On this page you will find summaries of research studies that were made possible by analysis of the data in the SHaRe registry.
Mulitdimensional structure-function relationships in human B-cardiac myosin from population-scale genetic variations.
In this study researchers looked at whether the genetic changes in the heart myosin that cause HCM tend to occur more often in certain areas of the molecule. In addition, the researchers looked at how different genetic changes contribute to differences in disease onset and disease outcomes of patients with Hypertrophic cardiomyopathy. Read more
Want to read the full study text? Find it here.