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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

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Showing 1-25 of 77 citing articles:

Patient stakeholder engagement in research: A narrative review to describe foundational principles and best practice activities
James D. Harrison, Andrew D. Auerbach, Wendy G. Anderson, et al.
Health Expectations (2019) Vol. 22, Iss. 3, pp. 307-316
Open Access | Times Cited: 188
Emerging Guidelines for Patient Engagement in Research
John Kirwan, Maarten de Wit, Lori Frank, et al.
Value in Health (2016) Vol. 20, Iss. 3, pp. 481-486
Open Access | Times Cited: 179
Patient and Public Engagement in Integrated Knowledge Translation Research: Are we there yet?
Davina Banner, Marc Bains, Sandra Carroll, et al.
Research Involvement and Engagement (2019) Vol. 5, Iss. 1
Open Access | Times Cited: 162
Designing a tool to support patient and public involvement in research projects: the Involvement Matrix
Dirk‐Wouter Smits, Karen van Meeteren, Martijn Klem, et al.
Research Involvement and Engagement (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 159
Patient and public involvement in research: a review of practical resources for young investigators
Ashokan Arumugam, Lawrence Rick Phillips, Ann Moore, et al.
BMC Rheumatology (2023) Vol. 7, Iss. 1
Open Access | Times Cited: 74
Quality of life in psoriatic arthritis
Tania Gudu, Laure Gossec
Expert Review of Clinical Immunology (2018) Vol. 14, Iss. 5, pp. 405-417
Open Access | Times Cited: 155
EULAR recommendations for the involvement of patient research partners in rheumatology research: 2023 update
Maarten de Wit, K. Aouad, Muriel Elhaï, et al.
Annals of the Rheumatic Diseases (2024), pp. ard-225566
Closed Access | Times Cited: 11
The 12-item Psoriatic Arthritis Impact of Disease Questionnaire: Construct Validity, Reliability, and Interpretability in a Clinical Setting
Marco Di Carlo, Andrea Becciolini, Valentina Lato, et al.
The Journal of Rheumatology (2016) Vol. 44, Iss. 3, pp. 279-285
Closed Access | Times Cited: 72
Practical guidance for engaging patients in health research, treatment guidelines and regulatory processes: results of an expert group meeting organized by the World Health Organization (WHO) and the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO)
Maarten de Wit, Cyrus Cooper, Peter Tugwell, et al.
Aging Clinical and Experimental Research (2019) Vol. 31, Iss. 7, pp. 905-915
Open Access | Times Cited: 62
Adolescent and young adult patients as co‐researchers: A scoping review
Kjersti J. Ø. Fløtten, Ana Isabel Fernandes Guerreiro, Ilaria Simonelli, et al.
Health Expectations (2021) Vol. 24, Iss. 4, pp. 1044-1055
Open Access | Times Cited: 48
A systematic review of measurement properties of patient reported outcome measures in psoriatic arthritis: A GRAPPA-OMERACT initiative
Pil Højgaard, Louise Klokker, Ana‐Maria Orbai, et al.
Seminars in Arthritis and Rheumatism (2017) Vol. 47, Iss. 5, pp. 654-665
Open Access | Times Cited: 59
PsAID12 Provisionally Endorsed at OMERACT 2018 as Core Outcome Measure to Assess Psoriatic Arthritis-specific Health-related Quality of Life in Clinical Trials
Ana‐Maria Orbai, Richard Holland, Ying Ying Leung, et al.
The Journal of Rheumatology (2018) Vol. 46, Iss. 8, pp. 990-995
Open Access | Times Cited: 51
Patient Preference Studies During Early Drug Development: Aligning Stakeholders to Ensure Development Plans Meet Patient Needs
Nigel S. Cook, Julie Cave, Anke‐Peggy Holtorf
Frontiers in Medicine (2019) Vol. 6
Open Access | Times Cited: 51
Successful Stepwise Development of Patient Research Partnership: 14 Years’ Experience of Actions and Consequences in Outcome Measures in Rheumatology (OMERACT)
Maarten de Wit, John Kirwan, Peter Tugwell, et al.
Patient (2016) Vol. 10, Iss. 2, pp. 141-152
Open Access | Times Cited: 50
Including the patient voice in the development and implementation of patient‐reported outcomes in cancer clinical trials
Bonnie Addario, Jan Geißler, Marcia K. Horn, et al.
Health Expectations (2019) Vol. 23, Iss. 1, pp. 41-51
Open Access | Times Cited: 38
A rapid realist review of patient engagement in patient-oriented research and health care system impacts: part one
Elaine Zibrowski, Tracey Carr, Shelagh McDonald, et al.
Research Involvement and Engagement (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 32
Patient-reported outcomes and patient-reported outcome measures in interstitial lung disease: where to go from here?
Meena Kalluri, Fabrizio Luppi, Ada Vancheri, et al.
European Respiratory Review (2021) Vol. 30, Iss. 160, pp. 210026-210026
Open Access | Times Cited: 28
Matching researchers’ needs and patients’ contributions: practical tips for meaningful patient engagement from the field of rheumatology
Casper Schoemaker, Dawn P. Richards, Maarten de Wit
Annals of the Rheumatic Diseases (2023) Vol. 82, Iss. 3, pp. 312-315
Open Access | Times Cited: 12
Development and early qualitative evidence of two novel patient-reported outcome instruments to assess daily functioning in people with early-stage Parkinson’s
Thomas Morel, Sophie Cleanthous, John Andrejack, et al.
Journal of Patient-Reported Outcomes (2023) Vol. 7, Iss. 1
Open Access | Times Cited: 11
Role of doctor-patient communication in rheumatology
R.A. Grekhov, А. В. Александров, I.А. Zborovskaya
Russian Journal of Preventive Medicine (2025) Vol. 28, Iss. 4, pp. 156-156
Closed Access
Validity and score interpretation of the 12-item Psoriatic Arthritis Impact of Disease: an analysis of pooled data from two phase 3 trials of bimekizumab in patients with psoriatic arthritis
Laure Gossec, Ana‐Maria Orbai, Laura C. Coates, et al.
RMD Open (2024) Vol. 10, Iss. 1, pp. e003548-e003548
Open Access | Times Cited: 3
Report of the GRAPPA-OMERACT Psoriatic Arthritis Working Group from the GRAPPA 2015 Annual Meeting
Ana‐Maria Orbai, Philip J. Mease, Maarten de Wit, et al.
The Journal of Rheumatology (2016) Vol. 43, Iss. 5, pp. 965-969
Open Access | Times Cited: 26
Assessing health-related quality of life in primary Sjögren’s syndrome—The PSS-QoL
Angelika Lackner, Martin Stradner, Josef Hermann, et al.
Seminars in Arthritis and Rheumatism (2017) Vol. 48, Iss. 1, pp. 105-110
Closed Access | Times Cited: 25
Effect of filgotinib on health-related quality of life in active psoriatic arthritis: a randomized phase 2 trial (EQUATOR)
Ana‐Maria Orbai, Alexis Ogdie, Laure Gossec, et al.
Lara D. Veeken (2019) Vol. 59, Iss. 7, pp. 1495-1504
Open Access | Times Cited: 24
Leveraging Patients’ Creative Ideas for Innovation in Health Care
Yuna S. H. Lee, Rachel Grob, Ingrid M. Nembhard, et al.
Milbank Quarterly (2023) Vol. 102, Iss. 1, pp. 233-269
Open Access | Times Cited: 8
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