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Demographic and prosocial intrapersonal characteristics of biobank participants and refusers: the findings of a survey in the Netherlands

Motives of contributing personal data for health research: (non-)participation in a Dutch biobank

Trust in Centralized Large-Scale Data Repository: A Qualitative Analysis

Does the GDPR have trust issues?

An analysis of the concept of solidarity from a Dutch and Japanese perspectives: solidariteit and kizuna

Written informed consent in health research is outdated

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Tracker rage on care sites not over: surfing behaviour still redirected

Donor legislation