scispace - formally typeset
W

Wilfried Renner

Researcher at Medical University of Graz

Publications -  224
Citations -  8647

Wilfried Renner is an academic researcher from Medical University of Graz. The author has contributed to research in topics: Genotype & Odds ratio. The author has an hindex of 42, co-authored 215 publications receiving 8104 citations. Previous affiliations of Wilfried Renner include University of Graz.

Papers
More filters
Journal ArticleDOI

Independent Association of Low Serum 25-Hydroxyvitamin D and 1,25-Dihydroxyvitamin D Levels With All-Cause and Cardiovascular Mortality

TL;DR: Low 25-hydroxyvitamin D levels were significantly correlated with variables of inflammation, oxidative burden, and cell adhesion, independent of coronary artery disease, physical activity level, Charlson Comorbidity Index, variables of mineral metabolism, and New York Heart Association functional class.
Journal ArticleDOI

A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels.

TL;DR: Three common mutations in the 3′ untranslated region of the VEGF gene are found; one of them, a 936 C/T exchange, may be an important determinant of V EGF plasma levels.
Journal ArticleDOI

New susceptibility locus for coronary artery disease on chromosome 3q22.3

Jeanette Erdmann, +60 more
- 01 Mar 2009 - 
TL;DR: A three-stage analysis of genome-wide SNP data in 1,222 German individuals with myocardial infarction and 1,298 controls is presented and suggestive association with a locus on 12q24.31 near HNF1A-C12orf43 is identified.
Journal ArticleDOI

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Cristian Pattaro, +735 more
TL;DR: A meta-analysis of genome-wide association studies for estimated glomerular filtration rate suggests that genetic determinants of eGFR are mediated largely through direct effects within the kidney and highlight important cell types and biological pathways.
Journal ArticleDOI

A common 936 c/t gene polymorphism of vascular endothelial growth factor is associated with decreased breast cancer risk

TL;DR: It is concluded that carriers of a VEGF 936T‐allele are at decreased risk for breast cancer, this, however, requiring further confirmation in a larger study.