Keilhauer CN - Search Results

1

Modelling the genetic risk in age-related macular degeneration.

Grassmann F, Fritsche LG, Keilhauer CN, Heid IM, Weber BH. Grassmann F, et al. Among authors: keilhauer cn. PLoS One. 2012;7(5):e37979. doi: 10.1371/journal.pone.0037979. Epub 2012 May 30. PLoS One. 2012. PMID: 22666427 Free PMC article.

2

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.

Rivera A, Fisher SA, Fritsche LG, Keilhauer CN, Lichtner P, Meitinger T, Weber BH. Rivera A, et al. Among authors: keilhauer cn. Hum Mol Genet. 2005 Nov 1;14(21):3227-36. doi: 10.1093/hmg/ddi353. Epub 2005 Sep 20. Hum Mol Genet. 2005. PMID: 16174643

3

Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).

Fisher SA, Rivera A, Fritsche LG, Keilhauer CN, Lichtner P, Meitinger T, Rudolph G, Weber BH. Fisher SA, et al. Among authors: keilhauer cn. Hum Mutat. 2007 Apr;28(4):406-13. doi: 10.1002/humu.20464. Hum Mutat. 2007. PMID: 17216616

4

Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.

Fritsche LG, Loenhardt T, Janssen A, Fisher SA, Rivera A, Keilhauer CN, Weber BH. Fritsche LG, et al. Among authors: keilhauer cn. Nat Genet. 2008 Jul;40(7):892-6. doi: 10.1038/ng.170. Epub 2008 May 30. Nat Genet. 2008. PMID: 18511946

5

Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene.

Fritsche LG, Freitag-Wolf S, Bettecken T, Meitinger T, Keilhauer CN, Krawczak M, Weber BH. Fritsche LG, et al. Among authors: keilhauer cn. Hum Mutat. 2009 Jul;30(7):1048-53. doi: 10.1002/humu.20957. Hum Mutat. 2009. PMID: 19384966

6

CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD.

Scholl HP, Fleckenstein M, Fritsche LG, Schmitz-Valckenberg S, Göbel A, Adrion C, Herold C, Keilhauer CN, Mackensen F, Mössner A, Pauleikhoff D, Weinberger AW, Mansmann U, Holz FG, Becker T, Weber BH. Scholl HP, et al. Among authors: keilhauer cn. PLoS One. 2009 Oct 12;4(10):e7418. doi: 10.1371/journal.pone.0007418. PLoS One. 2009. PMID: 19823576 Free PMC article.

7

An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD).

Fritsche LG, Lauer N, Hartmann A, Stippa S, Keilhauer CN, Oppermann M, Pandey MK, Köhl J, Zipfel PF, Weber BH, Skerka C. Fritsche LG, et al. Among authors: keilhauer cn. Hum Mol Genet. 2010 Dec 1;19(23):4694-704. doi: 10.1093/hmg/ddq399. Epub 2010 Sep 15. Hum Mol Genet. 2010. PMID: 20843825

8

Age-related macular degeneration with discordant late stage phenotypes in monozygotic twins.

Keilhauer CN, Fritsche LG, Weber BH. Keilhauer CN, et al. Ophthalmic Genet. 2011 Nov;32(4):237-44. doi: 10.3109/13816810.2011.592177. Epub 2011 Jul 8. Ophthalmic Genet. 2011. PMID: 21740222

9

A subgroup of age-related macular degeneration is associated with mono-allelic sequence variants in the ABCA4 gene.

Fritsche LG, Fleckenstein M, Fiebig BS, Schmitz-Valckenberg S, Bindewald-Wittich A, Keilhauer CN, Renner AB, Mackensen F, Mößner A, Pauleikhoff D, Adrion C, Mansmann U, Scholl HP, Holz FG, Weber BH. Fritsche LG, et al. Among authors: keilhauer cn. Invest Ophthalmol Vis Sci. 2012 Apr 30;53(4):2112-8. doi: 10.1167/iovs.11-8785. Invest Ophthalmol Vis Sci. 2012. PMID: 22427542

10

Keilhauer CN, Fritsche LG, Guthoff R, Haubitz I, Weber BH. Keilhauer CN, et al. Eur J Med Genet. 2013 Feb;56(2):72-9. doi: 10.1016/j.ejmg.2012.10.005. Epub 2012 Oct 25. Eur J Med Genet. 2013. PMID: 23103884

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