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Hemasphere|August 28, 2023
Targeted High-throughput Sequencing for Hematological Malignancies: A GBMHM Survey of Practice and Cost Evaluation in FranceMeryl Darlington, Pierre Sujobert, Olivier Kosmider, et al.
Blood|June 29, 2014
Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocationsJean-Baptiste Micol, Nicolas Duployez, Nicolas Boissel, 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.
Hemasphere|November 15, 2019
The Need for a Consensus Next-generation Sequencing Panel for Mature Lymphoid MalignanciesPierre Sujobert, Yannick Le Bris, Laurence de Leval, et al.
Blood|March 8, 2007
Postremission treatment of elderly patients with acute myeloid leukemia in first complete remission after intensive induction chemotherapy: results of the multicenter randomized Acute Leukemia French Association (ALFA) 9803 trialClaude Gardin, Pascal Turlure, Thierry Fagot, et al.
Blood|January 16, 2013
Clonal architecture of chronic myelomonocytic leukemiasRaphaël Itzykson, Olivier Kosmider, Aline Renneville, et al.
Cancers|May 5, 2021
The Impact of DNMT3A Status on NPM1 MRD Predictive Value and Survival in Elderly AML Patients Treated IntensivelyMaël Heiblig, Nicolas Duployez, Alice Marceau, et al.
American Journal of Hematology|July 18, 2013
Genome wide SNP array identified multiple mechanisms of genetic changes in Waldenstrom macroglobulinemiaStéphanie Poulain, Christophe Roumier, Sylvie Galiègue-Zouitina, et al.
Blood|October 21, 2017
Oncogenetic mutations combined with MRD improve outcome prediction in pediatric T-cell acute lymphoblastic leukemiaArnaud Petit, Amélie Trinquand, Sylvie Chevret, et al.
British Journal of Haematology|August 28, 2014
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndromeStéphanie Poulain, Eileen M Boyle, Christophe Roumier, et al.
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