Publicaciones en las que colabora con Javier Benítez Ortiz (13)

2018

  1. Whole exome sequencing identifies PLEC, EXO5 and DNAH7 as novel susceptibility genes in testicular cancer

    International Journal of Cancer, Vol. 143, Núm. 8, pp. 1954-1962

2017

  1. Genetic variation in the NEIL2 DNA glycosylase gene is associated with oxidative DNA damage in BRCA2 mutation carriers

    Oncotarget, Vol. 8, Núm. 70, pp. 114626-114636

2016

  1. DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

    Molecular Carcinogenesis, Vol. 55, Núm. 5, pp. 705-716

  2. Molecular insights into the OGG1 gene, a cancer risk modifier in BRCA1 and BRCA2 mutations carriers

    Oncotarget, Vol. 7, Núm. 18, pp. 25815-25825

2015

  1. Classifying early-onset colorectal cancer according to tumor location: New potential subcategories to explore

    American Journal of Cancer Research, Vol. 5, Núm. 7, pp. 2308-2313

  2. Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients

    Breast Cancer Research and Treatment, Vol. 149, Núm. 2, pp. 385-394

  3. Tumor MicroRNA expression profiling identifies circulating MicroRNAs for early breast cancer detection

    Clinical Chemistry, Vol. 61, Núm. 8, pp. 1098-1106

2014

  1. Age at onset should be a major criterion for subclassification of colorectal cancer

    Journal of Molecular Diagnostics, Vol. 16, Núm. 1, pp. 116-126

2013

  1. Short telomeres are frequent in hereditary breast tumors and are associated with high tumor grade

    Breast Cancer Research and Treatment, Vol. 141, Núm. 2, pp. 231-242

2012

  1. Shorter telomere length is associated with increased: Ovarian cancer risk in both familial and sporadic cases

    Journal of Medical Genetics, Vol. 49, Núm. 5, pp. 341-344

2011

  1. Early-onset colorectal cancer is an easy and effective tool to identify retrospectively Lynch syndrome

    Annals of Surgical Oncology, Vol. 18, Núm. 12, pp. 3285-3291

  2. Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

    Nature Genetics

  3. Genetic anticipation is associated with Telomere shortening in hereditary breast cancer

    PLoS Genetics, Vol. 7, Núm. 7