Rosemary E Gale

The impact of FLT3 internal tandem duplication mutant level, number, size, and interaction with NPM1 mutations in a large cohort of young adult patients with acute myeloid leukemia.

Adam J Mead, Robert K Hills, A. Mead, 2008, Blood.

Conflicting data on the prognostic significance of FLT3/TKD mutations in acute myeloid leukemia might be related to the incidence of biallelic disease.

Adam J Mead, Robert K Hills, A. Mead, 2008, Blood.

Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients.

Christine Kinnon, Christof von Kalle, Michael Hubank, 2008, The Journal of clinical investigation.

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia.

Christine Kinnon, Austen Worth, A. Worth, 2006, Blood.

Assessment of Minimal Residual Disease in Standard-Risk AML.

Yashma Patel, Robert K Hills, Hassan Farah, 2016, The New England journal of medicine.

Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds

Asim Khwaja, Arnold Pizzey, Bradley N Smith, 2009, British journal of haematology.