Publicaciones en colaboración con investigadores/as de Instituto Universitario de Oncologia del Principado de Asturias (42)

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

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. Transcriptomic clustering of critically ill COVID-19 patients

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

2022

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

    eLife, Vol. 11

  2. 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

  3. 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

  4. 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

  5. The FCGR2A rs1801274 polymorphism was associated with the risk of death among COVID-19 patients

    Clinical Immunology, Vol. 236

2021

  1. DNA genotyping of the ABO gene showed a significant association of the A-group (A1/A2 variants) with severe COVID-19.

    European Journal of Internal Medicine

  2. Familial hypercholesterolaemia in twin brothers born using in-vitro fertilisation with donor semen and ovules

    Anales de Pediatria, Vol. 94, Núm. 3, pp. 179-180

  3. The Interferon-induced transmembrane protein 3 gene (IFITM3) rs12252 C variant is associated with COVID-19

    Cytokine, Vol. 137

  4. Variant-genetic and transcript-expression analysis showed a role for the chemokine-receptor CCR5 in COVID-19 severity

    International Immunopharmacology, Vol. 98

2020

  1. Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome

    Gene, Vol. 762

2019

  1. MAPK inhibition and growth hormone: a promising therapy in XLH

    FASEB Journal, Vol. 33, Núm. 7, pp. 8349-8362

2018

  1. Marked alterations in the structure, dynamics and maturation of growth plate likely explain growth retardation and bone deformities of young Hyp mice

    Bone, Vol. 116, pp. 187-195

2014

  1. Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

    Nature Communications, Vol. 5

2012

  1. Growth hormone improves growth retardation induced by rapamycin without blocking its antiproliferative and antiangiogenic effects on rat growth plate

    PLoS ONE, Vol. 7, Núm. 4