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

Beate Skinningsrud

Department of Medical Genetics

Oslo University Hospital

Ullevål Hospital

Pb 4956 Nydalen

Norway

[email]@medisin.uio.no

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Medical Genetics, Oslo University Hospital, Ullevål Hospital, Pb 4956 Nydalen, Norway. 2008 - 2011
  • Institute of Medical Genetics, University of Oslo, Department of Medical Genetics, Ullevaal University Hospital, Norway. 2008

References

  1. Multiple Loci in the HLA Complex Are Associated with Addison's Disease. Skinningsrud, B., Lie, B.A., Lavant, E., Carlson, J.A., Erlich, H., Akselsen, H.E., Gervin, K., Wolff, A.B., Erichsen, M.M., Løvås, K., Husebye, E.S., Undlien, D.E. J. Clin. Endocrinol. Metab. (2011) [Pubmed]
  2. A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis. Skinningsrud, B., Lie, B.A., Husebye, E.S., Kvien, T.K., Førre, Ø., Flatø, B., Stormyr, A., Joner, G., Njølstad, P.R., Egeland, T., Undlien, D.E. Ann. Rheum. Dis. (2010) [Pubmed]
  3. X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene. Skinningsrud, B., Husebye, E.S., Gilfillan, G.D., Frengen, E., Erichsen, A., Gervin, K., Ormerod, E., Egeland, T., Undlien, D.E. J. Clin. Endocrinol. Metab. (2009) [Pubmed]
  4. Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease. Skinningsrud, B., Husebye, E.S., Gervin, K., Løvås, K., Blomhoff, A., Wolff, A.B., Kemp, E.H., Egeland, T., Undlien, D.E. Eur. J. Hum. Genet. (2008) [Pubmed]
  5. Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. Skinningsrud, B., Husebye, E.S., Pearce, S.H., McDonald, D.O., Brandal, K., Wolff, A.B., Løvås, K., Egeland, T., Undlien, D.E. J. Clin. Endocrinol. Metab. (2008) [Pubmed]
 
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