Touring art installation highlighting the stories of people with genetic conditions & their views on genomic medicine. Based on research of @imaginingfuture
'I:DNA – Evaluating the impact of public engagement with a multimedia art installation on genetic screening' an article on #ScienceOpen: https://t.co/o1cMEjMn6q
🚨BREAKING
We can confirm that USS is £7.4bn in surplus, and we are on track to restore UCU members pensions and significantly reduce the cost of their monthly contributions
We’ll use the coming months to ensure employers fulfil their obligations
Your action did this 💪
Seeking interviewees who have done health/social care research using telephone/video-call/other remote data collection methods. Please get in touch if you can help #ResearchMethods#qualitative#AcademicChatter#phdchat#aqhr Please RT
We knew octopuses were smart... but this is next level 🐙
@rowhoop and @ClareWilsonMed discuss the fascinating discovery that some cephalopods can alter their own genetic code...
Delighted to announce that I:DNA’s story (how it was first imagined and created out of research findings) is being featured at RareFest this year! @rarediseaseuk@warwickengages@stampcic#rarefest22 https://t.co/PQP5ZXbeVO
Do YOU want to help shape the future of #GenomicMedicine across our region?
We're encouraging applications to our Patient and Public Involvement panel.
Email [email protected] to apply today
Find out more:
https://t.co/L7WbmZBvwi
@NHSgms@rarediseaseuk@SWAN_UK
📢We are looking for two members of the public to join our expert oversight group. If you are interested in genetics and newborn screening, apply below. £75/ meeting (including prep time)📢
New paper with @horn_ruth_ : Why we need to explore the social and ethical implications of prenatal exome sequencing before we talk about implementation:
https://t.co/aFoispolM6
Registration now open for our first data workshop! Join us (online) 25th Nov for presentations from Felicity Boardman, Kriss Fearon and Amarpreet Kaur on 'perspectives of people living with genetic conditions' #ethics#sociogenomics#genomics@Ethixbird
Come & join us 25th November for our data sharing workshop (remote). An opportunity to discuss the perspectives of people w/genetic conditions as they appear in your own research as well as our presenters' work. @Ethixbird@CathyHerbrand@Corinna_Clark_ @Dr_A_Kaur @KrissFearon
Hot off the press: new paper with @gmt_88 on the responses of disabled people & their families to reproductive screening & testing. We compare data from parents of children with Down's Syndrome with data from people & families with genetic conditions.
https://t.co/yXH9uM0wW0
The QRDC study explores what happens to data quality when research interviews are conducted virtually (video/email/text) rather than in-person. Could you help us with this work as a public contributor? Payment of £25/hr for meetings and preparation.
https://t.co/cviw4TTpiV
We are so delighted that, after our tour (that reached 26,573 people in-person or online), I:DNA’s sculpture is now on display in the IBRB as part of Warwick’s sculpture collection https://t.co/kztN72WI4x
🪧New paper from the IF team🪧 Public, patient and professional attitudes to WGS in newborns: Expanding the notion of “benefit”: comparing public, parent, and professional attitudes towards whole genome sequencing in newborns https://t.co/mqqbC97Tpj