Corinna Clark
@Corinna_Clark_
Followers
36
Following
6
Statuses
24
Scientist, mum, gardener. Research interests - ethical & social impacts of genetics, public engagement, epidemiology, animal behaviour, welfare & ethics.
University of Warwick
Joined July 2022
0
0
1
Public & Patient Involvement is health research is so important and representation in PPI is vital
0
1
3
RT @HRA_Latest: We have published a report that looks at different ways to improve clinical research for participants. Our People-Centred…
0
43
0
RT @SergNetwork: Join us on 11th Sept 10-12 @ university of Warwick for the next SERG meeting! Presenters are Dr Rich Gorman (EPPiGEN) and…
0
4
0
RT @Sci_Ani: Discover how #diseases spread and how #vaccination programs are evaluated in this insightful animation from the MEMVIE project…
0
10
0
RT @EdMHill: ❓ Scientists help policy-makers make public health decisions, but who helps the scientists? 🗣️ Supported by @warwickengages…
0
1
0
You can read all about our recent MEMVIE project (PPIE in mathematical modelling for vaccination programmes) event as part of the Resonate Festival with Warwick Institute of Engagement here...@sophie_stan2
0
0
2
RT @ELSIhub: As part of our #ELSIabroad series, learn about #ELSI research in the United Kingdom with @felicityboardma Professor at Warwick…
0
1
0
New paper on healthcare professionals' views towards using next gen sequencing for Cystic Fibrosis newborn screening @ImaginingFuture @JaneChudleigh @LouiseCMoodyCU
0
0
2
Stakeholder Views of the Proposed Introduction of Next Generation Sequencing into the Cystic Fibrosis Screening Protocol in England #mdpiIJNS via @@IJNS_MDPI
0
0
0
RT @UFAW_1926: There is still time to complete our short online survey to help us understand how we can adapt to best meet the needs of tho…
0
6
0
Survey for UK-based healthcare professionals supporting people affected by Spinal Muscular Atrophy (any capacity e.g. neurologists/nurses/paediatricians/ GPs/surgeons/physios/counsellors/speech therapists...) Potential policy impact
0
2
1
Survey on whether all newborns should be offered screening for Spinal Muscular Atrophy (neuromuscular condition). Open to all UK residents, no knowledge of SMA or screening needed. Potential for impact on national screening policy
0
0
0
Looking for 2 members of the public to attend 3 online oversight meetings (£75 per meeting), anyone (UK) over 18 welcome, would especially love to hear from parents of younger children (10yrs and under). No knowledge of subject needed, just enthusiasm!
Would you like to contribute to research into the acceptability of genetic screening with future implications for all babies in the UK? We are looking for 2 members of the public to join our oversight group
0
1
1
RT @SergNetwork: MEETING POSTPONED. As SERG was due to take place on one of the recently announced UCU strike dates, we have taken the diff…
0
3
0
We are putting on a free art event for school-aged children (6+ years) in the Priors Shopping Centre, Leamington Spa, this Saturday (12th Nov) on theme of genetics and identity. See website for details @ImaginingFuture
0
0
0
@involveUK @UCL_CoPro @GaryHickey16 @NIHRinvolvement @PPI_Ignite_DCU @mhjmurray @EngageBritain @lynn_laidlaw @PatientVoicesUK @ARC_WM @BortoliS @Trial_Forge @elspeth_mathie @sophie_stan2 @carolin_sanders @ImaginingFuture @_I_DNA
Would you like to contribute to research into the acceptability of genetic screening with future implications for all babies in the UK? We are looking for 2 members of the public to join our oversight group
0
0
0