Publicaciones en colaboración con investigadores/as de Universitat de Girona (23)

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

  4. Plasma microrna expression profile for reduced ejection fraction in dilated cardiomyopathy

    Scientific Reports, Vol. 11, Núm. 1

  5. Rare variants associated with arrhythmogenic cardiomyopathy: Reclassification five years later

    Journal of Personalized Medicine, Vol. 11, Núm. 3, pp. 1-14

2020

  1. Genetic variants as sudden-death risk markers in inherited arrhythmogenic syndromes: Personalized genetic interpretation

    Journal of Clinical Medicine, Vol. 9, Núm. 6, pp. 1-9

  2. Peripheral microRNA panels to guide the diagnosis of familial cardiomyopathy

    Translational Research, Vol. 218, pp. 1-15

  3. Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

    EBioMedicine, Vol. 54

  4. Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?

    Forensic Science International: Genetics, Vol. 47

2018

  1. Plasma microRNAs as biomarkers for Lamin A/C-related dilated cardiomyopathy

    Journal of Molecular Medicine, Vol. 96, Núm. 8, pp. 845-856

2017

  1. Familial dilated cardiomyopathy: A multidisciplinary entity, from basic screening to novel circulating biomarkers

    International Journal of Cardiology, Vol. 228, pp. 870-880

2016

  1. Familial dilated cardiomyopathy caused by a novel frameshift in the BAG3 gene

    PLoS ONE, Vol. 11, Núm. 7