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 2022-08-01 to 2026-08-01.)

Article	Citations
	156
Exploring Benefits for Tibetan Cleft Lip and Palate Recipient Families From the Social Perspective of Healthcare Linkage	135
Decisions about adopting novel COVID‐19 vaccines among White adults in a rural state, USA: A qualitative study	133
Patient preferences for heart valve disease intervention	91
Expanding the boundaries of previously obtained informed consent in research: Views from participants in the Personalised Risk‐based Mammascreening study	84
Understanding Medicine Preferences of Older Adults: The Role of Messaging in a Multi‐Methods Experimental Survey	82
Look on the Bright Side: The Interactional Construction of a Survivor Identity in the Breast Cancer Clinic	71
Community views on the secondary use of general practice data: Findings from a mixed‐methods study	55
What Supports and Constrains the Implementation of Robust and Rapid Evaluation Within Local Government Public Health Systems?	51
A Joanna Briggs Institute Framework Approach to Shared Decision Making in End‐of‐Life	51
From Co‐Design to Quality Improvement: Using the Double Diamond Framework to Develop Primary Care Redesign Priorities for Hypertension Care	50
Co‐Design of a Community of Practice for People With Personal and Professional Expertise or Interest in Dementia in Australia	49
Co‐Developing User‐Centred Nutrition Educational Resources to Integrate Nutrition Into Multiple Sclerosis Care: A Collaborative Approach With Healthcare Professionals and Healthcare Consumers	46
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	45
Co‐Designing a Digital Stroke Prevention Platform: Leveraging Lived Experience and Expert Advice	43
Supporting patients to prepare for total knee replacement: Evidence‐, theory‐ and person‐based development of a ‘Virtual Knee School’ digital intervention	41
Factors Affecting the Integration of Dental Services Into Health and Social Care for People With Complex Needs	41
‘Nobody Has Ever Spoken to Me About PCD and Fertility Issues’: Fertility Experiences of People With Primary Ciliary Dyskinesia and Their Family Caregivers	40
Reducing long‐term use of benzodiazepine receptor agonists: In‐depth interview study with primary care stakeholders	40
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	38
Ripple Effects Mapping: Evaluating Multilevel Perspectives and Impacts of a Statewide Community–Academic Partnership Network on Covid‐19 Health Disparities	36
Identification and Applications of Key Elements in the Development of Pictorial Support for People With Aphasia After Stroke: A Co‐Design Approach	34
Hard to reach? Methodological challenges researching vulnerable, gang‐involved, young people	34
Powerless or Powerful? Healthcare Professionals' Construction of Agency in Patient and Family Engagement Accounts	32
An Application of Evidence‐Based Approaches to Engage Young People in the Design of a Global Mental Health Databank	30

Continuity Is Essential: The Experiences of Co‐Design Participants During the Implementation of a New Health Service	30
Participatory research with carers: A systematic review and narrative synthesis	29
Psychosocial Impact of Breast Density Notification Through Breast Cancer Screening: A Qualitative Interview Study	29
Indicators for adequate diabetes care for the indigenous communities of Ecuador	29