Anthony G. Robson
Anthony G. Robson
Consultant Electrophysiologist and Head of Electrophysiology, Moorfields Eye Hospital
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Phase 1 clinical study of an embryonic stem cell–derived retinal pigment epithelium patch in age-related macular degeneration
L da Cruz, K Fynes, O Georgiadis, J Kerby, YH Luo, A Ahmado, A Vernon, ...
Nature biotechnology 36 (4), 328, 2018
Biallelic mutation of BEST1 causes a distinct retinopathy in humans
R Burgess, ID Millar, BP Leroy, JE Urquhart, IM Fearon, E De Baere, ...
The American Journal of Human Genetics 82 (1), 19-31, 2008
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways
P Bakrania, M Efthymiou, JC Klein, A Salt, DJ Bunyan, A Wyatt, ...
The American Journal of Human Genetics 82 (2), 304-319, 2008
Congenital stationary night blindness: an analysis and update of genotype–phenotype correlations and pathogenic mechanisms
C Zeitz, AG Robson, I Audo
Progress in retinal and eye research 45, 58-110, 2015
Xanthophyll accumulation in the human retina during supplementation with lutein or zeaxanthin–the LUXEA (LUtein Xanthophyll Eye Accumulation) study
W Schalch, W Cohn, FM Barker, W Köpcke, J Mellerio, AC Bird, ...
Archives of biochemistry and biophysics 458 (2), 128-135, 2007
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans
Z Li, PI Sergouniotis, M Michaelides, DS Mackay, GA Wright, S Devery, ...
The American Journal of Human Genetics 85 (5), 711-719, 2009
Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity
AG Robson, Z Saihan, SA Jenkins, FW Fitzke, AC Bird, AR Webster, ...
British Journal of Ophthalmology 90 (4), 472-479, 2006
The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction
I Audo, AG Robson, GE Holder, AT Moore
Survey of ophthalmology 53 (1), 16-40, 2008
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update
AG Robson, M Michaelides, Z Saihan, AC Bird, AR Webster, AT Moore, ...
Documenta ophthalmologica 116 (2), 79-89, 2008
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity
AG Robson, A El-Amir, C Bailey, CA Egan, FW Fitzke, AR Webster, ...
Investigative ophthalmology & visual science 44 (8), 3544-3550, 2003
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness
C Zeitz, SG Jacobson, CP Hamel, K Bujakowska, M Neuillé, E Orhan, ...
The American Journal of Human Genetics 92 (1), 67-75, 2013
Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry
AG Robson, JD Moreland, D Pauleikhoff, T Morrissey, GE Holder, ...
Vision research 43 (16), 1765-1775, 2003
Phenotypic variation in enhanced S-cone syndrome
I Audo, M Michaelides, AG Robson, M Hawlina, V Vaclavik, JM Sandbach, ...
Investigative ophthalmology & visual science 49 (5), 2082-2093, 2008
Clinical and molecular characteristics of childhood-onset Stargardt disease
K Fujinami, J Zernant, RK Chana, GA Wright, K Tsunoda, Y Ozawa, ...
Ophthalmology 122 (2), 326-334, 2015
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause “cone dystrophy with supernormal rod electroretinogram” in humans
H Wu, JA Cowing, M Michaelides, SE Wilkie, G Jeffery, SA Jenkins, ...
The American Journal of Human Genetics 79 (3), 574-579, 2006
ISCEV guide to visual electrodiagnostic procedures
AG Robson, J Nilsson, S Li, S Jalali, AB Fulton, AP Tormene, GE Holder, ...
Documenta Ophthalmologica 136 (1), 1-26, 2018
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations
K Fujinami, N Lois, AE Davidson, DS Mackay, CR Hogg, EM Stone, ...
American journal of ophthalmology 155 (6), 1075-1088. e13, 2013
Electrophysiological characterisation and monitoring in the management of birdshot chorioretinopathy
GE Holder, AG Robson, C Pavesio, EM Graham
British Journal of Ophthalmology 89 (6), 709-718, 2005
Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuity
AG Robson, CA Egan, VA Luong, AC Bird, GE Holder, FW Fitzke
Investigative ophthalmology & visual science 45 (11), 4119-4125, 2004
Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function
K Fujinami, PI Sergouniotis, AE Davidson, G Wright, RK Chana, ...
American journal of ophthalmology 156 (3), 487-501. e1, 2013
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