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

Melanie J. Percy

Department of Haematology

Belfast City Hospital


United Kingdom


Name/email consistency: high



  • Department of Haematology, Belfast City Hospital, Belfast, United Kingdom. 2007 - 2009
  • Belfast City Hospital, Northern Ireland, United Kingdom. 2008


  1. Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. Percy, M.J., Rumi, E. Am. J. Hematol. (2009) [Pubmed]
  2. A gain-of-function mutation in the HIF2A gene in familial erythrocytosis. Percy, M.J., Furlow, P.W., Lucas, G.S., Li, X., Lappin, T.R., McMullin, M.F., Lee, F.S. N. Engl. J. Med. (2008) [Pubmed]
  3. Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis. Percy, M.J., Beer, P.A., Campbell, G., Dekker, A.W., Green, A.R., Oscier, D., Rainey, M.G., van Wijk, R., Wood, M., Lappin, T.R., McMullin, M.F., Lee, F.S. Blood (2008) [Pubmed]
  4. Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency. Percy, M.J., Lappin, T.R. Br. J. Haematol. (2008) [Pubmed]
  5. A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove. Percy, M.J., Furlow, P.W., Beer, P.A., Lappin, T.R., McMullin, M.F., Lee, F.S. Blood (2007) [Pubmed]
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