Relying on family history alone isn't enough. Knowing your patients' genetic variant status enables you to take action with increased screening and risk-reducing measures, so you can protect and preserve the health of your patients. Act now https://invit.ae/3EZbde2 #ActionOverAwareness #BreastCancerAwarenessMonth #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 Noah’s story here: https://invit.ae/3Y4hNJD #SCAmonth
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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://invit.ae/3XXM50o #BCAM
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There’s 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://invit.ae/4ek1Buw #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://invit.ae/4ek1Buw #genetictesting #GCchat
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Are you testing all of your ovarian cancer patients? Learn more about #genetictesting recommendations for your patient. https://invit.ae/4erpZdU #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 today: https://invit.ae/4ek1Buw #genetictesting #GCchat
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Congrats to ClinVar on reaching their 3 million milestone. This free, public database gathers information on genomic variations and their impact on human health. We're the #1 contributor, having submitted over 1.7 million genetic variant entries as of June 2024, aiming to promote transparency and improve patient care. Learn more about how we do it: https://invit.ae/3zK2pJA National Center for Biotechnology Information (NCBI)
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Ninety-five percent of rare diseases lack approved treatments. Better and deeper genetic datasets can help researchers make data-informed decisions as they strive to meet this urgent medical need. Learn how our huge set of de-identified patient data is helping #biopharma companies develop much-needed novel therapeutics. https://invit.ae/4exQkXk
Rare disease research benefits from large clinical and genomic datasets
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Genetic counselors are such a crucial part of a healthcare team, providing important information and support to patients and their families about their genetics. We’re thrilled about this positive step forward to ensure their services are captured accurately and consistently and to aid in health claims. Congratulations to everyone on this hard-won success. #GeneChat #NSGC24
🧬NEW: Genetic counselors have a new CPT® Code: 96041 launching January 2025! This is a positive step for our profession, ensuring genetic counselors can serve as vital healthcare partners for our provider colleagues and patients. Under the new code, billing will be based on the "total time” provided by the genetic counselor on the date of the encounter. In the coming weeks, NSGC will engage with members and external partners, including payors, starting with a can’t-miss plenary session on Sept. 19 at the #NSGC24 Annual Conference. We thank our volunteer and consultant teams, as well as ACMG - American College of Medical Genetics and Genomics for their efforts to help ensure that we can continue to deliver crucial services to our patients. Stay tuned for more resources as we transition to the new code going live in January 2025. #GeneChat
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