Chronicity rhetoric in health and welfare systems inhibits patient recovery: a qualitative, ethnographic study of fibromyalgia care
Cupit C. et al, (2025), Social Science and Medicine, 382
Mapping the Social Organisation of Neglect in the Case of Fibromyalgia: Using Smith's Sociology for People to Inform a Systems-Focused Literature Review
Cupit C. et al, (2025), Sociology of Health and Illness, 47
Overarching Priorities for Health and Care Research in the United Kingdom: A Coproduced Synthesis of James Lind Alliance ‘Top 10s’
Crocker JC. et al, (2024), Health Expectations, 27
Developing user personas to capture intersecting dimensions of disadvantage in older patients who are marginalised: a qualitative study
Husain L. et al, (2024), British Journal of General Practice, 74, e250 - e257
The ecomap: a tool for extending understanding in hermeneutic phenomenological research.
Jestico E. et al, (2023), Nurse Res, 31, 6 - 13
Safety implications of remote assessments for suspected COVID-19: qualitative study in UK primary care
Wieringa S. et al, (2023), BMJ Quality and Safety, 32, 732 - 741
How ‘significant others’ may support parents with decision-making about their child’s cancer care: An integrative literature review
Jestico ECL. et al, (2023), Journal of Clinical Nursing, 32, 1821 - 1840
Co-design and its consequences: developing a shared patient engagement framework in the IMI-PARADIGM project
Gunn CJ. et al, (2023), SCIENCE AND PUBLIC POLICY, 50, 1018 - 1028
Desperately Seeking Intersectionality in Digital Health Disparity Research: Narrative Review to Inform a Richer Theorization of Multiple Disadvantage
Husain L. et al, (2022), Journal of Medical Internet Research, 24
Planning and Evaluating Remote Consultation Services: A New Conceptual Framework Incorporating Complexity and Practical Ethics
Greenhalgh T. et al, (2021), Frontiers in Digital Health, 3
Could expanding the covid-19 case definition improve the UK’s pandemic response?
FINLAY T. et al, (2021), BMJ: British Medical Journal
Public involvement in the governance of population-level biomedical research: Unresolved questions and future directions
Erikainen S. et al, (2021), Journal of Medical Ethics, 47, 522 - 525
Could expanding the covid-19 case definition improve the UK's pandemic response?
Crozier A. et al, (2021), The BMJ, 374
Evaluation of patient engagement in medicine development: A multi-stakeholder framework with metrics
Vat LE. et al, (2021), Health Expectations, 24, 491 - 506
PNS232 What Constitutes the VALUE of Patient Engagement in the Development of New Medicines? Development of the Paradigm Monitoring and Evaluation Framework
Robinson P. et al, (2020), Value in Health, 23, S680 - S680
Evaluating the “return on patient engagement initiatives” in medicines research and development: A literature review
Vat LE. et al, (2020), Health Expectations, 23, 5 - 18
WHAT CONSTITUTES THE VALUE OF PATIENT ENGAGEMENT IN THE DEVELOPMENT OF NEW MEDICINES? DEVELOPMENT OF THE PARADIGM MONITORING AND EVALUATION FRAMEWORK
Robinson P. et al, (2020), VALUE IN HEALTH, 23, S680 - S680
Frameworks for supporting patient and public involvement in research: Systematic review and co-design pilot
Greenhalgh T. et al, (2019), Health expectations : an international journal of public participation in health care and health policy, 22, 785 - 801
Making the most of the waiting room: Electronic patient engagement, a mixed methods study.
Coathup V. et al, (2018), Digit Health, 4
Participant-centric initiatives and medical research: Scoping review protocol
Coathup V. et al, (2017), JMIR Research Protocols, 6