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

Year Number of Results
1967 1
1968 1
1972 1
1976 2
1977 2
1978 2
1980 1
1981 4
1982 1
1983 2
1984 2
1985 2
1986 5
1987 3
1988 4
1989 7
1990 4
1991 4
1992 5
1993 6
1994 4
1995 4
1996 2
1997 7
1998 10
1999 7
2000 11
2001 6
2002 4
2003 7
2004 10
2005 12
2006 1
2007 8
2008 7
2009 6
2010 6
2011 8
2012 7
2013 5
2014 2
2015 5
2016 19
2017 5
2018 11
2019 5
2020 6
2021 8
2022 5
2023 3
2024 2
2025 1

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Search Results

243 results

Results by year

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Page 1
Nonsyndromic Retinitis Pigmentosa Overview.
Fahim AT, Daiger SP, Weleber RG. Fahim AT, et al. Among authors: weleber rg. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301590 Free Books & Documents. Review.
Stargardt's macular dystrophy.
Weleber RG. Weleber RG. Arch Ophthalmol. 1994 Jun;112(6):752-4. doi: 10.1001/archopht.1994.01090180050033. Arch Ophthalmol. 1994. PMID: 8002831 No abstract available.
Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy Overview.
Kumaran N, Pennesi ME, Yang P, Trzupek KM, Schlechter C, Moore AT, Weleber RG, Michaelides M. Kumaran N, et al. Among authors: weleber rg. 2018 Oct 4 [updated 2023 Mar 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2018 Oct 4 [updated 2023 Mar 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 30285347 Free Books & Documents. Review.
Functional evaluation in inherited retinal disease.
Daich Varela M, Georgiou M, Hashem SA, Weleber RG, Michaelides M. Daich Varela M, et al. Among authors: weleber rg. Br J Ophthalmol. 2022 Nov;106(11):1479-1487. doi: 10.1136/bjophthalmol-2021-319994. Epub 2021 Nov 25. Br J Ophthalmol. 2022. PMID: 34824084 Review.
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, Dollfus H, Falana M, Giorda R, Golovleva I, Gottlob I, Heckenlively JR, Jacobson SG, Jones K, Jägle H, Janecke AR, Kellner U, Liskova P, Lorenz B, Martorell-Sampol L, Messias A, Meunier I, Belga Ottoni Porto F, Papageorgiou E, Plomp AS, de Ravel TJL, Reiff CM, Renner AB, Rosenberg T, Rudolph G, Salati R, Sener EC, Sieving PA, Stanzial F, Traboulsi EI, Tsang SH, Varsanyi B, Weleber RG, Zobor D, Stingl K, Wissinger B, Kohl S. Solaki M, et al. Among authors: weleber rg. Hum Mutat. 2022 Jul;43(7):832-858. doi: 10.1002/humu.24371. Epub 2022 Apr 14. Hum Mutat. 2022. PMID: 35332618 Review.
Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium.
Thompson DA, Ali RR, Banin E, Branham KE, Flannery JG, Gamm DM, Hauswirth WW, Heckenlively JR, Iannaccone A, Jayasundera KT, Khan NW, Molday RS, Pennesi ME, Reh TA, Weleber RG, Zacks DN; Monaciano Consortium. Thompson DA, et al. Among authors: weleber rg. Invest Ophthalmol Vis Sci. 2015 Feb 9;56(2):918-31. doi: 10.1167/iovs.14-16049. Invest Ophthalmol Vis Sci. 2015. PMID: 25667399 Free PMC article. Review.
Chromosome anomalies.
Hecht F, Weleber RG, Giblett ER. Hecht F, et al. Among authors: weleber rg. Lancet. 1967 Apr 15;1(7494):848. doi: 10.1016/s0140-6736(67)92816-4. Lancet. 1967. PMID: 4164314 No abstract available.
Ruvalcaba-Myhre-Smith syndrome.
Gretzula JC, Hevia O, Schachner LS, DiLiberti JH, Ruvalcaba RH, Schimschock JR, Weleber RG, Halal F, Lipson MH, Blumberg B, et al. Gretzula JC, et al. Among authors: weleber rg. Pediatr Dermatol. 1988 Feb;5(1):28-32. doi: 10.1111/j.1525-1470.1988.tb00880.x. Pediatr Dermatol. 1988. PMID: 3380760
243 results