Cambien F - Search Results

1

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. Among authors: cambien f. Hum Mol Genet. 2002 Feb 15;11(4):419-29. doi: 10.1093/hmg/11.4.419. Hum Mol Genet. 2002. PMID: 11854174

2

Inference of the strength of genotype-disease association from studies comparing offspring with and without parental history of disease.

Tiret L, Nicaud V, Ehnholm C, Havekes L, Menzel HJ, Ducimetiere P, Cambien F. Tiret L, et al. Among authors: cambien f. Ann Hum Genet. 1993 May;57(2):141-9. doi: 10.1111/j.1469-1809.1993.tb00895.x. Ann Hum Genet. 1993. PMID: 8368804

3

The P-selectin gene is highly polymorphic: reduced frequency of the Pro715 allele carriers in patients with myocardial infarction.

Herrmann SM, Ricard S, Nicaud V, Mallet C, Evans A, Ruidavets JB, Arveiler D, Luc G, Cambien F. Herrmann SM, et al. Among authors: cambien f. Hum Mol Genet. 1998 Aug;7(8):1277-84. doi: 10.1093/hmg/7.8.1277. Hum Mol Genet. 1998. PMID: 9668170

4

Sequence diversity in 36 candidate genes for cardiovascular disorders.

Cambien F, Poirier O, Nicaud V, Herrmann SM, Mallet C, Ricard S, Behague I, Hallet V, Blanc H, Loukaci V, Thillet J, Evans A, Ruidavets JB, Arveiler D, Luc G, Tiret L. Cambien F, et al. Am J Hum Genet. 1999 Jul;65(1):183-91. doi: 10.1086/302448. Am J Hum Genet. 1999. PMID: 10364531 Free PMC article.

5

SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery disease.

Tregouet DA, Barbaux S, Poirier O, Blankenberg S, Bickel C, Escolano S, Rupprecht HJ, Meyer J, Cambien F, Tiret L; AtheroGene group. Tregouet DA, et al. Among authors: cambien f. Ann Hum Genet. 2003 Nov;67(Pt 6):504-11. doi: 10.1046/j.1529-8817.2003.00053.x. Ann Hum Genet. 2003. PMID: 14641238

6

Exploration of multilocus effects in a highly polymorphic gene, the apolipoprotein (APOB) gene, in relation to plasma apoB levels.

Tahri-Daizadeh N, Tregouet DA, Nicaud V, Poirier O, Cambien F, Tiret L. Tahri-Daizadeh N, et al. Among authors: cambien f. Ann Hum Genet. 2004 Sep;68(Pt 5):405-18. doi: 10.1046/j.1529-8817.2004.00107.x. Ann Hum Genet. 2004. PMID: 15469418

7

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: cambien f. J Hypertens. 2002 Feb;20(2):229-35. doi: 10.1097/00004872-200202000-00012. J Hypertens. 2002. PMID: 11821707

8

Identification of new polymorphisms of the angiotensin I-converting enzyme (ACE) gene, and study of their relationship to plasma ACE levels by two-QTL segregation-linkage analysis.

Villard E, Tiret L, Visvikis S, Rakotovao R, Cambien F, Soubrier F. Villard E, et al. Among authors: cambien f. Am J Hum Genet. 1996 Jun;58(6):1268-78. Am J Hum Genet. 1996. PMID: 8651305 Free PMC article.

9

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: cambien f. Clin Genet. 1996 Oct;50(4):191-8. doi: 10.1111/j.1399-0004.1996.tb02624.x. Clin Genet. 1996. PMID: 9001797

10

Coronary heart disease and genetics in epidemiologist's view.

Cambien F, Poirier O, Mallet C, Tiret L. Cambien F, et al. Mol Med Today. 1997 May;3(5):197-203. doi: 10.1016/s1357-4310(97)01027-7. Mol Med Today. 1997. PMID: 9176882 Review.

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