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

Year Number of Results
1983 1
1988 3
1989 1
1990 5
1991 3
1992 3
1993 8
1994 2
1995 7
1996 9
1997 9
1998 11
1999 5
2000 13
2001 9
2002 7
2003 6
2004 18
2005 9
2006 5
2007 4
2008 9
2009 12
2010 4
2011 5
2012 11
2013 8
2014 5
2015 7
2016 9
2017 5
2018 3
2019 7
2020 14
2021 14
2022 12
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244 results
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Page 1
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Khan M, Cornelis SS, Pozo-Valero MD, Whelan L, Runhart EH, Mishra K, Bults F, AlSwaiti Y, AlTalbishi A, De Baere E, Banfi S, Banin E, Bauwens M, Ben-Yosef T, Boon CJF, van den Born LI, Defoort S, Devos A, Dockery A, Dudakova L, Fakin A, Farrar GJ, Sallum JMF, Fujinami K, Gilissen C, Glavač D, Gorin MB, Greenberg J, Hayashi T, Hettinga YM, Hoischen A, Hoyng CB, Hufendiek K, Jägle H, Kamakari S, Karali M, Kellner U, Klaver CCW, Kousal B, Lamey TM, MacDonald IM, Matynia A, McLaren TL, Mena MD, Meunier I, Miller R, Newman H, Ntozini B, Oldak M, Pieterse M, Podhajcer OL, Puech B, Ramesar R, Rüther K, Salameh M, Salles MV, Sharon D, Simonelli F, Spital G, Steehouwer M, Szaflik JP, Thompson JA, Thuillier C, Tracewska AM, van Zweeden M, Vincent AL, Zanlonghi X, Liskova P, Stöhr H, Roach JN, Ayuso C, Roberts L, Weber BHF, Dhaenens CM, Cremers FPM. Khan M, et al. Among authors: kellner u. Genet Med. 2020 Jul;22(7):1235-1246. doi: 10.1038/s41436-020-0787-4. Epub 2020 Apr 20. Genet Med. 2020. PMID: 32307445 Free article.
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
Schulz HL, Grassmann F, Kellner U, Spital G, Rüther K, Jägle H, Hufendiek K, Rating P, Huchzermeyer C, Baier MJ, Weber BH, Stöhr H. Schulz HL, et al. Among authors: kellner u. Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):394-403. doi: 10.1167/iovs.16-19936. Invest Ophthalmol Vis Sci. 2017. PMID: 28118664 Free PMC article.
Reply.
Marmor MF, Lai TY, Kellner U, Melles RB, Mieler WF. Marmor MF, et al. Among authors: kellner u. Ophthalmology. 2017 Mar;124(3):e29-e30. doi: 10.1016/j.ophtha.2016.06.063. Ophthalmology. 2017. PMID: 28219514 No abstract available.
[Toxic retinopathies].
Kellner U, Kellner S, Weinitz S, Farmand G. Kellner U, et al. Ophthalmologe. 2020 Dec;117(12):1247-1266. doi: 10.1007/s00347-020-01260-w. Ophthalmologe. 2020. PMID: 33211161 German.
[Hereditary retinal dystrophies].
Kellner U, Renner AB, Herbst SM, Kellner S, Weinitz S, Weber BH. Kellner U, et al. Klin Monbl Augenheilkd. 2012 Feb;229(2):171-93; quiz 194-6. doi: 10.1055/s-0031-1280461. Epub 2012 Jan 12. Klin Monbl Augenheilkd. 2012. PMID: 22241577 Review. German. No abstract available.
[Hereditary Macular Dystrophies].
Renner AB, Kellner U. Renner AB, et al. Among authors: kellner u. Klin Monbl Augenheilkd. 2016 Oct;233(10):1124-1141. doi: 10.1055/s-0042-100474. Epub 2016 Jul 6. Klin Monbl Augenheilkd. 2016. PMID: 27385259 Review. German.
244 results