Publikationen in Zusammenarbeit mit Forschern von Universitat de Girona (33)

2024

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

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

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. Results From Spain's 2022 Para Report Cards on Physical Activity of Children and Adolescents With Disabilities

    Adapted physical activity quarterly : APAQ, Vol. 40, Núm. 3, pp. 551-559

  4. 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. Predictive models for first-onset and persistence of depression and anxiety among university students

    Journal of Affective Disorders, Vol. 308, pp. 432-441

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

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

  6. 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

  6. Validation of an online version of the alcohol use disorders identification test (Audit) for alcohol screening in Spanish university students

    International Journal of Environmental Research and Public Health, Vol. 18, Núm. 10

  7. Ventricular Repolarization Parameters and Coronary Involvement in Kawasaki Disease

    Journal of Pediatrics, Vol. 236, pp. 108-112.e5

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. Mental disorders in Spanish university students: Prevalence, age-of-onset, severe role impairment and mental health treatment.

    Journal of Affective Disorders, Vol. 273, pp. 604-613