210 related articles for article (PubMed ID: 22369142)
1. Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5.
Nolan DK; Sutton B; Haynes C; Johnson J; Sebek J; Dowdy E; Crosslin D; Crossman D; Sketch MH; Granger CB; Seo D; Goldschmidt-Clermont P; Kraus WE; Gregory SG; Hauser ER; Shah SH
BMC Genet; 2012 Feb; 13():12. PubMed ID: 22369142
[TBL] [Abstract][Full Text] [Related]
2. Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.
Shah SH; Kraus WE; Crossman DC; Granger CB; Haines JL; Jones CJ; Mooser V; Huang L; Haynes C; Dowdy E; Vega GL; Grundy SM; Vance JM; Hauser ER
Ann Hum Genet; 2006 Nov; 70(Pt 6):738-48. PubMed ID: 17044848
[TBL] [Abstract][Full Text] [Related]
3. Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
Wang L; Hauser ER; Shah SH; Pericak-Vance MA; Haynes C; Crosslin D; Harris M; Nelson S; Hale AB; Granger CB; Haines JL; Jones CJ; Crossman D; Seo D; Gregory SG; Kraus WE; Goldschmidt-Clermont PJ; Vance JM
Am J Hum Genet; 2007 Apr; 80(4):650-63. PubMed ID: 17357071
[TBL] [Abstract][Full Text] [Related]
4. Genetic variation and association mapping for 12 agronomic traits in indica rice.
Lu Q; Zhang M; Niu X; Wang S; Xu Q; Feng Y; Wang C; Deng H; Yuan X; Yu H; Wang Y; Wei X
BMC Genomics; 2015 Dec; 16():1067. PubMed ID: 26673149
[TBL] [Abstract][Full Text] [Related]
5. Genetic and functional association of FAM5C with myocardial infarction.
Connelly JJ; Shah SH; Doss JF; Gadson S; Nelson S; Crosslin DR; Hale AB; Lou X; Wang T; Haynes C; Seo D; Crossman DC; Mooser V; Granger CB; Jones CJ; Kraus WE; Hauser ER; Gregory SG
BMC Med Genet; 2008 Apr; 9():33. PubMed ID: 18430236
[TBL] [Abstract][Full Text] [Related]
6. Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.
Minear MA; Crosslin DR; Sutton BS; Connelly JJ; Nelson SC; Gadson-Watson S; Wang T; Seo D; Vance JM; Sketch MH; Haynes C; Goldschmidt-Clermont PJ; Shah SH; Kraus WE; Hauser ER; Gregory SG
Hum Genet; 2011 Jun; 129(6):641-54. PubMed ID: 21298289
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.
Sutton BS; Crosslin DR; Shah SH; Nelson SC; Bassil A; Hale AB; Haynes C; Goldschmidt-Clermont PJ; Vance JM; Seo D; Kraus WE; Gregory SG; Hauser ER
Hum Mol Genet; 2008 May; 17(9):1318-28. PubMed ID: 18204052
[TBL] [Abstract][Full Text] [Related]
8. The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol.
Samani NJ; Braund PS; Erdmann J; Götz A; Tomaszewski M; Linsel-Nitschke P; Hajat C; Mangino M; Hengstenberg C; Stark K; Ziegler A; Caulfield M; Burton PR; Schunkert H; Tobin MD
J Mol Med (Berl); 2008 Nov; 86(11):1233-41. PubMed ID: 18649068
[TBL] [Abstract][Full Text] [Related]
9. A two-step genetic study on quantitative precursors of coronary artery disease in a homogeneous Indian population: case-control association discovery and validation by transmission-disequilibrium test.
Mallik S; Majumder PP
J Biosci; 2011 Dec; 36(5):857-68. PubMed ID: 22116284
[TBL] [Abstract][Full Text] [Related]
10. Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol.
Pare G; Serre D; Brisson D; Anand SS; Montpetit A; Tremblay G; Engert JC; Hudson TJ; Gaudet D
Am J Hum Genet; 2007 Apr; 80(4):673-82. PubMed ID: 17357073
[TBL] [Abstract][Full Text] [Related]
11. Replication and fine-mapping of genetic predictors of lipid traits in African-Americans.
Feng Q; Wei WQ; Levinson RT; Mosley JD; Stein CM
J Hum Genet; 2017 Oct; 62(10):895-901. PubMed ID: 28539666
[TBL] [Abstract][Full Text] [Related]
12. Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study.
Linsel-Nitschke P; Götz A; Erdmann J; Braenne I; Braund P; Hengstenberg C; Stark K; Fischer M; Schreiber S; El Mokhtari NE; Schaefer A; Schrezenmeir J; Rubin D; Hinney A; Reinehr T; Roth C; Ortlepp J; Hanrath P; Hall AS; Mangino M; Lieb W; Lamina C; Heid IM; Doering A; Gieger C; Peters A; Meitinger T; Wichmann HE; König IR; Ziegler A; Kronenberg F; Samani NJ; Schunkert H; ;
PLoS One; 2008 Aug; 3(8):e2986. PubMed ID: 18714375
[TBL] [Abstract][Full Text] [Related]
13. Association of the HNF1A polymorphisms and serum lipid traits, the risk of coronary artery disease and ischemic stroke.
Zhou YJ; Yin RX; Hong SC; Yang Q; Cao XL; Chen WX
J Gene Med; 2017 Jan; 19(1-2):. PubMed ID: 28035729
[TBL] [Abstract][Full Text] [Related]
14. Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease.
Tada H; Won HH; Melander O; Yang J; Peloso GM; Kathiresan S
Circ Cardiovasc Genet; 2014 Oct; 7(5):583-7. PubMed ID: 25170055
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide linkage analyses and candidate gene fine mapping for HDL3 cholesterol: the Framingham Study.
Yang Q; Lai CQ; Parnell L; Cupples LA; Adiconis X; Zhu Y; Wilson PW; Housman DE; Shearman AM; D'Agostino RB; Ordovas JM
J Lipid Res; 2005 Jul; 46(7):1416-25. PubMed ID: 15805549
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families.
Gao H; Li L; Rao S; Shen G; Xi Q; Chen S; Zhang Z; Wang K; Ellis SG; Chen Q; Topol EJ; Wang QK
PLoS One; 2014; 9(12):e113935. PubMed ID: 25485937
[TBL] [Abstract][Full Text] [Related]
17. Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.
Pranav Chand R; Kumar AS; Anuj K; Vishnupriya S; Mohan Reddy B
PLoS One; 2016; 11(6):e0153720. PubMed ID: 27257688
[TBL] [Abstract][Full Text] [Related]
18. Mendelian randomization studies in coronary artery disease.
Jansen H; Samani NJ; Schunkert H
Eur Heart J; 2014 Aug; 35(29):1917-24. PubMed ID: 24917639
[TBL] [Abstract][Full Text] [Related]
19. Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.
Shah SH; Freedman NJ; Zhang L; Crosslin DR; Stone DH; Haynes C; Johnson J; Nelson S; Wang L; Connelly JJ; Muehlbauer M; Ginsburg GS; Crossman DC; Jones CJ; Vance J; Sketch MH; Granger CB; Newgard CB; Gregory SG; Goldschmidt-Clermont PJ; Kraus WE; Hauser ER
PLoS Genet; 2009 Jan; 5(1):e1000318. PubMed ID: 19119412
[TBL] [Abstract][Full Text] [Related]
20. Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping.
Andrew T; Maniatis N; Carbonaro F; Liew SH; Lau W; Spector TD; Hammond CJ
PLoS Genet; 2008 Oct; 4(10):e1000220. PubMed ID: 18846214
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
