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Publications

A novel human fetal liver-derived model reveals that MLL-AF4 drives a distinct fetal gene expression program in infant ALL

Rice S. et al, (2020), bioRxiv

Effects of Tamoxifen on the Mutant Allele Burden and Disease Course in Patients with Myeloproliferative Neoplasms - Results of the Tamarin Study

Harrison C. et al, (2020), BLOOD, 136

Molecular Characterisation of Participants in the Phazar Trial Reveals Prognostic Impact of Mutations in Advanced-Phase-MPN

Brierley CK. et al, (2020), BLOOD, 136

Single-Cell Transcriptional Landscapes of Human Bone Marrow Reveal Distinct Erythroid Phenotypes Underpinned By Genotype in Diamond-Blackfan Anemia

Iskander D. et al, (2020), BLOOD, 136

Paracrine signalling by cardiac calcitonin controls atrial fibrogenesis and arrhythmia.

Moreira LM. et al, (2020), Nature, 587, 460 - 465

Predicting ultrahigh risk multiple myeloma by molecular profiling: an analysis of newly diagnosed transplant eligible myeloma XI trial patients.

Shah V. et al, (2020), Leukemia, 34, 3091 - 3096

A British Society for Haematology Guideline on the diagnosis and management of chronic myeloid leukaemia.

Smith G. et al, (2020), Br J Haematol, 191, 171 - 193

Modification of the Histone Landscape with JAK Inhibition in Myeloproliferative Neoplasms.

Greenfield G. et al, (2020), Cancers (Basel), 12

VALERIE: Visual-based inspection of alternative splicing events at single-cell resolution.

Wen WX. et al, (2020), PLoS Comput Biol, 16

Calcitonin paracrine signaling controls atrial fibrogenesis and arrhythmia

MOREIRA LM. et al, (2020), Nature

Spliceosome mutations are common in persons with myeloproliferative neoplasm-associated myelofibrosis with RBC-transfusion-dependence and correlate with response to pomalidomide

Chowdhury O., (2020), Leukemia

Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort.

Thaventhiran JED. et al, (2020), Nature, 584

SINGLE-CELL MULTI-OMIC ANALYSIS UNRAVELS GENETIC AND MOLECULAR HETEROGENEITY IN TRANSFORMED MYELOPROLIFERATIVE NEOPLASMS

Rodriguez-Meira A. et al, (2020), EXPERIMENTAL HEMATOLOGY, 88, S48 - S48

Artificial intelligence-based morphological fingerprinting of megakaryocytes: a new tool for assessing disease in MPN patients.

Sirinukunwattana K. et al, (2020), Blood Adv, 4, 3284 - 3294

Spliceosome mutations are common in persons with myeloproliferative neoplasm-associated myelofibrosis with RBC-transfusion-dependence and correlate with response to pomalidomide

MEAD A. et al, (2020), Leukemia

Whole-genome sequencing of a sporadic primary immunodeficiency cohort.

Thaventhiran JED. et al, (2020), Nature, 583, 90 - 95

Whole-genome sequencing of patients with rare diseases in a national health system.

Turro E. et al, (2020), Nature, 583, 96 - 102

A NOVEL IN VITRO PLATFORM FOR THE PRIORITISATION AND VALIDATION OF INHIBITORS OF BONE MARROW FIBROSIS USING HUMAN BONE MARROW (BM) STROMAL CELLS

COLOMBO M. et al, (2020), HemaSphere, 4, 1 - 1168

SINGLE-CELL MULTI-OMICS REVEALS ABERRANT MEGAKARYOCYTE-PROGENITOR (MKP) SUB-FRACTIONS IN MYELOFIBROSIS (MF) AND IDENTIFIES MUTANT CLONE-SPECIFIC TARGETS

PSAILA B. et al, (2020), HemaSphere, 4, 1 - 1168

Enhanced engraftment of human myelofibrosis stem and progenitor cells in MISTRG mice.

Lysenko V. et al, (2020), Blood Adv, 4, 2477 - 2488

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