Fundación Pública Galega de Medicina Xenómica

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. 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

11. 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

12. 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

13. 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

14. Digging deeper into East African human y chromosome lineages

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

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

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

16. Exfoliative cytology for diagnosing oral cancer

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

17. 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

18. Functional consequences of seven novel mutations in the CYP11B1 gene: Four mutations associated with nonclassic and three mutations causing classic 11β-hydroxylase deficiency

    Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 2, pp. 779-788

19. Genetic profile characterization of 10 X-STRs in four populations of the southeastern region of Brazil

    International Journal of Legal Medicine, Vol. 124, Núm. 5, pp. 427-432

20. Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant

    BMC Genetics, Vol. 11