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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.

Requested Article:

“Am I normal?” The Wishes of Patients With Lymphoma to Compare Their Patient-Reported Outcomes With Those of Their Peers
Simone Oerlemans, Lindy P. J. Arts, Nicole Horevoorts, et al.
Journal of Medical Internet Research (2017) Vol. 19, Iss. 8, pp. e288-e288
Open Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Cancer survivors not participating in observational patient-reported outcome studies have a lower survival compared to participants: the population-based PROFILES registry
Belle H. de Rooij, Nicole P. M. Ezendam, Floortje Mols, et al.
Quality of Life Research (2018) Vol. 27, Iss. 12, pp. 3313-3324
Open Access | Times Cited: 64
A Narrative Review on the Collection and Use of Electronic Patient-Reported Outcomes in Cancer Survivorship Care with Emphasis on Symptom Monitoring
Corina van den Hurk, Floortje Mols, Manuela Eicher, et al.
Current Oncology (2022) Vol. 29, Iss. 6, pp. 4370-4385
Open Access | Times Cited: 37
Visualization formats of patient-reported outcome measures in clinical practice: a systematic review about preferences and interpretation accuracy
Elaine A. C. Albers, Itske Fraterman, Iris Walraven, et al.
Journal of Patient-Reported Outcomes (2022) Vol. 6, Iss. 1
Open Access | Times Cited: 28
Reference data of the EORTC QLQ-C30 questionnaire: five consecutive annual assessments of approximately 2000 representative Dutch men and women
Floortje Mols, Olga Husson, Marije Oudejans, et al.
Acta Oncologica (2018) Vol. 57, Iss. 10, pp. 1381-1391
Open Access | Times Cited: 45
Electronic symptom monitoring in pediatric patients hospitalized for chemotherapy
Allison Barz Leahy, Lisa A. Schwartz, Yimei Li, et al.
Cancer (2021) Vol. 127, Iss. 16, pp. 2980-2989
Open Access | Times Cited: 23
Exploring Cancer Survivor Needs and Preferences for Communicating Personalized Cancer Statistics From Registry Data: Qualitative Multimethod Study
Ruben Vromans, Mies van Eenbergen, Gijs Geleijnse, et al.
JMIR Cancer (2021) Vol. 7, Iss. 4, pp. e25659-e25659
Open Access | Times Cited: 22
Measuring Clinical, Biological, and Behavioral Variables to Elucidate Trajectories of Patient-Reported Outcomes: The PROFILES Registry
Lonneke V. van de Poll‐Franse, Nicole Horevoorts, Dounya Schoormans, et al.
JNCI Journal of the National Cancer Institute (2022) Vol. 114, Iss. 6, pp. 800-807
Open Access | Times Cited: 14
More frequent use of health care services among distressed compared with nondistressed survivors of lymphoma and chronic lymphocytic leukemia: Results from the population‐based PROFILES registry
Lindy P. J. Arts, Simone Oerlemans, Lidwine W. Tick, et al.
Cancer (2018) Vol. 124, Iss. 14, pp. 3016-3024
Open Access | Times Cited: 24
Applying PRO Reference Values to Communicate Clinically Relevant Information at the Point-of-care
Roxanne E. Jensen, Jakob Bue Bjørner
Medical Care (2019) Vol. 57, Iss. Suppl 1, pp. S24-S30
Closed Access | Times Cited: 21
Communicating tailored risk information of cancer treatment side effects: Only words or also numbers?
Ruben Vromans, Steffen Pauws, Nadine Bol, et al.
BMC Medical Informatics and Decision Making (2020) Vol. 20, Iss. 1
Open Access | Times Cited: 19
Complementing clinical cancer registry data with patient reported outcomes: A feasibility study on routine electronic patient‐reported outcome assessment for the Austrian Myelome Registry
Monika Sztankay, Lucia Neppl, Lisa M. Wintner, et al.
European Journal of Cancer Care (2019) Vol. 28, Iss. 6
Open Access | Times Cited: 19
Lenalidomide maintenance for diffuse large B‐cell lymphoma patients responding to R‐CHOP: quality of life, dosing, and safety results from the randomised controlled REMARC study
Catherine Thiéblemont, Susannah Howlett, Olivier Casasnovas, et al.
British Journal of Haematology (2019) Vol. 189, Iss. 1, pp. 84-96
Open Access | Times Cited: 16
Need for numbers: assessing cancer survivors’ needs for personalized and generic statistical information
Ruben Vromans, Saar Hommes, Felix J. Clouth, et al.
BMC Medical Informatics and Decision Making (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 9
Web-Based Return of Individual Patient-Reported Outcome Results Among Patients With Lymphoma: Randomized Controlled Trial
Simone Oerlemans, Lindy P. J. Arts, Jacobien M. Kieffer, et al.
Journal of Medical Internet Research (2021) Vol. 23, Iss. 12, pp. e27886-e27886
Open Access | Times Cited: 11
BREAST-Q REACT: Qualitative Assessment of the Design, Functionality, and Clinical Utility of a New Score Interpretation Tool
Minji Kim, Jaime Gilliland, Mei-fan Parnes, et al.
Annals of Surgical Oncology (2024) Vol. 31, Iss. 7, pp. 4498-4511
Closed Access | Times Cited: 1
Monitoring potentially modifiable lifestyle factors in cancer survivors: A narrative review on currently available methodologies and innovations for large-scale surveillance
Jeroen W. G. Derksen, Sandra Beijer, Miriam Koopman, et al.
European Journal of Cancer (2018) Vol. 103, pp. 327-340
Closed Access | Times Cited: 11
Population-based cancer survivorship research: Experiences from Germany and the Netherlands
Melissa S. Y. Thong, Floortje Mols, Daniela Doege, et al.
Journal of Cancer Policy (2018) Vol. 15, pp. 87-91
Open Access | Times Cited: 9
How Returning Aggregate Research Results Impacts Interest in Research Engagement and Planned Actions Relevant to Health Care Decision Making: Cohort Study
Elissa R. Weitzman, Kara M. Magane, Lauren E. Wisk
Journal of Medical Internet Research (2018) Vol. 20, Iss. 12, pp. e10647-e10647
Open Access | Times Cited: 9
Effects of comparative information when communicating personalized risks of treatment outcomes: an experimental study
Ruben Vromans, Steffen Pauws, Lonneke V. van de Poll‐Franse, et al.
Journal of Risk Research (2022) Vol. 26, Iss. 3, pp. 324-343
Open Access | Times Cited: 5
Determinants and mediating mechanisms of quality of life and disease-specific symptoms among thyroid cancer patients: the design of the WaTCh study
Floortje Mols, Dounya Schoormans, Romana T. Netea‐Maier, et al.
Thyroid Research (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Patient-reported outcomes and psycho-oncological screening in hematology: a practical example of routine electronic monitoring
Jens Lehmann, Lisa M. Wintner, Monika Sztankay, et al.
memo - Magazine of European Medical Oncology (2020) Vol. 13, Iss. 3, pp. 285-293
Open Access | Times Cited: 4
Patient-Reported Outcome Measures in Breast Cancer Surgery
Minji Kim, Francis D. Graziano, Audree B. Tadros, et al.
Current Surgery Reports (2024) Vol. 12, Iss. 5, pp. 67-75
Closed Access
How Returning Aggregate Research Results Impacts Interest in Research Engagement and Planned Actions Relevant to Health Care Decision Making: Cohort Study (Preprint)
Elissa R. Weitzman, Kara M. Magane, Lauren E. Wisk
(2018)
Open Access | Times Cited: 1
Key concepts and opportunities
Benzi M. Kluger, Janis M. Miyasaki
Handbook of clinical neurology (2022), pp. 3-15
Closed Access | Times Cited: 1
Exploring Cancer Survivor Needs and Preferences for Communicating Personalized Cancer Statistics From Registry Data: Qualitative Multimethod Study (Preprint)
Ruben Vromans, Mies van Eenbergen, Gijs Geleijnse, et al.
(2020)
Open Access
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