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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Nicole Weisschuh

Centre for Ophthalmology

Institute for Ophthalmic Research

Molecular Genetics Laboratory

Tuebingen

Germany

[email]@uni-tuebingen.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Centre for Ophthalmology, Institute for Ophthalmic Research, Molecular Genetics Laboratory, Tuebingen, Germany. 2008 - 2009
  • Molecular Genetics Laboratory, University Eye Hospital, Tuebingen, Germany. 2005 - 2008

References

  1. A clinical and molecular genetic study of German patients with primary congenital glaucoma. Weisschuh, N., Wolf, C., Wissinger, B., Gramer, E. Am. J. Ophthalmol. (2009) [Pubmed]
  2. 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. Clin. Genet. (2008) [Pubmed]
  3. Variations in the WDR36 gene in German patients with normal tension glaucoma. Weisschuh, N., Wolf, C., Wissinger, B., Gramer, E. Mol. Vis. (2007) [Pubmed]
  4. Identification of genes that are linked with optineurin expression using a combined RNAi--microarray approach. Weisschuh, N., Alavi, M.V., Bonin, M., Wissinger, B. Exp. Eye Res. (2007) [Pubmed]
  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. Invest. Ophthalmol. Vis. Sci. (2006) [Pubmed]
  6. Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients. Weisschuh, N., Neumann, D., Wolf, C., Wissinger, B., Gramer, E. Mol. Vis. (2005) [Pubmed]
 
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