83 related articles for article (PubMed ID: 19955472)
1. 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]
2. Health-related disparities: influence of environmental factors.
Olden K; White SL
Med Clin North Am; 2005 Jul; 89(4):721-38. PubMed ID: 15925646
[TBL] [Abstract][Full Text] [Related]
3. [Genetic variation of the cholesterol ester transfer protein gene and the prevalence of coronary artery disease. The AtheroGene case control study].
Blankenberg S; Tiret L; Bickel C; Schlitt A; Jungmair W; Genth-Zotz S; Lubos E; Espinola-Klein C; Rupprecht HJ
Z Kardiol; 2004; 93 Suppl 4():IV16-23. PubMed ID: 15085362
[TBL] [Abstract][Full Text] [Related]
4. Translating genomic analyses into improved management of coronary artery disease.
Johansen CT; Lanktree MB; Hegele RA
Future Cardiol; 2010 Jul; 6(4):507-21. PubMed ID: 20608823
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. A comprehensive linkage analysis for myocardial infarction and its related risk factors.
Broeckel U; Hengstenberg C; Mayer B; Holmer S; Martin LJ; Comuzzie AG; Blangero J; Nürnberg P; Reis A; Riegger GA; Jacob HJ; Schunkert H
Nat Genet; 2002 Feb; 30(2):210-4. PubMed ID: 11818963
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide association studies in atherothrombosis.
Lotta LA
Eur J Intern Med; 2010 Apr; 21(2):74-8. PubMed ID: 20206874
[TBL] [Abstract][Full Text] [Related]
8. Association of cholesteryl ester transfer protein -629C > A polymorphism with high-density lipoprotein cholesterol levels in coronary artery disease patients.
Tanrikulu S; Ademoglu E; Gurdol F; Mutlu-Turkoglu U; Bilge AK; Nisanci Y
Cell Biochem Funct; 2009 Oct; 27(7):452-7. PubMed ID: 19784962
[TBL] [Abstract][Full Text] [Related]
9. Coronary artery disease: an example case study.
Barrett JH
Methods Mol Biol; 2011; 713():215-25. PubMed ID: 21153622
[TBL] [Abstract][Full Text] [Related]
10. The LDL receptor-related protein (LRP1/A2MR) and coronary atherosclerosis--novel genomic variants and functional consequences.
Schulz S; Schagdarsurengin U; Greiser P; Birkenmeier G; Müller-Werdan U; Hagemann M; Riemann D; Werdan K; Gläser C
Hum Mutat; 2002 Nov; 20(5):404. PubMed ID: 12402342
[TBL] [Abstract][Full Text] [Related]
11. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
Jensen HK
Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
[TBL] [Abstract][Full Text] [Related]
12. Genetics of myocardial infarction: a progress report.
Schunkert H; Erdmann J; Samani NJ
Eur Heart J; 2010 Apr; 31(8):918-25. PubMed ID: 20219748
[TBL] [Abstract][Full Text] [Related]
13. Toward a road map for global -omics: a primer on -omic technologies.
Coughlin SS
Am J Epidemiol; 2014 Dec; 180(12):1188-95. PubMed ID: 25409464
[TBL] [Abstract][Full Text] [Related]
14. Recent progress in understanding the genetic susceptibility to osteoporosis.
Zmuda JM; Cauley JA; Ferrell RE
Genet Epidemiol; 1999; 16(4):356-67. PubMed ID: 10207717
[TBL] [Abstract][Full Text] [Related]
15. Plasma triglycerides and type III hyperlipidemia are independently associated with premature familial coronary artery disease.
Hopkins PN; Wu LL; Hunt SC; Brinton EA
J Am Coll Cardiol; 2005 Apr; 45(7):1003-12. PubMed ID: 15808755
[TBL] [Abstract][Full Text] [Related]
16. Prediction of individual genetic risk of complex disease.
Wray NR; Goddard ME; Visscher PM
Curr Opin Genet Dev; 2008 Jun; 18(3):257-63. PubMed ID: 18682292
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factors.
Morabia A; Cayanis E; Costanza MC; Ross BM; Flaherty MS; Alvin GB; Das K; Gilliam TC
Hum Mol Genet; 2003 Nov; 12(21):2733-43. PubMed ID: 12966036
[TBL] [Abstract][Full Text] [Related]
19. A customized genetic approach to the number one killer: coronary artery disease.
Roberts R
Curr Opin Cardiol; 2008 Nov; 23(6):629-33. PubMed ID: 18830080
[TBL] [Abstract][Full Text] [Related]
20. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Weiss LA
Expert Rev Mol Diagn; 2009 Nov; 9(8):795-803. PubMed ID: 19895225
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]