Patients’ experiences and preferences for opt-in models and health professional involvement in biobanking consent: A cross-sectional survey of Australian cancer outpatients-Reference-Cited by-同舟云学术

Patients’ experiences and preferences for opt-in models and health professional involvement in biobanking consent: A cross-sectional survey of Australian cancer outpatients

Published:2018-03-23 Issue:1 Volume:15 Page:31-37
ISSN:1743-7555
Container-title:Asia-Pacific Journal of Clinical Oncology
language:en
Short-container-title:Asia-Pac J Clin Oncol

Author:

Fradgley Elizabeth A.¹²^ORCID,Chong Shu Er³,Cox Martine E.²,Gedye Craig³⁴,Paul Christine L.¹

Affiliation:

1. Priority Research Centre for Cancer Research Innovation and Translation; University of Newcastle; Callaghan NSW Australia

2. Priority Research Centre for Health Behaviour; University of Newcastle; Callaghan NSW Australia

3. School of Biomedical Sciences and Pharmacy; University of Newcastle; Callaghan NSW Australia

4. Calvary Mater Newcastle; Waratah NSW Australia

Funder

National Health and Medical Research Council

Hunter Medical Research Institute

Hunter Cancer Research Alliance

Cancer Institute NSW

University of Newcastle Australia

Publisher

Wiley

Subject

Oncology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ajco.12866/fullpdf

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3. Implementation of electronic consent at a biobank: an opportunity for precision medicine research;Boutin;J Pers Med,2016

4. Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era;Chalmers;BMC Med Ethics,2016

5. National Health and Medical Research Council Biobanks Information Paper 2010

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