Publicaciones en las que colabora con VICTOR QUESADA FERNANDEZ (23)

2022

  1. Author Correction: Comparative and demographic analysis of orang-utan genomes (Nature, (2011), 469, 7331, (529-533), 10.1038/nature09687)

    Nature

2015

  1. A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing

    Nature Communications, Vol. 6

  2. Non-coding recurrent mutations in chronic lymphocytic leukaemia

    Nature, Vol. 526, Núm. 7574, pp. 519-524

2014

  1. 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

  2. The common marmoset genome provides insight into primate biology and evolution

    Nature Genetics, Vol. 46, Núm. 8, pp. 850-857

  3. 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

  1. 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

  2. Frequent somatic mutations in components of the RNA processing machinery in chronic lymphocytic leukemia

    Leukemia

  3. 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

  4. POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia

    Nature Genetics, Vol. 45, Núm. 5, pp. 526-530

  5. Recurrent gene mutations in CLL

    Advances in Experimental Medicine and Biology, Vol. 792, pp. 87-107

  6. The genomic landscape of chronic lymphocytic leukemia: Clinical implications

    BMC Medicine, Vol. 11, Núm. 1

2012

  1. Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia

    Nature Genetics, Vol. 44, Núm. 11, pp. 1236-1242

  2. 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

  1. Comparative and demographic analysis of orang-utan genomes

    Nature, Vol. 469, Núm. 7331, pp. 529-533

  2. 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

  3. Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

    Nature, Vol. 475, Núm. 7354, pp. 101-105

2010

  1. 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

  2. International network of cancer genome projects

    Nature, Vol. 464, Núm. 7291, pp. 993-998

  3. The genome of a songbird

    Nature, Vol. 464, Núm. 7289, pp. 757-762