Virtual Panel Discussion: Practical Insights on Handling VUS-Europe
- Webinar | 25. 04. 24
From Ambiguity to Action: Practical Insights on Handling VUS
Understanding genetic variations and their implications is a cornerstone of advancing precision medicine. Yet, Variants of Uncertain Significance (VUS) remain a challenging gray area for clinicians and geneticists. How can we translate ambiguity into actionable insights for better patient care?
To address these pressing questions, 3billion, Inc. hosted a virtual panel discussion with some of Europe’s leading experts in genetics and genomic counseling. If you missed the live event, you can now watch the on-demand recording to gain practical insights into handling VUS in clinical practice.
What you’ll gain from this on-demand session:
- Expert insights from leading geneticists and genomic counselors across Europe
- Practical strategies for addressing VUS in clinical settings
- Shared experiences and solutions to common challenges with genomic uncertainty
- Actionable knowledge to improve patient care and diagnostic accuracy
Date Recorded: April 30, 2025
Duration: 1 hour
Location: Virtual (via Zoom)
By watching this on-demand session, you’ll gain valuable perspectives and tools to navigate the complexities of Variants of Uncertain Significance in genomic diagnostics and patient care.
Moderator
From Ambiguity to Action: Practical Insights on Handling VUS
- Speaker
- Hane Lee Ph.D.
- Role
- Chief Genomics Officer (CGO) at 3billion
Meet Our Panelists
From Ambiguity to Action: Practical Insights on Handling VUS
- Speaker
- Dr. Plaiasu Vasilica, MD, PhD
- Role
- Clinical Geneticist
From Ambiguity to Action: Practical Insights on Handling VUS
- Speaker
- Dr. Halyna Makukh, PhD
- Role
- Clinical Geneticist
From Ambiguity to Action: Practical Insights on Handling VUS
- Speaker
- Dr. Nedjeljka Zrno, MD
- Role
- Child Neurologist
From Ambiguity to Action: Practical Insights on Handling VUS
- Speaker
- Dr. GoHun Seo, MD
- Role
- Chief Medical Officer
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3billion Inc.
3billion is dedicated to creating a world where patients with rare diseases are not neglected in diagnosis and treatment.
