//
sign in
Profile
by @danabra.mov
Profile
by @dansshadow.bsky.social
Profile
by @jimpick.com
AviHandle
by @danabra.mov
AviHandle
by @dansshadow.bsky.social
AviHandle
by @katherine.computer
EventsList
by @katherine.computer
ProfileHeader
by @dansshadow.bsky.social
ProfileHeader
by @danabra.mov
ProfileMedia
by @danabra.mov
ProfilePlays
by @danabra.mov
ProfilePosts
by @danabra.mov
ProfilePosts
by @dansshadow.bsky.social
ProfileReplies
by @danabra.mov
Record
by @atsui.org
Skircle
by @danabra.mov
StreamPlacePlaylist
by @katherine.computer
+ new component
ProfilePosts









Loading...
Last week was the first #ReNUhopeConference It was an enormous privilege to meet many ReNU warriors (they give the best hugs!) and their families, and scientists and clinicians working on ReNU. ReNU Syndrome United have achieved so much in only a single year, building an incredible community šŸ’™
Amazing and exciting progress for rare conditions and families @uniquecharity.bsky.social. By all (clinicians, researchers and patients) working together will can continue to drive forward improved diagnosis, care and treatment for all.
Both translational and fundamental curiosity-driven research are needed to fuel the incredible progress we're seeing in genomic medicine; an important message in this article and and some lovely quotes from @sarahlwynn.bsky.social www.ft.com/content/25dd...
We are calling clinicians to propose rare genetic neurodevelopmental disorders, which they will be willing to lead development of a new guide, with assistance of our generative AI model. Propose a condition by 30th May: forms.office.com/e/j...
šŸ“¢ We're Hiring – Engagement & Communications Officer! 🌟 To apply and find out more click here: bit.ly/Uniquejob Join us in making a difference! #Hiring #CommunicationsOfficer #CharityJobs #RareDisorders
We were delighted to share this wonderful collaboration with the Julia Garnham Centre (JGC), Sheffield Children's NHS Foundation Trust and The University of Sheffield, aimed at increasing the number of Unique guides. Find them on our Disorder Guides page: rarechromo.org/disorder-gui...
A few weeks ago, I had an incredibly emotional call with James Coney, a writer for the Sunday Times whose son Charlie was in the @genomicsengland.bsky.social 100k project and was recently diagnosed with ReNU syndrome. This beautiful article tells their story ā¤ļø www.thetimes.com/article/0bcc...
10mo
May 29, 2025
May 29, 2025
May 8, 2025
Feb 14, 2025
3d
Mar 2, 2025
We must recognise and protect the pipelines that lead from research to real-world benefit
www.ft.com
Curiosity underlies a breakthrough in rare disease
A wonderful story of how 🧬 research can provide hope & answers to families affected by rare conditions. Enormous thanks to @nickywhiffin.bsky.social, Yuyang Chen & others whose work is dedicated to finding these answers for @uniquecharity.bsky.social families.
This beautiful drawing highlights what will be a wonderful evening celebrating science and a new gene discovery which has made such a difference to so many rare 🧬 families. @uniquecharity.bsky.social
Honoured to be included in this little gang! šŸ§¬ā¤ļø šŸ™ Looking forward to you joining us next year at #ESHG2026!
James Coney and his wife, Sarah, struggled not knowing why their 12-year-old was born with a severe learning disability. In their darkest moments, they blamed themselves. Then, out of the blue, came a...
My son Charlie — and the breakthrough that changed our lives
www.thetimes.com
Mar 2, 2025
Mar 21, 2025
Nicky Whiffin
Sarah Wynn
Caroline Wright
Unique
Unique
May 29, 2025
Sarah Wynn
Nicky Whiffin
Both translational and fundamental curiosity-driven research are needed to fuel the incredible progress we're seeing in genomic medicine; an important message in this article and and some lovely quotes from @sarahlwynn.bsky.social www.ft.com/content/25dd...
May 29, 2025
Sarah Wynn
Sarah Wynn
Sarah Wynn
We must recognise and protect the pipelines that lead from research to real-world benefit
www.ft.com
Curiosity underlies a breakthrough in rare disease
A few weeks ago, I had an incredibly emotional call with James Coney, a writer for the Sunday Times whose son Charlie was in the @genomicsengland.bsky.social 100k project and was recently diagnosed with ReNU syndrome. This beautiful article tells their story ā¤ļø www.thetimes.com/article/0bcc...
We are delighted to be hosting an evening of talks about the discovery of ReNU syndrome, at 17:30 on Tuesday 29th April at St Anne's College. Further information, and registration details can be found here: cpm.ox.ac.uk/event/the-di... We hope to see you there!
šŸ–¼ļø P25.064.D They're here! New approach to creating high-quality patient information at scale. Sheffield & Unique working with students, clinicians, families & AI Develop expert-reviewed guides for rare genetic conditions. #ESHG2026 šŸ“– rarechromo.org/disorder-gui...
Caroline Wright
Mar 2, 2025
Mar 20, 2025
4d
My son Charlie — and the breakthrough that changed our lives
James Coney and his wife, Sarah, struggled not knowing why their 12-year-old was born with a severe learning disability. In their darkest moments, they blamed themselves. Then, out of the blue, came a...
www.thetimes.com
Great picture from #ESHG2025 of three of my favorite UK superwomen of #Genomics Unique's @sarahlwynn.bsky.social, @genomicsengland.bsky.social Suzi Walker and @neygenomics.bsky.social Miranda Durkie
Nicky Whiffin
Centre for Personalised Medicine
May 24, 2025
James Fasham
Exeter Rare Disease