ELIECER
COTO GARCIA
Catedrático de Universidad
Hospital Universitario Central de Asturias
Oviedo, EspañaPublications in collaboration with researchers from Hospital Universitario Central de Asturias (321)
2025
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Assessing the association between common functional Nuclear Factor Kappa-b gene polymorphisms (NFKB1, NFKBIZ, NFKBIA) and Alzheimer´s disease
Behavioural Brain Research, Vol. 476
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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Identification of host endotypes using peripheral blood transcriptomics in a prospective cohort of patients with endocarditis
International Journal of Infectious Diseases, Vol. 148
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Immunoglobulin genes and severity of COVID-19
Immunogenetics, Vol. 76, Núm. 3, pp. 213-217
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Influence of the HLA-Cw6 Allele and IFIH1/MDA5 Gene Variants on the Cardiometabolic Risk Profile of Patients with Psoriatic Disease
Journal of Clinical Medicine, Vol. 13, Núm. 3
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NFKB1 variants were associated with the risk of Parkinson´s disease in male
Journal of Neural Transmission, Vol. 131, Núm. 7, pp. 773-779
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PCSK9 gene variations in the clinical setting of premature cardiovascular disease: A critical appraisal
International Journal of Cardiology, Vol. 413
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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
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Survival analysis and gender differences in hypertrophic cardiomyopathy proband patients referred for genetic testing
International Journal of Cardiology, Vol. 408
2023
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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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The IFIH1/MDA5 rs1990760 Gene Variant (946Thr) Differentiates Early- vs. Late-Onset Skin Disease and Increases the Risk of Arthritis in a Spanish Cohort of Psoriasis
International Journal of Molecular Sciences, Vol. 24, Núm. 19
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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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Common mitochondrial haplogroups as modifiers of the onset-age for critical COVID-19
Mitochondrion, Vol. 67, pp. 1-5
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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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Effects of IFIH1 rs1990760 variants on systemic inflammation and outcome in critically ill COVID-19 patients in an observational translational study
eLife, Vol. 11