These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
224 related articles for article (PubMed ID: 25333979)
1. 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]
2. The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population. Kashyap S; Kumar S; Agarwal V; Misra DP; Rai MK; Kapoor A Gene; 2018 Mar; 648():89-96. PubMed ID: 29309886 [TBL] [Abstract][Full Text] [Related]
3. Variants in 9p21 Predicts Severity of Coronary Artery Disease in a Chinese Han Population. Jing J; Su L; Zeng Y; Tang X; Wei J; Wang L; Zhou L Ann Hum Genet; 2016 Sep; 80(5):274-81. PubMed ID: 27461153 [TBL] [Abstract][Full Text] [Related]
4. Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population. Kalpana B; Murthy DK; Balakrishna N; Aiyengar MT Indian Heart J; 2019; 71(3):263-271. PubMed ID: 31543200 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Common SNP-based haplotype analysis of the 9p21.3 gene locus as predictor coronary artery disease in Tanzanian population. Akan G; Kisenge P; Sanga TS; Mbugi E; Adolf I; Turkcan MK; Janabi M; Atalar F Cell Mol Biol (Noisy-le-grand); 2019 Jul; 65(6):33-43. PubMed ID: 31472045 [TBL] [Abstract][Full Text] [Related]
9. Chromosome 9p21 rs10757278 polymorphism is associated with the risk of metabolic syndrome. Bayoglu B; Cakmak HA; Yuksel H; Can G; Karadag B; Ulutin T; Vural VA; Cengiz M Mol Cell Biochem; 2013 Jul; 379(1-2):77-85. PubMed ID: 23535969 [TBL] [Abstract][Full Text] [Related]
10. The assessment of the relationship between variations in the apelin gene and coronary artery disease in Turkish population. Pakizeh E; Çoşkunpınar E; Oltulu YM; Çakmak HA; İkitimur B; Işık Sağlam ZM; Karimova A; Vural VA Anatol J Cardiol; 2015 Sep; 15(9):716-21. PubMed ID: 25592107 [TBL] [Abstract][Full Text] [Related]
11. Polymorphism on chromosome 9p21.3 contributes to early-onset and severity of coronary artery disease in non-diabetic and type 2 diabetic patients. Wang W; Peng WH; Lu L; Zhang RY; Zhang Q; Wang LJ; Chen QJ; Shen WF Chin Med J (Engl); 2011 Jan; 124(1):66-71. PubMed ID: 21362310 [TBL] [Abstract][Full Text] [Related]
12. Association of polymorphisms in 9p21 region with CAD in North Indian population: replication of SNPs identified through GWAS. Kumar J; Yumnam S; Basu T; Ghosh A; Garg G; Karthikeyan G; Sengupta S Clin Genet; 2011 Jun; 79(6):588-93. PubMed ID: 20718794 [TBL] [Abstract][Full Text] [Related]
13. The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population. Cheng X; Shi L; Nie S; Wang F; Li X; Xu C; Wang P; Yang B; Li Q; Pan Z; Li Y; Xia H; Zheng C; Ke Y; Wu Y; Tang T; Yan X; Yang Y; Xia N; Yao R; Wang B; Ma X; Zeng Q; Tu X; Liao Y; Wang QK Diabetes; 2011 Feb; 60(2):680-4. PubMed ID: 21270277 [TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 18505420 [TBL] [Abstract][Full Text] [Related]
15. Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease. Schunkert H; Götz A; Braund P; McGinnis R; Tregouet DA; Mangino M; Linsel-Nitschke P; Cambien F; Hengstenberg C; Stark K; Blankenberg S; Tiret L; Ducimetiere P; Keniry A; Ghori MJ; Schreiber S; El Mokhtari NE; Hall AS; Dixon RJ; Goodall AH; Liptau H; Pollard H; Schwarz DF; Hothorn LA; Wichmann HE; König IR; Fischer M; Meisinger C; Ouwehand W; Deloukas P; Thompson JR; Erdmann J; Ziegler A; Samani NJ; Circulation; 2008 Apr; 117(13):1675-84. PubMed ID: 18362232 [TBL] [Abstract][Full Text] [Related]
16. Gene dosage of the common variant 9p21 predicts severity of coronary artery disease. Dandona S; Stewart AF; Chen L; Williams K; So D; O'Brien E; Glover C; Lemay M; Assogba O; Vo L; Wang YQ; Labinaz M; Wells GA; McPherson R; Roberts R J Am Coll Cardiol; 2010 Aug; 56(6):479-86. PubMed ID: 20670758 [TBL] [Abstract][Full Text] [Related]
17. Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease. Mendonça I; dos Reis RP; Pereira A; Café H; Serrão M; Sousa AC; Freitas AI; Guerra G; Freitas S; Freitas C; Ornelas I; Brehm A; Araújo JJ Rev Port Cardiol; 2011 Jun; 30(6):575-91. PubMed ID: 21874923 [TBL] [Abstract][Full Text] [Related]
18. The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease. Patel RS; Su S; Neeland IJ; Ahuja A; Veledar E; Zhao J; Helgadottir A; Holm H; Gulcher JR; Stefansson K; Waddy S; Vaccarino V; Zafari AM; Quyyumi AA Eur Heart J; 2010 Dec; 31(24):3017-23. PubMed ID: 20729229 [TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 26417150 [TBL] [Abstract][Full Text] [Related]
20. Polymorphisms in the long non-coding RNA CDKN2B-AS1 may contribute to higher systolic blood pressure levels in hypertensive patients. Bayoglu B; Yuksel H; Cakmak HA; Dirican A; Cengiz M Clin Biochem; 2016 Jul; 49(10-11):821-7. PubMed ID: 26944720 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]