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

Stamford, CT
Joined June 2009
Join us for our upcoming webinar! Get an approachable guide to exome sequencing - who to test, what to order and why - plus case studies and live Q&A. Designed for developmental-behavioral and general pediatricians. 🗓️November 11 🕒 3 p.m. ET Register: genedx.co/3WfLU3i
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More answers. Fewer diagnostic gaps. GeneDx is expanding its genome testing portfolio with long-read whole genome sequencing to identify complex genetic variation and solve difficult cases sooner. Learn more: genedx.co/4BpGvHd #Genomics #RareDisease #PrecisionMedicine
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When Olivia’s family spent years searching for answers, GeneDx trio exome sequencing helped uncover genetic findings that guided diagnoses and gave her family long-awaited clarity. Read her story: genedx.co/4yUhodP @csnk2a1org #DiagnosisDrivesAction #GeneticTesting
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At #ASHG2026, GeneDx is presenting 27 scientific abstracts demonstrating how exome and genome sequencing are advancing earlier diagnosis, accelerating discovery and helping inform more precise care. Read more about our research at ASHG: genedx.co/4yPwG2R
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Heading to Becker's 14th Annual CEO + CFO Roundtable? Connect with us to explore integrating genomics into broader health system priorities around quality, innovation, and patient outcomes. 📅November 2-5, 2026 📍Chicago, Illinois Meet with us: genedx.co/4sc199k
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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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