The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Bernd Hoppe

Correspondence and offprint requests to: Bernd Hoppe; E-mail:


Name/email consistency: high



  • Correspondence and offprint requests to: Bernd Hoppe; E-mail:. 2011 - 2012
  • University Hospital, Department of Pediatric and Adolescent Medicine, Division of Pediatric Nephrology, Kerpener Strasse 62, Germany. 2012
  • Division of Pediatric Nephrology, Children's Hospital Cologne, University of Cologne, Cologne, Germany. 2005 - 2010
  • University Children's Hospital Cologne, USA. 2005


  1. The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type III. Hoppe, B. Nephrol. Dial. Transplant. (2012) [Pubmed]
  2. An update on primary hyperoxaluria. Hoppe, B. Nat. Rev. Nephrol (2012) [Pubmed]
  3. Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation? Beck, B.B., Habbig, S., Dittrich, K., Stippel, D., Kaul, I., Koerber, F., Goebel, H., Salido, E.C., Kemper, M., Meyburg, J., Hoppe, B. Nephrol. Dial. Transplant. (2012) [Pubmed]
  4. Efficacy and safety of Oxalobacter formigenes to reduce urinary oxalate in primary hyperoxaluria. Hoppe, B., Groothoff, J.W., Hulton, S.A., Cochat, P., Niaudet, P., Kemper, M.J., Deschênes, G., Unwin, R., Milliner, D. Nephrol. Dial. Transplant. (2011) [Pubmed]
  5. Cardiorespiratory capacity in children and adolescents on maintenance haemodialysis. Schaar, B., Feldkötter, M., Nonn, J.M., Hoppe, B. Nephrol. Dial. Transplant. (2011) [Pubmed]
  6. Diagnostic examination of the child with urolithiasis or nephrocalcinosis. Hoppe, B., Kemper, M.J. Pediatr. Nephrol. (2010) [Pubmed]
  7. Evidence of true genotype-phenotype correlation in primary hyperoxaluria type 1. Hoppe, B. Kidney Int. (2010) [Pubmed]
  8. The primary hyperoxalurias. Hoppe, B., Beck, B.B., Milliner, D.S. Kidney Int. (2009) [Pubmed]
  9. Oxalobacter formigenes: a potential tool for the treatment of primary hyperoxaluria type 1. Hoppe, B., Beck, B., Gatter, N., von Unruh, G., Tischer, A., Hesse, A., Laube, N., Kaul, P., Sidhu, H. Kidney Int. (2006) [Pubmed]
  10. Is there a genotype-phenotype correlation in primary hyperoxaluria type 1?. Beck, B.B., Hoppe, B. Kidney Int. (2006) [Pubmed]
  11. Primary hyperoxaluria--the German experience. Hoppe, B., Latta, K., von Schnakenburg, C., Kemper, M.J. Am. J. Nephrol. (2005) [Pubmed]
  12. Absorptive hyperoxaluria leads to an increased risk for urolithiasis or nephrocalcinosis in cystic fibrosis. Hoppe, B., von Unruh, G.E., Blank, G., Rietschel, E., Sidhu, H., Laube, N., Hesse, A. Am. J. Kidney Dis. (2005) [Pubmed]
WikiGenes - Universities