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Items: 1 to 20 of 117


Stroke Risk Factors, Genetics, and Prevention.

Boehme AK, Esenwa C, Elkind MS.

Circ Res. 2017 Feb 3;120(3):472-495. doi: 10.1161/CIRCRESAHA.116.308398. Review.


Variants in ANRIL gene correlated with its expression contribute to myocardial infarction risk.

Cheng J, Cai MY, Chen YN, Li ZC, Tang SS, Yang XL, Chen C, Liu X, Xiong XD.

Oncotarget. 2017 Feb 21;8(8):12607-12619. doi: 10.18632/oncotarget.14721.


Challenges in Translating GWAS Results to Clinical Care.

Scheinfeldt LB, Schmidlen TJ, Gerry NP, Christman MF.

Int J Mol Sci. 2016 Aug 4;17(8). pii: E1267. doi: 10.3390/ijms17081267.


Genome-wide association analysis and replication of coronary artery disease in South Korea suggests a causal variant common to diverse populations.

Cho EY, Jang Y, Shin ES, Jang HY, Yoo YK, Kim S, Jang JH, Lee JY, Yun MH, Park MY, Chae JS, Lim JW, Shin DJ, Park S, Lee JH, Han BG, Rae KH, Cardon LR, Morris AP, Lee JE, Clarke GM.

Heart Asia. 2010 Sep 18;2(1):104-8. doi: 10.1136/ha.2009.001370. eCollection 2010.


The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease.

Kessler T, Vilne B, Schunkert H.

EMBO Mol Med. 2016 Jul 1;8(7):688-701. doi: 10.15252/emmm.201506174. Print 2016 Jul. Review.


9p21 locus rs10757278 is associated with advanced carotid atherosclerosis in a gender-specific manner.

Zivotić I, Djurić T, Stanković A, Djordjević A, Končar I, Davidović L, Alavantić D, Zivković M.

Exp Biol Med (Maywood). 2016 Jun;241(11):1210-6. doi: 10.1177/1535370216636718. Epub 2016 Mar 3.


The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.

Carey DJ, Fetterolf SN, Davis FD, Faucett WA, Kirchner HL, Mirshahi U, Murray MF, Smelser DT, Gerhard GS, Ledbetter DH.

Genet Med. 2016 Sep;18(9):906-13. doi: 10.1038/gim.2015.187. Epub 2016 Feb 11.


Analysis of Genomic Regions Associated With Coronary Artery Disease Reveals Continent-Specific Single Nucleotide Polymorphisms in North African Populations.

Zanetti D, Via M, Carreras-Torres R, Esteban E, Chaabani H, Anaibar F, Harich N, Habbal R, Ghalim N, Moral P.

J Epidemiol. 2016 May 5;26(5):264-71. doi: 10.2188/jea.JE20150034. Epub 2016 Jan 16.


Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.

Chen S, Wang X, Wang J, Zhao Y, Wang D, Tan C, Fa J, Zhang R, Wang F, Xu C, Huang Y, Li S, Yin D, Xiong X, Li X, Chen Q, Tu X, Yang Y, Xia Y, Xu C, Wang QK.

Atherosclerosis. 2016 Mar;246:148-156. doi: 10.1016/j.atherosclerosis.2016.01.008. Epub 2016 Jan 8.


Genetics of ischaemic stroke in young adults.

Terni E, Giannini N, Brondi M, Montano V, Bonuccelli U, Mancuso M.

BBA Clin. 2014 Dec 29;3:96-106. doi: 10.1016/j.bbacli.2014.12.004. eCollection 2015 Jun. Review.


The Relation between eNOS -786 C/T, 4 a/b, MMP-13 rs640198 G/T, Eotaxin 426 C/T, -384 A/G, and 67 G/A Polymorphisms and Long-Term Outcome in Patients with Coronary Artery Disease.

Kincl V, Máchal J, Drozdová A, Panovský R, Vašků A.

Dis Markers. 2015;2015:232048. doi: 10.1155/2015/232048. Epub 2015 Sep 30.


Polymorphism on Chromosome 9p21.3 Is Associated with Severity and Early-Onset CAD in Type 2 Diabetic Tunisian Population.

Abid K, Mili D, Kenani A.

Dis Markers. 2015;2015:792679. doi: 10.1155/2015/792679. Epub 2015 Aug 31.


A Lead ANRIL Polymorphism Is Associated with Elevated CRP Levels in Periodontitis: A Pilot Case-Control Study.

Teeuw WJ, Laine ML, Bizzarro S, Loos BG.

PLoS One. 2015 Sep 8;10(9):e0137335. doi: 10.1371/journal.pone.0137335. eCollection 2015.


Using Hamming Distance as Information for SNP-Sets Clustering and Testing in Disease Association Studies.

Wang C, Kao WH, Hsiao CK.

PLoS One. 2015 Aug 24;10(8):e0135918. doi: 10.1371/journal.pone.0135918. eCollection 2015.


The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey).

Helgeland Ø, Hertel JK, Molven A, Ræder H, Platou CG, Midthjell K, Hveem K, Nygård O, Njølstad PR, Johansson S.

Int J Endocrinol. 2015;2015:164652. doi: 10.1155/2015/164652. Epub 2015 May 18.


Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery.

Kertai MD, Li YJ, Li YW, Ji Y, Alexander J, Newman MF, Smith PK, Joseph D, Mathew JP, Podgoreanu MV; Duke Perioperative Genetics and Safety Outcomes (PEGASUS) Investigative Team.

BMJ Open. 2015 May 6;5(5):e006920. doi: 10.1136/bmjopen-2014-006920.


Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran.

Foroughmand AM, Nikkhah E, Galehdari H, Jadbabaee MH.

Cell J. 2015 Spring;17(1):89-98. Epub 2015 Apr 8.


The chromosome 9p21 variant interacts with vegetable and wine intake to influence the risk of cardiovascular disease: a population based cohort study.

Hindy G, Ericson U, Hamrefors V, Drake I, Wirfält E, Melander O, Orho-Melander M.

BMC Med Genet. 2014 Dec 31;15:1220. doi: 10.1186/s12881-014-0138-x. eCollection 2014.


Interaction of type 2 diabetes mellitus with chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case-control study in Chinese population.

Zhang LW, Li JP, Duan FF, Liu ZK, Zhan SY, Hu YH, Jiang J, Zhang Y, Huo Y, Chen DF.

BMC Cardiovasc Disord. 2014 Nov 27;14:170. doi: 10.1186/1471-2261-14-170.

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