Join us in honoring Rare Disease Day 2024! Michael Bray, PhD, MS, CGC, and Clinical Genetic Data Specialist shares profound insights into the journey of those living with rare diseases and our unwavering commitment to accelerate change. https://t.co/waH3kM8ayT #RareDiseaseDay

Feb 29th is #RareDiseaseDay. Are you ready? 300+ million people globally live with a rare disease - come together to advocate for equitable access to diagnosis, treatment, care, and social opportunities. Learn more at https://t.co/o7turYYiCn.

ThinkGenetic, Inc. leaders, Ruth Jacob O’Keefe and Dawn Laney are thrilled to be part of the #WorldSymposia this week. The event is designed to help researchers and clinicians expand knowledge and share information about lysosomal diseases.

Today, our CEO, Ruth Jacob O'Keefe, shared a short reflection on the past year at ThinkGenetic, expressing gratitude to our dedicated community for their unwavering commitment: https://t.co/mR5hU1tcsF #RareDisease #DigitalHealth

ThinkGenetic is pleased to announce the participation of CEO, Ruth O'Keefe, alongside Chief Genetic Officer, Dawn Laney at the upcoming 20th Annual #WORLDSymposia. We invite you to explore opportunities for connection with our leadership team. #LysosomalDisease #RareDiseases

Please welcome new Clinical Genetic Data Specialist, Michael Bray, MS, PhD, CGC to the clinical team. Michael has experience in genetic research with an emphasis on performing genetic analyses on data linked to de-identified electronic health records. #geneticcounseling

Finding the right diagnosis can be a lengthy, harrowing journey. Recent research by ThinkGenetic offers hope, showing how EHR data and an algorithm can identify patients at risk for rare genetic conditions. Learn more: https://t.co/ZxNLZX7kK5 #RareDisease #Healthcare #EHR

Join us at the Orphan Drugs & Rare Diseases Global Congress November 16-17 in Boston, MA. The two-day Congress aims to offer insights into how to improve the diagnostic process and access to treatments of Orphan Drugs and Rare Diseases. Learn more at https://t.co/9IAHjQOOkM

At #NSGC23 this week, Dawn Laney was honored as a nominee for the 2023 Heart of Genetic Counseling Award - a tribute to distinguished genetic counselors who provide exceptional and irreplaceable care to families dealing with major health challenges.

🔬 Today at #NSGC23, we reveal groundbreaking research on AADC deficiency. Join us at the Poster Gallery to learn how AI and EHRs identify patients at risk for rare diseases. Can't make it to NSGC? The results will be shared tomorrow at https://t.co/m6MdvLIXlZ! #RareDisease

Join us at the NSGC 2023 for two research poster discussions including how we used AI to identify patients at possible increased risk for Aromatic L-amino acid decarboxylase deficiency from Electronic Health Record data. Visit https://t.co/4X6mRsJBFi. #nsgc23 #raredisease

We're thrilled to announce the appointment of Ruth Jacob O'Keefe as our new CEO. This significant milestone in ThinkGenetic, Inc.'s journey represents our drive to continue innovating and driving progress in the rare disease space. Read more by visiting: https://t.co/uhy48YxWnp

Dive into the world of Large Language Models (LLMs). Corey Fournier, Senior Data Engineer at ThinkGenetic, reviews on LLMs and their compression in AI: https://t.co/Ivn3xdd1eZ #AI #LLM #Compression #ThinkGenetic #GeneticResearch

We believe that every individual's journey with genetic diseases is unique. Today we're sharing a heartfelt article from Jerry Walter, who shares his family's experience with Fabry disease. Read Jerry's moving story here: https://t.co/o1SbaBaZHH #FabryDisease #GeneticDisease

Congratulations to the 2023 Torch Award winners! We're especially proud of ThinkGenetic co-founder, Dawn Laney, who was one of those honored, for her dedication throughout her career to the rare disease community https://t.co/tNz83YQvfF #TorchAwards @SanofiUS #Fabry @raredisease

FDA approved the first drug for patients with fibrodysplasia ossificans progressive - a rare, autosomal dominant disease. The FDA granted this approval to @IpsenGroup Read the @US_FDA Announcement at https://t.co/s5V5GPzLdO #raredisease #Fibrodysplasia #FDA #FOP

A lab at Oregon Health & Science University offered Oregon residents free genetic screening and have completed screening for over 13,000 adults since 2018. Check out their process, findings, and hopes for future efforts here: https://t.co/EGGEAlENNo #research #genetics #genomics

Today is Chromosome 8p Day! If you haven’t signed up yet, there’s still time to join in on the second annual 8000 Steps for 8p! Check out https://t.co/5nfoUI2YdY for more information! #rare #genetics #genomics #chromosome8p #8000stepsfor8p

Happy CLOVES Awareness Day! Check out https://t.co/CdHYXWBmhX and @CLOVESSyndrome to find out how you can support and help raise awareness of CLOVES syndrome today! #raredisease #genetics #genomics #awareness #CLOVESsyndrome

Genetic counselors and GC students - did you know the @ThinkGeneticFdn is giving away funding to help you attend conferences or cover license fees right now? Go check it out and apply at