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

Consumer & Patient Education and Shared-Decision Making 

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Works citing "Managing the Personal Side of Health: How Patient Expertise Differs from the Expertise of Clinicians"

Andrea Hartzler, Wanda Pratt
J Med Internet Res 2011 (Aug 16); 13(3):e62 

According to Crossref, the following articles are citing this article (DOI 10.2196/jmir.1728):

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

1. Wolf CT, Veinot TC. Struggling for space and finding my place: An interactionist perspective on everyday use of biomedical information. Journal of the Association for Information Science and Technology 2014;:n/a [CrossRef]
2. Lederman R, Fan H, Smith S, Chang S. Who can you trust? Credibility assessment in online health forums. Health Policy and Technology 2014;3(1):13 [CrossRef]
3. Sanderson T, Angouri J. ‘I’m an expert in me and I know what I can cope with’: Patient expertise in rheumatoid arthritis. Communication & Medicine 2014;10(3) [CrossRef]
4. Davis JS, Zuber K. The Nephrology Interdisciplinary Team: An Education Synergism. Advances in Chronic Kidney Disease 2014;21(4):338 [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;65(7):1319 [CrossRef]
6. Frost J, Vermeulen IE, Beekers N. Anonymity Versus Privacy: Selective Information Sharing in Online Cancer Communities. Journal of Medical Internet Research 2014;16(5):e126 [CrossRef]
7. Dwyer AA, Quinton R, Morin D, Pitteloud N. Identifying the unmet health needs of patients with congenital hypogonadotropic hypogonadism using a web-based needs assessment: implications for online interventions and peer-to-peer support. Orphanet Journal of Rare Diseases 2014;9(1):83 [CrossRef]
8. Godbold N. Listening to bodies and watching machines: Developing health information skills, tools and services for people living with chronic kidney disease. Australian Academic & Research Libraries 2013;44(1):14 [CrossRef]
9. Huh J, Yetisgen-Yildiz M, Pratt W. Text classification for assisting moderators in online health communities. Journal of Biomedical Informatics 2013;46(6):998 [CrossRef]
10. Munson SA, Cavusoglu H, Frisch L, Fels S. Sociotechnical Challenges and Progress in Using Social Media for Health. Journal of Medical Internet Research 2013;15(10):e226 [CrossRef]
11. 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]
12. Abrahamson JA, Rubin VL. Discourse structure differences in lay and professional health communication. Journal of Documentation 2012;68(6):826 [CrossRef]
13. Rubenstein EL. “Things my doctor never told me”: Bridging information gaps in an online community. Proceedings of the American Society for Information Science and Technology 2012;49(1):1 [CrossRef]
14. Sabee CM, Bylund CL, Weber JG, Sonet E. The Association of Patients’ Primary Interaction Goals with Attributions for their Doctors’ Responses in Conversations about Online Health Research. Journal of Applied Communication Research 2012;40(3):271 [CrossRef]
15. Hewitt-Taylor J, Bond CS. What E-patients Want From the Doctor-Patient Relationship: Content Analysis of Posts on Discussion Boards. Journal of Medical Internet Research 2012;14(6):e155 [CrossRef]