Michalis Georgiou
Michalis Georgiou
Research Fellow, UCL IoO and Moorfields Eye Hospital. Ophthalmology Resident, UAMS.
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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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