J Mol Med (Berl)

The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol

Samani, N. J., Braund, P. S., Erdmann, J., Gotz, A., Tomaszewski, M., Linsel-Nitschke, P., Hajat, C., Mangino, M., Hengstenberg, C., Stark, K., Ziegler, A., Caulfield, M., Burton, P. R., Schunkert, H., Tobin, M. D.

J Mol Med (Berl). 2008 Nov;86(11):1233-41. doi: 10.1007/s00109-008-0387-2. Epub 2008 Jul 23.

http://www.ncbi.nlm.nih.gov/pubmed/18649068

Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction

Lieb, W., Zeller, T., Mangino, M., Gotz, A., Braund, P., Wenzel, J. J., Horn, C., Proust, C., Linsel-Nitschke, P., Amouyel, P., Bruse, P., Arveiler, D., Konig, I. R., Ferrieres, J., Ziegler, A., Balmforth, A. J., Evans, A., Ducimetiere, P., Cambien, F., Hengstenberg, C., Stark, K., Hall, A. S., Schunkert, H., Blankenberg, S., Samani, N. J., Erdmann, J., Tiret, L.

J Mol Med (Berl). 2008 Oct;86(10):1163-70. doi: 10.1007/s00109-008-0376-5. Epub 2008 Jul 1.

http://www.ncbi.nlm.nih.gov/pubmed/18592168

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., Gotz, A., Konig, I. R., Mayer, B., Fischer, M., Stritzke, J., Hengstenberg, C., Holmer, S. R., Doring, A., Lowel, H., Schunkert, H., Erdmann, J.

J Mol Med (Berl). 2006 Jan;84(1):88-96. Epub 2005 Nov 11.

http://www.ncbi.nlm.nih.gov/pubmed/16283142

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