Publications in collaboration with researchers from University of Chicago (29)

2020

  1. Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis

    American Journal of Respiratory and Critical Care Medicine, Vol. 201, Núm. 5, pp. 564-574

2018

  1. Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

    Nature Genetics

  2. Erratum to: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (Nature Genetics, (2018), 50, 8, (1072-1080), 10.1038/s41588-018-0157-1)

    Nature Genetics

2017

  1. Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study

    The Lancet Respiratory Medicine, Vol. 5, Núm. 11, pp. 869-880

  2. Association between telomere length and risk of cancer and non-neoplastic diseases a mendelian randomization study

    JAMA Oncology, Vol. 3, Núm. 5, pp. 636-651

2016

  1. Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene

    Journal of Allergy and Clinical Immunology, Vol. 137, Núm. 3, pp. 964-966

2015

  1. Lung transcriptomics during protective ventilatory support in sepsis-induced acute lung injury

    PLoS ONE, Vol. 10, Núm. 7

  2. Fine mapping of the myosin light chain kinase (MYLK) gene replicates the association with asthma in populations of Spanish descent

    Journal of Allergy and Clinical Immunology, Vol. 136, Núm. 4, pp. 1116-1118.e9

2014

  1. The NAMPT promoter is regulated by mechanical stress, signal transducer and activator of transcription 5, and acute respiratory distress syndrome-associated genetic variants

    American Journal of Respiratory Cell and Molecular Biology, Vol. 51, Núm. 5, pp. 660-667

  2. GADD45a promoter regulation by a functional genetic variant associated with acute lung injury

    PLoS ONE, Vol. 9, Núm. 6

2013

  1. Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: A genome-wide association study

    The Lancet Respiratory Medicine, Vol. 1, Núm. 4, pp. 309-317

  2. Functional promoter variants in sphingosine 1-phosphate receptor 3 associate with susceptibility to sepsis-associated acute respiratory distress syndrome

    American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 305, Núm. 7

2012

  1. An intronic MYLK variant associated with inflammatory lung disease regulates promoter activity of the smooth muscle myosin light chain kinase isoform

    Journal of Molecular Medicine, Vol. 90, Núm. 3, pp. 299-308

  2. African ancestry is associated with asthma risk in African Americans

    PLoS ONE, Vol. 7, Núm. 1

2011

  1. Type 2 deiodinase and host responses of sepsis and acute lung injury

    American Journal of Respiratory Cell and Molecular Biology, Vol. 45, Núm. 6, pp. 1203-1211

  2. Interleukin-1 receptor-associated kinase 3 gene associates with susceptibility to acute lung injury

    American Journal of Respiratory Cell and Molecular Biology, Vol. 45, Núm. 4, pp. 740-745

2010

  1. Functional variants of the sphingosine-1-phosphate receptor 1 gene associate with asthma susceptibility

    Journal of Allergy and Clinical Immunology, Vol. 126, Núm. 2

  2. An alternative method of acute lung injury classification for use in observational studies

    Chest, Vol. 138, Núm. 5, pp. 1054-1061

2009

  1. A common haplotype of the LBP gene predisposes to severe sepsis

    Critical Care Medicine, Vol. 37, Núm. 10, pp. 2759-2766

2008

  1. A common cortactin gene variation confers differential susceptibility to severe asthma

    Genetic Epidemiology, Vol. 32, Núm. 8, pp. 757-766