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Annales De Genetique|October 17, 2002
TPA stimulation culture for improved detection of t(11;14)(q13;q32) in mantle cell lymphomaEmmanuelle Barouk-Simonet, Joris Andrieux, Marie-Christine Copin, et al.
Blood|January 19, 2008
RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib resistanceCatherine Roche-Lestienne, Lauréline Deluche, Sélim Corm, et al.
British Journal of Haematology|October 20, 2010
Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemiaBenoîte Pérez, Olivier Kosmider, Bruno Cassinat, et al.
Haematologica|March 20, 2025
NPM1 mutation subtype switch in acute myeloid leukemiaBenjamin Podvin, Romane Joudinaud, Christophe Roumier, et al.
Cancer|October 10, 2013
Tolerability and efficacy of pegylated interferon-α-2a in combination with imatinib for patients with chronic-phase chronic myeloid leukemiaHyacinthe Johnson-Ansah, Joelle Guilhot, Philippe Rousselot, et al.
Oncotarget|August 28, 2016
Tetraspanin CD81 is an adverse prognostic marker in acute myeloid leukemiaThomas Boyer, Soizic Guihard, Christophe Roumier, et al.
Genes, Chromosomes & Cancer|September 4, 2008
Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: a complex chromosomal rearrangement of underestimated frequency in disease progression?Lauréline Deluche, Sami Joha, Sélim Corm, et al.
Oncotarget|October 17, 2015
Genetic polymorphisms associated with increased risk of developing chronic myelogenous leukemiaHeriberto Bruzzoni-Giovanelli, Juan R González, François Sigaux, et al.
Blood|August 19, 2011
Changes in the dynamics of the excess mortality rate in chronic phase-chronic myeloid leukemia over 1990-2007: a population studySelim Corm, Laurent Roche, Jean-Baptiste Micol, et al.
European Journal of Human Genetics : EJHG|June 17, 2018
Correction: Cost of cancer diagnosis using next-generation sequencing targeted gene panels in routine practice: a nationwide French studyPatricia Marino, Rajae Touzani, Lionel Perrier, et al.
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