ChristopherAllenFisherMD

PubMed

• Mutations in the chromatin-associated protein ATRX.
  Gibbons, R.J., Wada, T., Fisher, C.A., Malik, N., Mitson, M.J., Steensma, D.P., Fryer, A., Goudie, D.R., Krantz, I.D., Traeger-Synodinos, J.> ;Hum Mutat. 2008 Jun
• A novel molecular basis for beta thalassemia intermedia poses new questions about its pathophysiology.
  Premawardhena, A., Fisher, C.A., Olivieri, N.F., de Silva, S., Sloane-Stanley, J., Wood, W.G., Weatherall, D.J.> ;Blood. 2005 Nov 1
• Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.
  Salehi, R., Fisher, C. A., Bignell, P. A., Eslami, G., Old, J. M.> ;Hemoglobin. 2010
• A large deletion in the human alpha-globin cluster caused by a replication error is associated with an unexpectedly mild phenotype.
  Rugless, M. J., Fisher, C. A., Old, J. M., Sloane-Stanley, J., Ayyub, H., Higgs, D. R., Garrick, D.> ;Hum Mol Genet. 2008 Oct 1
• Hb Bart's in cord blood: an accurate indicator of alpha-thalassemia.
  Rugless, M. J., Fisher, C. A., Stephens, A. D., Amos, R. J., Mohammed, T., Old, J. M.> ;Hemoglobin. 2006
• A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
  Costa, D. B., Fisher, C. A., Miller, K. B., Pihan, G. A., Steensma, D. P., Gibbons, R. J., Higgs, D. R.> ;Eur J Haematol. 2006 May
• The molecular basis for the thalassaemias in Sri Lanka.
  Fisher, C. A., Premawardhena, A., de Silva, S., Perera, G., Rajapaksa, S., Olivieri, N. A., Old, J. M., Weatherall, D. J.> ;Br J Haematol. 2003 May
• Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mut...
  Steensma, D. P., Higgs, D. R., Fisher, C. A., Gibbons, R. J.> ;Blood. 2004 Mar 15
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