We are focussing our efforts on developing our LinkedIn following.
If you have a LinkedIn profile then be sure to connect with us to continue to receive updates from us:
https://t.co/nLWqZEGvy6
Matt Loose, of @UniofNottingham and @nottmhospitals speaks about long-read sequencing for brain tumours which is bringing time to diagnosis down from several weeks to just a few hours.
Here’s a piece on this work from earlier this year: https://t.co/mEBygZnMeW
#NHSGenomics2025
Excited to speak at the NHS Genomics Healthcare Summit today at 13:40: “Genomics & pathology – transforming pathways” — using cancer turnaround time data to drive service improvement. @RCPath#NHSGenomics#Pathology@East_Genomics@NHSgms
Looking forward to hearing our Patient and Public Voice (PPV) Panel Chair, Chris Hind speak at the @NHSgms Summit later today in a session on ‘Improving patient centric care - delivering equitable genomic services’.
#genomicsconversation#NHSGenomics2025
For many families, the journey to find a diagnosis is long and uncertain – often known as the #DiagnosticOdyssey. Discover what healthcare professionals can do to help shorten the journey via our online resource. https://t.co/SBUuBnpePo
Who might you meet at #RAREsummit25? 👋
Researchers, clinicians, biopharma, tech innovators, patient groups + those with lived experience.
Lots of opportunities to network & connect across the rare disease community.
Be part of the conversation.
Tickets: https://t.co/JEhhoHmMZK
Around 8 years after joining the 100,000 Genomes Project, Maria received a phone call telling her a diagnosis had been found for her son, Noah. RNU5B-1-related disorder is a recently discovered neurodevelopmental condition.
Read Noah's story: https://t.co/8NegM2WNEb
It's South Asian Heritage Month.
For this large and diverse group - almost 25% of the global population - conditions such as type 2 diabetes, cardiovascular disease and thalassaemia are more prevalent.
Some great work going on in this space: https://t.co/tgH6LsNrh0
"It would be a privilege to help translate this research into routine care, bringing the benefits of early genomic screening to all families across England"
Dr Meekai To shares her experience as Principal Clinician for the Generation Study, read below:
https://t.co/gRo64gcQ97
Breast cancer teams:
💻CanRisk training
🗓️8 Aug, 3pm
Join Dr Claire Searle from @nottmhospitals for a session on using CanRisk to calculate future risks of developing breast cancer using family history, genetic & other risk factors.
To register email: [email protected]
A selection of talks from the Genomics England Research Summit 2025 are now available to watch on YouTube, a chance to revisit key discussions and insights from the day.
Watch here: https://t.co/47wiv5B8cx
#GERS2025
A packed July newsletter for you, featuring:
🔹lab & Test Directory updates
🔹genomics in the NHS 10 Year Plan
🔹news, research & awareness dates
🔹events, education and training
Read it here: https://t.co/8khqJrcsnN
Join our mailing list here: https://t.co/gQ7gFJ8i9W