Publicacións (54) Publicacións nas que participase algún/ha investigador/a

2010

  1. A new approach to long QT syndrome mutation detection by Sequenom MassARRAY® system

    Electrophoresis, Vol. 31, Núm. 10, pp. 1648-1655

  2. A reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groups

    PLoS ONE, Vol. 5, Núm. 5

  3. A strong genetic association between the tumor necrosis factor locus and proliferative vitreoretinopathy: The Retina 4 Project

    Ophthalmology, Vol. 117, Núm. 12

  4. Análisis de genomas completos en genética de poblaciones humanas

    Memorias de la Real Sociedad Española de Historia Natural, Tomo 8, pp. 169-201

  5. Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

    Molecular Psychiatry, Vol. 15, Núm. 10, pp. 1023-1033

  6. Association of growth factors with arterial recanalization and clinical outcome in patients with ischemic stroke treated with tPA

    Journal of Thrombosis and Haemostasis, Vol. 8, Núm. 7, pp. 1567-1574

  7. Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women

    Journal of Psychiatric Research, Vol. 44, Núm. 11, pp. 717-724

  8. Association study of the serotoninergic system in migraine in the Spanish population

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 1, pp. 177-184

  9. BRCA1 5272-1G>A and BRCA2 5374delTATG are founder mutations of high relevance for genetic counselling in breast/ovarian cancer families of Spanish origin

    Clinical Genetics, Vol. 77, Núm. 1, pp. 60-69

  10. Beyond BRCA1 and BRCA2 wild-type breast and/or ovarian cancer families: Germline mutations in TP53 and PTEN

    Clinical Genetics

  11. CADASIL: Comunicación de una familia con una nueva mutación p.G296C en el exón 6 del gen Notch-3

    Revista de Neurologia, Vol. 51, Núm. 12, pp. 729-732

  12. COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer

    British Journal of Cancer, Vol. 102, Núm. 2, pp. 447-454

  13. Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: A two-stage case-control study

    Cancer Epidemiology Biomarkers and Prevention, Vol. 19, Núm. 2, pp. 619-623

  14. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

    Nature Genetics, Vol. 42, Núm. 2, pp. 132-136

  15. Digging deeper into East African human y chromosome lineages

    Human Genetics, Vol. 127, Núm. 5, pp. 603-613

  16. Erratum: COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (British Journal of Cancer 102 (447-454) DOI: 10.1038/sj.bjc.6605338))

    British Journal of Cancer

  17. Erratum: Prevalence of CYP2C9 polymorphisms in the south of Europe (Pharmacogenomics Journal (2009) DOI: 10.1038/tpj.2009.16))

    Pharmacogenomics Journal

  18. Estudios Farmacogenéticos del tratamiento con Antipsicóticos: Estado actual y perspectivas

    Actas Espanolas de Psiquiatria, Vol. 38, Núm. 5, pp. 301-316

  19. Exfoliative cytology for diagnosing oral cancer

    Biotechnic and Histochemistry, Vol. 85, Núm. 3, pp. 177-187

  20. Exploring the binding of Pt drugs to gold nanoparticles for controlled passive release of cisplatin.

    Journal of controlled release : official journal of the Controlled Release Society, Vol. 148, Núm. 1