Publicaciones en colaboración con investigadores/as de Universitat de Barcelona (15)

2023

  1. 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

2022

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

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

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

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

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

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

  4. 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. 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

  2. Personalized genetic diagnosis of congenital heart defects in newborns

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

  3. 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

2016

  1. Genetic basis of dilated cardiomyopathy

    International Journal of Cardiology, Vol. 224, pp. 461-472

2015

  1. A novel mutation in lamin A/C causing familial dilated cardiomyopathy associated with sudden cardiac death

    Journal of Cardiac Failure, Vol. 21, Núm. 3, pp. 217-225

2009

  1. Thigh and buttock exertional pain for the diagnosis of peripheral arterial disease

    European Journal of Internal Medicine, Vol. 20, Núm. 4, pp. 429-434