Publikationen in Zusammenarbeit mit Forschern von Hospital de Gran Canaria Dr. Negrin (64)

2024

  1. 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. PCSK6 and Survival in Idiopathic Pulmonary Fibrosis

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

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

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

  5. 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

  6. 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

  7. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

    Science immunology, Vol. 6, Núm. 62

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