Publicaciones en colaboración con investigadores/as de University of Liverpool (41)

2023

  1. Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia (Nature Genetics, (2022), 54, 11, (1621-1629), 10.1038/s41588-022-01192-y)

    Nature Genetics

  2. GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

    Nature, Vol. 617, Núm. 7962, pp. 764-768

2022

  1. Discovery of 42 genome-wide significant loci associated with dyslexia

    Nature Genetics, Vol. 54, Núm. 11, pp. 1621-1629

  2. 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. ADRB2 haplotypes and asthma exacerbations in children and young adults: An individual participant data meta-analysis

    Clinical and Experimental Allergy, Vol. 51, Núm. 9, pp. 1157-1171

  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 studies of exacerbations in children using long-acting beta2-agonists

    Pediatric Allergy and Immunology, Vol. 32, Núm. 6, pp. 1197-1207

  4. Genome-wide association study of asthma exacerbations despite inhaled corticosteroid use

    European Respiratory Journal, Vol. 57, Núm. 5

  5. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

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

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

2020

  1. Correction: Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritization (The Pharmacogenomics Journal, (2020), 20, 5, (621-628), 10.1038/s41397-019-0140-y)

    Pharmacogenomics Journal

  2. 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

  3. Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritisation

    Pharmacogenomics Journal, Vol. 20, Núm. 5, pp. 621-628

2019

  1. Genome-wide association study of inhaled corticosteroid response in admixed children with asthma

    Clinical and Experimental Allergy, Vol. 49, Núm. 6, pp. 789-798

  2. The p97–Ataxin 3 complex regulates homeostasis of the DNA damage response E3 ubiquitin ligase RNF8

    EMBO Journal, Vol. 38, Núm. 21

2018

  1. 17q21 variant increases the risk of exacerbations in asthmatic children despite inhaled corticosteroids use

    Allergy: European Journal of Allergy and Clinical Immunology

  2. Variants in genes coding for glutathione S-transferases and asthma outcomes in children

    Pharmacogenomics, Vol. 19, Núm. 8, pp. 707-713

2017

  1. Rationale and design of the multiethnic Pharmacogenomics in Childhood Asthma consortium

    Pharmacogenomics, Vol. 18, Núm. 10, pp. 931-943

2016

  1. Childhood asthma exacerbations and the Arg16 β2-receptor polymorphism: A meta-analysis stratified by treatment

    Journal of Allergy and Clinical Immunology, Vol. 138, Núm. 1, pp. 107-113.e5

  2. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy