H. Avet‐Loiseau

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Reactive plasmacytoses can mimick plasma cell leukemia: Therapeutical implications

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

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.

Genetic heterogeneity in multiple myeloma

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

Detection of nonrandom chromosomal changes in multiple myeloma by comparative genomic hybridization.

H. Avet‐Loiseau, R. Bataille, 1998, Blood.

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.

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.

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.

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

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

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.

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.

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.

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.

[Vertebral involvement and fetal alcohol syndrome].

B. Branger, N. Passuti, G. Picherot, 1991, Pediatrie.

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 .

13q14 deletions are not primary events in B-cell chronic lymphocytic leukemia: a study of 100 patients using fluorescence in situ hybridization.

R. Bataille, M. Devilder, J. Moisan, 1996, Clinical cancer research : an official journal of the American Association for Cancer Research.

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.

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.

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.

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.

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.

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.

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

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

Morphologic and molecular cytogenetics in neuroblastoma

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

Deletion of 5q31 is observed in megakaryocytic cells in patients with myelodysplastic syndromes and a del(5q), including the 5q‐ syndrome

R. Bataille, P. Talmant, R. Garand, 2000, Genes, chromosomes & cancer.

IgG‐secreting lymphoplasmacytoid leukaemia: a B‐cell disorder with extensively mutated VH genes undergoing Ig isotype‐switching frequently associated with trisomy 12

R. Bataille, A. Moreau, N. Robillard, 2000, British journal of haematology.

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.

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.

Mature B-cell lymphoblastic leukemia with MLL rearrangement: an uncommon and distinct subset of childhood acute leukemia

N. Dastugue, J. Harousseau, P. Talmant, 2008, Leukemia.

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

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

Clonal Hematologic Disorders in Down Syndrome A Review

J. Harousseau, H. Avet‐Loiseau, F. Méchinaud, 1995, Journal of pediatric hematology/oncology.

Genetic alterations in early‐onset invasive breast carcinomas: Correlation of c‐erbB‐2 amplification detected by fluorescence In situ hybridization with p53 accumulation and tumor phenotype

P. Fumoleau, M. Heymann, M. Fiche, 1999, 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.

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.

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.

Genetics and Cytogenetics of Multiple Myeloma

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

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

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

in minor cell populations during the course of

I. Martincorena, N. Munshi, H. Avet‐Loiseau, 2023 .

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

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

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.