Boote J, Wong R, Booth A: “Talking the talk or walking the walk?” A bibliometric review of the literature on public involvement in health research published between 1995 and 2009. Heal Expect 2015;18:44–57.
Price A, Biswas T, Biswas R: Person-centered healthcare in the information age: experiences from a user driven healthcare network. Eur J Pers Cent Healthc 2013;1:385.
Richards T, Snow R, Schroter S: Co-creating health: more than a dream. BMJ 2016;4550:i4550.
Crocker JC, Boylan A-M, Bostock J, Locock L: Is it worth it? Patient and public views on the impact of their involvement in health research and its assessment: a UK-based qualitative interview study. Heal Expect 2016, DOI: 10.1111/hex.12479.
Brett J, Staniszewska S, Mockford C, Herron-Marx S, Hughes J, Tysall C, et al: Mapping the impact of patient and public involvement on health and social care research: a systematic review. Heal Expect 2014;17:637–650.
Snow R, Crocker JC, Crowe S: Missed opportunities for impact in patient and carer involvement: a mixed methods case study of research priority setting. Res Involv Engagem 2015;1:7.
Price A, Liew SM, Kirkpatrick J, Price J, Lopreto T, Nelken Y: Mind the gap in clinical trials: a participatory action analysis with citizen collaborators. J Eval Clin Pract 2017;23:178–184.
Purkayastha S, Price A, Biswas R, Jai Ganesh AU, Otero P: From dyadic ties to information infrastructures: care-coordination between patients, providers, students and researchers. Yearb Med Inform 2015;10:68–74.
Bera K, Seth B, Biswas R: Conversational learning among medical students: harnessing the power of web 2.0 through user driven healthcare. Ann Neurosci 2013;20:37–38.
Sturmberg JP: Multimorbidity and chronic disease: an emergent perspective. J Eval Clin Pract 2014;20:508– 512.
Gabriel SE, Normand S-LT: Getting the methods right – the foundation of patient-centered outcomes research. N Engl J Med 2012;367:787–790.
