Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Publications

Recent publications published by researchers at the MRC WIMM.

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

Single-Cell Analyses Reveal Megakaryocyte-Biased Hematopoiesis in Myelofibrosis and Identify Mutant Clone-Specific Targets.

Psaila B. et al, (2020), Mol Cell, 78, 477 - 492.e8

A Novel Deletion in the RPL5 Gene in a Lebanese Child With Diamond Blackfan Anemia Unresponsive to Steroid Treatment.

Farah RA. et al, (2020), J Pediatr Hematol Oncol, 42, e235 - e237

H3K79me2/3 controls enhancer-promoter interactions and activation of the pan-cancer stem cell marker PROM1/CD133 in MLL-AF4 leukemia cells.

Godfrey L. et al, (2020), Leukemia

Heterogeneous disease-propagating stem cells in juvenile myelomonocytic leukemia.

Louka E. et al, (2020), BioRix

Whole-genome sequencing of rare disease patients in a national healthcare system

ROBERTS I. and WATKINS H., (2020), Nature

Germline variants in predisposition genes in children with Down syndrome and acute lymphoblastic leukemia.

Winer P. et al, (2020), Blood Adv, 4, 672 - 675

Single-cell analysis of bone marrow-derived CD34+ cells from children with sickle cell disease and thalassemia.

Hua P. et al, (2019), Blood, 134, 2111 - 2115

Trisomy 21 Driven Pro-Inflammatory Signalling in Fetal Bone Marrow May Play a Role in Perturbed B-Lymphopoiesis and Acute Lymphoblastic Leukemia of Down Syndrome

O'Byrne SI. et al, (2019), Blood, 134, 1206 - 1206

Decoding human fetal liver haematopoiesis.

Popescu D-M. et al, (2019), Nature, 574, 365 - 371

Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs.

O'Byrne S. et al, (2019), Blood, 134, 1059 - 1071

Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome.

Labuhn M. et al, (2019), Cancer Cell, 36

Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome.

Labuhn M. et al, (2019), Cancer Cell, 36, 123 - 138.e10

Impaired cellular and humoral immunity is a feature of Diamond-Blackfan anaemia; experience of 107 unselected cases in the United Kingdom.

Iskander D. et al, (2019), Br J Haematol, 186, 321 - 326

Unraveling the cellular origin and clinical prognostic markers of infant B-cell acute lymphoblastic leukemia using genome-wide analysis.

Agraz-Doblas A. et al, (2019), Haematologica, 104, 1176 - 1188

Germline selection shapes human mitochondrial DNA diversity.

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

Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children.

French CE. et al, (2019), Intensive Care Med, 45, 627 - 636

Single-cell assessment of transcriptome alterations induced by Scriptaid in early differentiated human haematopoietic progenitors during ex vivo expansion.

Hua P. et al, (2019), Sci Rep, 9

Addressing the need for an external quality assessment for next generation sequencing (NGS) in the diagnosis of rare inherited anaemias.

Roy N. et al, (2019), BRITISH JOURNAL OF HAEMATOLOGY, 185, 118 - 119

Load More

1
2
3
4
5
6
7
...
»

Include forthcoming?