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Escobar-Lopez L, Ochoa JP, Mirelis JG, Espinosa MA, Navarro M, Gallego-Delgado M, Barriales-Villa R, Robles-Mezcua A, Basurte-Elorz MT, Gutierrez Garcia-Moreno L, Climent V, Jimenez-Jaimez J, Mogollon-Jimenez MV, Lopez J, Pena-Pena ML, Garcia-Alvarez A, Brion M, Ripoll-Vera T, Palomino-Doza J, Tiron C, Idiazabal U, Brogger MN, Garcia-Hernandez S, Restrepo-Cordoba MA, Gonzalez-Lopez E, Mendez I, Sabater M, Villacorta E, Larranaga-Moreira JM, Abecia A, Fernandez AI, Garcia-Pinilla JM, Rodriguez-Palomares JF, Gimeno-Blanes JR, Bayes-Genis A, Lara-Pezzi E, Dominguez F, Garcia-Pavia P. Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy. J Am Coll Cardiol. 2021 Oct 26;78(17):1682-1699. doi: 10.1016/j.jacc.2021.08.039. PubMed PMID: 34674813.
AÑO: 2021; IF: 27.203
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34674813
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Bleijendaal H, Ramos LA, Lopes RR, Verstraelen TE, Baalman SWE, Oudkerk Pool MD, Tjong FVY, Melgarejo-Meseguer FM, Gimeno-Blanes FJ, Gimeno-Blanes JR, Amin AS, Winter MM, Marquering HA, Kok WEM, Zwinderman AH, Wilde AAM, Pinto YM. Computer versus cardiologist: Is a machine learning algorithm able to outperform an expert in diagnosing a phospholamban p.Arg14del mutation on the electrocardiogram? Heart Rhythm. 2021 Jan;18(1):79-87. doi: 10.1016/j.hrthm.2020.08.021. Epub 2020 Sep 8. PubMed PMID: 32911053.
AÑO: 2021; IF: 6.779
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Lopez Cuenca D, Orenes Moreno M, Olmo Conesa MC, Pastor Moreno A, Santos Mateo JJ, Munoz Esparza C, Navarro Penalver M, Castro Garcia FJ, Sabater Molina M, Gimeno Blanes JR. Reasons for refusing diagnostic tests and therapeutic recommendations and associated complications in inherited heart diseases. The RELUCTANT study. Rev Esp Cardiol (Engl Ed). 2021 Jun;74(6):526-532. doi: 10.1016/j.rec.2020.06.014. Epub 2020 Jul 22. English, Spanish. PubMed PMID: 32709565.
AÑO: 2021; IF: 6.975
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Lopez-Ayala JM, Gimeno-Blanes J, Lopez-Cuenca D, Molina MS, Gimeno-Blanes JR. Electrocardiographic Screening of Arrhythmogenic Cardiomyopathy in Genotype-Positive and Phenotype-Negative Relatives. Front Cardiovasc Med. 2021 May 7;8:646391. doi: 10.3389/fcvm.2021.646391. eCollection 2021. PubMed PMID: 34026867; PubMed Central PMCID: PMC8137826.
AÑO: 2021; IF: 5.846
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Lopes LR, Garcia-Hernandez S, Lorenzini M, Futema M, Chumakova O, Zateyshchikov D, Isidoro-Garcia M, Villacorta E, Escobar-Lopez L, Garcia-Pavia P, Bilbao R, Dobarro D, Sandin-Fuentes M, Catalli C, Gener Querol B, Mezcua A, Garcia Pinilla J, Bloch Rasmussen T, Ferreira-Aguar A, Revilla-Marti P, Basurte Elorz MT, Bautista Paves A, Ramon Gimeno J, Figueroa AV, Franco-Gutierrez R, Fuentes-Canamero ME, Martinez Moreno M, Ortiz-Genga M, Piqueras-Flores J, Analia Ramos K, Rudzitis A, Ruiz-Guerrero L, Stein R, Triguero-Bocharan M, de la Higuera L, Ochoa JP, Abu-Bonsrah D, Kwok CYT, Smith JB, Porrello ER, Akhtar MM, Jager J, Ashworth M, Syrris P, Elliott DA, Monserrat L, Elliott PM. Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy. Eur Heart J. 2021 Aug 21;42(32):3063-3073. doi: 10.1093/eurheartj/ehab424. PubMed PMID: 34263907; PubMed Central PMCID: PMC8380059.
AÑO: 2021; IF: 35.855
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