Herrmann SM - 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: herrmann sm. Hum Mol Genet. 2002 Feb 15;11(4):419-29. doi: 10.1093/hmg/11.4.419. Hum Mol Genet. 2002. PMID: 11854174

2

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. Hum Mol Genet. 1998 Aug;7(8):1277-84. doi: 10.1093/hmg/7.8.1277. Hum Mol Genet. 1998. PMID: 9668170

3

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. Among authors: herrmann sm. Am J Hum Genet. 1999 Jul;65(1):183-91. doi: 10.1086/302448. Am J Hum Genet. 1999. PMID: 10364531 Free PMC article.

4

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

5

Polymorphisms of the endothelin-A and -B receptor genes in relation to blood pressure and myocardial infarction: the Etude Cas-Témoins sur l'Infarctus du Myocarde (ECTIM) Study.

Nicaud V, Poirier O, Behague I, Herrmann SM, Mallet C, Troesch A, Bouyer J, Evans A, Luc G, Ruidavets JB, Arveiler D, Bingham A, Tiret L, Cambien F. Nicaud V, et al. Among authors: herrmann sm. Am J Hypertens. 1999 Mar;12(3):304-10. doi: 10.1016/s0895-7061(98)00255-6. Am J Hypertens. 1999. PMID: 10192234 Clinical Trial.

6

Polymorphisms of the endothelial nitric oxide synthase gene - no consistent association with myocardial infarction in the ECTIM study.

Poirier O, Mao C, Mallet C, Nicaud V, Herrmann SM, Evans A, Ruidavets JB, Arveiler D, Luc G, Tiret L, Soubrier F, Cambien F. Poirier O, et al. Among authors: herrmann sm. Eur J Clin Invest. 1999 Apr;29(4):284-90. doi: 10.1046/j.1365-2362.1999.00451.x. Eur J Clin Invest. 1999. PMID: 10231340

7

Identification of two polymorphisms in the early growth response protein-1 gene: possible association with lipid variables.

Brand E, Herrmann SM, Nicaud V, Evans A, Ruidavets JB, Arveiler D, Luc G, Cambien F, Soubrier F. Brand E, et al. Among authors: herrmann sm. J Mol Med (Berl). 2000;78(2):81-6. doi: 10.1007/s001090000074. J Mol Med (Berl). 2000. PMID: 10794543

8

Polymorphisms in the genes encoding platelet-derived growth factor A and alpha receptor.

Herrmann SM, Ricard S, Nicaud V, Brand E, Behague I, Blanc H, Ruidavets JB, Evans A, Arveiler D, Luc G, Poirier O, Cambien F. Herrmann SM, et al. J Mol Med (Berl). 2000;78(5):287-92. doi: 10.1007/s001090000111. J Mol Med (Berl). 2000. PMID: 10954201

9

Polymorphisms of the human matrix gla protein (MGP) gene, vascular calcification, and myocardial infarction.

Herrmann SM, Whatling C, Brand E, Nicaud V, Gariepy J, Simon A, Evans A, Ruidavets JB, Arveiler D, Luc G, Tiret L, Henney A, Cambien F. Herrmann SM, et al. Arterioscler Thromb Vasc Biol. 2000 Nov;20(11):2386-93. doi: 10.1161/01.atv.20.11.2386. Arterioscler Thromb Vasc Biol. 2000. PMID: 11073842

10

The histidin-rich glycoprotein Pro186/Ser polymorphism is not related to myocardial infarction in the ECTIM study.

Herrmann SM, Poirier O, Nicaud V, Ruidavets JB, Evans A, Arveiler D, Luc G, Bara L, Cambien F. Herrmann SM, et al. Thromb Haemost. 1998 Feb;79(2):359-61. Thromb Haemost. 1998. PMID: 9493591

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