Publikationen, an denen er mitarbeitet María Torres Español (25)

2023

  1. DNA polymorphisms associated with lactase persistence, self-perceived symptoms of lactose intolerance, milk and dairy consumption, and ancestry, in the Uruguayan population

    American Journal of Human Biology, Vol. 35, Núm. 6

2017

  1. A new panel of SNPs to assess thyroid carcinoma risk: A pilot study in a Brazilian admixture population

    BMC Medical Genetics, Vol. 18, Núm. 1

  2. Correction: A european spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics (PLoS ONE (2016) 11:9 (e0162866) DOI: 10.1371/journal.pone.0162866)

    PLoS ONE

2016

  1. A European spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics

    PLoS ONE, Vol. 11, Núm. 9

  2. Development of a methylation marker set for forensic age estimation using analysis of public methylation data and the Agena Bioscience EpiTYPER system

    Forensic Science International: Genetics, Vol. 24, pp. 65-74

2015

  1. Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors

    International Journal of Cancer, Vol. 136, Núm. 6, pp. E685-E696

2014

  1. Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set

    Forensic Science International: Genetics, Vol. 11, Núm. 1, pp. 13-25

  2. Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Markers

    PLoS Genetics, Vol. 10, Núm. 7

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

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

  4. High-throughput genotyping assay for the large-scale genetic characterization of Cryptosporidium parasites from human and bovine samples

    Parasitology, Vol. 141, Núm. 4, pp. 491-500

2013

  1. Association of thromboxane A1 synthase (TBXAS1) gene polymorphism with acute urticaria induced by nonsteroidal anti-inflammatory drugs

    Journal of Allergy and Clinical Immunology, Vol. 132, Núm. 4, pp. 989-991

2012

  1. Development of a panel of genome-wide ancestry informative markers to study admixture throughout the americas

    PLoS Genetics, Vol. 8, Núm. 3

2010

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

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

  2. 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

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

    Clinical Genetics

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

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

  5. 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