Publicaciones (394) Publicaciones de ELIECER COTO GARCIA

2024

  1. 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

  2. NFKB1 variants were associated with the risk of Parkinson´s disease in male

    Journal of Neural Transmission

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  2. Age-dependent effect of the IFIH1/MDA5 gene variants on the risk of critical COVID-19

    Immunogenetics, Vol. 75, Núm. 2, pp. 91-98

  3. 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

  4. Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia

    Journal of Clinical Medicine, Vol. 12, Núm. 3

  5. 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

  6. Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients

    Journal of Clinical Medicine, Vol. 12, Núm. 3

  7. 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

  8. Transcriptomic clustering of critically ill COVID-19 patients

    The European respiratory journal, Vol. 61, Núm. 1

2022

  1. A first update on mapping the human genetic architecture of COVID-19

    Nature

  2. Association of the Genetic Variation in the Long Non‐Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy

    Life, Vol. 12, Núm. 6

  3. Common mitochondrial haplogroups as modifiers of the onset-age for critical COVID-19

    Mitochondrion, Vol. 67, pp. 1-5

  4. Different Phenotypes in Monozygotic Twins, Carriers of the Same Pathogenic Variant for Hypertrophic Cardiomyopathy

    Life, Vol. 12, Núm. 9

  5. Effects of IFIH1 rs1990760 variants on systemic inflammation and outcome in critically ill COVID-19 patients in an observational translational study

    eLife, Vol. 11

  6. Emergence of New SARS-CoV2 Omicron Variants after the Change of Surveillance and Control Strategy

    Microorganisms, Vol. 10, Núm. 10

  7. 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

  8. 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

  9. Hereditary angioedema caused by a novel intronic variant of SERPING1

    Pediatric Allergy and Immunology

  10. 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