Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?
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"Let's get the best quality research we can": public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study.The risk of re-identification versus the need to identify individuals in rare disease researchComparison of consumers' views on electronic data sharing for healthcare and researchPatient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative StudySharing my health data: a survey of data sharing preferences of healthy individualsThe use of electronic patient records for medical research: conflicts and contradictionsPatient and public attitudes towards informed consent models and levels of awareness of Electronic Health Records in the UKWillingness to share personal health record data for care improvement and public health: a survey of experienced personal health record usersAssessing subject privacy and data confidentiality in an emerging region for clinical trials: United Arab Emirates.The acceptability of conducting data linkage research without obtaining consent: lay people's views and justifications.Sharing medical data for health research: the early personal health record experience.Public preferences about secondary uses of electronic health information.Consent for use of clinical leftover biosample: a survey among Chinese patients and the general publicMolecular genetic testing and the future of clinical genomics.Public trust in health information sharing: implications for biobanking and electronic health record systemsGPs' approaches to documenting stigmatising information: a qualitative study.Are Patients With Cancer Less Willing to Share Their Health Information? Privacy, Sensitivity, and Social PurposeFactors affecting willingness to share electronic health data among California consumers.Joint replacement recipients' views about health information privacy.Patient informed governance of distributed research networks: results and discussion from six patient focus groupsUse of electronic patient records for research: views of patients and staff in general practice.Stepping Up to the Plate: An Agenda for Research and Policy Action on Electronic Medical Records in Canadian Primary Healthcare.Does consent bias research?Patient preferences toward an interactive e-consent application for research using electronic health records.When Patient Engagement and Research Ethics Collide: Lessons from a Dementia Forum.Patients' attitudes to informed consent for genomic research with donated samples.
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P2860
Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?
description
2009 nî lūn-bûn
@nan
2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Consent for use of personal in ...... blic differ in their opinions?
@ast
Consent for use of personal in ...... blic differ in their opinions?
@en
type
label
Consent for use of personal in ...... blic differ in their opinions?
@ast
Consent for use of personal in ...... blic differ in their opinions?
@en
prefLabel
Consent for use of personal in ...... blic differ in their opinions?
@ast
Consent for use of personal in ...... blic differ in their opinions?
@en
P2093
P2860
P50
P356
P1433
P1476
Consent for use of personal in ...... blic differ in their opinions?
@en
P2093
Cathy Charles
Donald J Willison
Jennifer Ranford
Valerie Steeves
P2860
P2888
P356
10.1186/1472-6939-10-10
P577
2009-07-24T00:00:00Z
P5875
P6179
1021703139