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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. 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]
 
2. 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]
 
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. 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]
 
5. 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]
 
6. 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]
 
7. 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]
 
8. 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]
 
9. 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]