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The AASPIRE practice-based guidelines for the inclusion of autistic adults in research as co-researchers and study participants

Autism : the international journal of research and practice, 2019-11, Vol.23 (8), p.2007-2019

2019

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The ethics and regulatory landscape of including vulnerable populations in pragmatic clinical trials

Clinical trials (London, England), 2015-10, Vol.12 (5), p.503-510

2015

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Publication Pressure and Scientific Misconduct in Medical Scientists

Journal of empirical research on human research ethics, 2014-12, Vol.9 (5), p.64-71

2014

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Community-Based Participatory Research Conceptual Model: Community Partner Consultation and Face Validity

Qualitative health research, 2016-01, Vol.26 (1), p.117-135

2016

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A comparison of institutional review board professionals’ and patients’ views on consent for research on medical practices

Clinical trials (London, England), 2016-10, Vol.13 (5), p.555-565

2016

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How do clinical research coordinators learn Good Clinical Practice? A mixed-methods study of factors that predict uptake of knowledge

Clinical trials (London, England), 2020-04, Vol.17 (2), p.166-175

2020

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What constitutes meaningful engagement for patients and families as partners on research teams?

Journal of health services research & policy, 2018-07, Vol.23 (3), p.158-167

2018

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The Challenges of Participant Photography: A Critical Reflection on Methodology and Ethics in Two Cultural Contexts

Qualitative health research, 2017-05, Vol.27 (6), p.923-937

2017

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What should autism research focus upon? Community views and priorities from the United Kingdom

Autism : the international journal of research and practice, 2014-10, Vol.18 (7), p.756-770

2014

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Writing Usable Qualitative Health Research Findings

Qualitative health research, 2012-10, Vol.22 (10), p.1404-1413

2012

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The under reporting of recruitment strategies in research with children with life-threatening illnesses: A systematic review

Palliative Medicine, 2017-05, Vol.31 (5), p.419-436

2017

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Barriers to healthcare: Instrument development and comparison between autistic adults and adults with and without other disabilities

Autism : the international journal of research and practice, 2017-11, Vol.21 (8), p.972-984

2017

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Stakeholder Perspectives on Creating and Maintaining Trust in Community–Academic Research Partnerships

Health education & behavior, 2017-02, Vol.44 (1), p.182-191

2017

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A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent

Clinical trials (London, England), 2017-02, Vol.14 (1), p.94-102

2017

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Establishing the Psychometric Properties of Constructs in a Community-Based Participatory Research Conceptual Model

American journal of health promotion, 2015-05, Vol.29 (5), p.e188-e202

2015

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Overcoming Barriers to the Recruitment of Nurses as Participants in Health Care Research

Qualitative health research, 2011-12, Vol.21 (12), p.1705-1718

2011

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Research Ethics Committees and Participatory Action Research With Young People: The Politics of Voice

Journal of empirical research on human research ethics, 2016-04, Vol.11 (2), p.122-128

2016

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‘I’m sure we made it a better study…’: Experiences of adults with intellectual disabilities and parent carers of patient and public involvement in a health research study

Journal of intellectual disabilities, 2019-03, Vol.23 (1), p.78-96

2019

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Factor Structure of the Clinical Research Appraisal Inventory (CRAI)

Evaluation & the health professions, 2014-03, Vol.37 (1), p.71-82

2014

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Exploring the Hidden Barriers in Knowledge Translation: A Case Study Within an Academic Community

Qualitative health research, 2015-11, Vol.25 (11), p.1506-1517

2015

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A New Measure of Research Participant Burden: Brief Report

Journal of empirical research on human research ethics, 2014-10, Vol.9 (4), p.46-49

2014

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Health research participants’ preferences for receiving research results

Clinical trials (London, England), 2016-12, Vol.13 (6), p.582-591

2016

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A Seat at the Table: Designing an Activity-Based Community Advisory Committee With People Living With HIV Who Use Drugs

Qualitative health research, 2019-06, Vol.29 (7), p.1029-1042

2019

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“Respect the way I need to communicate with you”: Healthcare experiences of adults on the autism spectrum

Autism : the international journal of research and practice, 2015-10, Vol.19 (7), p.824-831

2015

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Engaging Gypsy, Roma, and Traveller Communities in Research: Maximizing Opportunities and Overcoming Challenges

Qualitative health research, 2019-07, Vol.29 (9), p.1324-1333

2019

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The AASPIRE practice-based guidelines for the inclusion of autistic adults in research as co-researchers and study participants

The ethics and regulatory landscape of including vulnerable populations in pragmatic clinical trials

Publication Pressure and Scientific Misconduct in Medical Scientists

Community-Based Participatory Research Conceptual Model: Community Partner Consultation and Face Validity

A comparison of institutional review board professionals’ and patients’ views on consent for research on medical practices

How do clinical research coordinators learn Good Clinical Practice? A mixed-methods study of factors that predict uptake of knowledge

What constitutes meaningful engagement for patients and families as partners on research teams?

The Challenges of Participant Photography: A Critical Reflection on Methodology and Ethics in Two Cultural Contexts

What should autism research focus upon? Community views and priorities from the United Kingdom

Writing Usable Qualitative Health Research Findings

The under reporting of recruitment strategies in research with children with life-threatening illnesses: A systematic review

Barriers to healthcare: Instrument development and comparison between autistic adults and adults with and without other disabilities

Stakeholder Perspectives on Creating and Maintaining Trust in Community–Academic Research Partnerships

A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent

Establishing the Psychometric Properties of Constructs in a Community-Based Participatory Research Conceptual Model

Overcoming Barriers to the Recruitment of Nurses as Participants in Health Care Research

Research Ethics Committees and Participatory Action Research With Young People: The Politics of Voice

‘I’m sure we made it a better study…’: Experiences of adults with intellectual disabilities and parent carers of patient and public involvement in a health research study

Factor Structure of the Clinical Research Appraisal Inventory (CRAI)

Exploring the Hidden Barriers in Knowledge Translation: A Case Study Within an Academic Community

A New Measure of Research Participant Burden: Brief Report

Health research participants’ preferences for receiving research results

A Seat at the Table: Designing an Activity-Based Community Advisory Committee With People Living With HIV Who Use Drugs

“Respect the way I need to communicate with you”: Healthcare experiences of adults on the autism spectrum

Engaging Gypsy, Roma, and Traveller Communities in Research: Maximizing Opportunities and Overcoming Challenges

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