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Clinical Genetics|July 7, 2020
De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopeniaJan Hendrik Niemann, Chen Du, Susanne Morlot, et al.
Haematologica|December 15, 2018
Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemiaAna C Glembotsky, Dominika Sliwa, Dominique Bluteau, et al.
Blood|December 3, 2015
Effect of lenalidomide treatment on clonal architecture of myelodysplastic syndromes without 5q deletionVirginie Chesnais, Aline Renneville, Andrea Toma, et al.
Genes, Chromosomes & Cancer|February 20, 2019
A recurrent clonally distinct Burkitt lymphoma case highlights genetic key events contributing to oncogenesisDominique Penther, Pierre-Julien Viailly, Sylvain Latour, et al.
Blood|September 6, 2019
Germline DDX41 mutations define a significant entity within adult MDS/AML patientsMarie Sébert, Marie Passet, Anna Raimbault, et al.
Clinical Case Reports|May 19, 2023
Hairy cell leukemia with isolated bone lesionsLaura Cailly, Cécile Gruchet, Elsa Maitre, et al.
Leukemia|June 26, 2020
Clonal dominance is an adverse prognostic factor in acute myeloid leukemia treated with intensive chemotherapyMarco Cerrano, Matthieu Duchmann, Rathana Kim, et al.
American Journal of Hematology|July 4, 2026
High Proportion of PNH Type II Neutrophils Is Associated With Thrombosis in Patients Displaying a PNH Clone ≥ 1Orianne Wagner-Ballon, Anne-Catherine Lhoumeau, Anna Raimbault, et al.
Blood|August 21, 2020
p53 activation during ribosome biogenesis regulates normal erythroid differentiationSalomé Le Goff, Ismael Boussaid, Celia Floquet, et al.
Blood|November 18, 2017
A landscape of germ line mutations in a cohort of inherited bone marrow failure patientsOlivier Bluteau, Marie Sebert, Thierry Leblanc, et al.
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