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Page 1
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Homsy J, Zaidi S, Shen Y, Ware JS, Samocha KE, Karczewski KJ, DePalma SR, McKean D, Wakimoto H, Gorham J, Jin SC, Deanfield J, Giardini A, Porter GA Jr, Kim R, Bilguvar K, López-Giráldez F, Tikhonova I, Mane S, Romano-Adesman A, Qi H, Vardarajan B, Ma L, Daly M, Roberts AE, Russell MW, Mital S, Newburger JW, Gaynor JW, Breitbart RE, Iossifov I, Ronemus M, Sanders SJ, Kaltman JR, Seidman JG, Brueckner M, Gelb BD, Goldmuntz E, Lifton RP, Seidman CE, Chung WK. Homsy J, et al. Among authors: seidman jg, seidman ce. Science. 2015 Dec 4;350(6265):1262-6. doi: 10.1126/science.aac9396. Science. 2015. PMID: 26785492 Free PMC article.
Genetic causes of human heart failure.
Morita H, Seidman J, Seidman CE. Morita H, et al. J Clin Invest. 2005 Mar;115(3):518-26. doi: 10.1172/JCI24351. J Clin Invest. 2005. PMID: 15765133 Free PMC article. Review.
Cardiac myosin-binding protein-C phosphorylation and cardiac function.
Sadayappan S, Gulick J, Osinska H, Martin LA, Hahn HS, Dorn GW 2nd, Klevitsky R, Seidman CE, Seidman JG, Robbins J. Sadayappan S, et al. Among authors: seidman jg, seidman ce. Circ Res. 2005 Nov 25;97(11):1156-63. doi: 10.1161/01.RES.0000190605.79013.4d. Epub 2005 Oct 13. Circ Res. 2005. PMID: 16224063 Free PMC article.
Cardiovascular genomics.
Sabatine MS, Seidman JG, Seidman CE. Sabatine MS, et al. Among authors: seidman jg, seidman ce. Circulation. 2006 Mar 21;113(11):e450-5. doi: 10.1161/CIRCULATIONAHA.105.560151. Circulation. 2006. PMID: 16549641 No abstract available.
Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics.
Alcalai R, Seidman JG, Seidman CE. Alcalai R, et al. Among authors: seidman jg, seidman ce. J Cardiovasc Electrophysiol. 2008 Jan;19(1):104-10. doi: 10.1111/j.1540-8167.2007.00965.x. Epub 2007 Oct 4. J Cardiovasc Electrophysiol. 2008. PMID: 17916152 Review.
585 results