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Page 1
Genetic association analyses highlight biological pathways underlying mitral valve prolapse.
Dina C, Bouatia-Naji N, Tucker N, Delling FN, Toomer K, Durst R, Perrocheau M, Fernandez-Friera L, Solis J; PROMESA investigators; Le Tourneau T, Chen MH, Probst V, Bosse Y, Pibarot P, Zelenika D, Lathrop M, Hercberg S, Roussel R, Benjamin EJ, Bonnet F, Lo SH, Dolmatova E, Simonet F, Lecointe S, Kyndt F, Redon R, Le Marec H, Froguel P, Ellinor PT, Vasan RS, Bruneval P, Markwald RR, Norris RA, Milan DJ, Slaugenhaupt SA, Levine RA, Schott JJ, Hagege AA; MVP-France; Jeunemaitre X; Leducq Transatlantic MITRAL Network. Dina C, et al. Among authors: ellinor pt. Nat Genet. 2015 Oct;47(10):1206-11. doi: 10.1038/ng.3383. Epub 2015 Aug 24. Nat Genet. 2015. PMID: 26301497 Free PMC article.
Risk stratification in the long-QT syndrome.
Ellinor PT, Milan DJ, MacRae CA. Ellinor PT, et al. N Engl J Med. 2003 Aug 28;349(9):908-9; author reply 908-9. doi: 10.1056/NEJM200308283490916. N Engl J Med. 2003. PMID: 12944579 No abstract available.
Factors affecting error in integration of electroanatomic mapping with CT and MR imaging during catheter ablation of atrial fibrillation.
Heist EK, Chevalier J, Holmvang G, Singh JP, Ellinor PT, Milan DJ, D'Avila A, Mela T, Ruskin JN, Mansour M. Heist EK, et al. Among authors: ellinor pt. J Interv Card Electrophysiol. 2006 Oct;17(1):21-7. doi: 10.1007/s10840-006-9060-2. Epub 2007 Jan 25. J Interv Card Electrophysiol. 2006. PMID: 17252200 Clinical Trial.
Cardiac sodium channel mutation in atrial fibrillation.
Ellinor PT, Nam EG, Shea MA, Milan DJ, Ruskin JN, MacRae CA. Ellinor PT, et al. Heart Rhythm. 2008 Jan;5(1):99-105. doi: 10.1016/j.hrthm.2007.09.015. Epub 2007 Sep 19. Heart Rhythm. 2008. PMID: 18088563
Development of a risk score for atrial fibrillation (Framingham Heart Study): a community-based cohort study.
Schnabel RB, Sullivan LM, Levy D, Pencina MJ, Massaro JM, D'Agostino RB Sr, Newton-Cheh C, Yamamoto JF, Magnani JW, Tadros TM, Kannel WB, Wang TJ, Ellinor PT, Wolf PA, Vasan RS, Benjamin EJ. Schnabel RB, et al. Among authors: ellinor pt. Lancet. 2009 Feb 28;373(9665):739-45. doi: 10.1016/S0140-6736(09)60443-8. Lancet. 2009. PMID: 19249635 Free PMC article.
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
Benjamin EJ, Rice KM, Arking DE, Pfeufer A, van Noord C, Smith AV, Schnabel RB, Bis JC, Boerwinkle E, Sinner MF, Dehghan A, Lubitz SA, D'Agostino RB Sr, Lumley T, Ehret GB, Heeringa J, Aspelund T, Newton-Cheh C, Larson MG, Marciante KD, Soliman EZ, Rivadeneira F, Wang TJ, Eiríksdottir G, Levy D, Psaty BM, Li M, Chamberlain AM, Hofman A, Vasan RS, Harris TB, Rotter JI, Kao WH, Agarwal SK, Stricker BH, Wang K, Launer LJ, Smith NL, Chakravarti A, Uitterlinden AG, Wolf PA, Sotoodehnia N, Köttgen A, van Duijn CM, Meitinger T, Mueller M, Perz S, Steinbeck G, Wichmann HE, Lunetta KL, Heckbert SR, Gudnason V, Alonso A, Kääb S, Ellinor PT, Witteman JC. Benjamin EJ, et al. Among authors: ellinor pt. Nat Genet. 2009 Aug;41(8):879-81. doi: 10.1038/ng.416. Epub 2009 Jul 13. Nat Genet. 2009. PMID: 19597492 Free PMC article.
536 results