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476 results

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Page 1
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL; NHLBI Exome Sequencing Project; Girelli D, Martinelli N, Farlow DN, DePristo MA, Roberts R, Stewart AF, Saleheen D, Danesh J, Epstein SE, Sivapalaratnam S, Hovingh GK, Kastelein JJ, Samani NJ, Schunkert H, Erdmann J, Shah SH, Kraus WE, Davies R, Nikpay M, Johansen CT, Wang J, Hegele RA, Hechter E, Marz W, Kleber ME, Huang J, Johnson AD, Li M, Burke GL, Gross M, Liu Y, Assimes TL, Heiss G, Lange EM, Folsom AR, Taylor HA, Olivieri O, Hamsten A, Clarke R, Reilly DF, Yin W, Rivas MA, Donnelly P, Rossouw JE, Psaty BM, Herrington DM, Wilson JG, Rich SS, Bamshad MJ, Tracy RP, Cupples LA, Rader DJ, Reilly MP, Spertus JA, Cresci S, Hartiala J, Tang WH, Hazen SL, Allayee H, Reiner AP, Carlson CS, Kooperberg C, Jackson RD, Boerwinkle E, Lander ES, Schwartz SM, Siscovick DS, McPherson R, Tybjaerg-Hansen A, Abecasis GR, Watkins H, Nickerson DA, Ardissino D, Sunyaev SR, O'Donnell CJ, Altshuler D, Gabriel S, Kathiresan S. Do R, et al. Among authors: kathiresan s. Nature. 2015 Feb 5;518(7537):102-6. doi: 10.1038/nature13917. Epub 2014 Dec 10. Nature. 2015. PMID: 25487149 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