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

Gert Matthijs

Center for Human Genetics

University of Leuven



Name/email consistency: high



  • Center for Human Genetics, University of Leuven, Belgium. 1996 - 2006


  1. The European opposition against the BRCA gene patents. Matthijs, G. Fam. Cancer (2006) [Pubmed]
  2. Research network: EUROGLYCANET: a European network focused on congenital disorders of glycosylation. Matthijs, G. Eur. J. Hum. Genet. (2005) [Pubmed]
  3. The prenatal diagnosis of congenital disorders of glycosylation (CDG). Matthijs, G., Schollen, E., Van Schaftingen, E. Prenat. Diagn. (2004) [Pubmed]
  4. Congenital disorders of glycosylation. Matthijs, G. Trends Biochem. Sci. (2000) [Pubmed]
  5. Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia). Matthijs, G., Schollen, E., Bjursell, C., Erlandson, A., Freeze, H., Imtiaz, F., Kjaergaard, S., Martinsson, T., Schwartz, M., Seta, N., Vuillaumier-Barrot, S., Westphal, V., Winchester, B. Hum. Mutat. (2000) [Pubmed]
  6. Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A. Matthijs, G., Schollen, E., Van Schaftingen, E., Cassiman, J.J., Jaeken, J. Am. J. Hum. Genet. (1998) [Pubmed]
  7. PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13. Matthijs, G., Schollen, E., Pirard, M., Budarf, M.L., Van Schaftingen, E., Cassiman, J.J. Genomics (1997) [Pubmed]
  8. Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome). Matthijs, G., Schollen, E., Pardon, E., Veiga-Da-Cunha, M., Jaeken, J., Cassiman, J.J., Van Schaftingen, E. Nat. Genet. (1997) [Pubmed]
  9. Evidence for genetic heterogeneity in the carbohydrate-deficient glycoprotein syndrome type I (CDG1). Matthijs, G., Legius, E., Schollen, E., Vandenberk, P., Jaeken, J., Barone, R., Fiumara, A., Visser, G., Lambert, M., Cassiman, J.J. Genomics (1996) [Pubmed]
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