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.
Register once to receive every episode delivered directly to your inbox before it is released.
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
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.
Register once to receive every episode delivered directly to your inbox before it is released.
This CEU webinar will provide a case-based review of primary immune disorders, highlighting clinical features and natural history patterns associated with major categories of primary immune disorders. Attendees will explore the role of genomic sequencing in diagnosis and characterization, as well as how genomic sequencing results can inform patient management, treatment considerations, and counseling for patients and families.
As genomic testing becomes more integrated into neonatal care, NICU teams play an important role in helping patients and families navigate complex clinical journeys. This webinar will explore practical applications of rapid genomesequencing in the NICU and discuss how earlier genetic insights can influence care coordination, interdisciplinary workflows, and family communication.
Description:
Genetic testing can help general pediatricians uncover an underlying cause sooner when a child presents with broad or nonspecific developmental concerns. In this webinar, Dr. Tommy Martin discusses why AAP-aligned genetic testing should be considered earlier in the care journey, how it can help clarify next steps for children with global developmental delay or intellectual disability, and what general pediatricians need to know to bring testing into practice with confidence.
Description:
This CEU webinar will explore key counseling considerations in prenatal genomic sequencing. Attendees will gain a deeper understanding of the range of potential fetal and parental findings identified through prenatal genomic testing, including their clinical implications. The session will also address critical considerations for transition of care and multidisciplinary coordination when results reveal genetic findings requiring ongoing management.
Speakers:
Lisa Gurry, Chief Business Officer, GeneDx and Colton Frazer, Senior Health Economics & Outcomes Research Scientist, GeneDx
Description:
Genomic data is rapidly reshaping drug development, but not all data delivers the same value. For biopharma teams, the ability to accurately identify patients, understand disease burden, and make confident development decisions depends on integrating clinically validated genomic insights with real-world data.
This webinar will explore how integrating clinical-grade genomic data with longitudinal insights can fuel drug discovery, accelerate precise clinical trials, advance HEOR research, and generate evidence to deliver value across the drug development lifecycle.
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