The importance of being expert
The quest for cancer information on the Internet
Bibliographic Data
| ID | 4601112 |
|---|---|
| Authors | Sue Ziebland (0000-0002-6496-4859, University of Oxford, corresponding author) |
| Year | 2004 |
| Volume | 59 |
| Issue | 9 |
| Pages | 1783-1793 |
| Publication date | 2004-11-01 |
| Peer Reviewed | Yes |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Social Science & Medicine (JOURNAL) |
| Journal identifiers | ISSN: 0277-9536 • E-ISSN: 1873-5347 |
| Publisher | Elsevier BV (PUBLISHER) |
| DOI | 10.1016/j.socscimed.2004.02.019 |
| PMID | 15312914 |
| OpenAlex | W1973389377 |
| Language | EN |
| Citations received | 77 |
| References cited | 19 |
Breast cancer · Cancer · Competence (human resources · Health care · Internet privacy · Narrative · Political science · Public relations · Sociology of health and illness · The Internet · World Wide Web · Computer Science · Focus Groups and Qualitative Methods · Health Literacy and Information Accessibility · Medicine · Patient-Provider Communication in Healthcare · Psychology · Social Psychology
O desenvolvimento das tecnologias de informação e comunicação
Health and Illness in a Connected World
Making sense of qualitative data analysis
Saber lego y experto en salud
Digitalization and co-creation of healthcare value
Lessening the Evils, Online
Curating the digital space
The Association Among Gender, Computer Use and Online Health Searching, and Mental Health
Constructing the digital patient
Genetics, cyberspace and bioethics
Questioning context
Application du concept de responsabilisation personnelle aux usages sociaux des technologies d’information et de communication en santé
Vital scientific puzzle or lived uncertainty? Professional and lived approaches to the uncertainties of ageing with HIV
Reflections on the centrality of power in medical sociology
“I like to be an informed person but…” negotiating responsibility for treatment decisions in cancer care
Paradoxical bodies
Self‐directed learning and prostate cancer
L’expertise profane dans la prise en charge hospitalière du VIH/Sida au Cameroun
Public Claims about Automatic External Defibrillators
My health is not a job’
How will e-health affect patient participation in the clinic? A review of e-health studies and the current evidence for changes in the relationship between medical professionals and patients
Practicing Patienthood Online
Maternal Devices”, Social Media and the Self-Management of Pregnancy, Mothering and Child Health
Public and User Participation in Public Service Delivery
Making sense of patient expertise
Pain as performance
The thing about pain
Using online mining techniques to inform formative evaluations
Internet Community Group Participation
Social Media’s Role in Peacebuilding and Post-Conflict Recovery
Fathers sharing about early parental support in health-care - virtual discussions on an Internet forum
Gender as a context for interpreting the self‐directed learning experiences of prostate and breast cancer patients
Les savoirs profanes et l'intelligence du Web
A Masked Truth? Public Discussions about Face Masks on a French Health Forum
Mastery, Isolation, or Acceptance
The Imitation Game as a Method for Exploring Knowledge(s) of Chronic Illness
Internet Recruitment and E-Mail Interviews in Qualitative Studies
Digital mediation of candidacy in maternity care
You become a slightly better doctor
Network gatekeeping
I knew before I was told
Internet marketing of bariatric surgery
Internet na promoção da saúde
Keep complaining til someone listens
Expert or experiential knowledge? How knowledge informs situated action in childcare practices
Talking About Looking
Online Health Information Seeking in the Context of the Medical Consultation in Switzerland
Use of Social Media Among Individuals Who Suffer From Post-Traumatic Stress
Making it All Normal
Online boundary-work
A paradox in healthcare service development
Similarities and differences in the meanings children and their parents attach to epilepsy medications
Demanding patient or demanding encounter
Combining patient talk about internet use during primary care consultations with retrospective accounts. A qualitative analysis of interactional and interview data
A platform for goodness, not for badness
From 'parallel world' to 'trading zone
The digital divide
The role of the Internet in cancer patients' engagement with complementary and alternative treatments
Online self-expression and experimentation as 'reflectivism
A internet, o paciente expert e a prática médica
Education for type 2 diabetes mellitus self-care
Patients receiving ambulatory care
The Forms and Uses of Acquired Prostate Cancer Expertise Among Prostate Cancer Survivors
Women, Pregnancy, and Health Information Online
Understanding our potential research publics
Information creation on online drug forums
The devil you know
Understanding fear of cancer recurrence in terms of damage to 'everyday health competence
One wants to know what a chromosome is
Everyday health and the internet
Producing genetic knowledge and citizenship through the Internet
The challenge of fitting in
Ordinary people only
Trusting blindly can be the biggest risk of all
The mundane realities of the everyday lay use of the internet for health, and their consequences for media convergence
The vaccination debate in the 'post-truth' era
Health information work and the enactment of care in couples and families affected by Multiple Sclerosis
Empirical Studies Assessing the Quality of Health Information for Consumers on the World Wide Web
Virtual Community Care? Social Policy and the Emergence of Computer Mediated Social Support
Consumer health information seeking on the Internet
The Story of My Illness
Accounts of health and illness
The genesis of chronic illness
Doctor in the house
| Unique citing works | 77 |
|---|---|
| Citations per year | 3,67 |
| Citation span | 2005 - 2025 (21) |
| Citation velocity | recent |
| Highly cited | No |
| Citation types | Neutral: 76 |