Publicaciones en las que colabora con Elena Arbelo Lainez (10)

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

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

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

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

    EBioMedicine, Vol. 54

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

    Forensic Science International: Genetics, Vol. 47