Carlos Alberto
Flores Infante
External Researcher
Itahisa
Marcelino Rodríguez
Reader
Publications by the researcher in collaboration with Itahisa Marcelino Rodríguez (16)
2024
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A genome-wide association study of adults with community-acquired pneumonia
Respiratory Research, Vol. 25, Núm. 1
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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
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A catalog of the genetic causes of hereditary angioedema in the Canary Islands (Spain)
Frontiers in Immunology, Vol. 13
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Admixture Mapping of Sepsis in European Individuals With African Ancestries
Frontiers in Medicine, Vol. 9
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Developing CIRdb as a catalog of natural genetic variation in the Canary Islanders
Scientific Reports, Vol. 12, Núm. 1
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Evaluation of a whole-exome sequencing pipeline and benchmarking of causal germline variant prioritizers
Human Mutation, Vol. 43, Núm. 12, pp. 2010-2020
2021
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First census of patients with hereditary angioedema in the canary islands
Journal of Clinical Medicine, Vol. 10, Núm. 20
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Genetic ancestry inference and its application for the genetic mapping of human diseases
International Journal of Molecular Sciences, Vol. 22, Núm. 13
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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
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Whole-Blood Mitochondrial DNA Copies Are Associated With the Prognosis of Acute Respiratory Distress Syndrome After Sepsis
Frontiers in Immunology, Vol. 12
2020
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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
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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
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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
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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
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Bradykinin-mediated angioedema: An update of the genetic causes and the impact of genomics
Frontiers in Genetics, Vol. 10, Núm. SEP
2018
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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