Transform patient care with rapid #genome #sequencing, recommended as a first-line test by the International Precision Child Health Partnership, the American College of Medical Genetics and Genomics, and the National Society of Genetic Counselors. Learn more at https://genedx.co/3T04ZST.
About us
At GeneDx, we believe that everyone deserves personalized, targeted medical care—and that it all begins with a genetic diagnosis. Fueled by one of the world’s largest rare disease data sets, our industry-leading exome and genome tests translate complex genomic data into clinical answers that unlock personalized health plans, accelerate drug discovery, and improve health system efficiencies. It all starts with a single test.
- Website
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https://www.genedx.com
External link for GeneDx
- Industry
- Biotechnology Research
- Company size
- 1,001-5,000 employees
- Headquarters
- Stamford, CT
- Type
- Public Company
- Specialties
- genetic testing, rare genetic disorders, molecular diagnostics, whole genome sequencing, next generation sequencing, neonatal screening, whole exome sequencing, genome, genetics, artificial intelligence, and exome
Locations
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Primary
333 Ludlow Street
8th Floor
Stamford, CT 06902, US
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207 Perry Pkwy
Gaithersburg, Maryland 20877, US
Employees at GeneDx
Updates
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GeneDx reposted this
We envision a world where any genetic disorder is diagnosed quickly to prevent disease progression and ensure long and healthy lives for all. Our team at GeneDx is translating our leadership in exome to pave the way for a genome future. Proud of our team and what's ahead in service of patients. https://lnkd.in/eQ_m7a5W
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Easier. More accessible. Non-invasive. Simplified #genome #sequencing sample collection with buccal (cheek swab) samples for patients. Because one less blood draw really does make a difference. Learn more at https://genedx.co/4fsqN2K
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GeneDx reposted this
Over the past few years, we have successfully transformed GeneDx into a driving force in genetic diagnostics, and we haven’t gotten here alone. Our patients and their families, our customers, collaborators, our team members, and shareholders make all of it possible, and I want to thank them for their ongoing dedication and support. We are painting a vision for a better future in healthcare: one where every family can benefit from earlier diagnosis of disease through genomics, and with another successful quarter under our belt, we are one step closer to realizing that future. https://lnkd.in/euCJ8mCK
GeneDx Reports Second Quarter 2024 Financial Results and Business Highlights | GeneDx
ir.genedx.com
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The faster you receive answers, the sooner you can take action. We're proud to announce that our rapid genome sequencing will provide written results in as soon as 5 days, enabling even more timely diagnosis and treatment decisions. Learn more: https://genedx.co/4fsqN2K
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📣 GeneDx's Q2 2024 financial results are now available. Join us today for our earnings call, where we'll discuss our financial and operating performance. For more details, read our press release: https://genedx.co/4d3ZDh5
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Why are many patients with #epilepsy still receiving narrow testing, like multi-gene panels? Oftentimes, it’s about opening doors. GeneDx’s Epilepsy Partnership Program helps eligible pediatric patients access guideline-backed #exome sequencing, even if they’re uninsured or their insurance provider denies coverage. Your patients deserve answers—and not to worry about access to exome sequencing. Learn more at https://genedx.co/467Sbih
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Did you know that rapid genome sequencing doesn’t just help identify a diagnosis earlier? It's also been shown to reduce healthcare costs up to $15,786 per child in the #NICU. Learn more about rapid genome’s potential benefits for you and your patients at https://genedx.co/4feROqC.
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Ordering a #trio—testing a patient and two family members—can boost the power of #exome by: ✔️doubling the chances of finding a #genetic #diagnosis ✔️decreasing the time it takes to receive results Bottom line: By comparing the #DNA of relatives, ordering trios can make it more likely—and faster—to find answers for your patients and their families.
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Every day we hear remarkable stories about the impact whole genome sequencing (WGS) and whole exome sequencing (WES) have on our patients. A diagnosis can lead to better patient care plans, therapies, communities and so much more. Thank you to Liz Strouse for sharing her son Tiem’s story. GeneDx is thrilled to see Florida open access to biomarker testing for patients seeking answers in all areas in medicine as we celebrate the 1 year anniversary of the Andrew John Anderson Rapid Genome Sequencing Program. Thank you to the Tampa Bay Times for sharing Tiem’s story, hopefully other parents on a diagnostic odyssey can read this story and get one step closer to answers. And thank you to Ashley Arthur, our market access leader, for advocating for these families. https://lnkd.in/eEwc2vTz
Florida hopes to reduce ‘diagnostic odyssey’ for children with rare diseases
tampabay.com