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Page 1
Association of angiotensin-converting enzyme 2 (ACE2) gene polymorphisms with parameters of left ventricular hypertrophy in men. Results of the MONICA Augsburg echocardiographic substudy.
Lieb W, Graf J, Götz A, König IR, Mayer B, Fischer M, Stritzke J, Hengstenberg C, Holmer SR, Döring A, Löwel H, Schunkert H, Erdmann J. Lieb W, et al. Among authors: gotz a. J Mol Med (Berl). 2006 Jan;84(1):88-96. doi: 10.1007/s00109-005-0718-5. Epub 2005 Nov 11. J Mol Med (Berl). 2006. PMID: 16283142
Association between arterial pressure and coronary artery calcification.
Mayer B, Lieb W, Radke PW, Götz A, Fischer M, Bässler A, Doehring LC, Aherrahrou Z, Liptau H, Erdmann J, Holmer S, Hense HW, Hengstenberg C, Schunkert H. Mayer B, et al. Among authors: gotz a. J Hypertens. 2007 Aug;25(8):1731-8. doi: 10.1097/HJH.0b013e328165cbb6. J Hypertens. 2007. PMID: 17620972
Lack of association between the MEF2A gene and myocardial infarction.
Lieb W, Mayer B, König IR, Borwitzky I, Götz A, Kain S, Hengstenberg C, Linsel-Nitschke P, Fischer M, Döring A, Wichmann HE, Meitinger T, Kreutz R, Ziegler A, Schunkert H, Erdmann J. Lieb W, et al. Among authors: gotz a. Circulation. 2008 Jan 15;117(2):185-91. doi: 10.1161/CIRCULATIONAHA.107.728485. Epub 2007 Dec 17. Circulation. 2008. PMID: 18086930
Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population.
Linsel-Nitschke P, Götz A, Medack A, König IR, Bruse P, Lieb W, Mayer B, Stark K, Hengstenberg C, Fischer M, Baessler A, Ziegler A, Schunkert H, Erdmann J. Linsel-Nitschke P, et al. Among authors: gotz a. Clin Sci (Lond). 2008 Nov;115(10):309-15. doi: 10.1042/CS20070468. Clin Sci (Lond). 2008. PMID: 18318662
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study.
Linsel-Nitschke P, Götz A, Erdmann J, Braenne I, Braund P, Hengstenberg C, Stark K, Fischer M, Schreiber S, El Mokhtari NE, Schaefer A, Schrezenmeir J, Rubin D, Hinney A, Reinehr T, Roth C, Ortlepp J, Hanrath P, Hall AS, Mangino M, Lieb W, Lamina C, Heid IM, Doering A, Gieger C, Peters A, Meitinger T, Wichmann HE, König IR, Ziegler A, Kronenberg F, Samani NJ, Schunkert H; Wellcome Trust Case Control Consortium (WTCCC); Cardiogenics Consortium. Linsel-Nitschke P, et al. Among authors: gotz a. PLoS One. 2008 Aug 20;3(8):e2986. doi: 10.1371/journal.pone.0002986. PLoS One. 2008. PMID: 18714375 Free PMC article.
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
Schunkert H, Götz A, Braund P, McGinnis R, Tregouet DA, Mangino M, Linsel-Nitschke P, Cambien F, Hengstenberg C, Stark K, Blankenberg S, Tiret L, Ducimetiere P, Keniry A, Ghori MJ, Schreiber S, El Mokhtari NE, Hall AS, Dixon RJ, Goodall AH, Liptau H, Pollard H, Schwarz DF, Hothorn LA, Wichmann HE, König IR, Fischer M, Meisinger C, Ouwehand W, Deloukas P, Thompson JR, Erdmann J, Ziegler A, Samani NJ; Cardiogenics Consortium. Schunkert H, et al. Among authors: gotz a. Circulation. 2008 Apr 1;117(13):1675-84. doi: 10.1161/CIRCULATIONAHA.107.730614. Epub 2008 Mar 24. Circulation. 2008. PMID: 18362232 Free PMC article.
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: gotz a. 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
278 results