Search results (21)
« Back to PublicationsSFX-01 is therapeutic against myeloproliferative disorders caused by activating mutations in Shp2.
Journal article
Cho H-J. et al, (2025), EMBO Mol Med, 17, 2115 - 2136
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
Neutrophilic erythrophagocytosis in a child with paroxysmal cold hamoglobinuria.
Journal article
Pervaiz O. et al, (2022), EJHaem, 3, 1394 - 1395
In utero origin of myelofibrosis presenting in adult monozygotic twins.
Journal article
Sousos N. et al, (2022), Nat Med, 28, 1207 - 1211
Deciphering TP53 mutant Cancer Evolution with Single-Cell Multi-Omics
Preprint
Rodriguez-Meira A. et al, (2022)
Heterogeneous disease-propagating stem cells in juvenile myelomonocytic leukemia.
Journal article
Louka E. et al, (2021), J Exp Med, 218
Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
Other
Thaventhiran JED. et al, (2020), Nature, 584
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
Unravelling Intratumoral Heterogeneity through High-Sensitivity Single-Cell Mutational Analysis and Parallel RNA Sequencing.
Journal article
Rodriguez-Meira A. et al, (2019), Mol Cell, 73, 1292 - 1305.e8
Heterogeneous disease-propagating stem cells in juvenile myelomonocytic leukemia
Journal article
Louka E. et al, (2019)
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
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
