Publikationen, an denen er mitarbeitet Ariel Callero Viera (9)

2022

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

    Frontiers in Immunology, Vol. 13

2021

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

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

  2. 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. 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

  2. Corrigendum: Bradykinin-Mediated Angioedema: An Update of the Genetic Causes and the Impact of Genomics (Frontiers in Genetics, (2019), 10, 10.3389/fgene.2019.00900)

    Frontiers in Genetics

  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

  4. The genomics and metagenomics of asthma severity (GEMAS) study: Rationale and design

    Journal of Personalized Medicine, Vol. 10, Núm. 3, pp. 1-16

2019

  1. Bradykinin-mediated angioedema: An update of the genetic causes and the impact of genomics

    Frontiers in Genetics, Vol. 10, Núm. SEP

2016

  1. Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene

    Journal of Allergy and Clinical Immunology, Vol. 137, Núm. 3, pp. 964-966