Renner W - Search Results

1

Effect of the rs2259816 polymorphism in the HNF1A gene on circulating levels of c-reactive protein and coronary artery disease (the ludwigshafen risk and cardiovascular health study).

Kleber ME, Grammer TB, Renner W, März W. Kleber ME, et al. Among authors: renner w. BMC Med Genet. 2010 Nov 9;11:157. doi: 10.1186/1471-2350-11-157. BMC Med Genet. 2010. PMID: 21062467 Free PMC article.

2

Association of angiotensinogen haplotypes with angiotensinogen levels but not with blood pressure or coronary artery disease: the Ludwigshafen Risk and Cardiovascular Health Study.

Renner W, Nauck M, Winkelmann BR, Hoffmann MM, Scharnagl H, Mayer V, Boehm BO, März W; LURIC Study team. Renner W, et al. J Mol Med (Berl). 2005 Mar;83(3):235-9. doi: 10.1007/s00109-004-0618-0. Epub 2004 Dec 15. J Mol Med (Berl). 2005. PMID: 15599691

3

Role of the interleukin-6 -174 G>C gene polymorphism in retinal artery occlusion.

Weger M, Steinbrugger I, Haas A, März W, El-Shabrawi Y, Weger W, Schmut O, Renner W. Weger M, et al. Among authors: renner w. Stroke. 2005 Feb;36(2):249-52. doi: 10.1161/01.STR.0000151329.84830.37. Epub 2004 Dec 16. Stroke. 2005. PMID: 15604420

4

Association analysis of the polymorphism T1128C in the signal peptide of neuropeptide Y in a Swedish hypertensive population.

Renner W, Grammer T, Hoffmann MM, Nauck MS, Winkelmann BR, Boehm BO, März W. Renner W, et al. J Hypertens. 2004 Dec;22(12):2398-9; author reply 2399-400. doi: 10.1097/00004872-200412000-00025. J Hypertens. 2004. PMID: 15614037 No abstract available.

5

The serotonin transporter gene polymorphism is not associated with smoking behavior.

Trummer O, Köppel H, Wascher TC, Grünbacher G, Gutjahr M, Stanger O, Ramschak-Schwarzer S, Boehm BO, Winkelmann BR, März W, Renner W. Trummer O, et al. Among authors: renner w. Pharmacogenomics J. 2006 Nov-Dec;6(6):397-400. doi: 10.1038/sj.tpj.6500389. Epub 2006 May 16. Pharmacogenomics J. 2006. PMID: 16702982

6

The angiotensin-I converting enzyme I/D polymorphism is not associated with type 2 diabetes in individuals undergoing coronary angiography. (The Ludwigshafen Risk and Cardiovascular Health Study).

Grammer TB, Renner W, von Karger S, Boehm BO, Winkelmann BR, Maerz W. Grammer TB, et al. Among authors: renner w. Mol Genet Metab. 2006 Aug;88(4):378-83. doi: 10.1016/j.ymgme.2006.01.008. Epub 2006 Jun 12. Mol Genet Metab. 2006. PMID: 16765625

7

The MHC2TA -168A>G gene polymorphism is not associated with rheumatoid arthritis in Austrian patients.

Yazdani-Biuki B, Brickmann K, Wohlfahrt K, Mueller T, März W, Renner W, Gutjahr M, Langsenlehner U, Krippl P, Wascher TC, Paulweber B, Graninger W, Brezinschek HP. Yazdani-Biuki B, et al. Among authors: renner w. Arthritis Res Ther. 2006;8(4):R97. doi: 10.1186/ar1974. Arthritis Res Ther. 2006. PMID: 16776848 Free PMC article.

8

G-protein beta3 subunit (GNB3) gene polymorphisms and cardiovascular disease: the Ludwigshafen Risk and Cardiovascular Health (LURIC) study.

Renner W, Hoffmann MM, Grünbacher G, Winkelmann BR, Boehm BO, März W. Renner W, et al. Atherosclerosis. 2007 May;192(1):108-12. doi: 10.1016/j.atherosclerosis.2006.07.001. Epub 2006 Aug 14. Atherosclerosis. 2007. PMID: 16908025

9

Alanine to serine polymorphism at position 986 of the calcium-sensing receptor associated with coronary heart disease, myocardial infarction, all-cause, and cardiovascular mortality.

März W, Seelhorst U, Wellnitz B, Tiran B, Obermayer-Pietsch B, Renner W, Boehm BO, Ritz E, Hoffmann MM. März W, et al. Among authors: renner w. J Clin Endocrinol Metab. 2007 Jun;92(6):2363-9. doi: 10.1210/jc.2006-0071. Epub 2007 Mar 20. J Clin Endocrinol Metab. 2007. PMID: 17374704

10

Association of complement factor H Y402H gene polymorphism with different subtypes of exudative age-related macular degeneration.

Wegscheider BJ, Weger M, Renner W, Steinbrugger I, März W, Mossböck G, Temmel W, El-Shabrawi Y, Schmut O, Jahrbacher R, Haas A. Wegscheider BJ, et al. Among authors: renner w. Ophthalmology. 2007 Apr;114(4):738-42. doi: 10.1016/j.ophtha.2006.07.048. Ophthalmology. 2007. PMID: 17398321

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