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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 2
2005 2
2006 3
2007 2
2008 2
2009 2
2010 7
2011 5
2012 6
2013 9
2014 9
2015 9
2016 5
2017 6
2018 13
2019 20
2020 13
2021 20
2022 7
2023 3
2024 14
2025 17
2026 6

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160 results

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Page 1
Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.
Fujinami K, Strauss RW, Chiang JP, Audo IS, Bernstein PS, Birch DG, Bomotti SM, Cideciyan AV, Ervin AM, Marino MJ, Sahel JA, Mohand-Said S, Sunness JS, Traboulsi EI, West S, Wojciechowski R, Zrenner E, Michaelides M, Scholl HPN; ProgStar Study Group; ProgStar Study Group. Fujinami K, et al. Br J Ophthalmol. 2019 Mar;103(3):390-397. doi: 10.1136/bjophthalmol-2018-312064. Epub 2018 Jun 20. Br J Ophthalmol. 2019. PMID: 29925512 Free PMC article.
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC).
Sharon D, Ben-Yosef T, Goldenberg-Cohen N, Pras E, Gradstein L, Soudry S, Mezer E, Zur D, Abbasi AH, Zeitz C, Cremers FPM, Khan MI, Levy J, Rotenstreich Y, Birk OS, Ehrenberg M, Leibu R, Newman H, Shomron N, Banin E, Perlman I. Sharon D, et al. Among authors: zeitz c. Hum Mutat. 2020 Jan;41(1):140-149. doi: 10.1002/humu.23903. Epub 2019 Sep 15. Hum Mutat. 2020. PMID: 31456290
Extensive macular atrophy with pseudodrusen-like appearance (EMAP) clinical characteristics, diagnostic criteria, and insights from allied inherited retinal diseases and age-related macular degeneration.
Antropoli A, Bianco L, Romano F, Trinco A, Arrigo A, Benadji A, Atia R, Palacci O, Dagostinoz D, Devisme C, Condroyer C, Antonio A, Bosello F, Casati S, Salvetti AP, Zaffalon C, Gaudric A, Sahel JA, Staurenghi G, Bandello F, Sennlaub F, Zeitz C, Meunier I, Battaglia Parodi M, Audo I. Antropoli A, et al. Among authors: zeitz c. Prog Retin Eye Res. 2025 Jan;104:101320. doi: 10.1016/j.preteyeres.2024.101320. Epub 2024 Nov 25. Prog Retin Eye Res. 2025. PMID: 39603590 Free article. Review.
Shedding light on myopia by studying complete congenital stationary night blindness.
Zeitz C, Roger JE, Audo I, Michiels C, Sánchez-Farías N, Varin J, Frederiksen H, Wilmet B, Callebert J, Gimenez ML, Bouzidi N, Blond F, Guilllonneau X, Fouquet S, Léveillard T, Smirnov V, Vincent A, Héon E, Sahel JA, Kloeckener-Gruissem B, Sennlaub F, Morgans CW, Duvoisin RM, Tkatchenko AV, Picaud S. Zeitz C, et al. Prog Retin Eye Res. 2023 Mar;93:101155. doi: 10.1016/j.preteyeres.2022.101155. Epub 2023 Jan 19. Prog Retin Eye Res. 2023. PMID: 36669906 Free article. Review.
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration.
Sangermano R, Gupta P, Price C, Han J, Navarro J, Condroyer C, Place EM, Antonio A, Mukai S, Zanlonghi X, Sahel JA, DiTroia S, O'Heir E, Duncan JL, Pierce EA, Zeitz C, Audo I, Huckfeldt RM, Bujakowska KM. Sangermano R, et al. Among authors: zeitz c. NPJ Genom Med. 2024 Nov 8;9(1):58. doi: 10.1038/s41525-024-00439-3. NPJ Genom Med. 2024. PMID: 39516462 Free PMC article.
DRD2 activation inhibits choroidal neovascularization in patients with Parkinson's disease and age-related macular degeneration.
Mathis T, Baudin F, Mariet AS, Augustin S, Bricout M, Przegralek L, Roubeix C, Benzenine É, Blot G, Nous C, Kodjikian L, Mauget-Faÿsse M, Sahel JA, Plevin R, Zeitz C, Delarasse C, Guillonneau X, Creuzot-Garcher C, Quantin C, Hunot S, Sennlaub F. Mathis T, et al. Among authors: zeitz c. J Clin Invest. 2024 Jul 16;134(17):e174199. doi: 10.1172/JCI174199. J Clin Invest. 2024. PMID: 39012703 Free PMC article.
Eyes shut homolog (EYS): Connecting molecule to disease.
Marques JP, Santos Sousa I, Patrício D, Simões BF, Chukwunalu O, Zeitz C, Audo I, Collin RWJ, Quinn PMJ, Ambrósio AF, Alves CH. Marques JP, et al. Among authors: zeitz c. Prog Retin Eye Res. 2025 Sep;108:101391. doi: 10.1016/j.preteyeres.2025.101391. Epub 2025 Aug 15. Prog Retin Eye Res. 2025. PMID: 40819709 Free article. Review.
Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosa.
Bianco L, Navarro J, Michiels C, Sangermano R, Condroyer C, Antonio A, Antropoli A, Andrieu C, Place EM, Pierce EA, El Shamieh S, Smirnov V, Kalatzis V, Mansard L, Roux AF, Bocquet B, Sahel JA, Meunier I, Bujakowska KM, Audo I, Zeitz C. Bianco L, et al. Among authors: zeitz c. Genet Med. 2025 Jun;27(6):101418. doi: 10.1016/j.gim.2025.101418. Epub 2025 Mar 19. Genet Med. 2025. PMID: 40119724 Free article.
160 results