Publications (229) Carlos Alberto Flores Infante publications

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2025

  1. A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity

    Journal of Experimental Medicine, Vol. 222, Núm. 2

  2. A tiered strategy to identify relevant genetic variants in familial pulmonary fibrosis: a proof of concept for the clinical practice

    European Journal of Human Genetics

  3. Clinical value of circulating bioactive adrenomedullin for prediction of outcome and hydrocortisone response in sepsis patients—a post-hoc analysis of the HYPRESS trial

    Infection

  4. Genetic variability of Shiga toxin-producing Escherichia coli strains isolated from Paraguayan cattle

    Microbiology spectrum, Vol. 13, Núm. 10, pp. e0059625

  5. Genome-wide association study of susceptibility to acute respiratory distress syndrome

    eBioMedicine, Vol. 120

  6. IFNγ in human sepsis: a scoping review

    Annals of Intensive Care, Vol. 15, Núm. 1

  7. Pharmacogenomic Study of SARS-CoV-2 Treatments: Identifying Polymorphisms Associated with Treatment Response in COVID-19 Patients

    Biomedicines, Vol. 13, Núm. 3

  8. Small variant benchmark from a complete assembly of X and Y chromosomes

    Nature communications, Vol. 16, Núm. 1, pp. 497

  9. Tracheal Aspirate Metagenomics Reveals Association of Antibiotic Resistance with Nonpulmonary Sepsis Mortality

    American Journal of Respiratory Cell and Molecular Biology

  10. Whole Exome Sequencing in Drug-Induced Angioedema Caused by Angiotensin-Converting Enzyme Inhibitors: A Pilot Study in Five Patients

    Journal of Clinical Medicine, Vol. 14, Núm. 5

2024

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

    Respiratory Research, Vol. 25, Núm. 1

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

    ERJ Open Research, Vol. 10, Núm. 1

  3. Defining the Differential Corticosteroid Response Basis from Multiple Omics Approaches

    International Journal of Molecular Sciences, Vol. 25, Núm. 24

  4. Does HLA explain the high incidence of childhood-onset type 1 diabetes in the Canary Islands? The role of Asp57 DQB1 molecules

    BMC pediatrics, Vol. 24, Núm. 1, pp. 569

  5. 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

  6. Genomic epidemiology of the primary methicillin-resistant Staphylococcus aureus clones causing invasive infections in Paraguayan children

    Microbiology Spectrum, Vol. 12, Núm. 4

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

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

  8. Modelling the demographic history of human North African genomes points to a recent soft split divergence between populations

    Genome Biology, Vol. 25, Núm. 1

  9. Novel risk loci for COVID-19 hospitalization among admixed American populations

    eLife, Vol. 13

  10. SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency

    Journal of Experimental Medicine, Vol. 221, Núm. 9