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Single-cell multi-omics identifies chronic inflammation as a driver of TP53-mutant leukemic evolution.

Journal article

Rodriguez-Meira A. et al, (2023), Nat Genet, 55, 1531 - 1541

In utero origin of myelofibrosis presenting in adult monozygotic twins.

Journal article

Sousos N. et al, (2022), Nat Med, 28, 1207 - 1211

Heterogeneous disease-propagating stem cells in juvenile myelomonocytic leukemia.

Journal article

Louka E. et al, (2021), J Exp Med, 218

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

Journal article

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

Carfilzomib therapy for relapsed myeloma: results of a UK multicentre experience.

Journal article

Djebbari F. et al, (2020), Br J Haematol, 188, e57 - e60

Germline selection shapes human mitochondrial DNA diversity.

Journal article

Wei W. et al, (2019), Science, 364

Whole genome sequencing for the investigation of rare anaemias: Challenges and real-world outcomes

Conference paper

Brierley C. et al, (2019), BRITISH JOURNAL OF HAEMATOLOGY, 185, 115 - 116

Single Cell Analysis Resolves Genetic and Transcriptional Heterogeneity in Myeloproliferative Neoplasms

Conference paper

Rodriguez-Meira A. et al, (2018), Experimental Hematology, 64

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures.

Journal article

Ito Y. et al, (2018), Am J Hum Genet, 103, 144 - 153