Beyond trust: Amplifying unheard voices on concerns about harm resulting from health data-sharing

by Stephanie Mulrine, Mwenza Blell, Madeleine Murtagh
Published 2021-10-01

Direct-to-Consumer Genetic Testing's Red Herring: “Genetic Ancestry” and Personalized Medicine

by Mwenza Blell, M. A. Hunter, M. A. Hunter
Published 2019-03-01

What does engagement mean to participants in longitudinal cohort studies? A qualitative study

by Cynthia A. Ochieng, Joel T. Minion, Andrew Turner, Mwenza Blell, Madeleine J. Murtagh
Published 2021-06-01

The ECOUTER methodology for stakeholder engagement in translational research

by Madeleine J. Murtagh, Joel T. Minion, Andrew Turner, Rebecca C. Wilson, Mwenza Blell, Cynthia Ochieng, Barnaby Murtagh, Stephanie Roberts, Oliver W. Butters, Paul R Burton
Published 2017-04-01

Return of individual research results from genomic research: A systematic review of stakeholder perspectives

by Danya F. Vears, Joel T. Minion, Stephanie J. Roberts, James Cummings, Mavis Machirori, Mwenza Blell, Isabelle Budin-Ljøsne, Lorraine Cowley, Stephanie O. M. Dyke, Clara Gaff, Robert Green, Alison Hall, Amber L. Johns, Bartha M. Knoppers, Stephanie Mulrine, Christine Patch, Eva Winkler, Madeleine J. Murtagh
Published 2021-01-01

Return of individual research results from genomic research: A systematic review of stakeholder perspectives.

by Danya F Vears, Joel T Minion, Stephanie J Roberts, James Cummings, Mavis Machirori, Mwenza Blell, Isabelle Budin-Ljøsne, Lorraine Cowley, Stephanie O M Dyke, Clara Gaff, Robert Green, Alison Hall, Amber L Johns, Bartha M Knoppers, Stephanie Mulrine, Christine Patch, Eva Winkler, Madeleine J Murtagh
Published 2021-01-01