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

Year Number of Results
1946 1
1947 1
1948 2
1949 1
1950 2
1951 3
1952 2
1953 1
1954 2
1955 4
1956 6
1957 1
1958 3
1959 3
1960 5
1961 6
1962 4
1964 2
1965 5
1966 4
1967 4
1968 2
1969 1
1970 2
1972 1
1976 3
1977 2
1978 2
1982 4
1983 4
1984 1
1985 4
1987 1
1988 2
1989 3
1990 3
1991 2
1992 1
1993 4
1994 3
1995 5
1996 3
1997 3
1998 4
1999 5
2000 7
2001 9
2002 13
2003 13
2004 8
2005 8
2006 8
2007 5
2008 5
2009 5
2010 7
2011 13
2012 29
2013 15
2014 4
2015 8
2016 5
2017 4
2018 4
2019 5
2020 8
2021 13
2022 12
2023 10
2024 3

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334 results

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Page 1
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, Bala E, Lee KE, Hunter DJ, Sardell RJ, Mitchell P, Merriam JE, Cipriani V, Hoffman JD, Schick T, Lechanteur YT, Guymer RH, Johnson MP, Jiang Y, Stanton CM, Buitendijk GH, Zhan X, Kwong AM, Boleda A, Brooks M, Gieser L, Ratnapriya R, Branham KE, Foerster JR, Heckenlively JR, Othman MI, Vote BJ, Liang HH, Souzeau E, McAllister IL, Isaacs T, Hall J, Lake S, Mackey DA, Constable IJ, Craig JE, Kitchner TE, Yang Z, Su Z, Luo H, Chen D, Ouyang H, Flagg K, Lin D, Mao G, Ferreyra H, Stark K, von Strachwitz CN, Wolf A, Brandl C, Rudolph G, Olden M, Morrison MA, Morgan DJ, Schu M, Ahn J, Silvestri G, Tsironi EE, Park KH, Farrer LA, Orlin A, Brucker A, Li M, Curcio CA, Mohand-Saïd S, Sahel JA, Audo I, Benchaboune M, Cree AJ, Rennie CA, Goverdhan SV, Grunin M, Hagbi-Levi S, Campochiaro P, Katsanis N, Holz FG, Blond F, Blanché H, Deleuze JF, Igo RP Jr, Truitt B, Peachey NS, Meuer SM, Myers CE, Moore EL, Klein R, Hauser MA, Postel EA, Courtenay MD, Schwartz SG, Kovach JL, Scott WK, Liew G, Tan AG, Gopinath B, Merriam JC, Smith RT, K… See abstract for full author list ➔ Fritsche LG, et al. Among authors: rudolph g. Nat Genet. 2016 Feb;48(2):134-43. doi: 10.1038/ng.3448. Epub 2015 Dec 21. Nat Genet. 2016. PMID: 26691988 Free PMC article.
Achromatopsia: Genetics and Gene Therapy.
Michalakis S, Gerhardt M, Rudolph G, Priglinger S, Priglinger C. Michalakis S, et al. Among authors: rudolph g. Mol Diagn Ther. 2022 Jan;26(1):51-59. doi: 10.1007/s40291-021-00565-z. Epub 2021 Dec 3. Mol Diagn Ther. 2022. PMID: 34860352 Free PMC article. Review.
[Gene therapy in ophthalmology].
Priglinger CS, Gerhardt MJ, Rudolph G, Priglinger SG, Michalakis S. Priglinger CS, et al. Among authors: rudolph g. Ophthalmologie. 2023 Aug;120(8):867-882. doi: 10.1007/s00347-023-01883-9. Epub 2023 Jul 7. Ophthalmologie. 2023. PMID: 37418021 Review. German.
Comitant strabismus.
Schworm HD, Rudolph G. Schworm HD, et al. Among authors: rudolph g. Curr Opin Ophthalmol. 2000 Oct;11(5):310-7. doi: 10.1097/00055735-200010000-00004. Curr Opin Ophthalmol. 2000. PMID: 11148695 Review.
Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies.
Glöckle N, Kohl S, Mohr J, Scheurenbrand T, Sprecher A, Weisschuh N, Bernd A, Rudolph G, Schubach M, Poloschek C, Zrenner E, Biskup S, Berger W, Wissinger B, Neidhardt J. Glöckle N, et al. Among authors: rudolph g. Eur J Hum Genet. 2014 Jan;22(1):99-104. doi: 10.1038/ejhg.2013.72. Epub 2013 Apr 17. Eur J Hum Genet. 2014. PMID: 23591405 Free PMC article.
Complications of shoulder arthroscopy.
Moen TC, Rudolph GH, Caswell K, Espinoza C, Burkhead WZ Jr, Krishnan SG. Moen TC, et al. Among authors: rudolph gh. J Am Acad Orthop Surg. 2014 Jul;22(7):410-9. doi: 10.5435/JAAOS-22-07-410. J Am Acad Orthop Surg. 2014. PMID: 24966247 Review.
[Ophthalmology and genetics].
Rudolph G. Rudolph G. Klin Monbl Augenheilkd. 2013 Mar;230(3):221-2. doi: 10.1055/s-0032-1328289. Epub 2013 Mar 18. Klin Monbl Augenheilkd. 2013. PMID: 23508751 German. No abstract available.
[Posterior embryotoxon].
Gandorfer A, Rudolph G, Boergen KP, Kampik A. Gandorfer A, et al. Among authors: rudolph g. Ophthalmologe. 2000 Mar;97(3):226-7. doi: 10.1007/s003470050518. Ophthalmologe. 2000. PMID: 10789182 German. No abstract available.
[Corneal disease in childhood-Hereditary, degenerative or infectious?].
Brunner BS, Kassumeh S, Rudolph G, Priglinger SG, Messmer EM. Brunner BS, et al. Among authors: rudolph g. Ophthalmologie. 2023 Aug;120(8):811-817. doi: 10.1007/s00347-023-01897-3. Epub 2023 Jul 12. Ophthalmologie. 2023. PMID: 37438454 Review. German.
334 results