OOIR: Observatory of International Research

Papers

(The H4-Index of Health Expectations is 26. 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 2021-07-01 to 2025-07-01.)

Article	Citations
	147
Inside Front Cover: Volume 25 Issue 1	109
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	83
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	75
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	70
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	68
Feasibility of a best–worst scaling exercise to set priorities for autism research	63
Indicators for adequate diabetes care for the indigenous communities of Ecuador	60
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	58
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	52
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	48
Just a story? Leadership, lived experience and integrated care	45
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	44
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	43
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	38
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	36
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	36
Acceptability of risk stratification within population‐based cancer screening from the perspective of the general public: A mixed‐methods systematic review	35
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	33
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	31
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	31
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	31
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	30
Trauma‐informed co‐production: Collaborating and combining expertise to improve access to primary care with women with complex needs	29
Patient preferences for heart valve disease intervention	29

Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	27
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	26
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	26
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	26
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	26