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Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Glessner JT, Bick AG, Ito K, Homsy J, Rodriguez-Murillo L, Fromer M, Mazaika E, Vardarajan B, Italia M, Leipzig J, DePalma SR, Golhar R, Sanders SJ, Yamrom B, Ronemus M, Iossifov I, Willsey AJ, State MW, Kaltman JR, White PS, Shen Y, Warburton D, Brueckner M, Seidman C, Goldmuntz E, Gelb BD, Lifton R, Seidman J, Hakonarson H, Chung WK. Glessner JT, et al. Among authors: seidman j, seidman c. Circ Res. 2014 Oct 24;115(10):884-896. doi: 10.1161/CIRCRESAHA.115.304458. Epub 2014 Sep 9. Circ Res. 2014. PMID: 25205790 Free PMC article. Clinical Trial.
Genetic causes of human heart failure.
Morita H, Seidman J, Seidman CE. Morita H, et al. Among authors: seidman j, seidman ce. 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. Circulation. 2006 Mar 21;113(11):e450-5. doi: 10.1161/CIRCULATIONAHA.105.560151. Circulation. 2006. PMID: 16549641 No abstract available.
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Greenway SC, Pereira AC, Lin JC, DePalma SR, Israel SJ, Mesquita SM, Ergul E, Conta JH, Korn JM, McCarroll SA, Gorham JM, Gabriel S, Altshuler DM, Quintanilla-Dieck Mde L, Artunduaga MA, Eavey RD, Plenge RM, Shadick NA, Weinblatt ME, De Jager PL, Hafler DA, Breitbart RE, Seidman JG, Seidman CE. Greenway SC, et al. Among authors: seidman jg, seidman ce. Nat Genet. 2009 Aug;41(8):931-5. doi: 10.1038/ng.415. Epub 2009 Jul 13. Nat Genet. 2009. PMID: 19597493 Free PMC article.
Locus for familial migrainous vertigo disease maps to chromosome 5q35.
Bahmad F Jr, DePalma SR, Merchant SN, Bezerra RL, Oliveira CA, Seidman CE, Seidman JG. Bahmad F Jr, et al. Ann Otol Rhinol Laryngol. 2009 Sep;118(9):670-6. doi: 10.1177/000348940911800912. Ann Otol Rhinol Laryngol. 2009. PMID: 19810609 Free PMC article.
Genetics of hypertrophic cardiomyopathy.
Konno T, Chang S, Seidman JG, Seidman CE. Konno T, et al. Curr Opin Cardiol. 2010 May;25(3):205-9. doi: 10.1097/HCO.0b013e3283375698. Curr Opin Cardiol. 2010. PMID: 20124998 Free PMC article. Review.
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