230 related articles for article (PubMed ID: 23616109)
21. Molecular genetics of coronary artery disease.
Ozaki K; Tanaka T
J Hum Genet; 2016 Jan; 61(1):71-7. PubMed ID: 26134515
[TBL] [Abstract][Full Text] [Related]
22. Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders.
Björkegren JLM; Kovacic JC; Dudley JT; Schadt EE
J Am Coll Cardiol; 2015 Mar; 65(8):830-845. PubMed ID: 25720628
[TBL] [Abstract][Full Text] [Related]
23. Shared genetic aetiology of coronary artery disease and atherosclerotic stroke - 2015.
Kessler T; Erdmann J; Dichgans M; Schunkert H
Curr Atheroscler Rep; 2015 Apr; 17(4):498. PubMed ID: 25690589
[TBL] [Abstract][Full Text] [Related]
24. Gene scanning and heart attack risk.
Barth AS; Tomaselli GF
Trends Cardiovasc Med; 2016 Apr; 26(3):260-5. PubMed ID: 26277204
[TBL] [Abstract][Full Text] [Related]
25. FHL5 Controls Vascular Disease-Associated Gene Programs in Smooth Muscle Cells.
Wong D; Auguste G; Lino Cardenas CL; Turner AW; Chen Y; Song Y; Ma L; Perry RN; Aherrahrou R; Kuppusamy M; Yang C; Mosquera JV; Dube CJ; Khan MD; Palmore M; Kalra J; Kavousi M; Peyser PA; Matic L; Hedin U; Manichaikul A; Sonkusare SK; Civelek M; Kovacic JC; Björkegren JLM; Malhotra R; Miller CL
Circ Res; 2023 Apr; 132(9):1144-1161. PubMed ID: 37017084
[TBL] [Abstract][Full Text] [Related]
26. [Importance of modern genome-wide studies for the risk of myocardial infarction].
Kessler T; Erdmann J; Schunkert H
Internist (Berl); 2014 Feb; 55(2):141-7. PubMed ID: 24399470
[TBL] [Abstract][Full Text] [Related]
27. Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.
Wauters E; Carruthers KF; Buysschaert I; Dunbar DR; Peuteman G; Belmans A; Budaj A; Van de Werf F; Lambrechts D; Fox KA
Eur Heart J; 2013 Apr; 34(13):993-1001. PubMed ID: 23161703
[TBL] [Abstract][Full Text] [Related]
28. The impact of susceptibility loci for coronary artery disease on other vascular domains and recurrence risk.
Tragante V; Doevendans PA; Nathoe HM; van der Graaf Y; Spiering W; Algra A; de Borst GJ; de Bakker PI; Asselbergs FW;
Eur Heart J; 2013 Oct; 34(37):2896-904. PubMed ID: 23828831
[TBL] [Abstract][Full Text] [Related]
29. Molecular genetics of coronary artery disease: measuring the phenotype.
Samani NJ
Clin Sci (Lond); 1998 Dec; 95(6):645-6. PubMed ID: 9831687
[No Abstract] [Full Text] [Related]
30. Druggability of Coronary Artery Disease Risk Loci.
Tragante V; Hemerich D; Alshabeeb M; Brænne I; Lempiäinen H; Patel RS; den Ruijter HM; Barnes MR; Moore JH; Schunkert H; Erdmann J; Asselbergs FW
Circ Genom Precis Med; 2018 Aug; 11(8):e001977. PubMed ID: 30354342
[TBL] [Abstract][Full Text] [Related]
31. The discovery of genes implicated in myocardial infarction.
Ouwehand WH;
J Thromb Haemost; 2009 Jul; 7 Suppl 1():305-7. PubMed ID: 19630822
[TBL] [Abstract][Full Text] [Related]
32. Invited commentary: genetic variants and individual- and societal-level risk factors.
Coughlin SS
Am J Epidemiol; 2010 Jan; 171(1):24-6. PubMed ID: 19955472
[TBL] [Abstract][Full Text] [Related]
33. 2018 George Lyman Duff Memorial Lecture: Genetics and Genomics of Coronary Artery Disease: A Decade of Progress.
McPherson R
Arterioscler Thromb Vasc Biol; 2019 Oct; 39(10):1925-1937. PubMed ID: 31462092
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Genetics of myocardial infarction.
Topol EJ
J Invasive Cardiol; 2004 Jul; 16(7 Suppl):32S-35S. PubMed ID: 23573570
[TBL] [Abstract][Full Text] [Related]
36. Plasma levels of the anti-coagulation protein C and the risk of ischaemic heart disease. A Mendelian randomisation study.
Schooling CM; Zhong Y
Thromb Haemost; 2017 Jan; 117(2):262-268. PubMed ID: 27882376
[TBL] [Abstract][Full Text] [Related]
37. Association of Connexin37 C1019T with myocardial infarction and coronary artery disease: a meta-analysis.
Wen D; Du X; Nie SP; Dong JZ; Ma CS
Exp Gerontol; 2014 Oct; 58():203-7. PubMed ID: 24937033
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. [Identification of risk genes for myocardial infarction by genome wide association studies].
Linsel-Nitschke P; Erdmann J; Schunkert H
Hamostaseologie; 2010 Nov; 30(4):230-5. PubMed ID: 21057710
[TBL] [Abstract][Full Text] [Related]
40. [Molecular genetics of coronary artery diseases].
Ozaki K; Tanaka T
Nihon Rinsho; 2016 Jun; 74 Suppl 4 Pt 1():306-13. PubMed ID: 27534188
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
