publication venue for
- ‘It reshaped how I will do research’: A qualitative exploration of team members’ experiences with youth and family engagement in a randomized controlled trial 2021
- Priority measures for publicly reporting primary care performance: Results of public engagement through deliberative dialogues in 3 Canadian provinces. 23:1213-1223. 2020
- Preparing for patient partnership: A scoping review of patient partner engagement and evaluation in research. 23:523-539. 2020
- Exploring transitions in care from pulmonary rehabilitation to home for persons with chronic obstructive pulmonary disease: A descriptive qualitative study. 23:414-422. 2020
- Citizen perspectives on the use of publicly reported primary care performance information: Results from citizen‐patient dialogues in three Canadian provinces. 22:974-982. 2019
- Ethnic differences in psychosis—Lay epidemiology explanations. 22:965-973. 2019
- Supporting the evaluation of public and patient engagement in health system organizations: Results from an implementation research study. 22:1132-1143. 2019
- Evaluating community deliberations about health research priorities. 22:772-784. 2019
- Codesigning health and other public services with vulnerable and disadvantaged populations: Insights from an international collaboration. 22:284-297. 2019
- Co-designing for quality: Creating a user-driven tool to improve quality in youth mental health services. 21:1013-1023. 2018
- How do adolescents with cerebral palsy participate? Learning from their personal experiences. 21:1024-1034. 2018
- Patient and public engagement in research and health system decision making: A systematic review of evaluation tools. 21:1075-1084. 2018
- Talking to the people that really matter about their participation in pandemic clinical research: A qualitative study in four European countries. 21:387-395. 2018
- How and why should we engage parents as co-researchers in health research? A scoping review of current practices. 20:543-554. 2017
- ‘Who is on your health-care team?’ Asking individuals with heart failure about care team membership and roles. 20:198-210. 2017
- Supporting quality public and patient engagement in health system organizations: development and usability testing of the Public and Patient Engagement Evaluation Tool. 19:817-827. 2016
- ‘Talk to me’: a mixed methods study on preferred physician behaviours during end-of-life communication from the patient perspective. 19:883-896. 2016
- Citizen expectations of ‘academic entrepreneurship’ in health research: public science, practical benefit. 18:2356-2374. 2015
- The development of scales to measure childhood cancer survivors' readiness for transition to long‐term follow‐up care as adults. 18:1941-1955. 2015
- Values and preferences for oral antithrombotic therapy in patients with atrial fibrillation: physician and patient perspectives. 18:2318-2327. 2015
- How oncologists communicate information to women with recurrent ovarian cancer in the context of treatment decision making in the medical encounter. 18:1066-1080. 2015
- Is the Give Youth a Voice questionnaire an appropriate measure of teen-centred care in paediatric oncology: a Rasch measurement theory analysis. 18:1686-1697. 2015
- Understanding why patients with immune thrombocytopenia are deeply divided on splenectomy. 17:809-817. 2014
- Assessing the conceptual clarity and evidence base of quality criteria/standards developed for evaluating decision aids. 17:232-243. 2014
- Fair reckoning: a qualitative investigation of responses to an economic health resource allocation survey. 17:174-185. 2014
- Consumer involvement in systematic reviews of comparative effectiveness research. 16:323-337. 2013
- Physician‐related facilitators and barriers to patient involvement in treatment decision making in early stage breast cancer: perspectives of physicians and patients. 16:373-384. 2013
- Patients’ decision making to accept or decline an implantable cardioverter defibrillator for primary prevention of sudden cardiac death. 16:69-79. 2013
- The integration of citizens into a science/policy network in genetics: governance arrangements and asymmetry in expertise. 14:261-271. 2011
- A treatment decision aid may increase patient trust in the diabetes specialist. TheStatin Choicerandomized trial. 12:38-44. 2009
- Can I accurately predict the impact of an illness and its treatment on my future subjective well-being? A complex question that does not have a simple answer. 9:252-254. 2006
- A shared treatment decision-making approach between patients with chronic conditions and their clinicians: the case of diabetes. 9:25-36. 2006
- Consumer-driven health care: Building partnerships in research. 8:352-359. 2005
- From rhetoric to reality: including patient voices in supportive cancer care planning. 8:195-209. 2005
- Treatment decision aids: conceptual issues and future directions. 8:114-125. 2005
- Self-reported use of shared decision-making among breast cancer specialists and perceived barriers and facilitators to implementing this approach. 7:338-348. 2004
- Providing evidence-based information to patients in general practice and pharmacies: what is the acceptability, usefulness and impact on drug use?. 6:281-289. 2003
- Using disease risk estimates to guide risk factor interventions: field test of a patient workbook for self-assessing coronary risk. 5:3-15. 2002
- Whose priorities count? Comparison of community-identified health problems and Burden-of-Disease-assessed health priorities in a district in Uganda. 5:55-62. 2002
- Clinical decision-making in the context of chronic illness. 3:6-16. 2000
- Editorial: special conference issue. 3:1-5. 2000
- Lessons learned from the Decision Board: a unique and evolving decision aid. 3:69-76. 2000
- Attitudes to randomized clinical trials amongst out‐patients attending a medical oncology clinic. 2:33-43. 1999
- Finding harmony within dissonance: Engaging patients, family/caregivers and service providers in research to fundamentally restructure relationships through integrative dynamics 2020