OOIR: Observatory of International Research

Papers

(The H4-Index of Health Expectations is 28. 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 2021-09-01 to 2025-09-01.)

Article	Citations
	161
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	115
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	87
Feasibility of a best–worst scaling exercise to set priorities for autism research	86
Indicators for adequate diabetes care for the indigenous communities of Ecuador	80
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	78
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	65
Developing a novel co‐produced methodology to understand ‘real‐world’ help‐seeking in online peer–peer communities by young people experiencing emotional abuse and neglect	62
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	57
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	48
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	46
Just a story? Leadership, lived experience and integrated care	44
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	40
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	38
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	37
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	35
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	35
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	34
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	33
Inside Front Cover: Volume 25 Issue 1	32
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	32
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	32
Patient preferences for heart valve disease intervention	31
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	31
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	30

An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	29
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey	28
Identifying Common Patient‐Oriented Priorities for Child and Adolescent Health Research and Care: A Systematic Review of Priority Setting Partnerships	28
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event	28