UNIOVI-PEDIATRIA
OVIPED
Centro de Investigacion Biomedica en Red de Enfermedades Respiratorias
Madrid, EspañaPublicacions en col·laboració amb investigadors/es de Centro de Investigacion Biomedica en Red de Enfermedades Respiratorias (20)
2024
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Chromosome-Y haplogroups in Asturias (Northern Spain) and their association with severe COVID-19
Molecular Genetics and Genomics, Vol. 299, Núm. 1
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Immunoglobulin genes and severity of COVID-19
Immunogenetics, Vol. 76, Núm. 3, pp. 213-217
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Retrospective variant reclassification and resequencing in hypertrophic cardiomyopathy: a reference unit centre experience
European Journal of Preventive Cardiology, Vol. 31, Núm. 6, pp. e38-e41
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Age-dependent effect of the IFIH1/MDA5 gene variants on the risk of critical COVID-19
Immunogenetics, Vol. 75, Núm. 2, pp. 91-98
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Chromosome Y Haplogroup R Was Associated with the Risk of Premature Myocardial Infarction with ST-Elevation: Data from the CholeSTEMI Registry
Journal of Clinical Medicine, Vol. 12, Núm. 14
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Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia
Journal of Clinical Medicine, Vol. 12, Núm. 3
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Mitochondrial Heteroplasmy as a Marker for Premature Coronary Artery Disease: Analysis of the Poly-C Tract of the Control Region Sequence
Journal of Clinical Medicine, Vol. 12, Núm. 6
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Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients
Journal of Clinical Medicine, Vol. 12, Núm. 3
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Transcriptomic clustering of critically ill COVID-19 patients
The European respiratory journal, Vol. 61, Núm. 1
2022
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Association of the Genetic Variation in the Long Non‐Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 6
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Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 9
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FURIN gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID-19
Journal of Medical Virology, Vol. 94, Núm. 8, pp. 3589-3595
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Genetic variants in the NF-κB signaling pathway (NFKB1, NFKBIA, NFKBIZ) and risk of critical outcome among COVID-19 patients
Human Immunology, Vol. 83, Núm. 8-9, pp. 613-617
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IGHG3 hinge length variation was associated with the risk of critical disease and death in a Spanish COVID-19 cohort
Genes and Immunity, Vol. 23, Núm. 6, pp. 205-208
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KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort
Life, Vol. 12, Núm. 4
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The FCGR2A rs1801274 polymorphism was associated with the risk of death among COVID-19 patients
Clinical Immunology, Vol. 236
2021
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The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19
Cytokine, Vol. 137
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Variant-genetic and transcript-expression analysis showed a role for the chemokine-receptor CCR5 in COVID-19 severity
International Immunopharmacology, Vol. 98