Article metrics
PDF
Other content recommended for you
- Informing research participants of research results: analysis of Canadian university based research ethics board policies
- Returning research results to individuals who are incarcerated in the USA
- Attitudes of African-American parents about biobank participation and return of results for themselves and their children
- Reconsenting paediatric research participants for use of identifying data
- Return of participant-level clinical trial results to participants: pilot of a simplified centralised approach
- Awareness, experiences and perceptions regarding genetic testing and the return of genetic and genomics results in a hypothetical research context among patients in Uganda: a qualitative study
- Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial
- The return of individual research findings in paediatric genetic research
- Sickle Cell Disease Genomics of Africa (SickleGenAfrica) Network: ethical framework and initial qualitative findings from community engagement in Ghana, Nigeria and Tanzania
- Ethics of ‘Counting Me In’: framing the implications of direct-to-patient genomics research