Invitae
@Invitae
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Bringing comprehensive genetic information into mainstream medicine to improve healthcare. To read our community guidelines, visit https://t.co/EhmweQKgU7
San Francisco
Joined January 2012
For the first time, doctors used a gene-editing therapy tailored to a baby’s life-threatening, genetic disorder, a step toward more personalized care for rare disease patients:
npr.org
For the first time, doctors have created a customized treatment using the revolutionary gene-editing technique known as CRISPR to treat a baby with a rare, life-threatening genetic disorder.
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When Meaghen stopped meeting developmental milestones, her mother Marissa began a search for answers. A genetic test helped reveal the true source of Meaghen’s condition and helped Marissa become a better advocate for her daughter. Read her story here:
blog.invitae.com
When little Meaghen stopped meeting her developmental milestones, a genetic test helped her parents find better support
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Ten years after testing positive for a BRCA2 variant, cancer has touched Amanda’s family in more ways than one. She reflects on how preventive measures helped protect her health and why open communication with her kids is key. Read Amanda’s story:
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Join us in celebrating Genetic Counselor Awareness Day! We honor the incredible contributions of genetic counselors and the invaluable role they play in healthcare. Let's show our appreciation for all that they do. #GeneticCounselorAwarenessDay Invitae is now part of Labcorp.
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Want to learn about mainstreaming models for cancer risk assessment and genetic testing? Join us Saturday, Nov 16 at #CGAIGC2024 for our symposium from 12:30–1:30 pm. Click here to learn more: https://t.co/VYbfeMsFPJ Invitae is part of #Labcorp
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Join us at booth #650 at ASHG to learn how we’re transforming variant classification with the power of machine learning to reclassify uncertain results. https://t.co/D5rNUSUNm8
#ASHG #VUSReclassification Invitae is now part of Labcorp.
jamanetwork.com
This cohort study analyzes the rates at which clinical genetic variants are reclassified and the types of evidence that enable reclassification among individuals who undergo genetic testing for...
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Attending #CGAIGC24? Stop by booth #3 to learn how we can help inform #colorectalcancer #gicancer #polyposis care with our hereditary cancer #GeneticTesting.
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Planning for #ASHG? Visit booth #650 to learn about the latest updates to Invitae Generation™ and our variant classification methods. Learn more: https://t.co/CaJoEgldGn
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As far as Sarah knew, breast cancer didn’t run in her family. The results of one genetic test changed everything: Sarah discovered she was positive for BRCA1, which significantly increased her lifetime risk of developing breast and ovarian cancer.
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Insights gained from genetic testing for hereditary cancer can impact medical recommendations. In fact, the American Society of Breast Surgeons (ASBrS) recommends genetic testing for all patients with breast cancer. Learn more: https://t.co/b1LP6hlY14
#BCAM
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When Noah began having cardiac arrests at 18 months old, his doctors couldn’t figure out why. An exome sequencing test helped reveal the genetic source of his cardiac arrests and gave his parents more certainty about how to protect his health. Read more:
blog.invitae.com
How exome sequencing helped reveal the surprising triggers of a rare cardiac condition
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As we honor and support survivors and patients during Breast Cancer Awareness Month, take a moment to explore how #genetictesting can be a powerful tool for helping your patients take care of their health. Learn how we make testing easy: https://t.co/b1LP6hlY14
#BCAM
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There is still time to register. Join us for this live webinar presented on October 10 at 12 pm ET/9 am PT and earn CEUs by attending. Register: https://t.co/sTCGBsJOLx
#genetictesting #GCchat
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Interested in exploring Sherloc? Join us for a live webinar presented on October 10 at 12 pm ET/9 am PT and earn CEUs by attending. Register now: https://t.co/sTCGBsJOLx
#genetictesting #GCchat
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Are you testing all of your ovarian cancer patients? Learn more about #genetictesting recommendations for your patient. https://t.co/uec4OKwd5k
#OvarianCancerAwarenessMonth
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The evolution of Sherloc: Insights into the innovative and scalable approaches impacting variant classification. Join us for this live webinar presented on October 10 at 12 pm ET/9 am PT and earn CEUs by attending. Register: https://t.co/sTCGBsJOLx
#genetictesting #GCchat
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Large genetic datasets can help researchers and biopharma teams develop much-needed treatments for rare diseases. Learn how our huge set of de-identified patient data helps support these efforts.
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Attending #NSGC24? Join us and professional resume writer, Carey Hunter, MA, CPRW, at booth #527 for mini-workshops between sessions and personalized resume advice. Submit your resume in advance to guarantee a professional review https://t.co/JuZhQD3fPV
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A new clinical utility study shows that genetic test results can affect treatment and follow-up recommendations for patients with prostate cancer. Read the study:
auajournals.org
Purpose:Identification of pathogenic germline variants in patients with prostate cancer can help inform treatment selection, screening for secondary malignancies, and cascade testing. Limited...
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