
Julian G Barwell
@julianbarwell
Consultant Clinical Geneticist and Honorary Professor in Cancer Studies
ID: 840532110003822592
http://eastgenomics.org.uk/ 11-03-2017 11:57:26
579 Tweet
575 Followers
435 Following


Many rare conditions are really not so rare. Fragile X affects 1 in 4k ♂️ and 1 in 6k ♀️, with 1 in 600 and 1 in 250 being carriers. 👂 Julian G Barwell taking to BBC Leicester Ady Dayman - youtube.com/watch?v=2dyFp3… 👀LeicestershireLive: leicestermercury.co.uk/news/leicester… #fragileXawarenessday


News| New app launched to support estimated 175,000 people in the UK with Lynch Syndrome 👉 le.ac.uk/news/2024/octo… The app will help people to monitor and manage their condition, alongside their treating clinicians. #CitizensOfChange| Julian G Barwell| Lynch Syndrome UK

TUNE IN NOW: the last episode of #TheRoadtoGenome Series 3 is live, a fantastic interview with Chris Hind chair of the Patient & Public Voice Forum for NHS East Genomics sharing his journey with #Haemochromatosis & the power of the Patient Voice. Listen ney-genomics.org.uk/about-genomics…

Geneticist Julian G Barwell spoke to BBC Radio 5 Live about MP Richard Holden MP's call to ban first-cousin marriage in the UK. Interview from 2h 27m: bbc.co.uk/sounds/play/m0…



Series 4 of The Road to Genome opens up with a great chat with rapping Consultant Clinical Geneticist, Prof Julian G Barwell Episode available on Mon 13 Jan (a NY treat!). Series available on all podcast platforms - or listen on North East & Yorkshire Genomics website - ney-genomics.org.uk/about-genomics…



It's a Cracker! Series 4 of The Road to Genome begins today & it's a cracking interview with rapping Consultant Clinical Geneticist Professor Julian G Barwell. It's a New Year's treat & mic drop interview Listen in: eu1.hubs.ly/H0fMjc90 or wherever you get your podcasts







What an incredible day of science, innovation, and empowerment at the Lynch Syndrome UK conference on #LynchSyndromeDay2025. The pace of progress in this space is truly inspiring, and I was honoured to be part of it working in partnership with those living with Lynch syndrome.





