On 25th of September, International Ataxia Awareness Day, we at the Oxford-Harrington Rare Disease Centre stand together with the global Ataxia community on the path towards developing innovative therapeutic approaches.

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Progress in rare disease starts with people coming together. We're delighted to welcome the rare disease community to the Oxford-Harrington Rare Disease Centre Symposium 2026 for two days of collaboration, shared learning and new ideas. #RareDisease

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Scholarship and short-talk deadlines are approaching (30 Sept) for @keystoneSymposia.bsky.social Genetic Medicines to Treat Cardiovascular Disease, this January in Keystone. A great line up of speakers. See key dates: keysym.us/KSCardioGeneMed27 #KSCardioGeneMed27

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How does an embryo generate the right cells in the right place? Delighted to share our latest findings on how neural crest cells acquire vagal or trunk identities Spoiler alert: The timing & combination of CDXs preconfigures cell identity & distinct HOX states www.biorxiv.org/content/10.6...

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How do we move beyond the idea of the ‘average patient’ in medicine? In this episode of The Digital Twin Theory, Professor Blanca Rodriguez explores how digital twins, AI and computational modelling can support more personalised, equitable healthcare. Listen now: open.spotify.com/episode/0RDN...

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