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)

Gerhard Binder

University Children's Hospital Tuebingen

Paediatric Endocrinology

Hoppe-Seyler-Strasse 1




Name/email consistency: high



  • University Children's Hospital Tuebingen, Paediatric Endocrinology, Hoppe-Seyler-Strasse 1, Tuebingen, Germany. 2008 - 2011
  • Paediatric Endocrinology, University Children's Hospital, Tubingen, Germany. 2005 - 2009


  1. Silver-Russell syndrome. Binder, G., Begemann, M., Eggermann, T., Kannenberg, K. Best Pract. Res. Clin. Endocrinol. Metab. (2011) [Pubmed]
  2. Noonan syndrome, the Ras-MAPK signalling pathway and short stature. Binder, G. Horm. Res. (2009) [Pubmed]
  3. Response to growth hormone in short children with Noonan syndrome: correlation to genotype. Binder, G. Horm. Res. (2009) [Pubmed]
  4. Effects of dehydroepiandrosterone therapy on pubic hair growth and psychological well-being in adolescent girls and young women with central adrenal insufficiency: a double-blind, randomized, placebo-controlled phase III trial. Binder, G., Weber, S., Ehrismann, M., Zaiser, N., Meisner, C., Ranke, M.B., Maier, L., Wudy, S.A., Hartmann, M.F., Heinrich, U., Bettendorf, M., Doerr, H.G., Pfaeffle, R.W., Keller, E. J. Clin. Endocrinol. Metab. (2009) [Pubmed]
  5. The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alteration. Binder, G., Seidel, A.K., Martin, D.D., Schweizer, R., Schwarze, C.P., Wollmann, H.A., Eggermann, T., Ranke, M.B. J. Clin. Endocrinol. Metab. (2008) [Pubmed]
  6. Homozygosity of the d3-growth hormone receptor polymorphism is associated with a high total effect of GH on growth and a low BMI in girls with Turner syndrome. Binder, G., Trebar, B., Baur, F., Schweizer, R., Ranke, M.B. Clin. Endocrinol. (Oxf) (2008) [Pubmed]
  7. The course of neonatal cholestasis in congenital combined pituitary hormone deficiency. Binder, G., Martin, D.D., Kanther, I., Schwarze, C.P., Ranke, M.B. J. Pediatr. Endocrinol. Metab. (2007) [Pubmed]
  8. Catch-up growth in autosomal dominant isolated growth hormone deficiency (IGHD type II). Binder, G., Iliev, D.I., Mullis, P.E., Ranke, M.B. Growth Horm. IGF Res. (2007) [Pubmed]
  9. IGF-II serum levels are normal in children with Silver-Russell syndrome who frequently carry epimutations at the IGF2 locus. Binder, G., Seidel, A.K., Weber, K., Haase, M., Wollmann, H.A., Ranke, M.B., Eggermann, T. J. Clin. Endocrinol. Metab. (2006) [Pubmed]
  10. The d3-growth hormone (GH) receptor polymorphism is associated with increased responsiveness to GH in Turner syndrome and short small-for-gestational-age children. Binder, G., Baur, F., Schweizer, R., Ranke, M.B. J. Clin. Endocrinol. Metab. (2006) [Pubmed]
  11. PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndrome. Binder, G., Neuer, K., Ranke, M.B., Wittekindt, N.E. J. Clin. Endocrinol. Metab. (2005) [Pubmed]
WikiGenes - Universities