ELIECER
COTO GARCIA
Catedrático de Universidad
Centro de Investigacion Biomedica en Red de Enfermedades Respiratorias
Madrid, EspañaPublications en collaboration avec des chercheurs de Centro de Investigacion Biomedica en Red de Enfermedades Respiratorias (20)
2024
-
Chromosome-Y haplogroups in Asturias (Northern Spain) and their association with severe COVID-19
Molecular Genetics and Genomics, Vol. 299, Núm. 1
-
Immunoglobulin genes and severity of COVID-19
Immunogenetics, Vol. 76, Núm. 3, pp. 213-217
-
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
-
A second update on mapping the human genetic architecture of COVID-19
Nature
-
Age-dependent effect of the IFIH1/MDA5 gene variants on the risk of critical COVID-19
Immunogenetics, Vol. 75, Núm. 2, pp. 91-98
-
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
-
Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia
Journal of Clinical Medicine, Vol. 12, Núm. 3
-
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
-
Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients
Journal of Clinical Medicine, Vol. 12, Núm. 3
-
Transcriptomic clustering of critically ill COVID-19 patients
The European respiratory journal, Vol. 61, Núm. 1
2022
-
Association of the Genetic Variation in the Long Non‐Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 6
-
Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy
Life, Vol. 12, Núm. 9
-
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
-
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
-
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
-
KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort
Life, Vol. 12, Núm. 4
-
The FCGR2A rs1801274 polymorphism was associated with the risk of death among COVID-19 patients
Clinical Immunology, Vol. 236
2021
-
The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19
Cytokine, Vol. 137
-
Variant-genetic and transcript-expression analysis showed a role for the chemokine-receptor CCR5 in COVID-19 severity
International Immunopharmacology, Vol. 98