GeneDx

GeneDx Paving the way for faster diagnoses & more precise care plans through genomic & clinical insights.

We see a world where every genetic condition is understood, and every patient receives the care they need to live their healthiest life through genomics. ​

GeneDx combines unmatched clinical expertise, advanced technology, and the power of GeneDx Infinity™, the world’s largest rare disease genomic dataset. This unparalleled foundation powers GeneDx’s ExomeDx™ and GenomeDx™ tests – ranked #1 by ex

pert geneticists and granted FDA Breakthrough Device Designation – enabling clinicians to deliver precise, fast, and actionable diagnoses. ​

With over 25 years of innovation, more than 4,800 genetic diseases diagnosed, and over 1,000 scientific publications, we’re building the genomic intelligence network that’s shaping the future of precision medicine: for patients, providers, and partners alike.

09/04/2026

Celebrating our August #1 Mindset Winners! 🎉

These five outstanding teammates demonstrate the values that help our teams, customers, and work move forward:

🏆 Tori Al-Hark, #1 Mindset Champion
Creates a supportive environment where teammates feel respected, encouraged, and empowered to grow.

🤝 Karlie Kaier, Cross-Functional Collaborator
Bridges technical operations, quality requirements, and compliance with professionalism and patience.

🌟 Naho Harada, Customer Impact Star
Builds trust through clear communication while advocating for clients and the best possible patient care.

💡 Philippe Soares, Innovation Driver
Shares deep technical expertise and fuels AI innovation to help our team work more efficiently.

🔄 Sarah Waltho, Best Pivot
Used adaptability, problem-solving, and collaboration to help achieve a positive outcome for her customer and GeneDx.

Congratulations to all of our winners, and thank you for making a meaningful impact every day!

Ahead of Canadian Association of Genetic Counsellors (CAGC) Annual Education Conference coming soon, we’re highlighting ...
09/02/2026

Ahead of Canadian Association of Genetic Counsellors (CAGC) Annual Education Conference coming soon, we’re highlighting the power of collaboration to accelerate rare disease discovery.

GeneDx and Canadian partners have contributed to 15 peer-reviewed publications in the past ~18 months, including work that helped upgrade six genes and expand diagnostic knowledge for patients worldwide.

Read our blog on the topic and visit us at to learn more about the real-world impact of GeneMatcher-facilitated collaborations.

https://genedx.co/4ydewrD

09/01/2026

September is NICU Awareness Month.

This month, we recognize the extraordinary clinicians, care teams, and families navigating some of the most complex and challenging moments in newborn care.

For critically ill infants, time matters. When a genetic condition is suspected, rapid genomic sequencing can help deliver answers sooner, supporting informed care decisions and providing greater clarity for families during times of uncertainty. Rapid results can be available in as soon as 48 hours, helping care teams act when every moment counts.

As we honor the resilience of NICU families and the dedication of the professionals who care for them, we're reminded of the importance of expanding access to the tools and insights that can help bring answers faster.

https://genedx.co/4guT7V5

Sometimes finding the answer means looking beyond the initial result.After a skeletal dysplasia panel identified one pat...
08/31/2026

Sometimes finding the answer means looking beyond the initial result.

After a skeletal dysplasia panel identified one pathogenic variant and one variant of uncertain significance (VUS), Mateo's family was still left without a definitive diagnosis.

Exome testing through GeneDx classified the VUS as likely pathogenic, providing a conclusive diagnosis of NPR2-related acromesomelic dysplasia and ending years of uncertainty.

Read Mateo's story and see how variant data within the GeneDx Infinity database can help unlock answers for more families.

https://genedx.co/4cELQPW

08/28/2026

🚀 Looking for your next opportunity to make an impact?

At GeneDx, we're helping people find answers faster through genomic insights that can change lives. We're growing our team and hiring for several key roles across commercial, clinical, and laboratory functions:

✅ Regional Account Executive, Specialty (DC/Alexandria) https://genedx.co/4cJ2Nsx
✅ Strategic Account Director, NICU (NYC) https://genedx.co/4zy6vit
✅ Assistant Clinical Analyst I (Remote US) https://genedx.co/4xoH95k
✅ Workforce Supervisor, Commercial Production Lab https://genedx.co/3UhSLIG

If you're passionate about advancing healthcare, collaborating with exceptional colleagues, and helping bring answers to patients and families, we'd love to hear from you.

Explore our current openings and apply today: 🔗 https://genedx.co/4oIgGfz

NICU nurses are often at the center of care coordination and family communication. In partnership with National Associat...
08/27/2026

NICU nurses are often at the center of care coordination and family communication. In partnership with National Association of Neonatal Nurses (NANN), GeneDx hosted this educational webinar exploring how rapid genomic sequencing can support care planning, interdisciplinary collaboration, and family-centered conversations throughout the NICU journey.

Hear practical insights from former bedside NICU nurse Kiley Moran on integrating genomic testing into neonatal care workflows. View now: https://genedx.co/3RYeUuV

Join us for the next installment in our webinar series: A case-based tour of primary immune disorders: Practical approac...
08/26/2026

Join us for the next installment in our webinar series: A case-based tour of primary immune disorders: Practical approaches for diagnosis and management

📆 Thursday, September 10, 2026 at 12 PM ET

📍With Nicholas Rider, DO, FCIS, FAAAAI

This session will explore:

• Clinical features and natural history patterns associated with major categories of primary immune disorders
• The role of genomic sequencing in the diagnosis and characterization of primary immune disorders
• How genomic sequencing results can influence patient management, treatment considerations, and counseling for patients and families

CEU credit is available.

Register now: https://genedx.co/468jYzY

08/25/2026

The need for earlier genetic answers is clear:

👧 Over 450,000 children in the U.S. live with epilepsy.
🧒 More than 1 million children live with intellectual disability.
🧬 Up to 50% of developmental delay, intellectual disability, and epilepsy cases may have a genetic cause.
📆 About 1 in 4 pediatric patients wait more than a year for a genetics appointment.

To help address these barriers, we've introduced a new clinician-guided offering that allows eligible families to initiate exome testing online through a simplified digital experience. Families are connected with licensed healthcare providers who can review medical information, determine clinical appropriateness, order testing, and return results, helping more children access expert-guided genetic testing without lengthy specialty-care delays.

Earlier answers can help guide treatment decisions, reduce unnecessary testing, support coordinated care, and provide families with a clearer path forward.

Get started today ⬇️
https://www.genedx.com/patients/access-genetic-testing

When Mora began missing developmental milestones, her family kept asking questions — and exome testing helped provide an...
08/21/2026

When Mora began missing developmental milestones, her family kept asking questions — and exome testing helped provide answers before a medical crisis occurred. Her early SYNGAP1 diagnosis enabled proactive seizure monitoring, earlier specialist care, and a clearer path forward.

Read Mora’s story and see how a genetic diagnosis can drive action.
https://genedx.co/45JUwRl

08/20/2026

For busy pediatricians, every step that makes genetic testing easier and faster can help move patients and families closer to answers.

That’s why GeneDx launched Easy Order, a new guided experience in the Provider Portal for eligible ExomeDx™ orders with CMA. The streamlined workflow helps general pediatricians caring for patients with global developmental delay (GDD) or intellectual disability (ID) submit more complete orders, reduce avoidable back-and-forth, and spend less time on administrative steps.

With fewer workflow interruptions, providers can get back to patient care sooner, spending more time with patients and families.

Read more: https://genedx.co/4bYmSuD

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Gaithersburg, MD

Opening Hours

Monday 8am - 8pm
Tuesday 8am - 8pm
Wednesday 8am - 8pm
Thursday 8am - 8pm
Friday 8am - 8pm

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+13015192100

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