Publicaciones en colaboración con investigadores/as de Imperial College London (18)

2024

  1. Association study of human leukocyte antigen variants and idiopathic pulmonary fibrosis

    ERJ Open Research, Vol. 10, Núm. 1

  2. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

    Human Genetics and Genomics Advances, Vol. 5, Núm. 3

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  2. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

    Nature, Vol. 623, Núm. 7988, pp. 803-813

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

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

  4. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

    Journal of Experimental Medicine, Vol. 220, Núm. 5

  5. PCSK6 and Survival in Idiopathic Pulmonary Fibrosis

    American journal of respiratory and critical care medicine, Vol. 207, Núm. 11, pp. 1515-1524

  6. The causal relationship between gastro-oesophageal reflux disease and idiopathic pulmonary fibrosis: a bidirectional two-sample Mendelian randomisation study

    European Respiratory Journal, Vol. 61, Núm. 5

2022

  1. Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis

    Thorax, Vol. 77, Núm. 8, pp. 829-833

  2. Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics

    Cell Genomics, Vol. 2, Núm. 10

2021

  1. Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations

    American Journal of Respiratory and Critical Care Medicine

2020

  1. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  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. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

2018

  1. 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

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

    Nature Genetics

2017

  1. 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

  2. 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