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

Reinhard Schneppenheim

University Medical Center Hamburg-Eppendorf

Department of Pediatric Hematology and Oncology

Martinistrasse 52

D-20246 Hamburg



Name/email consistency: high



  • University Medical Center Hamburg-Eppendorf, Department of Pediatric Hematology and Oncology, Martinistrasse 52, D-20246 Hamburg, Germany. 2006
  • University Children's Hospital Hamburg, Division of Paediatric Haematology and Oncology, Germany. 2000 - 2005
  • Department of Pediatric Hematology and Oncology, Center of Gynecology, Obstetrics and Pediatrics, University Hospital Hamburg-Eppendorf, Germany. 2005
  • Paediatric Oncology, University Children's Hospital, Hamburg, Germany. 2004
  • Children's University Hospital, Hamburg-Eppendorf; Lab Association Prof Arndt and Partners, Coagulation Laboratory, Hamburg, Germany. 2003


  1. A common origin of the 4143insA ADAMTS13 mutation. Schneppenheim, R., Kremer Hovinga, J.A., Becker, T., Budde, U., Karpman, D., Brockhaus, W., Hrachovinová, I., Korczowski, B., Oyen, F., Rittich, S., von Rosen, J., Tjønnfjord, G.E., Pimanda, J.E., Wienker, T.F., Lämmle, B. Thromb. Haemost. (2006) [Pubmed]
  2. Phenotypic and genotypic diagnosis of von Willebrand disease: a 2004 update. Schneppenheim, R., Budde, U. Semin. Hematol. (2005) [Pubmed]
  3. The evolving classification of von Willebrand disease. Schneppenheim, R. Blood Coagul. Fibrinolysis (2005) [Pubmed]
  4. Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization. Schneppenheim, R., Lenk, H., Obser, T., Oldenburg, J., Oyen, F., Schneppenheim, S., Schwaab, R., Will, K., Budde, U. Thromb. Haemost. (2004) [Pubmed]
  5. von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Schneppenheim, R., Budde, U., Oyen, F., Angerhaus, D., Aumann, V., Drewke, E., Hassenpflug, W., Häberle, J., Kentouche, K., Kohne, E., Kurnik, K., Mueller-Wiefel, D., Obser, T., Santer, R., Sykora, K.W. Blood (2003) [Pubmed]
  6. Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 families. Schneppenheim, R., Federici, A.B., Budde, U., Castaman, G., Drewke, E., Krey, S., Mannucci, P.M., Riesen, G., Rodeghiero, F., Zieger, B., Zimmermann, R. Thromb. Haemost. (2000) [Pubmed]
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