Publicaciones en las que colabora con Miguel Urioste Azcorra (14)

2022

  1. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients

    Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1

2019

  1. Clinical and molecular comparative study of colorectal cancer based on age-of-onset and tumor location: Two main criteria for subclassifying colorectal cancer

    International Journal of Molecular Sciences, Vol. 20, Núm. 4

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. Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene

    Journal of the National Cancer Institute, Vol. 107, Núm. 5

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

2012

  1. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

    Clinical Cancer Research, Vol. 18, Núm. 10, pp. 2828-2837

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

    PLoS Genetics, Vol. 7, Núm. 7