Publicaciones en colaboración con investigadores/as de Centro Nacional de Investigaciones Oncológicas (5)

2013

  1. DNA methylation signatures identify biologically distinct thyroid cancer subtypes

    Journal of Clinical Endocrinology and Metabolism, Vol. 98, Núm. 7, pp. 2811-2821

2012

  1. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

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

2010

  1. SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

    The Lancet Oncology, Vol. 11, Núm. 4, pp. 366-372