C. Allen

发表

Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia

C. Chelala, D. Linch, J. Cazier, 2008, Genes, chromosomes & cancer.

Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party.

T. A. Lister, J. Fitzgibbon, R. Hills, 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

TP53 gene mutation is frequent in patients with acute myeloid leukemia and complex karyotype, and is associated with very poor prognosis

R. Hills, D. Linch, D. Bowen, 2009, Leukemia.

X chromosome inactivation analysis reveals a difference in the biology of ET patients with JAK2 and CALR mutations.

D. Linch, R. Gale, C. Allen, 2014, Blood.

Prevalence and timing of TP53 mutations in del(17p) myeloma and effect on survival

G. Ryland, J. Sive, N. Rabin, 2017, Blood Cancer Journal.

The use of monoclonal antibodies UCH/β and UCHγ for the antenatal diagnosis of /β‐thalassaemia

P. Beverley, E. Huehns, P. Beverley, 1987 .

LYMPHOID NEOPLASIA Activation of the LMO2 oncogene through a somatically acquired neomorphic promoter in T-cell acute lymphoblastic leukemia

R. Young, A. Look, A. Pizzey, 2017 .

Genetically distinct leukemic stem cells in human CD34− acute myeloid leukemia are arrested at a hemopoietic precursor-like stage

P. Vyas, A. Mead, C. Craddock, 2016, The Journal of experimental medicine.

WT1 mutations in T-ALL.

A. Ferrando, R. Pieters, T. Palomero, 2009, Blood.

WT 1 mutations in TALL

A. Ferrando, R. Pieters, T. Palomero, 2009 .

Notch-1 Mutations Are Secondary Events in Some Patients with T-Cell Acute Lymphoblastic Leukemia

L. Foroni, D. Linch, M. Mansour, 2007, Clinical Cancer Research.

Notch-1Mutations Are Secondary Events in Some Patients with T-Cell Acute Lymphoblastic Leukemia

L. Foroni, D. Linch, M. Mansour, 2007 .

Prognostic implications of NOTCH1 and FBXW7 mutations in adults with T-cell acute lymphoblastic leukemia treated on the MRC UKALLXII/ECOG E2993 protocol.

A. Ferrando, M. Sulis, M. Tallman, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Activation of the LMO2 oncogene through a somatically acquired neomorphic promoter in T-cell acute lymphoblastic leukemia.

R. Young, A. Look, A. Pizzey, 2016, Blood.

Simpson's Paradox and the Impact of Different DNMT3A Mutations on Outcome in Younger Adults With Acute Myeloid Leukemia.

R. Hills, D. Linch, A. Burnett, 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

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.

The importance of relative mutant level for evaluating impact on outcome of KIT, FLT3 and CBL mutations in core-binding factor acute myeloid leukemia

R. Hills, D. Linch, A. Burnett, 2013, Leukemia.

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

A. Mead, R. Hills, D. Linch, 2013 .

Mutation of the Wilms’ Tumor 1 Gene Is a Poor Prognostic Factor Associated with Chemoresistance in Normal Karyotype Acute Myeloid Leukemia.

T. A. Lister, J. Fitzgibbon, R. Hills, 2007 .

Plasma cell neoplasm associated chronic neutrophilic leukemia with membrane proximal and truncating CSF3R mutations

A. Khwaja, K. Yong, R. Gale, 2014, Leukemia & lymphoma.

Variable outcome and methylation status according to CEBPA mutant type in double-mutated acute myeloid leukemia patients and the possible implications for treatment

A. Feber, R. Hills, D. Linch, 2017, Haematologica.

1 Activation of the LMO 2 oncogene through a somatically acquired 1 neomorphic promoter in T-Cell Acute Lymphoblastic Leukemia 2 3

R. Young, A. Look, A. Pizzey, 2017 .

The use of monoclonal antibodies UCH beta and UCH gamma for the antenatal diagnosis of beta-thalassaemia.

P. Beverley, E. Huehns, R. Gale, 1987, British journal of haematology.

Mutations in a Large Cohort of Young Adult Patients with Core Binding Factor Acute Myeloid Leukemia: Impact on Outcome and the Selection of Patients for Alternative Treatment Including Transplantation in First Complete Remission

R. Hills, D. Linch, A. Moorman, 2011 .

KIR gene haplotype: an independent predictor of clinical outcome in MDS patients.

R. Hills, K. Rezvani, D. Marin, 2016, Blood.