VICTOR
QUESADA FERNANDEZ
Profesor Contratado Doctor
Universitat de Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Universitat de Barcelona (18)
2019
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Association of the POT1 Germline Missense Variant p.I78T with Familial Melanoma
JAMA Dermatology, Vol. 155, Núm. 5, pp. 604-609
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
2015
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A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing
Nature Communications, Vol. 6
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Molecular pathogenesis of CLL and its evolution
International Journal of Hematology, Vol. 101, Núm. 3, pp. 219-228
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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
2014
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Mutations in TLR/MYD88 pathway identify a subset of young chronic lymphocytic leukemia patients with favorable outcome
Blood, Vol. 123, Núm. 24, pp. 3790-3796
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Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia
Genome Research, Vol. 24, Núm. 2, pp. 212-226
2013
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Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia
Leukemia
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Functional analysis of sucrase-isomaltase mutations from chronic lymphocytic leukemia patients
Human Molecular Genetics, Vol. 22, Núm. 11, pp. 2273-2282
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NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome
Leukemia, Vol. 27, Núm. 5, pp. 1100-1106
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POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia
Nature Genetics, Vol. 45, Núm. 5, pp. 526-530
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Recurrent gene mutations in CLL
Advances in Experimental Medicine and Biology, Vol. 792, pp. 87-107
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The genomic landscape of chronic lymphocytic leukemia: Clinical implications
BMC Medicine, Vol. 11, Núm. 1
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
2011
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Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
Nature, Vol. 475, Núm. 7354, pp. 101-105
2010
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International network of cancer genome projects
Nature, Vol. 464, Núm. 7291, pp. 993-998