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Items: 1 to 20 of 83

1.

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 Jr, Haynes C, Goldschmidt-Clermont PJ, Shah SH, Kraus WE, Hauser ER, Gregory SG.

Hum Genet. 2011 Jun;129(6):641-54. doi: 10.1007/s00439-011-0959-z. Epub 2011 Feb 5.

2.

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 1;17(9):1318-28. doi: 10.1093/hmg/ddn020. Epub 2008 Jan 18.

3.

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 Jr, Granger CB, Seo D, Goldschmidt-Clermont P, Kraus WE, Gregory SG, Hauser ER, Shah SH.

BMC Genet. 2012 Feb 27;13:12. doi: 10.1186/1471-2156-13-12.

4.

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.

Chen SN, Ballantyne CM, Gotto AM Jr, Marian AJ.

BMC Cardiovasc Disord. 2009 Jan 27;9:3. doi: 10.1186/1471-2261-9-3.

5.

Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.

Crosslin DR, Shah SH, Nelson SC, Haynes CS, Connelly JJ, Gadson S, Goldschmidt-Clermont PJ, Vance JM, Rose J, Granger CB, Seo D, Gregory SG, Kraus WE, Hauser ER.

Hum Genet. 2009 Mar;125(2):217-29. doi: 10.1007/s00439-008-0619-0. Epub 2009 Jan 8.

6.

Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.

Wang L, Hauser ER, Shah SH, Seo D, Sivashanmugam P, Exum ST, Gregory SG, Granger CB, Haines JL, Jones CJ, Crossman D, Haynes C, Kraus WE, Freedman NJ, Pericak-Vance MA, Goldschmidt-Clermont PJ, Vance JM.

Ann Hum Genet. 2008 Jul;72(Pt 4):443-53. doi: 10.1111/j.1469-1809.2008.00433.x. Epub 2008 Jul 3.

7.

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. doi: 10.1371/journal.pgen.1000318. Epub 2009 Jan 2.

8.

Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease.

Horne BD, Camp NJ, Anderson JL, Mower CP, Clarke JL, Kolek MJ, Carlquist JF; Intermountain Heart Collaborative Study Group..

J Am Coll Cardiol. 2007 May 22;49(20):2053-60. Epub 2007 May 4.

9.

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. Epub 2007 Feb 8.

10.

Biological and genetic interaction between tenascin C and neuropeptide S receptor 1 in allergic diseases.

Orsmark-Pietras C, Melén E, Vendelin J, Bruce S, Laitinen A, Laitinen LA, Lauener R, Riedler J, von Mutius E, Doekes G, Wickman M, van Hage M, Pershagen G, Scheynius A, Nyberg F, Kere J; PARSIFAL Genetics Study Group..

Hum Mol Genet. 2008 Jun 1;17(11):1673-82. doi: 10.1093/hmg/ddn058. Epub 2008 Feb 27.

PMID:
18305139
11.

IL-24 gene polymorphisms are associated with cardiometabolic parameters and cardiovascular risk factors but not with premature coronary artery disease: the genetics of atherosclerotic disease Mexican study.

Vargas-Alarcón G, Posadas-Romero C, Villarreal-Molina T, Alvarez-León E, Angeles-Martinez J, Posadas-Sanchez R, Monroy-Muñoz I, Luna-Fuentes S, González-Salazar C, Ramirez-Bello J, Cardoso-Saldaña G, Medina-Urrutia A, Kimura-Hayama E.

J Interferon Cytokine Res. 2014 Sep;34(9):659-66. doi: 10.1089/jir.2013.0081. Epub 2014 Feb 19.

12.

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 22;9:33. doi: 10.1186/1471-2350-9-33.

13.

Polymorphisms in the IL6 gene in Asian Indian families with premature coronary artery disease--the Indian Atherosclerosis Research Study.

Maitra A, Shanker J, Dash D, John S, Sannappa PR, Rao VS, Ramanna JK, Kakkar VV.

Thromb Haemost. 2008 May;99(5):944-50. doi: 10.1160/TH07-11-0686.

PMID:
18449426
14.

Association of polymorphisms in the ALOX15B gene with coronary artery disease.

Wuest SJ, Horn T, Marti-Jaun J, Kühn H, Hersberger M.

Clin Biochem. 2014 Apr;47(6):349-55. doi: 10.1016/j.clinbiochem.2013.12.013. Epub 2013 Dec 27.

PMID:
24373925
15.

Polymorphisms in dipeptidyl peptidase IV gene are associated with the risk of myocardial infarction in patients with atherosclerosis.

Aghili N, Devaney JM, Alderman LO, Zukowska Z, Epstein SE, Burnett MS.

Neuropeptides. 2012 Dec;46(6):367-71. doi: 10.1016/j.npep.2012.10.001. Epub 2012 Oct 31.

PMID:
23122333
16.

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 15;16(8):887-99. Epub 2007 Feb 26.

PMID:
17324965
17.

A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits.

Muiya NP, Wakil S, Al-Najai M, Tahir AI, Baz B, Andres E, Al-Boudari O, Al-Tassan N, Al-Shahid M, Meyer BF, Dzimiri N.

Gene. 2014 Jul 10;544(2):152-8. doi: 10.1016/j.gene.2014.04.064. Epub 2014 Apr 28.

PMID:
24786211
18.

Association of alpha2-Heremans-Schmid glycoprotein polymorphisms with subclinical atherosclerosis.

Lehtinen AB, Burdon KP, Lewis JP, Langefeld CD, Ziegler JT, Rich SS, Register TC, Carr JJ, Freedman BI, Bowden DW.

J Clin Endocrinol Metab. 2007 Jan;92(1):345-52. Epub 2006 Oct 24.

PMID:
17062776
19.

Single nucleotide polymorphisms of ERβ and coronary atherosclerotic disease in Chinese Han women.

Shen C, Chen Z, Mahmoodurrahman M, Chen X.

Int J Clin Exp Pathol. 2015 Feb 1;8(2):2044-50. eCollection 2015 Feb 1.

20.

Low frequency haplotypes of E-selectin polymorphisms G2692A and C1901T give increased protection from coronary artery disease.

Gorący J, Gorący I, Kaczmarczyk M, Parczewski M, Brykczyński M, Clark J, Safranow K, Ciechanowicz A.

Med Sci Monit. 2011 Jun;17(6):CR334-40.

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