Human and Molecular Genetics Center

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Broeckel Lab

 
Ulrich Broeckel, MD
Associate Professor, Pediatrics
Specialization: Human Genetics of Complex Disease
Tel: (414) 456-4409
Dr. Broeckel's CV
Email Dr. Broeckel

 


Research Interests

The Broeckel lab focuses on the identification and functional evaluation of genes involved in cardiovascular diseases. We have an ongoing research project focused on left ventricular hypertrophy, myocardial infarction and coronary artery disease, end-stage renal disease, and hypertension.

We use state of the art genome-wide association (GWA) studies to identify genes involved in cardiovascular diseases. While GWA studies provide only evidence for association, we also establish various platforms to subsequently evaluate the function of identified genes.

We also pursue large scale epidemiological studies in clinical cohorts. This allows us to evaluate the effect and impact of SNPs identified in GWA studies with regard to their clinical relevance. For this project the Broeckel lab contributes one MCW component to the Wisconsin Genomics Initiative, a consortium including our group and MCW as well as the Marshfield Clinic and the University of Wisconsin, Madison and Milwaukee.

The Individualized Medicine Institute (IMI)

Ongoing studies are:
  • HyperGen: Genetic Epidemiology of Left Ventricular Hypertrophy Genetics of CRP in Myocardial Function (NHLBI)
  • Genetics of Myocardial Infarction and Related Risk factors (NHLBI)
  • Molecular Genetics of Hypertension
  • Genetic Predisposition to End-Stage Renal Disease Epidemiology
  • The Wisconsin Genomics Initiative

 


Click here for Dr. Broeckel's  Faculty Collaboration Database profile page,
which includes an up to date listing of his publications.
 

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