Hengstenberg C - Search Results

1

A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.

Davies RW, Wells GA, Stewart AF, Erdmann J, Shah SH, Ferguson JF, Hall AS, Anand SS, Burnett MS, Epstein SE, Dandona S, Chen L, Nahrstaedt J, Loley C, König IR, Kraus WE, Granger CB, Engert JC, Hengstenberg C, Wichmann HE, Schreiber S, Tang WH, Ellis SG, Rader DJ, Hazen SL, Reilly MP, Samani NJ, Schunkert H, Roberts R, McPherson R. Davies RW, et al. Among authors: hengstenberg c. Circ Cardiovasc Genet. 2012 Apr 1;5(2):217-25. doi: 10.1161/CIRCGENETICS.111.961243. Epub 2012 Feb 7. Circ Cardiovasc Genet. 2012. PMID: 22319020 Free PMC article.

2

A comprehensive linkage analysis for myocardial infarction and its related risk factors.

Broeckel U, Hengstenberg C, Mayer B, Holmer S, Martin LJ, Comuzzie AG, Blangero J, Nürnberg P, Reis A, Riegger GA, Jacob HJ, Schunkert H. Broeckel U, et al. Among authors: hengstenberg c. Nat Genet. 2002 Feb;30(2):210-4. doi: 10.1038/ng827. Epub 2002 Jan 30. Nat Genet. 2002. PMID: 11818963

3

[Genetic factors in myocardial infarction--Results from a candidate gene and a genome-wide approach between beta blockers].

Hengstenberg C, Bröckel U, Holmer S, Mayer B, Fischer M, Baessler A, Erdmann J, Lieb W, Löwel H, Riegger G, Schunkert H. Hengstenberg C, et al. Herz. 2002 Nov;27(7):649-61. doi: 10.1007/s00059-002-2432-1. Herz. 2002. PMID: 12439636 German.

4

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations: prediction of clinical status--is molecular genetics a new tool for the management of hypertrophic cardiomyopathy in clinical practice?

Hengstenberg C, Erdmann J, Charron P. Hengstenberg C, et al. Cardiovasc Res. 2003 Feb;57(2):298-301. doi: 10.1016/s0008-6363(02)00781-2. Cardiovasc Res. 2003. PMID: 12566102 No abstract available.

5

Association of polymorphisms of the apolipoprotein(a) gene with lipoprotein(a) levels and myocardial infarction.

Holmer SR, Hengstenberg C, Kraft HG, Mayer B, Pöll M, Kürzinger S, Fischer M, Löwel H, Klein G, Riegger GA, Schunkert H. Holmer SR, et al. Among authors: hengstenberg c. Circulation. 2003 Feb 11;107(5):696-701. doi: 10.1161/01.cir.0000048125.79640.77. Circulation. 2003. PMID: 12578871

6

Lack of association of a 9 bp insertion/deletion polymorphism within the bradykinin 2 receptor gene with myocardial infarction.

Fischer M, Lieb W, Marold D, Berthold M, Baessler A, Lowel H, Hense HW, Hengstenberg C, Holmer S, Schunkert H, Erdmann J. Fischer M, et al. Among authors: hengstenberg c. Clin Sci (Lond). 2004 Nov;107(5):505-11. doi: 10.1042/CS20040129. Clin Sci (Lond). 2004. PMID: 15301669

7

No association of interleukin-6 gene polymorphism (-174 G/C) with myocardial infarction or traditional cardiovascular risk factors.

Lieb W, Pavlik R, Erdmann J, Mayer B, Holmer SR, Fischer M, Baessler A, Hengstenberg C, Loewel H, Doering A, Riegger GA, Schunkert H. Lieb W, et al. Among authors: hengstenberg c. Int J Cardiol. 2004 Nov;97(2):205-12. doi: 10.1016/j.ijcard.2003.07.038. Int J Cardiol. 2004. PMID: 15458685

8

Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction.

Fischer M, Broeckel U, Holmer S, Baessler A, Hengstenberg C, Mayer B, Erdmann J, Klein G, Riegger G, Jacob HJ, Schunkert H. Fischer M, et al. Among authors: hengstenberg c. Circulation. 2005 Feb 22;111(7):855-62. doi: 10.1161/01.CIR.0000155611.41961.BB. Epub 2005 Feb 14. Circulation. 2005. PMID: 15710764

9

Association of the T8590C polymorphism of CYP4A11 with hypertension in the MONICA Augsburg echocardiographic substudy.

Mayer B, Lieb W, Götz A, König IR, Aherrahrou Z, Thiemig A, Holmer S, Hengstenberg C, Doering A, Loewel H, Hense HW, Schunkert H, Erdmann J. Mayer B, et al. Among authors: hengstenberg c. Hypertension. 2005 Oct;46(4):766-71. doi: 10.1161/01.HYP.0000182658.04299.15. Epub 2005 Sep 6. Hypertension. 2005. PMID: 16144986

10

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: hengstenberg c. 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

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