AI helps genetics professionals navigate genomic data at scale, but human expertise is essential. AI, diverse data, and clinical insight can shorten the diagnostic odyssey and improve patient care.
Read the article: genedx.co/3Wsbwdi
#GenomicMedicine #AI #RareDisease
Heading to #SDBP2026? Connect with our team and discover how exome and genome sequencing can help uncover earlier answers for children with developmental and behavioral conditions.
📅October 23-27, 2026
📍New Orleans, Louisiana
Meet with us: genedx.co/3Vi2yyW
Families searching for answers face enough uncertainty. For those who have met their deductible, year-end may be an important time to consider recommended genetic testing before benefits reset.
Learn how timing can help make testing more accessible.
genedx.co/4hBtFxu
We're heading to #ASHG26 with one of our strongest scientific programs yet.
Visit us at Booth #616 to connect with our team about how we're delivering more precise genetic answers for patients and families.
Learn more: genedx.co/4hs9fHd
#RareDisease #PrecisionMedicine
In this episode of 48 hours that changed the case, Dr. Linda Genen discusses a real, anonymized case where ultraRapid genome sequencing identified a de novo pathogenic variant in the GLUD1 gene and helped inform targeted management.
▶️ genedx.co/3TJdEfS
#NICU #GLUD1

ALT This image is a promotional graphic featuring a person in professional attire. The text highlights a discussion about "GLUD1 / Glutamate dehydrogenase hyperinsulinism" and the phrase "48 hours that changed the case." It mentions Dr. Linda Genen, MD, MPH, who is identified as a neonatologist and Chief Medical Officer at GeneDx.
At #breakthroughs26, GeneDx CEO Katherine Stueland joined healthcare leaders to discuss improving outcomes, reducing costs and building a more sustainable system.
#GeneDx #breakthroughs26 #GenomicMedicine #HealthcareTransformation
Sunshine Genetics enrolled its first Florida families, launching a newborn screening pilot to explore how genome sequencing may support earlier identification of genetic conditions. GeneDx is proud to provide sequencing and interpretation.
#NBS #GeneDx
genedx.co/4yGdXYe
Could genomic testing help identify the cause of a child's unexplained critical illness?
Our new Pediatric Critical Care resource page highlights when rapid genome sequencing may be appropriate in the PICU.
genedx.co/3VLJIQL
#PediatricCriticalCare #GenomeSequencing #PICU
At ICoNS 2026, GeneDx has shared new GUARDIAN and BRIDGES-NBS evidence advancing scalable genomic newborn screening. As a sequencing and interpretation partner, GeneDx is helping move gNBS from research toward broader clinical use.
#NBS #GeneDx
genedx.co/4dVAoA4
Headed to #CHNC2026 in Denver? Stop by our booth to learn how exome and genome sequencing can help uncover the genetic causes of complex and unexplained conditions in critically ill infants.
📆 October 20-21
📍 Denver, CO
Meet with us ⬇️
genedx.co/3Vlr4z5

ALT Flyer for the Children's Hospital Neonatal Consortium (CHNC) Conference, October 19-21, 2026, in Denver, Colorado. Text invites attendees to visit GeneDx for insights on genetic causes in critically ill infants, highlighting clinical evidence and management improvements for NICU patients. Includes decorative elements and a heart symbol.
Oregon will soon enroll families in BRIDGES-NBS, a nationwide study exploring how genome sequencing may support earlier insights for newborns. GeneDx is proud to provide sequencing and interpretation for the study.
#NewbornScreening #RareDisease #GeneDx
genedx.co/4zlIt9G
NEWS: Introducing Prenatal Exome-to-Genome Reflex, giving care teams a flexible way to begin with exome and reflex to genome when additional info is needed, without a new order or specimen.
Learn how this approach supports real-world prenatal care: genedx.co/4hhQEO2
Miss our webinar with Endpoints?
Listen to experts from GeneDx and Komodo Health explore how clinically interpreted genomic data and claims-based insights work together to help biopharma teams generate real-world evidence.
Watch now: genedx.co/4yUwsI9
#DrugDevelopment
At #MHPA26, GeneDx presented SAVES-Kids findings showing stepwise testing added 19 months and $2,039 before ES/GS for children covered by Medicaid.
Read more here: genedx.co/4AGQsiY
#MHPA26 #GeneticTesting #Medicaid #PrecisionMedicine #RareDisease #HealthEquity #Genomics
Genomic testing is becoming easier to integrate into everyday pediatric care. At #AAP2026, GeneDx is introducing Easy Order—a streamlined way for pediatricians to order exome and chromosomal microarray testing.
Learn more: genedx.co/4y2OkzJ
#Pediatrics #GeneticTesting
Headed to #CAGC2026 in Halifax? Stop by Booth #3 to explore the latest data, product updates, and insights in genomic testing.
Don't miss: The Diagnostic Yield of Exome and Genome Sequencing: Context Matters
📍 October 14 | 12:15-1:15 PM
Learn more ⬇️
genedx.co/4xpwqGP
Heading the 55th #CNSAM?
📅 October 14-16
📍Montreal, Canada
🧬Booth #601
Meet with our team to learn how exome sequencing can help identify the underlying genetic causes of unexplained pediatric neurologic and neurodevelopmental conditions: genedx.co/3V4Md0p
On #NICUAwarenessDay, these messages of hope, handwritten by NICU nurses at #NANN2026, are a reminder for families that they are not alone.
Thank you NICU nurses for your exceptional care and support when families need it most. 💚
genedx.co/3TRvsFA
Rare disease research starts with the right data—and combining genomic and longitudinal claims insights can provide a more complete view of the patient journey.
ICYMI watch our full Endpoints webinar on demand: genedx.co/4yUwsI9
#RareDisease #Genomics #RealWorldEvidence
It's not too late. Join Dr. Arie Weinstock for a case-based webinar exploring how genomic testing can help identify the underlying cause of epilepsy in children and young adults and inform care decisions.
📅 Oct 1 | 11 AM ET
genedx.co/3UZgfCJ
#Epilepsy #GeneticTesting














