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 2021-08-01 to 2025-08-01.)

Article	Citations
	156
Assessing the experience of person‐centred coordinated care of people with chronic conditions in the Netherlands: Validation of the Dutch P3CEQ	110
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	84
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	81
Feasibility of a best–worst scaling exercise to set priorities for autism research	74
Indicators for adequate diabetes care for the indigenous communities of Ecuador	73
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	65
Children's Communication Choices About Musculoskeletal Pain and Injury: Insights From a Public Involvement Event	61
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	61
Cocreation with Dutch patients of decision‐relevant information to support shared decision‐making about adjuvant treatment in breast cancer care	55
Patient co‐design of digital health storytelling tools for multimorbidity: A phenomenological study	48
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	47
The dyadic self‐care experience of stroke survivors and their caregivers: A qualitative descriptive study	46
Evaluating meaningful impact of Patient and Public Involvement: A Q methodology study among researchers and young people with a chronic condition	43
Talking Trials: An arts‐based exploration of attitudes to clinical trials amongst minority ethnic members of the South Riverside Community of Cardiff	38
Youth engagement in mental health research: A systematic review	38
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	37
Just a story? Leadership, lived experience and integrated care	37
The Relationship Between Healthcare System Distrust and Intention to Use Violence Against Health Professionals: The Mediating Role of Health News Perceptions	35
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	32
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	32
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	32
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	32
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	32
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	32

Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	31
Participatory research with carers: A systematic review and narrative synthesis	29
Struggling with capital: Recovery after severe traumatic brain injury among working‐age individuals in Denmark	28