Wissinger B - Search Results

1

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. Among authors: wissinger b. 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

2

Macular dystrophy with protan genotype and phenotype studied with cone type specific ERGs.

Scholl HP, Kremers J, Wissinger B. Scholl HP, et al. Among authors: wissinger b. Curr Eye Res. 2001 Mar;22(3):221-8. doi: 10.1076/ceyr.22.3.221.5514. Curr Eye Res. 2001. PMID: 11462159

3

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. Among authors: wissinger b. Mol Vis. 2005 Apr 18;11:284-7. Mol Vis. 2005. PMID: 15851979 Free article.

4

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: wissinger b. Br J Ophthalmol. 2005 Oct;89(10):1258-64. doi: 10.1136/bjo.2004.063933. Br J Ophthalmol. 2005. PMID: 16170112 Free PMC article.

5

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. Among authors: wissinger b. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3846-52. doi: 10.1167/iovs.06-0343. Invest Ophthalmol Vis Sci. 2006. PMID: 16936096

6

A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy.

Alavi MV, Bette S, Schimpf S, Schuettauf F, Schraermeyer U, Wehrl HF, Ruttiger L, Beck SC, Tonagel F, Pichler BJ, Knipper M, Peters T, Laufs J, Wissinger B. Alavi MV, et al. Among authors: wissinger b. Brain. 2007 Apr;130(Pt 4):1029-42. doi: 10.1093/brain/awm005. Epub 2007 Feb 21. Brain. 2007. PMID: 17314202

7

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

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

8

Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T. Wissinger B, et al. Invest Ophthalmol Vis Sci. 2008 Feb;49(2):751-7. doi: 10.1167/iovs.07-0471. Invest Ophthalmol Vis Sci. 2008. PMID: 18235024

9

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. Among authors: wissinger b. 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

10

Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy.

Fuhrmann N, Alavi MV, Bitoun P, Woernle S, Auburger G, Leo-Kottler B, Yu-Wai-Man P, Chinnery P, Wissinger B. Fuhrmann N, et al. Among authors: wissinger b. J Med Genet. 2009 Feb;46(2):136-44. doi: 10.1136/jmg.2008.062570. J Med Genet. 2009. PMID: 19181907

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