Publicaciones en colaboración con investigadores/as de National Cancer Institute (24)

2024

  1. 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

2023

  1. CanScreen5, a global repository for breast, cervical and colorectal cancer screening programs

    Nature Medicine, Vol. 29, Núm. 5, pp. 1135-1145

2022

  1. A unifying hypothesis for PNMZL and PTFL: morphological variants with a common molecular profile

    Blood Advances, Vol. 6, Núm. 16, pp. 4661-4674

  2. Genomic profiling for clinical decision making in lymphoid neoplasms

    Blood

2021

  1. MAPK and JAK-STAT pathways dysregulation in plasmablastic lymphoma

    Haematologica, Vol. 106, Núm. 10, pp. 2682-2693

2020

  1. Follicular lymphoma t(14;18)-negative is genetically a heterogeneous disease

    Blood Advances, Vol. 4, Núm. 22, pp. 5652-5665

2019

  1. Burkitt-like lymphoma with 11q aberration: A germinal center-derived lymphoma genetically unrelated to Burkitt lymphoma

    Haematologica, Vol. 104, Núm. 9, pp. 1822-1829

  2. CCND2 and CCND3 hijack immunoglobulin light-chain enhancers in cyclin D12 mantle cell lymphoma

    Blood, Vol. 133, Núm. 9, pp. 940-951

2018

  1. CREBBP gene mutations are frequently detected in in situ follicular neoplasia

    Blood

  2. 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

  1. Improved classification of leukemic B-cell lymphoproliferative disorders using a transcriptional and genetic classifier

    Haematologica

  2. 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

  1. Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell Lineage

    Cancer Cell, Vol. 30, Núm. 5, pp. 806-821

  2. 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

2014

  1. A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma

    Blood, Vol. 123, Núm. 8, pp. 1187-1198

2013

  1. CCND2 rearrangements are the most frequent genetic events in cyclin D1 - mantle cell lymphoma

    Blood, Vol. 121, Núm. 8, pp. 1394-1402

  2. Follicular lymphomas in children and young adults: A comparison of the pediatric variant with usual follicular lymphoma

    American Journal of Surgical Pathology, Vol. 37, Núm. 3, pp. 333-343

  3. Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

    Nature Genetics, Vol. 45, Núm. 8, pp. 868-876

  4. 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

  5. MicroRNA expression profiles identify subtypes of mantle cell lymphoma with different clinicobiological characteristics

    Clinical Cancer Research, Vol. 19, Núm. 12, pp. 3121-3129