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

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

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

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

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

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

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

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

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

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

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

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

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