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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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Martinez-Sole J, Sabater-Molina M, Braza-Boils A, Santos-Mateo JJ, Molina P, Martinez-Dolz L, Gimeno JR, Zorio E. Facts and Gaps in Exercise Influence on Arrhythmogenic Cardiomyopathy: New Insights From a Meta-Analysis Approach. Front Cardiovasc Med. 2021 Oct 18;8:702560. doi: 10.3389/fcvm.2021.702560. eCollection 2021. Erratum In: Front Cardiovasc Med. 2022 Feb 04;8:816280. PubMed PMID: 34733888; PubMed Central PMCID: PMC8558346.
AÑO: 2021; IF: 2.9
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Sabater Molina M, Nicolas Rocamora E, Bendicho AI, Vazquez EG, Zorio E, Rodriguez FD, Gil Ortuno C, Rodriguez AI, Sanchez-Lopez AJ, Jara Rubio R, Moreno-Docon A, Marcos PJ, Garcia Pavia P, Villa RB, Gimeno Blanes JR. Polymorphisms in ACE, ACE2, AGTR1 genes and severity of COVID-19 disease. PLoS One. 2022 Feb 4;17(2):e0263140. doi: 10.1371/journal.pone.0263140. eCollection 2022. PubMed PMID: 35120165; PubMed Central PMCID: PMC8815985.
AÑO: 2022; IF: 3.7
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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. 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 Mar;54(3):232-239. doi: 10.1038/s41588-021-01007-6. Epub 2022 Feb 24. Erratum In: Nat Genet. 2022 May;54(5):735. PubMed PMID: 35210625; PubMed Central PMCID: PMC9376964.
AÑO: 2022; IF: 30.8
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Martinez-Campelo L, Cruz R, Blanco-Verea A, Moscoso I, Ramos-Luis E, Lage R, Alvarez-Barredo M, Sabater-Molina M, Penafiel-Verdu P, Jimenez-Jaimez J, Rodriguez-Manero M, Brion M. Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome. PLoS One. 2022 Mar 1;17(3):e0263469. doi: 10.1371/journal.pone.0263469. eCollection 2022. PubMed PMID: 35231055; PubMed Central PMCID: PMC8887717.
AÑO: 2022; IF: 3.7
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