Unlocking STXBP1 through Electronic Medical Records

Julia Xian posts a follow-up blog from her STXBP1 Summit + presentation here.

Understanding the EMR. Several weeks ago, I gave a presentation at the STXBP1 Summit conference, the third annual meeting since the first in 2019 – a time when I had just entered the field of neurogenetics. It has been fascinating to follow one of the neurodevelopmental genes with the “fastest growing knowledge,” with the expanded scope of clinical studies and emergence of novel avenues for targeted gene therapies on the horizon. However, one of the many projects our STXBP1 team is currently working on takes a somewhat atypical approach – we aimed to map the natural disease history of STXBP1-related disorders based entirely on reconstructed Electronic Medical Records (EMR). Here are some of the challenges we have had to confront and what we learned searching for meaning in the depth of the EMR.” Read the full post.

Julie Xian is a Data Scientist in the Helbig Lab at Children’s Hospital of Philadelphia (CHOP).

Previous
Previous

Uplifting Athletes and STXBP1 Foundation Fund $20,000 Grant to Dr. Alex Felix at University of Pennsylvania

Next
Next

The 2022 STXBP1 Summit – a personal reflection by Dr. Ingo Helbig