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Leukemia Research|December 9, 2016
High-throughput sequencing in acute lymphoblastic leukemia: Follow-up of minimal residual disease and emergence of new clonesMikaël Salson, Mathieu Giraud, Aurélie Caillault, et al.
Haematologica|April 13, 2004
Partial duplication of the MLL oncogene in patients with aggressive acute myeloid leukemiaConstantina Sambani, Roberta La Starza, Christophe Roumier, et al.
Blood|April 10, 2009
High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorderClaude Preudhomme, Aline Renneville, Violaine Bourdon, et al.
Oncotarget|October 15, 2013
High imatinib dose overcomes insufficient response associated with ABCG2 haplotype in chronic myelogenous leukemia patientsMarc Delord, Philippe Rousselot, Jean Michel Cayuela, et al.
Oncotarget|May 12, 2012
BCL2L10 is a predictive factor for resistance to azacitidine in MDS and AML patientsThomas Cluzeau, Guillaume Robert, Nicolas Mounier, et al.
European Journal of Haematology|October 17, 2017
Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemiaNicolas Duployez, Wadih Abou Chahla, Sophie Lejeune, et al.
Oncotarget|January 20, 2018
Role of IRF4 in resistance to immunomodulatory (IMid) compounds<sup>®</sup> in Waldenström's macroglobulinemiaElisabeth Bertrand, Nathalie Jouy, Salomon Manier, et al.
Hemasphere|May 8, 2024
Induction of AML cell differentiation using HOXA9/DNA binding inhibitors as a potential therapeutic option for HOXA9-dependent AMLMélanie Lambert, Samy Jambon, Mohamed A Bouhlel, et al.
Leukemia Research|October 16, 2015
Quantification of EVI1 transcript levels in acute myeloid leukemia by RT-qPCR analysis: A study by the ALFA GroupThomas Smol, Olivier Nibourel, Alice Marceau-Renaut, et al.
Haematologica|January 25, 2012
Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survivalCsaba Bödör, Aline Renneville, Matthew Smith, et al.
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