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Jean-Luc Laï

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Violaine Havelange; Christian Herens; Jean-Luc Laï; Jeanne-Marie Libouton; Eric Lippert; Lucienne Michaux; Francine Mugneret; N Nadal; Dominique Penther; Hélène A Poirel; Martine Raphael; Christine Terré; Ivan Théate; Isabelle Tigaud; Geneviève Ameye; Laurence Baranger; Carole Barin; Christine Cabrol; Evelyne Callet-Bauchu; Marie-Agnès Collonge-Rame; Nicole Dastugue; Anne Hagemeijer
Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement.
Sami Joha; Véronique Dauphin; frederic lepretre; Sélim Corm; Franck E Nicolini; Christophe Roumier; Olivier Nibourel; Nathalie Grardel; Véronique Maguer-Satta; Thierry Idziorek; Martin Figeac; Jean-Luc Laï; Bruno Quesnel; Gabriel Etienne; François Guilhot; Eric Lippert; Claude Preudhomme; Catherine Roche-Lestienne
Genomic characterization of Imatinib resistance in CD34+ cell populations from chronic myeloid leukaemia patients.
Lauréline Deluche; Sami Joha; Sélim Corm; Agnès Daudignon; Sandrine Geffroy; Sabine Quief; Céline Villenet; Jean-Pierre Kerckaert; Jean-Luc Laï; Claude Preudhomme; Catherine Roche-Lestienne
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?

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2013: Violaine Havelange; Christian Herens; Jean-Luc Laï; Jeanne-Marie Libouton; Eric Lippert; Lucienne Michaux; Francine Mugneret; N Nadal; Dominique Penther; Hélène A Poirel; Martine Raphael; Christine Terré; Ivan Théate; Isabelle Tigaud; Geneviève Ameye; Laurence Baranger; Carole Barin; Christine Cabrol; Evelyne Callet-Bauchu; Marie-Agnès Collonge-Rame; Nicole Dastugue; Anne Hagemeijer
Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement.
Genes, chromosomes & cancer 2013;52(1):81-92.
2011: Sami Joha; Véronique Dauphin; frederic lepretre; Sélim Corm; Franck E Nicolini; Christophe Roumier; Olivier Nibourel; Nathalie Grardel; Véronique Maguer-Satta; Thierry Idziorek; Martin Figeac; Jean-Luc Laï; Bruno Quesnel; Gabriel Etienne; François Guilhot; Eric Lippert; Claude Preudhomme; Catherine Roche-Lestienne
Genomic characterization of Imatinib resistance in CD34+ cell populations from chronic myeloid leukaemia patients.
Leukemia research 2011;35(4):448-58.
2008: Lauréline Deluche; Sami Joha; Sélim Corm; Agnès Daudignon; Sandrine Geffroy; Sabine Quief; Céline Villenet; Jean-Pierre Kerckaert; Jean-Luc Laï; Claude Preudhomme; Catherine Roche-Lestienne
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?
Genes, chromosomes & cancer 2008;47(12):1110-7.
2008: Steven Richebourg; Olivier Theisen; Isabelle Plantier; Anne Parry; Valérie Soenen-Cornu; Pascale Lepelley; Claude Preudhomme; Aline Renneville; Jean-Luc Laï; Catherine Roche-Lestienne
Chronic myeloproliferative disorder with t(8;22)(p11;q11) can mime clonal cytogenetic evolution of authentic chronic myelogeneous leukemia.
Genes, chromosomes & cancer 2008;47(10):915-8.
2008: Steven Richebourg; Virginie Eclache; Christine Perot; Marie-France Portnoi; Jacqueline Van den Akker; Christine Terré; Odile Maareck; Valérie Soenen; Franck Viguié; Jean-Luc Laï; Joris Andrieux; Sélim Corm; Catherine Roche-Lestienne
Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL1 or BCR deletion status or response to imatinib therapy.
Cancer genetics and cytogenetics 2008;182(2):95-102.
2008: Catherine Roche-Lestienne; Lauréline Deluche; Sélim Corm; Isabelle Tigaud; Sami Joha; Nathalie Philippe; Sandrine Geffroy; Jean-Luc Laï; Franck-Emmanuel Nicolini; Claude Preudhomme
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 resistance.
Blood 2008;111(7):3735-41.
2008: Isabelle Luquet; Jean-Luc Laï; Carole Barin; Laurence Baranger; Chrystèle Bilhou-Nabera; Eric Lippert; C Gervais; Pascaline Talmant; Pascale Cornillet-Lefebvre; Christine Perot; N Nadal; Marie-Joëlle Mozziconacci; Marina Lafage-Pochitaloff; Virginie Eclache; Francine Mugneret; C Lefebvre; Christian Herens; F Speleman; Hélène A Poirel; Isabelle Tigaud; Christine Cabrol; Philippe Rousselot; Sylvie Daliphard; Michèle Imbert; Richard Garand; Frank Geneviève; Roland Berger; Christine Terre
Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity: a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH).
Leukemia 2008;22(1):132-7.
2007: Joris Andrieux; Catherine Roche-Lestienne; Sandrine Geffroy; desterke christophe; Nathalie Grardel; Isabelle Plantier; Dominik Selleslag; Jean-Loup Demory; Jean-Luc Laï; Xavier Leleu; Caroline Le Bousse-Kerdiles; Peter Vandenberghe
Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis.
Cancer genetics and cytogenetics 2007;178(1):11-6.
2006: Aline Renneville; Bruno Quesnel; A Charpentier; Louis Terriou; A Crinquette; Jean-Luc Laï; C Cossement; P Lionne-Huyghe; C Rose; Francis Bauters; Claude Preudhomme
High occurrence of JAK2 V617 mutation in refractory anemia with ringed sideroblasts associated with marked thrombocytosis.
Leukemia 2006;20(11):2067-70.
2006: Joris Andrieux; Chrystèle Bilhou-Nabera; Eric Lippert; Marie-Caroline Le Bousse-Kerdiles; Brigitte Dupriez; Nathalie Grardel; Olivier Pierre-Louis; desterke christophe; Vincent Praloran; Jean-Luc Laï; Jean-Loup Demory
Expression of HMGA2 in PB leukocytes and purified CD34+ cells from controls and patients with Myelofibrosis and myeloid metaplasia.
Leukemia & lymphoma 2006;47(9):1956-9.
2006: Catherine Roche-Lestienne; Nicole Dastugue; Steven Richebourg; Blandine Roquefeuil; Jean-Hugues Dalle; Jean-Luc Laï; Joris Andrieux
Acute megakaryoblastic leukemia with der(7)t(5;7)(q11;p11 approximately p12) associated with Down syndrome: a fourth case report.
Cancer genetics and cytogenetics 2006;169(2):184-6.
2006: Catherine Roche-Lestienne; Steven Richebourg; Jean-Luc Laï; Joris Andrieux; Valérie Soenen-Cornu; Sandrine Geffroy
Isolated tetrasomy 13: a fifth case report of a rare chromosome abnormality associated with poorly differentiated acute myeloid leukemia.
Cancer genetics and cytogenetics 2006;168(2):181-2.
2006: Joris Andrieux; Sandrine Geffroy; Chrystèle Bilhou-Nabera; Brigitte Dupriez; Jean-Loup Demory; Francis Bauters; Jean-Luc Laï; Nicole Dastugue
Cryptic 6p21.3 duplications and triplication involving HMGA1 partially masked by add 6p in four cases of myelodysplasia.
Cancer genetics and cytogenetics 2006;164(1):84-7.
2005: Selim Corm; Valeria Biggio; Catherine Roche-Lestienne; Jean-Luc Laï; Ibrahim Yakoub-Agha; Noël Philippe; Franck E Nicolini; Thierry Facon; Claude Preudhomme
Coexistence of AML1/RUNX1 and BCR-ABL point mutations in an imatinib-resistant form of CML.
Leukemia 2005;19(11):1991-2.
2005: Frédéric Nicodème; Sandrine Geffroy; Massimo Conti; Bruno Delobel; Valérie Soenen; Nathalie Grardel; Henri Porte; Marie-Christine Copin; Jean-Luc Laï; Joris Andrieux
Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3).
Genes, chromosomes & cancer 2005;44(2):154-60.
2005: Catherine Roche-Lestienne; S Lepers; Valérie Soenen-Cornu; Jean-Emmanuel Kahn; Jean-Luc Laï; E Hachulla; F Drupt; A-L Demarty; Anne Roumier; Martine Gardembas; M Dib; Noël Philippe; Nathalie Cambier; S Barete; C Libersa; Olivier Bletry; Pierre-Yves Hatron; Bruno Quesnel; Christian Rose; K Maloum; Odile Blanchet; Pierre Fenaux; Lionel Prin; Claude Preudhomme
Molecular characterization of the idiopathic hypereosinophilic syndrome (HES) in 35 French patients with normal conventional cytogenetics.
Leukemia 2005;19(5):792-8.
2005: Emmanuelle Barouk-Simonet; Valérie Soenen-Cornu; Christophe Roumier; Alain Cosson; Jean-Luc Laï; Pierre Fenaux; Claude Preudhomme
Role of multiplex FISH in identifying chromosome involvement in myelodysplastic syndromes and acute myeloid leukemias with complex karyotypes: a report on 28 cases.
Cancer genetics and cytogenetics 2005;157(2):118-26.
2005: María D Odero; Francis H Grand; S Iqbal; F Ross; J P Roman; José L Vizmanos; Joris Andrieux; Jean-Luc Laï; María J Calasanz; Nicholas C P Cross
Disruption and aberrant expression of HMGA2 as a consequence of diverse chromosomal translocations in myeloid malignancies.
Leukemia 2005;19(2):245-52.
2005: Catherine Roche-Lestienne; Stéphane Darré; Jean-Luc Laï; Thierry Facon; Joëlle Guilhot; Claude Preudhomme
Factors predicting molecular and cytogenetic response in chronic myeloid leukemia patients treated with imatinib.
Haematologica 2005;90(1):131-3.
2004: Stéphane Depil; Xavier Leleu; Jean-Baptiste Micol; Céline Berthon; Jean-Luc Laï; Francis Bauters; Bruno Quesnel; Thierry Facon
Abnormal cytogenetics and significant bone marrow plasmacytosis are predictive of early progression and short survival in patients with low tumor mass asymptomatic multiple myeloma.
Leukemia & lymphoma 2004;45(12):2481-4.
2004: Christiane Charrin; Xavier Thomas; Martine Ffrench; Quoc-Hung Le; Joris Andrieux; Marie-Joëlle Mozziconacci; Jean-Luc Laï; Chrystèle Bilhou-Nabera; Lucienne Michaux; Alain BERNHEIM; Christian Bastard; Hossein Mossafa; Christine Perot; Odile Maarek; Claude Boucheix; Véronique Lheritier; André Delannoy; Denis Fière; Nicole Dastugue
A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL).
Blood 2004;104(8):2444-51.
2004: Lucie Lafay-Cousin; Valérie Soenen; Françoise Mazingue; Claude Preudhomme; Jean-Luc Laï; Joris Andrieux
Chromosomal insertion involving MLL in childhood acute myeloblastic leukemia (M4).
Cancer genetics and cytogenetics 2004;150(2):153-5.
2004: Joris Andrieux; Jean-Loup Demory; Brigitte Dupriez; Sabine Quief; Isabelle Plantier; Christophe Roumier; Francis Bauters; Jean-Luc Laï; Jean-Pierre Kerckaert
Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia.
Genes, chromosomes & cancer 2004;39(1):82-7.
2003: Joris Andrieux; Sandra Fert-Ferrer; Marie-Christine Copin; Pauline Huyghe; Pierre Pocachard; James Lespinasse; Francis Bauters; Jean-Luc Laï; Bruno Quesnel
Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32).
Cancer genetics and cytogenetics 2003;145(1):65-9.
2003: Anne Roumier; Nathalie Grardel; Jean-Luc Laï; I Becqueriaux; K Ghomari; Aurore de Lavareille; Florence Roufosse; Lionel Prin; Monique Capron
Hypereosinophilia with abnormal T cells, trisomy 7 and elevated TARC serum level.
Haematologica 2003;88(7):ECR24.
2003: Catherine Roche-Lestienne; Jean-Luc Laï; Stéphane Darré; Thierry Facon; Claude Preudhomme
A mutation conferring resistance to imatinib at the time of diagnosis of chronic myelogenous leukemia.
The New England journal of medicine 2003;348(22):2265-6.
2003: Joris Andrieux; Jean-Loup Demory; Marie Thérèse Caulier; Philippe Agape; Marc Wetterwald; Francis Bauters; Jean-Luc Laï
Karyotypic abnormalities in myelofibrosis following polycythemia vera.
Cancer genetics and cytogenetics 2003;140(2):118-23.
2002: Jean-Hugues Dalle; L Mortier; Christophe Roumier; Jean-Luc Laï; Benoit Catteau; Emmanuel Delaporte; Brigitte Nelken
[Cutaneous symptoms revealing a monoblastic leukemia].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2002;9(10):1046-9.
2002: Joris Andrieux; Jean-Loup Demory; Pierre Morel; Isabelle Plantier; Brigitte Dupriez; Marie Thérèse Caulier; Francis Bauters; Jean-Luc Laï
Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia.
Cancer genetics and cytogenetics 2002;137(1):68-71.
2002: Catherine Roche-Lestienne; Valérie Soenen-Cornu; Nathalie Grardel-Duflos; Jean-Luc Laï; Noël Philippe; Thierry Facon; Pierre Fenaux; Claude Preudhomme
Several types of mutations of the Abl gene can be found in chronic myeloid leukemia patients resistant to STI571, and they can pre-exist to the onset of treatment.
Blood 2002;100(3):1014-8.
2002: Emmanuelle Barouk-Simonet; Joris Andrieux; Marie-Christine Copin; Nathalie Grardel-Duflos; Pauline Huyghe; Jean-Hugues Patte; Claude Preudhomme; Bruno Quesnel; Jean-Luc Laï
TPA stimulation culture for improved detection of t(11;14)(q13;q32) in mantle cell lymphoma.
Annales de génétique 2002;45(3):165-8.
2002: Jean-Hugues Dalle; Martine Fournier; Brigitte Nelken; Françoise Mazingue; Jean-Luc Laï; Francis Bauters; Pierre Fenaux; Bruno Quesnel
p16(INK4a) immunocytochemical analysis is an independent prognostic factor in childhood acute lymphoblastic leukemia.
Blood 2002;99(7):2620-3.
2001: Thierry Facon; Hervé Avet-Loiseau; Gaëlle Guillerm; P Moreau; Frank Geneviève; Marc Zandecki; Jean-Luc Laï; Xavier Leleu; Jean-Pierre Jouet; Francis Bauters; Jean-Luc Harousseau; Régis Bataille; Jean-Yves Mary
Chromosome 13 abnormalities identified by FISH analysis and serum beta2-microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy.
Blood 2001;97(6):1566-71.
2000: Nathalie Cambier; Valérie Soenen-Cornu; Jean-Luc Laï; Alain Cosson; Pierre Fenaux; Claude Preudhomme
Investigation of minimal residual disease in adult Ph1 positive acute lymphoblastic leukemia by a combination of cell sorting and fluorescence in situ hybridization: a preliminary study on 6 cases.
Haematologica 2000;85(6):664-5.
2000: Claude Preudhomme; Christophe Roumier; M P Hildebrand; E Dallery-Prudhomme; Danièle Lantoine; Jean-Luc Laï; Agnès Daudignon; C Adenis; Francis Bauters; Pierre Fenaux; Jean-Pierre Kerckaert; Sylvie Galiègue-Zouitina
Nonrandom 4p13 rearrangements of the RhoH/TTF gene, encoding a GTP-binding protein, in non-Hodgkin's lymphoma and multiple myeloma.
Oncogene 2000;19(16):2023-32.
2000: Christophe Roumier; Sylvie Galiègue-Zouitina; Christian Bastard; Valérie Soenen; Jean-Luc Laï; Claude Denis; Gérard Buchonnet; Jean-Pierre Kerckaert; Alain Cosson; Pierre Fenaux; Claude Preudhomme
FISH analysis with a YAC probe improves detection of LAZ3/BCL6 rearrangement in non-Hodgkin's lymphoma.
The hematology journal : the official journal of the European Haematology Association / EHA 2000;1(2):117-25.
1999: Sylvie Galiègue-Zouitina; Sabine Quief; M P Hildebrand; Claude Denis; L Detourmignies; Jean-Luc Laï; Jean-Pierre Kerckaert
Nonrandom fusion of L-plastin(LCP1) and LAZ3(BCL6) genes by t(3;13)(q27;q14) chromosome translocation in two cases of B-cell non-Hodgkin lymphoma.
Genes, chromosomes & cancer 1999;26(2):97-105.
1999: D Duflos-Delaplace; Jean-Luc Laï; Brigitte Nelken; Franck Genevieve; Anne-Sophie Defachelles; Marc Zandecki
Transient leukemoid disorder in a newborn with Down syndrome followed 19 months later by an acute myeloid leukemia: demonstration of the same structural change in both instances with clonal evolution.
Cancer genetics and cytogenetics 1999;113(2):166-71.
1999: Agnès Daudignon; H Bisiau; F Le Baron; Jean-Luc Laï; Marc Wetterwald; Sylvie Galiègue-Zouitina; P Morel; Patrick Duthilleul
Four cases of follicular lymphoma with t(14;18)(q32;q21) and t(3;4)(q27;p13) with LAZ3 (BCL6) rearrangement.
Cancer genetics and cytogenetics 1999;111(2):157-60.
1999: Franck Genevieve; Marc Zandecki; Jean-Luc Laï; Bernadette Hennache; J L Faucompre; L Stalnikiewicz; Francis Bauters; Thierry Facon
Evaluation of minimal residual disease by interphase FISH in multiple myeloma: does complete remission exist?
Leukemia 1999;13(4):641-4.
1999: Xavier Leleu; Jean-Pierre Jouet; Isabelle Plantier; Marc Zandecki; Jean-Luc Laï; D Mucha; J P Lejeune; Francis Bauters; T Facon
Isolated neurological relapse following stem cell transplantation in plasma cell leukemia: a report of two cases.
Leukemia 1999;13(2):307-9.
1998: Jean-Luc Laï; L Michaux; N Dastugue; F Vasseur; Agnès Daudignon; T Facon; Francis Bauters; Marc Zandecki
Cytogenetics in multiple myeloma: a multicenter study of 24 patients with t(11;14)(q13;q32) or its variant.
Cancer genetics and cytogenetics 1998;104(2):133-8.
1998: Jean-Luc Laï; Agnès Daudignon; Jean-Pierre Kerckaert; Sylvie Galiègue-Zouitina; L Detourmignies; P Morel; Francis Bauters; Pierre Fenaux
Translocation (3;13)(q27;q14): a nonrandom and probably secondary structural change in non-Hodgkin lymphomas.
Cancer genetics and cytogenetics 1998;103(2):140-3.
1998: Valérie Soenen; Claude Preudhomme; Christophe Roumier; Jean-Luc Laï; Pascale Lepelley; T Facon; D Pagniez; Pierre Fenaux
Myelodysplasia during the course of myeloma. Restriction of 17p deletion and p53 overexpression to myeloid cells.
Leukemia 1998;12(2):238-41.
1998: Valérie Soenen; Claude Preudhomme; Christophe Roumier; Agnès Daudignon; Jean-Luc Laï; Pierre Fenaux
17p Deletion in acute myeloid leukemia and myelodysplastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ.
Blood 1998;91(3):1008-15.
1998: Y Sterkers; Claude Preudhomme; Jean-Luc Laï; Jean-Loup Demory; Marie Thérèse Caulier; Eric Wattel; Dominique Bordessoule; Francis Bauters; Pierre Fenaux
Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: high proportion of cases with 17p deletion.
Blood 1998;91(2):616-22.
1997: Marc Zandecki; Jean-Luc Laï; Frank Geneviève; F Bernardi; H Volle-Rémy; Odile Blanchet; M François; Alain Cosson; Francis Bauters; Thierry Facon
Several cytogenetic subclones may be identified within plasma cells from patients with monoclonal gammopathy of undetermined significance, both at diagnosis and during the indolent course of this condition.
Blood 1997;90(9):3682-90.
1997: Marc Zandecki; F Bernardi; Franck Genevieve; Jean-Luc Laï; Claude Preudhomme; M Flactif; Alain Cosson; Francis Bauters; Thierry Facon
Involvement of peripheral blood cells in multiple myeloma: chromosome changes are the rule within circulating plasma cells but not within B lymphocytes.
Leukemia 1997;11(7):1034-9.
1996: Marc Zandecki; Jean-Luc Laï; Thierry Facon
Multiple myeloma: almost all patients are cytogenetically abnormal.
British journal of haematology 1996;94(2):217-27.
1995: M Flactif; Marc Zandecki; Jean-Luc Laï; F Bernardi; V Obein; Francis Bauters; Thierry Facon
Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myeloma.
Leukemia 1995;9(12):2109-14.
1995: Marc Zandecki; V Obein; F Bernardi; Valérie Soenen; M Flactif; Jean-Luc Laï; M François; Thierry Facon
Monoclonal gammopathy of undetermined significance: chromosome changes are a common finding within bone marrow plasma cells.
British journal of haematology 1995;90(3):693-6.
1995: Jean-Luc Laï; Marc Zandecki; J Y Mary; F Bernardi; V Izydorczyk; M Flactif; P Morel; J P Jouet; Francis Bauters; Thierry Facon
Improved cytogenetics in multiple myeloma: a study of 151 patients including 117 patients at diagnosis.
Blood 1995;85(9):2490-7.
1994: M Flactif; Jean-Luc Laï; Pierre Fenaux
Reassessment of an apparent t(12;17)(p11;p11) as an unbalanced t(17;21)(p11;q11) in a case of B-cell chronic lymphocytic leukemia by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1994;78(1):108-11.
1994: M Flactif; Jean-Luc Laï; Marc Zandecki; F Bernardi; N Trillot; Francis Bauters; Thierry Facon
Two cases of t(1;16)(p11;p11) in multiple myeloma: confirmation by chromosome painting.
Cancer genetics and cytogenetics 1994;76(1):10-4.
1994: Marc Zandecki; F Bernardi; Jean-Luc Laï; Thierry Facon; V Izydorczyk; Francis Bauters; Alain Cosson
Image analysis in multiple myeloma at diagnosis. Correlation with cytogenetic study.
Cancer genetics and cytogenetics 1994;74(2):115-9.
1993: Eric Wattel; Jean-Luc Laï; Mohamed Hebbar; Claude Preudhomme; D Grahek; P Morel; Francis Bauters; Pierre Fenaux
De novo myelodysplastic syndrome (MDS) with deletion of the long arm of chromosome 20: a subtype of MDS with distinct hematological and prognostic features?
Leukemia research 1993;17(11):921-6.
1993: L Detourmignies; Eric Wattel; Jean-Luc Laï; Francis Bauters; Pierre Fenaux
Is there still a role for low-dose cytosine arabinoside in de novo acute myeloid leukemia in the elderly? A report on 77 cases.
Annals of hematology 1993;66(5):235-40.
1992: Claude Preudhomme; T Facon; Marc Zandecki; M Vanrumbeke; Jean-Luc Laï; E Nataf; M H Loucheux-Lefebvre; Jean-Pierre Kerckaert; P Fenaux
Rare occurrence of P53 gene mutations in multiple myeloma.
British journal of haematology 1992;81(3):440-3.
1992: Pierre Fenaux; Claude Preudhomme; Jean-Luc Laï; I Quiquandon; P Jonveaux; M Vanrumbeke; C Sartiaux; P Morel; M H Loucheux-Lefebvre; Francis Bauters
Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis.
Leukemia 1992;6(4):246-50.
1992: Pierre Fenaux; Claude Preudhomme; I Quiquandon; P Jonveaux; Jean-Luc Laï; M Vanrumbeke; M H Loucheux-Lefebvre; Francis Bauters; Roland Berger; Jean-Pierre Kerckaert
Mutations of the P53 gene in acute myeloid leukaemia.
British journal of haematology 1992;80(2):178-83.
1991: P Jonveaux; Pierre Fenaux; I Quiquandon; J M Pignon; Jean-Luc Laï; M H Loucheux-Lefebvre; Michel Goossens; Francis Bauters; Roland Berger
Mutations in the p53 gene in myelodysplastic syndromes.
Oncogene 1991;6(12):2243-7.
1991: Pierre Fenaux; P Jonveaux; I Quiquandon; Jean-Luc Laï; J M Pignon; M H Loucheux-Lefebvre; Francis Bauters; Roland Berger; Jean-Pierre Kerckaert
P53 gene mutations in acute myeloid leukemia with 17p monosomy.
Blood 1991;78(7):1652-7.
1990: Jean-Luc Laï; Z Aissaoui; C Collyn-d'Hooghe; M H Delfau; B Grandchamp; P Fenaux; J P Jouet; B Desablens; M Deminatti; M H Loucheux-Lefebvre
Chronic myeloid leukemia with unusual variant Ph translocation (22;22)(q11;q13). Two cases with chimeric BCR-ABL transcripts.
Cancer genetics and cytogenetics 1990;48(2):209-16.
1990: Jean-Luc Laï; Marc Zandecki; Pierre Fenaux; F Le Baron; Francis Bauters; Alain Cosson; M Deminatti
Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemia. A possible association with acquired pseudo-Pelger-Huët anomaly and small vacuolated granulocytes.
Cancer genetics and cytogenetics 1990;46(2):173-83.
1990: M H Delfau; Jean-Pierre Kerckaert; M Collyn d'Hooghe; Pierre Fenaux; Jean-Luc Laï; J P Jouet; B Grandchamp
Detection of minimal residual disease in chronic myeloid leukemia patients after bone marrow transplantation by polymerase chain reaction.
Leukemia 1990;4(1):1-5.
1990: P Fenaux; Jean-Luc Laï; C Preudhomme; J P Jouet; M Deminatti; F Bauters
Is translocation (8;21) a "favorable" cytogenetic rearrangement in acute myeloid leukemia?
Nouvelle revue française d'hématologie 1990;32(3):179-82.
1990: Jean-Pierre Kerckaert; Martine Duterque-Coquillaud; M Collyn-d'Hooghe; P Morel; Marie-Ange Majérus; Jean-Luc Laï; Pierre Fenaux; Francis Bauters; Brigitte Debuire; M H Loucheux-Lefebvre
Polymorphism of the proto-oncogene ETS-1 in hematological malignancies.
Leukemia 1990;4(1):16-9.
1989: Pierre Fenaux; M H Estienne; Jean-Luc Laï; R Beuscart; Brigitte Dupriez; Jean-Pierre Jouet; Francis Bauters
[Acquired idiopathic sideroblastic anemia. Apropos of 39 cases].
La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne 1989;10(4):323-9.
1989: Jean-Luc Laï; M H Estienne; Pierre Fenaux; Pascale Lepelley; J J Huart; Francis Bauters; M Deminatti
Translocation t(10;17)(p13;q12) in two cases of acute nonlymphocytic leukemia with phagocytic activity of blasts. A new cytogenetic entity?
Cancer genetics and cytogenetics 1989;39(1):45-53.
1989: Jean-Luc Laï; Pierre Fenaux; M H Estienne; J J Huart; J B Savary; Pascale Lepelley; Jean-Pierre Jouet; Brigitte Nelken; Francis Bauters; M Deminatti
Translocation t(1;19)(q23;p13) in acute lymphoblastic leukemia. A report on six new cases and an unusual t(17;19)(q11;q13), with special reference to prognostic factors.
Cancer genetics and cytogenetics 1989;37(1):9-17.
1988: Jean-Loup Demory; Brigitte Dupriez; Pierre Fenaux; Jean-Luc Laï; R Beuscart; Jean-Pierre Jouet; M Deminatti; Francis Bauters
Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: a report on 47 cases.
Blood 1988;72(3):855-9.
1988: Jean-Luc Laï; Pierre Fenaux; J P Pollet; M H Estienne; J B Savary; J J Huart; M Deminatti
Acute lymphocytic leukemia with 9p anomalies. A report of four additional cases and review of the literature.
Cancer genetics and cytogenetics 1988;33(1):99-109.
1988: Marc Zandecki; Jean-Luc Laï; F Mazingue; Pascale Lepelley; O Chassaing; J P Farriaux; M Deminatti; Alain Cosson
Congenital acute monoblastic leukemia with double translocation (8;16) (p11;p13) and (16;20) (q13;p13).
Nouvelle revue française d'hématologie 1988;30(4):247-50.
1987: Jean-Luc Laï; Pierre Fenaux; Marc Zandecki; J B Savary; M H Estienne; Jean-Pierre Jouet; Francis Bauters; M Deminatti
Promyelocytic blast crisis of Philadelphia-positive thrombocythemia with translocations (9;22) and (15;17).
Cancer genetics and cytogenetics 1987;29(2):311-4.
1987: Jean-Luc Laï; Marc Zandecki; J P Jouet; J B Savary; A Lambiliotte; F Bauters; Alain Cosson; M Deminatti
Three cases of translocation (8;16)(p11;p13) observed in acute myelomonocytic leukemia: a new specific subgroup?
Cancer genetics and cytogenetics 1987;27(1):101-9.
1987: Jean-Luc Laï; J P Jouet; J B Savary; P Fenaux; F Bauters; M Deminatti
Chronic myelogenous leukemia with t(9;22) and t(8;11): a new chromosome anomaly.
Cancer genetics and cytogenetics 1987;25(1):103-7.
1987: Jean-Luc Laï; P Fenaux; J B Savary; J P Jouet; P Le Pelley; F Bauters; M Deminatti
Translocation (1;7) in a case of secondary chronic myelomonocytic leukemia.
Cancer genetics and cytogenetics 1987;24(2):355-7.
1987: Jean-Luc Laï; Jean-Pierre Jouet; Marc Zandecki; J B Savary; Pierre Fenaux; Pascale Lepelley; Brigitte Nelken; Francis Bauters; M Deminatti
[(9;11) (p21;q23) translocation: apropos of 2 new cases seen in acute undifferentiated monoblastic AML5a leukemia].
Nouvelle revue française d'hématologie 1987;29(5):303-6.
1987: Marc Zandecki; Brigitte Dupriez; Jean-Luc Laï; Pierre Fenaux; Thierry Facon; Pascale Lepelley; M H Estienne; J J Huart; Jean-Pierre Jouet
[Acute lymphoblastic leukemia, Burkitt-cell type, after Hodgkin's disease. Study of 2 cases].
Nouvelle revue française d'hématologie 1987;29(6):365-9.
1985: Jean-Luc Laï; J P Jouet; F Bauters; M Deminatti
Chronic myelogenous leukemia with translocation (8;22): report of a new case.
Cancer genetics and cytogenetics 1985;17(4):365-6.
1983: Jean-Luc Laï; J P Jouet; Marc Zandecki; J J Huart; F Bauters; M Deminatti
[Burkitt's acute lymphoblastic leukemia. Incidence and cytogenetic aspects].
Nouvelle revue française d'hématologie 1983;25(5):303-9.
1983: Jean-Luc Laï; Marc Zandecki; J Weill; Alain Cosson; C Ponte; M Deminatti
[Transient leukoblastosis and dysmegakariocytopoiesis with clone 46, XX+21, t(5;7), in a newborn infant with trisomy 21].
Nouvelle revue française d'hématologie 1983;25(6):363-7.