Publications (25) Carlos Alberto Flores Infante publications

filter_list Allergy and Immunology

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

2022

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

    Frontiers in Medicine, Vol. 9

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

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

  5. Targeted analysis of genomic regions enriched in African ancestry reveals novel classical HLA alleles associated with asthma in Southwestern Europeans

    Scientific Reports, Vol. 11, Núm. 1

2020

  1. 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. Genomic predictors of asthma phenotypes and treatment response

    Frontiers in Pediatrics, Vol. 7, Núm. FEB

  2. Role of genomics in asthma exacerbations

    Current Opinion in Pulmonary Medicine, Vol. 25, Núm. 1, pp. 101-112

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. A pathway-based association study reveals variants from Wnt signalling genes contributing to asthma susceptibility

    Clinical and Experimental Allergy, Vol. 47, Núm. 5, pp. 618-626

  2. Rationale and design of the multiethnic Pharmacogenomics in Childhood Asthma consortium

    Pharmacogenomics, Vol. 18, Núm. 10, pp. 931-943

2016

  1. Copy number variation in ALOX5 and PTGER1 is associated with NSAIDs-induced urticaria and/or angioedema

    Pharmacogenetics and Genomics, Vol. 26, Núm. 6, pp. 280-287

  2. Genetic variants of thymic stromal lymphopoietin in nonsteroidal anti-inflammatory drug-induced urticaria/ angioedema

    International Archives of Allergy and Immunology, Vol. 169, Núm. 4, pp. 249-255

2014

  1. Variants of CEP68 gene are associated with acute urticaria/angioedema induced by multiple non-steroidal anti-inflammatory drugs

    PLoS ONE, Vol. 9, Núm. 3

2013

  1. Assessing the Validity of Asthma Associations for Eight Candidate Genes and Age at Diagnosis Effects

    PLoS ONE, Vol. 8, Núm. 9