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García-Giustiniani D, Arad M, Ortíz-Genga M, Barriales-Villa R, Fernández X, Rodríguez-García I, Mazzanti A, Veira E, Maneiro E, Rebolo P, Lesende I, Cazón L, Freimark D, Gimeno-Blanes JR, Seidman C, Seidman J, McKenna W, Monserrat L. Phenotype and prognostic correlations of the converter region mutations affecting the ? myosin heavy chain. Heart. 2015 Jul;101(13):1047-53. doi: 10.1136/heartjnl-2014-307205. PubMed PMID: 25935763; PubMed Central PMCID: PMC4484257.
AÑO: 2015; IF: 5.693
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López-Ayala JM, Boven L, van den Wijngaard A, Peñafiel-Verdú P, van Tintelen JP, Gimeno JR. Phospholamban p.arg14del mutation in a Spanish family with arrhythmogenic cardiomyopathy: evidence for a European founder mutation. Rev Esp Cardiol (Engl Ed). 2015 Apr;68(4):346-9. doi: 10.1016/j.rec.2014.11.012. PubMed PMID: 25700660.
AÑO: 2015; IF: 4.596
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Muñoz-Esparza C, García-Molina E, Salar-Alcaraz M, Peñafiel-Verdú P, Sánchez-Muñoz JJ, Martínez Sánchez J, Cabañas-Perianes V, Valdés Chávarri M, García Alberola A, Gimeno-Blanes JR. Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. Rev Esp Cardiol (Engl Ed). 2015 Oct;68(10):861-8. doi: 10.1016/j.rec.2014.10.022. PubMed PMID: 25819988.
AÑO: 2015; IF: 4.596
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Lopez-Ayala JM, Pastor-Quirante F, Gonzalez-Carrillo J, Lopez-Cuenca D, Sanchez-Munoz JJ, Oliva-Sandoval MJ, Gimeno JR. Genetics of myocarditis in arrhythmogenic right ventricular dysplasia. Heart Rhythm. 2015 Apr;12(4):766-73. doi: 10.1016/j.hrthm.2015.01.001. PubMed PMID: 25616123.
AÑO: 2015; IF: 4.391
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Jiménez-Jáimez J, Peinado R, Grima EZ, Segura F, Moriña P, Sánchez Muñoz JJ, Mazuelos F, Cózar R, Gimeno JR, Heras RP, Monserrat L, Domingo D, Ortiz-Genga M, Fernández Pastor J, Álvarez M, Tercedor L. Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study). Am J Cardiol. 2015 Sep 15;116(6):894-9. doi: 10.1016/j.amjcard.2015.06.030. PubMed PMID: 26189708.
AÑO: 2015; IF: 3.154
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