GeneDx (@genedx) 's Twitter Profile
GeneDx

@genedx

GeneDx is paving the way for faster diagnoses and more precise care plans through genomic and clinical insights.

ID: 46161991

linkhttps://www.genedx.com/ calendar_today10-06-2009 17:03:43

4,4K Tweet

6,6K Followers

837 Following

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For babies in the NICU, their story has just begun. Find #answers that help get them out of the #NICU and onto the next chapter of their story. Learn how GeneDx can help.

For babies in the NICU, their story has just begun. Find #answers that help get them out of the #NICU and onto the next chapter of their story. Learn how GeneDx can help.
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Families want answers. #rWGS can help you get to the root cause of a #NICU patient’s condition - and can direct more personalized treatment. Learn how you can implement comprehensive genetic testing by visiting the GeneDx booth at the Nemours Children's Neonatology Conference.

Families want answers. #rWGS can help you get to the root cause of a #NICU patient’s condition - and can direct more personalized treatment. Learn how you can implement comprehensive genetic testing by visiting the GeneDx booth at the Nemours Children's Neonatology Conference.
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Are you a healthcare provider working in a #NICU? Do you want to implement rapid genetic testing, but lack genetic specialist support? Learn how to interpret #genetic results & discuss them with caregivers, with insights from a panel of experts. bit.ly/3KV9ZEj

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Incorporating #genomic #sequencing into your workflow doesn’t have to be complicated. Instead, let us do the heavy lifting. We can assist with: ✅ selecting appropriate tests ✅ answering clinical questions ✅ reporting patient-centric results ✅ guiding potential next steps

Incorporating #genomic #sequencing into your workflow doesn’t have to be complicated. Instead, let us do the heavy lifting. We can assist with:
✅ selecting appropriate tests
✅ answering clinical questions
✅ reporting patient-centric results
✅ guiding potential next steps
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Five. That’s how many uninformative tests the average child with neurodevelopmental disorders undergoes in search of a #genetic diagnosis. Find critical information sooner by ordering #exome first. Test once, discover more, and help your #patients get the care they need earlier.

Five. That’s how many uninformative tests the average child with neurodevelopmental disorders undergoes in search of a #genetic diagnosis. Find critical information sooner by ordering #exome first. Test once, discover more, and help your #patients get the care they need earlier.
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There’s no place like home for the #holidays. But for the most vulnerable patients, this isn’t always possible. Give them the gift of #genetic insights that can help inform diagnosis, direct treatment, & make sure they’re back where they belong: in the arms of their loved ones.

There’s no place like home for the #holidays. But for the most vulnerable patients, this isn’t always possible. Give them the gift of #genetic insights that can help inform diagnosis, direct treatment, & make sure they’re back where they belong: in the arms of their loved ones.
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New year. New insights. New direction. The understanding gained through #genetic testing can hold so much promise for #patients and their families. That’s why for 2024, we’re committed to finding more answers for more patients.

New year. New insights. New direction. The understanding gained through #genetic testing can hold so much promise for #patients and their families. That’s why for 2024, we’re committed to finding more answers for more patients.
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9 state Medicaid programs now cover rapid whole #genome #sequencing (rWGS) in the pediatric inpatient setting. Utah joins a growing list of states who recognize the importance of offering rWGS in the NICU & PICU to provide a rapid diagnosis for the most vulnerable patients.

9 state Medicaid programs now cover rapid whole #genome #sequencing (rWGS) in the pediatric inpatient setting. 

Utah joins a growing list of states who recognize the importance of offering rWGS in the NICU & PICU to provide a rapid diagnosis for the most vulnerable patients.
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GeneDx's 2023 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 here: genedx.co/3wkToVP

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More patients need #genetic testing than there are genetics experts. How do we ensure they get the care they need? Join us for a collaborative brainstorming session at the 2024 #ACMG meeting, as we discuss patient access outside of the genetics clinic. ➡️ genedx.co/3wERK1B

More patients need #genetic testing than there are genetics experts. How do we ensure they get the care they need? Join us for a collaborative brainstorming session at the 2024 #ACMG meeting, as we discuss patient access outside of the genetics clinic.
➡️ genedx.co/3wERK1B
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📣Join us at the American College of Medical Genetics (#ACMG) Annual Meeting as we present new data demonstrating the clinical superiority of #ExomeSequencing. Exome finds answers that other tests can miss. Read more in our full press release: genedx.co/3TAFeJm

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We’re taking the stage with Egetis Therapeutics and Effie Parks at World Orphan Drug Congress USA! Join us for a panel discussion on April 25 at 1:00pm to learn how we can bring new therapies to patients, faster, by working together. We’re looking forward to connecting in Boston!

We’re taking the stage with <a href="/Egetis_EGTX/">Egetis Therapeutics</a> and <a href="/OnceUponAGene/">Effie Parks</a> at <a href="/OrphanConf/">World Orphan Drug Congress USA</a>! Join us for a panel discussion on April 25 at 1:00pm to learn how we can bring new therapies to patients, faster, by working together. We’re looking forward to connecting in Boston!
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Our latest Vanguards of Health Care episode dropped last week featuring GeneDx's CEO Katherine Stueland. She shared how they're trying to make multi-gene panels a thing of the past with exome testing and her views on testing's future. Listen here: open.spotify.com/episode/4AvjTW…

Our latest Vanguards of Health Care episode dropped last week featuring <a href="/GeneDx/">GeneDx</a>'s CEO Katherine Stueland. She shared how they're trying to make multi-gene panels a thing of the past with exome testing and her views on testing's future.

Listen here:
open.spotify.com/episode/4AvjTW…
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GeneDx's Q1 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. genedx.co/3wkWCZG

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This is the last month to earn your CME credit! Learn about the expanding and vital role of rapid #Genomic sequencing in the NICU in the webcast: A #NICU Clinician's Guide to Rapid Whole #Genome Sequencing—before the webinar expires on May 24. bit.ly/3KV9ZEj

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Exome sequencing is more likely to find a #genetic #diagnosis for epilepsy patients. It’s recommended as a first-line test for individuals with unexplained #epilepsy by the National Society of Genetic Counselors and endorsed by the American Epilepsy Society.

Exome sequencing is more likely to find a #genetic #diagnosis for epilepsy patients. It’s recommended as a first-line test for individuals with unexplained #epilepsy by the National Society of Genetic Counselors and endorsed by the American Epilepsy Society.
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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: genedx.co/3SxxZ46

📣 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: genedx.co/3SxxZ46
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Coming soon: Faster turnaround for rapid genome sequencing, buccal sample types accepted for patients receiving genome, and more. The result? Accelerated diagnoses for patients. For more details, read our press release: genedx.co/3SvXsea

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Join us for a satellite symposium at the NSGC 43rd Annual Conference, where we'll explore different paths that help patients gain access and find answers, sooner. We look forward to seeing you there!​ Register now: genedx.co/3X9kv0V

Join us for a satellite symposium at the NSGC 43rd Annual Conference, where we'll explore different paths that help patients gain access and find answers, sooner. We look forward to seeing you there!​

Register now: genedx.co/3X9kv0V