Author

Julien Mozziconacci

Observed names: J Mozziconacci, M J Mozziconacci, M MOZZICONACCI, M-J Mozziconacci, M. J. Mozziconacci, M. Mozziconacci, M.-J. Mozziconacci, M.J. Mozziconacci, M.‐J. MOZZICONACCI, MARIE-JOELLE MOZZICONACCI, MJ MOZZICONACCI, MJ Mozziconacci, Marie-Joelle Garraud-Mozziconacci, Marie-Joelle Moziconacci, Marie-Joelle Moziconnacci, Marie-Joelle Mozzicconacci, Marie-Joelle Mozziconacci, Marie-Joelle. Mozziconacci, Marie-Joëlle Mozziconacci, Marie-Joëlle Mozziconacci, Marie-Jo�lle Mozziconacci, Marie-joelle Mozziconacci, Marie‐Joelle Mozicconacci, Marie‐Joelle Mozziconacci, Marie‐Joëlle Mozziconacci, Marie‐Jöelle Mozziconacci, Mozziconacci Marie-Joelle, Mozziconacci Mj, Mozziconacci, Marie-Joëlle, marie‐joelle mozziconnaci

Institutions: Centre National de la Recherche Scientifique, Inserm, Sorbonne Université, Muséum national d'Histoire naturelle, Institut Paoli-Calmettes, Structure et Instabilité des Génomes

Observed institutions: Centre National de la Recherche Scientifique, Inserm, Aix-Marseille Université, Centre Hospitalier Universitaire de Toulouse, Sorbonne Université, Centre Hospitalier Universitaire de Besançon, Institut universitaire du cancer de Toulouse Oncopole, Centre Hospitalier Universitaire d'Angers, Muséum national d'Histoire naturelle, Centre de Recherche en Cancérologie de Marseille, Institut Paoli-Calmettes, Hôpital d'Hautepierre, Hôpital de la Timone, Structure et Instabilité des Génomes, University of Genoa

ORCID: 0000-0001-5652-0302

Observed ORCID: 0000-0001-5652-0302

OpenAlex ID: A5011027517

Mutations of polycomb‐associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia

2009 · Véronique Gelsi‐Boyer, Virginie Trouplin, et al. · British Journal of Haematology · 589

Defective expression and function of natural killer cell–triggering receptors in patients with acute myeloid leukemia

2002 · Régis T. Costello, Simona Sivori, et al. · Blood · 525

Mutations of ASXL1 gene in myeloproliferative neoplasms

2009 · N Carbuccia, A Murati, et al. · Leukemia · 338

Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party. Groupe Français de Cytogénétique Hématologique, Groupe de Français d'Hematologie Cellulaire, UK Cancer Cytogenetics Group and BIOMED 1 European Community-Concerted Action "Molecular Cytogenetic Diagnosis in Haematological Malignancies".

2000 · D Grimwade, A Biondi, et al. · PubMed · 325

Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases

2012 · Véronique Gelsi-Boyer, Mandy Brecqueville, et al. · Journal of Hematology & Oncology · 291

Comprehensive Profiling of 8p11-12 Amplification in Breast Cancer

2005 · Véronique Gelsi-Boyer, Béatrice Orsetti, et al. · Molecular Cancer Research · 236

ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia

2010 · Véronique Gelsi‐Boyer, Virginie Trouplin, et al. · British Journal of Haematology · 225

A new morphologic classification system for acute promyelocytic leukemia distinguishes cases with underlying PLZF/RARA gene rearrangements.

2000 · D Sainty, V Liso, et al. · PubMed · 189

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder

2009 · Claude Preudhomme, Aline Renneville, et al. · Blood · 181

Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias

2010 · Julien Rocquain, Nadine Carbuccia, et al. · BMC Cancer · 180

Comorbidity is an independent predictor of complete remission in elderly patients receiving induction chemotherapy for acute myeloid leukemia

2007 · Anne Etienne, Benjamin Esterni, et al. · Cancer · 171

Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms

2012 · Mandy Brecqueville, Jérôme Rey, et al. · Genes Chromosomes and Cancer · 168

Prognostic value of TP53 gene mutations in myelodysplastic syndromes and acute myeloid leukemia treated with azacitidine

2014 · Cecile Bally, Lionel Adès, et al. · Leukemia Research · 166

Myeloid malignancies: mutations, models and management

2012 · Anne Murati, Mandy Brecqueville, et al. · BMC Cancer · 163

Gene expression profiling identifies molecular subgroups among nodal peripheral T-cell lymphomas

2005 · B Ballester, O Ramuz, et al. · Oncogene · 152

Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenstrom's macroglobulinemia

2012 · F. Nguyen-Khac, J. Lambert, et al. · Haematologica · 151

Distinct and Complementary Information Provided by Use of Tissue and DNA Microarrays in the Study of Breast Tumor Markers

2002 · Christophe Ginestier, Emmanuelle Charafe-Jauffret, et al. · American Journal Of Pathology · 143

Report of 34 patients with clonal chromosomal abnormalities in Philadelphia-negative cells during imatinib treatment of Philadelphia-positive chronic myeloid leukemia

2004 · C Terre, V Eclache, et al. · Leukemia · 140

NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique

2006 · S P Romana, I Radford-Weiss, et al. · Leukemia · 137

Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1genes

2008 · Véronique Gelsi-Boyer, Virginie Trouplin, et al. · BMC Cancer · 135

Leukemia : Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K

2008 · Isabelle Luquet, Jia‐Qi Lai, et al. · 129

Differential association of calreticulin type 1 and type 2 mutations with myelofibrosis and essential thrombocytemia: relevance for disease evolution

2014 · X Cabagnols, J P Defour, et al. · Leukemia · 128

Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogénétique Hématologique study

2010 · Etienne Coyaud, Stephanie Struski, et al. · Blood · 125

Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias

2009 · N Carbuccia, V Trouplin, et al. · Leukemia · 121

Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia

2015 · I Antony-Debré, N Duployez, et al. · Leukemia · 108

Works count: 216

Citation count: 9,184

H-index: 53

I10-index: 121