C05-GUARD – Genes Underlying Aortic valve Disease
Aortic valve stenosis (AS) develops in the context of a bi- or tricuspid aortic valve formation. Genetic factors are involved in the development of both AS types. However, the genetic architecture is heterogeneous and depends on the effect size and frequency of the underlying disease variants/mutations. Through our scientific network GUARD (www.guard-net.de), we carried out two large genome-wide association studies (GWAS) that led to the identification of common risk variants for the development of both AS types. We now aim to identify the entire spectrum of genetic risk factors for bi- and tricuspid AS and to analyse them together with other disease-relevant data sets using modern systems biology approaches.
Contacts
Prof. Dr. Markus M. Nöthen
Biomedical Center I, Building 13, ground floor
Institute of Human Genetics
University Hospital Bonn
Venusberg-Campus 1
53127 Bonn
Jun.-Prof. Dr. Maximilian Billmann
Building 76
Institute of Human Genetics
University Hospital Bonn
Venusberg-Campus 1
53127 Bonn
PD Dr. Baravan Al-Kassou
Building 26
Medical Clinic and Polyclinic II
Heart Center
University Hospital Bonn
Venusberg-Campus 1
53127 Bonn
Prof. Dr. Johannes Schumacher
Center for Human Genetics
Philipps-University Marburg
Baldingerstraße
35033 Marburg
Dr. Sandeep Grover
Institut for Human Genetics
University Hospital Bonn
Venusberg-Campus 1
53127 Bonn