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Page 1
Heritability of Atrial Fibrillation.
Weng LC, Choi SH, Klarin D, Smith JG, Loh PR, Chaffin M, Roselli C, Hulme OL, Lunetta KL, Dupuis J, Benjamin EJ, Newton-Cheh C, Kathiresan S, Ellinor PT, Lubitz SA. Weng LC, et al. Among authors: kathiresan s. Circ Cardiovasc Genet. 2017 Dec;10(6):e001838. doi: 10.1161/CIRCGENETICS.117.001838. Circ Cardiovasc Genet. 2017. PMID: 29237688 Free PMC article.
On the significance of linkage studies of complex traits.
Newton-Cheh C, Larson M, Kathiresan S, O'Donnell C. Newton-Cheh C, et al. Among authors: kathiresan s. Am J Hum Genet. 2004 Jul;75(1):151-2; author reply 152-4. doi: 10.1086/422220. Am J Hum Genet. 2004. PMID: 15164311 Free PMC article. No abstract available.
On the interpretation of genetic association studies.
Kathiresan S, Newton-Cheh C, Gerszten RE. Kathiresan S, et al. Eur Heart J. 2004 Aug;25(16):1378-81. doi: 10.1016/j.ehj.2004.06.035. Eur Heart J. 2004. PMID: 15321696 No abstract available.
Common genetic variation at the endothelial nitric oxide synthase locus and relations to brachial artery vasodilator function in the community.
Kathiresan S, Larson MG, Vasan RS, Guo CY, Vita JA, Mitchell GF, Keyes MJ, Newton-Cheh C, Musone SL, Lochner AL, Drake JA, Levy D, O'Donnell CJ, Hirschhorn JN, Benjamin EJ. Kathiresan S, et al. Circulation. 2005 Sep 6;112(10):1419-27. doi: 10.1161/CIRCULATIONAHA.105.544619. Epub 2005 Aug 29. Circulation. 2005. PMID: 16129794
Aging syndrome genes and premature coronary artery disease.
Low AF, O'Donnell CJ, Kathiresan S, Everett B, Chae CU, Shaw SY, Ellinor PT, MacRae CA. Low AF, et al. Among authors: kathiresan s. BMC Med Genet. 2005 Oct 31;6:38. doi: 10.1186/1471-2350-6-38. BMC Med Genet. 2005. PMID: 16262891 Free PMC article.
476 results