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Annual report
How DPUK is adapting to rapid change
Publications
Researchers at DPUK and other institutions worldwide have published articles based on their work using DPUK resources. Here we list a wide selection of research papers that have either been funded or enabled by DPUK. You can search by author and topic.
Clinical Studies Register
Our Clinical Studies Register comprises more than 58,000 research participants who have already undergone extensive characterisation and have pre-existing consent for re-contact through their parent DPUK cohort.
Great Minds
Great Minds is a register of over 13,000 highly characterised research volunteers. It is a resource available for researchers enabling precision-matching for studies.
Great Minds Members Event - Decoding Dementia: Biomarkers, Big Data, and the Future of Diagnosis
This special Great Minds event brought together leading experts to explore how biomarkers, big data, and artificial intelligence are transforming dementia research and diagnosis. Our distinguished panel discussed the remarkable developments in blood-based biomarkers over the past five years, examined their clinical validity and readiness for NHS implementation, and explored the potential of AI in dementia care. The event provided valuable insights into how these innovations are shaping the future of personalised medicine and early detection in dementia.
DPUK Datathons
DPUK Datathons are FREE ONLINE EVENTS. They are a key part of our data analyst training programme, placing researchers in multidisciplinary teams to generate valuable new findings in dementia research using cohorts in the DPUK Data Portal.
Deep and Frequent Phenotyping
The Deep and Frequent Phenotyping study has been described as one of the most significant current areas of research in dementia.
TDF Register Volunteers
The DPUK Trials Delivery Framework Register serves as a national repository of valuable information, including memory scores, clinical history, brain scan results, and medications, collected from local research registers at patients' local sites. By agreeing to place their data in the Register, individuals gain the opportunity to be contacted for future research studies within the Trials Delivery Framework that align with their suitability.