1295 related articles for article (PubMed ID: 17478679)
1. A common variant on chromosome 9p21 affects the risk of myocardial infarction.
Helgadottir A; Thorleifsson G; Manolescu A; Gretarsdottir S; Blondal T; Jonasdottir A; Jonasdottir A; Sigurdsson A; Baker A; Palsson A; Masson G; Gudbjartsson DF; Magnusson KP; Andersen K; Levey AI; Backman VM; Matthiasdottir S; Jonsdottir T; Palsson S; Einarsdottir H; Gunnarsdottir S; Gylfason A; Vaccarino V; Hooper WC; Reilly MP; Granger CB; Austin H; Rader DJ; Shah SH; Quyyumi AA; Gulcher JR; Thorgeirsson G; Thorsteinsdottir U; Kong A; Stefansson K
Science; 2007 Jun; 316(5830):1491-3. PubMed ID: 17478679
[TBL] [Abstract][Full Text] [Related]
2. The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.
Wahlstrand B; Orho-Melander M; Delling L; Kjeldsen S; Narkiewicz K; Almgren P; Hedner T; Melander O
J Hypertens; 2009 Apr; 27(4):769-73. PubMed ID: 19293724
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.
Smith JG; Melander O; Lövkvist H; Hedblad B; Engström G; Nilsson P; Carlson J; Berglund G; Norrving B; Lindgren A
Circ Cardiovasc Genet; 2009 Apr; 2(2):159-64. PubMed ID: 20031580
[TBL] [Abstract][Full Text] [Related]
5. Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.
Ozaki K; Ohnishi Y; Iida A; Sekine A; Yamada R; Tsunoda T; Sato H; Sato H; Hori M; Nakamura Y; Tanaka T
Nat Genet; 2002 Dec; 32(4):650-4. PubMed ID: 12426569
[TBL] [Abstract][Full Text] [Related]
6. Association between the coronary artery disease risk locus on chromosome 9p21.3 and abdominal aortic aneurysm.
Bown MJ; Braund PS; Thompson J; London NJ; Samani NJ; Sayers RD
Circ Cardiovasc Genet; 2008 Oct; 1(1):39-42. PubMed ID: 20031540
[TBL] [Abstract][Full Text] [Related]
7. Association between PPARalpha gene polymorphisms and myocardial infarction.
Reinhard W; Stark K; Sedlacek K; Fischer M; Baessler A; Neureuther K; Weber S; Kaess B; Wiedmann S; Mitsching S; Lieb W; Erdmann J; Meisinger C; Doering A; Tolle R; Jeron A; Riegger G; Hengstenberg C
Clin Sci (Lond); 2008 Nov; 115(10):301-8. PubMed ID: 18336366
[TBL] [Abstract][Full Text] [Related]
8. Common genetic variation in the prothrombin gene, hormone therapy, and incident nonfatal myocardial infarction in postmenopausal women.
Hindorff LA; Psaty BM; Carlson CS; Heckbert SR; Lumley T; Smith NL; Lemaitre RN; Rieder MJ; Nickerson DA; Reiner AP
Am J Epidemiol; 2006 Apr; 163(7):600-7. PubMed ID: 16467413
[TBL] [Abstract][Full Text] [Related]
9. Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors.
Wiedmann S; Neureuther K; Stark K; Reinhard W; Kallmünzer B; Baessler A; Fischer M; Linsel-Nitschke P; Erdmann J; Schunkert H; Hengstenberg C
Obesity (Silver Spring); 2009 Jul; 17(7):1390-5. PubMed ID: 19197259
[TBL] [Abstract][Full Text] [Related]
10. Chromosome 9p21 and cardiovascular disease: the story unfolds.
Samani NJ; Schunkert H
Circ Cardiovasc Genet; 2008 Dec; 1(2):81-4. PubMed ID: 20031549
[No Abstract] [Full Text] [Related]
11. The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factors.
Stark K; Neureuther K; Sedlacek K; Hengstenberg W; Fischer M; Baessler A; Wiedmann S; Jeron A; Holmer S; Erdmann J; Schunkert H; Hengstenberg C
Clin Sci (Lond); 2007 Aug; 113(4):213-8. PubMed ID: 17472578
[TBL] [Abstract][Full Text] [Related]
12. A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality.
Ellis KL; Pilbrow AP; Frampton CM; Doughty RN; Whalley GA; Ellis CJ; Palmer BR; Skelton L; Yandle TG; Palmer SC; Troughton RW; Richards AM; Cameron VA
Circ Cardiovasc Genet; 2010 Jun; 3(3):286-93. PubMed ID: 20400779
[TBL] [Abstract][Full Text] [Related]
13. Candidate gene polymorphisms and the 9p21 locus in acute coronary syndromes.
Tousoulis D; Briasoulis A; Papageorgiou N; Antoniades C; Stefanadis C
Trends Mol Med; 2008 Oct; 14(10):441-9. PubMed ID: 18786860
[TBL] [Abstract][Full Text] [Related]
14. Variant on 9p21 is strongly associated with coronary artery disease but lacks association with myocardial infarction and disease severity in a population in Western India.
Bhanushali AA; Parmar N; Contractor A; Shah VT; Das BR
Arch Med Res; 2011 Aug; 42(6):469-74. PubMed ID: 21925557
[TBL] [Abstract][Full Text] [Related]
15. Polymorphisms in the paraoxonase and endothelial nitric oxide synthase genes and the risk of early-onset myocardial infarction.
Morray B; Goldenberg I; Moss AJ; Zareba W; Ryan D; McNitt S; Eberly SW; Glazko G; Mathew J
Am J Cardiol; 2007 Apr; 99(8):1100-5. PubMed ID: 17437735
[TBL] [Abstract][Full Text] [Related]
16. Common variation in cytochrome P450 epoxygenase genes and the risk of incident nonfatal myocardial infarction and ischemic stroke.
Marciante KD; Totah RA; Heckbert SR; Smith NL; Lemaitre RN; Lumley T; Rice KM; Hindorff LA; Bis JC; Hartman B; Psaty BM
Pharmacogenet Genomics; 2008 Jun; 18(6):535-43. PubMed ID: 18496133
[TBL] [Abstract][Full Text] [Related]
17. [Genetic variants, cardiovascular risk and genome-wide association studies].
Companioni O; Rodríguez Esparragón F; Fernández-Aceituno AM; Rodríguez Pérez JC
Rev Esp Cardiol; 2011 Jun; 64(6):509-14. PubMed ID: 21550161
[TBL] [Abstract][Full Text] [Related]
18. Haplotypes of the caspase-1 gene, plasma caspase-1 levels, and cardiovascular risk.
Blankenberg S; Godefroy T; Poirier O; Rupprecht HJ; Barbaux S; Bickel C; Nicaud V; Schnabel R; Kee F; Morrison C; Evans A; Lackner KJ; Cambien F; Münzel T; Tiret L;
Circ Res; 2006 Jul; 99(1):102-8. PubMed ID: 16778130
[TBL] [Abstract][Full Text] [Related]
19. Common polymorphisms in the cannabinoid CB2 receptor gene (CNR2) are not associated with myocardial infarction and cardiovascular risk factors.
Reinhard W; Stark K; Neureuther K; Sedlacek K; Fischer M; Baessler A; Weber S; Kaess B; Wiedmann S; Erdmann J; Lieb W; Jeron A; Riegger G; Hengstenberg C
Int J Mol Med; 2008 Aug; 22(2):165-74. PubMed ID: 18636169
[TBL] [Abstract][Full Text] [Related]
20. Associations with myocardial infarction of six polymorphisms selected from a three-stage genome-wide association study.
Horne BD; Carlquist JF; Muhlestein JB; Nicholas ZP; Anderson JL;
Am Heart J; 2007 Nov; 154(5):969-75. PubMed ID: 17967605
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
