Publikationen, an denen er mitarbeitet Itahisa Marcelino Rodríguez (16)

2024

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

    Respiratory Research, Vol. 25, Núm. 1

  2. 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

2022

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

    Frontiers in Immunology, Vol. 13

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

    Frontiers in Medicine, Vol. 9

  3. Developing CIRdb as a catalog of natural genetic variation in the Canary Islanders

    Scientific Reports, Vol. 12, Núm. 1

  4. Evaluation of a whole-exome sequencing pipeline and benchmarking of causal germline variant prioritizers

    Human Mutation, Vol. 43, Núm. 12, pp. 2010-2020

2021

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

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

  2. Genetic ancestry inference and its application for the genetic mapping of human diseases

    International Journal of Molecular Sciences, Vol. 22, Núm. 13

  3. 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

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

    Frontiers in Immunology, Vol. 12

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. 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

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

    Frontiers in Genetics, Vol. 10, Núm. SEP

2018

  1. Genomic analyses of human European diversity at the southwestern edge: Isolation, African influence and disease associations in the Canary Islands

    Molecular Biology and Evolution, Vol. 35, Núm. 12, pp. 3010-3026