Bioaraba
Centro de investigación
Kiel University
Kiel, AlemaniaPublicaciones en colaboración con investigadores/as de Kiel University (26)
2022
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A unifying hypothesis for PNMZL and PTFL: morphological variants with a common molecular profile
Blood Advances, Vol. 6, Núm. 16, pp. 4661-4674
2019
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CCND2 and CCND3 hijack immunoglobulin light-chain enhancers in cyclin D12 mantle cell lymphoma
Blood, Vol. 133, Núm. 9, pp. 940-951
2017
2016
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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
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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
2015
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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
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A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
Forensic Science International: Genetics, Vol. 12, pp. 12-23
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Clinical utility gene card for: Transient Neonatal Diabetes Mellitus, 6q24-related
European Journal of Human Genetics, Vol. 22, Núm. 9, pp. 1153
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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
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CCND2 rearrangements are the most frequent genetic events in cyclin D1 - mantle cell lymphoma
Blood, Vol. 121, Núm. 8, pp. 1394-1402
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Continent-Wide Decoupling of Y-Chromosomal Genetic Variation from Language and Geography in Native South Americans
PLoS Genetics, Vol. 9, Núm. 4
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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
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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
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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
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Molecular genetics of lymphomas in children and young adults
Hematological Malignancies: In Children, Adolescents and Young Adults (World Scientific Publishing Co.), pp. 153-168
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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
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Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease
Leukemia
2011
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A unique case of follicular lymphoma provides insights to the clonal evolution from follicular lymphoma in situ to manifest follicular lymphoma
Blood
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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
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Epigenetic activation of SOX11 in Lymphoid Neoplasms by Histone modifications
PLoS ONE, Vol. 6, Núm. 6