Weisschuh N - Search Results

1

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: weisschuh n. Sci Rep. 2017 Aug 1;7(1):6992. doi: 10.1038/s41598-017-07117-8. Sci Rep. 2017. PMID: 28765526 Free PMC article.

2

Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients.

Weisschuh N, Neumann D, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Mol Vis. 2005 Apr 18;11:284-7. Mol Vis. 2005. PMID: 15851979 Free article.

3

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.

Schuster A, Weisschuh N, Jägle H, Besch D, Janecke AR, Zierler H, Tippmann S, Zrenner E, Wissinger B. Schuster A, et al. Among authors: weisschuh n. Br J Ophthalmol. 2005 Oct;89(10):1258-64. doi: 10.1136/bjo.2004.063933. Br J Ophthalmol. 2005. PMID: 16170112 Free PMC article.

4

Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations.

Weisschuh N, Dressler P, Schuettauf F, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3846-52. doi: 10.1167/iovs.06-0343. Invest Ophthalmol Vis Sci. 2006. PMID: 16936096

5

Variations in the WDR36 gene in German patients with normal tension glaucoma.

Weisschuh N, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Mol Vis. 2007 May 16;13:724-9. Mol Vis. 2007. PMID: 17563723 Free PMC article.

6

Identification of genes that are linked with optineurin expression using a combined RNAi--microarray approach.

Weisschuh N, Alavi MV, Bonin M, Wissinger B. Weisschuh N, et al. Exp Eye Res. 2007 Oct;85(4):450-61. doi: 10.1016/j.exer.2007.06.012. Epub 2007 Jun 27. Exp Eye Res. 2007. PMID: 17663987

7

A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly.

Weisschuh N, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Clin Genet. 2008 Nov;74(5):476-80. doi: 10.1111/j.1399-0004.2008.01025.x. Epub 2008 May 21. Clin Genet. 2008. PMID: 18498376

8

A clinical and molecular genetic study of German patients with primary congenital glaucoma.

Weisschuh N, Wolf C, Wissinger B, Gramer E. Weisschuh N, et al. Am J Ophthalmol. 2009 Apr;147(4):744-53. doi: 10.1016/j.ajo.2008.11.008. Epub 2009 Feb 4. Am J Ophthalmol. 2009. PMID: 19195637

9

Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma.

Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Gramer G, Wissinger B, Weisschuh N. Wolf C, et al. Among authors: weisschuh n. J Glaucoma. 2010 Feb;19(2):136-41. doi: 10.1097/IJG.0b013e31819f9330. J Glaucoma. 2010. PMID: 19373106

10

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study.

Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Reinthal E, Wissinger B, Weisschuh N. Wolf C, et al. Among authors: weisschuh n. BMC Med Genet. 2009 Sep 15;10:91. doi: 10.1186/1471-2350-10-91. BMC Med Genet. 2009. PMID: 19754948 Free PMC article.

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