Live and on-demand webinars
Join an upcoming webinar or view our library of on-demand recordings. From genetics 101 to genomic-based newborn screening, we’ve got you covered!
In pediatric critical care settings, patients may present with complex symptoms that do not point to a clear diagnosis. 48 hours that changed the case follows real, anonymized patient cases where ultraRapid genome sequencing helped uncover genomic answers in just 48 hours.
Hosted by Dr. Linda Genen, each episode examines one case, the diagnostic uncertainty clinicians faced, and how earlier genomic insights helped care teams make more informed care decisions. From cases involving neurologic, metabolic, cardiac, and other complex presentations, the series highlights the clinical value of knowing sooner.
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Upcoming webinars
In this webinar, attendees will explore genetic testing strategies for children and young adults with epilepsy, with insights relevant to pediatricians, pediatric and adult neurologists, geneticists, genetic counselors, developmental behavioral pediatricians and other clinicians involved in diagnostic evaluation.
Arie Weinstock, Professor of Clinical Neurology at the State University of New York at Buffalo and Director of the Epilepsy Program and Long-Term Monitoring at Oishei Children’s Hospital, will use pediatric and young adult neurology cases to illustrate how genetic testing, including genomic sequencing with trio analysis (parental samples), can help identify the underlying cause of disease. A genetic diagnosis can end the diagnostic odyssey and allow tailored therapy.
Rare disease research begins with understanding the underlying biology. GeneDx Infinity - the world's largest clinically interpreted rare disease database - combines clinically generated genomic data and expert interpretation to help biopharma identify the right patients and better understand disease biology. When linked with Komodo Health's longitudinal claims-based data, researchers gain a more complete view of the patient journey, connecting genetic insights to treatment patterns, healthcare utilization, and long-term outcomes.
Join experts from GeneDx and Komodo Health to explore how integrated genomic and claims-based data can improve patient finding, enable more precise rare disease cohorts, and generate higher-confidence real-world evidence across the drug development lifecycle. The session will also demonstrate how GeneDx Infinity and Komodo's AI-first capabilities, including Marmot, help transform complex datasets into actionable insights for discovery, clinical development, and post-launch evidence generation.
Past webinars
Abigail Sassaman, MS, CGC (Medical Science Liaison at GeneDx) was joined by Dr. Samantha Vergano, MD, FACMG, FAAP (Associate Medical Director, Outpatient Services – Genetic Medicine at Seattle Children’s) for a timely conversation on what’s changing and how clinicians can confidently implement the new recommendations.
Learn why an expert on neurogenetics and rare disease recommends ordering exome for patients. Join Dr. Isabella Herman as she explains the importance of exome sequencing at this webinar.
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