Speaker(s):
Kelly Schiabor Barrett, PhD, Senior Staff Scientist, Helix, Discloses the following: Helix ["Employment Affiliation"]
Matthew Levy, PhD, Staff Research Scientist, Helix, Discloses the following: Helix ["Employment Affiliation"]
Learning Objectives:
At the conclusion of this session, the participant should be able to:
- Describe how linked genomic and EHR data can be used to measure the real-world impact of established genetic interventions, including population screening programs and pharmacogenomics.
- Identify examples of novel genetic associations with clinical actionability, including variant-specific treatment selection, that have emerged from clinicogenomic datasets.
- Explain how a clinicogenomic dataset can be used to both build and prospectively validate genetic risk tools for conditions where direct biomarker measurement is unavailable or underutilized.
Disclosure of Relevant Financial Relationships with/without Commercial Interests:
The Planning Committee consisting of Juliann Savatt, MS, LCGC, Melissa Kelly, MS, LCGC, Marc Williams, MD, and Cara McCormick, MPH have no identified disclosures.
CE Committee Member/Content Reviewers have nothing to disclose: Christen Mowad, MD, Alison Mowery, DNP, CRNP
Any/All relevant financial relationships have been mitigated.
Content Disclosure:
This presentation/content is HIPAA compliant.
Commercial Support for this Session:
None
Session date:
09/14/2026 - 12:00pm to 1:00pm EDT
Location:
Virtual via Microsoft Teams
Danville, PA
17822
United States
See map: Google Maps
Add to calendar:
- 1.00 AMA PRA Category 1 Credit™
- 1.00 Participation Credit

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