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

Focus Groups and Qualitative Research for Human Factors Research (772) Ethics, Privacy, and Legal Issues (457) Electronic/Mobile Data Capture, Internet-based Survey & Research Methodology (788) Secondary Use of Clinical Data for Research and Surveillance (320) Big Data (219) Policy (51) Health Information Exchange (78)

Published on in Vol 9, No 3 (2022): Jul-Sep

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/36797, first published .
Patients’ and Publics’ Preferences for Data-Intensive Health Research Governance: Survey Study

Patients’ and Publics’ Preferences for Data-Intensive Health Research Governance: Survey Study

Patients’ and Publics’ Preferences for Data-Intensive Health Research Governance: Survey Study

Authors of this article:

Sam H A Muller1 Author Orcid Image ;   Ghislaine J M W van Thiel1 Author Orcid Image ;   Marilena Vrana2 Author Orcid Image ;   Menno Mostert1 Author Orcid Image ;   Johannes J M van Delden1 Author Orcid Image
Article Authors Cited by (6) Tweetations (11) Metrics

Sam H A Muller   1 , MSc ;   Ghislaine J M W van Thiel   1 , MSc, PhD ;   Marilena Vrana   2 , MA ;   Menno Mostert   1 , LLM, PhD ;   Johannes J M van Delden   1 , MD, PhD

1 Department of Medical Humanities, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands

2 European Heart Network, Brussels, Belgium

Corresponding Author:

  • Sam H A Muller, MSc
  • Department of Medical Humanities
  • Julius Center for Health Sciences and Primary Care
  • University Medical Center Utrecht, Utrecht University
  • Universiteitsweg 100
  • Utrecht, 3584 CX
  • Netherlands
  • Phone: 31 623034456
  • Email: s.h.a.muller-4@umcutrecht.nl