Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 48
Times Cited: 48
Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M Fullerton, Hank Greely, Mats G Hansson, Sara Hull, Scott Kim, Bernie Lo, Rebecca Pentz, Laura Rodriguez, Carol Weil, Benjamin S Wilfond, David Wendler. Am J Bioeth 2015
Times Cited: 122
Times Cited: 122
List of shared articles
Times cited
An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots.
Erin Rothwell, Aaron Goldenberg, Erin Johnson, Naomi Riches, Beth Tarini, Jeffrey R Botkin. J Empir Res Hum Res Ethics 2017
Erin Rothwell, Aaron Goldenberg, Erin Johnson, Naomi Riches, Beth Tarini, Jeffrey R Botkin. J Empir Res Hum Res Ethics 2017
Informed Consent in the Newly Established Biobank.
Judita Kinkorová, Ondřej Topolčan, Radek Kučera. Int J Environ Res Public Health 2019
Judita Kinkorová, Ondřej Topolčan, Radek Kučera. Int J Environ Res Public Health 2019
Is it ethical to prevent secondary use of stored biological samples and data derived from consenting research participants? The case of Malawi.
Randy G Mungwira, Wongani Nyangulu, James Misiri, Steven Iphani, Ruby Ng'ong'ola, Chawanangwa M Chirambo, Francis Masiye, Joseph Mfutso-Bengo. BMC Med Ethics 2015
Randy G Mungwira, Wongani Nyangulu, James Misiri, Steven Iphani, Ruby Ng'ong'ola, Chawanangwa M Chirambo, Francis Masiye, Joseph Mfutso-Bengo. BMC Med Ethics 2015
"Still Rather Hazy at Present": Citizens' and Physicians' Views on Returning Results from Biobank Research Using Broad Consent.
Gaia Barazzetti, Samuele Cavalli, Lazare Benaroyo, Alain Kaufmann. Genet Test Mol Biomarkers 2017
Gaia Barazzetti, Samuele Cavalli, Lazare Benaroyo, Alain Kaufmann. Genet Test Mol Biomarkers 2017
Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
From "Informed" to "Engaged" Consent: Risks and Obligations in Consent for Participation in a Health Data Repository.
Elizabeth Bromley, Alexandra Mendoza-Graf, Sandra Berry, Camille Nebeker, Dmitry Khodyakov. J Law Med Ethics 2020
Elizabeth Bromley, Alexandra Mendoza-Graf, Sandra Berry, Camille Nebeker, Dmitry Khodyakov. J Law Med Ethics 2020
Regulating the Secondary Use of Data for Research: Arguments Against Genetic Exceptionalism.
Andrea Martani, Lester Darryl Geneviève, Christiane Pauli-Magnus, Stuart McLennan, Bernice Simone Elger. Front Genet 2019
Andrea Martani, Lester Darryl Geneviève, Christiane Pauli-Magnus, Stuart McLennan, Bernice Simone Elger. Front Genet 2019
Reflections on dynamic consent in biomedical research: the story so far.
Harriet J A Teare, Megan Prictor, Jane Kaye. Eur J Hum Genet 2020
Harriet J A Teare, Megan Prictor, Jane Kaye. Eur J Hum Genet 2020
Biomedical Big Data: New Models of Control Over Access, Use and Governance.
Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017