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577 results

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Page 1
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies.
Reichart D, Lindberg EL, Maatz H, Miranda AMA, Viveiros A, Shvetsov N, Gärtner A, Nadelmann ER, Lee M, Kanemaru K, Ruiz-Orera J, Strohmenger V, DeLaughter DM, Patone G, Zhang H, Woehler A, Lippert C, Kim Y, Adami E, Gorham JM, Barnett SN, Brown K, Buchan RJ, Chowdhury RA, Constantinou C, Cranley J, Felkin LE, Fox H, Ghauri A, Gummert J, Kanda M, Li R, Mach L, McDonough B, Samari S, Shahriaran F, Yapp C, Stanasiuk C, Theotokis PI, Theis FJ, van den Bogaerdt A, Wakimoto H, Ware JS, Worth CL, Barton PJR, Lee YA, Teichmann SA, Milting H, Noseda M, Oudit GY, Heinig M, Seidman JG, Hubner N, Seidman CE. Reichart D, et al. Among authors: seidman jg, seidman ce. Science. 2022 Aug 5;377(6606):eabo1984. doi: 10.1126/science.abo1984. Epub 2022 Aug 5. Science. 2022. PMID: 35926050 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.
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.
Comparative proteomics profiling of a phospholamban mutant mouse model of dilated cardiomyopathy reveals progressive intracellular stress responses.
Gramolini AO, Kislinger T, Alikhani-Koopaei R, Fong V, Thompson NJ, Isserlin R, Sharma P, Oudit GY, Trivieri MG, Fagan A, Kannan A, Higgins DG, Huedig H, Hess G, Arab S, Seidman JG, Seidman CE, Frey B, Perry M, Backx PH, Liu PP, MacLennan DH, Emili A. Gramolini AO, et al. Among authors: seidman jg, seidman ce. Mol Cell Proteomics. 2008 Mar;7(3):519-33. doi: 10.1074/mcp.M700245-MCP200. Epub 2007 Nov 30. Mol Cell Proteomics. 2008. PMID: 18056057 Free article.
Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting.
Fox AA, Collard CD, Shernan SK, Seidman CE, Seidman JG, Liu KY, Muehlschlegel JD, Perry TE, Aranki SF, Lange C, Herman DS, Meitinger T, Lichtner P, Body SC. Fox AA, et al. Among authors: seidman jg, seidman ce. Anesthesiology. 2009 Apr;110(4):738-47. doi: 10.1097/aln.0b013e31819c7496. Anesthesiology. 2009. PMID: 19326473 Free PMC article.
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. Among authors: seidman jg, seidman ce. Ann Otol Rhinol Laryngol. 2009 Sep;118(9):670-6. doi: 10.1177/000348940911800912. Ann Otol Rhinol Laryngol. 2009. PMID: 19810609 Free PMC article.
577 results