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Citing this Article

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

Works citing "Patient-reported Outcomes as a Source of Evidence in Off-Label Prescribing: Analysis of Data From PatientsLikeMe"

According to Crossref, the following articles are citing this article (DOI 10.2196/jmir.1643):

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

  1. Wicks P, Stamford J, Grootenhuis MA, Haverman L, Ahmed S. Innovations in e-health. Quality of Life Research 2014;23(1):195
    CrossRef
  2. Eggleston EM, Weitzman ER. Innovative Uses of Electronic Health Records and Social Media for Public Health Surveillance. Current Diabetes Reports 2014;14(3)
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  3. Bauer DC, Gaff C, Dinger ME, Caramins M, Buske FA, Fenech M, Hansen D, Cobiac L. Genomics and personalised whole-of-life healthcare. Trends in Molecular Medicine 2014;20(9):479
    CrossRef
  4. Kazmer MM, Lustria MLA, Cortese J, Burnett G, Kim J, Ma J, Frost J. Distributed knowledge in an online patient support community: Authority and discovery. Journal of the Association for Information Science and Technology 2014;65(7):1319
    CrossRef
  5. Dal Pan GJ. Ongoing Challenges in Pharmacovigilance. Drug Safety 2014;37(1):1
    CrossRef
  6. O'Neill B, Ziebland S, Valderas J, Lupiáñez-Villanueva F. User-Generated Online Health Content: A Survey of Internet Users in the United Kingdom. Journal of Medical Internet Research 2014;16(4):e118
    CrossRef
  7. Keller B, Labrique A, Jain KM, Pekosz A, Levine O. Mind the Gap: Social Media Engagement by Public Health Researchers. Journal of Medical Internet Research 2014;16(1):e8
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  8. Capurro D, Cole K, Echavarría MI, Joe J, Neogi T, Turner AM. The Use of Social Networking Sites for Public Health Practice and Research: A Systematic Review. Journal of Medical Internet Research 2014;16(3):e79
    CrossRef
  9. Moorhead SA, Hazlett DE, Harrison L, Carroll JK, Irwin A, Hoving C. A New Dimension of Health Care: Systematic Review of the Uses, Benefits, and Limitations of Social Media for Health Communication. Journal of Medical Internet Research 2013;15(4):e85
    CrossRef
  10. Saunders DR, Bex PJ, Woods RL. Crowdsourcing a Normative Natural Language Dataset: A Comparison of Amazon Mechanical Turk and In-Lab Data Collection. Journal of Medical Internet Research 2013;15(5):e100
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  11. Vincent A, Benzo RP, Whipple MO, McAllister SJ, Erwin PJ, Saligan LN. Beyond pain in fibromyalgia: insights into the symptom of fatigue. Arthritis Research & Therapy 2013;15(6):221
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  12. Marrie RA, Salter AR, Tyry T, Fox RJ, Cutter GR. Preferred Sources of Health Information in Persons With Multiple Sclerosis: Degree of Trust and Information Sought. Journal of Medical Internet Research 2013;15(4):e67
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  13. Vayena E, Mastroianni A, Kahn J. Caught in the Web: Informed Consent for Online Health Research. Science Translational Medicine 2013;5(173):173fs6
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  14. Subirats L, Ceccaroni L, Lopez-Blazquez R, Miralles F, García-Rudolph A, Tormos JM. Circles of Health: Towards an advanced social network about disabilities of neurological origin. Journal of Biomedical Informatics 2013;46(6):1006
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  15. Hesse BW, Cole GE, Powe BD. Partnering Against Cancer Today: A Blueprint for Coordinating Efforts Through Communication Science. JNCI Monographs 2013;2013(47):233
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  16. Tozzi AE, Mingarelli R, Agricola E, Gonfiantini M, Pandolfi E, Carloni E, Gesualdo F, Dallapiccola B. The internet user profile of Italian families of patients with rare diseases: a web survey. Orphanet Journal of Rare Diseases 2013;8(1):76
    CrossRef
  17. Karamanlis DA, Tzitzis PM, Bratsas CA, Bamidis PD. Personal health records in the preclinical medical curriculum: modeling student responses in a simple educational environment utilizing Google Health. BMC Medical Education 2012;12(1):88
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  18. Cascade E, Marr P, Winslow M, Burgess A, Nixon M. Conducting Research on the Internet: Medical Record Data Integration with Patient-Reported Outcomes. Journal of Medical Internet Research 2012;14(5):e137
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  19. Coleman JJ, McDowell SE. An agenda for UK clinical pharmacology: The potential of the internet. British Journal of Clinical Pharmacology 2012;73(6):953
    CrossRef
  20. Dal Pan GJ. Monitoring the Safety of Medicines Used Off-Label. Clinical Pharmacology & Therapeutics 2012;91(5):787
    CrossRef
  21. Vayena E, Mastroianni A, Kahn J. Ethical Issues in Health Research With Novel Online Sources. American Journal of Public Health 2012;102(12):2225
    CrossRef
  22. Swan M. Crowdsourced Health Research Studies: An Important Emerging Complement to Clinical Trials in the Public Health Research Ecosystem. Journal of Medical Internet Research 2012;14(2):e46
    CrossRef
  23. Nakamura C, Bromberg M, Bhargava S, Wicks P, Zeng-Treitler Q. Mining Online Social Network Data for Biomedical Research: A Comparison of Clinicians’ and Patients’ Perceptions About Amyotrophic Lateral Sclerosis Treatments. Journal of Medical Internet Research 2012;14(3):e90
    CrossRef
  24. Wicks P, Keininger DL, Massagli MP, la Loge CD, Brownstein C, Isojärvi J, Heywood J. Perceived benefits of sharing health data between people with epilepsy on an online platform. Epilepsy & Behavior 2012;23(1):16
    CrossRef
  25. Lowenthal J, Hull SC, Pearson SD. The Ethics of Early Evidence — Preparing for a Possible Breakthrough in Alzheimer's Disease. New England Journal of Medicine 2012;367(6):488
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  26. Samal L, Saha S, Chander G, Korthuis PT, Sharma RK, Sharp V, Cohn J, Moore RD, Beach MC. Internet Health Information Seeking Behavior and Antiretroviral Adherence in Persons Living with HIV/AIDS. AIDS Patient Care and STDs 2011;25(7):445
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  27. Frost JH. The case for using social media to aggregate patient experiences with off-label prescriptions. Expert Review of Pharmacoeconomics & Outcomes Research 2011;11(4):371
    CrossRef
  28. Wicks P, Massagli M, Kulkarni A, Dastani H. Use of an Online Community to Develop Patient-Reported Outcome Instruments: The Multiple Sclerosis Treatment Adherence Questionnaire (MS-TAQ). Journal of Medical Internet Research 2011;13(1):e12
    CrossRef