Ferran
Nadeu
Publications by the researcher in collaboration with Ferran Nadeu (18)
2024
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Large B-cell lymphomas with CCND1 rearrangement have different immunoglobulin gene breakpoints and genomic profile than mantle cell lymphoma
Blood Cancer Journal, Vol. 14, Núm. 1
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MYC-rearranged mature B-cell lymphomas in children and young adults are molecularly Burkitt Lymphoma
Blood Cancer Journal, Vol. 14, Núm. 1
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Testicular large B-cell lymphoma is genetically similar to PCNSL and distinct from nodal DLBCL
HemaSphere, Vol. 8, Núm. 10
2023
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Intravascular Large B-Cell Lymphoma Genomic Profile Is Characterized by Alterations in Genes Regulating NF-κB and Immune Checkpoints
American Journal of Surgical Pathology, Vol. 47, Núm. 2, pp. 202-211
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MALAT1 expression is associated with aggressive behavior in indolent B-cell neoplasms
Scientific Reports, Vol. 13, Núm. 1
2022
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Revised International Prognostic Index and genetic alterations are associated with early failure to R-CHOP in patients with diffuse large B-cell lymphoma
British Journal of Haematology, Vol. 196, Núm. 3, pp. 589-598
2021
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MAPK and JAK-STAT pathways dysregulation in plasmablastic lymphoma
Haematologica, Vol. 106, Núm. 10, pp. 2682-2693
2020
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Cryptic insertions of the immunoglobulin light chain enhancer region near CCND1 in t(11;14)-negative mantle cell lymphoma
Haematologica
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Distinct molecular profile of IRF4-rearranged large B-cell lymphoma
Blood, Vol. 135, Núm. 4, pp. 274-286
2019
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Burkitt-like lymphoma with 11q aberration: A germinal center-derived lymphoma genetically unrelated to Burkitt lymphoma
Haematologica, Vol. 104, Núm. 9, pp. 1822-1829
2018
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A comprehensive flow-cytometry-based immunophenotypic characterization of Burkitt-like lymphoma with 11q aberration
Modern Pathology, Vol. 31, Núm. 5, pp. 732-743
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Clinical impact of the subclonal architecture and mutational complexity in chronic lymphocytic leukemia
Leukemia, Vol. 32, Núm. 3, pp. 645-653
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Integrating genomic alterations in diffuse large B-cell lymphoma identifies new relevant pathways and potential therapeutic targets
Leukemia, Vol. 32, Núm. 3, pp. 675-684
2017
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Mutations of MAP2K1 are frequent in pediatric-type follicular lymphoma and result in ERK pathway activation
Blood, Vol. 130, Núm. 3, pp. 323-327
2016
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Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia
Blood, Vol. 127, Núm. 17, pp. 2122-2130
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Genome-wide analysis of pediatric-type follicular lymphoma reveals low genetic complexity and recurrent alterations of TNFRSF14 gene
Blood, Vol. 128, Núm. 8, pp. 1101-1111
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NOTCH1, TP53, and MAP2K1 mutations in splenic diffuse red pulp small B-cell lymphoma are associated with progressive disease
American Journal of Surgical Pathology, Vol. 40, Núm. 2, pp. 192-201
2013
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Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
Proceedings of the National Academy of Sciences of the United States of America, Vol. 110, Núm. 45, pp. 18250-18255