Explore our sister journals here.

Maintenance Notice

Due to necessary scheduled maintenance, the JMIR Publications website will be unavailable from Wednesday, July 01, 2020 at 8:00 PM to 10:00 PM EST. We apologize in advance for any inconvenience this may cause you.

Who will be affected?

Citing this Article

Right click to copy or hit: ctrl+c (cmd+c on mac)

Published on 20.11.17 in Vol 6, No 2 (2017): Jul-Dec

This paper is in the following e-collection/theme issue:

Works citing "Shaping an Effective Health Information Website on Rare Diseases Using a Group Decision-Making Tool: Inclusion of the Perspectives of Patients, Their Family Members, and Physicians"

Ana Babac, Svenja Litzkendorf, Katharina Schmidt, Frédéric Pauer, Kathrin Damm, Martin Frank, Johann-Matthias Graf von der Schulenburg

Interact J Med Res 2017 (Nov 20); 6(2):e23 

According to Crossref, the following articles are citing this article (DOI 10.2196/ijmr.7352):

(note that this is only a small subset of citations)

  1. Bernhoff G, Saripanidis C, Bertilson BC. “As If Neck Injuries Did Not Exist”: An Interview Study of Patients’ and Relatives’ Perceptions of Web Information on and Management of Whiplash Injuries in Sweden. Interactive Journal of Medical Research 2019;8(2):e9881
    CrossRef
  2. Hong S, Wang L, Zhao D, Zhang Y, Chen Y, Tan J, Liang L, Zhu T. Clinical utility in infants with suspected monogenic conditions through next‐generation sequencing. Molecular Genetics & Genomic Medicine 2019;7(6)
    CrossRef
  3. Walewski JL, Donovan D, Nori M. How many zebras are there, and where are they hiding in medical literature? A literature review of publications on rare diseases. Expert Opinion on Orphan Drugs 2019;7(11):513
    CrossRef
  4. Babac A, Damm K, Graf von der Schulenburg J. Patient-reported data informing early benefit assessment of rare diseases in Germany: A systematic review. Health Economics Review 2019;9(1)
    CrossRef
  5. Babac A, von Friedrichs V, Litzkendorf S, Zeidler J, Damm K, Graf von der Schulenburg J. Integrating patient perspectives in medical decision-making: a qualitative interview study examining potentials within the rare disease information exchange process in practice. BMC Medical Informatics and Decision Making 2019;19(1)
    CrossRef
  6. Bleyer AJ, Kidd K, Robins V, Martin L, Taylor A, Santi A, Tsoumas G, Hunt A, Swain E, Abbas M, Akinbola E, Vidya S, Moossavi S, Bleyer AJ, Živná M, Hartmannová H, Hodaňová K, Vyleťal P, Votruba M, Harden M, Blumenstiel B, Greka A, Kmoch S. Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases. Genetics in Medicine 2020;22(1):142
    CrossRef
  7. . ‘Negative’ clinical trials in rare diseases and beyond: reclassification and potential solutions. Future Rare Diseases 2021;1(1)
    CrossRef
  8. Wollmann K, der Keylen PV, Tomandl J, Meerpohl JJ, Sofroniou M, Maun A, Voigt-Radloff S. The information needs of internet users and their requirements for online health information—A scoping review of qualitative and quantitative studies. Patient Education and Counseling 2021;104(8):1904
    CrossRef
  9. Nori M, Fisher-Vance D, Wuerth L, Colenso R, Donovan DJ. The global role of patients, advocates and caregivers in rare diseases. Future Rare Diseases 2022;2(2)
    CrossRef
  10. Lu K, Liao H. A survey of group decision making methods in Healthcare Industry 4.0: bibliometrics, applications, and directions. Applied Intelligence 2022;52(12):13689
    CrossRef