CARLOS
LOPEZ OTIN
Catedrático de Universidad
Hospital Clinic Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Hospital Clinic Barcelona (26)
2020
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Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma
Leukemia, Vol. 34, Núm. 11, pp. 3007-3018
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The proliferative history shapes the DNA methylome of B-cell tumors and predicts clinical outcome
Nature Cancer, Vol. 1, Núm. 11, pp. 1066-1081
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
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Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomics
Nature Communications, Vol. 10, Núm. 1
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Mutations in the RAS-BRAF-MAPK-ERK pathway define a specific subgroup of patients with adverse clinical features and provide new therapeutic options in chronic lymphocytic leukemia
Haematologica, Vol. 104, Núm. 3, pp. 576-586
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Precise in vivo genome editing via single homology arm donor mediated intron-targeting gene integration for genetic disease correction
Cell Research, Vol. 29, Núm. 10, pp. 804-819
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The U1 spliceosomal RNA is recurrently mutated in multiple cancers
Nature, Vol. 574, Núm. 7780, pp. 712-716
2018
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Altered patterns of global protein synthesis and translational fidelity in RPS15-mutated chronic lymphocytic leukemia
Blood, Vol. 132, Núm. 22, pp. 2375-2388
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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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The mutational landscape of small lymphocytic lymphoma compared to non-early stage chronic lymphocytic leukemia
Leukemia and Lymphoma, Vol. 59, Núm. 10, pp. 2318-2326
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The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia
Nature Medicine, Vol. 24, Núm. 6, pp. 868-880
2016
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
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Mutations in CHD2 cause defective association with active chromatin in chronic lymphocytic leukemia
Blood, Vol. 126, Núm. 2, pp. 195-202
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Non-coding recurrent mutations in chronic lymphocytic leukaemia
Nature, Vol. 526, Núm. 7574, pp. 519-524
2012
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Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia
Nature Genetics, Vol. 44, Núm. 11, pp. 1236-1242
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Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
Nature Genetics, Vol. 44, Núm. 1, pp. 47-52
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Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, Vol. 8, Núm. 4, pp. 445-544
2011
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Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
Nature, Vol. 475, Núm. 7354, pp. 101-105