Publicacións (97) Publicacións nas que participase algún/ha investigador/a

2011

  1. A SNP multiplex for the simultaneous prediction of biogeographic ancestry and pigmentation type

    Forensic Science International: Genetics Supplement Series, Vol. 3, Núm. 1

  2. A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy

    Neuromuscular Disorders, Vol. 21, Núm. 4, pp. 254-262

  3. A novel mutation in the OFD1 (Cxorf5) gene may contribute to oral phenotype in patients with oral-facial-digital syndrome type 1

    Oral Diseases, Vol. 17, Núm. 6, pp. 610-614

  4. A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving azathioprine

    Journal of Gastrointestinal and Liver Diseases, Vol. 20, Núm. 3, pp. 247-253

  5. A putative "hepitype" in the ATM gene associated with chronic lymphocytic leukemia risk

    Genes Chromosomes and Cancer, Vol. 50, Núm. 11, pp. 887-895

  6. A rapid analytical method based on microwave-assisted extraction for the determination of drugs of abuse in vitreous humor

    Analytical and Bioanalytical Chemistry, Vol. 401, Núm. 7, pp. 2177-2186

  7. A statistical framework for the interpretation of mtdna mixtures: Forensic and medical applications

    PLoS ONE, Vol. 6, Núm. 10

  8. A study of East Timor variability using the SNPforID 52-plex SNP panel

    Forensic Science International: Genetics, Vol. 5, Núm. 1

  9. A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22

    British Journal of Cancer, Vol. 105, Núm. 6, pp. 870-875

  10. An update of in Silico tools for the prediction of pathogenesis in Missense variants

    Current Bioinformatics, Vol. 6, Núm. 2, pp. 185-198

  11. Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): Evidence of founder effects

    British Journal of Dermatology, Vol. 165, Núm. 4, pp. 906-911

  12. Analysis of global variability in 15 established and 5 new European Standard Set (ESS) STRs using the CEPH human genome diversity panel

    Forensic Science International: Genetics, Vol. 5, Núm. 3, pp. 155-169

  13. Antioxidant properties of dimethyl sulfoxide and its viability as a solvent in the evaluation of neuroprotective antioxidants

    Journal of Pharmacological and Toxicological Methods, Vol. 63, Núm. 2, pp. 209-215

  14. Análisis de la demanda asistencial en Urgencias pediátricas en un Centro de Salud semiurbano de Galicia

    Revista Espanola de Pediatria, Vol. 67, Núm. 5, pp. 251-256

  15. Análisis de la demanda asistencial en Urgencias pediátricas en un Centro de Salud semiurbano de Galicia

    Revista española de pediatría: clínica e investigación, Vol. 67, Núm. 5, pp. 251-256

  16. Bioanalytical procedures and recent developments in the determination of opiates/opioids in human biological samples

    Analytical and Bioanalytical Chemistry, Vol. 400, Núm. 6, pp. 1665-1690

  17. Bipolar electrothermal vessel sealing system and 5-mm 2 expandable trocar approach in pediatric laparoscopic varicocelectomy: A successful time-effective technical refinement

    Surgical Laparoscopy, Endoscopy and Percutaneous Techniques, Vol. 21, Núm. 5

  18. CAMT in a female with developmental delay, facial malformations and central nervous system anomalies

    Pediatric Blood and Cancer, Vol. 56, Núm. 3, pp. 452-453

  19. CYP2D6 genotyping by liquid chromatography-electrospray ionization mass spectrometry

    Analytical and Bioanalytical Chemistry, Vol. 400, Núm. 8, pp. 2361-2370

  20. Call for participation in the neurogenetics consortium within the Human Variome Project

    Neurogenetics, Vol. 12, Núm. 3, pp. 169-173