Today on #EctodermalDysplasia Awareness Day, we share how Genomenon’s founder & CSO turned his diagnosis into Mastermind—a genomic intelligence platform now used by 2k+ labs to improve rare disease diagnosis 📖 Read more: www.genomenon.com/blog/the-sto... #RareDiseaseDay #Blog

February is Heart Month ♥️ Genomenon offers free access to curated variant insights on TNNC1, MYBPC3, and 9 rare disease genes to support research and patient care. Search Mastermind today! 🧬 Sign up for free: mastermind.genomenon.com/users/sign_u...

#HeartMonth #RareDiseaseDay #Genomics

Every February 4th #WorldCancerDay unites the globe to raise awareness & advance cancer research. We harness genomics to drive precision medicine, empowering researchers with our Cancer Knowledgebase (CKB) 🧬🌎🔎 Read our latest blog to learn how: bit.ly/4jJKqWb

February is #RareDiseaseMonth, a time to support those facing rare genetic conditions. To advance research and care, we're offering free access to curated variant insights on 12 key genes starting Feb 1!

🧬🖥️ Sign up free today & start searching: mastermind.genomenon.com/users/sign_u...

🧬 Know someone who feels fully rested after just 4 hours of sleep? They might have a rare genetic variant in the BHLHE41 (DEC2) gene! #BHLHE41 is a transcription factor that regulates circadian rhythms and sleep duration. Learn more in Mastermind: mastermind.genomenon.com/gene?gene=bh...

Our Cancer Knowledgebase (CKB) now covers clinical trials in 39 countries, including 25 new in Europe, boosting access to genomically relevant trials. Learn more in our latest blog!

www.genomenon.com/blog/ckbs-gl...

Did you know? 🧬 PLA2G6 gene variants cause #INAD, a rare neurodegenerative disorder. Early genetic testing is vital. Access free PLA2G6 variant insights this December in Mastermind! mastermind.genomenon.com/gene?gene=pl...