; Sarah Hull; Keren Carss; Arundhati Dev-Borman; Christina Chakarova; Kinga Bujakowska; L. Ingeborgh van den Born; Anthony G. Robson; Graham E. Holder; Michel Michaelides; Frans P. M. Cremers; Eric Pierce; F. Lucy Raymond; Anthony T. Moore; Andrew R. Webster
TAGS: alleles, mutation, retinal dystrophies, homozygote
Invest. Ophthalmol. Vis. Sci.. 2016; 57(11):4806-4813. doi: https://doi.org/10.1167/iovs.16-19687

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2013

Phenotypic variability in paediatric cases of enhanced S-cone syndrome (ESCS)

Gavin Arno; Panagiotis Sergouniotis; Arundhati Dev Borman; Aman Chandra; Graham Holder; Anthony Robson; Andrew Webster; Anthony Moore

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1319. doi:

ARVO Annual Meeting Abstract June 2013

Evidence of the role of ADAMTS18 in ocular development

Aman Chandra; Gavin Arno; Panagiotis Sergouniotis; Arundhati Dev Borman; Andrew Webster; Anthony Moore

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1346. doi:

Genetics June 2012

Early Onset Retinal Dystrophy Due to Mutations in LRAT : Molecular Analysis and Detailed Phenotypic Study

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Arundhati Dev Borman; Louise A. Ocaka; Donna S. Mackay; Caterina Ripamonti; Robert H. Henderson; Phillip Moradi; Georgina Hall; Graeme C. Black; Anthony G. Robson; Graham E. Holder; Andrew R. Webster; Fred Fitzke; Andrew Stockman; Anthony T. Moore
TAGS: mutation, phenotype, retinal dystrophies, perimetry
Invest. Ophthalmol. Vis. Sci.. 2012; 53(7):3927-3938. doi: https://doi.org/10.1167/iovs.12-9548

Genetics May 2011

Screening of SPATA7 in Patients with Leber Congenital Amaurosis and Severe Childhood-Onset Retinal Dystrophy Reveals Disease-Causing Mutations

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Donna S. Mackay; Louise A. Ocaka; Arundhati Dev Borman; Panagiotis I. Sergouniotis; Robert H. Henderson; Phillip Moradi; Anthony G. Robson; Dorothy A. Thompson; Andrew R. Webster; Anthony T. Moore
TAGS: child, leber's amaurosis, mutation, retinal dystrophies, screening, family, exons
Invest. Ophthalmol. Vis. Sci.. 2011; 52(6):3032-3038. doi: https://doi.org/10.1167/iovs.10-7025

ARVO Annual Meeting Abstract April 2011

Childhood Onset Retinal Dystrophy Due To LRAT Mutations

Arundhati Dev Borman; Louise Ocaka; Donna S. Mackay; Caterina Ripamonti; Anthony G. Robson; Graeme Black; Andrew R. Webster; Fred Fitzke; Andrew Stockman; Anthony T. Moore

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5380. doi:

Retina March 2011

A Survey of DNA Variation of C2ORF71 in Probands with Progressive Autosomal Recessive Retinal Degeneration and Controls

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Panagiotis I. Sergouniotis; Zheng Li; Donna S. Mackay; Genevieve A. Wright; Arundhati Dev Borman; Sophie R. Devery; Anthony T. Moore; Andrew R. Webster
TAGS: autosomal recessive inheritance, dna, high-resolution melt curve analysis, polymerase chain reaction, proband, retinal degeneration, surveys, dideoxy chain termination dna sequencing
Invest. Ophthalmol. Vis. Sci.. 2011; 52(3):1880-1886. doi: https://doi.org/10.1167/iovs.10-6043

Includes: Supplemental Content

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Online ISSN: 1552-5783

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

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