Publicaciones en colaboración con investigadores/as de Hospital de Gran Canaria Dr. Negrin (33)

2023

  1. Admixture mapping of severe asthma exacerbations in Hispanic/Latino children and youth

    Thorax, Vol. 78, Núm. 3, pp. 233-241

  2. Alpha-1 antitrypsin deficiency and Pi*S and Pi*Z SERPINA1 variants are associated with asthma exacerbations

    Pulmonology

  3. Epigenome-Wide Association Studies of the Fractional Exhaled Nitric Oxide and Bronchodilator Drug Response in Moderate-to-Severe Pediatric Asthma

    Biomedicines, Vol. 11, Núm. 3

  4. Epigenomic response to albuterol treatment in asthma-relevant airway epithelial cells

    Clinical Epigenetics, Vol. 15, Núm. 1

  5. Human genetics influences microbiome composition involved in asthma exacerbations despite inhaled corticosteroid treatment

    Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 3, pp. 799-806.e6

  6. Multi-omic approach associates blood methylome with bronchodilator drug response in pediatric asthma

    Journal of Allergy and Clinical Immunology, Vol. 151, Núm. 6, pp. 1503-1512

  7. Novel insights into the whole-blood DNA methylome of asthma in ethnically diverse children and youth

    The European respiratory journal, Vol. 62, Núm. 6

2022

  1. Multi-ancestry genome-wide association study of asthma exacerbations

    Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, Vol. 33, Núm. 6, pp. e13802

2021

  1. A deoxyribonuclease 1–like 3 genetic variant associates with asthma exacerbations

    Journal of Allergy and Clinical Immunology, Vol. 147, Núm. 3, pp. 1095-1097.e10

  2. Combined analysis of transcriptomic and genetic data for the identification of loci involved in glucocorticosteroid response in asthma

    Allergy: European Journal of Allergy and Clinical Immunology, Vol. 76, Núm. 4, pp. 1238-1243

  3. Genome-wide association study reveals a novel locus for asthma with severe exacerbations in diverse populations

    Pediatric Allergy and Immunology, Vol. 32, Núm. 1, pp. 106-115

  4. Identification of robo2 as a potential locus associated with inhaled corticosteroid response in childhood asthma

    Journal of Personalized Medicine, Vol. 11, Núm. 8

  5. Role of sex on the genetic susceptibility to childhood asthma in latinos and african americans

    Journal of Personalized Medicine, Vol. 11, Núm. 11

2020

  1. Admixture mapping of asthma in southwestern Europeans with North African ancestry influences

    American journal of physiology. Lung cellular and molecular physiology, Vol. 318, Núm. 5, pp. L965-L975

  2. Precision medicine in childhood asthma: Omic studies of treatment response

    International Journal of Molecular Sciences, Vol. 21, Núm. 8

  3. The genomics and metagenomics of asthma severity (GEMAS) study: Rationale and design

    Journal of Personalized Medicine, Vol. 10, Núm. 3, pp. 1-16

2017

  1. A pathway-based association study reveals variants from Wnt signalling genes contributing to asthma susceptibility

    Clinical and Experimental Allergy, Vol. 47, Núm. 5, pp. 618-626

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. Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis

    Critical Care, Vol. 19, Núm. 1

  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