A citation-based method for searching scientific literature

Edward S Dove, Yann Joly, Bartha M Knoppers. Genome Biol 2012
Times Cited: 25







List of co-cited articles
144 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
94
24

A review of the key issues associated with the commercialization of biobanks.
Timothy Caulfield, Sarah Burningham, Yann Joly, Zubin Master, Mahsa Shabani, Pascal Borry, Allan Becker, Michael Burgess, Kathryn Calder, Christine Critchley,[...]. J Law Biosci 2014
51
24

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
249
24

DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
70
20

Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
112
20

Public and biobank participant attitudes toward genetic research participation and data sharing.
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
177
20

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
132
20

Research ethics: Treat donors as partners in biobank research.
Krishanu Saha, J Benjamin Hurlbut. Nature 2011
28
16

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
232
16

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
69
16




From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
221
16

A solidarity-based approach to the governance of research biobanks.
Barbara Prainsack, Alena Buyx. Med Law Rev 2013
41
16

Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
137
16


The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
103
16

Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative Study.
Karen Spencer, Caroline Sanders, Edgar A Whitley, David Lund, Jane Kaye, William Gregory Dixon. J Med Internet Res 2016
81
16

Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research.
Hawys Williams, Karen Spencer, Caroline Sanders, David Lund, Edgar A Whitley, Jane Kaye, William G Dixon. JMIR Med Inform 2015
59
16

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V Campbell, Calvin W L Ho, Kazuto Kato, Jusaku Minari, Chih-Hsing Ho, Colin Mitchell,[...]. BMC Med Ethics 2016
61
16

Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
113
16


From patients to partners: participant-centric initiatives in biomedical research.
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
168
12

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
56
12


Consent and research governance in biobanks: evidence from focus groups with medical researchers.
E A Whitley, N Kanellopoulou, J Kaye. Public Health Genomics 2012
28
12

Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and “personalized” medicine?
Wylie Burke, Hilary Burton, Alison E Hall, Mohamed Karmali, Muin J Khoury, Bartha Knoppers, Eric M Meslin, Fiona Stanley, Caroline F Wright, Ronald L Zimmern. Genet Med 2010
61
12

Community engagement in biobanking: Experiences from the eMERGE Network.
Amy A Lemke, Joel T Wu, Carol Waudby, Jill Pulley, Carol P Somkin, Susan Brown Trinidad. Genom Soc Policy 2010
38
12

Connecting the public with biobank research: reciprocity matters.
Herbert Gottweis, George Gaskell, Johannes Starkbaum. Nat Rev Genet 2011
37
12

Public preferences regarding informed consent models for participation in population-based genomic research.
Jodyn Platt, Juli Bollinger, Rachel Dvoskin, Sharon L R Kardia, David Kaufman. Genet Med 2014
58
12

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
493
12

Ethics. Identifiability in genomic research.
William W Lowrance, Francis S Collins. Science 2007
113
12

Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
139
12

Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
60
12

Governing UK Biobank: the importance of ensuring public trust.
Richard Tutton, Jane Kaye, Klaus Hoeyer. Trends Biotechnol 2004
31
12

Informed consent in the genomics era.
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
57
12

Biobanks and the phantom public.
Herbert Gottweis, Haidan Chen, Johannes Starkbaum. Hum Genet 2011
26
12

Towards 'Engagement 2.0': Insights from a study of dynamic consent with biobank participants.
Harriet Ja Teare, Michael Morrison, Edgar A Whitley, Jane Kaye. Digit Health 2015
26
12

Should the 14-day rule for embryo research become the 28-day rule?
John B Appleby, Annelien L Bredenoord. EMBO Mol Med 2018
27
12

Biobank governance in the post-genomic age.
Herbert Gottweis, Georg Lauss. Per Med 2010
20
15

Organoids as hybrids: ethical implications for the exchange of human tissues.
Sarah N Boers, Johannes J M van Delden, Annelien L Bredenoord. J Med Ethics 2019
20
15

Ethical issues in human organoid and gastruloid research.
Megan Munsie, Insoo Hyun, Jeremy Sugarman. Development 2017
41
12

The hope and the hype of organoid research.
Meritxell Huch, Juergen A Knoblich, Matthias P Lutolf, Alfonso Martinez-Arias. Development 2017
180
12

Biobanking: the foundation of personalized medicine.
Robert E Hewitt. Curr Opin Oncol 2011
167
12


Induced pluripotent stem cells in disease modelling and drug discovery.
R Grant Rowe, George Q Daley. Nat Rev Genet 2019
211
12

Human tissues in a dish: The research and ethical implications of organoid technology.
Annelien L Bredenoord, Hans Clevers, Juergen A Knoblich. Science 2017
147
12

Consent for governance in the ethical use of organoids.
Sarah N Boers, Annelien L Bredenoord. Nat Cell Biol 2018
21
14

Every participant is a PI. Citizen science and participatory governance in population studies.
Alena Buyx, Lorenzo Del Savio, Barbara Prainsack, Henry Völzke. Int J Epidemiol 2017
19
15


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.