Universitat de Girona-ko ikertzaileekin lankidetzan egindako argitalpenak (32)

2025

  1. Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes

    iScience, Vol. 28, Núm. 5

  2. MicroRNA-143-3p and miR-452-5p: A Fingerprint for the Diagnosis of Aortic Stenosis in the Geriatric Population

    Biomedicines, Vol. 13, Núm. 3

  3. MicroRNAs unlock mystery of arrhythmogenic cardiomyopathy

    Kardiologia Polska

2024

  1. A narrative review of inherited arrhythmogenic syndromes in young population: Role of genetic diagnosis in exercise recommendations

    BMJ Open Sport and Exercise Medicine, Vol. 10, Núm. 3

  2. Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic Diagnosis

    Biomedicines, Vol. 12, Núm. 11

  3. Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy

    International Journal of Molecular Sciences, Vol. 25, Núm. 7

  4. Interpreting the actionable clinical role of rare variants associated with short QT syndrome

    Human Genetics, Vol. 143, Núm. 12, pp. 1499-1508

  5. Role of miRNA–mRNA Interactome in Pathophysiology of Arrhythmogenic Cardiomyopathy

    Biomedicines, Vol. 12, Núm. 8

  6. The Protective Role of miR-130b-3p Against Palmitate-Induced Lipotoxicity in Cardiomyocytes Through PPARγ Pathway

    International Journal of Molecular Sciences, Vol. 25, Núm. 22

2023

  1. Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death

    Frontiers in Medicine, Vol. 10

  2. Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort

    International Journal of Legal Medicine, Vol. 137, Núm. 2, pp. 345-351

  3. Role of microRNAs in arrhythmogenic cardiomyopathy: translation as biomarkers into clinical practice

    Translational Research, Vol. 259, pp. 72-82

2022

  1. A microRNA Signature for the Diagnosis of Statins Intolerance

    International Journal of Molecular Sciences, Vol. 23, Núm. 15

  2. Clinical impact of rare variants associated with inherited channelopathies: a 5-year update

    Human Genetics, Vol. 141, Núm. 10, pp. 1579-1589

  3. Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes

    Journal of Personalized Medicine, Vol. 12, Núm. 2

  4. The Role of MicroRNAs in Dilated Cardiomyopathy: New Insights for an Old Entity

    International Journal of Molecular Sciences, Vol. 23, Núm. 21

  5. miR-16-5p Suppression Protects Human Cardiomyocytes against Endoplasmic Reticulum and Oxidative Stress-Induced Injury

    International Journal of Molecular Sciences, Vol. 23, Núm. 3

2021

  1. Circulating circRNA as biomarkers for dilated cardiomyopathy etiology

    Journal of Molecular Medicine, Vol. 99, Núm. 12, pp. 1711-1725

  2. Malignant arrhythmogenic role associated with rbm20: A comprehensive interpretation focused on a personalized approach

    Journal of Personalized Medicine, Vol. 11, Núm. 2, pp. 1-17

  3. Personalized genetic diagnosis of congenital heart defects in newborns

    Journal of Personalized Medicine, Vol. 11, Núm. 6