Publicacións nas que colabora con María Torres Español (10)

2014

  1. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

    Nature Genetics, Vol. 46, Núm. 8, pp. 826-836

2010

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

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

  2. Identification of a novel mutation in the human PDE6A gene in autosomal recessive retinitis pigmentosa: Homology with the nmf28/nmf28 mice model

    Clinical Genetics

  3. LARGE-SCALE MUTATION SCREENING IN SUDDEN CARDIAC DEATH (SCD)

    ACTA MEDICINAE LEGALIS ET SOCIALIS (UNIV COIMBRA), pp. 211-217

  4. New technologies in the genetic approach to sudden cardiac death in the young

    Forensic Science International, Vol. 203, Núm. 1-3, pp. 15-24

2008

  1. Analyses of variants located in estrogen metabolism genes (ESR1, ESR2, COMT and APOE) and schizophrenia

    Schizophrenia Research, Vol. 100, Núm. 1-3, pp. 308-315

  2. Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction

    Journal of Psychiatric Research, Vol. 42, Núm. 4, pp. 278-288

2006

  1. SUMO4 and MAP3K7IP2 single nucleotide polymorphisms and susceptibility to rheumatoid arthritis

    Journal of Rheumatology, Vol. 33, Núm. 6, pp. 1048-1051

2005

  1. Relative efficiency of the linkage disequilibrium mapping approach in detecting candidate genes for schizophrenia in different european populations

    Genomics, Vol. 86, Núm. 3, pp. 280-286

2003

  1. Typing Y-chromosome single nucleotide polymorphisms with DNA microarray technology

    International Congress Series, Vol. 1239, Núm. C, pp. 21-25