Publicacións (69) Publicacións nas que participase algún/ha investigador/a

2018

  1. Agaricus bisporus supplementation reduces high-fat diet-induced body weight gain and fatty liver development

    Journal of Physiology and Biochemistry, Vol. 74, Núm. 4, pp. 635-646

  2. A imparable revolución da Medicina Personalizada

    Revista Real Academia Galega de Ciencias, Núm. 37, pp. 24-25

  3. A transcriptome-wide association study among 97,898 women to identify candidate susceptibility genes for epithelial ovarian cancer risk

    Cancer Research, Vol. 78, Núm. 18, pp. 5419-5430

  4. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

    Nature Genetics, Vol. 50, Núm. 7, pp. 968-978

  5. ABCA12 mutations in patients with autosomal recessive congenital ichthyosis: evidence of a founder effect in the Spanish population and phenotype-genotype implications

    Journal of Dermatological Science

  6. Ancestry analysis in rural Brazilian populations of African descent

    Forensic Science International: Genetics, Vol. 36, pp. 160-166

  7. Assessment of genotyping tools applied in genetic susceptibility studies of periodontal disease: A systematic review

    Archives of Oral Biology, Vol. 92, pp. 38-50

  8. Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

    Nature Genetics, Vol. 50, Núm. 7, pp. 928-936

  9. Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1

    American Journal of Kidney Diseases, Vol. 72, Núm. 3, pp. 411-418

  10. BRCA1 and BRCA2 5′ noncoding region variants identified in breast cancer patients alter promoter activity and protein binding

    Human Mutation, Vol. 39, Núm. 12, pp. 2025-2039

  11. Computational tools for splicing defect prediction in breast/ovarian cancer genes: How efficient are they at predicting RNA alterations?

    Frontiers in Genetics, Vol. 9, Núm. SEP

  12. Congenital hyperinsulinism in two siblings with ABCC8 mutation: Same genotype, different phenotypes

    Archives of Endocrinology and Metabolism, Vol. 62, Núm. 5, pp. 560-565

  13. De novo mutations (DNMs) in autism spectrum disorder (ASD): Pathway and network analysis

    Frontiers in Genetics, Vol. 9, Núm. SEP

  14. Determination and diagnostic value of CA9 mRNA in peripheral blood of patients with oral leukoplakia

    Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 33, Núm. 1, pp. 951-955

  15. Development of an isotoxic decision support system integrating genetic markers of toxicity for the implantation of a rectum spacer

    Acta Oncologica, Vol. 57, Núm. 11, pp. 1499-1505

  16. El póster científico como herramienta docente: Experiencia con alumnado de máster

    Experiencias pedagógicas e innovación educativa: aportaciones desde la praxis docente e investigadora (Octaedro), pp. 1742-1750

  17. El valor de la prueba de ADN

    Genética forense, del laboratorio a los tribunales (Díaz de Santos), pp. 445-470

  18. Erratum: Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia (British Journal of Cancer (2017) 117 (1215-1223) DOI: 10.1038/bjc.2017.240)

    British Journal of Cancer

  19. FKBP5 polymorphisms and hypothalamic-pituitary-adrenal axis negative feedback in major depression and obsessive-compulsive disorder

    Journal of Psychiatric Research, Vol. 104, pp. 227-234

  20. Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

    Nature Communications, Vol. 9, Núm. 1