Jo Brett

The GRIPP checklist: Strengthening the quality of patient and public involvement reporting in research

Rosemary Barber, S. Staniszewska, J. Brett, 2011, International Journal of Technology Assessment in Health Care.

Developing the evidence base of patient and public involvement in health and social care research

Jim Elliott, Rosemary Barber, Peter Beresford, 2011 .

Reaching consensus on reporting patient and public involvement (PPI) in research: methods and lessons learned from the development of reporting guidelines

Iveta Simera, David Moher, Colin Tysall, 2017, BMJ Open.

A systematic mapping review of effective interventions for communicating with, supporting and providing information to parents of preterm infants

Mary Newburn, S. Staniszewska, N. Jones, 2011, BMJ Open.

A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities

Colin Tysall, S. Staniszewska, J. Brett, 2014, The Patient - Patient-Centered Outcomes Research.

The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines.

Julie Roberts, Ian Bullock, Kate Seers, 2014, International journal for quality in health care : journal of the International Society for Quality in Health Care.

Patient and Public Involvement in Patient-Reported Outcome Measures

S. Staniszewska, J. Brett, K. Haywood, 2012, The Patient - Patient-Centered Outcomes Research.

The PIRICOM study : a systematic review of the conceptualisation, measurement, impact and outcomes of patients and public involvement in health and social care research

Helen R. Bayliss, Kate Seers, K. Seers, 2010 .