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

Mark I. Rees

Department of Molecular Medicine

University of Auckland Medical School

Postbag 92019


New Zealand


Name/email consistency: high



  • Department of Molecular Medicine, University of Auckland Medical School, Postbag 92019, Auckland, New Zealand. 2001 - 2003
  • Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff, UK. 2000


  1. Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia. Rees, M.I., Harvey, K., Ward, H., White, J.H., Evans, L., Duguid, I.C., Hsu, C.C., Coleman, S.L., Miller, J., Baer, K., Waldvogel, H.J., Gibbon, F., Smart, T.G., Owen, M.J., Harvey, R.J., Snell, R.G. J. Biol. Chem. (2003) [Pubmed]
  2. Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia. Rees, M.I., Lewis, T.M., Vafa, B., Ferrie, C., Corry, P., Muntoni, F., Jungbluth, H., Stephenson, J.B., Kerr, M., Snell, R.G., Schofield, P.R., Owen, M.J. Hum. Genet. (2001) [Pubmed]
  3. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). Rees, M.I., Watts, P., Fenton, I., Clarke, A., Snell, R.G., Owen, M.J., Gray, J. Hum. Genet. (2000) [Pubmed]
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