Empowering healthier lives through genetic testing & genomics 💙 Experts in exome & genome sequencing 🧬

Stamford, CT
Joined June 2009
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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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