| Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy JS Gill, M Georgiou, A Kalitzeos, AT Moore, M Michaelides British Journal of Ophthalmology 103 (5), 711-720, 2019 | 168 | 2019 |
| Genetic basis of inherited retinal disease in a molecularly characterized cohort of more than 3000 families from the United Kingdom N Pontikos, G Arno, N Jurkute, E Schiff, R Ba-Abbad, S Malka, A Gimenez, ... Ophthalmology 127 (10), 1384-1394, 2020 | 150 | 2020 |
| Treatments for dry age-related macular degeneration: therapeutic avenues, clinical trials and future directions TAC de Guimaraes, MD Varela, M Georgiou, M Michaelides British Journal of Ophthalmology 106 (3), 297-304, 2022 | 135 | 2022 |
| Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options N Hirji, J Aboshiha, M Georgiou, J Bainbridge, M Michaelides Ophthalmic genetics 39 (2), 149-157, 2018 | 102 | 2018 |
| Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options N Rahman, M Georgiou, KN Khan, M Michaelides British Journal of Ophthalmology 104 (4), 451-460, 2020 | 96 | 2020 |
| Gene therapy for neovascular age-related macular degeneration: rationale, clinical trials and future directions TAC de Guimaraes, M Georgiou, JWB Bainbridge, M Michaelides British Journal of Ophthalmology 105 (2), 151-157, 2021 | 84 | 2021 |
| Inherited retinal diseases: Therapeutics, clinical trials and end points—A review M Georgiou, K Fujinami, M Michaelides Clinical & Experimental Ophthalmology 49 (3), 270-288, 2021 | 82 | 2021 |
| Adaptive optics imaging of inherited retinal diseases M Georgiou, A Kalitzeos, EJ Patterson, A Dubra, J Carroll, M Michaelides British Journal of Ophthalmology 102 (8), 1028-1035, 2018 | 78 | 2018 |
| Structural variants create new topological-associated domains and ectopic retinal enhancer-gene contact in dominant retinitis pigmentosa SE de Bruijn, A Fiorentino, D Ottaviani, S Fanucchi, US Melo, ... The American Journal of Human Genetics 107 (5), 802-814, 2020 | 76 | 2020 |
| Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approaches V Berry, M Georgiou, K Fujinami, R Quinlan, A Moore, M Michaelides British Journal of Ophthalmology 104 (10), 1331-1337, 2020 | 57 | 2020 |
| Prospective cohort study of childhood-onset Stargardt disease: fundus autofluorescence imaging, progression, comparison with adult-onset disease, and disease symmetry M Georgiou, T Kane, P Tanna, Z Bouzia, N Singh, A Kalitzeos, ... American journal of ophthalmology 211, 159-175, 2020 | 51 | 2020 |
| Deep phenotyping of PDE6C-associated achromatopsia M Georgiou, AG Robson, N Singh, N Pontikos, T Kane, N Hirji, ... Investigative ophthalmology & visual science 60 (15), 5112-5123, 2019 | 50 | 2019 |
| Adaptive optics retinal imaging in CNGA3-associated achromatopsia: retinal characterization, interocular symmetry, and intrafamilial variability M Georgiou, KM Litts, A Kalitzeos, CS Langlo, T Kane, N Singh, ... Investigative Ophthalmology & Visual Science 60 (1), 383-396, 2019 | 48 | 2019 |
| Leber congenital amaurosis/early-onset severe retinal dystrophy: current management and clinical trials MD Varela, TAC de Guimaraes, M Georgiou, M Michaelides British Journal of Ophthalmology 106 (4), 445-451, 2022 | 44 | 2022 |
| Characterization of retinal structure in ATF6-associated achromatopsia RR Mastey, M Georgiou, CS Langlo, A Kalitzeos, EJ Patterson, T Kane, ... Investigative ophthalmology & visual science 60 (7), 2631-2640, 2019 | 44 | 2019 |
| Longitudinal assessment of retinal structure in achromatopsia patients with long-term follow-up N Hirji, M Georgiou, A Kalitzeos, JW Bainbridge, N Kumaran, J Aboshiha, ... Investigative ophthalmology & visual science 59 (15), 5735-5744, 2018 | 44 | 2018 |
| GUCY2D-associated Leber congenital amaurosis: a retrospective natural history study in preparation for trials of novel therapies Z Bouzia, M Georgiou, S Hull, AG Robson, K Fujinami, T Rotsos, ... American journal of ophthalmology 210, 59-70, 2020 | 43 | 2020 |
| Autosomal recessive bestrophinopathy: clinical features, natural history, and genetic findings in preparation for clinical trials G Casalino, KN Khan, M Armengol, G Wright, N Pontikos, M Georgiou, ... Ophthalmology 128 (5), 706-718, 2021 | 37 | 2021 |
| Juvenile batten disease (CLN3): detailed ocular phenotype, novel observations, delayed diagnosis, masquerades, and prospects for therapy GA Wright, M Georgiou, AG Robson, N Ali, A Kalhoro, SMK Holthaus, ... Ophthalmology Retina 4 (4), 433-445, 2020 | 35 | 2020 |
| Cross-sectional and longitudinal assessment of the ellipsoid zone in childhood-onset Stargardt disease P Tanna, M Georgiou, RW Strauss, N Ali, N Kumaran, A Kalitzeos, ... Translational Vision Science & Technology 8 (2), 1-1, 2019 | 35 | 2019 |
Michel MichaelidesUCL Institute of Ophthalmology and Moorfields Eye HospitalVerified email at ucl.ac.uk
