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Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
Trégouët DA, König IR, Erdmann J, Munteanu A, Braund PS, Hall AS, Grosshennig A, Linsel-Nitschke P, Perret C, DeSuremain M, Meitinger T, Wright BJ, Preuss M, Balmforth AJ, Ball SG, Meisinger C, Germain C, Evans A, Arveiler D, Luc G, Ruidavets JB, Morrison C, van der Harst P, Schreiber S, Neureuther K, Schäfer A, Bugert P, El Mokhtari NE, Schrezenmeir J, Stark K, Rubin D, Wichmann HE, Hengstenberg C, Ouwehand W; Wellcome Trust Case Control Consortium; Cardiogenics Consortium; Ziegler A, Tiret L, Thompson JR, Cambien F, Schunkert H, Samani NJ. Trégouët DA, et al. Among authors: luc g. Nat Genet. 2009 Mar;41(3):283-5. doi: 10.1038/ng.314. Epub 2009 Feb 8. Nat Genet. 2009. PMID: 19198611
Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach.
Barbaux S, Tregouet DA, Nicaud V, Poirier O, Perret C, Godefroy T, Francomme C, Combadiere C, Arveiler D, Luc G, Ruidavets JB, Evans AE, Kee F, Morrison C, Tiret L, Brand-Herrmann SM, Cambien F. Barbaux S, et al. Among authors: luc g. J Mol Med (Berl). 2007 Nov;85(11):1271-80. doi: 10.1007/s00109-007-0234-x. Epub 2007 Jul 19. J Mol Med (Berl). 2007. PMID: 17634906
Large scale association analysis of novel genetic loci for coronary artery disease.
Coronary Artery Disease Consortium; Samani NJ, Deloukas P, Erdmann J, Hengstenberg C, Kuulasmaa K, McGinnis R, Schunkert H, Soranzo N, Thompson J, Tiret L, Ziegler A. Coronary Artery Disease Consortium, et al. Arterioscler Thromb Vasc Biol. 2009 May;29(5):774-80. doi: 10.1161/ATVBAHA.108.181388. Epub 2009 Jan 22. Arterioscler Thromb Vasc Biol. 2009. PMID: 19164808 Free PMC article.
Sequence polymorphisms in the apolipoprotein(a) gene and their association with lipoprotein(a) levels and myocardial infarction. The ECTIM Study.
Brazier L, Tiret L, Luc G, Arveiler D, Ruidavets JB, Evans A, Chapman J, Cambien F, Thillet J. Brazier L, et al. Among authors: luc g. Atherosclerosis. 1999 Jun;144(2):323-33. doi: 10.1016/s0021-9150(98)00333-5. Atherosclerosis. 1999. PMID: 10407493
In addition to apo(a) phenotyping, five previously described polymorphisms of the apo(a) gene were genotyped: a (TTTTA)n repeat at position -1400 from the ATG, a G/A at -914, a C/T at -49, a G/A at -21 and a Met/Thr affecting amino acid 4168. As reported earlier [Pa …
In addition to apo(a) phenotyping, five previously described polymorphisms of the apo(a) gene were genotyped: a (TTTTA)n repeat at position …
DNA polymorphisms in linkage disequilibrium at the 3' end of the human APO AII gene: relationships with lipids, apolipoproteins and coronary heart disease.
Dupuy-Gorce AM, Desmarais E, Vigneron S, Buresi C, Nicaud V, Evans A, Luc G, Arveiler D, Marqués-Vidal P, Cambien F, Tiret L, Crastes de Paulet A, Roizés G. Dupuy-Gorce AM, et al. Among authors: luc g. Clin Genet. 1996 Oct;50(4):191-8. doi: 10.1111/j.1399-0004.1996.tb02624.x. Clin Genet. 1996. PMID: 9001797
226 results