VICTOR
QUESADA FERNANDEZ
Profesor Contratado Doctor
XOSE ANTON
SUAREZ PUENTE
Catedrático de Universidad
Publicaciones en las que colabora con XOSE ANTON SUAREZ PUENTE (23)
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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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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The common marmoset genome provides insight into primate biology and evolution
Nature Genetics, Vol. 46, Núm. 8, pp. 850-857
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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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Biología molecular, evolución y enfermedad en la Era Genómica
F. Javier Fortea Pérez: Universitatis Ovetensis Magister. Estudios en homenaje (Ediciones de la Universidad de Oviedo), pp. 565-574
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Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia
Leukemia
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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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Comparative and demographic analysis of orang-utan genomes
Nature, Vol. 469, Núm. 7331, pp. 529-533
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Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome
American Journal of Human Genetics, Vol. 88, Núm. 5, pp. 650-656
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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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Comparative genomic analysis of the zebra finch degradome provides new insights into evolution of proteases in birds and mammals
BMC Genomics, Vol. 11, Núm. 1
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International network of cancer genome projects
Nature, Vol. 464, Núm. 7291, pp. 993-998
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The genome of a songbird
Nature, Vol. 464, Núm. 7289, pp. 757-762