#WorldBrainDay is a reminder of how far we’ve come & how far we still need to go in understanding complex brain disorders 🧠 Explore 535 genes and 36,000+ variants from top neuro panels in #MastermindGIP mastermind.genomenon.com/users/sign_up/…

The latest update from the Cancer Knowledgebase (#CKB) shows continued momentum in evidence-based cancer genomics. 👉 Explore how CKB supports faster decisions and smarter strategies in #precisionmedicine: genomenon.com/somatic-curati…

#ICYMI See the latest webinar with UCB on 'Real-World Evidence for Precision Therapeutics' & learn how our work accelerates accurate diagnosis & also reduces barriers to genetic testing, ultimately improving patient outcomes & informing care strategies genomenon.com/resource/real-…

👓 August is Children's Eye Health and Safety Month & through September we’re making EYS and 32 other clinically important genes freely available in #MastermindGIP! 🧬 Start searching today: mastermind.genomenon.com/users/sign_up/…

❔ Did you know? Germline variants in the #PALB2 gene significantly increase breast cancer risk - often nearly as much as variants in #BRCA1 and #BRCA2. Explore the most comprehensive, curated PALB2 data available - completely free in Mastermind! mastermind.genomenon.com/users/sign_up/…

With the Cancer Knowledgebase #CKB - a Variant of Uncertain Significance #VUS isn’t a final answer - it’s a starting point. It marks where science still has room to grow & where our work continues. Learn more: ckb.genomenon.com/?utm_source=x&…

August is Autoinflammatory Disease Awareness Month! Familial Mediterranean Fever #FMF is a genetic disorder caused by pathogenic variants in the MEFV gene 🧬 Free through September - access #MEFV in Mastermind & 32 other clinically significant genes: mastermind.genomenon.com/users/sign_up/…

In genomics, context is everything. A variant's relevance can shift dramatically based on the latest research. That’s why maintenance is not an afterthought; it’s a core part of what makes #CKB trustworthy. Read how we keep CKB accurate, current & trusted:genomenon.com/blog/cancer-kn…

🧬 Variants in #RYR2 can cause #CPVT - a hidden heart disorder where the first sign may be sudden death. Early testing & family screening can save lives. Explore this gene in #MastermindGIP 🔎 mastermind.genomenon.com/gene?gene=ryr2…

One of the richest sources of #RealWorldEvidence is hiding in plain sight: the scientific literature. Learn why overlooking it means missing opportunity: genomenon.com/blog/scientifi…

August is #AppendixCancer Awareness Month. Variants in BRAF, GNAS, KRAS & ATM drive this rare disease - explore 50 curated cancer genes free in #CKB CORE: ckb.genomenon.com/?utm_source=x&…

Today is SATB2-Associated Syndrome Awareness Day! 🧬 #SATB2 variants cause a rare syndrome affecting brain, facial, and speech development. Free through September: Explore SATB2 + 32 genes in #MastermindGIP mastermind.genomenon.com/users/sign_up/…

🧬 #ABCB1 encodes P-glycoprotein, a “drug pump” moving chemo drugs out of cells. Variants can alter response - sometimes the difference between a drug that works and one that fails #GeneFact #Genomics #CancerResearch #CKB

We are pleased to announce our strategic partnership with Genomenon. This collaboration allows the Mastermind Genomic Intelligence Platform and Cancer Knowledgebase to integrate seamlessly into the VarSeq Suite. 📣 Read the full press release here: bit.ly/3HEZnLn

In honor of #CharcotMarieTooth Awareness Month the LMNA gene 🧬 is free to explore in #MastermindGIP throughout September. Not a user yet? Create your free account: mastermind.genomenon.com/users/sign_up/…

Every baby deserves the best possible start in life. 💙 That’s why Newborn Screening Awareness Month matters to us at Genomenon. 👉 Learn how we’re helping shape the future of #NBS genomenon.com/blog/future-ne…

By drawing on functional studies, case series, patient registries & decades of literature, #RWE provides the missing context to reclassify uncertain variants as pathogenic or benign - turning ambiguity into actionable knowledge. See the latest #blog: bit.ly/4nljehY

Today we honor those living with #LaforaDisease, their families & the researchers striving for breakthroughs. Awareness is the first step toward better care and better therapies. Get Mastermind PRO & access this valuable data: bit.ly/475omB2 #FightLafora

❔How do you take 20,000+ oncology tests a year and make the results faster, consistent, and actionable? Read the latest #webinar recap with #CKB & Northwestern Medicine: bit.ly/46y7lPX

#GLUT1DeficiencySyndrome is a rare neurological disorder caused by pathogenic variants in the SLC2A1 gene 🧬 This along with 32 other clinically relevant genes are freely available in Mastermind CORE through December. Get started today with a free account: bit.ly/4pUnl6i