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

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Gregor Kuhlenbäumer

Leibniz Institute of Atherosclerosis Research

University of Münster

Münster

Germany

[email]@uni-muenster.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Leibniz Institute of Atherosclerosis Research, University of Münster, Münster, Germany. 2007
  • Department of Neurology, University of Münster, Albert-Schweitzer-Str 33, 48129 Münster, Germany. 2002 - 2006
  • Department of Neurology, University of Münster, Germany. 2004
  • Klinik und Poliklinik für Neurologie Westfälische Wilhelms Universität Münster, Germany. 2001

References

  1. Association between single nucleotide polymorphisms in the lysyl oxidase-like 1 gene and spontaneous cervical artery dissection. Kuhlenbäumer, G., Friedrichs, F., Kis, B., Berlit, P., Maintz, D., Nassenstein, I., Nabavi, D., Dittrich, R., Stoll, M., Ringelstein, B. Cerebrovasc. Dis. (2007) [Pubmed]
  2. Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohort. Kuhlenbäumer, G., Berger, K., Huge, A., Lange, E., Kessler, C., John, U., Funke, H., Nabavi, D.G., Stögbauer, F., Ringelstein, E.B., Stoll, M. J. Neurol. Neurosurg. Psychiatr. (2006) [Pubmed]
  3. Mutations in SEPT9 cause hereditary neuralgic amyotrophy. Kuhlenbäumer, G., Hannibal, M.C., Nelis, E., Schirmacher, A., Verpoorten, N., Meuleman, J., Watts, G.D., De Vriendt, E., Young, P., Stögbauer, F., Halfter, H., Irobi, J., Goossens, D., Del-Favero, J., Betz, B.G., Hor, H., Kurlemann, G., Bird, T.D., Airaksinen, E., Mononen, T., Serradell, A.P., Prats, J.M., Van Broeckhoven, C., De Jonghe, P., Timmerman, V., Ringelstein, E.B., Chance, P.F. Nat. Genet. (2005) [Pubmed]
  4. Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14. Kuhlenbäumer, G., Lüdemann, P., Schirmacher, A., De Vriendt, E., Hünermund, G., Young, P., Hund-Georgiadis, M., Schuierer, G., Möller, H., Ringelstein, E.B., Van Broeckhoven, C., Timmerman, V., Stögbauer, F. Neurology (2004) [Pubmed]
  5. Clinical features and molecular genetics of hereditary peripheral neuropathies. Kuhlenbäumer, G., Young, P., Hünermund, G., Ringelstein, B., Stögbauer, F. J. Neurol. (2002) [Pubmed]
  6. Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals. Kuhlenbäumer, G., Kress, W., Ringelstein, E.B., Stögbauer, F. J. Neurol. (2001) [Pubmed]
 
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