Publicacións en colaboración con investigadores/as de Hospital de Gran Canaria Dr. Negrin (66)

2024

  1. A genome-wide association study of adults with community-acquired pneumonia

    Respiratory Research, Vol. 25, Núm. 1

  2. Erratum: Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (Genome medicine (2023) 15 1 (22))

    Genome medicine

2023

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

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

  2. Genetic Determinants of the Acute Respiratory Distress Syndrome

    Journal of Clinical Medicine, Vol. 12, Núm. 11

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

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

  4. PCSK6 and Survival in Idiopathic Pulmonary Fibrosis

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

  5. Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival from Sepsis

    Critical Care Explorations, Vol. 5, Núm. 11, pp. E0997

  6. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

    Genome Medicine, Vol. 15, Núm. 1

  7. Xanthine oxidoreductase gene polymorphisms are associated with high risk of sepsis and organ failure

    Respiratory Research, Vol. 24, Núm. 1

2022

  1. A catalog of the genetic causes of hereditary angioedema in the Canary Islands (Spain)

    Frontiers in Immunology, Vol. 13

  2. A genome-wide association study of survival in patients with sepsis

    Critical Care, Vol. 26, Núm. 1

  3. A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection

    Nature Immunology, Vol. 23, Núm. 2, pp. 159-164

  4. Admixture Mapping of Sepsis in European Individuals With African Ancestries

    Frontiers in Medicine, Vol. 9

  5. Wilson Disease Prevalence: Discrepancy Between Clinical Records, Registries and Mutation Carrier Frequency

    Journal of pediatric gastroenterology and nutrition, Vol. 74, Núm. 2, pp. 192-199

2021

  1. Clinical and biological markers for predicting ARDS and outcome in septic patients

    Scientific Reports, Vol. 11, Núm. 1

  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. First census of patients with hereditary angioedema in the canary islands

    Journal of Clinical Medicine, Vol. 10, Núm. 20

  4. From Your Nose to Your Toes: A Review of Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic‒Associated Pernio

    Journal of Investigative Dermatology, Vol. 141, Núm. 12, pp. 2791-2796

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

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

  6. Whole-Blood Mitochondrial DNA Copies Are Associated With the Prognosis of Acute Respiratory Distress Syndrome After Sepsis

    Frontiers in Immunology, Vol. 12