| 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 | 178 | 2022 |
| 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 | 94 | 2021 |
| 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 | 65 | 2022 |
| Artificial intelligence in retinal disease: clinical application, challenges, and future directions M Daich Varela, S Sen, TAC De Guimaraes, N Kabiri, N Pontikos, ... Graefe's Archive for Clinical and Experimental Ophthalmology 261 (11), 3283-3297, 2023 | 48 | 2023 |
| Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies … M Georgiou, AG Robson, K Fujinami, TAC de Guimarães, ... Progress in retinal and eye research 100, 101244, 2024 | 35 | 2024 |
| KCNV2 retinopathy: clinical features, molecular genetics and directions for future therapy TACD Guimaraes, M Georgiou, AG Robson, M Michaelides Ophthalmic Genetics 41 (3), 208-215, 2020 | 35 | 2020 |
| Structural evaluation in inherited retinal diseases MD Varela, B Esener, SA Hashem, TAC de Guimaraes, M Georgiou, ... British Journal of Ophthalmology 105 (12), 1623-1631, 2021 | 30 | 2021 |
| SynthEye: investigating the impact of synthetic data on artificial intelligence-assisted gene diagnosis of inherited retinal disease YA Veturi, W Woof, T Lazebnik, I Moghul, P Woodward-Court, SK Wagner, ... Ophthalmology Science 3 (2), 100258, 2023 | 28 | 2023 |
| KCNV2-associated retinopathy: genetics, electrophysiology, and clinical course—KCNV2 Study Group Report 1 M Georgiou, AG Robson, K Fujinami, SM Leo, A Vincent, F Nasser, ... American journal of ophthalmology 225, 95-107, 2021 | 24 | 2021 |
| KCNV2-associated retinopathy: detailed retinal phenotype and structural endpoints—KCNV2 Study Group Report 2 M Georgiou, K Fujinami, A Vincent, F Nasser, S Khateb, ME Vargas, ... American Journal of Ophthalmology 230, 1-11, 2021 | 20 | 2021 |
| Inherited causes of combined vision and hearing loss: clinical features and molecular genetics TAC de Guimaraes, E Arram, AF Shakarchi, M Georgiou, M Michaelides British Journal of Ophthalmology 107 (10), 1403-1414, 2023 | 18 | 2023 |
| RP2-associated X-linked retinopathy: clinical findings, molecular genetics, and natural history M Georgiou, AG Robson, K Jovanovic, TAC de Guimarães, N Ali, ... Ophthalmology 130 (4), 413-422, 2023 | 15 | 2023 |
| Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene) Q Nguyen, W Woof, N Kabiri, S Sen, MD Varela, TAC De Guimaraes, ... BMJ open 13 (3), e071043, 2023 | 15 | 2023 |
| Stargardt misdiagnosis: How ocular genetics helps MB Ibanez IV, TAC de Guimaraes, J Capasso, N Bello, AV Levin American Journal of Medical Genetics Part A 185 (3), 814-819, 2021 | 10 | 2021 |
| Eye2Gene: prediction of causal inherited retinal disease gene from multimodal imaging using deep-learning N Pontikos, W Woof, A Veturi, B Javanmardi, M Ibarra-Arellano, A Hustinx, ... | 9 | 2022 |
| AAV5-RPGR (botaretigene sparoparvovec) gene therapy for X-linked retinitis pigmentosa (XLRP) demonstrates localized improvements in static perimetry M Michaelides, J Xu, D Wang, P Wong, A Fung, A Forbes, S Naylor, ... Investigative Ophthalmology & Visual Science 63 (7), 3846-3846, 2022 | 9 | 2022 |
| CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History TAC De Guimarães, AG Robson, IMC de Guimaraes, Y Laich, N Aychoua, ... Investigative Ophthalmology & Visual Science 65 (8), 27-27, 2024 | 4 | 2024 |
| Best vitelliform macular dystrophy natural history study report 1: clinical features and genetic findings Y Laich, M Georgiou, K Fujinami, MD Varela, Y Fujinami-Yokokawa, ... Ophthalmology 131 (7), 845-854, 2024 | 4 | 2024 |
| Sex distributions in Non-ABCA4 autosomal macular dystrophies AV Mishra, S Vermeirsch, S Lin, MP Martin-Gutierrez, M Simcoe, ... Investigative Ophthalmology & Visual Science 65 (5), 9-9, 2024 | 4 | 2024 |
| Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3000 Inherited Retinal Disease Patients from the United Kingdom W Woof, TAC de Guimarães, S Al-Khuzaei, MD Varela, S Sen, P Bagga, ... medRxiv, 2024.03. 24.24304809, 2024 | 4 | 2024 |
