Absolute privilege going to the fantastic Naseby Church of England primary school on monday to open science week talking about DNA and our relationship with Nature. With our book, DNA models, poems and raps we discussed how we don’t just live on Earth, we are Earth.

Great to be at Naseby explaining ACT & G. The language of life & biology Teaching that Watson and Crick, with a two sided letter. Showed that in the natural world and life, the simpler the better Loved sharing our new children's book And a huge thank you to the head, Mrs Cook

Do you have Lynch Syndrome? Are you a clinician with an interest in LS? Register your free place at our Lynch Syndrome event in Nottingham, 22 April 2024. Virtual joining option available. Meet our fantastic speakers for patient and clinician sessions: events.eahsn.org/LynchSyndromeP…

🔊NEW PAPER🔊 Our review paper of pharmacological management of Fragile X Syndrome is now available in full 😀Please RT! Professor Rohit Shankar Dr Lisa Burrows RN(MH) Julian G Barwell CIDER Research SAPPHIRE research LPT Research Team NDP SIG Link: doi.org/10.1080/146565…

Nominations for our annual UHL Recognition Awards are now open – including the Patient’s Choice Award. If you've experienced exceptional care from a UHL colleague or team, here's your chance to show appreciation: leicestershospitals.nhs.uk/aboutus/our-pu… #UHLRecognition #NHSheroes

A great honour to be presenting at the East Genomics Lynch Syndrome conference in Nottingham on our Lynch syndrone App. We have just received ethics and so should be able to release on Apple and Google very soon #eastgenomics

Honoured to be presenting today at the Royal College of Physicians 'Future of Medicine Conference' on ethical dilemmas in genetics and genomic medicine.

Delighted to be presenting at the Royal Society of Medicine today to discuss genetic and genomic testing for those without a clear diagnosis. Careful descriptive phenotyping and consent are key here

Thank you to everyone that attended our R14 National MDT session this afternoon. We shared an animation created by Matthew Wakeling showing the process of short read whole genome sequencing that received a lot of positive feedback - here it is 🧬🧬🧬 youtube.com/watch?v=x_Xs5N…

Do you have Lynch Syndrome or a Rare Condition? Join us on 22 May to find out about: ✅Cambridge Rare Disease Network (CamRARE) patient passport ✅Lynch Syndrome UK patient passport ✅Leicester's Hospitals developed LS patient app Register your FREE place: events.eahsn.org/GenomicsBITEIn…

We helped this lady over-turn this decision to reject her application because of her family history BBC News - Army backtracks on teen rejected over breast-cancer gene - BBC News bbc.co.uk/news/articles/…

Amazing to see so many people at the What is DNA? Book launch at Walker's book store in Oakham this evening! Thanks so much to everyone who attended and sent good wishes and to the many people that helped Neeta and I write it xxx

Pleased to see this published in Eye Journal - we demonstrated improved feasibility of handheld OCT in children with craniosynostosis: nature.com/articles/s4143… Noor Ul Owase Jeelani Robert Henderson Mervyn Thomas Catey Bunce💙 Great Ormond Street Hospital Eye Department GOSH Craniofacial Research Unit

We've a great line-up of sessions & speakers for our online Genomics Showcase events next month: 🧬Cancer - Mon 8 July 🧬Rare & Inherited Conditions - Wed 10 July 🧬Prenatal & Paediatric - Thu 11 July Register your free place(s) here: events.eahsn.org/NHSEastGenomic…

Hi 🕷️Jude Brown! We’re researching experiences of cancer genetic risk and social media and are looking to interview people who share content about Lynch Syndrome on Twitter. Would you be interested in talking to us? If so we can send you more info via DM/email. Thanks so much!

Diagnosis of a rare disease is not a destination, it’s the beginning. Julian G Barwell speaking with Alex and Chris McQuade on Fragile X syndrome and the journey travelled by the patient and family. UKCRF Network #crfconf24 Rare Diseases Ireland HealthResearchBoard

Six talks in 7 days including pharmacogenetic prescribing solutions, rare disease Apps, plans for a holistic national fragile X syndrome hub, future research infrastructure, schools outreach and a podcast on familial prostate cancer: Mapping a vision of 21st century healthcare

At US national Fragile X conference and learning how to set up an integrated and holistic care hub in the UK, underpinned by access to research.

We are interviewing! Do you write about #BRCA and/or #Lynchsyndrome on social media? We would like to hear about how you do it! We are trying to understand how social media can contribute to personal experiences of learning about or coping with #hereditarycancer👇

Here is a new character I am working on, rapping would you believe about the structure of DNA, complementing our educational and fun book for children age 8-12 called 'What is DNA?' available on amazon. Neeta Kulkarni Chris Hind NHS East Genomics