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de Frutos F, Ochoa JP, Navarro-Penalver M, Baas A, Bjerre JV, Zorio E, Mendez I, Lorca R, Verdonschot JAJ, Garcia-Granja PE, Bilinska Z, Fatkin D, Fuentes-Canamero ME, Garcia-Pinilla JM, Garcia-Alvarez MI, Girolami F, Barriales-Villa R, Diez-Lopez C, Lopes LR, Wahbi K, Garcia-Alvarez A, Rodriguez-Sanchez I, Rekondo-Olaetxea J, Rodriguez-Palomares JF, Gallego-Delgado M, Meder B, Kubanek M, Hansen FG, Restrepo-Cordoba MA, Palomino-Doza J, Ruiz-Guerrero L, Sarquella-Brugada G, Perez-Perez AJ, Bermudez-Jimenez FJ, Ripoll-Vera T, Rasmussen TB, Jansen M, Sabater-Molina M, Elliot PM, Garcia-Pavia P; European Genetic Cardiomyopathies Initiative Investigators. Natural History of MYH7-Related Dilated Cardiomyopathy. J Am Coll Cardiol. 2022 Oct 11;80(15):1447-1461. doi: 10.1016/j.jacc.2022.07.023. Epub 2022 Aug 22. PubMed PMID: 36007715.
AÑO: 2022; IF: 24.0
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36007715
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Bermudez-Jimenez FJ, Carriel V, Santos-Mateo JJ, Fernandez A, Garcia-Hernandez S, Ramos KA, Piqueras-Flores J, Cabrera-Romero E, Barriales-Villa R, de la Higuera Romero L, Alcala Lopez JE, Gimeno Blanes JR, Sanchez-Porras D, Campos F, Alaminos M, Oyonarte-Ramirez JM, Alvarez M, Tercedor L, Brodehl A, Jimenez-Jaimez J. ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium. Rev Esp Cardiol (Engl Ed). 2023 May;76(5):301-311. doi: 10.1016/j.rec.2022.08.002. Epub 2022 Aug 8. English, Spanish. PubMed PMID: 35952944.
AÑO: 2023; IF: 7.2
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Bayonas-Ruiz A, Munoz-Franco FM, Sabater-Molina M, Oliva-Sandoval MJ, Gimeno JR, Bonacasa B. Current therapies for hypertrophic cardiomyopathy: a systematic review and meta-analysis of the literature. ESC Heart Fail. 2023 Feb;10(1):8-23. doi: 10.1002/ehf2.14142. Epub 2022 Oct 1. PubMed PMID: 36181355; PubMed Central PMCID: PMC9871697.
AÑO: 2023; IF: 3.2
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Guler MN, Tscheiller NM, Sabater-Molina M, Gimeno JR, Nebigil CG. Evidence for reciprocal network interactions between injured hearts and cancer. Front Cardiovasc Med. 2022 Jul 15;9:929259. doi: 10.3389/fcvm.2022.929259. eCollection 2022. PubMed PMID: 35911555; PubMed Central PMCID: PMC9334681.
AÑO: 2022; IF: 3.6
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Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, Anys S, Minois D, Arnaud M, Duchateau J, Wijeyeratne YD, Muir A, Papadakis M, Castelletti S, Torchio M, Ortuno CG, Lacunza J, Giachino DF, Cerrato N, Martins RP, Campuzano O, Van Dooren S, Thollet A, Kyndt F, Mazzanti A, Clementy N, Bisson A, Corveleyn A, Stallmeyer B, Dittmann S, Saenen J, Noel A, Honarbakhsh S, Rudic B, Marzak H, Rowe MK, Federspiel C, Le Page S, Placide L, Milhem A, Barajas-Martinez H, Beckmann BM, Krapels IP, Steinfurt J, Winkel BG, Jabbari R, Shoemaker MB, Boukens BJ, Skoric-Milosavljevic D, Bikker H, Manevy F, Lichtner P, Ribases M, Meitinger T, Muller-Nurasyid M; KORA-Study Group; Veldink JH, van den Berg LH, Van Damme P, Cusi D, Lanzani C, Rigade S, Charpentier E, Baron E, Bonnaud S, Lecointe S, Donnart A, Le Marec H, Chatel S, Karakachoff M, Bezieau S, London B, Tfelt-Hansen J, Roden D, Odening KE, Cerrone M, Chinitz LA, Volders PG, van de Berg MP, Laurent G, Faivre L, Antzelevitch C, Kaab S, Arnaout AA, Dupuis JM, Pasquie JL, Billon O, Roberts JD, Jesel L, Borggrefe M, Lambiase PD, Mansourati J, Loeys B, Leenhardt A, Guicheney P, Maury P, Schulze-Bahr E, Robyns T, Breckpot J, Babuty D, Priori SG, Napolitano C; Nantes Referral Center for inherited cardiac arrhythmia; de Asmundis C, Brugada P, Brugada R, Arbelo E, Brugada J, Mabo P, Behar N, Giustetto C, Molina MS, Gimeno JR, Hasdemir C, Schwartz PJ, Crotti L, McKeown PP, Sharma S, Behr ER, Haissaguerre M, Sacher F, Rooryck C, Tan HL, Remme CA, Postema PG, Delmar M, Ellinor PT, Lubitz SA, Gourraud JB, Tanck MW, George AL Jr, MacRae CA, Burridge PW, Dina C, Probst V, Wilde AA, Schott JJ, Redon R, Bezzina CR. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat Genet. 2022 May;54(5):735. doi: 10.1038/s41588-022-01079-y. No abstract available. PubMed PMID: 35474365.
AÑO: 2022; IF: 30.8
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