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

Bernd Wissinger

Molecular Genetics Laboratory

Institute for Ophthalmic Research

Centre for Ophthalmology

University Clinics Tübingen



Name/email consistency: high



  • Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University Clinics Tübingen, Germany. 1998 - 2011
  • Molekulargenetisches Labor, Abt Pathophysiologie des Sehens und Neuroophthalmologie, Tübingen, Germany. 2001
  • Molekulargenetisches Labor, Universitäts-Augenklinik, Tübingen, Germany. 1997 - 1998


  1. Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. Wissinger, B., Schaich, S., Baumann, B., Bonin, M., Jägle, H., Friedburg, C., Varsányi, B., Hoyng, C.B., Dollfus, H., Heckenlively, J.R., Rosenberg, T., Rudolph, G., Kellner, U., Salati, R., Plomp, A., De Baere, E., Andrassi-Darida, M., Sauer, A., Wolf, C., Zobor, D., Bernd, A., Leroy, B.P., Enyedi, P., Cremers, F.P., Lorenz, B., Zrenner, E., Kohl, S. Hum. Mutat. (2011) [Pubmed]
  2. 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. Invest. Ophthalmol. Vis. Sci. (2008) [Pubmed]
  3. CNGA3 mutations in hereditary cone photoreceptor disorders. Wissinger, B., Gamer, D., Jägle, H., Giorda, R., Marx, T., Mayer, S., Tippmann, S., Broghammer, M., Jurklies, B., Rosenberg, T., Jacobson, S.G., Sener, E.C., Tatlipinar, S., Hoyng, C.B., Castellan, C., Bitoun, P., Andreasson, S., Rudolph, G., Kellner, U., Lorenz, B., Wolff, G., Verellen-Dumoulin, C., Schwartz, M., Cremers, F.P., Apfelstedt-Sylla, E., Zrenner, E., Salati, R., Sharpe, L.T., Kohl, S. Am. J. Hum. Genet. (2001) [Pubmed]
  4. Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11. Wissinger, B., Jägle, H., Kohl, S., Broghammer, M., Baumann, B., Hanna, D.B., Hedels, C., Apfelstedt-Sylla, E., Randazzo, G., Jacobson, S.G., Zrenner, E., Sharpe, L.T. Genomics (1998) [Pubmed]
  5. New aspects of an old theme: the genetic basis of human color vision. Wissinger, B., Sharpe, L.T. Am. J. Hum. Genet. (1998) [Pubmed]
  6. Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy. Wissinger, B., Besch, D., Baumann, B., Fauser, S., Christ-Adler, M., Jurklies, B., Zrenner, E., Leo-Kottler, B. Biochem. Biophys. Res. Commun. (1997) [Pubmed]
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