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 "Use of an Online Community to Develop Patient-Reported Outcome Instruments: The Multiple Sclerosis Treatment Adherence Questionnaire (MS-TAQ)"

Paul Wicks, Michael Massagli, Amit Kulkarni, Homa Dastani
J Med Internet Res 2011 (Jan 24); 13(1):e12 

According to Crossref, the following articles are citing this article (DOI 10.2196/jmir.1687):

(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. Wicks P, Sulham KA, Gnanasakthy A. Quality of Life in Organ Transplant Recipients Participating in an Online Transplant Community. The Patient - Patient-Centered Outcomes Research 2014;7(1):73 [CrossRef]
3. Little M, Wicks P, Vaughan T, Pentland A. Quantifying Short-Term Dynamics of Parkinson’s Disease Using Self-reported Symptom Data From an Internet Social Network. Journal of Medical Internet Research 2013;15(1):e20 [CrossRef]
4. Ožura A, Kovač L, Šega S. Adherence to disease-modifying therapies and attitudes regarding disease in patients with multiple sclerosis. Clinical Neurology and Neurosurgery 2013;115:S6 [CrossRef]
5. Jones JL, Scheidt DJ, Kaushal RS, Carroll CA. Assessing the role of patient support services on adherence rates in patients using glatiramer acetate for relapsing-remitting multiple sclerosis. Journal of Medical Economics 2013;16(2):213 [CrossRef]
6. Oprescu F, Campo S, Lowe J, Andsager J, Morcuende JA. Online Information Exchanges for Parents of Children With a Rare Health Condition: Key Findings From an Online Support Community. Journal of Medical Internet Research 2013;15(1):e16 [CrossRef]
7. Wicks P, Vaughan TE, Massagli MP. The multiple sclerosis rating scale, revised (MSRS-R): Development, refinement, and psychometric validation using an online community. Health and Quality of Life Outcomes 2012;10(1):70 [CrossRef]
8. Haase R, Schultheiss T, Kempcke R, Thomas K, Ziemssen T. Use and Acceptance of Electronic Communication by Patients With Multiple Sclerosis: A Multicenter Questionnaire Study. Journal of Medical Internet Research 2012;14(5):e135 [CrossRef]
9. Kennedy CM, Powell J, Payne TH, Ainsworth J, Boyd A, Buchan I. Active Assistance Technology for Health-Related Behavior Change: An Interdisciplinary Review. Journal of Medical Internet Research 2012;14(3):e80 [CrossRef]
10. 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]
11. 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]
12. Lejbkowicz I, Caspi O, Miller A. Participatory medicine and patient empowerment towards personalized healthcare in multiple sclerosis. Expert Review of Neurotherapeutics 2012;12(3):343 [CrossRef]