Publicaciones en colaboración con investigadores/as de Kiel University (24)

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

2019

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

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

2017

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

    Haematologica

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. 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

2015

  1. A B-cell epigenetic signature defines three biologic subgroups of chronic lymphocytic leukemia with clinical impact

    Leukemia, Vol. 29, Núm. 3, pp. 598-605

2014

  1. Clinical utility gene card for: Transient Neonatal Diabetes Mellitus, 6q24-related

    European Journal of Human Genetics, Vol. 22, Núm. 9, pp. 1153

  2. Increasing genomic and epigenomic complexity in the clonal evolution from in situ to manifest t(14;18)-positive follicular lymphoma

    Leukemia, Vol. 28, Núm. 5, pp. 1103-1112

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. High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas

    Genes Chromosomes and Cancer, Vol. 52, Núm. 2, pp. 150-155

  3. 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

  4. Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas

    Haematologica, Vol. 98, Núm. 8, pp. 1237-1241

2012

  1. Molecular genetics of lymphomas in children and young adults

    Hematological Malignancies: In Children, Adolescents and Young Adults (World Scientific Publishing Co.), pp. 153-168

  2. Molecular subsets of mantle cell lymphoma defined by the IGHV mutational status and SOX11 expression have distinct biologic and clinical features

    Cancer Research, Vol. 72, Núm. 20, pp. 5307-5316

  3. Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease

    Leukemia

2011

  1. A unique case of follicular lymphoma provides insights to the clonal evolution from follicular lymphoma in situ to manifest follicular lymphoma

    Blood

  2. Clinical, pathological and genetic features of primary mediastinal large B-cell lymphomas and mediastinal gray zone lymphomas in children

    Haematologica, Vol. 96, Núm. 2, pp. 262-268

  3. Epigenetic activation of SOX11 in Lymphoid Neoplasms by Histone modifications

    PLoS ONE, Vol. 6, Núm. 6

  4. Follicular lymphoma grade 3B

    Best Practice and Research: Clinical Haematology, Vol. 24, Núm. 2, pp. 111-119

  5. Follicular lymphoma grade 3B is a distinct neoplasm according to cytogenetic and immunohistochemical profiles

    Haematologica, Vol. 96, Núm. 9, pp. 1327-1334