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Items: 1 to 20 of 48

1.

[Genetic basis of ischemic heart disease. Do women have distinctive characteristics?].

Notarangelo MF, Coppini L, Guidorossi A, Giacalone R, Merlini PA.

G Ital Cardiol (Rome). 2012 Jun;13(6):386-95. doi: 10.1714/1073.11755. Italian.

PMID:
22622116
2.

Clinical features and outcomes of women with unstable ischemic heart disease: observations from metabolic efficiency with ranolazine for less ischemia in non-ST-elevation acute coronary syndromes-thrombolysis in myocardial infarction 36 (MERLIN-TIMI 36).

Mega JL, Hochman JS, Scirica BM, Murphy SA, Sloan S, McCabe CH, Merlini P, Morrow DA.

Circulation. 2010 Apr 27;121(16):1809-17. doi: 10.1161/CIRCULATIONAHA.109.897231. Epub 2010 Apr 12.

3.

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.

Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C.

Hum Mol Genet. 2007 Apr 15;16(8):887-99. Epub 2007 Feb 26.

PMID:
17324965
4.

9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population.

Ding H, Xu Y, Wang X, Wang Q, Zhang L, Tu Y, Yan J, Wang W, Hui R, Wang CY, Wang DW.

Circ Cardiovasc Genet. 2009 Aug;2(4):338-46. doi: 10.1161/CIRCGENETICS.108.810226. Epub 2009 May 28.

5.

Genetic contributors toward increased risk for ischemic heart disease.

Nordlie MA, Wold LE, Kloner RA.

J Mol Cell Cardiol. 2005 Oct;39(4):667-79. Review.

PMID:
16087188
6.

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.

Topol EJ, McCarthy J, Gabriel S, Moliterno DJ, Rogers WJ, Newby LK, Freedman M, Metivier J, Cannata R, O'Donnell CJ, Kottke-Marchant K, Murugesan G, Plow EF, Stenina O, Daley GQ.

Circulation. 2001 Nov 27;104(22):2641-4.

7.

[Pathophysiology of ischemic heart disease in women].

Andreotti F, Rio T, Gianmarinaro M, Navarese EP, Marchese N, Crea F.

G Ital Cardiol (Rome). 2012 Jun;13(6):396-400. doi: 10.1714/1073.11756. Italian.

PMID:
22622117
8.

Genomic risk variants at 1p13.3, 1q41, and 3q22.3 are associated with subsequent cardiovascular outcomes in healthy controls and in established coronary artery disease.

Ellis KL, Frampton CM, Pilbrow AP, Troughton RW, Doughty RN, Whalley GA, Ellis CJ, Skelton L, Thomson J, Yandle TG, Richards AM, Cameron VA.

Circ Cardiovasc Genet. 2011 Dec;4(6):636-46. doi: 10.1161/CIRCGENETICS.111.960336. Epub 2011 Oct 7.

9.

Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.

Smith JG, Melander O, Lövkvist H, Hedblad B, Engström G, Nilsson P, Carlson J, Berglund G, Norrving B, Lindgren A.

Circ Cardiovasc Genet. 2009 Apr;2(2):159-64. doi: 10.1161/CIRCGENETICS.108.835173. Epub 2009 Feb 12.

10.

CD14 C-260T gene polymorphism and ischemic heart disease susceptibility: a HuGE review and meta-analysis.

Zhang HF, Zhong BL, Zhu WL, Xie SL, Qiu LX, Zhu LG, Wang Y, Lei L.

Genet Med. 2009 Jun;11(6):403-8. doi: 10.1097/GIM.0b013e3181a16cb0. Review.

PMID:
19346955
11.

Fibrinogen gene haplotypes in relation to risk of coronary events and coronary and extracoronary atherosclerosis: the Rotterdam Study.

Kardys I, Uitterlinden AG, Hofman A, Witteman JC, de Maat MP.

Thromb Haemost. 2007 Feb;97(2):288-95.

PMID:
17264959
12.

Identifying the susceptibility genes for coronary artery disease: from hyperbole through doubt to cautious optimism.

Hamsten A, Eriksson P.

J Intern Med. 2008 May;263(5):538-52. doi: 10.1111/j.1365-2796.2008.01958.x. Review.

13.

A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis.

Suzuki S, Yoshimura M, Nakayama M, Abe K, Yamamuro M, Nagayoshi Y, Kojima S, Kaikita K, Sugiyama S, Yasue H, Ogawa H.

Pharmacogenet Genomics. 2007 Nov;17(11):919-30.

PMID:
18075462
14.

Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events.

Predazzi IM, Martínez-Labarga C, Vecchione L, Mango R, Ciccacci C, Amati F, Ottoni C, Crawford MH, Rickards O, Romeo F, Novelli G.

Ann Hum Biol. 2010 Apr;37(2):136-48. doi: 10.3109/03014460903393857.

PMID:
19961348
15.

Inflammatory cytokine gene variants in coronary artery disease patients in Greece.

Manginas A, Tsiavou A, Chaidaroglou A, Giamouzis G, Degiannis D, Panagiotakos D, Cokkinos DV.

Coron Artery Dis. 2008 Dec;19(8):575-82. doi: 10.1097/MCA.0b013e32831286e8.

PMID:
19005292
16.

Genetic variation associated with ischemic heart failure: a HuGE review and meta-analysis.

Kitsios G, Zintzaras E.

Am J Epidemiol. 2007 Sep 15;166(6):619-33. Epub 2007 Jul 21. Review.

PMID:
17644825
17.

Angiotensinogen mutations and risk for ischemic heart disease, myocardial infarction, and ischemic cerebrovascular disease. Six case-control studies from the Copenhagen City Heart Study.

Sethi AA, Tybjaerg-Hansen A, Grønholdt ML, Steffensen R, Schnohr P, Nordestgaard BG.

Ann Intern Med. 2001 May 15;134(10):941-54.

PMID:
11352695
18.

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.

Chen SN, Ballantyne CM, Gotto AM Jr, Marian AJ.

BMC Cardiovasc Disord. 2009 Jan 27;9:3. doi: 10.1186/1471-2261-9-3.

19.

The genetic basis of coronary artery disease: from candidate genes to whole genome analysis.

Franchini M, Peyvandi F, Mannucci PM.

Trends Cardiovasc Med. 2008 Jul;18(5):157-62. doi: 10.1016/j.tcm.2008.04.003. Review.

PMID:
18790385
20.

Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.

Wang Y, Fu W, Xie F, Wang Y, Chu X, Wang H, Shen M, Wang Y, Wang Y, Sun W, Lei R, Yang L, Wu H, Foo J, Liu J, Jin L, Huang W.

J Hum Genet. 2010 Aug;55(8):490-4. doi: 10.1038/jhg.2010.53. Epub 2010 May 20.

PMID:
20485444

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