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Roland Berger

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Molecular Sequence Data

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Publications

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Su Xinying; Della-Valle Véronique; Delabesse Eric; Azgui Zahia; Berger Roland; Merle-Béral Hélène; Bernard Olivier A; Nguyen-Khac Florence
Transcriptional activation of the cardiac homeobox gene CSX1/NKX2-5 in a B-cell chronic lymphoproliferative disorder.
Petit Arnaud; Radford Isabelle; Waill Marie-Christine; Romana Serge; Berger Roland
NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
Luquet I; Laï J L; Barin C; Baranger L; Bilhou-Nabera C; Lippert E; Gervais C; Talmant P; Cornillet-Lefebvre P; Perot C; Nadal N; Mozziconacci M J; Lafage-Pochitaloff M; Eclache V; Mugneret F; Lefebvre C; Herens C; Speleman F; Poirel H; Tigaud I; Cabrol C; Rousselot P; Daliphard S; Imbert M; Garand R; Geneviève F; Berger R; Terre C;
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: Su Xinying; Della-Valle Véronique; Delabesse Eric; Azgui Zahia; Berger Roland; Merle-Béral Hélène; Bernard Olivier A; Nguyen-Khac Florence
Transcriptional activation of the cardiac homeobox gene CSX1/NKX2-5 in a B-cell chronic lymphoproliferative disorder.
Haematologica 2008;93(7):1081-5.
2008: Petit Arnaud; Radford Isabelle; Waill Marie-Christine; Romana Serge; Berger Roland
NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
Cancer genetics and cytogenetics 2008;180(1):43-6.
2008: Luquet I; Laï J L; Barin C; Baranger L; Bilhou-Nabera C; Lippert E; Gervais C; Talmant P; Cornillet-Lefebvre P; Perot C; Nadal N; Mozziconacci M J; Lafage-Pochitaloff M; Eclache V; Mugneret F; Lefebvre C; Herens C; Speleman F; Poirel H; Tigaud I; Cabrol C; Rousselot P; Daliphard S; Imbert M; Garand R; Geneviève F; Berger R; Terre C;
Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity: a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2008;22(1):132-7.
2007: Berger Roland; Bernard Olivier A
Jumping translocations.
Genes, chromosomes & cancer 2007;46(8):717-23.
2007: Lessard M; Hélias C; Struski S; Perrusson N; Uettwiller F; Mozziconacci M-J; Lafage-Pochitaloff M; Dastugue N; Terré C; Brizard F; Cornillet-Lefebvre P; Mugneret F; Barin C; Herry A; Luquet I; Desangles F; Michaux L; Verellen-Dumoulin C; Perrot C; Van den Akker J; Lespinasse J; Eclache V; Berger R;
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: Malinge Sebastien; Ben-Abdelali Raouf; Settegrana Catherine; Radford-Weiss Isabelle; Debre Marianne; Beldjord Kheira; Macintyre Elizabeth A; Villeval Jean-Luc; Vainchenker William; Berger Roland; Bernard Olivier A; Delabesse Eric; Penard-Lacronique Virginie
Novel activating JAK2 mutation in a patient with Down syndrome and B-cell precursor acute lymphoblastic leukemia.
Blood 2007;109(5):2202-4.
2007: Berger R; Bernard O A
Interleukin-2 receptor beta chain locus rearrangement in a T-cell acute lymphoblastic leukemia.
Pathologie-biologie 2007;55(1):56-8.
2007: Berger R
[Human cytogenetics. From 1956 to 2006]
Pathologie-biologie 2007;55(1):1-12.
2006: Su Xin-Ying; Della-Valle Véronique; Andre-Schmutz Isabelle; Lemercier Claudie; Radford-Weiss Isabelle; Ballerini Paola; Lessard Michel; Lafage-Pochitaloff Marina; Mugneret Francine; Berger Roland; Romana Serge P; Bernard Olivier A; Penard-Lacronique Virginie
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: Chapiro Elise; Russell Lisa; Radford-Weiss Isabelle; Bastard Christian; Lessard Michel; Struski Stephanie; Cave Helene; Fert-Ferrer Sandra; Barin Carole; Maarek Odile; Della-Valle Veronique; Strefford Jonathan C; Berger Roland; Harrison Christine J; Bernard Olivier A; Nguyen-Khac Florence
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: Su Xinying; Drabkin Harry; Clappier Emmanuelle; Morgado Ester; Busson Maryvonne; Romana Serge; Soulier Jean; Berger Roland; Bernard Olivier A; Lavau Catherine
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: Jeandidier Eric; Dastugue Nicole; Mugneret Francine; Lafage-Pochitaloff Marina; Mozziconacci Marie-Joëlle; Herens Christian; Michaux Lucienne; Verellen-Dumoulin Christine; Talmant Pascaline; Cornillet-Lefebvre Pascale; Luquet Isabelle; Charrin Christiane; Barin Carole; Collonge-Rame Marie-Agnès; Pérot Christine; Van den Akker Jacqueline; Grégoire Marie-José; Jonveaux P; Baranger Laurence; Eclache-Saudreau Virginie; Pagès Marie-Pierre; Cabrol Christine; Terré Christine; Berger Roland;
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: Romana S P; Radford-Weiss I; Ben Abdelali R; Schluth C; Petit A; Dastugue N; Talmant P; Bilhou-Nabera C; Mugneret F; Lafage-Pochitaloff M; Mozziconacci M-J; Andrieu J; Lai J-L; Terre C; Rack K; Cornillet-Lefebvre P; Luquet I; Nadal N; Nguyen-Khac F; Perot C; Van den Akker J; Fert-Ferrer S; Cabrol C; Charrin C; Tigaud I; Poirel H; Vekemans M; Bernard O A; Berger R;
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(4):696-706.
2006: Berger Roland; Busson Maryvonne; Romana Serge P
A cryptic chromosome 19 abnormality in a patient with Ph-positive acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 2006;165(1):79-80.
2006: Berger R; Busson M; Baranger L; Hélias C; Lessard M; Dastugue N; Speleman F
Loss of the NPM1 gene in myeloid disorders with chromosome 5 rearrangements.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(2):319-21.
2006: Berger Roland; Busson Maryvonne; Dastugue Nicole; Radford-Weiss Isabelle; Michaux Lucienne; Hagemeijer Anne; Quilichini Benoît; Benattar Laurence; Bernard Olivier; Romana Serge P
Acute megakaryoblastic leukemia and loss of the RUNX1 gene.
Cancer genetics and cytogenetics 2006;164(1):71-3.
2005: Lessard M; Struski S; Leymarie V; Flandrin G; Lafage-Pochitaloff M; Mozziconacci M-J; Talmant P; Bastard C; Charrin C; Baranger L; Hélias C; Cornillet-Lefebvre P; Mugneret F; Cabrol C; Pagès M-P; Fert-Ferret D; Nguyen-Khac F; Quilichini B; Barin C; Berger R;
Cytogenetic study of 75 erythroleukemias.
Cancer genetics and cytogenetics 2005;163(2):113-22.
2005: Nguyen-Khac Florence; Davi Frédéric; Receveur Aline; Maloum Karim; Morel Véronique; Le Garff-Tavernier Magali; Ong Jeanne; Berger Roland; Leblond Véronique; Merle-Béral Hélène
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: Ballerini P; Busson M; Fasola S; van den Akker J; Lapillonne H; Romana S P; Marynen P; Bernard O A; Landman-Parker J; Berger R
NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2005;19(3):468-70.
2004: Su Xin Ying; Busson Maryvonne; Della Valle Véronique; Ballerini Paola; Dastugue Nicole; Talmant Pascaline; Ferrando Adolfo A; Baudry-Bluteau Dominique; Romana Serge; Berger Roland; Bernard Olivier A
Various types of rearrangements target TLX3 locus in T-cell acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2004;41(3):243-9.
2004: Receveur Aline; Ong Jeanne; Merlin Laurent; Azgui Zahia; Merle-Béral Hélène; Berger Roland; Nguyen-Khac Florence
Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.
Annales de génétique 2004;47(4):423-7.
2004: Busson Maryvonne; Romana Serge; Nguyen Khac Florence; Bernard Olivier; Berger Roland
Cryptic translocations involving chromosome 20 in polycythemia vera.
Annales de génétique 2004;47(4):365-71.
2004: Valle V Della; Guglielmi L; Busson M; Zwarthoff E C; Berger R; Bernard O A
Expression of the MN1-TEL fusion protein in the human UCSD/AML1 leukemic cell line.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2004;18(9):1558-60.
2003: Ballerini P; Blaise A; Mercher T; Pellegrino B; Perot C; van den Akker J; Gatbois E; Adam M; Douay L; Berger R; Bernard O; Landman-Parker J
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 : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2003;17(6):1193-6.
2003: Li Xiaxin; Leteurtre François; Rocha Vanderson; Guardiola Philippe; Berger Roland; Daniel Marie-Therese; Noguera Maria Helena; Maarek Odile; Roux Gwenaëlle L E; de la Salmonière Pauline; Richard Patrice; Gluckman Eliane
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: Mercher T; Courtois G; Berger R; Bernard O A
[Molecular basis of the t(1;22)(p13;q13) specific for human acute megakaryoblastic leukemia]
Pathologie-biologie 2003;51(1):27-32.
2003: Roumier Christophe; Eclache Virginie; Imbert Michelle; Davi Frederic; MacIntyre Elizabeth; Garand Richard; Talmant Pascaline; Lepelley Pascale; Lai Jean Luc; Casasnovas Olivier; Maynadie Marc; Mugneret Francine; Bilhou-Naberra Chrystele; Valensi Francoise; Radford Isabelle; Mozziconacci Marie Joelle; Arnoulet Christine; Duchayne Eliane; Dastugue Nicole; Cornillet Pascale; Daliphard Sylvie; Garnache Francine; Boudjerra Najiba; Jouault Helene; Fenneteau Odile; Pedron Béatrice; Berger Roland; Flandrin Georges; Fenaux Pierre; Preudhomme Claude;
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.
2002: Busson-Le Coniat Maryvonne; Boucher Nathalie; Blanché Hélène; Thomas Gilles; Berger Roland
Chromosome studies of in vitro senescent lymphocytes: nonrandom trisomy 2.
Annales de génétique 2002;45(4):193-6.
2002: Nguyen Khac Florence; Waill Marie Christine; Romana Serge P; Radford-Weiss Isabelle; Busson Maryvonne; Collonge-Rame Marie Agnès; Ribadeau-Dumas Antoine; Piffaut Marie-Claude; Daniel Marie-Thérèse; Davi Frédéric; Merle-Béral Hélène; Berger Roland; Arock Michel
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: Ballerini Paola; Blaise Annick; Busson-Le Coniat Maryvonne; Su Xin Ying; Zucman-Rossi Jessica; Adam Mircea; van den Akker Jacqueline; Perot Christine; Pellegrino Beatrice; Landman-Parker Judith; Douay Luc; Berger Roland; Bernard Olivier A
HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis.
Blood 2002;100(3):991-7.
2002: Dastugue Nicole; Lafage-Pochitaloff Marina; Pagès Marie-Pierre; Radford Isabelle; Bastard Christian; Talmant Pascaline; Mozziconacci Marie Joelle; Léonard Claude; Bilhou-Nabéra Christelle; Cabrol Christine; Capodano Anne-Marie; Cornillet-Lefebvre Pascale; Lessard Michel; Mugneret Francine; Pérot Christine; Taviaux Sylvie; Fenneteaux Odile; Duchayne Eliane; Berger Roland;
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: Paulien Sylvie; Maarek Odile; Daniel Marie Thérèse; Berger Roland
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: Mercher Thomas; Busson-Le Coniat Maryvonne; Nguyen Khac Florence; Ballerini Paola; Mauchauffé Martine; Bui Hung; Pellegrino Béatrice; Radford Isabelle; Valensi Françoise; Mugneret Francine; Dastugue Nicole; Bernard Olivier A; Berger Roland
Recurrence of OTT-MAL fusion in t(1;22) of infant AML-M7.
Genes, chromosomes & cancer 2002;33(1):22-8.
2001: Busson-Le Coniat M; Nguyen Khac F; Daniel M T; Bernard O A; Berger R
Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2001;32(3):244-9.
2001: Berger R; Busson M; Daniel M T
B-cell acute lymphoblastic leukemia with tandem t(14;14)(q11;q32).
Cancer genetics and cytogenetics 2001;130(1):84-6.
2001: Bernard O A; Busson-LeConiat M; Ballerini P; Mauchauffé M; Della Valle V; Monni R; Nguyen Khac F; Mercher T; Penard-Lacronique V; Pasturaud P; Gressin L; Heilig R; Daniel M T; Lessard M; Berger R
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 : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(10):1495-504.
2001: Mercher T; Coniat M B; Monni R; Mauchauffe M; Nguyen Khac F; Gressin L; Mugneret F; Leblanc T; Dastugue N; Berger R; Bernard O A
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: Monni R; Santos S C; Mauchauffe M; Berger R; Ghysdael J; Gouilleux F; Gisselbrecht S; Bernard O; Penard-Lacronique V
The TEL-Jak2 oncoprotein induces Socs1 expression and altered cytokine response in Ba/F3 cells.
Oncogene 2001;20(7):849-58.
2000: Salmon-Nguyen F; Busson M; Daniel M; Leblanc T; Bernard O A; Berger R
CALM-AF10 fusion gene in leukemias: simple and inversion-associated translocation (10;11).
Cancer genetics and cytogenetics 2000;122(2):137-40.
2000: Poirel H; Lopez R G; Lacronique V; Della Valle V; Mauchauffé M; Berger R; Ghysdael J; Bernard O A
Characterization of a novel ETS gene, TELB, encoding a protein structurally and functionally related to TEL.
Oncogene 2000;19(41):4802-6.
2000: Salomon-Nguyen F; Busson-Le Coniat M; Lafage Pochitaloff M; Mozziconacci J; Berger R; Bernard O A
AML1-MTG16 fusion gene in therapy-related acute leukemia with t(16;21)(q24;q22): two new cases.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(9):1704-5.
2000: Busson Le Coniat M; Brizard F; Smadja N V; Maarek O; Der Sarkissian H; Berger R
Interstitial telomere repeats in translocations of hematopoietic disorders.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(9):1630-3.
2000: Salomon-Nguyen F; Della-Valle V; Mauchauffe M; Busson-Le Coniat M; Ghysdael J; Berger R; Bernard O A
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: Paulien S; Busson-Le Coniat M; Berger R
Acute megakaryocytic leukaemia with acquired polysomy 21 and translocation t(1;21).
Annales de génétique 2000;43(2):99-104.
2000: Lacronique V; Boureux A; Monni R; Dumon S; Mauchauffé M; Mayeux P; Gouilleux F; Berger R; Gisselbrecht S; Ghysdael J; Bernard O A
Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells.
Blood 2000;95(6):2076-83.
2000: Berger R; Coniat M B
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: Busson-Le Coniat M; Salomon-Nguyen F; Dastugue N; Maarek O; Lafage-Pochitaloff M; Mozziconacci M J; Baranger L; Brizard F; Radford I; Jeanpierre M; Bernard O A; Berger R
Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders: rearrangements of DNA satellite II and new recurrent translocations.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1999;13(12):1975-81.
1999: Romana S; Poirel H; Della Valle V; Mauchauffé M; Busson-Le Coniat M; Berger R; Bernard O A
Molecular analysis of chromosomal breakpoints in three examples of chromosomal translocation involving the TEL gene.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1999;13(11):1754-9.
1999: Maarek O; Salabelle A; Le Coniat M B; Daniel M T; Berger R
Chromosome 16 inversion-associated translocation: two new cases.
Cancer genetics and cytogenetics 1999;114(2):126-9.
1999: Terré C; Garcia I; Bastie J N; Mayeur D; Decombe L; Gruyer P; Berger R; Castaigne S
A case of chronic neutrophilic leukemia with deletion (11)(q23).
Cancer genetics and cytogenetics 1999;110(1):70-1.
1999: Busson-Le Coniat M; Salomon-Nguyen F; Hillion J; Bernard O A; Berger R
MLL-AF1q fusion resulting from t(1;11) in acute leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1999;13(2):302-6.
1998: Bernard O A; Hillion J; Le Coniat M; Berger R
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: Poirel H; Lacronique V; Mauchauffé M; Le Coniat M; Raffoux E; Daniel M T; Erickson P; Drabkin H; MacLeod R A; Drexler H G; Ghysdael J; Berger R; Bernard O A
Analysis of TEL proteins in human leukemias.
Oncogene 1998;16(22):2895-903.
1998: Salomon-Nguyen F; Brizard F; Le Coniat M; Radford I; Berger R; Brizard A
Abnormalities of the short arm of chromosome 12 in T cell prolymphocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(6):972-5.
1997: Lacronique V; Boureux A; Valle V D; Poirel H; Quang C T; Mauchauffé M; Berthou C; Lessard M; Berger R; Ghysdael J; Bernard O A
A TEL-JAK2 fusion protein with constitutive kinase activity in human leukemia.
Science (New York, N.Y.) 1997;278(5341):1309-12.
1997: Hillion J; Le Coniat M; Jonveaux P; Berger R; Bernard O A
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: Berger R; Le Coniat M; Lacronique V; Daniel M T; Lessard M; Berthou C; Marynen P; Bernard O
Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: a report including three novel translocations involving the TEL/ETV6 gene.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(9):1400-3.
1997: Le Coniat M; Della Valle V; Marynen P; Berger R
A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(8):1360-3.
1997: Leblanc T; Berger R
Molecular cytogenetics of childhood acute myelogenous leukaemias.
European journal of haematology 1997;59(1):1-13.
1997: Duprez E; Tong J H; Dérré J; Chen S J; Berger R; Chen Z; Lanotte M
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: Poirel H; Oury C; Carron C; Duprez E; Laabi Y; Tsapis A; Romana S P; Mauchauffe M; Le Coniat M; Berger R; Ghysdael J; Bernard O A
The TEL gene products: nuclear phosphoproteins with DNA binding properties.
Oncogene 1997;14(3):349-57.
1996: Bernard O A; Romana S P; Poirel H; Berger R
Molecular cytogenetics of t(12;21) (p13;q22).
Leukemia & lymphoma 1996;23(5-6):459-65.
1996: Leblanc T; Le Coniat M; Flexor M; Baruchel A; Daniel M T; Berger R
An interstitial 11q23 deletion proven to be a rearrangement interrupting the MLL gene in an infant with acute myeloblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(11):1844-6.
1996: Maarek O; Jonveaux P; Le Coniat M; Derré J; Berger R
Faconi anemia and bone marrow clonal chromosome abnormalities.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(11):1700-4.
1996: Jonveaux P; Daniel M T; Martel V; Maarek O; Berger R
Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphoma.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(9):1453-5.
1996: Berger R; Jonveaux P
Clonal chromosome abnormalities in Fanconi anemia.
Hematology and cell therapy 1996;38(4):291-6.
1996: Della Valle V; le Coniat M; Soulard M; Nguyen V C; Berger R; Larsen C J
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: Tigaud I; Charrin C; Berger R; Jonveaux P
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: Berger R; Le Coniat M; Romana S P; Jonveaux P
Secondary acute myeloblastic leukemia with t(16;21) (q24;q22). involving the AML1 gene.
Hematology and cell therapy 1996;38(2):183-6.
1996: Le Coniat M; Choi D S; Maroteaux L; Launay J M; Berger R
The 5-HT2B receptor gene maps to 2q36.3-2q37.1.
Genomics 1996;32(1):172-3.
1996: Jonveaux P; Le Coniat M; Derre J; Flexor M A; Daniel M T; Berger R
Chromosome microdissection in leukemia: a powerful tool for the analysis of complex chromosomal rearrangements.
Genes, chromosomes & cancer 1996;15(1):26-33.
1996: Berger R; Flexor M; Le Coniat M; Larsen C J
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: Romana S P; Le Coniat M; Poirel H; Marynen P; Bernard O; Berger R
Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(1):167-70.
1996: Berger R; Le Coniat M; Flexor M A; Leblanc T
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.
1995: Romana S P; Poirel H; Leconiat M; Flexor M A; Mauchauffé M; Jonveaux P; Macintyre E A; Berger R; Bernard O A
High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia.
Blood 1995;86(11):4263-9.
1995: Le Coniat M; Romana S P; Berger R
Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia.
Genes, chromosomes & cancer 1995;14(3):204-9.
1995: Bernard O A; Romana S P; Schichman S A; Mauchauffé M; Jonveaux P; Berger R
Partial duplication of HRX in acute leukemia with trisomy 11.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(9):1487-90.
1995: Romana S P; Mauchauffé M; Le Coniat M; Chumakov I; Le Paslier D; Berger R; Bernard O A
The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion.
Blood 1995;85(12):3662-70.
1995: Daniel M T; Tigaud I; Flexor M A; Nogueira M E; Berger R; Jonveaux P
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: Poirel H; Jonveaux P; Daniel M T; Berger R
Trisomy 14: a recurring cytogenetic abnormality associated with myeloid disorders.
Leukemia & lymphoma 1995;17(5-6):455-7.
1995: Berger R; Flexor M; Le Coniat M; Derré J; Leblanc T
Translocation (2;3)(p22;q28) is associated with myeloid disorders.
Cancer genetics and cytogenetics 1995;79(2):130-2.
1995: Le Coniat M; Berger R
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: Rousseau-Merck M F; Duro D; Berger R; Thiesen H J
Chromosomal localization of two KOX zinc finger genes on chromosome bands 7q21-q22.
Annales de génétique 1995;38(2):81-4.
1994: Jonveaux P; Hillion J; Bernard O; Le Coniat M; Derré J; Flexor M; Larsen C J; Berger R
Distinct MLL gene rearrangements associated with successive acute monocytic and lymphoblastic leukemias in the same patient.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(12):2224-7.
1994: Leblanc T; Hillion J; Derré J; Le Coniat M; Baruchel A; Daniel M T; Berger R
Translocation t(11;11)(q13;q23) and HRX gene rearrangement associated with therapy-related leukemia in a child previously treated with VP16.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(10):1646-8.
1994: Hébert J; Cayuela J M; Daniel M T; Berger R; Sigaux F
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: Brizard F; Brizard A; Guilhot F; Tanzer J; Berger R
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 : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(6):1005-11.
1994: Jonveaux P; Fenaux P; Berger R
Trisomy 6 as the sole chromosome abnormality in myeloid disorders.
Cancer genetics and cytogenetics 1994;74(2):150-2.
1994: Laabi Y; Gras M P; Brouet J C; Berger R; Larsen C J; Tsapis A
The BCMA gene, preferentially expressed during B lymphoid maturation, is bidirectionally transcribed.
Nucleic acids research 1994;22(7):1147-54.
1994: Cherif D; Bernard O; Paulien S; James M R; Le Paslier D; Berger R
Hunting 11q23 deletions with fluorescence in situ hybridization (FISH).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(4):578-86.
1994: Bernard O A; Mauchauffe M; Mecucci C; Van den Berghe H; Berger R
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: Hébert J; Jonveaux P; d'Agay M F; Berger R
Cytogenetic studies in patients with Richter's syndrome.
Cancer genetics and cytogenetics 1994;73(1):65-8.
1994: Romana S P; Le Coniat M; Berger R
t(12;21): a new recurrent translocation in acute lymphoblastic leukemia.
Genes, chromosomes & cancer 1994;9(3):186-91.
1994: Carbonnel F; Lavergne A; Messing B; Tsapis A; Berger R; Galian A; Nemeth J; Brouet J C; Rambaud J C
Extensive small intestinal T-cell lymphoma of low-grade malignancy associated with a new chromosomal translocation.
Cancer 1994;73(4):1286-91.
1994: Cherif D; Der-Sarkissian H; Berger R
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: Berger R
Translocation t(8;21)(q22;q22): cytogenetics and molecular biology.
Nouvelle revue française d'hématologie 1994;36 Suppl 1():S67-9.
1993: Rousseau-Merck M F; Hillion J; Jonveaux P; Couillin P; Seité P; Thiesen H J; Berger R
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: Séité P; Hillion J; d'Agay M F; Berger R; Larsen C J
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: Bernard O; Groettrup M; Mugneret F; Berger R; Azogui O
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 : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(10):1645-53.
1993: Jonveaux P; Daniel M T; Berger R
5q- anomaly preceding acute myeloblastic leukemia with 53 chromosomes without chromosome 5 abnormality.
Cancer genetics and cytogenetics 1993;70(2):146-7.
1993: Romana S P; Cherif D; Le Coniat M; Derré J; Flexor M A; Berger R
In situ hybridization to interphase nuclei in acute leukemia.
Genes, chromosomes & cancer 1993;8(2):98-103.
1993: Berger R; Le Coniat M; Gendron M C
Fanconi anemia. Chromosome breakage and cell cycle studies.
Cancer genetics and cytogenetics 1993;69(1):13-6.
1993: Le Coniat M; Romana S P; Bernard O; Flexor M A; Hillion J; Cherif D; Berger R
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: Antonini P; Linares G; Gaillard N; Venuat A M; Schlumberger M; Travagli J P; Caillou B; Berger R; Parmentier C
Cytogenetic characterization of a new human papillary thyroid carcinoma permanent cell line (GLAG-66).
Cancer genetics and cytogenetics 1993;67(2):117-22.
1993: Séité P; Hillion J; Leroux D; Berger R; Larsen C J
Common sequence in chromosome translocations affecting B- and T-cell malignancies: a novel recombination site?
Genes, chromosomes & cancer 1993;6(4):253-4.
1993: Fermand J P; Mitjavila M T; Le Couedic J P; Tsapis A; Berger R; Modigliani R; Seligmann M; Brouet J C; Vainchenker W
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: Baurmann H; Cherif D; Berger R
Interphase cytogenetics by fluorescent in situ hybridization (FISH) for characterization of monosomy-7-associated myeloid disorders.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(3):384-91.
1993: Séité P; Hillion J; d'Agay M F; Gaulard P; Cazals D; Badoux F; Berger R; Larsen C J
BCL2 gene activation and protein expression in follicular lymphoma: a report on 64 cases.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(3):410-7.
1993: Larsen C J; Seite P; Hillion J; D'Agay M F; Berger R
Some recent aspects of the molecular biology of human lymphoma.
Nouvelle revue française d'hématologie 1993;35(1):37-40.
1993: Cherif D; Romana S; Der-Sarkissian H; Jones C; Berger R
Chromosome painting in acute monocytic leukemia.
Genes, chromosomes & cancer 1993;6(2):107-12.
1993: Rousseau-Merck M F; Atger M; Loosfelt H; Milgrom E; Berger R
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: Seité P; Leroux D; Hillion J; Monteil M; Berger R; Mathieu-Mahul D; Larsen C J
Molecular analysis of a variant 18;22 translocation in a case of lymphocytic lymphoma.
Genes, chromosomes & cancer 1993;6(1):39-44.
1993: Romana S P; Tachdjian G; Druart L; Cohen D; Berger R; Chérif D
A simple method for prenatal diagnosis of trisomy 21 on uncultured amniocytes.
European journal of human genetics : EJHG 1993;1(3):245-51.
1992: Duprez E; Ruchaud S; Houge G; Martin-Thouvenin V; Valensi F; Kastner P; Berger R; Lanotte M
A retinoid acid 'resistant' t(15;17) acute promyelocytic leukemia cell line: isolation, morphological, immunological, and molecular features.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(12):1281-7.
1992: Berger R; Daniel M T; Jonveaux P; Baruchel A
Relapse as acute monoblastic leukemia (AML-M5) of t(6;9) acute myeloblastic leukemia (AML-M2).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(11):1227-8.
1992: Laâbi Y; Gras M P; Carbonnel F; Brouet J C; Berger R; Larsen C J; Tsapis A
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: Berger R; Le Coniat M; Derré J; Flexor M A; Hillion J
Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia.
Cancer genetics and cytogenetics 1992;63(2):97-9.
1992: Bernard O; Azogui O; Lecointe N; Mugneret F; Berger R; Larsen C J; Mathieu-Mahul D
A third tal-1 promoter is specifically used in human T cell leukemias.
The Journal of experimental medicine 1992;176(4):919-25.
1992: Antonini P; Vénuat A M; Caillou B; Berger R; Schlumberger M; Bernheim A; Parmentier C
Cytogenetic studies on 19 papillary thyroid carcinomas.
Genes, chromosomes & cancer 1992;5(3):206-11.
1992: Rousseau-Merck M F; Tunnacliffe A; Berger R; Ponder B A; Thiesen H J
A cluster of expressed zinc finger protein genes in the pericentromeric region of human chromosome 10.
Genomics 1992;13(3):845-8.
1992: Berger R; Le Coniat M; Derré J; Flexor M A
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: Berger R; Le Coniat M; Derré J
5q- anomaly in acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1992;61(2):201-3.
1992: Jonveaux P; Berger R
Chromosome studies in plasma cell leukemia and multiple myeloma in transformation.
Genes, chromosomes & cancer 1992;4(4):321-5.
1992: Le Coniat M; Soulard M; Della Valle V; Larsen C J; Berger R
Localization of the human gene encoding heterogeneous nuclear RNA ribonucleoprotein G (hnRNP-G) to chromosome 6p12.
Human genetics 1992;88(5):593-5.
1992: Cherif D; Der-Sarkissian H; Derré J; Tokino T; Nakamura Y; Berger R
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: Berger R; Dombret H
New variant translocation in acute myelomonocytic leukemia with bone marrow eosinophilia.
Cancer genetics and cytogenetics 1992;58(2):204-5.
1992: Fenaux P; Preudhomme C; Quiquandon I; Jonveaux P; Laï J L; Vanrumbeke M; Loucheux-Lefebvre M H; Bauters F; Berger R; Kerckaert J P
Mutations of the P53 gene in acute myeloid leukaemia.
British journal of haematology 1992;80(2):178-83.
1992: Fenaux P; Jonveaux P; Quiquandon I; Preudhomme C; Lai J L; Vanrumbeke M; Loucheux-Lefebvre M H; Bauters F; Berger R; Kerckaert J P
Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(1):42-6.
1992: Daniel M T; Jonveaux P; Berger R
Relapse as acute monocytic leukaemia of acute lymphoblastic leukaemia with t(4;11).
Nouvelle revue française d'hématologie 1992;34(4):347-8.
1991: Jonveaux P; Fenaux P; Quiquandon I; Pignon J M; Laï J L; Loucheux-Lefebvre M H; Goossens M; Bauters F; Berger R
Mutations in the p53 gene in myelodysplastic syndromes.
Oncogene 1991;6(12):2243-7.
1991: Fenaux P; Jonveaux P; Quiquandon I; Laï J L; Pignon J M; Loucheux-Lefebvre M H; Bauters F; Berger R; Kerckaert J P
P53 gene mutations in acute myeloid leukemia with 17p monosomy.
Blood 1991;78(7):1652-7.
1991: Berger R; Le Coniat M; Derré J; Vecchione D; Jonveaux P
Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities.
Genes, chromosomes & cancer 1991;3(5):332-7.
1991: Kemper O; Derré J; Cherif D; Engelmann H; Wallach D; Berger R
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: Bernard O; Lecointe N; Jonveaux P; Souyri M; Mauchauffé M; Berger R; Larsen C J; Mathieu-Mahul D
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: Baruchel A; Daniel M T; Schaison G; Berger R
Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation.
Cancer genetics and cytogenetics 1991;54(2):239-43.
1991: Hillion J; Larsen C J; Berger R
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: Derré J; Kemper O; Cherif D; Nophar Y; Berger R; Wallach D
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: Berger R; Le Coniat M; Derré J; Vecchione D
Partial deletion of chromosome 2 in non-Hodgkin lymphoma.
Cancer genetics and cytogenetics 1991;53(1):113-7.
1991: Seite P; Huebner K; Rousseau-Merck M F; Berger R; Thiesen H J
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: Antonini P; Vénuat A M; Linares G; Caillou B; Schlumberger M; Travagli J P; Berger R; Parmentier C
Cytogenetic abnormalities in thyroid adenomas.
Cancer genetics and cytogenetics 1991;52(2):157-64.
1991: Miglierina R; Le Coniat M; Berger R
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: Lanotte M; Martin-Thouvenin V; Najman S; Balerini P; Valensi F; Berger R
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: Rousseau-Merck M F; Zahraoui A; Touchot N; Tavitian A; Berger R
Chromosome assignment of four RAS-related RAB genes.
Human genetics 1991;86(4):350-4.
1991: Hillion J; Flexor M A; Larsen C J; Berger R
Studies of BCR rearrangements in Philadelphia-positive acute leukemia.
Cancer genetics and cytogenetics 1991;51(2):259-67.
1991: Rousseau-Merck M F; Huebner K; Berger R; Thiesen H J
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: Berger R
Chromosomal abnormalities in T-cell malignant lymphoma.
Bulletin du cancer 1991;78(3):283-90.
1991: Jonveaux P; Le Coniat M; Derré J; Vecchione D; Berger R
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: Jonveaux P; Le Coniat M; Grausz D; Berger R
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: Derré J; Cherif D; Le Coniat M; Julier C; Berger R
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: Jonveaux P; Le Coniat M; Derré J; Vecchione D; Berger R
Deletion of (7p13p14) in non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1990;50(1):53-6.
1990: Rousseau-Merck M F; Misrahi M; Loosfelt H; Atger M; Milgrom E; Berger R
Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31.
Genomics 1990;8(2):233-6.
1990: Jonveaux P; Berger R
Chromosomal deletions in non-Hodgkin's malignant lymphomas.
Cancer genetics and cytogenetics 1990;49(2):265-9.
1990: Cherif D; Julier C; Delattre O; Derré J; Lathrop G M; Berger R
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: Cherif D; Berger R
New localizations of VH sequences by in situ hybridization with biotinylated probes.
Genes, chromosomes & cancer 1990;2(2):103-8.
1990: Grausz D; Lanotte M; Valensi F; Hillion J; Chen S J; Chen Z; Morinet F; Berger R
A new Ph1+, bcr cell line derived from a patient with ALL-L1 gained autonomy in culture concomitant to CD23 expression.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(5):359-64.
1990: Berger R; Chen S J; Chen Z
Philadelphia-positive acute leukemia. Cytogenetic and molecular aspects.
Cancer genetics and cytogenetics 1990;44(2):143-52.
1990: Berger R; Le Coniat M; Vecchione D; Derré J; Chen S J
Cytogenetic studies of 44 T-cell acute lymphoblastic leukemias.
Cancer genetics and cytogenetics 1990;44(1):69-75.
1990: Schaison G; Leverger G; Bernheim A; Daniel M T; Flandrin G; Berger R
Cytogenetic study of 130 childhood acute nonlymphocytic leukemias.
Haematology and blood transfusion 1990;33():157-8.
1990: Rousseau-Merck M F; Misrahi M; Atger M; Loosfelt H; Milgrom E; Berger R
Localization of the human luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chromosome 2p21.
Cytogenetics and cell genetics 1990;54(1-2):77-9.
1990: Castaigne S; Chomienne C; Daniel M T; Berger R; Miclea J M; Ballerini P; Degos L
Retinoic acids in the treatment of acute promyelocytic leukemia.
Nouvelle revue française d'hématologie 1990;32(1):36-8.
1990: Rousseau-Merck M F; Pizon V; Tavitian A; Berger R
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: Jonveaux P; Berger R
Microdissection and microcloning of human banded chromosomes.
Nouvelle revue française d'hématologie 1990;32(6):455-7.
1990: Miglierina R; Le Coniat M; Gendron M; Berger R
Diagnosis of Fanconi's anemia by flow cytometry.
Nouvelle revue française d'hématologie 1990;32(6):391-3.
1989: Le Coniat M; Alcaide-Loridan C; Fellous M; Berger R
Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23-6q24.
Human genetics 1989;84(1):92-4.
1989: Rousseau-Merck M F; Zahraoui A; Bernheim A; Touchot N; Miglierina R; Tavitian A; Berger R
Chromosome mapping of the human ras-related rab3A gene to 19p13.2.
Genomics 1989;5(4):694-8.
1989: Berger R; Le Coniat M; Derré J; Vecchione D
Secondary nonrandom chromosomal abnormalities of band 13q34 in Burkitt lymphoma-leukemia.
Genes, chromosomes & cancer 1989;1(2):115-8.
1989: Chen S J; Chen Z; Font M P; d'Auriol L; Larsen C J; Berger R
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: Chomienne C; Ballerini P; Balitrand N; Amar M; Bernard J F; Boivin P; Daniel M T; Berger R; Castaigne S; Degos L
Retinoic acid therapy for promyelocytic leukaemia.
Lancet 1989;2(8665):746-7.
1989: Le Coniat M; Souyri M; Vigon I; Wendling F; Tambourin P; Berger R
The human homolog of the myeloproliferative virus maps to chromosome band 1p34.
Human genetics 1989;83(2):194-6.
1989: Berger R
Homozygosity for 8pter----q22 in acute myeloblastic leukemia with t(8;21)(q22;q22).
Genes, chromosomes & cancer 1989;1(1):112-4.
1989: Antonini P; Venuat A M; Linares G; Caillou B; Berger R; Parmentier C
A translocation (7;10)(q35;q21) in a differentiated papillary carcinoma of the thyroid.
Cancer genetics and cytogenetics 1989;41(1):139-44.
1989: Berger R; Le Coniat M; Derré J; Vecchione D; Chen S J
Chromosomal rearrangement on chromosome 11q14-q21 in T cell acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(8):560-2.
1989: Pellet P; Berger R; Bernheim A; Brouet J C; Tsapis A
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: Chen S J; Chen Z; Hillion J; Grausz D; Loiseau P; Flandrin G; Berger R
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: Chen S J; Chen Z; d'Auriol L; Le Coniat M; Grausz D; Berger R
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: Cherif D; Lavialle C; Modjtahedi N; Le Coniat M; Berger R; Brison O
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.
1989: Chen S J; Chen Z; Derré J; Le Coniat M; Valensi F; Sigaux F; Berger R
Are most secondary acute lymphoblastic leukemias mixed acute leukemias?
Nouvelle revue française d'hématologie 1989;31(1):17-22.
1989: Berger R; Bernheim A
Cytogenetics of acute nonlymphocytic leukemia in relapse.
Nouvelle revue française d'hématologie 1989;31(2):153-4.
1989: Bernheim A; Berger R
Cytogenetics acquisitions in malignant lymphomas.
Nouvelle revue française d'hématologie 1989;31(2):140-1.
1988: Baranger L; Berger R
Translocation t(11;11)(p15;p15) in a case of acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1988;36(2):225-6.
1988: Berger R; Baranger L; Bernheim A; Valensi F; Flandrin G;
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: Chen S J; Chen Z; Grausz J D; Hillion J; d'Auriol L; Flandrin G; Larsen C J; Berger R
Molecular cloning of a 5' segment of the genomic phl gene defines a new breakpoint cluster region (bcr2) in Philadelphia-positive acute leukemias.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(10):634-41.
1988: Berger R; Le Coniat M; Derré J; Vecchione D; Pacot A; Chen S J; Baranger L; Bernheim A
Cytogenetic studies on acute nonlymphocytic leukemia in relapse.
Cancer genetics and cytogenetics 1988;34(1):11-8.
1988: Cherif D; Le Coniat M; Suarez H G; Bernheim A; Berger R
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: Rousseau-Merck M F; Bernheim A; Chardin P; Miglierina R; Tavitian A; Berger R
The ras-related ral gene maps to chromosome 7p15-22.
Human genetics 1988;79(2):132-6.
1988: Chen S J; Flandrin G; Daniel M T; Valensi F; Baranger L; Grausz D; Bernheim A; Chen Z; Sigaux F; Berger R
Philadelphia-positive acute leukemia: lineage promiscuity and inconsistently rearranged breakpoint cluster region.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(5):261-73.
1988: Larsen C J; Mathieu-Mahul D; Bernard O; Soudon J; Mauchauffé M; Bernheim A; Berger R
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 : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(4):247-8.
1988: Bernard O; Larsen C J; Hampe A; Mauchauffé M; Berger R; Mathieu-Mahul D
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: Rousseau-Merck M F; Simon-Chazottes D; Arpin M; Pringault E; Louvard D; Guénet J L; Berger R
Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1.
Human genetics 1988;78(2):130-3.
1988: Leverger G; Bernheim A; Daniel M T; Flandrin G; Schaison G; Berger R
Cytogenetic study of 130 childhood acute nonlymphocytic leukemias.
Medical and pediatric oncology 1988;16(4):227-32.
1987: Rousseau-Merck M F; Misrahi M; Loosfelt H; Milgrom E; Berger R
Localization of the human progesterone receptor gene to chromosome 11q22-q23.
Human genetics 1987;77(3):280-2.
1987: Berger R; Flandrin G; Bernheim A; Le Coniat M; Vecchione D; Pacot A; Derré J; Daniel M T; Valensi F; Sigaux F
Cytogenetic studies on 519 consecutive de novo acute nonlymphocytic leukemias.
Cancer genetics and cytogenetics 1987;29(1):9-21.
1987: Cramer P; Vainchenker W; Brouet J C; Berger R
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: Le Coniat M; Vecchione D; Pacot A; Bernheim A; Berger R; Gardet P; Parmentier C
Cytogenetic studies on patients with medullary carcinoma of the thyroid.
Cancer genetics and cytogenetics 1987;25(2):303-7.
1987: Fermand J P; Sigaux F; Tsapis A; Mathieu-Mahul D; Schmitt C; Daniel M T; Seligmann M; Berger R; Brouet J C
T cell-derived blast crisis in chronic myelocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1987;1(3):210-2.
1986: Berger R; Bernheim A; Le Coniat M; Vecchione D; Pacot A; Daniel M T; Flandrin G
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: Mathieu-Mahul D; Caubet J F; Bernheim A; Mauchauffé M; Palmer E; Berger R; Larsen C J
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: Caubet J F; Mathieu-Mahul D; Bernheim A; Larsen C J; Berger R
Human proto-oncogene c-mos maps to 8q11.
The EMBO journal 1985;4(9):2245-8.
1985: Caubet J F; Mathieu-Mahul D; Bernheim A; Larsen C J; Berger R
[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: Mathieu-Mahul D; Xu D Q; Saule S; Lidereau R; Galibert F; Berger R; Mauchauffé M; Larsen C J
An EcoRI restriction fragment length polymorphism (RFLP) in the human c-erb A locus.
Human genetics 1985;71(1):41-4.
1983: Berger R; Bernheim A; Le Coniat M; Vecchione D; Pacot A; Flandrin G
[Cytogenetics and acute non-lymphoblastic leukemias. Value of short-term cultures]
Nouvelle revue française d'hématologie 1983;25(2):81-6.
1981: Berger R; Bernheim A; Schaison G
Discrepancy between G and R bands. Example of an acute non-lymphocytic leukemia.
Human genetics 1981;59(1):84-6.

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