Meet our CEO!

Meet our software developer! 💻

Meet our BD Associate!

Did you know 50% of all rare disease patients are children? #FactFriday

Meet our CTO!

Meet Cheyanne Perry Suarez, our Patient Community Manager!

It’s Global Niemann-Pick Awareness Day.

Why Drug Developers Are Launching Sponsored Testing Programs With Probably Genetic bit.ly/3vDIPbU

Understanding the lives of #raredisease patients is imperative for those researching and developing treatments for rare diagnoses. ➤ bit.ly/3q75WuX

Did you know? • #RareDisease affects 350 million people worldwide. 🌎

PRESS RELEASE: SynGAP Research Fund deploys #CouldItBeSYNGAP1 screening tool in partnership with Probably Genetic! Share this tool with #epilepsy #autism and other #specialneeds communities. #SYNGAP1 eurekalert.org/news-releases/…

Follow us on Instagram! #ProbablyGenetic #Instagram

Most, but not all, genetic disorders begin in childhood. The frequency of childhood genetic disorders is under recognized, yet awareness is imperative for early intervention and treatment. That’s why Probably Genetic makes it our goal to shorten the diagnostic odyssey! #Genetics

Probably Genetic has had quite a few new hires recently! We are thrilled to be adding to our team. ⁣Stay tuned for future posts to get to know our team of dedicated individuals!

Meet Jancie!

Meet our Associate Product Manager! #ProbablyGenetic

We have partnered with Probably Genetic to launch a US-based, no-cost genetic testing program for eligible individuals diagnosed with #FTD or experiencing FTD-like symptoms. If you or anyone in your community might benefit from this opportunity, please see bit.ly/3CNho4C

Congrats to Mike Graglia 🌻 and the SynGAP Research Fund (SRF) team for getting covered in Newsweek! If you want to understand what it means to be undiagnosed, to get a diagnosis for a condition without a treatment, and to make people take on your cause and work on therapeutics, read this article.

We are so excited to partner with Probably Genetic Their FREE #genetictesting program includes genetic counseling. bit.ly/3GW2VoT If you know someone with #cerebralpalsy or #epilepsy who has not had whole exome sequencing, PLEASE share this with them! #CTNNB1

We are offering no-cost genetic testing for individuals with pediatric-onset seizure and movement disorders. If you or a loved one experience seizures, movement difficulties, or have received a cerebral palsy diagnosis apply for testing here: bit.ly/3NhxmJG