Michalis Georgiou
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Also affiliated: National Health Service (2021–2022); Massachusetts Eye and Ear Infirmary (2026); Moorfields Eye Hospital NHS Foundation Trust (2017–2026); Harvard University (2026); Duke University (2025); University of Arkansas Medical Center (2021–2024); National Institute for Health and Care Research (2025); NIHR Moorfields Biomedical Research Centre (2025–2026); Moorfields Eye Charity (2021); Moorfields Eye Hospital (2018–2026); University College London (2017–2026); Erasmus University Rotterdam (2021)
Biomedical Subjects
Links
Biography and Research Information
Metrics
- h-index: 33
- Publications: 117
- Citations: 3,513
Selected Publications
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Stargardt macular dystrophy (2026)
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Best Vitelliform Macular Dystrophy Natural History Study Report 2 (2025)
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PDE6A-Associated Retinitis Pigmentosa, Clinical Characteristics, Genetics, and Natural History (2024)
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Clinical, Genetic, and Histopathological Characteristics of CRX-associated Retinal Dystrophies (2024)
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Phase 1/2 AAV5-hRKp.RPGR (Botaretigene Sparoparvovec) Gene Therapy: Safety and Efficacy in RPGR-Associated X-Linked Retinitis Pigmentosa (2024)
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A patient with albinism and retinitis pigmentosa, a case report (2024)
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IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural History (2024)
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Congenital Stationary Night Blindness (2024)
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Fractal Changes of the Retinal Microvasculature in Syphilitic Uveitis (2024)
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Cataract Surgery Outcomes in Retinitis Pigmentosa A Comparative Clinical Database Study (2024)
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Best Vitelliform Macular Dystrophy Natural History Study Report 1 (2024)
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Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes (2024)
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RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers (2023)
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RBP3-Retinopathy—Inherited High Myopia and Retinal Dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping (2023)
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First-in-Human Gene Therapy Trial of AAV8-hCARp.hCNGB3 in Adults and Children With CNGB3-associated Achromatopsia (2023)