A three-year university degree in England now costs a student approximately £90,000, including tuition fees and a “minimum standard” of living expenses, according to new research
https://t.co/Wy4IhY2Rz4
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👉 https://t.co/jyuYjq6PUC
Very few people seem to understand university finances and, distressingly, this includes many academics and most policymakers. This is an attempt to condense the key points you need to know. https://t.co/gxJOEXfSuc
Just highlighting the link for donations to the Michael Mosley Fellowship https://t.co/KIO3htWc94 ,which is being administered by the charity of which I am a trustee, the Chronic Disease Research Foundation.
AI-authored abstracts ‘more authentic’ than human-written ones
Higher ratings for AI-authored abstracts should not obscure the need for engaging prose with a ‘human touch’, says study co-author https://t.co/7T1HOGc9bX
Awesome study showing the power of rare-variant analysis to discover new biology, even in a common-variant "saturated" trait like height. The largest effect allele had a 7cm impact!
Amazing work by @GarethHawkes1 @rnbeaumont1 @AlisaManningPhD @mnweedon and many more
@BehrElijah, Professor in Cardiovascular Medicine and Honorary Consultant Cardiologist at St George's, was featured on @TheBHF 's Heartbeat programme, discussing the tragic reality of sudden cardiac death.
The Generation Study is a ground-breaking research study in partnership with the NHS which will sequence the whole genomes of up to 100,000 newborn babies and look for 200+ rare conditions in early childhood.
Find out more: https://t.co/rLJv2SJ6ya
@DHSCgovuk@NHSEngland
Announcing the Michael Mosley Memorial Research Fund, created by Dr Michael Mosley’s family in partnership with the Chronic Disease Research Foundation (of which I am a trustee)
The associated JustGiving page is here:
https://t.co/KIO3htWc94
Now online! Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders https://t.co/d3ot80grzD
The @acgs_news position statement: Rare disease genomic testing in the UK and Ireland: promoting timely and equitable access, is online https://t.co/rwujz5zKiz Collaborative best practice guidance involving @Unique_charity@NHSgms@WalesGenePark@GeneticAlliance@GenQA & others🧵
Protein mislocalization of missense variants is common and primarily driven by effects on protein stability and membrane insertion rather than disruptions of trafficking signals or specific interaction https://t.co/y6VQiMMhYd?
Curious about biomedical science? 🧬 🔬
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