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

Peter Huppke

Department of Pediatrics and Pediatric Neurology

Faculty of Medicine

Georg August University




Name/email consistency: high



  • Department of Pediatrics and Pediatric Neurology, Faculty of Medicine, Georg August University, Göttingen, Germany. 2005 - 2012
  • Neuropediatric Department and Department of Genetic Epidemiology, Institute of Human Genetics, Georg-August-Universität Göttingen, Göttingen, Germany. 2003
  • Abteilung Kinderheilkunde, Schwerpunkt Neuropädiatrie, Georg-August-Universität Göttingen, Germany. 2000 - 2002
  • Neuropediatric Department, Georg-August-Universität Göttingen, Germany. 2002


  1. Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutase. Huppke, P., Brendel, C., Korenke, G.C., Marquardt, I., Donsante, A., Yi, L., Hicks, J.D., Steinbach, P.J., Wilson, C., Elpeleg, O., Møller, L.B., Christodoulou, J., Kaler, S.G., Gärtner, J. Hum. Mutat. (2012) [Pubmed]
  2. Neuromyelitis optica and NMO-IgG in European pediatric patients. Huppke, P., Blüthner, M., Bauer, O., Stark, W., Reinhardt, K., Huppke, B., Gärtner, J. Neurology (2010) [Pubmed]
  3. A practical guide to pediatric multiple sclerosis. Huppke, P., Gärtner, J. Neuropediatrics (2010) [Pubmed]
  4. Immunoglobulin therapy in idiopathic hypothalamic dysfunction. Huppke, P., Heise, A., Rostasy, K., Huppke, B., Gärtner, J. Pediatr. Neurol. (2009) [Pubmed]
  5. Treatment of epilepsy in Rett syndrome. Huppke, P., Köhler, K., Brockmann, K., Stettner, G.M., Gärtner, J. Eur. J. Paediatr. Neurol. (2007) [Pubmed]
  6. Very mild cases of Rett syndrome with skewed X inactivation. Huppke, P., Maier, E.M., Warnke, A., Brendel, C., Laccone, F., Gärtner, J. J. Med. Genet. (2006) [Pubmed]
  7. Perisylvian polymicrogyria in Landau-Kleffner syndrome. Huppke, P., Kallenberg, K., Gärtner, J. Neurology (2005) [Pubmed]
  8. Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2. Huppke, P., Ohlenbusch, A., Brendel, C., Laccone, F., Gärtner, J. Am. J. Med. Genet. A (2005) [Pubmed]
  9. Molecular diagnosis of Rett syndrome. Huppke, P., Gärtner, J. J. Child Neurol. (2005) [Pubmed]
  10. Indication for genetic testing: a checklist for Rett syndrome. Huppke, P., Köhler, K., Laccone, F., Hanefeld, F. J. Pediatr. (2003) [Pubmed]
  11. The spectrum of phenotypes in females with Rett Syndrome. Huppke, P., Held, M., Laccone, F., Hanefeld, F. Brain Dev. (2003) [Pubmed]
  12. Influence of mutation type and location on phenotype in 123 patients with Rett syndrome. Huppke, P., Held, M., Hanefeld, F., Engel, W., Laccone, F. Neuropediatrics (2002) [Pubmed]
  13. Altered methylation pattern of the G6 PD promoter in Rett syndrome. Huppke, P., Bohlander, S., Krämer, N., Laccone, F., Hanefeld, F. Neuropediatrics (2002) [Pubmed]
  14. Eosinophilic fasciitis leading to painless contractures. Huppke, P., Wilken, B., Brockmann, K., Sattler, B., Hanefeld, F. Eur. J. Pediatr. (2002) [Pubmed]
  15. Two brothers with Hennekam syndrome and cerebral abnormalities. Huppke, P., Christen, H.J., Sattler, B., Hanefeld, F. Clin. Dysmorphol. (2000) [Pubmed]
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