A citation-based method for searching scientific literature

Mark Sheehan. Public Health Ethics 2011
Times Cited: 64



Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
Times Cited: 229




List of shared articles



Times cited

Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
120



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

Participatory Disease Surveillance Systems: Ethical Framework.
Lester Darryl Geneviève, Andrea Martani, Tenzin Wangmo, Daniela Paolotti, Carl Koppeschaar, Charlotte Kjelsø, Caroline Guerrisi, Marco Hirsch, Olivia Woolley-Meza, Paul Lukowicz,[...]. J Med Internet Res 2019
7

Sampling populations of humans across the world: ELSI issues.
Bartha Maria Knoppers, Ma'n H Zawati, Emily S Kirby. Annu Rev Genomics Hum Genet 2012
36


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

International Charter of principles for sharing bio-specimens and data.
Deborah Mascalzoni, Edward S Dove, Yaffa Rubinstein, Hugh J S Dawkins, Anna Kole, Pauline McCormack, Simon Woods, Olaf Riess, Franz Schaefer, Hanns Lochmüller,[...]. Eur J Hum Genet 2015
73


Sample and data sharing barriers in biobanking: consent, committees, and compromises.
Flora Colledge, Kirsten Persson, Bernice Elger, David Shaw. Ann Diagn Pathol 2014
13


Biomedical Big Data: New Models of Control Over Access, Use and Governance.
Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
31




Improving the informed consent process in international collaborative rare disease research: effective consent for effective research.
Sabina Gainotti, Cathy Turner, Simon Woods, Anna Kole, Pauline McCormack, Hanns Lochmüller, Olaf Riess, Volker Straub, Manuel Posada, Domenica Taruscio,[...]. Eur J Hum Genet 2016
25


Editorial - ethical practice and genomic research.
Janet Seeley, Michael Parker. Glob Bioeth 2020
0

Can dynamic consent facilitate the protection of biomedical big data in biobanking in Malaysia?
Mohammad Firdaus Abdul Aziz, Aimi Nadia Mohd Yusof. Asian Bioeth Rev 2019
2

Evaluating the consent preferences of UK research volunteers for genetic and clinical studies.
Susan E Kelly, Timothy D Spector, Lynn F Cherkas, Barbara Prainsack, Juliette M Harris. PLoS One 2015
25