Publicacións (41) Publicacións nas que participase algún/ha investigador/a

2014

  1. A Rb1 promoter variant with reduced activity contributes to osteosarcoma susceptibility in irradiated mice

    Molecular Cancer, Vol. 13, Núm. 1

  2. A collaborative European exercise on mRNA-based body fluid/skin typing and interpretation of DNA and RNA results

    Forensic Science International: Genetics, Vol. 10, Núm. 1, pp. 40-48

  3. A genome-wide study of modern-day Tuscans: Revisiting Herodotus's theory on the origin of the Etruscans

    PLoS ONE, Vol. 9, Núm. 9

  4. A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

    Journal of Medical Genetics, Vol. 51, Núm. 7, pp. 475-478

  5. Alcohol consumption and survival after a breast cancer diagnosis: A literature-based meta-analysis and collaborative analysis of data for 29,239 cases

    Cancer Epidemiology Biomarkers and Prevention, Vol. 23, Núm. 6, pp. 934-945

  6. Brugada syndrome and p.E61X_RANGRF

    Cardiology Journal, Vol. 21, Núm. 2, pp. 121-127

  7. Characterisation of a subpopulation of sperm with massive nuclear damage, as recognised with the sperm chromatin dispersion test

    Andrologia, Vol. 46, Núm. 6, pp. 602-609

  8. Choroidal thickness in diabetic retinopathy: The influence of antiangiogenic therapy

    Retina, Vol. 34, Núm. 6, pp. 1199-1207

  9. Clinical characteristics of reticular pseudodrusen in the fellow eye of patients with unilateral neovascular age-related macular degeneration

    Ophthalmology, Vol. 121, Núm. 9, pp. 1748-1755

  10. Comprehensive analyses of DNA repair pathways, smoking and bladder cancer risk in Los Angeles and Shanghai

    International Journal of Cancer, Vol. 135, Núm. 2, pp. 335-347

  11. Development of a forensic skin colour predictive test

    Forensic Science International: Genetics, Vol. 13, pp. 34-44

  12. Dietary sources of N-nitroso compounds and bladder cancer risk: Findings from the Los Angeles bladder cancer study

    International Journal of Cancer, Vol. 134, Núm. 1, pp. 125-135

  13. Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia

    Clinical Genetics, Vol. 85, Núm. 2, pp. 154-158

  14. Exploring iris colour prediction and ancestry inference in admixed populations of South America

    Forensic Science International: Genetics, Vol. 13, pp. 3-9

  15. Genome-wide DNA methylation analysis of articular chondrocytes reveals a cluster of osteoarthritic patients

    Annals of the Rheumatic Diseases, Vol. 73, Núm. 4, pp. 668-677

  16. Genome-wide association study identifies multiple loci associated with bladder cancer risk

    Human Molecular Genetics, Vol. 23, Núm. 5

  17. Genome-wide interaction study of smoking and bladder cancer risk

    Carcinogenesis, Vol. 35, Núm. 8, pp. 1737-1744

  18. Genética de la muerte súbita inexplicada

    Medicina Clinica, Vol. 142, Núm. 6, pp. 265-269

  19. Global population variability in Qiagen Investigator HDplex STRs

    Forensic Science International: Genetics, Vol. 8, Núm. 1, pp. 36-43

  20. Identification of genetic alterations, as causative genetic defects in long QT syndrome, using next generation sequencing technology

    PLoS ONE, Vol. 9, Núm. 12