From our team to yours, we wish you a happy and healthy holiday!

Meet us at the Forbes Healthcare Summit today in NYC & learn how we're tackling real-world challenges of extracting and synthesizing data from the literature, and how AI plus expert curation can make that tractable! 📧 [email protected]

🤝 Meet the team at AMP 2025 at Booth 433 for live demos of our platforms for germline and somatic variant interpretation, the Cancer Knowledgebase (CKB) and Mastermind! #AMPath2025 #AMP2025 #CKB #MastermindGIP

Attending #AMPath2025? Join us this morning at 10am EST in 156AB Level 1 for our corporate workshop: 'Revealing the Value of Literature-Based Real-World Evidence - Transforming Trial Design, Label Expansion, and Clinical Decision-Making' & visit Booth 433 this week to say hello! 👋

Going to #AMPath2025 in Boston? 👋 Find Genomemon at Booth #433 and let’s chat about your work and how we can provide support! amp25.amp.org

🗓️ Tomorrow! Meet us in Theater 2 at 10:15am EDT for our #ASHG25 CoLab talk with #GoldenHelix on Automating Genomic Workflows ⚙️ Hear how our partnership enhances genomic interpretation & delivers high-confidence, literature-backed insights to clinical laboratories worldwide.

October is Healthy Lung Month 🫁 Access curated literature, variant insights & clinical context for KCNK3, ENG & CFTR in #MastermindGIP plus 30 additional clinically relevant genes through December 🧬 Get started with a free account today: bit.ly/3W6L2uI

Meet us at #ASHG25 this week in Boston! 🤝 Live demos of #MastermindGIP and #CKB at Booth 1258, check out our CoLab with Golden Helix on Thursday in Theater 2 & ask us about our poster submission! Connect with the team to learn how we're making genomic evidence actionable 🧬

Attending #ASHG25? Stop by Booth 1258 for live demos, join us for a CoLab talk with #GoldenHelix & see our poster on 'Proportions of Missense, De Novo, and Disease Subtype Observations in Patients with COL1A1 & COL1A2 related Osteogenesis Imperfecta from the Literature'🧬

#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/48cZYP6

❔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/4mHDtpb

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/4gUvXWC

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:

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 www.genomenon.com/blog/future-...

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_u...

🧬 #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

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_u...

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=b...

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

🧬 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=ry...

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: www.genomenon.com/blog/cancer-...

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_u...

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=b...

❔ 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_u...

👓 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_u...

#ICYMI Watch last month's webinar with UCB on 'Real-World Evidence for Precision Therapeutics' & learn how our partnership accelerates accurate diagnosis but also reduces barriers to genetic testing, ultimately improving patient outcomes & informing care strategies www.genomenon.com/resource/rea...

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: www.genomenon.com/somatic-cura...

#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_u...

Rare but relentless #bonecancer demands our attention! July is Bone Cancer Awareness Month. Dive deeper into variants to curated evidence, treatment options, and active clinical trials in #CKB 🔎🧬 ckb.genomenon.com?utm_source=b...

We're excited to announce our partnership with UCB to accelerate research and diagnosis for thymidine kinase 2 deficiency (TK2d)—a devastating but underdiagnosed rare mitochondrial disease. Read the #pressrelease ➡️ www.genomenon.com/news-press-e...

33 genes. 10 new! All free in Mastermind CORE through Sept 30 🔎 Explore rare disease insights & curated variant data now in our latest #blog 🧬 www.genomenon.com/blog/fueling...

We're at the #FestivalofGenomics & #BioData in Boston - Let's meet to discuss how we uncover the genomic drivers of genetic disease and cancer—transforming complex genetic data into clear, actionable insights! 🤝📧[email protected]

Today is #SickleCellAwareness Day! We're offering free access to curated HBB variant data to support care & research in #MastermindGIP. Our latest blog outlines what's included: www.genomenon.com/blog/sickle-...

📣 #LatestNews 📣 Intelliseq Integrates Genomenon’s Cancer Knowledgebase #CKB into #iFlow Platform to Advance Somatic Variant Interpretation. Read the full #PR 👉 www.genomenon.com/news-press-e...

Today is #CDKL5 Awareness Day. Gain access to curated CDKL5 variant insights to support early diagnosis in #Mastermind Genomic Intelligence Platform today: 🔗 mastermind.genomenon.com?utm_source=b...

📣 #PressRelease Learn how our genomic intelligence is driving actionable outcomes in translational research in this newly published study co-authored with RectifyPharma & DTR Labs: www.genomenon.com/news-press-e...

🧬 MC1R isn’t just the red hair gene—it’s a game changer. People with #MC1R variants often need more anesthesia, feel pain more intensely & burn in the sun much faster. 1 gene, 3 systems: appearance, pain, and protection. Explore now in #MastermindGIP mastermind.genomenon.com/gene?gene=mc...

Solid tumors are driven by genomics, not location. #CKB delivers curated variant insights to power precision #oncology🔬 Learn how CKB delivers the genomic precision needed to drive smarter decisions in our latest #blog: www.genomenon.com/blog/decodin...

#LatestNews 📣 Genomenon, Inc. to Participate in BIO 2025 in Boston to Highlight Real World Evidence for Precision Therapeutics - read the full announcement: www.genomenon.com/news-press-e... #BIO2025 #PressRelease #Genomics #RWE #PrecisionMedicine

🗓️ Register now for our next live webinar June 26th: Real-World Evidence for Precision Therapeutics. Gain insights into providing actionable evidence that accelerates drug discovery & enables more targeted patient identification. Meet the panelists: www.genomenon.com/resource/rea...

As part of #BattenDisease Awareness Day we’re offering free access to expertly curated variant data for the CLN3 gene in #MastermindGIP 🧬 Our latest blog shares a story of a family searching for answers—and holding onto hope. See more & explore #CLN3: www.genomenon.com/blog/batten-...

🧬 Variants in the DRD4 gene—part of the dopamine receptor family—have been linked to novelty-seeking and risk-taking behaviors in several studies. That’s why some call it the 'adventure gene'. Explore DRD4 in Mastermind: mastermind.genomenon.com/gene?gene=dr...

🤝 Meet with the Genomenon team at #BIO2025, June 16-19 in Boston! Let’s collaborate through the BIO Partnering™ system—because the world can’t wait. #Genomics #PrecisionMedicine #Innovation

In our latest blog, published in light of #Melanoma and #SkinCancerAwarenessMonth we explore the genetic blueprint driving the deadliest form of skin cancer—and how these insights are reshaping diagnosis, treatment, and outcomes. Read more: www.genomenon.com/blog/the-gen...

Celebrate #CysticFibrosis Awareness Month with free access to CFTR and 32 other curated genes in #MastermindCORE—available through June 30: mastermind.genomenon.com/users/sign_u...

Are you a mosquito magnet? 🦟 Your ABO gene may be the reason—type O blood attracts more bites! Blame your DNA & explore more: mastermind.genomenon.com/gene?gene=abo

🧬✔️ We’ve made curated content for 33 high-impact genes available within #MastermindCORE — spanning key clinical areas such as hereditary cancer, neurodevelopmental disorders & complement-mediated conditions 🔗 Read more in our latest #blog www.genomenon.com/blog/fueling...

We support the #Resolution4Rare to bring urgent attention to the 300M+ living with rare diseases. Early diagnosis starts with better data! www.rarediseasesinternational.org/wha-resoluti...

🎉 Today marks 11 years since Genomenon began its journey to bring genomic intelligence to the forefront of precision medicine—and what a journey it’s been! Take a look at more of our milestones from last year's blog: www.genomenon.com/blog/genomen...

👁‍🗨 Did you know? PAX6 is essential for eye development? Variants can cause aniridia—absence of the iris. Explore this 🧬 & more in #MastermindGIP: mastermind.genomenon.com/gene?gene=pa...