Tiret L - Search Results

1

Lack of association between complement factor H polymorphisms and coronary artery disease or myocardial infarction.

Nicaud V, Francomme C, Ruidavets JB, Luc G, Arveiler D, Kee F, Evans A, Morrison C, Blankenberg S, Cambien F, Tiret L. Nicaud V, et al. Among authors: tiret l. J Mol Med (Berl). 2007 Jul;85(7):771-5. doi: 10.1007/s00109-007-0185-2. Epub 2007 Mar 30. J Mol Med (Berl). 2007. PMID: 17396242

2

Impact of pathogen burden in patients with coronary artery disease in relation to systemic inflammation and variation in genes encoding cytokines.

Georges JL, Rupprecht HJ, Blankenberg S, Poirier O, Bickel C, Hafner G, Nicaud V, Meyer J, Cambien F, Tiret L; AtheroGene Group. Georges JL, et al. Among authors: tiret l. Am J Cardiol. 2003 Sep 1;92(5):515-21. doi: 10.1016/s0002-9149(03)00717-3. Am J Cardiol. 2003. PMID: 12943869

3

Interleukin-18 and the risk of coronary heart disease in European men: the Prospective Epidemiological Study of Myocardial Infarction (PRIME).

Blankenberg S, Luc G, Ducimetière P, Arveiler D, Ferrières J, Amouyel P, Evans A, Cambien F, Tiret L; PRIME Study Group. Blankenberg S, et al. Among authors: tiret l. Circulation. 2003 Nov 18;108(20):2453-9. doi: 10.1161/01.CIR.0000099509.76044.A2. Epub 2003 Oct 27. Circulation. 2003. PMID: 14581397

4

In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarction.

Tregouet DA, Ricard S, Nicaud V, Arnould I, Soubigou S, Rosier M, Duverger N, Poirier O, Macé S, Kee F, Morrison C, Denèfle P, Tiret L, Evans A, Deleuze JF, Cambien F. Tregouet DA, et al. Among authors: tiret l. Arterioscler Thromb Vasc Biol. 2004 Apr;24(4):775-81. doi: 10.1161/01.ATV.0000121573.29550.1a. Epub 2004 Feb 12. Arterioscler Thromb Vasc Biol. 2004. PMID: 14962947

5

Platelet-activating factor-acetylhydrolase and PAF-receptor gene haplotypes in relation to future cardiovascular event in patients with coronary artery disease.

Ninio E, Tregouet D, Carrier JL, Stengel D, Bickel C, Perret C, Rupprecht HJ, Cambien F, Blankenberg S, Tiret L. Ninio E, et al. Among authors: tiret l. Hum Mol Genet. 2004 Jul 1;13(13):1341-51. doi: 10.1093/hmg/ddh145. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115767

6

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: tiret l. 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

7

Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.

Lieb W, Zeller T, Mangino M, Götz A, Braund P, Wenzel JJ, Horn C, Proust C, Linsel-Nitschke P, Amouyel P, Bruse P, Arveiler D, König IR, Ferrières J, Ziegler A, Balmforth AJ, Evans A, Ducimetière P, Cambien F, Hengstenberg C, Stark K, Hall AS, Schunkert H, Blankenberg S, Samani NJ, Erdmann J, Tiret L. Lieb W, et al. Among authors: tiret l. J Mol Med (Berl). 2008 Oct;86(10):1163-70. doi: 10.1007/s00109-008-0376-5. Epub 2008 Jul 1. J Mol Med (Berl). 2008. PMID: 18592168

8

Molecular and functional characterization of polymorphisms in the secreted phospholipase A2 group X gene: relevance to coronary artery disease.

Gora S, Perret C, Jemel I, Nicaud V, Lambeau G, Cambien F, Ninio E, Blankenberg S, Tiret L, Karabina SA. Gora S, et al. Among authors: tiret l. J Mol Med (Berl). 2009 Jul;87(7):723-33. doi: 10.1007/s00109-009-0483-y. Epub 2009 Jun 3. J Mol Med (Berl). 2009. PMID: 19495570 Free PMC article.

9

Polymorphisms of the beta2 -adrenoceptor (ADRB2) gene and essential hypertension: the ECTIM and PEGASE studies.

Herrmann SM, Nicaud V, Tiret L, Evans A, Kee F, Ruidavets JB, Arveiler D, Luc G, Morrison C, Hoehe MR, Paul M, Cambien F. Herrmann SM, et al. Among authors: tiret l. J Hypertens. 2002 Feb;20(2):229-35. doi: 10.1097/00004872-200202000-00012. J Hypertens. 2002. PMID: 11821707

10

Heterogeneity of linkage disequilibrium in human genes has implications for association studies of common diseases.

Tiret L, Poirier O, Nicaud V, Barbaux S, Herrmann SM, Perret C, Raoux S, Francomme C, Lebard G, Trégouët D, Cambien F. Tiret L, et al. Hum Mol Genet. 2002 Feb 15;11(4):419-29. doi: 10.1093/hmg/11.4.419. Hum Mol Genet. 2002. PMID: 11854174

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