Investigating the Extent to Which Patients Should Control Access to Patient Records for Research: A Deliberative Process Using Citizens’ Juries

Public responses to the sharing and linkage of health data for research purposes: a systematic review and thematic synthesis of qualitative studies

(2016) Mhairi Aitken et al.   BMC Medical Ethics

Long-Term Mental Health Outcomes of Military Service

(2016) Beverly P. Bergman et al.   JOURNAL OF CLINICAL PSYCHIATRY

Recent trends in the incidence of anxiety and prescription of anxiolytics and hypnotics in children and young people: An e-cohort study

(2015) A. John et al.   JOURNAL OF AFFECTIVE DISORDERS

The social licence for research: whycare.dataran into trouble

(2015) Pam Carter et al.   JOURNAL OF MEDICAL ETHICS

Thinking outside the 'knowledge deficit' box: Scientists could achieve more fulfilled professional lives by embracing the skills needed for effective interaction with the public

(2014) C. Pouliot et al.   EMBO REPORTS

The use of citizens' juries in health policy decision-making: A systematic review

(2014) Jackie Street et al.   SOCIAL SCIENCE & MEDICINE

“Let’s get the best quality research we can”: public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study

(2013) Elizabeth M Hill et al.   BMC Medical Research Methodology

Impact of Scotland’s Comprehensive, Smoke-Free Legislation on Stroke

(2013) Daniel F. Mackay et al.   PLoS One

National electronic health records and the digital disruption of moral orders

(2013) Karin Garrety et al.   SOCIAL SCIENCE & MEDICINE

‘Nothing is really safe’: a focus group study on the processes of anonymizing and sharing of health data for research purposes

(2010) Gill Haddow et al.   JOURNAL OF EVALUATION IN CLINICAL PRACTICE

Alternatives to project-specific consent for access to personal information for health research: Insights from a public dialogue

(2008) Donald J Willison et al.   BMC Medical Ethics

Engaging the public in priority-setting for health technology assessment: findings from a citizens’ jury

(2008) Devidas Menon et al.   HEALTH EXPECTATIONS

Research on Medical Records without Informed Consent

(2008) Franklin G. Miller   JOURNAL OF LAW MEDICINE & ETHICS