Upcoming webinar

Democratizing precision neurology:
Expanding first-line genome access for every child in need
Date: Tuesday, November 17, 2026
Time: 12:00 PM ET | 9:00 AM PT
Webinar duration: 60 minutes
Registrants will receive a recording of the webinar approximately one week after the event.
Learn more about:
In child neurology, defining an underlying genetic etiology is often stalled by fragmented approaches to testing, including tiered, single-gene, or panel testing. A broad “genome-first” model has the potential to simplify clinical workflows by replacing multiple diagnostic steps with a single, highly comprehensive test—helping clinicians reach diagnostic clarity sooner for children with complex neurodevelopmental disorders, refractory epilepsies, or unexplained tone anomalies.

During this session, our speakers will:

  • Examine the clinical justification for adopting broad genomic sequencing as an initial diagnostic tool
  • Explore which patient phenotypes may benefit most
  • Discuss the importance of expanding access to testing to help reduce diagnostic disparities
  • Demonstrate how a “one-test” strategy can provide clinicians with insights to guide personalized management earlier in a child’s care journey

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Hear from our speakers:


Kristina Julich
Kristina Julich, MD
Chief, Pediatric Neurogenetics Center
UT Austin Pediatric Neurosciences
Dell Children's Medical Center
Brian Schoenfeld
Brian Schoenfeld, MS, LCGC
Director, Medical Science
Rare Disease, Natera
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