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NOS1AP is a genetic modifier of the long-QT syndrome.
Crotti L, Monti MC, Insolia R, Peljto A, Goosen A, Brink PA, Greenberg DA, Schwartz PJ, George AL Jr. Crotti L, et al. Among authors: insolia r. Circulation. 2009 Oct 27;120(17):1657-63. doi: 10.1161/CIRCULATIONAHA.109.879643. Epub 2009 Oct 12. Circulation. 2009. PMID: 19822806 Free PMC article.
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ. Crotti L, et al. Among authors: insolia r. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Wang DW, Rhodes TE, George AL Jr, Schwartz PJ. Arnestad M, et al. Among authors: insolia r. Circulation. 2007 Jan 23;115(3):361-7. doi: 10.1161/CIRCULATIONAHA.106.658021. Epub 2007 Jan 8. Circulation. 2007. PMID: 17210839
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.
Crotti L, Spazzolini C, Schwartz PJ, Shimizu W, Denjoy I, Schulze-Bahr E, Zaklyazminskaya EV, Swan H, Ackerman MJ, Moss AJ, Wilde AA, Horie M, Brink PA, Insolia R, De Ferrari GM, Crimi G. Crotti L, et al. Among authors: insolia r. Circulation. 2007 Nov 20;116(21):2366-75. doi: 10.1161/CIRCULATIONAHA.107.726950. Epub 2007 Nov 5. Circulation. 2007. PMID: 17984373
Prevalence of the congenital long-QT syndrome.
Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G, Gabbarini F, Goulene K, Insolia R, Mannarino S, Mosca F, Nespoli L, Rimini A, Rosati E, Salice P, Spazzolini C. Schwartz PJ, et al. Among authors: insolia r. Circulation. 2009 Nov 3;120(18):1761-7. doi: 10.1161/CIRCULATIONAHA.109.863209. Epub 2009 Oct 19. Circulation. 2009. PMID: 19841298 Free PMC article.
Long-QT syndrome: from genetics to management.
Schwartz PJ, Crotti L, Insolia R. Schwartz PJ, et al. Among authors: insolia r. Circ Arrhythm Electrophysiol. 2012 Aug 1;5(4):868-77. doi: 10.1161/CIRCEP.111.962019. Circ Arrhythm Electrophysiol. 2012. PMID: 22895603 Free PMC article. Review. No abstract available.
Gene symbol: KCNH2. Disease: Long QT syndrome.
Crotti L, Crotti L, Pedrazzini M, Insolia R, Ferrandi C, Cuoretti A, Gandolfi E, Celano G, Dagradi F, Schwartz PJ. Crotti L, et al. Among authors: insolia r. Hum Genet. 2008 Jun;123(5):540. Hum Genet. 2008. PMID: 20960613 No abstract available.
Gene symbol: KCNQ1. Disease: Long QT syndrome.
Crotti L, Insolia R, Ferrandi C, Pedrazzini M, Cuoretti A, Gandolfi E, Sanzo A, Dagradi F, Schwartz PJ. Crotti L, et al. Among authors: insolia r. Hum Genet. 2008 Jun;123(5):541. Hum Genet. 2008. PMID: 20960614 No abstract available.
Gene symbol: KCNH2. Disease: Long QT syndrome.
Crotti L, Pedrazzini M, Insolia R, Ferrandi C, Cuoretti A, Celano G, Gandolfi E, Dagradi F, Schwartz PJ. Crotti L, et al. Among authors: insolia r. Hum Genet. 2008 Jun;123(5):541. Hum Genet. 2008. PMID: 20960616 Free article. No abstract available.
27 results