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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 2
2025 5
2026 0

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338 results

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Page 1
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.
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.
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries.
Gorman BR, Voloudakis G, Igo RP Jr, Kinzy T, Halladay CW, Bigdeli TB, Zeng B, Venkatesh S, Cooke Bailey JN, Crawford DC, Markianos K, Dong F, Schreiner PA, Zhang W; VA Million Veteran Program; International AMD Genomics Consortium (IAMDGC); Hadi T, Anger MD, Stockwell A, Melles RB, Yin J, Choquet H, Kaye R, Patasova K, Patel PJ, Yaspan BL, Jorgenson E, Hysi PG, Lotery AJ, Gaziano JM, Tsao PS, Fliesler SJ, Sullivan JM, Greenberg PB, Wu WC, Assimes TL, Pyarajan S, Roussos P, Peachey NS, Iyengar SK. Gorman BR, et al. Nat Genet. 2024 Dec;56(12):2659-2671. doi: 10.1038/s41588-024-01764-0. Epub 2024 Dec 2. Nat Genet. 2024. PMID: 39623103
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.
Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic Neuropathy.
Yu-Wai-Man P, Newman NJ, Biousse V, Carelli V, Moster ML, Vignal-Clermont C, Klopstock T, Sadun AA, Sergott RC, Hage R, Degli Esposti S, La Morgia C, Priglinger C, Karanja R, Taiel M, Sahel JA; LHON Study Group. Yu-Wai-Man P, et al. JAMA Ophthalmol. 2025 Feb 1;143(2):99-108. doi: 10.1001/jamaophthalmol.2024.5375. JAMA Ophthalmol. 2025. PMID: 39699886 Free PMC article. Clinical Trial.
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.
[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.
Diagnosis of Inherited Retinal Diseases.
Birtel J, Yusuf IH, Priglinger C, Rudolph G, Charbel Issa P. Birtel J, et al. Among authors: rudolph g. Klin Monbl Augenheilkd. 2021 Mar;238(3):249-259. doi: 10.1055/a-1388-7236. Epub 2021 Mar 30. Klin Monbl Augenheilkd. 2021. PMID: 33784788 English, German.
[Congenital cranial dysinnervation disorders (CCDD)].
Nentwich MM, Nentwich MF, Maertz J, Brandlhuber U, Rudolph G. Nentwich MM, et al. Among authors: rudolph g. Klin Monbl Augenheilkd. 2015 Mar;232(3):275-80. doi: 10.1055/s-0041-100772. Epub 2015 Mar 24. Klin Monbl Augenheilkd. 2015. PMID: 25803556 Review. German.
338 results