Publications (25) Carlos Alberto Flores Infante publications

filter_list Internal Medicine

2024

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

    Respiratory Research, Vol. 25, Núm. 1

2023

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

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

  2. 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

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

    Critical Care, Vol. 26, Núm. 1

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

    Frontiers in Medicine, Vol. 9

  3. From Samples to Germline and Somatic Sequence Variation: A Focus on Next-Generation Sequencing in Melanoma Research

    Life, Vol. 12, Núm. 11

  4. Transactive Response DNA-Binding Protein (TARDBP/TDP-43) Regulates Cell Permissivity to HIV-1 Infection by Acting on HDAC6

    International Journal of Molecular Sciences, Vol. 23, Núm. 11

2021

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

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

  2. 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

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

    European Respiratory Journal, Vol. 57, Núm. 5

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

    Frontiers in Immunology, Vol. 12

  5. 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. Evaluation of whole-exome enrichment solutions: Lessons from the high-end of the short-read sequencing scale

    Journal of Clinical Medicine, Vol. 9, Núm. 11, pp. 1-22

  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. Interactive web-based resource for annotation of genetic variants causing hereditary angioedema (HADA): Database development, implementation, and validation

    Journal of Medical Internet Research, Vol. 22, Núm. 10

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. Whole-exome sequencing identifies somatic mutations associated with mortality in metastatic clear cell kidney carcinoma

    Frontiers in Genetics, Vol. 10, Núm. MAY

2017

  1. 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

2015

  1. Altered profile of circulating endothelial-derived microparticles in ventilator-induced lung injury

    Critical Care Medicine, Vol. 43, Núm. 12, pp. e551-e559