Healx @healx
AI-powered and patient-inspired. We accelerate the discovery and development of #raredisease treatments. healx.ai Cambridge, UK Joined April 2014-
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NEWS! Today we are deepening our relationship with long-term partner @ChildrensTumor to advance #neurofibromatosis type 1 treatments. We will receive investment from CTF to support our lead compound to clinical trials. Find out more: bit.ly/3xr28tY #nf #endnf #ai
As we approach Rare Disease Day on Thursday February 29th, here is an update on our fundraising efforts for @timothysyndromealliance.... We smashed our target 🥳 but more is always welcome! Donate here! justgiving.com/page/ellie-dan… #RareDiseaseDay #timothysyndrome #fundraising
Progress in Fragile X Syndrome research, a complex neurodevelopmental disorder. Healx's AI-approach discovered a potential combo therapy which has shown promise in improving cognition and autism-like behaviours in in vivo models. Read more tinyurl.com/5zurbvd3 #AIforGood
As part of Corporate Social Responsibility, our chosen charity for 2024 is @TimothySyndrome Our fundraising efforts will play a pivotal role in supporting the TSA. Hoping our collaborative efforts make a positive impact over the next 12 months! justgiving.com/page/ellie-dan…
Healx named as one of @BloombergUK’s ‘Startups to Watch’ - 25 startups picked from 1,500+ applicants. Criteria included companies that are growing fast + working on something unique - which we certainly are! Drug discovery for #rarediseases powered by #AI rb.gy/kn584
How AI Could Make Every Disease A Rare Disease hubs.li/Q01L-NBG0 Written by @TimGuilliams of @healx
In an exclusive interview, Viagra co-creator Dr. David Brown talks about his passion for entrepreneurialism, the mind-blowing benefits of machine learning and how big pharma needs a change in mindset… campdenfb.com/article/dr-dav… #machinelearning #interview #pharma #viagra @healx
New estimates find there are close to 10,000 rare diseases - not 7,000 as we previously thought 🤯 Learn how our Senior Scientist, Mariavi Ruiz, assessed the most recent research to make sense of all the statistics 👇 healx.ai/blog/how-many-…
HAPPY RARE DISEASE DAY!! 😍🩺🦓 Do you have your stripes at the ready?! 🌈🌈Today we are asking you to #showyourstripes for #rarediseaseday ALL DAY to raise awareness for those living with rare conditions! Remember to tag us @M4RareDiseases!!
Today is #RareDiseaseDay!🎉 In just half an hour we launch our report, share our #CareForRare campaign and begin our day of raising awareness for the 3.5 million people living with a rare condition in the UK. With your help, we can make this year the biggest yet! Who's with us?
Bruce Bloom, Chief Collaboration Officer at @healx , discusses Rare Disease Day, his work at Cures Within Reach & AI opening up the field of drug discovery Read more: bit.ly/3SE93Xw #RareDiseaseDay #biotech #pharma
Today is #RareDiseaseDay🎗️🦓 300 million people have a rare disease - half of them are children. And 90% of rare diseases have no treatment. We want to change that. increasing awareness of rare diseases is a critical step on the path to better support and new treatments👇
Tomorrow it's #RareDiseaseDay 2023! 💡 Light up at 7 pm wherever you are to raise awareness for people living with a rare disease! 🏛️ Find a monument being lit up near you: cutt.ly/MPUWDKx 🏠 Find out how to light up your home: cutt.ly/zPlxnHb #LightUpForRare
This is me… #RareDiseaseDay tea party hand wreath 2023 Thank you to everyone who joined us today, to those who baked & helped out. What a wonderful afternoon celebrating our uniqueness & our togetherness! Special to meet new families today. Taking our next steps together 💜
Opinion: 2022 was a breakthrough year for understanding rare diseases. 2023 needs to be better trib.al/9hhKBVU
🚨NEW DATASET alert! The Neurofibromatosis Open Science Initiative (@nfopensci) just released the first dataset (cbioportal.org/study/summary?…) of plexiform neurofibroma and other NF1-linked tumors to @cbioportal!
Will the United States #AI Bill Of Rights help fix artificial intelligence's bias problem? Our CEO & Co-founder @TimGuilliams thinks much more needs to be done. Read more👇 forbes.com/sites/forbeste…
The @healx team nailed it 🙌 The growing #CACNA1C community now have an accurate and validated Wikipedia source to learn from and enhance with their own insights and citations. en.wikipedia.org/wiki/CACNA1C-r… @neurosciencecu @JFGUnderwood @RebeccaJLevyMD
#ParkNews This in depth @Labiotech_eu piece explores the practice of drug repurposing for rare diseases and features @healx's approach to computational drug repurposing. ow.ly/H89p50MzWm4
With omics, phenotyping, and a graph-based approach, @healx advances a hypothesis-free model of drug discovery. Instead of looking at one drug’s action on one disease, it looks into multiple possibilities for enhancing, repurposing, or combining drugs. labiotech.eu/in-depth/drug-…
Beacon for Rare Disea.. @RareBeacon
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Cambridge Rare Diseas.. @camraredisease
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EveryLife Foundation @EveryLifeOrg
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22K Followers 2K Following European Pharmaceuticals Industry correspondent @Reuters. Previously reporting from Africa and the Middle East for @Reuters @FT @AP since 2010.
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7K Followers 835 Following The Children's Tumor Foundation is dedicated to ending NF, a group of genetic conditions that cause tumors to grow all over the body, through research.
Timothy Syndrome Alli.. @tsa_charity
379 Followers 1K Following We're dedicated to improving the diagnosis, treatment and care of those living with #CACNA1C-related disorders including #TimothySyndrome and #LongQT8.
OpenAI @OpenAI
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67 Followers 378 Following The best membrane protein reagents around. All are made in-house and coming straight from our lab to yours. Toxins, antibodies, growth factors, and more.
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Aoife Campbell 👩�.. @AoifeCampbell18
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Ovid Therapeutics @OvidRx
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Misa Ogura @misa_ogura
333 Followers 599 Following Senior ML Engineer @healx | Ex. Cancer Cell Biologist | Co-founder & CTO of @womendrivendev | She/her | Gender nonconforming
Dan Mason @iamdanmason
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Dr Elizabeth Coker @LizzieCoker
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Sara Friedman @sarafriedmannn
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Founders Forum Group @Founders_Forum
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KCL Rare Diseases @S4RDKCL
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16K Followers 2K Following The leading voice for decision-makers throughout the global biopharma ecosystem. Follow us on LinkedIn for exclusive insights & analysis: https://t.co/V33Z1gfUfZ
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36K Followers 4K Following In-depth reporting on startup Europe, for startup Europe. 🇪🇺 Subscribe to Sifted Pro for vital market intelligence: https://t.co/M3g11175y3
Innovative Health Ini.. @IHIEurope
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MELLODDY Consortium @MELLODDY_IMI
637 Followers 42 Following MELLODDY is seeking to accelerate drug discovery using machine learning in a new model of collaboration between traditional competitors
Exciting news! @healx is proud to enhance its partnership with @ChildrensTumor Foundation to advance treatments for #NF1, reaffirming our mission to make a meaningful impact in the lives of rare disease patients. bit.ly/3xr28tY #RareDisease #PatientImpact #AI
NEWS! Today we are deepening our relationship with long-term partner @ChildrensTumor to advance #neurofibromatosis type 1 treatments. We will receive investment from CTF to support our lead compound to clinical trials. Find out more: bit.ly/3xr28tY #nf #endnf #ai
"The group is very important on a human level, it allows discussion, sharing and support. It was an unexpected discovery in 2023, immense gratitude." In 2023 we connected with 38 more #CACNA1C individuals. Help us signpost to more in 2024. #RareDiseases #TimothySyndrome #LongQT8
"Having a safe place to ask questions with people who know about my babies syndrome has been so comforting for us and we are so grateful for the #TimothySyndrome / #LongQT8/ #CACNA1C-related disorder community." 🌈 Together, we're stronger. #RareDiseases #Community
Progress in Fragile X Syndrome research, a complex neurodevelopmental disorder. Healx's AI-approach discovered a potential combo therapy which has shown promise in improving cognition and autism-like behaviours in in vivo models. Read more tinyurl.com/5zurbvd3 #AIforGood
How AI Could Make Every Disease A Rare Disease hubs.li/Q01L-NBG0 Written by @TimGuilliams of @healx
In an exclusive interview, Viagra co-creator Dr. David Brown talks about his passion for entrepreneurialism, the mind-blowing benefits of machine learning and how big pharma needs a change in mindset… campdenfb.com/article/dr-dav… #machinelearning #interview #pharma #viagra @healx
HAPPY RARE DISEASE DAY!! 😍🩺🦓 Do you have your stripes at the ready?! 🌈🌈Today we are asking you to #showyourstripes for #rarediseaseday ALL DAY to raise awareness for those living with rare conditions! Remember to tag us @M4RareDiseases!!
Today is #RareDiseaseDay!🎉 In just half an hour we launch our report, share our #CareForRare campaign and begin our day of raising awareness for the 3.5 million people living with a rare condition in the UK. With your help, we can make this year the biggest yet! Who's with us?
Bruce Bloom, Chief Collaboration Officer at @healx , discusses Rare Disease Day, his work at Cures Within Reach & AI opening up the field of drug discovery Read more: bit.ly/3SE93Xw #RareDiseaseDay #biotech #pharma
Thank you for your support of #RareDiseaseDay @healx
Today is #RareDiseaseDay🎗️🦓 300 million people have a rare disease - half of them are children. And 90% of rare diseases have no treatment. We want to change that. increasing awareness of rare diseases is a critical step on the path to better support and new treatments👇
Tomorrow it's #RareDiseaseDay 2023! 💡 Light up at 7 pm wherever you are to raise awareness for people living with a rare disease! 🏛️ Find a monument being lit up near you: cutt.ly/MPUWDKx 🏠 Find out how to light up your home: cutt.ly/zPlxnHb #LightUpForRare
Time for Africa and Europe to mark #RareDiseaseDay 2023! TV broadcasts, radio podcasts, public transport visuals… Through various means, the community is sharing our call for equity everywhere! Are you also ready to share your colours 💙💚💜? 👉 rarediseaseday.org/category/event…
It is now #RareDiseaseDay across the globe 🌍 📌 Organise and post your event: cutt.ly/98d6NtE ✨ Join the Global Chain of Lights & #LightUpForRare: cutt.ly/zPlxnHb 📖 Share your story: cutt.ly/s8d612W 🔥 Share our resources: cutt.ly/M8d69nH
This is me… #RareDiseaseDay tea party hand wreath 2023 Thank you to everyone who joined us today, to those who baked & helped out. What a wonderful afternoon celebrating our uniqueness & our togetherness! Special to meet new families today. Taking our next steps together 💜
3 wishes for #RareDiseaseDay Chelsea Wong of RARE Youth Revolution, said: - For people to stop underestimating the patient - For healthcare professionals to listen to us - To stop seeing us as people who are sad all the time and can't have hopes, hobbies and passions.
.@healx want to progress 100 rare disease treatments by 2025 with #AI. After a seed round, they were seeking capital to accelerate growth. Funding from @atomico and @balderton made it possible. Read more about #DigitalHealth businesses in our portfolio: bit.ly/3LVUQjy
What do you have planned for Rare Disease Day this year?💡From our own #showyourstripes sock campaign to tea parties, here's just 7 ways you can gear up for February 28th! m4rd.org/2023/02/01/7-t…
Opinion: 2022 was a breakthrough year for understanding rare diseases. 2023 needs to be better trib.al/9hhKBVU
🚨NEW DATASET alert! The Neurofibromatosis Open Science Initiative (@nfopensci) just released the first dataset (cbioportal.org/study/summary?…) of plexiform neurofibroma and other NF1-linked tumors to @cbioportal!
The @healx team nailed it 🙌 The growing #CACNA1C community now have an accurate and validated Wikipedia source to learn from and enhance with their own insights and citations. en.wikipedia.org/wiki/CACNA1C-r… @neurosciencecu @JFGUnderwood @RebeccaJLevyMD
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