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Meeting Abstract (8)
Journal Articles (3)

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Investigative Ophthalmology & Visual Science (11)

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ARVO Annual Meeting Abstract (8)
Retina (2)
Biochemistry and Molecular Biology (1)

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Eye Anatomy and Disorders (3)
Genetics (3)
Retina (3)
Biochemistry and Molecular Biology (1)
Imaging (1)
Multidisciplinary Ophthalmic Imaging (1)
Visual Psychophysics and Physiological Optics (1)

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eye (2)
family (2)
macular dystrophy (2)
mutation (2)
retinal cone (2)
arm of chromosome (1)
atrophy (1)
genetic linkage analysis (1)
macular disorders (1)
maps (1)

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ARVO Annual Meeting Abstract June 2024

Reinforced random-walk model of retinal angiogenesis

Cassandra DuBose Corry; Brandon Pace; Kelsey Bradshaw; Elizabeth Vargis

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):5673.

ARVO Annual Meeting Abstract June 2021

A computational model of neovascularization in wet age related macular degeneration

Kelsey Bradshaw; Andrew Kjar; Michael Cotner; Jacilyn Fielding; Teren Teeples; Zhen Zhang; Elizabeth Vargis

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):2711.

ARVO Annual Meeting Abstract June 2020

A computational model of the effect of VEGF production in wet age-related macular degeneration on neovascularization

Kelsey Bradshaw; Elizabeth Vargis; Zhen Zang

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):5404.

Retina September 2010

The PROM1 Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

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Michel Michaelides; Marie-Claire Gaillard; Pascal Escher; Leila Tiab; Matthew Bedell; François-Xavier Borruat; Daniel Barthelmes; Ruben Carmona; Kang Zhang; Edward White; Michelle McClements; Anthony G. Robson; Graham E. Holder; Keith Bradshaw; David M. Hunt; Andrew R. Webster; Anthony T. Moore; Daniel F. Schorderet; Francis L. Munier
TAGS: eye, family, macular disorders, macular dystrophy, mutation, retinal cone, rod photoreceptors, atrophy, phenotype
Invest. Ophthalmol. Vis. Sci.. 2010; 51(9):4771-4780. https://doi.org/10.1167/iovs.09-4561

ARVO Annual Meeting Abstract April 2010

Contribution of Post-Receptoral Cells to the Cone A-Wave of the Human ERG in CSNB and Auto-Immune Retinopathy

K. Bradshaw; R. Hanitzsch

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):3274.

ARVO Annual Meeting Abstract May 2006

Post–Receptoral Components of the Human Cone–Driven ERG

K. Bradshaw

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1665.

Biochemistry and Molecular Biology June 2005

Identification of Novel RPGR ORF15 Mutations in X-linked Progressive Cone-Rod Dystrophy (XLCORD) Families

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Neil D. Ebenezer; Michel Michaelides; Sharon A. Jenkins; Isabelle Audo; Andrew R. Webster; Michael E. Cheetham; Andrew Stockman; Eamonn R. Maher; John R. Ainsworth; John R. Yates; Keith Bradshaw; Graham E. Holder; Anthony T. Moore; Alison J. Hardcastle
TAGS: family, mutation, progressive cone-rod dystrophy, x-linked inheritance, retinitis pigmentosa, retinal cone
Invest. Ophthalmol. Vis. Sci.. 2005; 46(6):1891-1898. https://doi.org/10.1167/iovs.04-1482

ARVO Annual Meeting Abstract May 2005

Cone–Rod Dystrophy, Intra–Familial Variability and Incomplete Penetrance Associated With the R172W Mutation in the Peripherin/RDS Gene

M. Michaelides; G.E. Holder; K. Bradshaw; D.M. Hunt; A.T. Moore

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1791.

ARVO Annual Meeting Abstract May 2004

ERG responses to full–field stimuli recorded with skin and corneal electrodes in healthy volunteers and in children with retinal dystrophies.

S.P. Meredith; A. Fulton; R. Hansen; A. Reddy; K. Bradshaw; A. Moore

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):801.

ARVO Annual Meeting Abstract May 2003

An Autosomal Dominant Bull’s-Eye Macular Dystrophy (MCDR2) That Maps to Chromosome 4p

M. Michaelides; S. Johnson; A. Poulson; K. Bradshaw; C. Bellmann; D.M. Hunt; A.T. Moore

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):1495.

Retina April 2003

An Autosomal Dominant Bull’s-Eye Macular Dystrophy (MCDR2) that Maps to the Short Arm of Chromosome 4

PDF

Michel Michaelides; Samantha Johnson; Arabella Poulson; Keith Bradshaw; Caren Bellmann; David M. Hunt; Anthony T. Moore
TAGS: arm of chromosome, eye, macular dystrophy, maps, genetic linkage analysis
Invest. Ophthalmol. Vis. Sci.. 2003; 44(4):1657-1662. https://doi.org/10.1167/iovs.02-0941

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Translational Vision Science & Technology

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