A citation-based method for searching scientific literature

Mark Sheehan. Public Health Ethics 2011
Times Cited: 64



Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
Times Cited: 132




List of shared articles



Times cited

Citizens' views on sharing their health data: the role of competence, reliability and pursuing the common good.
Minerva C Rivas Velarde, Petros Tsantoulis, Claudine Burton-Jeangros, Monica Aceti, Pierre Chappuis, Samia Hurst-Majno. BMC Med Ethics 2021
0

Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature.
Alma Husedzinovic, Dominik Ose, Christoph Schickhardt, Stefan Fröhling, Eva C Winkler. Eur J Hum Genet 2015
28

Participant views on consent in cancer genetics research: preparing for the precision medicine era.
Karen L Edwards, Diane M Korngiebel, Lesley Pfeifer, Deborah Goodman, Anne Renz, Lari Wenzel, Deborah J Bowen, Celeste M Condit. J Community Genet 2016
8

Broad consent in practice: lessons learned from a hospital-based biobank for prospective research on genomic and medical data.
Gaia Barazzetti, Francesca Bosisio, Daria Koutaissoff, Brenda Spencer. Eur J Hum Genet 2020
3

Participant-Centric Initiatives: Tools to Facilitate Engagement In Research.
Nicholas Anderson, Caleb Bragg, Andrea Hartzler, Kelly Edwards. Appl Transl Genom 2012
21

Extending the surrogacy analogy: applying the advance directive model to biobanks.
Stephanie Solomon, Ann Mongoven. Public Health Genomics 2015
2

Attitudes of Costa Rican individuals towards donation of personal genetic data for research.
Gabriela Chavarria-Soley, Fernanda Francis-Cartin, Fabiola Jimenez-Gonzalez, Alejandro Ávila-Aguirre, Maria Jose Castro-Gomez, Lauren Robarts, Anna Middleton, Henriette Raventós. Per Med 2021
0