| Long-term effect of gene therapy on Leber’s congenital amaurosis JWB Bainbridge, MS Mehat, V Sundaram, SJ Robbie, SE Barker, ... New England Journal of Medicine 372 (20), 1887-1897, 2015 | 785 | 2015 |
| A prospective randomized trial of intravitreal bevacizumab or laser therapy in the management of diabetic macular edema (BOLT study): 12-month data: report 2 M Michaelides, A Kaines, RD Hamilton, S Fraser-Bell, R Rajendram, ... Ophthalmology 117 (6), 1078-1086. e2, 2010 | 703 | 2010 |
| A comparison of the causes of blindness certifications in England and Wales in working age adults (16–64 years), 1999–2000 with 2009–2010 G Liew, M Michaelides, C Bunce BMJ open 4 (2), e004015, 2014 | 630 | 2014 |
| A 2-year prospective randomized controlled trial of intravitreal bevacizumab or laser therapy (BOLT) in the management of diabetic macular edema: 24-month data: report 3 R Rajendram, S Fraser-Bell, A Kaines, M Michaelides, RD Hamilton, ... Archives of ophthalmology 130 (8), 972-979, 2012 | 523 | 2012 |
| Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ... The American Journal of Human Genetics 100 (1), 75-90, 2017 | 408 | 2017 |
| Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options P Tanna, RW Strauss, K Fujinami, M Michaelides British Journal of Ophthalmology 101 (1), 25-30, 2017 | 368 | 2017 |
| 100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report 100,000 Genomes Project Pilot Investigators New England Journal of Medicine 385 (20), 1868-1880, 2021 | 362 | 2021 |
| Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions N Kumaran, AT Moore, RG Weleber, M Michaelides British journal of ophthalmology 101 (9), 1147-1154, 2017 | 303 | 2017 |
| Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice Z Yang, Y Chen, C Lillo, J Chien, Z Yu, M Michaelides, M Klein, ... The Journal of clinical investigation 118 (8), 2908-2916, 2008 | 289 | 2008 |
| The cone dysfunction syndromes M Michaelides, DM Hunt, AT Moore British Journal of Ophthalmology 88 (2), 291-297, 2004 | 285 | 2004 |
| Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis M Michaelides, AJ Hardcastle, DM Hunt, AT Moore Survey of ophthalmology 51 (3), 232-258, 2006 | 271 | 2006 |
| Retinal toxicity associated with hydroxychloroquine and chloroquine: risk factors, screening, and progression despite cessation of therapy M Michaelides, NB Stover, PJ Francis, RG Weleber Archives of ophthalmology 129 (1), 30-39, 2011 | 222 | 2011 |
| 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 | 220 | 2018 |
| Acute retinal necrosis: a national population-based study to assess the incidence, methods of diagnosis, treatment strategies and outcomes in the UK MN Muthiah, M Michaelides, CS Child, SM Mitchell British Journal of Ophthalmology 91 (11), 1452-1455, 2007 | 216 | 2007 |
| Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia S Kohl, D Zobor, WC Chiang, N Weisschuh, J Staller, IG Menendez, ... Nature genetics 47 (7), 757-765, 2015 | 215 | 2015 |
| The genetics of inherited macular dystrophies M Michaelides, DM Hunt, AT Moore Journal of medical genetics 40 (9), 641-650, 2003 | 215 | 2003 |
| 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 | 211 | 2009 |
| Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes KN Khan, OA Mahroo, RS Khan, MD Mohamed, M McKibbin, A Bird, ... Progress in retinal and eye research 53, 70-106, 2016 | 202 | 2016 |
| Retinitis pigmentosa-associated cystoid macular oedema: pathogenesis and avenues of intervention S Strong, G Liew, M Michaelides British journal of ophthalmology 101 (1), 31-37, 2017 | 186 | 2017 |
| Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta DA Parry, AJ Mighell, W El-Sayed, RC Shore, IK Jalili, H Dollfus, ... The american journal of human genetics 84 (2), 266-273, 2009 | 186 | 2009 |
