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Results by year

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

Year Number of Results
1976 2
1977 3
1978 2
1979 3
1981 3
1983 2
1984 5
1985 2
1986 8
1987 8
1988 8
1989 7
1990 3
1991 11
1992 11
1993 17
1994 14
1995 16
1996 10
1997 23
1998 20
1999 23
2000 19
2001 20
2002 13
2003 6
2004 18
2005 14
2006 15
2007 15
2008 12
2009 12
2010 27
2011 21
2012 22
2013 20
2014 15
2015 15
2016 8
2017 23
2018 21
2019 25
2020 21
2021 17
2022 15
2023 9
2024 6

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Search Results

561 results

Results by year

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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. Among authors: zrenner e. 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.
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C. Bonnet C, et al. Among authors: zrenner e. Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27. Eur J Hum Genet. 2016. PMID: 27460420 Free PMC article.
Bioengineering strategies for restoring vision.
Cehajic-Kapetanovic J, Singh MS, Zrenner E, MacLaren RE. Cehajic-Kapetanovic J, et al. Among authors: zrenner e. Nat Biomed Eng. 2023 Apr;7(4):387-404. doi: 10.1038/s41551-021-00836-4. Epub 2022 Jan 31. Nat Biomed Eng. 2023. PMID: 35102278 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: zrenner e. 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.
Neuroimaging the retina.
Pugh EN Jr, Baehr W, Zrenner E. Pugh EN Jr, et al. Among authors: zrenner e. Vision Res. 2005 Dec;45(28):3431. doi: 10.1016/j.visres.2005.09.040. Epub 2005 Nov 10. Vision Res. 2005. PMID: 16289207 Free article. No abstract available.
CNGB1-related rod-cone dystrophy: A mutation review and update.
Nassisi M, Smirnov VM, Solis Hernandez C, Mohand-Saïd S, Condroyer C, Antonio A, Kühlewein L, Kempf M, Kohl S, Wissinger B, Nasser F, Ragi SD, Wang NK, Sparrow JR, Greenstein VC, Michalakis S, Mahroo OA, Ba-Abbad R, Michaelides M, Webster AR, Degli Esposti S, Saffren B, Capasso J, Levin A, Hauswirth WW, Dhaenens CM, Defoort-Dhellemmes S, Tsang SH, Zrenner E, Sahel JA, Petersen-Jones SM, Zeitz C, Audo I. Nassisi M, et al. Among authors: zrenner e. Hum Mutat. 2021 Jun;42(6):641-666. doi: 10.1002/humu.24205. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33847019 Free PMC article. Review.
[Electronic Retina Implants - an Abandoned Dream?].
Faber H, Bartz-Schmidt KU, Stett A, Zrenner E, Stingl K. Faber H, et al. Among authors: zrenner e. Klin Monbl Augenheilkd. 2020 Mar;237(3):288-293. doi: 10.1055/a-1021-5040. Epub 2020 Mar 17. Klin Monbl Augenheilkd. 2020. PMID: 32182631 Review. German.
Will retinal implants restore vision?
Zrenner E. Zrenner E. Science. 2002 Feb 8;295(5557):1022-5. doi: 10.1126/science.1067996. Science. 2002. PMID: 11834821 Review.
CDHR1 mutations in retinal dystrophies.
Stingl K, Mayer AK, Llavona P, Mulahasanovic L, Rudolph G, Jacobson SG, Zrenner E, Kohl S, Wissinger B, Weisschuh N. Stingl K, et al. Among authors: zrenner e. Sci Rep. 2017 Aug 1;7(1):6992. doi: 10.1038/s41598-017-07117-8. Sci Rep. 2017. PMID: 28765526 Free PMC article.
561 results