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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. Chan K, et al. Among authors: shen wf, shen gq. J Am Coll Cardiol. 2013 Mar 5;61(9):957-70. doi: 10.1016/j.jacc.2012.10.051. Epub 2013 Jan 23. J Am Coll Cardiol. 2013. PMID: 23352782 Free PMC article.
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. Shen GQ, et al. Am J Hum Genet. 2007 Oct;81(4):780-91. doi: 10.1086/521581. Epub 2007 Aug 31. Am J Hum Genet. 2007. PMID: 17847002 Free PMC article.
113 results