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Roland Berger

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Xinying Su; Véronique Della-Valle; Eric Delabesse; Zahia Azgui; Roland Berger; Hélène Merle-Béral; Olivier A Bernard; Florence Nguyen Khac
Transcriptional activation of the cardiac homeobox gene CSX1/NKX2-5 in a B-cell chronic lymphoproliferative disorder.
Arnaud Petit; Isabelle Radford; Marie-Christine Perrier Waill; Serge Romana; Roland Berger
NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
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).

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All Publications

2008: Xinying Su; Véronique Della-Valle; Eric Delabesse; Zahia Azgui; Roland Berger; Hélène Merle-Béral; Olivier A Bernard; Florence Nguyen Khac
Transcriptional activation of the cardiac homeobox gene CSX1/NKX2-5 in a B-cell chronic lymphoproliferative disorder.
Haematologica 2008;93(7):1081-5.
2008: Arnaud Petit; Isabelle Radford; Marie-Christine Perrier Waill; Serge Romana; Roland Berger
NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
Cancer genetics and cytogenetics 2008;180(1):43-6.
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: Roland Berger; Olivier A Bernard
Jumping translocations.
Genes, chromosomes & cancer 2007;46(8):717-23.
2007: michel lessard; Catherine Hélias; Stéphanie Struski; N Perrusson; Françoise Uettwiller; Marie-Joëlle Mozziconacci; Marina Lafage-Pochitaloff; Nicole Dastugue; Christine Terré; Françoise Brizard; Pascale Cornillet-Lefebvre; Francine Mugneret; Carole Barin; Angèle Herry; Isabelle Luquet; F Desangles; Lucienne Michaux; Christine Verellen-Dumoulin; C Perrot; Jacqueline van den Akker; James Lespinasse; Virginie Eclache; Roland Berger
Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?
Cancer genetics and cytogenetics 2007;176(1):1-21.
2007: Sebastien Malinge; Raouf Ben-Abdelali; Catherine Settegrana; Isabelle Radford-Weiss; Marianne Debre; Kheira Beldjord; Elizabeth Macintyre; Jean-Luc Villeval; William Vainchenker; Roland Berger; Olivier A Bernard; Eric Delabesse; Virginie Penard-Lacronique
Novel activating JAK2 mutation in a patient with Down syndrome and B-cell precursor acute lymphoblastic leukemia.
Blood 2007;109(5):2202-4.
2007: Roland Berger; O A Bernard
Interleukin-2 receptor beta chain locus rearrangement in a T-cell acute lymphoblastic leukemia.
Pathologie-biologie 2007;55(1):56-8.
2007: Roland Berger
[Human cytogenetics. From 1956 to 2006].
Pathologie-biologie 2007;55(1):1-12.
2006: Xin Ying Su; Véronique Della Valle; Isabelle Andre-Schmutz; Claudie Lemercier; Isabelle Radford-Weiss; Paola Ballerini; michel lessard; Marina Lafage-Pochitaloff; Francine Mugneret; Roland Berger; Serge Romana; Olivier A Bernard; Virginie Penard-Lacronique
HOX11L2/TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32).
Blood 2006;108(13):4198-201.
2006: Elise Chapiro; Lisa Russell; Isabelle Radford-Weiss; Christian Bastard; michel lessard; Stéphanie Struski; Helene Cave; Sandra Fert-Ferrer; Carole Barin; Odile Maarek; Véronique Della Valle; Jon C Strefford; Roland Berger; Christine J Harrison; Olivier A Bernard; Florence Nguyen Khac
Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia.
Blood 2006;108(10):3560-3.
2006: Xinying Su; Harry A Drabkin; Emmanuelle Clappier; Ester Morgado; Maryvonne Busson; Serge Romana; Jean Soulier; Roland Berger; Olivier A Bernard; Catherine Lavau
Transforming potential of the T-cell acute lymphoblastic leukemia-associated homeobox genes HOXA13, TLX1, and TLX3.
Genes, chromosomes & cancer 2006;45(9):846-55.
2006: Eric Jeandidier; Nicole Dastugue; Francine Mugneret; Marina Lafage-Pochitaloff; Marie-Joëlle Mozziconacci; Christian Herens; Lucienne Michaux; Christine Verellen-Dumoulin; Pascaline Talmant; Pascale Cornillet-Lefebvre; Isabelle Luquet; Christiane Charrin; Carole Barin; Marie-Agnès Collonge-Rame; Christine Pérot; Jacqueline van den Akker; Marie-José Grégoire; Philippe Jonveaux; Laurence Baranger; Virginie Eclache-Saudreau; Marie-Pierre Pagès; Christine Cabrol; Christine Terré; Roland Berger
Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique Hématologique.
Cancer genetics and cytogenetics 2006;166(1):1-11.
2006: Serge Romana; Isabelle Radford-Weiss; Raouf Ben-Abdelali; C Schluth; A Petit; Nicole Dastugue; Pascaline Talmant; Chrystèle Bilhou-Nabera; Francine Mugneret; Marina Lafage-Pochitaloff; Marie-Joëlle Mozziconacci; J Andrieu; Jean-Luc Lai; Christine Terre; KA Rack; Pascale Cornillet-Lefebvre; Isabelle Luquet; N Nadal; Florence Nguyen Khac; Christine Perot; Jacqueline van den Akker; Sandra Fert-Ferrer; Christine Cabrol; Christiane Charrin; Isabelle Tigaud; Hélène A Poirel; Michel Vekemans; Olivier A Bernard; Roland Berger
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.
Leukemia 2006;20(4):696-706.
2006: Roland Berger; Maryvonne Busson; Serge P Romana
A cryptic chromosome 19 abnormality in a patient with Ph-positive acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 2006;165(1):79-80.
2006: Roland Berger; Maryvonne Busson; Laurence Baranger; Catherine Hélias; michel lessard; Nicole Dastugue; F Speleman
Loss of the NPM1 gene in myeloid disorders with chromosome 5 rearrangements.
Leukemia 2006;20(2):319-21.
2006: Roland Berger; Maryvonne Busson; Nicole Dastugue; Isabelle Radford-Weiss; Lucienne Michaux; Anne Hagemeijer; Benoît Quilichini; Laurence Benattar; Olivier Bernard; Serge Romana
Acute megakaryoblastic leukemia and loss of the RUNX1 gene.
Cancer genetics and cytogenetics 2006;164(1):71-3.
2005: michel lessard; Stéphanie Struski; Vincent Leymarie; Georges Flandrin; Marina Lafage-Pochitaloff; Marie-Joëlle Mozziconacci; Pascaline Talmant; Christian Bastard; Christiane Charrin; Laurence Baranger; Catherine Hélias; Pascale Cornillet-Lefebvre; Francine Mugneret; Christine Cabrol; Marie-Pierre Pagès; D Fert-Ferret; Florence Nguyen Khac; B Quilichini; Carole Barin; Roland Berger
Cytogenetic study of 75 erythroleukemias.
Cancer genetics and cytogenetics 2005;163(2):113-22.
2005: Florence Nguyen Khac; Frédéric Davi; Aline Receveur; Karim Maloum; Véronique Morel; Magali Le Garff-Tavernier; Jeanne Ong; Roland Berger; Véronique Leblond; Hélène Merle-Béral
Burkitt-type acute leukemia in a patient with B-prolymphocytic leukemia: evidence for a common origin.
Cancer genetics and cytogenetics 2005;159(1):74-8.
2005: Paola Ballerini; Maryvonne Busson; Sylvie Fasola; Jacqueline van den Akker; Hélène Lapillonne; Serge Romana; P Marynen; Olivier A Bernard; Judith Landman-Parker; Roland Berger
NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance.
Leukemia 2005;19(3):468-70.
2004: Xin Ying Su; Maryvonne Busson; Véronique Della Valle; Paola Ballerini; Nicole Dastugue; Pascaline Talmant; Adolfo Ferrando; Dominique Baudry-Bluteau; Serge Romana; Roland Berger; Olivier A Bernard
Various types of rearrangements target TLX3 locus in T-cell acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2004;41(3):243-9.
2004: Aline Receveur; Jeanne Ong; Laurent Merlin; Zahia Azgui; Hélène Merle-Béral; Roland Berger; Florence Nguyen Khac
Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.
Annales de génétique 2004;47(4):423-7.
2004: Maryvonne Busson; Serge Romana; Florence Nguyen Khac; Olivier Bernard; Roland Berger
Cryptic translocations involving chromosome 20 in polycythemia vera.
Annales de génétique 2004;47(4):365-71.
2004: V Della Valle; L Guglielmi; Maryvonne Busson; E C Zwarthoff; Roland Berger; Olivier A Bernard
Expression of the MN1-TEL fusion protein in the human UCSD/AML1 leukemic cell line.
Leukemia 2004;18(9):1558-60.
2003: Paola Ballerini; Annick Blaise; Thomas Mercher; Béatrice Pellegrino; Christine Perot; Jacqueline van den Akker; E Gatbois; Mircéa Adam; Luc Douay; Roland Berger; O Bernard; Judith Landman-Parker
A novel real-time RT-PCR assay for quantification of OTT-MAL fusion transcript reliable for diagnosis of t(1;22) and minimal residual disease (MRD) detection.
Leukemia 2003;17(6):1193-6.
2003: Xiaxin Li; François Leteurtre; Vanderson Rocha; Philippe Guardiola; Roland Berger; Marie-Thérèse Daniel; Maria Helena Noguera; Odile Maarek; Gwenaëlle L E Roux; Pauline De La Salmonière; Patrice Richard; Eliane Gluckman
Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia.
British journal of haematology 2003;120(5):836-45.
2003: Christophe Roumier; Virginie Eclache; Michèle Imbert; Frédéric Davi; Elizabeth Macintyre; Richard Garand; Pascaline Talmant; Pascale Lepelley; Jean-Luc Lai; Olivier Casasnovas; Marc Maynadie; Francine Mugneret; Chrystele Bilhou-Naberra; Françoise Valensi; Isabelle Radford; Marie-Joëlle Mozziconacci; Christine Arnoulet; Eliane Duchayne; Nicole Dastugue; Pascale Cornillet; Sylvie Daliphard; Francine Garnache; Najiba Boudjerra; Hélène Jouault; Odile Fenneteau; Béatrice Pedron; Roland Berger; Georges Flandrin; Pierre Fenaux; Claude Preudhomme
M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: a report of 59 cases by the Groupe Français d'Hématologie Cellulaire (GFHC) and the Groupe Français de Cytogénétique Hématologique (GFCH).
Blood 2003;101(4):1277-83.
2003: Thomas Mercher; G Courtois; Roland Berger; Olivier A Bernard
[Molecular basis of the t(1;22)(p13;q13) specific for human acute megakaryoblastic leukemia].
Pathologie-biologie 2003;51(1):27-32.
2002: Maryvonne Busson-Le Coniat; Nathalie Boucher; Hélène Blanché; Gilles Thomas; Roland Berger
Chromosome studies of in vitro senescent lymphocytes: nonrandom trisomy 2.
Annales de génétique 2002;45(4):193-6.
2002: Florence Nguyen Khac; Marie-Christine Perrier Waill; Serge Romana; Isabelle Radford-Weiss; Maryvonne Busson; Marie-Agnès Collonge-Rame; Antoine Ribadeau Dumas; Marie-Claude Piffaut; Marie-Thérèse Daniel; Frédéric Davi; Hélène Merle-Béral; Roland Berger; Michel AROCK
Identical abnormality of the short arm of chromosome 18 in two Philadelphia-positive chronic myelocytic leukemia patients with erythroblastic transformation, resulting in duplication of BCR-ABL1 fusion.
Cancer genetics and cytogenetics 2002;138(1):22-6.
2002: Paola Ballerini; Annick Blaise; Maryvonne Busson-Le Coniat; Xin Ying Su; Jessica Zucman-Rossi; Mircéa Adam; Jacqueline van den Akker; Christine Perot; Béatrice Pellegrino; Judith Landman-Parker; Luc Douay; Roland Berger; Olivier A Bernard
HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis.
Blood 2002;100(3):991-7.
2002: Nicole Dastugue; Marina Lafage-Pochitaloff; Marie-Pierre Pagès; Isabelle Radford; Christian Bastard; Pascaline Talmant; Marie-Joëlle Mozziconacci; Claude Léonard; Christelle Bilhou-Nabéra; Christine Cabrol; Anne-Marie Capodano; Pascale Cornillet-Lefebvre; michel lessard; Francine Mugneret; Christine Pérot; Sylvie Taviaux; Odile Fenneteaux; Eliane Duchayne; Roland Berger
Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématologique (GFCH).
Blood 2002;100(2):618-26.
2002: Sylvie Paulien; Odile Maarek; Marie-Thérèse Daniel; Roland Berger
A novel translocation, t(9;21)(q13;q22) rearranging the RUNX1 gene in acute myelomonocytic leukemia.
Annales de génétique 2002;45(2):67-9.
2002: Thomas Mercher; Maryvonne Busson-Le Coniat; Florence Nguyen Khac; Paola Ballerini; Martine Mauchauffé; Hung Bui; Béatrice Pellegrino; Isabelle Radford; Françoise Valensi; Francine Mugneret; Nicole Dastugue; Olivier A Bernard; Roland Berger
Recurrence of OTT-MAL fusion in t(1;22) of infant AML-M7.
Genes, chromosomes & cancer 2002;33(1):22-8.
2001: Maryvonne Busson-Le Coniat; Florence Nguyen Khac; Marie-Thérèse Daniel; Olivier A Bernard; Roland Berger
Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2001;32(3):244-9.
2001: Roland Berger; Maryvonne Busson; Marie-Thérèse Daniel
B-cell acute lymphoblastic leukemia with tandem t(14;14)(q11;q32).
Cancer genetics and cytogenetics 2001;130(1):84-6.
2001: Olivier A Bernard; M Busson-LeConiat; Paola Ballerini; Martine Mauchauffé; Véronique Della Valle; R Monni; Florence Nguyen Khac; Thomas Mercher; Virginie Penard-Lacronique; P Pasturaud; L Gressin; R Heilig; Marie-Thérèse Daniel; michel lessard; Roland Berger
A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia.
Leukemia 2001;15(10):1495-504.
2001: Thomas Mercher; M B Coniat; R Monni; M Mauchauffe; Florence Nguyen Khac; L Gressin; Francine Mugneret; Thierry Leblanc; Nicole Dastugue; Roland Berger; Olivier A Bernard
Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(10):5776-9.
2001: R Monni; SC Santos; M Mauchauffe; Roland Berger; Jacques Ghysdael; Fabrice Gouilleux; Sylvie Gisselbrecht; Olivier Bernard; Virginie Penard-Lacronique
The TEL-Jak2 oncoprotein induces Socs1 expression and altered cytokine response in Ba/F3 cells.
Oncogene 2001;20(7):849-58.
2000: F Salmon-Nguyen; Maryvonne Busson; M Daniel; Thierry Leblanc; Olivier A Bernard; Roland Berger
CALM-AF10 fusion gene in leukemias: simple and inversion-associated translocation (10;11).
Cancer genetics and cytogenetics 2000;122(2):137-40.
2000: Hélène A Poirel; Rodolphe G Lopez; V Lacronique; Véronique Della Valle; Martine Mauchauffé; Roland Berger; Jacques Ghysdael; Olivier A Bernard
Characterization of a novel ETS gene, TELB, encoding a protein structurally and functionally related to TEL.
Oncogene 2000;19(41):4802-6.
2000: F Salomon-Nguyen; Maryvonne Busson-Le Coniat; Marina Lafage-Pochitaloff; J Mozziconacci; Roland Berger; Olivier A Bernard
AML1-MTG16 fusion gene in therapy-related acute leukemia with t(16;21)(q24;q22): two new cases.
Leukemia 2000;14(9):1704-5.
2000: Maryvonne Busson-Le Coniat; Françoise Brizard; N V Smadja; Odile Maarek; H Der Sarkissian; Roland Berger
Interstitial telomere repeats in translocations of hematopoietic disorders.
Leukemia 2000;14(9):1630-3.
2000: F Salomon-Nguyen; Véronique Della Valle; M Mauchauffe; Maryvonne Busson-Le Coniat; Jacques Ghysdael; Roland Berger; Olivier A Bernard
The t(1;12)(q21;p13) translocation of human acute myeloblastic leukemia results in a TEL-ARNT fusion.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(12):6757-62.
2000: S Paulien; M Busson-Le Coniat; Roland Berger
Acute megakaryocytic leukaemia with acquired polysomy 21 and translocation t(1;21).
Annales de génétique 2000;43(2):99-104.
2000: V Lacronique; anthony boureux; R Monni; S Dumon; Martine Mauchauffé; Patrick Mayeux; Fabrice Gouilleux; Roland Berger; Sylvie Gisselbrecht; Jacques Ghysdael; Olivier A Bernard
Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells.
Blood 2000;95(6):2076-83.
2000: Roland Berger; M B Coniat
Uneven frequencies of secondary chromosomal abnormalities in acute myeloid leukemias with t(8;21), t(15;17), and inv(16).
Cancer genetics and cytogenetics 2000;117(2):159-62.
1999: Maryvonne Busson-Le Coniat; F Salomon-Nguyen; Nicole Dastugue; Odile Maarek; Marina Lafage-Pochitaloff; Marie-Joëlle Mozziconacci; Laurence Baranger; Françoise Brizard; Isabelle Radford; M Jeanpierre; Olivier A Bernard; Roland Berger
Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders: rearrangements of DNA satellite II and new recurrent translocations.
Leukemia 1999;13(12):1975-81.
1999: Serge Romana; Hélène A Poirel; Véronique Della Valle; Martine Mauchauffé; Maryvonne Busson-Le Coniat; Roland Berger; Olivier A Bernard
Molecular analysis of chromosomal breakpoints in three examples of chromosomal translocation involving the TEL gene.
Leukemia 1999;13(11):1754-9.
1999: Odile Maarek; A Salabelle; MB Le Coniat; Marie-Thérèse Daniel; Roland Berger
Chromosome 16 inversion-associated translocation: two new cases.
Cancer genetics and cytogenetics 1999;114(2):126-9.
1999: Christine Terré; Isabel Garcia; Jean-Noël Bastie; D Mayeur; L Decombe; P Gruyer; Roland Berger; Sylvie Castaigne
A case of chronic neutrophilic leukemia with deletion (11)(q23).
Cancer genetics and cytogenetics 1999;110(1):70-1.
1999: Maryvonne Busson-Le Coniat; F Salomon-Nguyen; J Hillion; Olivier A Bernard; Roland Berger
MLL-AF1q fusion resulting from t(1;11) in acute leukemia.
Leukemia 1999;13(2):302-6.
1998: Olivier A Bernard; J Hillion; MB Le Coniat; Roland Berger
A new case of translocation t(6;11)(q21;q23) in a therapy-related acute myeloid leukemia resulting in an MLL-AF6q21 fusion.
Genes, chromosomes & cancer 1998;22(3):221-4.
1998: Hélène A Poirel; V Lacronique; Martine Mauchauffé; MB Le Coniat; Emmanuel Raffoux; Marie-Thérèse Daniel; Paul F Erickson; Harry A Drabkin; R A MacLeod; H G Drexler; Jacques Ghysdael; Roland Berger; Olivier A Bernard
Analysis of TEL proteins in human leukemias.
Oncogene 1998;16(22):2895-903.
1998: F Salomon-Nguyen; Françoise Brizard; M Le Coniat; Isabelle Radford; Roland Berger; André Brizard
Abnormalities of the short arm of chromosome 12 in T cell prolymphocytic leukemia.
Leukemia 1998;12(6):972-5.
1997: V Lacronique; anthony boureux; V D Valle; Hélène A Poirel; Christine Tran Quang; Martine Mauchauffé; C Berthou; michel lessard; Roland Berger; Jacques Ghysdael; Olivier A Bernard
A TEL-JAK2 fusion protein with constitutive kinase activity in human leukemia.
Science (New York, N.Y.) 1997;278(5341):1309-12.
1997: J Hillion; MB Le Coniat; P Jonveaux; Roland Berger; Olivier A Bernard
AF6q21, a novel partner of the MLL gene in t(6;11)(q21;q23), defines a forkhead transcriptional factor subfamily.
Blood 1997;90(9):3714-9.
1997: Roland Berger; MB Le Coniat; V Lacronique; Marie-Thérèse Daniel; michel lessard; C Berthou; P Marynen; Olivier Bernard
Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: a report including three novel translocations involving the TEL/ETV6 gene.
Leukemia 1997;11(9):1400-3.
1997: M Le Coniat; V Della Valle; P Marynen; Roland Berger
A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia.
Leukemia 1997;11(8):1360-3.
1997: T Leblanc; Roland Berger
Molecular cytogenetics of childhood acute myelogenous leukaemias.
European journal of haematology 1997;59(1):1-13.
1997: E Duprez; Jian-Hua Tong; J Dérré; S J Chen; Roland Berger; Z Chen; Michel Lanotte
JEM-1, a novel gene encoding a leucine-zipper nuclear factor upregulated during retinoid-induced maturation of NB4 promyelocytic leukaemia.
Oncogene 1997;14(13):1563-70.
1997: Hélène A Poirel; C Oury; Clemence Carron; E Duprez; Yacine LAABI; Andréas Tsapis; Serge Romana; M Mauchauffe; MB Le Coniat; Roland Berger; Jacques Ghysdael; Olivier A Bernard
The TEL gene products: nuclear phosphoproteins with DNA binding properties.
Oncogene 1997;14(3):349-57.
1996: O A Bernard; Serge Romana; Hélène A Poirel; Roland Berger
Molecular cytogenetics of t(12;21) (p13;q22).
Leukemia & lymphoma 1996;23(5-6):459-65.
1996: Thierry Leblanc; MB Le Coniat; M Flexor; André Baruchel; Marie-Thérèse Daniel; Roland Berger
An interstitial 11q23 deletion proven to be a rearrangement interrupting the MLL gene in an infant with acute myeloblastic leukemia.
Leukemia 1996;10(11):1844-6.
1996: Odile Maarek; P Jonveaux; MB Le Coniat; J Derré; Roland Berger
Faconi anemia and bone marrow clonal chromosome abnormalities.
Leukemia 1996;10(11):1700-4.
1996: P Jonveaux; Marie-Thérèse Daniel; V Martel; Odile Maarek; Roland Berger
Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphoma.
Leukemia 1996;10(9):1453-5.
1996: Roland Berger; P Jonveaux
Clonal chromosome abnormalities in Fanconi anemia.
Hematology and cell therapy 1996;38(4):291-6.
1996: V Della Valle; M le Coniat; M Soulard; V C Nguyen; Roland Berger; C J Larsen
Dual localization of the human gene encoding hnRNP I/PTB protein to chromosomes 19p13.3 and 14q23.
Human genetics 1996;98(2):210-3.
1996: Isabelle Tigaud; Christiane Charrin; Roland Berger; P Jonveaux
Partial deletion of the long arm of chromosome 5: a fluorescence in situ hybridization study using band-specific painting probes generated by chromosome microdissection.
Cancer genetics and cytogenetics 1996;89(2):126-8.
1996: Roland Berger; MB Le Coniat; Serge Romana; P Jonveaux
Secondary acute myeloblastic leukemia with t(16;21) (q24;q22). involving the AML1 gene.
Hematology and cell therapy 1996;38(2):183-6.
1996: MB Le Coniat; Doo-Sup Choi; Luc Maroteaux; Jean-Marie Launay; Roland Berger
The 5-HT2B receptor gene maps to 2q36.3-2q37.1.
Genomics 1996;32(1):172-3.
1996: Roland Berger; MB Le Coniat; M A Flexor; Thierry Leblanc
Translocation t(10;11) involving the MLL gene in acute myeloid leukemia. Importance of fluorescence in situ hybridization (FISH) analysis.
Annales de génétique 1996;39(3):147-51.
1996: P Jonveaux; MB Le Coniat; J Derre; M A Flexor; Marie-Thérèse Daniel; Roland Berger
Chromosome microdissection in leukemia: a powerful tool for the analysis of complex chromosomal rearrangements.
Genes, chromosomes & cancer 1996;15(1):26-33.
1996: Roland Berger; M Flexor; MB Le Coniat; C J Larsen
Presence of three recurrent chromosomal reaarrangements, t(2;3)(p12;q37), del(8)(q24), and t(14;18), in an acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1996;86(1):76-9.
1996: Serge Romana; MB Le Coniat; Hélène A Poirel; P Marynen; O Bernard; Roland Berger
Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21).
Leukemia 1996;10(1):167-70.
1995: Serge Romana; Hélène A Poirel; M Leconiat; M A Flexor; Martine Mauchauffé; P Jonveaux; Elizabeth Macintyre; Roland Berger; O A Bernard
High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia.
Blood 1995;86(11):4263-9.
1995: MB Le Coniat; Serge Romana; Roland Berger
Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia.
Genes, chromosomes & cancer 1995;14(3):204-9.
1995: O A Bernard; Serge Romana; S A Schichman; Martine Mauchauffé; P Jonveaux; Roland Berger
Partial duplication of HRX in acute leukemia with trisomy 11.
Leukemia 1995;9(9):1487-90.
1995: Serge Romana; Martine Mauchauffé; MB Le Coniat; I Chumakov; D Le Paslier; Roland Berger; O A Bernard
The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion.
Blood 1995;85(12):3662-70.
1995: Marie-Thérèse Daniel; Isabelle Tigaud; M A Flexor; M E Nogueira; Roland Berger; P Jonveaux
Leukaemic non-Hodgkin's lymphomas with hyperdiploid cells and t(11;14)(q13;q32): a subtype of mantle cell lymphoma?
British journal of haematology 1995;90(1):77-84.
1995: Hélène A Poirel; P Jonveaux; Marie-Thérèse Daniel; Roland Berger
Trisomy 14: a recurring cytogenetic abnormality associated with myeloid disorders.
Leukemia & lymphoma 1995;17(5-6):455-7.
1995: Roland Berger; M Flexor; MB Le Coniat; J Derré; Thierry Leblanc
Translocation (2;3)(p22;q28) is associated with myeloid disorders.
Cancer genetics and cytogenetics 1995;79(2):130-2.
1995: MB Le Coniat; Roland Berger
The proteinase 3 (PRTN3) gene is localized on 19p13.3 and is distal to the E2A gene.
Annales de génétique 1995;38(4):231-3.
1995: M F Rousseau-Merck; D Duro; Roland Berger; H J Thiesen
Chromosomal localization of two KOX zinc finger genes on chromosome bands 7q21-q22.
Annales de génétique 1995;38(2):81-4.
1994: P Jonveaux; J Hillion; O Bernard; MB Le Coniat; J Derré; M Flexor; C J Larsen; Roland Berger
Distinct MLL gene rearrangements associated with successive acute monocytic and lymphoblastic leukemias in the same patient.
Leukemia 1994;8(12):2224-7.
1994: Thierry Leblanc; J Hillion; J Derré; MB Le Coniat; André Baruchel; Marie-Thérèse Daniel; Roland Berger
Translocation t(11;11)(q13;q23) and HRX gene rearrangement associated with therapy-related leukemia in a child previously treated with VP16.
Leukemia 1994;8(10):1646-8.
1994: J Hébert; Jean-Michel Cayuela; Marie-Thérèse Daniel; Roland Berger; François Sigaux
Detection of minimal residual disease in acute myelomonocytic leukemia with abnormal marrow eosinophils by nested polymerase chain reaction with allele specific amplification.
Blood 1994;84(7):2291-6.
1994: Françoise Brizard; André Brizard; françois guilhot; J Tanzer; Roland Berger
Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias.
Leukemia 1994;8(6):1005-11.
1994: P Jonveaux; P Fenaux; Roland Berger
Trisomy 6 as the sole chromosome abnormality in myeloid disorders.
Cancer genetics and cytogenetics 1994;74(2):150-2.
1994: Yacine LAABI; M P Gras; J C Brouet; Roland Berger; C J Larsen; Andréas Tsapis
The BCMA gene, preferentially expressed during B lymphoid maturation, is bidirectionally transcribed.
Nucleic acids research 1994;22(7):1147-54.
1994: D Cherif; O Bernard; S Paulien; MR James; D Le Paslier; Roland Berger
Hunting 11q23 deletions with fluorescence in situ hybridization (FISH).
Leukemia 1994;8(4):578-86.
1994: O A Bernard; M Mauchauffe; C Mecucci; H Van den Berghe; Roland Berger
A novel gene, AF-1p, fused to HRX in t(1;11)(p32;q23), is not related to AF-4, AF-9 nor ENL.
Oncogene 1994;9(4):1039-45.
1994: J Hébert; P Jonveaux; M F d'Agay; Roland Berger
Cytogenetic studies in patients with Richter's syndrome.
Cancer genetics and cytogenetics 1994;73(1):65-8.
1994: Serge Romana; MB Le Coniat; Roland Berger
t(12;21): a new recurrent translocation in acute lymphoblastic leukemia.
Genes, chromosomes & cancer 1994;9(3):186-91.
1994: Franck Carbonnel; A Lavergne; Bernard Messing; Andréas Tsapis; Roland Berger; A Galian; J Nemeth; J C Brouet; Jean-Claude Rambaud
Extensive small intestinal T-cell lymphoma of low-grade malignancy associated with a new chromosomal translocation.
Cancer 1994;73(4):1286-91.
1994: D Cherif; H Der-Sarkissian; Roland Berger
Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nuclei.
Human genetics 1994;93(1):1-6.
1994: Roland Berger
Translocation t(8;21)(q22;q22): cytogenetics and molecular biology.
Nouvelle revue française d'hématologie 1994;36 Suppl 1():S67-9.
1993: M F Rousseau-Merck; J Hillion; P Jonveaux; P Couillin; P Seité; H J Thiesen; Roland Berger
Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19.
Human genetics 1993;92(6):583-7.
1993: P Séité; J Hillion; M F d'Agay; Roland Berger; C J Larsen
BCL2 complex rearrangement in follicular lymphoma: translocation mbr/JH and deletion in the vcr region of the same BCL2 allele.
Oncogene 1993;8(11):3073-80.
1993: P Jonveaux; M T Daniel; Roland Berger
5q- anomaly preceding acute myeloblastic leukemia with 53 chromosomes without chromosome 5 abnormality.
Cancer genetics and cytogenetics 1993;70(2):146-7.
1993: O Bernard; M Groettrup; F Mugneret; Roland Berger; Orly Azogui
Molecular analysis of T-cell receptor transcripts in a human T-cell leukemia bearing a t(1;14) and an inv(7); cell surface expression of a TCR-beta chain in the absence of alpha chain.
Leukemia 1993;7(10):1645-53.
1993: Serge Romana; D Cherif; MB Le Coniat; J Derré; M A Flexor; Roland Berger
In situ hybridization to interphase nuclei in acute leukemia.
Genes, chromosomes & cancer 1993;8(2):98-103.
1993: Roland Berger; MB Le Coniat; M C Gendron
Fanconi anemia. Chromosome breakage and cell cycle studies.
Cancer genetics and cytogenetics 1993;69(1):13-6.
1993: MB Le Coniat; Serge Romana; O Bernard; M A Flexor; J Hillion; D Cherif; Roland Berger
A novel translocation, t(9;11)(q33;q23) involving the HRX gene in an acute monocytic leukemia.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1993;316(7):692-7.
1993: P Antonini; G Linares; N Gaillard; AM Venuat; Martin Schlumberger; J P Travagli; B Caillou; Roland Berger; Claude Parmentier
Cytogenetic characterization of a new human papillary thyroid carcinoma permanent cell line (GLAG-66).
Cancer genetics and cytogenetics 1993;67(2):117-22.
1993: P Séité; J Hillion; Dominique Leroux; Roland Berger; C J Larsen
Common sequence in chromosome translocations affecting B- and T-cell malignancies: a novel recombination site?
Genes, chromosomes & cancer 1993;6(4):253-4.
1993: Jean-Paul Fermand; M T Mitjavila; Jean-Pierre Le Couedic; A Tsapis; Roland Berger; Robert Modigliani; M Seligmann; Jean-Claude Brouet; William Vainchenker
Role of granulocyte-macrophage colony-stimulating factor, interleukin-3 and interleukin-5 in the eosinophilia associated with T cell lymphoma.
British journal of haematology 1993;83(3):359-64.
1993: H Baurmann; D Cherif; Roland Berger
Interphase cytogenetics by fluorescent in situ hybridization (FISH) for characterization of monosomy-7-associated myeloid disorders.
Leukemia 1993;7(3):384-91.
1993: P Séité; J Hillion; M F d'Agay; P Gaulard; D Cazals; F Badoux; Roland Berger; C J Larsen
BCL2 gene activation and protein expression in follicular lymphoma: a report on 64 cases.
Leukemia 1993;7(3):410-7.
1993: C J Larsen; P Seite; J Hillion; M F D'Agay; Roland Berger
Some recent aspects of the molecular biology of human lymphoma.
Nouvelle revue française d'hématologie 1993;35(1):37-40.
1993: D Cherif; Serge Romana; H Der-Sarkissian; C Jones; Roland Berger
Chromosome painting in acute monocytic leukemia.
Genes, chromosomes & cancer 1993;6(2):107-12.
1993: M F Rousseau-Merck; M Atger; Hugues Loosfelt; E Milgrom; Roland Berger
The chromosomal localization of the human follicle-stimulating hormone receptor gene (FSHR) on 2p21-p16 is similar to that of the luteinizing hormone receptor gene.
Genomics 1993;15(1):222-4.
1993: Serge Romana; Gérard Tachdjian; L Druart; D Cohen; Roland Berger; D Chérif
A simple method for prenatal diagnosis of trisomy 21 on uncultured amniocytes.
European journal of human genetics : EJHG 1993;1(3):245-51.
1993: P Seité; Dominique Leroux; J Hillion; M Monteil; Roland Berger; D Mathieu-Mahul; C J Larsen
Molecular analysis of a variant 18;22 translocation in a case of lymphocytic lymphoma.
Genes, chromosomes & cancer 1993;6(1):39-44.
1992: E Duprez; S Ruchaud; Gunnar Houge; V Martin-Thouvenin; Françoise Valensi; P Kastner; Roland Berger; Michel Lanotte
A retinoid acid 'resistant' t(15;17) acute promyelocytic leukemia cell line: isolation, morphological, immunological, and molecular features.
Leukemia 1992;6(12):1281-7.
1992: Roland Berger; M T Daniel; P Jonveaux; A Baruchel
Relapse as acute monoblastic leukemia (AML-M5) of t(6;9) acute myeloblastic leukemia (AML-M2).
Leukemia 1992;6(11):1227-8.
1992: Yacine LAABI; M P Gras; Franck Carbonnel; J C Brouet; Roland Berger; C J Larsen; Andréas Tsapis
A new gene, BCM, on chromosome 16 is fused to the interleukin 2 gene by a t(4;16)(q26;p13) translocation in a malignant T cell lymphoma.
The EMBO journal 1992;11(11):3897-904.
1992: Roland Berger; MB Le Coniat; J Derré; M A Flexor; J Hillion
Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia.
Cancer genetics and cytogenetics 1992;63(2):97-9.
1992: O Bernard; Orly Azogui; N Lecointe; F Mugneret; Roland Berger; C J Larsen; D Mathieu-Mahul
A third tal-1 promoter is specifically used in human T cell leukemias.
The Journal of experimental medicine 1992;176(4):919-25.
1992: P Antonini; Anne-Marie Vénuat; B Caillou; Roland Berger; Martin Schlumberger; Alain BERNHEIM; Claude Parmentier
Cytogenetic studies on 19 papillary thyroid carcinomas.
Genes, chromosomes & cancer 1992;5(3):206-11.
1992: Roland Berger; MB Le Coniat; J Derré; M A Flexor
Loss of chromosome 22 in patients with refractory anemia with excess of blasts (RAEB) in transformation and acute leukemia after RAEB.
Cancer genetics and cytogenetics 1992;61(2):210-2.
1992: Roland Berger; MB Le Coniat; J Derré
5q- anomaly in acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1992;61(2):201-3.
1992: M F Rousseau-Merck; A Tunnacliffe; Roland Berger; Bruce A J Ponder; H J Thiesen
A cluster of expressed zinc finger protein genes in the pericentromeric region of human chromosome 10.
Genomics 1992;13(3):845-8.
1992: P Jonveaux; Roland Berger
Chromosome studies in plasma cell leukemia and multiple myeloma in transformation.
Genes, chromosomes & cancer 1992;4(4):321-5.
1992: M Le Coniat; M Soulard; V Della Valle; C J Larsen; Roland Berger
Localization of the human gene encoding heterogeneous nuclear RNA ribonucleoprotein G (hnRNP-G) to chromosome 6p12.
Human genetics 1992;88(5):593-5.
1992: D Cherif; H Der-Sarkissian; J Derré; T Tokino; Y Nakamura; Roland Berger
The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11).
Genes, chromosomes & cancer 1992;4(2):107-12.
1992: Roland Berger; H Dombret
New variant translocation in acute myelomonocytic leukemia with bone marrow eosinophilia.
Cancer genetics and cytogenetics 1992;58(2):204-5.
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.
1992: Pierre Fenaux; P Jonveaux; I Quiquandon; Claude Preudhomme; Jean-Luc Lai; M Vanrumbeke; M H Loucheux-Lefebvre; Francis Bauters; Roland Berger; Jean-Pierre Kerckaert
Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases.
Leukemia 1992;6(1):42-6.
1992: Marie-Thérèse Daniel; P Jonveaux; Roland Berger
Relapse as acute monocytic leukaemia of acute lymphoblastic leukaemia with t(4;11).
Nouvelle revue française d'hématologie 1992;34(4):347-8.
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.
1991: Roland Berger; MB Le Coniat; J Derré; D Vecchione; P Jonveaux
Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities.
Genes, chromosomes & cancer 1991;3(5):332-7.
1991: O Kemper; J Derré; D Cherif; Hartmut Engelmann; David Wallach; Roland Berger
The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2-p36.3.
Human genetics 1991;87(5):623-4.
1991: O Bernard; N Lecointe; P Jonveaux; M Souyri; Martine Mauchauffé; Roland Berger; C J Larsen; D Mathieu-Mahul
Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5' part of the tal-1 gene.
Oncogene 1991;6(8):1477-88.
1991: André Baruchel; Marie-Thérèse Daniel; Gérard Schaison; Roland Berger
Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation.
Cancer genetics and cytogenetics 1991;54(2):239-43.
1991: J Hillion; C J Larsen; Roland Berger
Hemizygous deletion of the 3' end of the RB1 gene in a case of Philadelphia positive-acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1991;54(2):197-203.
1991: J Derré; O Kemper; D Cherif; Y Nophar; Roland Berger; David Wallach
The gene for the type 1 tumor necrosis factor receptor (TNF-R1) is localized on band 12p13.
Human genetics 1991;87(2):231-3.
1991: Roland Berger; MB Le Coniat; J Derré; D Vecchione
Partial deletion of chromosome 2 in non-Hodgkin lymphoma.
Cancer genetics and cytogenetics 1991;53(1):113-7.
1991: P Seite; K Huebner; M F Rousseau-Merck; Roland Berger; H J Thiesen
Two human genes encoding zinc finger proteins, ZNF 12 (KOX 3) and ZNF 26 (KOX 20), map to chromosome 7p22-p21 and 12q24.33, respectively.
Human genetics 1991;86(6):585-90.
1991: P Antonini; Anne-Marie Vénuat; G Linares; B Caillou; Martin Schlumberger; J P Travagli; Roland Berger; Claude Parmentier
Cytogenetic abnormalities in thyroid adenomas.
Cancer genetics and cytogenetics 1991;52(2):157-64.
1991: R Miglierina; MB Le Coniat; Roland Berger
A simple diagnostic test for Fanconi anemia by flow cytometry.
Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology 1991;3(2):111-8.
1991: Michel Lanotte; V Martin-Thouvenin; S Najman; P Balerini; Françoise Valensi; Roland Berger
NB4, a maturation inducible cell line with t(15;17) marker isolated from a human acute promyelocytic leukemia (M3).
Blood 1991;77(5):1080-6.
1991: M F Rousseau-Merck; Ahmed Zahraoui; N Touchot; A Tavitian; Roland Berger
Chromosome assignment of four RAS-related RAB genes.
Human genetics 1991;86(4):350-4.
1991: J Hillion; M A Flexor; C J Larsen; Roland Berger
Studies of BCR rearrangements in Philadelphia-positive acute leukemia.
Cancer genetics and cytogenetics 1991;51(2):259-67.
1991: Roland Berger
Chromosomal abnormalities in T-cell malignant lymphoma.
Bulletin du cancer 1991;78(3):283-90.
1991: P Jonveaux; MB Le Coniat; J Derré; D Vecchione; Roland Berger
Loss of genetic material from the short arm of chromosome 12 is a frequent secondary abnormality in non-Hodgkin's lymphoma.
Hematologic pathology 1991;5(1):21-6.
1991: M F Rousseau-Merck; K Huebner; Roland Berger; H J Thiesen
Chromosomal localization of two human zinc finger protein genes, ZNF24 (KOX17) and ZNF29 (KOX26), to 18q12 and 17p13-p12, respectively.
Genomics 1991;9(1):154-61.
1991: P Jonveaux; MB Le Coniat; D Grausz; Roland Berger
Lack of mutations in the TP53 tumor suppressor gene exons 5 to 8 in Fanconi's anemia.
Nouvelle revue française d'hématologie 1991;33(5):343-5.
1990: J Derré; D Cherif; MB Le Coniat; Cécile Julier; Roland Berger
In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemia.
Genes, chromosomes & cancer 1990;2(4):341-4.
1990: P Jonveaux; MB Le Coniat; J Derré; D Vecchione; Roland Berger
Deletion of (7p13p14) in non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1990;50(1):53-6.
1990: P Jonveaux; Roland Berger
Chromosomal deletions in non-Hodgkin's malignant lymphomas.
Cancer genetics and cytogenetics 1990;49(2):265-9.
1990: M F Rousseau-Merck; Micheline Misrahi; Hugues Loosfelt; M Atger; E Milgrom; Roland Berger
Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31.
Genomics 1990;8(2):233-6.
1990: D Cherif; Cécile Julier; O Delattre; J Derré; G Mark Lathrop; Roland Berger
Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(17):6639-43.
1990: D Cherif; Roland Berger
New localizations of VH sequences by in situ hybridization with biotinylated probes.
Genes, chromosomes & cancer 1990;2(2):103-8.
1990: D Grausz; M Lanotte; Françoise Valensi; J Hillion; S J Chen; Z Chen; F Morinet; Roland Berger
A new Ph1+, bcr cell line derived from a patient with ALL-L1 gained autonomy in culture concomitant to CD23 expression.
Leukemia 1990;4(5):359-64.
1990: Roland Berger; S J Chen; Z Chen
Philadelphia-positive acute leukemia. Cytogenetic and molecular aspects.
Cancer genetics and cytogenetics 1990;44(2):143-52.
1990: Gérard Schaison; Guy Leverger; Alain BERNHEIM; Marie-Thérèse Daniel; G Flandrin; Roland Berger
Cytogenetic study of 130 childhood acute nonlymphocytic leukemias.
Haematology and blood transfusion 1990;33():157-8.
1990: Roland Berger; MB Le Coniat; D Vecchione; J Derré; S J Chen
Cytogenetic studies of 44 T-cell acute lymphoblastic leukemias.
Cancer genetics and cytogenetics 1990;44(1):69-75.
1990: M F Rousseau-Merck; Micheline Misrahi; M Atger; Hugues Loosfelt; E Milgrom; Roland Berger
Localization of the human luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chromosome 2p21.
Cytogenetics and cell genetics 1990;54(1-2):77-9.
1990: Sylvie Castaigne; Christine Chomienne; Marie-Thérèse Daniel; Roland Berger; J M Miclea; P Ballerini; Laurent Degos
Retinoic acids in the treatment of acute promyelocytic leukemia.
Nouvelle revue française d'hématologie 1990;32(1):36-8.
1990: M F Rousseau-Merck; V Pizon; A Tavitian; Roland Berger
Chromosome mapping of the human RAS-related RAP1A, RAP1B, and RAP2 genes to chromosomes 1p12----p13, 12q14, and 13q34, respectively.
Cytogenetics and cell genetics 1990;53(1):2-4.
1990: P Jonveaux; Roland Berger
Microdissection and microcloning of human banded chromosomes.
Nouvelle revue française d'hématologie 1990;32(6):455-7.
1990: R Miglierina; MB Le Coniat; M Gendron; Roland Berger
Diagnosis of Fanconi's anemia by flow cytometry.
Nouvelle revue française d'hématologie 1990;32(6):391-3.
1989: MB Le Coniat; C Alcaide-Loridan; M Fellous; Roland Berger
Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23-6q24.
Human genetics 1989;84(1):92-4.
1989: M F Rousseau-Merck; Ahmed Zahraoui; Alain BERNHEIM; N Touchot; R Miglierina; A Tavitian; Roland Berger
Chromosome mapping of the human ras-related rab3A gene to 19p13.2.
Genomics 1989;5(4):694-8.
1989: Roland Berger; MB Le Coniat; J Derré; D Vecchione
Secondary nonrandom chromosomal abnormalities of band 13q34 in Burkitt lymphoma-leukemia.
Genes, chromosomes & cancer 1989;1(2):115-8.
1989: S J Chen; Z Chen; M P Font; L d'Auriol; C J Larsen; Roland Berger
Structural alterations of the BCR and ABL genes in Ph1 positive acute leukemias with rearrangements in the BCR gene first intron: further evidence implicating Alu sequences in the chromosome translocation.
Nucleic acids research 1989;17(19):7631-42.
1989: Christine Chomienne; P Ballerini; Nicole Balitrand; M Amar; J F Bernard; P Boivin; Marie-Thérèse Daniel; Roland Berger; Sylvie Castaigne; Laurent Degos
Retinoic acid therapy for promyelocytic leukaemia.
Lancet 1989;2(8665):746-7.
1989: MB Le Coniat; M Souyri; I Vigon; Françoise Wendling; P Tambourin; Roland Berger
The human homolog of the myeloproliferative virus maps to chromosome band 1p34.
Human genetics 1989;83(2):194-6.
1989: Roland Berger
Homozygosity for 8pter----q22 in acute myeloblastic leukemia with t(8;21)(q22;q22).
Genes, chromosomes & cancer 1989;1(1):112-4.
1989: P Antonini; AM Venuat; G Linares; B Caillou; Roland Berger; Claude Parmentier
A translocation (7;10)(q35;q21) in a differentiated papillary carcinoma of the thyroid.
Cancer genetics and cytogenetics 1989;41(1):139-44.
1989: Roland Berger; MB Le Coniat; J Derré; D Vecchione; S J Chen
Chromosomal rearrangement on chromosome 11q14-q21 in T cell acute lymphoblastic leukemia.
Leukemia 1989;3(8):560-2.
1989: P Pellet; Roland Berger; Alain BERNHEIM; Jean-Claude Brouet; A Tsapis
Molecular analysis of a t(9;14)(p11;q32) translocation occurring in a case of human alpha heavy chain disease.
Oncogene 1989;4(5):653-7.
1989: S J Chen; Z Chen; J Hillion; D Grausz; Pascale Loiseau; G Flandrin; Roland Berger
Ph1-positive, bcr-negative acute leukemias: clustering of breakpoints on chromosome 22 in the 3' end of the BCR gene first intron.
Blood 1989;73(5):1312-5.
1989: S J Chen; Z Chen; L d'Auriol; MB Le Coniat; D Grausz; Roland Berger
Ph1+bcr- acute leukemias: implication of Alu sequences in a chromosomal translocation occurring in the new cluster region within the BCR gene.
Oncogene 1989;4(2):195-202.
1989: S J Chen; Z Chen; J Derré; MB Le Coniat; F Valensi; F Sigaux; Roland Berger
Are most secondary acute lymphoblastic leukemias mixed acute leukemias?
Nouvelle revue française d'hématologie 1989;31(1):17-22.
1989: Roland Berger; Alain BERNHEIM
Cytogenetics of acute nonlymphocytic leukemia in relapse.
Nouvelle revue française d'hématologie 1989;31(2):153-4.
1989: Alain BERNHEIM; Roland Berger
Cytogenetics acquisitions in malignant lymphomas.
Nouvelle revue française d'hématologie 1989;31(2):140-1.
1989: D Cherif; C Lavialle; N Modjtahedi; MB Le Coniat; Roland Berger; Olivier Brison
Selection of cells with different chromosomal localizations of the amplified c-myc gene during in vivo and in vitro growth of the breast carcinoma cell line SW 613-S.
Chromosoma 1989;97(4):327-33.
1988: L Baranger; Roland Berger
Translocation t(11;11)(p15;p15) in a case of acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1988;36(2):225-6.
1988: Roland Berger; L Baranger; Alain BERNHEIM; Françoise Valensi; G Flandrin; A Berheimm
Cytogenetics of T-cell malignant lymphoma. Report of 17 cases and review of the chromosomal breakpoints.
Cancer genetics and cytogenetics 1988;36(1):123-30.
1988: S J Chen; Z Chen; J D Grausz; J Hillion; L d'Auriol; G Flandrin; C J Larsen; Roland Berger
Molecular cloning of a 5' segment of the genomic phl gene defines a new breakpoint cluster region (bcr2) in Philadelphia-positive acute leukemias.
Leukemia 1988;2(10):634-41.
1988: Roland Berger; MB Le Coniat; J Derré; D Vecchione; A Pacot; S J Chen; L Baranger; Alain BERNHEIM
Cytogenetic studies on acute nonlymphocytic leukemia in relapse.
Cancer genetics and cytogenetics 1988;34(1):11-8.
1988: D Cherif; MB Le Coniat; H G Suarez; Alain BERNHEIM; Roland Berger
Chromosomal localization of amplified c-myc in a human colon adenocarcinoma cell line with a biotinylated probe.
Cancer genetics and cytogenetics 1988;33(2):245-9.
1988: M F Rousseau-Merck; Alain BERNHEIM; P Chardin; R Miglierina; A Tavitian; Roland Berger
The ras-related ral gene maps to chromosome 7p15-22.
Human genetics 1988;79(2):132-6.
1988: S J Chen; G Flandrin; Marie-Thérèse Daniel; Françoise Valensi; L Baranger; D Grausz; Alain BERNHEIM; Z Chen; François Sigaux; Roland Berger
Philadelphia-positive acute leukemia: lineage promiscuity and inconsistently rearranged breakpoint cluster region.
Leukemia 1988;2(5):261-73.
1988: C J Larsen; D Mathieu-Mahul; O Bernard; J Soudon; Martine Mauchauffé; Alain BERNHEIM; Roland Berger
Two human leukemic T cell lines with a t(8;14)(q24;q11) translocation (KE-37R and SKW3 cells) may have a common origin.
Leukemia 1988;2(4):247-8.
1988: O Bernard; C J Larsen; A Hampe; Martine Mauchauffé; Roland Berger; D Mathieu-Mahul
Molecular mechanisms of a t(8;14)(q24;q11) translocation juxtaposing c-myc and TcR-alpha genes in a T-cell leukaemia: involvement of a V alpha internal heptamer.
Oncogene 1988;2(2):195-200.
1988: M F Rousseau-Merck; D Simon-Chazottes; Monique Arpin; Eric Pringault; Daniel Louvard; Jean-Louis Guénet; Roland Berger
Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1.
Human genetics 1988;78(2):130-3.
1988: Guy Leverger; Alain BERNHEIM; Marie-Thérèse Daniel; G Flandrin; Gérard Schaison; Roland Berger
Cytogenetic study of 130 childhood acute nonlymphocytic leukemias.
Medical and pediatric oncology 1988;16(4):227-32.
1987: M F Rousseau-Merck; Micheline Misrahi; Hugues Loosfelt; E Milgrom; Roland Berger
Localization of the human progesterone receptor gene to chromosome 11q22-q23.
Human genetics 1987;77(3):280-2.
1987: Roland Berger; G Flandrin; Alain BERNHEIM; MB Le Coniat; D Vecchione; A Pacot; J Derré; M T Daniel; F Valensi; F Sigaux
Cytogenetic studies on 519 consecutive de novo acute nonlymphocytic leukemias.
Cancer genetics and cytogenetics 1987;29(1):9-21.
1987: P Cramer; William Vainchenker; Jean-Claude Brouet; Roland Berger
Cytogenetic study of myeloid and erythroid colonies in chronic myeloid leukaemia with stable Ph1 mosaicism.
British journal of haematology 1987;67(1):51-4.
1987: MB Le Coniat; D Vecchione; A Pacot; Alain Bernheim; Roland Berger; P Gardet; C Parmentier
Cytogenetic studies on patients with medullary carcinoma of the thyroid.
Cancer genetics and cytogenetics 1987;25(2):303-7.
1987: Jean-Paul Fermand; François Sigaux; A Tsapis; D Mathieu-Mahul; C Schmitt; Marie-Thérèse Daniel; M Seligmann; Roland Berger; Jean-Claude Brouet
T cell-derived blast crisis in chronic myelocytic leukemia.
Leukemia 1987;1(3):210-2.
1986: Roland Berger; Alain BERNHEIM; MB Le Coniat; D Vecchione; A Pacot; M T Daniel; G Flandrin
Abnormalities of the short arm of chromosome 12 in acute nonlymphocytic leukemia and dysmyelopoietic syndrome.
Cancer genetics and cytogenetics 1986;19(3-4):281-9.
1985: D Mathieu-Mahul; J F Caubet; Alain BERNHEIM; Martine Mauchauffé; E Palmer; Roland Berger; C J Larsen
Molecular cloning of a DNA fragment from human chromosome 14(14q11) involved in T-cell malignancies.
The EMBO journal 1985;4(13A):3427-33.
1985: J F Caubet; D Mathieu-Mahul; Alain BERNHEIM; C J Larsen; Roland Berger
Human proto-oncogene c-mos maps to 8q11.
The EMBO journal 1985;4(9):2245-8.
1985: J F Caubet; D Mathieu-Mahul; Alain BERNHEIM; C J Larsen; Roland Berger
[Rearrangement of the c-myc proto-oncogene locus in a cell line of T-lymphoblastic origin].
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1985;300(5):171-6.
1985: D Mathieu-Mahul; D Q Xu; S Saule; R Lidereau; F Galibert; Roland Berger; Martine Mauchauffé; C J Larsen
An EcoRI restriction fragment length polymorphism (RFLP) in the human c-erb A locus.
Human genetics 1985;71(1):41-4.
1983: Roland Berger; Alain BERNHEIM; MB Le Coniat; D Vecchione; A Pacot; G Flandrin
[Cytogenetics and acute non-lymphoblastic leukemias. Value of short-term cultures].
Nouvelle revue française d'hématologie 1983;25(2):81-6.
1981: Roland Berger; Alain BERNHEIM; Gérard Schaison
Discrepancy between G and R bands. Example of an acute non-lymphocytic leukemia.
Human genetics 1981;59(1):84-6.