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

Medicine 2.0: Social Media, Open, Participatory, Collaborative Medicine 


Advertisement: Preregister now for the Medicine 2.0 Congress

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

Jeana Frost, Sally Okun, Timothy Vaughan, James Heywood, Paul Wicks
J Med Internet Res 2011 (Jan 21); 13(1):e6 

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. 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 [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) [CrossRef]
 
3. Wicks P, Stamford J, Grootenhuis MA, Haverman L, Ahmed S. Innovations in e-health. Quality of Life Research 2014;23(1):195 [CrossRef]
 
4. Dal Pan GJ. Ongoing Challenges in Pharmacovigilance. Drug Safety 2014;37(1):1 [CrossRef]
 
5. 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;:n/a [CrossRef]
 
6. 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]
 
7. Vayena E, Mastroianni A, Kahn J. Caught in the Web: Informed Consent for Online Health Research. Science Translational Medicine 2013;5(173):173fs6 [CrossRef]
 
8. 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]
 
9. 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]
 
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 [CrossRef]
 
11. 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 [CrossRef]
 
12. Hesse BW, Cole GE, Powe BD. Partnering Against Cancer Today: A Blueprint for Coordinating Efforts Through Communication Science. JNCI Monographs 2013;2013(47):233 [CrossRef]
 
13. 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 [CrossRef]
 
14. 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 [CrossRef]
 
15. 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]
 
16. Dal Pan GJ. Monitoring the Safety of Medicines Used Off-Label. Clinical Pharmacology & Therapeutics 2012;91(5):787 [CrossRef]
 
17. 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 [CrossRef]
 
18. 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]
 
19. 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]
 
20. 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]
 
21. 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 [CrossRef]
 
22. 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 [CrossRef]
 
23. 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]
 
24. 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]
 
25. 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 [CrossRef]
 
26. 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]