Inherited retinal diseases: Therapeutics, clinical trials and end points—A review von Georgiou, Michalis, Fujinami, Kaoru, Michaelides, Michel

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Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options von Rahman, Najiha, Georgiou, Michalis, Khan, Kamron N, Michaelides, Michel

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Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy von Gill, Jasdeep S, Georgiou, Michalis, Kalitzeos, Angelos, Moore, Anthony T, Michaelides, Michel

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Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approaches von Berry, Vanita, Georgiou, Michalis, Fujinami, Kaoru, Quinlan, Roy, Moore, Anthony, Michaelides, Michel

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Gene therapy for neovascular age-related macular degeneration: rationale, clinical trials and future directions von Guimaraes, Thales Antonio Cabral de, Georgiou, Michalis, Bainbridge, James W B, Michaelides, Michel

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Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom von Pontikos, Nikolas, Arno, Gavin, Jurkute, Neringa, Schiff, Elena, Ba-Abbad, Rola, Malka, Samantha, Gimenez, Ainoa, Georgiou, Michalis, Wright, Genevieve, Armengol, Monica, Knight, Hannah, Katz, Menachem, Moosajee, Mariya, Yu-Wai-Man, Patrick, Moore, Anthony T., Michaelides, Michel, Webster, Andrew R., Mahroo, Omar A.

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Leber congenital amaurosis/early-onset severe retinal dystrophy: current management and clinical trials von Daich Varela, Malena, Cabral de Guimaraes, Thales Antonio, Georgiou, Michalis, Michaelides, Michel

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Inherited causes of combined vision and hearing loss: clinical features and molecular genetics von Guimaraes, Thales Antonio Cabral de, Arram, Elizabeth, Shakarchi, Ahmed F, Georgiou, Michalis, Michaelides, Michel

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Adaptive optics imaging of inherited retinal diseases von Georgiou, Michalis, Kalitzeos, Angelos, Patterson, Emily J, Dubra, Alfredo, Carroll, Joseph, Michaelides, Michel

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Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa von de Bruijn, Suzanne E., Fiorentino, Alessia, Ottaviani, Daniele, Fanucchi, Stephanie, Melo, Uirá S., Corral-Serrano, Julio C., Mulders, Timo, Georgiou, Michalis, Rivolta, Carlo, Pontikos, Nikolas, Arno, Gavin, Roberts, Lisa, Greenberg, Jacquie, Albert, Silvia, Gilissen, Christian, Aben, Marco, Rebello, George, Mead, Simon, Raymond, F. Lucy, Corominas, Jordi, Smith, Claire E.L., Kremer, Hannie, Downes, Susan, Black, Graeme C., Webster, Andrew R., Inglehearn, Chris F., van den Born, L. Ingeborgh, Koenekoop, Robert K., Michaelides, Michel, Ramesar, Raj S., Hoyng, Carel B., Mundlos, Stefan, Mhlanga, Musa M., Cremers, Frans P.M., Cheetham, Michael E., Roosing, Susanne, Hardcastle, Alison J.

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GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel Therapies von Bouzia, Zaina, Georgiou, Michalis, Hull, Sarah, Robson, Anthony G., Fujinami, Kaoru, Rotsos, Tryfon, Pontikos, Nikolas, Arno, Gavin, Webster, Andrew R., Hardcastle, Alison J., Fiorentino, Alessia, Michaelides, Michel

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An Artificial Intelligence System for Optimizing Radioactive Iodine Therapy Dosimetry von Georgiou, Michalis F, Nielsen, Joshua A, Chiriboga, Rommel, Kuker, Russ A

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CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History von Daich Varela, Malena, Georgiou, Michalis, Alswaiti, Yahya, Kabbani, Jamil, Fujinami, Kaoru, Fujinami-Yokokawa, Yu, Khoda, Shaheeni, Mahroo, Omar A., Robson, Anthony G., Webster, Andrew R., AlTalbishi, Alaa, Michaelides, Michel

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Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History von Georgiou, Michalis, Grewal, Parampal S., Narayan, Akshay, Alser, Muath, Ali, Naser, Fujinami, Kaoru, Webster, Andrew R., Michaelides, Michel

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Structural evaluation in inherited retinal diseases von Daich Varela, Malena, Esener, Burak, Hashem, Shaima A, Cabral de Guimaraes, Thales Antonio, Georgiou, Michalis, Michaelides, Michel

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Characterization of Retinal Structure in ATF6-Associated Achromatopsia von Mastey, Rebecca R, Georgiou, Michalis, Langlo, Christopher S, Kalitzeos, Angelos, Patterson, Emily J, Kane, Thomas, Singh, Navjit, Vincent, Ajoy, Moore, Anthony T, Tsang, Stephen H, Lin, Jonathan H, Young, Marielle P, Hartnett, M Elizabeth, Héon, Elise, Kohl, Susanne, Michaelides, Michel, Carroll, Joseph

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Leveraging Programmatic Collaboration for a Radiopharmaceutical Clinic von Kunos, Charles A, Martin, Molly E, Georgiou, Michalis F, Kuker, Russ A, Chauhan, Aman

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Gastric Emptying Scintigraphy Protocol Optimization Using Machine Learning for the Detection of Delayed Gastric Emptying von Georgiou, Michalis F, Sfakianaki, Efrosyni, Diaz-Kanelidis, Monica N, Moshiree, Baha

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KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course—KCNV2 Study Group Report 1 von Georgiou, Michalis, Robson, Anthony G., Fujinami, Kaoru, Leo, Shaun M., Vincent, Ajoy, Nasser, Fadi, Cabral De Guimarães, Thales Antônio, Khateb, Samer, Pontikos, Nikolas, Fujinami-Yokokawa, Yu, Liu, Xiao, Tsunoda, Kazushige, Hayashi, Takaaki, Vargas, Mauricio E., Thiadens, Alberta A.H.J., de Carvalho, Emanuel R., Nguyen, Xuan-Thanh-An, Arno, Gavin, Mahroo, Omar A., Martin-Merida, Maria Inmaculada, Jimenez-Rolando, Belen, Gordo, Gema, Carreño, Ester, Ayuso, Carmen, Sharon, Dror, Kohl, Susanne, Huckfeldt, Rachel M., Wissinger, Bernd, Boon, Camiel J.F., Banin, Eyal, Pennesi, Mark E., Khan, Arif O., Webster, Andrew R., Zrenner, Eberhart, Héon, Elise, Michaelides, Michel

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IMPG2-associated unilateral adult onset vitelliform macular dystrophy von Georgiou, Michalis, Chauhan, Muhammad Z., Michaelides, Michel, Uwaydat, Sami H.

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