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Items: 1 to 20 of 291

1.

Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction risk.

Fan M, Dandona S, McPherson R, Allayee H, Hazen SL, Wells GA, Roberts R, Stewart AF.

Circ Cardiovasc Genet. 2013 Aug;6(4):372-80. doi: 10.1161/CIRCGENETICS.113.000104. Epub 2013 May 31.

2.

Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.

Horne BD, Carlquist JF, Muhlestein JB, Bair TL, Anderson JL.

Circ Cardiovasc Genet. 2008 Dec;1(2):85-92. doi: 10.1161/CIRCGENETICS.108.793158.

3.

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

Shen GQ, Li L, Rao S, Abdullah KG, Ban JM, Lee BS, Park JE, Wang QK.

Arterioscler Thromb Vasc Biol. 2008 Feb;28(2):360-5. Epub 2007 Nov 29.

4.

Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease.

Gong Y, Beitelshees AL, Cooper-DeHoff RM, Lobmeyer MT, Langaee TY, Wu J, Cresci S, Province MA, Spertus JA, Pepine CJ, Johnson JA.

Circ Cardiovasc Genet. 2011 Apr;4(2):169-78. doi: 10.1161/CIRCGENETICS.110.959296. Epub 2011 Mar 3.

5.

Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.

Anderson JL, Horne BD, Kolek MJ, Muhlestein JB, Mower CP, Park JJ, May HT, Camp NJ, Carlquist JF.

Am Heart J. 2008 Dec;156(6):1155-1162.e2. doi: 10.1016/j.ahj.2008.07.006. Epub 2008 Oct 11.

PMID:
19033013
6.

A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.

Shen GQ, Girelli D, Li L, Rao S, Archacki S, Olivieri O, Martinelli N, Park JE, Chen Q, Topol EJ, Wang QK.

Circ Cardiovasc Genet. 2014 Aug;7(4):514-20. doi: 10.1161/CIRCGENETICS.113.000321. Epub 2014 May 27.

7.

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.

8.

Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.

Chan K, Patel RS, Newcombe P, Nelson CP, Qasim A, Epstein SE, Burnett S, Vaccarino VL, Zafari AM, Shah SH, Anderson JL, Carlquist JF, Hartiala J, Allayee H, Hinohara K, Lee BS, Erl A, Ellis KL, Goel A, Schaefer AS, El Mokhtari NE, Goldstein BA, Hlatky MA, Go AS, Shen GQ, Gong Y, Pepine C, Laxton RC, Whittaker JC, Tang WH, Johnson JA, Wang QK, Assimes TL, Nöthlings U, Farrall M, Watkins H, Richards AM, Cameron VA, Muendlein A, Drexel H, Koch W, Park JE, Kimura A, Shen WF, Simpson IA, Hazen SL, Horne BD, Hauser ER, Quyyumi AA, Reilly MP, Samani NJ, Ye S.

J Am Coll Cardiol. 2013 Mar 5;61(9):957-70. doi: 10.1016/j.jacc.2012.10.051. Epub 2013 Jan 23.

9.

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.

10.

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease.

Patel RS, Su S, Neeland IJ, Ahuja A, Veledar E, Zhao J, Helgadottir A, Holm H, Gulcher JR, Stefansson K, Waddy S, Vaccarino V, Zafari AM, Quyyumi AA.

Eur Heart J. 2010 Dec;31(24):3017-23. doi: 10.1093/eurheartj/ehq272. Epub 2010 Aug 20.

11.

9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population.

Ding H, Xu Y, Wang X, Wang Q, Zhang L, Tu Y, Yan J, Wang W, Hui R, Wang CY, Wang DW.

Circ Cardiovasc Genet. 2009 Aug;2(4):338-46. doi: 10.1161/CIRCGENETICS.108.810226. Epub 2009 May 28.

12.

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
13.

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.

Shen GQ, Li L, Girelli D, Seidelmann SB, Rao S, Fan C, Park JE, Xi Q, Li J, Hu Y, Olivieri O, Marchant K, Barnard J, Corrocher R, Elston R, Cassano J, Henderson S, Hazen SL, Plow EF, Topol EJ, Wang QK.

Am J Hum Genet. 2007 Oct;81(4):780-91. Epub 2007 Aug 31.

14.

Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease.

Virani SS, Brautbar A, Lee VV, MacArthur E, Morrison AC, Grove ML, Nambi V, Frazier L, Wilson JM, Willerson JT, Boerwinkle E, Ballantyne CM.

Circ J. 2012;76(4):950-6. Epub 2012 Feb 9.

15.

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

Schunkert H, Götz A, Braund P, McGinnis R, Tregouet DA, Mangino M, Linsel-Nitschke P, Cambien F, Hengstenberg C, Stark K, Blankenberg S, Tiret L, Ducimetiere P, Keniry A, Ghori MJ, Schreiber S, El Mokhtari NE, Hall AS, Dixon RJ, Goodall AH, Liptau H, Pollard H, Schwarz DF, Hothorn LA, Wichmann HE, König IR, Fischer M, Meisinger C, Ouwehand W, Deloukas P, Thompson JR, Erdmann J, Ziegler A, Samani NJ; Cardiogenics Consortium.

Circulation. 2008 Apr 1;117(13):1675-84. doi: 10.1161/CIRCULATIONAHA.107.730614. Epub 2008 Mar 24.

16.

Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locus.

Zollbrecht C, Grassl M, Fenk S, Höcherl R, Hubauer U, Reinhard W, Esslinger UB, Ebert S, Langmann T, Stark K, Hengstenberg C.

Atherosclerosis. 2013 Apr;227(2):244-9. doi: 10.1016/j.atherosclerosis.2012.12.030. Epub 2013 Jan 17.

PMID:
23375685
17.

Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese.

Peng WH, Lu L, Zhang Q, Zhang RY, Wang LJ, Yan XX, Chen QJ, Shen WF.

Clin Chem Lab Med. 2009;47(8):917-22. doi: 10.1515/CCLM.2009.215.

PMID:
19548844
18.

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; SMART study group.

Eur Heart J. 2013 Oct;34(37):2896-904. doi: 10.1093/eurheartj/eht222. Epub 2013 Jul 4.

19.

Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction.

van Setten J, Isgum I, Smolonska J, Ripke S, de Jong PA, Oudkerk M, de Koning H, Lammers JW, Zanen P, Groen HJ, Boezen HM, Postma DS, Wijmenga C, Viergever MA, Mali WP, de Bakker PI.

Atherosclerosis. 2013 Jun;228(2):400-5. doi: 10.1016/j.atherosclerosis.2013.02.039. Epub 2013 Mar 13.

20.

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.

Scheffold T, Kullmann S, Huge A, Binner P, Ochs HR, Schöls W, Thale J, Motz W, Hegge FJ, Stellbrink C, Dorsel T, Gülker H, Heuer H, Dinh W, Stoll M, Haltern G; Forschungsverbund Herz-Kreislauf in NRW (Research Consortium Heart and Circulation in North Rhine-Westphalia).

BMC Cardiovasc Disord. 2011 Mar 7;11:9. doi: 10.1186/1471-2261-11-9.

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