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Journal Articles

SET-NUP214 is a recurrent γδ lineage-specific fusion transcript associated with corticosteroid/chemotherapy resistance in adult T-ALL

Raouf Ben Abdelali, Anne Roggy, Thibaut Leguay, Agata Cieslak, Aline Renneville, Aurore Touzart, Anne Banos, Edouard Randriamalala, Denis Caillot, Bruno Lioure, Alain Devidas, Hossein Mossafa, Claude Preudhomme, Norbert Ifrah, Hervé Dombret, Elizabeth Macintyre, Vahid Asnafi

Blood (2014) 123 (12): 1860–1863.

https://doi.org/10.1182/blood-2013-08-521518

Published: 2014

Includes: Supplemental data

Journal Articles

Towards a Purely Oncogenetic Risk Classification of Adult T-ALL: a GRAALL Study

Blood (2012) 120 (21): 881.

https://doi.org/10.1182/blood.V120.21.881.881

Published: 2012

Journal Articles

Coexistance of Multiple Myeloma and Myelodysplastic Syndrome or Lymphoid Diseases At Diagnosis: Evidence for Two Clonal and Independent Chromose Abnormalities

Hossein Mossafa, PhD, Sabine Defasque, Jr., MD, Christine Fourcade, Sr., JeanPierre Hurst, Sr., Bertrand Joly

Blood (2011) 118 (21): 5063.

https://doi.org/10.1182/blood.V118.21.5063.5063

Published: 2011

Journal Articles

A Fully Automated Method for Isolating Highly Enriched Population of Multiple Myeloma Plasma Cell From Whole Bone Marrow for Enhanced Sensitivity in Downstream Assays

Hossein Mossafa, PhD, Sabine Defasque, Jr., MD, Hamid Belaouni, Sr., MD, Adrian Arechiga, Sr., PhD

Blood (2011) 118 (21): 5064.

https://doi.org/10.1182/blood.V118.21.5064.5064

Published: 2011

Journal Articles

Cytogenetic Abnormalities In a Cohort of 171 Patients with Waldenström Macroglobulinemia Before Treatment: Clinical and Biological Correlations

Blood (2010) 116 (21): 801.

https://doi.org/10.1182/blood.V116.21.801.801

Published: 2010

Journal Articles

Pangenomic Study In Patients with Persistent Polyclonal Binucleated B-Cell Lymphocytosis (PPBL)

Edouard Cornet, MD, Karine Courel, Jean-François Lesesve, MD, Xavier Troussard, MD, Hossein Mossafa, PhD

Blood (2010) 116 (21): 2405.

https://doi.org/10.1182/blood.V116.21.2405.2405

Published: 2010

Journal Articles

Clinical-grade production of human mesenchymal stromal cells: occurrence of aneuploidy without transformation

Karin Tarte, Julien Gaillard, Jean-Jacques Lataillade, Loic Fouillard, Martine Becker, Hossein Mossafa, Andrei Tchirkov, Hélène Rouard, Catherine Henry, Marie Splingard, Joelle Dulong, Delphine Monnier, Patrick Gourmelon, Norbert-Claude Gorin, Luc Sensebé, on behalf of Société Française de Greffe de Moelle et Thérapie Cellulaire

Blood (2010) 115 (8): 1549–1553.

https://doi.org/10.1182/blood-2009-05-219907

Published: 2010

Includes: Supplemental data

Journal Articles

Deletions of Chromosomes 6q and 13q, and Trisomy 4 Are the Most Common Cytogenetic Abnormalities in Waldenstrom Macroglobulinemia. Preliminary Results of a Multicentric Study.

Blood (2008) 112 (11): 1771.

https://doi.org/10.1182/blood.V112.11.1771.1771

Published: 2008

Journal Articles

High Frequency of the JAK2 V617F Mutation in Patients with Trisomy of Chromosome 9.

Hossein Mossafa, III, PHD, Hamid Belaouni, II, MD, Veronique Saada, PHD, Christine Fourcade, Sr., MD, J. Pierre Hurst, Sr., MD, Driss Chaoui, III, MD

Blood (2008) 112 (11): 1749.

https://doi.org/10.1182/blood.V112.11.1749.1749

Published: 2008

Journal Articles

Gene Expression Profiling of Persistent Polyclonal B-Cell Lymphocytosis Using Whole Genome Microarrays.

Charles H. Lawrie, DPhil, Xavier Troussard, Hossein Mossafa, Chris Hatton

Blood (2006) 108 (11): 4289.

https://doi.org/10.1182/blood.V108.11.4289.4289

Published: 2006

Journal Articles

c-Myc Amplification in Non Hodgkin’s-Lymphomas with Burkitt-Like Features Is Associated with a Poor Prognosis.

Hossein Mossafa, MD, Diane Damotte, MD, Anne Vincenneau, MD, Isabelle Amouroux, MD, Nareth Athken, MD, Arache Djnabian, MD, Roland Jeandel, MD, Eli Khoury, MD, Jean-Michel Martelli, MD, Thierry Samson, MD, Sylvie Tapia, MD, Georges Flandrin, Xavier Troussard

Blood (2004) 104 (11): 3266.

https://doi.org/10.1182/blood.V104.11.3266.3266

Published: 2004

Journal Articles

A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL)

Christiane Charrin, Xavier Thomas, Martine Ffrench, Quoc-Hung Le, Joris Andrieux, Marie-Joelle Mozziconacci, Jean-Luc Laï, Chrystele Bilhou-Nabera, Lucienne Michaux, Alain Bernheim, Christian Bastard, Hossein Mossafa, Christine Perot, Odile Maarek, Claude Boucheix, Véronique Lheritier, André Delannoy, Denis Fière, Nicole Dastugue

Blood (2004) 104 (8): 2444–2451.

https://doi.org/10.1182/blood-2003-04-1299

Published: 2004

NARROW

SET-NUP214 is a recurrent γδ lineage-specific fusion transcript associated with corticosteroid/chemotherapy resistance in adult T-ALL

Towards a Purely Oncogenetic Risk Classification of Adult T-ALL: a GRAALL Study

Coexistance of Multiple Myeloma and Myelodysplastic Syndrome or Lymphoid Diseases At Diagnosis: Evidence for Two Clonal and Independent Chromose Abnormalities

A Fully Automated Method for Isolating Highly Enriched Population of Multiple Myeloma Plasma Cell From Whole Bone Marrow for Enhanced Sensitivity in Downstream Assays

Cytogenetic Abnormalities In a Cohort of 171 Patients with Waldenström Macroglobulinemia Before Treatment: Clinical and Biological Correlations

Pangenomic Study In Patients with Persistent Polyclonal Binucleated B-Cell Lymphocytosis (PPBL)

Clinical-grade production of human mesenchymal stromal cells: occurrence of aneuploidy without transformation

Deletions of Chromosomes 6q and 13q, and Trisomy 4 Are the Most Common Cytogenetic Abnormalities in Waldenstrom Macroglobulinemia. Preliminary Results of a Multicentric Study.

High Frequency of the JAK2 V617F Mutation in Patients with Trisomy of Chromosome 9.

Gene Expression Profiling of Persistent Polyclonal B-Cell Lymphocytosis Using Whole Genome Microarrays.

c-Myc Amplification in Non Hodgkin’s-Lymphomas with Burkitt-Like Features Is Associated with a Poor Prognosis.

A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL)

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American Society of Hematology

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ASH Publications

American Society of Hematology

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