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Ortiz-Genga MF, Cuenca S, Dal Ferro M, Zorio E, Salgado-Aranda R, Climent V, Padrón-Barthe L, Duro-Aguado I, Jiménez-Jáimez J, Hidalgo-Olivares VM, García-Campo E, Lanzillo C, Suárez-Mier MP, Yonath H, Marcos-Alonso S, Ochoa JP, Santomé JL, García-Giustiniani D, Rodríguez-Garrido JL, Domínguez F, Merlo M, Palomino J, Peña ML, Trujillo JP, Martín-Vila A, Stolfo D, Molina P, Lara-Pezzi E, Calvo-Iglesias FE, Nof E, Calò L, Barriales-Villa R, Gimeno-Blanes JR, Arad M, García-Pavía P, Monserrat L. Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. J Am Coll Cardiol. 2016 Dec 6;68(22):2440-2451. doi: 10.1016/j.jacc.2016.09.927. PubMed PMID: 27908349.
AÑO: 2016; IF: 19.896
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Manrique-Rodriguez, S.; de la Rubia-Nieto, A.; Garcia-Robles, J. A.; Goicoechea-Diezhandino, M.; Gimeno-Blanes, J. A.; Pernia-Lopez, M. S.; Pellicer-Franco, C.; Sanjurjo-Saez, M.. Individualized therapy in patients with Fabry disease: is it a feasible strategy for rare diseases?. EXPERT OPINION ON ORPHAN DRUGS. DEC 2016; 4(12):1199-1206. 10.1080/21678707.2016.1253468
AÑO: 2016; IF: 0.559
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O'Mahony C, Jichi F, Monserrat L, Ortiz-Genga M, Anastasakis A, Rapezzi C, Biagini E, Gimeno JR, Limongelli G, McKenna WJ, Omar RZ, Elliott PM; Hypertrophic Cardiomyopathy Outcomes Investigators*. Inverted U-Shaped Relation Between the Risk of Sudden Cardiac Death and Maximal Left Ventricular Wall Thickness in Hypertrophic Cardiomyopathy. Circ Arrhythm Electrophysiol. 2016 Jun;9(6). pii: e003818. doi: 10.1161/CIRCEP.115.003818. PubMed PMID: 27217341.
AÑO: 2016; IF: 5.41
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Lopez-Ayala JM, Ortiz-Genga M, Gomez-Milanes I, Lopez-Cuenca D, Ruiz-Espejo F, Sanchez-Munoz JJ, Oliva-Sandoval MJ, Monserrat L, Gimeno JR. A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy. Clin Genet. 2015 Aug;88(2):172-6. doi: 10.1111/cge.12458. PubMed PMID: 25041374.
AÑO: 2015; IF: 3.892
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Moreno C, Oliveras A, de la Cruz A, Bartolucci C, Muñoz C, Salar E, Gimeno JR, Severi S, Comes N, Felipe A, González T, Lambiase P, Valenzuela C. A new KCNQ1 mutation at the S5 segment that impairs its association with KCNE1 is responsible for short QT syndrome. Cardiovasc Res. 2015 Sep 1;107(4):613-23. doi: 10.1093/cvr/cvv196. PubMed PMID: 26168993.
AÑO: 2015; IF: 5.465
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