414 related articles for article (PubMed ID: 18048406)
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;
Hum Mol Genet; 2008 Mar; 17(6):806-14. PubMed ID: 18048406
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 18048766
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 23729007
[TBL] [Abstract][Full Text] [Related]
4. The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.
Chen SN; Ballantyne CM; Gotto AM; Marian AJ
BMC Cardiovasc Disord; 2009 Jan; 9():3. PubMed ID: 19173706
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 19956784
[TBL] [Abstract][Full Text] [Related]
6. 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; 544(2):152-8. PubMed ID: 24786211
[TBL] [Abstract][Full Text] [Related]
7. Genetic and epigenetic associations of ANRIL with coronary artery disease and risk factors.
Xu B; Xu Z; Chen Y; Lu N; Shu Z; Tan X
BMC Med Genomics; 2021 Oct; 14(1):240. PubMed ID: 34615528
[TBL] [Abstract][Full Text] [Related]
8. 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; ;
BMC Med Genet; 2010 Apr; 11():60. PubMed ID: 20403154
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 15209773
[TBL] [Abstract][Full Text] [Related]
10. Associations between low serum levels of ANRIL and some common gene SNPs in Iranian patients with premature coronary artery disease.
Taheri Bajgan E; Zahedmehr A; Shakerian F; Maleki M; Bakhshandeh H; Mowla SJ; Malakootian M
Sci Rep; 2024 Jan; 14(1):1244. PubMed ID: 38218954
[TBL] [Abstract][Full Text] [Related]
11. 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; 470(7333):264-8. PubMed ID: 21307941
[TBL] [Abstract][Full Text] [Related]
12. 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; 16(8):887-99. PubMed ID: 17324965
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 21744264
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 21372283
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 25333979
[TBL] [Abstract][Full Text] [Related]
16. 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; 9(6):e100339. PubMed ID: 24967709
[TBL] [Abstract][Full Text] [Related]
17. 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; 300(20):2389-97. PubMed ID: 19033589
[TBL] [Abstract][Full Text] [Related]
18. Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
Cunnington MS; Santibanez Koref M; Mayosi BM; Burn J; Keavney B
PLoS Genet; 2010 Apr; 6(4):e1000899. PubMed ID: 20386740
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 20858033
[TBL] [Abstract][Full Text] [Related]
20. 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; 7(1):15. PubMed ID: 23738802
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]