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Martin Figeac
Martin Figeac
Université de Lille
Verified email at univ-lille.fr
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Year
Activating mutations in genes related to TCR signaling in angioimmunoblastic and other follicular helper T-cell–derived lymphomas
D Vallois, MPD Dobay, RD Morin, F Lemonnier, E Missiaglia, M Juilland, ...
Blood, The Journal of the American Society of Hematology 128 (11), 1490-1502, 2016
2392016
Comprehensive mutational profiling of core binding factor acute myeloid leukemia
N Duployez, A Marceau-Renaut, N Boissel, A Petit, M Bucci, S Geffroy, ...
Blood, The Journal of the American Society of Hematology 127 (20), 2451-2459, 2016
2172016
Next-Generation Sequencing in Diffuse Large B-Cell Lymphoma Highlights Molecular Divergence and Therapeutic Opportunities: a LYSA StudyTargeted NGS Details DLBCL Divergence and …
S Dubois, PJ Viailly, S Mareschal, E Bohers, P Bertrand, P Ruminy, ...
Clinical cancer research 22 (12), 2919-2928, 2016
2042016
Beneficial effects of exercise in a transgenic mouse model of Alzheimer's disease-like Tau pathology
K Belarbi, S Burnouf, FJ Fernandez-Gomez, C Laurent, S Lestavel, ...
Neurobiology of disease 43 (2), 486-494, 2011
1712011
Autocrine Induction of Invasive and Metastatic Phenotypes by the MIF-CXCR4 Axis in Drug-Resistant Human Colon Cancer CellsMIF, CXCR4, and Aggressive Drug-Resistant Colon Cancer …
AF Dessein, L Stechly, N Jonckheere, P Dumont, D Monté, E Leteurtre, ...
Cancer research 70 (11), 4644-4654, 2010
1262010
Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations
JB Micol, N Duployez, N Boissel, A Petit, S Geffroy, O Nibourel, ...
Blood, The Journal of the American Society of Hematology 124 (9), 1445-1449, 2014
1232014
Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations
JB Micol, N Duployez, N Boissel, A Petit, S Geffroy, O Nibourel, ...
Blood, The Journal of the American Society of Hematology 124 (9), 1445-1449, 2014
1232014
Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations
JB Micol, N Duployez, N Boissel, A Petit, S Geffroy, O Nibourel, ...
Blood, The Journal of the American Society of Hematology 124 (9), 1445-1449, 2014
1232014
IDH1/2 but not DNMT3A mutations are suitable targets for minimal residual disease monitoring in acute myeloid leukemia patients: a study by the Acute Leukemia French Association
H Debarri, D Lebon, C Roumier, M Cheok, A Marceau-Renaut, O Nibourel, ...
Oncotarget 6 (39), 42345, 2015
1022015
Genomic Landscape of CXCR4 Mutations in Waldenström MacroglobulinemiaCXCR4 Mutation in Waldenström Macroglobulinemia
S Poulain, C Roumier, A Venet-Caillault, M Figeac, C Herbaux, G Marot, ...
Clinical Cancer Research 22 (6), 1480-1488, 2016
1002016
Biological and Clinical Relevance of Associated Genomic Alterations in MYD88 L265P and non-L265P–Mutated Diffuse Large B-Cell Lymphoma: Analysis of 361 CasesMYD88 L265P and non …
S Dubois, PJ Viailly, E Bohers, P Bertrand, P Ruminy, V Marchand, ...
Clinical Cancer Research 23 (9), 2232-2244, 2017
862017
Recurrent mutations of the exportin 1 gene (XPO1) and their impact on selective inhibitor of nuclear export compounds sensitivity in primary mediastinal B‐cell lymphoma
F Jardin, A Pujals, L Pelletier, E Bohers, V Camus, S Mareschal, S Dubois, ...
American journal of hematology 91 (9), 923-930, 2016
862016
Accurate classification of germinal center B-cell–like/activated B-cell–like diffuse large B-cell lymphoma using a simple and rapid reverse transcriptase–multiplex ligation …
S Mareschal, P Ruminy, C Bagacean, V Marchand, M Cornic, JP Jais, ...
The Journal of Molecular Diagnostics 17 (3), 273-283, 2015
692015
Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1/S transition in CD4+ CD56+ haematodermic neoplasms and contribute …
F Jardin, M Callanan, D Penther, P Ruminy, X Troussard, JP Kerckaert, ...
Leukemia 23 (4), 698-707, 2009
682009
Fast multiclonal clusterization of V (D) J recombinations from high-throughput sequencing
M Giraud, M Salson, M Duez, C Villenet, S Quief, A Caillault, N Grardel, ...
BMC genomics 15 (1), 1-12, 2014
672014
BAP1 is altered by copy number loss, mutation, and/or loss of protein expression in more than 70% of malignant peritoneal mesotheliomas
N Leblay, F Leprêtre, N Le Stang, A Gautier-Stein, L Villeneuve, S Isaac, ...
Journal of Thoracic Oncology 12 (4), 724-733, 2017
612017
Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease
E Mutez, A Nkiliza, K Belarbi, A de Broucker, C Vanbesien-Mailliot, ...
Neurobiology of disease 63, 165-170, 2014
552014
Next-generation sequencing of FLT3 internal tandem duplications for minimal residual disease monitoring in acute myeloid leukemia.
JE Bibault, M Figeac, N Hélevaut, C Rodriguez, S Quief, S Sebda, ...
Oncotarget 6 (26), 22812-22821, 2015
542015
Beneficial Effect of a Selective Adenosine A2A Receptor Antagonist in the APPswe/PS1dE9 Mouse Model of Alzheimer’s Disease
E Faivre, JE Coelho, K Zornbach, E Malik, Y Baqi, M Schneider, L Cellai, ...
Frontiers in molecular neuroscience 11, 235, 2018
532018
Neurofibromatosis‐1 gene deletions and mutations in de novo adult acute myeloid leukemia
E Boudry‐Labis, C Roche‐Lestienne, O Nibourel, N Boissel, C Terre, ...
American journal of hematology 88 (4), 306-311, 2013
532013
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