H. Avet-Loiseau

发表

Ploidy, as detected by fluorescence in situ hybridization, defines different subgroups in multiple myeloma

F. Magrangeas, J. Harousseau, N. Robillard, 2005, Leukemia.

Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia

H. Cavé, B. Grandchamp, F. Méchinaud, 2001, Leukemia.

Amplification of band q22 of chromosome 21, including AML1, in older children with acute lymphoblastic leukemia: an emerging molecular cytogenetic subgroup

J. Soulier, A. Baruchel, V. Najfeld, 2003, Leukemia.

Morphologic and molecular cytogenetics in neuroblastoma

A. Bernheim, M. Leibovitch, H. Avet-Loiseau, 1995, Cancer.

Detection of t(11;14) using interphase molecular cytogenetics in mantle cell lymphoma and atypical chronic lymphocytic leukemia

M. Batzer, R. Bataille, H. Avet-Loiseau, 1998, Genes, chromosomes & cancer.

Comparative genomic hybridization is a powerful tool, complementary to cytogenetics, to identify chromosomal abnormalities in childhood acute lymphoblastic leukaemia

R. Bataille, J. Harousseau, P. Talmant, 1997, British journal of haematology.

Cytogenetically aberrant cells in the stem cell compartment (CD34+lin-) in acute myeloid leukemia.

M. Slovak, C. Willman, D. Head, 1995, Blood.

International Myeloma Working Group molecular classification of multiple myeloma: spotlight review

B. Barlogie, J. Shaughnessy, G. Morgan, 2009, Leukemia.

p16(INK4a) and p15(INK4b) gene methylations in plasma cells from monoclonal gammopathy of undetermined significance.

B. Quesnel, P. Fenaux, G. Guillerm, 2001, Blood.

Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors.

R. Bataille, F. Magrangeas, S. Minvielle, 2001, Blood.

Genetics and Cytogenetics of Multiple Myeloma

Bart Barlogie, Rafael Fonseca, Herve Avet-Loiseau, 2004, Cancer Research.

N-Myc gene amplification is a major prognostic factor in localized neuroblastoma: results of the French NBL 90 study. Neuroblastoma Study Group of the Société Francaise d'Oncologie Pédiatrique.

O. Delattre, D. Frappaz, H. Avet-Loiseau, 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Molecular cytogenetic abnormalities in multiple myeloma and plasma cell leukemia measured using comparative genomic hybridization

M. Pallavicini, J. Feusner, H. Avet-Loiseau, 1997, Genes, chromosomes & cancer.

Reactive plasmacytoses can mimick plasma cell leukemia: Therapeutical implications

R. Bataille, C. Pellat-deceunynck, P. Moreau, 2007, Leukemia & lymphoma.

Cytogenetic, interphase, and multicolor fluorescence in situ hybridization analyses in primary plasma cell leukemia: a study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myélome and the Groupe Français de Cytogénétique Hématologique.

R. Bataille, H. Avet-Loiseau, E. Callet‐Bauchu, 2001, Blood.

Genetic heterogeneity in multiple myeloma

F. Magrangeas, S. Wuillème, L. Lodé, 2005, Leukemia.

Biological and prognostic impact of APOBEC-induced mutations in the spectrum of plasma cell dyscrasias and multiple myeloma cell lines

E. Pinatel, P. Tarpey, N. Bolli, 2017, Leukemia.

High incidence of translocations t(11;14)(q13;q32) and t(4;14)(p16;q32) in patients with plasma cell malignancies.

R. Bataille, Jian-yong Li, T. Facon, 1998, Cancer research.

CD4 (cid:1) , CD56 (cid:1) DC2 acute leukemia is characterized by recurrent clonal chromosomal changes affecting 6 major targets: a study of 21 cases by the Groupe Franc¸ais de Cytoge´ne´tique He´matologique

M. Callanan, V. Eclache, N. Dastugue, 2002 .

Absence of mutations in cereblon (CRBN) and DNA damage-binding protein 1 (DDB1) genes and significance for IMiD therapy

A. Madan, R. Orlowski, H. Avet-Loiseau, 2013, Leukemia.

Additional copies of a 25 Mb chromosomal region originating from 17q23.1‐17qter are present in 90% of high‐grade neuroblastomas

D. Le Paslier, A. Bernheim, G. Danglot, 1996, Genes, chromosomes & cancer.

Amplification of AML1 gene is present in childhood acute lymphoblastic leukemia but not in adult, and is not associated with AML1 gene mutation

C. Preudhomme, C. Roumier, N. Milpied, 2002, Leukemia.

Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization.

R. Bataille, Jian-yong Li, A. Moreau, 1999, The American journal of pathology.

CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS Monosomy 13 Is Associated With the Transition of Monoclonal Gammopathy of Undetermined Signiﬁcance to Multiple Myeloma

R. Bataille, B. Grosbois, Jian-yong Li, 2022 .

Large deletions 5′ to the ETO breakpoint are recurrent events in patients with t(8;21) acute myeloid leukemia

R. Bataille, N. Dastugue, P. Talmant, 2002, Leukemia.

14q32 chromosomal translocations: a hallmark of plasma cell dyscrasias?

F. Magrangeas, S. Minvielle, H. Avet-Loiseau, 2000, The hematology journal : the official journal of the European Haematology Association.

Is t(14;18)(q32;q21) a constant finding in follicular lymphoma? An interphase FISH study on 63 patients

A. Moreau, A. Moreau, N. Milpied, 2003, Leukemia.

High incidence of N and K‐Ras activating mutations in multiple myeloma and primary plasma cell leukemia at diagnosis

D Puthier, R. Bataille, M. Devilder, 2001, Human mutation.

14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesis of multiple myeloma. Intergroupe Francophone du Myélome.

R. Bataille, B. Grosbois, H. Avet-Loiseau, 1999, Cancer research.

Fluorescence in situ hybridization on peripheral-blood specimens is a reliable method to evaluate cytogenetic response in chronic myeloid leukemia.

R. Bataille, P. Moreau, J. Harousseau, 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

CD33 is expressed on plasma cells of a significant number of myeloma patients, and may represent a therapeutic target

F. Magrangeas, N. Robillard, S. Wuillème, 2005, Leukemia.

Finding new human minisatellite sequences in the vicinity of long CA-rich sequences.

E. Petit, Y. Hauck, G. Vergnaud, 1999, Genome research.

Gene amplifications detected by fluorescence in situ hybridization in pure intraductal breast carcinomas: Relation to morphology, cell proliferation and expression of breast cancer‐related genes

B. Dutrillaux, H. Avet-Loiseau, P. Fumoleau, 2000, International journal of cancer.

Comparative genomic hybridization detects genomic abnormalities in 80% of follicular lymphomas

R. Bataille, H. Avet-Loiseau, A. Moreau, 1997, British journal of haematology.