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

Esther van de Vosse

Department of Infectious Diseases

C5-P, Leiden University Medical Center

Albinusdreef 2



Name/email consistency: high



  • Department of Infectious Diseases, C5-P, Leiden University Medical Center, Albinusdreef 2, Netherlands. 2005 - 2011


  1. Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation. van de Vosse, E., Verhard, E.M., Tool, A.J., de Visser, A.W., Kuijpers, T.W., Hiemstra, P.S., van Dissel, J.T. Ann. Hematol. (2011) [Pubmed]
  2. Mycobacterium bovis BCG-itis and cervical lymphadenitis due to Salmonella enteritidis in a patient with complete interleukin-12/-23 receptor beta1 deficiency. van de Vosse, E., Ottenhoff, T.H., de Paus, R.A., Verhard, E.M., de Boer, T., van Dissel, J.T., Kuijpers, T.W. Infection (2010) [Pubmed]
  3. Distribution of CFTR variations in an Indonesian enteric fever cohort. van de Vosse, E., de Visser, A.W., Al-Attar, S., Vossen, R., Ali, S., van Dissel, J.T. Clin. Infect. Dis. (2010) [Pubmed]
  4. A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation. van de Vosse, E., van Wengen, A., van Geelen, J.A., de Boer, M., Roos, D., van Dissel, J.T. J. Hum. Genet. (2009) [Pubmed]
  5. Antisense-mediated exon skipping to correct IL-12Rbeta1 deficiency in T cells. van de Vosse, E., Verhard, E.M., de Paus, R.A., Platenburg, G.J., van Deutekom, J.C., Aartsma-Rus, A., van Dissel, J.T. Blood (2009) [Pubmed]
  6. Genetic deficiencies of innate immune signalling in human infectious disease. van de Vosse, E., van Dissel, J.T., Ottenhoff, T.H. Lancet. Infect. Dis (2009) [Pubmed]
  7. Targets of anticytokine therapy and the risk of infections in humans and mice. van de Vosse, E., van Agtmael, M.A. Curr. Opin. Rheumatol (2007) [Pubmed]
  8. Susceptibility to typhoid fever is associated with a polymorphism in the cystic fibrosis transmembrane conductance regulator (CFTR). van de Vosse, E., Ali, S., de Visser, A.W., Surjadi, C., Widjaja, S., Vollaard, A.M., van Dissel, J.T. Hum. Genet. (2005) [Pubmed]
  9. Molecular complementation of IL-12Rbeta1 deficiency reveals functional differences between IL-12Rbeta1 alleles including partial IL-12Rbeta1 deficiency. van de Vosse, E., de Paus, R.A., van Dissel, J.T., Ottenhoff, T.H. Hum. Mol. Genet. (2005) [Pubmed]
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