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Items: 1 to 20 of 107

1.

Single variants can explain the association between coronary heart disease and haplotypes in the apolipoprotein(a) locus.

Shiffman D, Louie JZ, Rowland CM, Malloy MJ, Kane JP, Devlin JJ.

Atherosclerosis. 2010 Sep;212(1):193-6. doi: 10.1016/j.atherosclerosis.2010.05.009. Epub 2010 May 13.

PMID:
20605575
2.

Interaction effects between Paraoxonase 1 variants and cigarette smoking on risk of coronary heart disease in a Singaporean Chinese population.

Han Y, Dorajoo R, Ke T, Ayala B, Chang X, Khor CC, van Dam RM, Yuan JM, Koh WP, Liu J, Goh DY, Friedlander Y, Heng CK.

Atherosclerosis. 2015 May;240(1):40-5. doi: 10.1016/j.atherosclerosis.2015.01.042. Epub 2015 Feb 25.

3.
4.

Genetic variants associated with Lp(a) lipoprotein level and coronary disease.

Clarke R, Peden JF, Hopewell JC, Kyriakou T, Goel A, Heath SC, Parish S, Barlera S, Franzosi MG, Rust S, Bennett D, Silveira A, Malarstig A, Green FR, Lathrop M, Gigante B, Leander K, de Faire U, Seedorf U, Hamsten A, Collins R, Watkins H, Farrall M; PROCARDIS Consortium.

N Engl J Med. 2009 Dec 24;361(26):2518-28. doi: 10.1056/NEJMoa0902604.

5.

Two rare variants explain association with acute myocardial infarction in an extended genomic region including the apolipoprotein(A) gene.

Koch W, Mueller JC, Schrempf M, Wolferstetter H, Kirchhofer J, Schömig A, Kastrati A.

Ann Hum Genet. 2013 Jan;77(1):47-55. doi: 10.1111/j.1469-1809.2012.00739.x.

6.

APOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy men.

Ken-Dror G, Talmud PJ, Humphries SE, Drenos F.

Mol Med. 2010 Sep-Oct;16(9-10):389-99. doi: 10.2119/molmed.2010.00044. Epub 2010 May 20.

7.

A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease.

Luke MM, Kane JP, Liu DM, Rowland CM, Shiffman D, Cassano J, Catanese JJ, Pullinger CR, Leong DU, Arellano AR, Tong CH, Movsesyan I, Naya-Vigne J, Noordhof C, Feric NT, Malloy MJ, Topol EJ, Koschinsky ML, Devlin JJ, Ellis SG.

Arterioscler Thromb Vasc Biol. 2007 Sep;27(9):2030-6. Epub 2007 Jun 14.

8.

Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men.

Ken-Dror G, Drenos F, Humphries SE, Talmud PJ, Hingorani AD, Kivimäki M, Kumari M, Bauer KA, Morrissey JH, Ireland HA.

J Thromb Haemost. 2010 Nov;8(11):2394-403. doi: 10.1111/j.1538-7836.2010.04035.x.

9.

Positive correlation between variants of lipid metabolism‑related genes and coronary heart disease.

Zhang LN, Liu PP, Zhou J, Huang RS, Yuan F, Fei LJ, Huang Y, Xu L, Hao LM, Qiu XJ, Le Y, Yang X, Xu W, Huang X, Ye M, Lian J, Duan S.

Mol Med Rep. 2013 Jul;8(1):260-6. doi: 10.3892/mmr.2013.1454. Epub 2013 May 2.

10.

[Advances in the Association between Apolipoprotein (a) Gene Polymorphisms and Coronary Heart Disease].

Zhu L, L Z, Song YY.

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2015 Aug;37(4):482-8. doi: 10.3881/j.issn.1000-503X.2015.04.020. Chinese.

11.

Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart disease.

Maubaret CG, Salpea KD, Romanoski CE, Folkersen L, Cooper JA, Stephanou C, Li KW, Palmen J, Hamsten A, Neil A, Stephens JW, Lusis AJ, Eriksson P, Talmud PJ, Humphries SE; Simon Broome Research Group; EARSII consortium.

PLoS One. 2013 Dec 12;8(12):e83122. doi: 10.1371/journal.pone.0083122. eCollection 2013.

12.

Lipoprotein(a) genetic variants associated with coronary and peripheral vascular disease but not with stroke risk in the Heart Protection Study.

Hopewell JC, Clarke R, Parish S, Armitage J, Lathrop M, Hager J, Collins R; Heart Protection Study Collaborative Group.

Circ Cardiovasc Genet. 2011 Feb;4(1):68-73. doi: 10.1161/CIRCGENETICS.110.958371. Epub 2011 Jan 20.

13.

Functional SNPs in HSPA1A gene predict risk of coronary heart disease.

He M, Guo H, Yang X, Zhang X, Zhou L, Cheng L, Zeng H, Hu FB, Tanguay RM, Wu T.

PLoS One. 2009;4(3):e4851. doi: 10.1371/journal.pone.0004851. Epub 2009 Mar 31.

14.

A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.

Kyriakou T, Seedorf U, Goel A, Hopewell JC, Clarke R, Watkins H, Farrall M; PROCARDIS Consortium.

Arterioscler Thromb Vasc Biol. 2014 Sep;34(9):2095-9. doi: 10.1161/ATVBAHA.114.303462. Epub 2014 Jun 12.

15.

Four genetic polymorphisms of paraoxonase gene and risk of coronary heart disease: a meta-analysis based on 88 case-control studies.

Wang M, Lang X, Zou L, Huang S, Xu Z.

Atherosclerosis. 2011 Feb;214(2):377-85. doi: 10.1016/j.atherosclerosis.2010.11.028. Epub 2010 Nov 26.

PMID:
21146823
16.

Associations between single nucleotide polymorphisms on chromosome 9p21 and risk of coronary heart disease in Chinese Han population.

Zhou L, Zhang X, He M, Cheng L, Chen Y, Hu FB, Wu T.

Arterioscler Thromb Vasc Biol. 2008 Nov;28(11):2085-9. doi: 10.1161/ATVBAHA.108.176065. Epub 2008 Aug 28.

17.

Plasminogen activator inhibitor-1 gene: selection of tagging single nucleotide polymorphisms and association with coronary heart disease.

Su S, Chen S, Zhao J, Huang J, Wang X, Chen R, Gu D.

Arterioscler Thromb Vasc Biol. 2006 Apr;26(4):948-54. Epub 2006 Jan 19.

18.

Meta-analyses of HFE variants in coronary heart disease.

Lian J, Xu L, Huang Y, Le Y, Jiang D, Yang X, Xu W, Huang X, Dong C, Ye M, Zhou J, Duan S.

Gene. 2013 Sep 15;527(1):167-73. doi: 10.1016/j.gene.2013.06.034. Epub 2013 Jun 20.

PMID:
23792061
19.

Renalase gene polymorphism in patients with hypertension and concomitant coronary heart disease.

Li X, Jiang W, Li L, Huang R, Yang Q, Yang Y, Hong Y, Tang X.

Kidney Blood Press Res. 2014;39(1):9-16. doi: 10.1159/000355771. Epub 2014 Apr 30.

20.

LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography.

Santos PC, Bueno CT, Lemos PA, Krieger JE, Pereira AC.

Lipids Health Dis. 2014 Apr 29;13:74. doi: 10.1186/1476-511X-13-74.

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