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Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.
Campuzano O, Fernandez-Falgueras A, Sarquella-Brugada G, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Coll M, Fiol V, Iglesias A, Perez-Serra A, Mates J, Del Olmo B, Ferrer C, Alcalde M, Puigmulé M, Mademont-Soler I, Pico F, Lopez L, Tiron C, Brugada J, Brugada R. Campuzano O, et al. Among authors: brugada r, brugada j. Front Genet. 2019 May 15;10:450. doi: 10.3389/fgene.2019.00450. eCollection 2019. Front Genet. 2019. PMID: 31156706 Free PMC article.
Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
Mates J, Mademont-Soler I, Fernandez-Falgueras A, Sarquella-Brugada G, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Coll M, Fiol V, Iglesias A, Perez-Serra A, Olmo BD, Alcalde M, Puigmulé M, Pico F, Lopez L, Ferrer C, Tiron C, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O. Mates J, et al. Among authors: brugada r, brugada j. Forensic Sci Int Genet. 2020 Jul;47:102281. doi: 10.1016/j.fsigen.2020.102281. Epub 2020 Mar 20. Forensic Sci Int Genet. 2020. PMID: 32248082 Review.
Genetics of channelopathies associated with sudden cardiac death.
Campuzano O, Sarquella-Brugada G, Brugada R, Brugada J. Campuzano O, et al. Among authors: brugada r, brugada j. Glob Cardiol Sci Pract. 2015 Oct 13;2015(3):39. doi: 10.5339/gcsp.2015.39. eCollection 2015. Glob Cardiol Sci Pract. 2015. PMID: 26566530 Free PMC article. Review.
Brugada syndrome and p.E61X_RANGRF.
Campuzano O, Berne P, Selga E, Allegue C, Iglesias A, Brugada J, Brugada R. Campuzano O, et al. Among authors: brugada r, brugada j. Cardiol J. 2014;21(2):121-7. doi: 10.5603/CJ.a2013.0125. Epub 2013 Oct 21. Cardiol J. 2014. PMID: 24142675
Brugada Syndrome and PKP2: Evidences and uncertainties.
Campuzano O, Fernández-Falgueras A, Iglesias A, Brugada R. Campuzano O, et al. Among authors: brugada r. Int J Cardiol. 2016 Jul 1;214:403-5. doi: 10.1016/j.ijcard.2016.03.194. Epub 2016 Apr 7. Int J Cardiol. 2016. PMID: 27085656
Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.
Toro R, Pérez-Serra A, Campuzano O, Moncayo-Arlandi J, Allegue C, Iglesias A, Mangas A, Brugada R. Toro R, et al. Among authors: brugada r. PLoS One. 2016 Jul 8;11(7):e0158730. doi: 10.1371/journal.pone.0158730. eCollection 2016. PLoS One. 2016. PMID: 27391596 Free PMC article.
Familial dilated cardiomyopathy: A multidisciplinary entity, from basic screening to novel circulating biomarkers.
de Gonzalo-Calvo D, Quezada M, Campuzano O, Perez-Serra A, Broncano J, Ayala R, Ramos M, Llorente-Cortes V, Blasco-Turrión S, Morales FJ, Gonzalez P, Brugada R, Mangas A, Toro R. de Gonzalo-Calvo D, et al. Among authors: brugada r. Int J Cardiol. 2017 Feb 1;228:870-880. doi: 10.1016/j.ijcard.2016.11.045. Epub 2016 Nov 8. Int J Cardiol. 2017. PMID: 27889554 Review.
Genetics of familial atrial fibrillation.
Campuzano O, Brugada R. Campuzano O, et al. Among authors: brugada r. Europace. 2009 Oct;11(10):1267-71. doi: 10.1093/europace/eup199. Epub 2009 Aug 6. Europace. 2009. PMID: 19666641 Review.
404 results