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Items: 1 to 20 of 138

1.

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

Broadbent HM, Peden JF, Lorkowski S, Goel A, Ongen H, Green F, Clarke R, Collins R, Franzosi MG, Tognoni G, Seedorf U, Rust S, Eriksson P, Hamsten A, Farrall M, Watkins H; PROCARDIS consortium..

Hum Mol Genet. 2008 Mar 15;17(6):806-14. Epub 2007 Nov 29.

PMID:
18048406
2.

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

Shen GQ, Li L, Rao S, Abdullah KG, Ban JM, Lee BS, Park JE, Wang QK.

Arterioscler Thromb Vasc Biol. 2008 Feb;28(2):360-5. Epub 2007 Nov 29.

3.

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.

4.

A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits.

Muiya NP, Wakil S, Al-Najai M, Tahir AI, Baz B, Andres E, Al-Boudari O, Al-Tassan N, Al-Shahid M, Meyer BF, Dzimiri N.

Gene. 2014 Jul 10;544(2):152-8. doi: 10.1016/j.gene.2014.04.064. Epub 2014 Apr 28.

PMID:
24786211
5.

Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.

Horne BD, Carlquist JF, Muhlestein JB, Bair TL, Anderson JL.

Circ Cardiovasc Genet. 2008 Dec;1(2):85-92. doi: 10.1161/CIRCGENETICS.108.793158.

6.

Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population.

Gori F, Specchia C, Pietri S, Crociati L, Barlera S, Franciosi M, Nicolucci A, Signorini S, Brambilla P, Franzosi MG; GISSI Prevenzione Investigators.; SIBioC-GISSI Prevenzione Group..

BMC Med Genet. 2010 Apr 19;11:60. doi: 10.1186/1471-2350-11-60.

7.

9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response.

Harismendy O, Notani D, Song X, Rahim NG, Tanasa B, Heintzman N, Ren B, Fu XD, Topol EJ, Rosenfeld MG, Frazer KA.

Nature. 2011 Feb 10;470(7333):264-8. doi: 10.1038/nature09753.

8.

Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction risk.

Fan M, Dandona S, McPherson R, Allayee H, Hazen SL, Wells GA, Roberts R, Stewart AF.

Circ Cardiovasc Genet. 2013 Aug;6(4):372-80. doi: 10.1161/CIRCGENETICS.113.000104. Epub 2013 May 31.

9.

The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non-insulin-dependent) diabetes mellitus.

Lacquemant C, Froguel P, Lobbens S, Izzo P, Dina C, Ruiz J.

Diabet Med. 2004 Jul;21(7):776-81.

PMID:
15209773
10.

Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population.

Çakmak HA, Bayoğlu B, Durmaz E, Can G, Karadağ B, Cengiz M, Vural VA, Yüksel H.

Anatol J Cardiol. 2015 Mar;15(3):196-203. doi: 10.5152/akd.2014.5285. Epub 2014 Apr 8.

11.

Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease.

Gong Y, Beitelshees AL, Cooper-DeHoff RM, Lobmeyer MT, Langaee TY, Wu J, Cresci S, Province MA, Spertus JA, Pepine CJ, Johnson JA.

Circ Cardiovasc Genet. 2011 Apr;4(2):169-78. doi: 10.1161/CIRCGENETICS.110.959296. Epub 2011 Mar 3.

12.

Identification of susceptibility variants in ADIPOR1 gene associated with type 2 diabetes, coronary artery disease and the comorbidity of type 2 diabetes and coronary artery disease.

Jin Z, Pu L, Sun L, Chen W, Nan N, Li H, Zhu H, Yang X, Wang N, Hui J, Zhang Y, Zhou Q, Zhao F, Yang F, Shi X, Zhu X, Yang Y, Zhang W, Zheng C, Li X, Yang D, Jia R, Meng S, Yang Z.

PLoS One. 2014 Jun 26;9(6):e100339. doi: 10.1371/journal.pone.0100339. eCollection 2014.

13.

Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes.

Doria A, Wojcik J, Xu R, Gervino EV, Hauser TH, Johnstone MT, Nolan D, Hu FB, Warram JH.

JAMA. 2008 Nov 26;300(20):2389-97. doi: 10.1001/jama.2008.649.

14.

Haplotypes on 9p21 modify the risk for coronary artery disease among Indians.

AshokKumar M, Emmanuel C, Dhandapany PS, Rani DS, SaiBabu R, Cherian KM, Thangaraj K.

DNA Cell Biol. 2011 Feb;30(2):105-10. doi: 10.1089/dna.2010.1046. Epub 2010 Sep 21.

PMID:
20858033
15.

Association of +45(T/G) and +276(G/T) polymorphisms in the adiponectin gene with coronary artery disease in a population of Iranian patients with type 2 diabetes.

Esteghamati A, Mansournia N, Nakhjavani M, Mansournia MA, Nikzamir A, Abbasi M.

Mol Biol Rep. 2012 Apr;39(4):3791-7. doi: 10.1007/s11033-011-1156-9. Epub 2011 Jul 10.

PMID:
21744264
16.

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.

17.

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
18.

New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3.

Alshahid M, Wakil SM, Al-Najai M, Muiya NP, Elhawari S, Gueco D, Andres E, Hagos S, Mazhar N, Meyer BF, Dzimiri N.

Hum Genomics. 2013 Jun 5;7:15. doi: 10.1186/1479-7364-7-15.

19.

Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk.

Jansen H, Loley C, Lieb W, Pencina MJ, Nelson CP, Kathiresan S, Peloso GM, Voight BF, Reilly MP, Assimes TL, Boerwinkle E, Hengstenberg C, Laaksonen R, McPherson R, Roberts R, Thorsteinsdottir U, Peters A, Gieger C, Rawal R, Thompson JR, König IR; CARDIoGRAM consortium., Vasan RS, Erdmann J, Samani NJ, Schunkert H.

Atherosclerosis. 2015 Aug;241(2):419-26. doi: 10.1016/j.atherosclerosis.2015.05.033. Epub 2015 Jun 3.

20.

Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).

Abdullah KG, Li L, Shen GQ, Hu Y, Yang Y, MacKinlay KG, Topol EJ, Wang QK.

Ann Hum Genet. 2008 Sep;72(Pt 5):654-7. doi: 10.1111/j.1469-1809.2008.00454.x. Epub 2008 May 26.

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