| 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), 328-337, 2018 | 665 | 2018 |
| 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 | 346 | 2018 |
| 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 | 342 | 2015 |
| 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 | 329 | 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 | 300 | 2008 |
| ISCEV Standard for full-field clinical electroretinography (2022 update) AG Robson, LJ Frishman, J Grigg, R Hamilton, BG Jeffrey, M Kondo, S Li, ... Documenta Ophthalmologica 144 (3), 165-177, 2022 | 280 | 2022 |
| Transplantation of human embryonic stem cell-derived retinal pigment epithelial cells in macular degeneration MS Mehat, V Sundaram, C Ripamonti, AG Robson, AJ Smith, S Borooah, ... Ophthalmology 125 (11), 1765-1775, 2018 | 245 | 2018 |
| 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 | 216 | 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 | 198 | 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 | 193 | 2007 |
| ISCEV Standard for clinical electro-oculography (2017 update) PA Constable, M Bach, LJ Frishman, BG Jeffrey, AG Robson, ... Documenta Ophthalmologica 134, 1-9, 2017 | 185 | 2017 |
| 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 | 176 | 2006 |
| 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 | 174 | 2013 |
| 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 | 163 | 2008 |
| 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 | 161 | 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 | 153 | 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 | 152 | 2013 |
| 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 | 138 | 2006 |
| 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 | 131 | 2008 |
| 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 | 125 | 2003 |
