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| 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 | 336 | 2015 |
| ISCEV guide to visual electrodiagnostic procedures AG Robson, J Nilsson, S Li, S Jalali, AB Fulton, AP Tormene, GE Holder, ... Documenta Ophthalmologica 136, 1-26, 2018 | 335 | 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 | 327 | 2008 |
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| 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 | 213 | 2009 |
| 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 | 194 | 2015 |
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| ISCEV Standard for clinical electro-oculography (2017 update) PA Constable, M Bach, LJ Frishman, BG Jeffrey, AG Robson, ... Documenta Ophthalmologica 134, 1-9, 2017 | 179 | 2017 |
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| 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 | 174 | 2006 |
| 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, 79-89, 2008 | 161 | 2008 |
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