Publications by authors named "Stephanie Struski"

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Retrospective analysis of a cohort of 41 B-cell prolymphocytic leukemia patients: impact of genetics and targeted therapies (a FILO study).
Caroline Algrin, Louis Pérol, Elise Chapiro, Lucile Baseggio, Karim Maloum, Stéphanie Struski

Haematologica· June 2023

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The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11.
Marina Lafage-Pochitaloff, Bastien Gerby, Véronique Baccini, Laetitia Largeaud, Vincent Fregona, Stéphanie Struski

Blood Adv· January 2022

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Myeloid malignancies with translocation t(4;12)(q11-13;p13): molecular landscape, clonal hierarchy and clinical outcomes.
Vincent Parinet, Elise Chapiro, Audrey Bidet, Baptiste Gaillard, Odile Maarek, Stéphanie Struski

J Cell Mol Med· October 2021

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Clinical and biological features of B-cell neoplasms with CDK6 translocations: an association with a subgroup of splenic marginal zone lymphomas displaying frequent CD5 expression, prolymphocytic cells, and TP53 abnormalities.
Baptiste Gailllard, Pascale Cornillet-Lefebvre, Quoc-Hung Le, Karim Maloum, Mélanie Pannetier, Stéphanie Struski

Br J Haematol· April 2021

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Cytogenetically masked fusion and concomitant deletion in a case of acute myeloid leukemia with a complex karyotype.
Benoît Ducourneau, Laurène Fenwarth, Nicolas Duployez, Juliette Lambert, Stéphanie Struski

Leuk Lymphoma· July 2020

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Subsequent development of histiocytic sarcoma and follicular lymphoma: cytogenetics and next-generation sequencing analyses provide evidence for transdifferentiation of early common lymphoid precursor-a case report and review of literature.
Sarah Péricart, Charlotte Waysse, Aurore Siegfried, Stephanie Struski, Eric Delabesse

Virchows Arch· April 2020

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Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53.
Elise Chapiro, Elodie Pramil, M'boyba Diop, Damien Roos-Weil, Clémentine Dillard, Stéphanie Struski

Blood· November 2019

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Poor prognosis of chromosome 7 clonal aberrations in Philadelphia-negative metaphases and relevance of potential underlying myelodysplastic features in chronic myeloid leukemia.
Audrey Bidet, Stéphanie Dulucq, Thomas Smol, Alice Marceau-Renaut, Stéphane Morisset, Stéphanie Struski

Haematologica· June 2019

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7q22 deletion in myeloid malignancies: be attentive to the design of the FISH probe.
Stéphanie Struski, Isabelle Luquet

Ann Biol Clin (Paris)· April 2019

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Mutational and cytogenetic analyses of 188 CLL patients with trisomy 12: A retrospective study from the French Innovative Leukemia Organization (FILO) working group.
Damien Roos-Weil, Florence Nguyen-Khac, Sylvie Chevret, Cyrille Touzeau, Clémence Roux, Stéphanie Struski

Genes Chromosomes Cancer· November 2018

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"Double-hit" chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain.
Elise Chapiro, Claude Lesty, Clémentine Gabillaud, Eric Durot, Simon Bouzy, Stéphanie Struski

Am J Hematol· March 2018

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Major prognostic value of complex karyotype in addition to TP53 and IGHV mutational status in first-line chronic lymphocytic leukemia.
Yannick Le Bris, Stéphanie Struski, Romain Guièze, Caroline Rouvellat, Naïs Prade

Hematol Oncol· December 2017

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Cytogenetics in the management of chronic lymphocytic leukemia: an update by the Groupe francophone de cytogénétique hématologique (GFCH).
Florence Nguyen-Khac, Claire Borie, Evelyne Callet-Bauchu, Virginie Eclache, Stéphanie Struski

Ann Biol Clin (Paris)· October 2016

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A novel cryptic insertion of CBFB into MYH11: importance of FISH probe design.
Audrey Bidet, Elodie Laharanne, Stéphanie Struski, Isabelle Luquet, Eric Lippert

Cancer Genet· February 2015

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14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma.
Adrien Cosson, Elise Chapiro, Nabila Belhouachi, Hong-Anh Cung, Boris Keren, Stephanie Struski

Genes Chromosomes Cancer· August 2014

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Chromosomal translocations involving the IGH@ locus in B-cell precursor acute lymphoblastic leukemia: 29 new cases and a review of the literature.
Elise Chapiro, Isabelle Radford-Weiss, Hong-Anh Cung, Nicole Dastugue, Nathalie Nadal, Stephanie Struski

Cancer Genet· May 2013

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Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenström's macroglobulinemia.
Florence Nguyen-Khac, Jerome Lambert, Elise Chapiro, Aurore Grelier, Sarah Mould, Stéphanie Struski

Haematologica· April 2013

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Specific chromosomal IG translocations have different prognoses in chronic lymphocytic leukemia.
Florence Nguyen-Khac, Elise Chapiro, Claude Lesty, Aurore Grelier, Isabelle Luquet, Stéphanie Struski

Am J Blood Res· August 2012

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Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course.
Natalie Put, Katrien Van Roosbroeck, Peter Konings, Peter Meeus, Caroline Brusselmans, Stéphanie Struski

Ann Hematol· June 2012

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Refinement of 1p36 alterations not involving PRDM16 in myeloid and lymphoid malignancies.
Francois P Duhoux, Geneviève Ameye, Virginie Lambot, Christian Herens, Frédéric Lambert, Stéphanie Struski

PLoS One· February 2012

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PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies.
Francois P Duhoux, Geneviève Ameye, Carmen P Montano-Almendras, Khadija Bahloula, Marie J Mozziconacci, Stéphanie Struski

Br J Haematol· January 2012

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Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infants.
Cathy Quelen, Eric Lippert, Stephanie Struski, Cécile Demur, Gwendoline Soler

Blood· May 2011

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Chromosomal abnormalities in transformed Ph-negative myeloproliferative neoplasms are associated to the transformation subtype and independent of JAK2 and the TET2 mutations.
Florence Nguyen-Khac, Claude Lesty, Virginie Eclache, Lucile Couronné, Olivier Kosmider, Stephanie Struski

Genes Chromosomes Cancer· October 2010

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Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogenetique Hematologique study.
Etienne Coyaud, Stephanie Struski, Nais Prade, Julien Familiades, Ruth Eichner

Blood· April 2010

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Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stages.
Elise Chapiro, Nathalie Leporrier, Isabelle Radford-Weiss, Christian Bastard, Hossein Mossafa, Stéphanie Struski

Leuk Res· January 2010

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