New Published Research

Data from the Monogenic Diabetes Registry leads to many published papers. Here are a few of our most recent publications. Click the title to view:

• A case report of IPEX Syndrome caused by a small deletion in FOXP3 gene

• The pros/cons of trialing a sulfonylurea before genetic testing in cases of neonatal diabetes

• A case report detailing how one teenager struggling with medication adherence led to a genetic diagnosis of GCK-MODY

• A next-generation sequencing approach to genetic testing

• Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes

• Sulfonylurea use improves but does not always normalize insulin secretion in 6q24-related transient neonatal diabetes

• Intronic mutation in INS gene causes diabetes through a novel mechanism

• Online monogenic diabetes discussion group: supporting families and fueling new research

Since November 2014, our team has given over 15 presentations on monogenic diabetes, including traveling to Canada, India, Israel, Egypt, and Ireland.