Michel Michaelides
Michel Michaelides
UCL Institute of Ophthalmology and Moorfields Eye Hospital
Verified email at
Cited by
Cited by
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
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
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
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
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
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
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
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
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
The cone dysfunction syndromes
M Michaelides, DM Hunt, AT Moore
British Journal of Ophthalmology 88 (2), 291-297, 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
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
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
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
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
The genetics of inherited macular dystrophies
M Michaelides, DM Hunt, AT Moore
Journal of medical genetics 40 (9), 641-650, 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
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
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
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
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