OOIR: Observatory of International Research

Papers

(The H4-Index of Health Expectations is 29. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-10-01 to 2025-10-01.)

Article	Citations
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	169
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	124
Feasibility of a best–worst scaling exercise to set priorities for autism research	96
	92
Development of an inflammatory bowel disease (IBD) Patient‐Reported Experience Measure (PREM): A patient‐led consensus work and ‘think aloud’ study for a quality improvement programme	82
Continuity Is Essential: The Experiences of Co‐Design Participants During the Implementation of a New Health Service	81
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	68
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	64
Indicators for adequate diabetes care for the indigenous communities of Ecuador	62
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event	52
Identifying Common Patient‐Oriented Priorities for Child and Adolescent Health Research and Care: A Systematic Review of Priority Setting Partnerships	47
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey	46
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	43
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	40
Preferences for Peer Support Amongst Families Engaged in Paediatric Screening Programmes: The Perspectives of Parents Involved in Screening for Type 1 Diabetes in Children Aged 3–13	40
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	39
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	38
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	35
Inside Front Cover: Volume 25 Issue 1	35
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	34
Participatory research with carers: A systematic review and narrative synthesis	33
Youth engagement in mental health research: A systematic review	33
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	32
Ripple Effects Mapping: Evaluating Multilevel Perspectives and Impacts of a Statewide Community–Academic Partnership Network on Covid‐19 Health Disparities	31
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	30

Just a story? Leadership, lived experience and integrated care	30
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	30
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	29
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	29