Publicaciones en colaboración con investigadores/as de Instituto de Investigación Sanitaria del Principado de Asturias (49)

2025

  1. 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

  1. Chromosome-Y haplogroups in Asturias (Northern Spain) and their association with severe COVID-19

    Molecular Genetics and Genomics, Vol. 299, Núm. 1

  2. Identification of host endotypes using peripheral blood transcriptomics in a prospective cohort of patients with endocarditis

    International Journal of Infectious Diseases, Vol. 148

  3. Immunoglobulin genes and severity of COVID-19

    Immunogenetics, Vol. 76, Núm. 3, pp. 213-217

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

    Journal of Neural Transmission, Vol. 131, Núm. 7, pp. 773-779

  5. New challenges in specialized health training related to skills in telemedicine and information and communication technologies

    Educacion Medica

  6. PCSK9 gene variations in the clinical setting of premature cardiovascular disease: A critical appraisal

    International Journal of Cardiology, Vol. 413

  7. 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

  8. Survival analysis and gender differences in hypertrophic cardiomyopathy proband patients referred for genetic testing

    International Journal of Cardiology, Vol. 408

2023

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

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

  2. 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

  3. Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia

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

  4. 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

  5. Nutritional Assessment and Support in Children with Chronic Kidney Disease: The Benefits of Working with a Registered Dietitian

    Nutrients, Vol. 15, Núm. 3

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

    Life, Vol. 12, Núm. 6

  2. Cellular and Molecular Alterations Underlying Abnormal Bone Growth in X-Linked Hypophosphatemia

    International Journal of Molecular Sciences, Vol. 23, Núm. 2

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

    Mitochondrion, Vol. 67, pp. 1-5