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Ian R. Peake

Royal Hallamshire Hospital

57

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Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort.

2013 Thrombosis and Haemostasis
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Copy number variation is a significant contributor to type 1 VWD pathogenesis in the EU MCMDM-1VWD cohort

2011
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Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort

2010 Haematologica
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Facile and rapid analysis of three DNA polymorphisms within the human factor IX gene using the polymerase chain reaction

2008 British Journal of Haematology
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Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemia

2004 British Journal of Haematology
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Mutational analysis of class III receptor tyrosine kinases (C-KIT, C-FMS, FLT3) in idiopathic myelofibrosis.

2003 British Journal of Haematology
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The Molecular Basis of Hemophilia A: Genotype-Phenotype Relationships and Inhibitor Development

2003 Seminars in Thrombosis and Hemostasis
- Anne Goodeve
- Ian R. Peake
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c‐FMS mutational analysis in acute myeloid leukaemia

2003 British Journal of Haematology
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Can full-length wild-type von Willebrand factor (VWF) or the VWF propeptide rescue secretion of the R273W VWF variant associated with quantitative deficiency?

2003 Journal of Thrombosis and Haemostasis
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Oestrogenic repression of human coagulation factor VII expression mediated through an oestrogen response element sequence motif in the promoter region

2002 Human Molecular Genetics
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Citations (26)