A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
42

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
208
39

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
227
35


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
117
32

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
39
32

Broad Consent for Research With Biological Samples: Workshop Conclusions.
Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M Fullerton, Hank Greely, Mats G Hansson, Sara Hull, Scott Kim,[...]. Am J Bioeth 2015
133
25



Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
64
21

Ethical endgames: broad consent for narrow interests; open consent for closed minds.
Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm. Camb Q Healthc Ethics 2011
18
22

Informed consent and routinisation.
Thomas Ploug, Soren Holm. J Med Ethics 2013
21
19


The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
110
14

Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach.
Menno Mostert, Annelien L Bredenoord, Monique C I H Biesaart, Johannes J M van Delden. Eur J Hum Genet 2016
34
14

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
76
14


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
104
10



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
157
10

Research on medical records without informed consent.
Franklin G Miller. J Law Med Ethics 2008
32
10

Routinisation of informed consent in online health care systems.
Thomas Ploug, Søren Holm. Int J Med Inform 2015
8
37

Does consent bias research?
Mark A Rothstein, Abigail B Shoben. Am J Bioeth 2013
27
11

Ethical challenges of big data in public health.
Effy Vayena, Marcel Salathé, Lawrence C Madoff, John S Brownstein. PLoS Comput Biol 2015
98
10


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
50
7



Bringing the Common Rule into the 21st Century.
Kathy L Hudson, Francis S Collins. N Engl J Med 2015
45
7

Readability standards for informed-consent forms as compared with actual readability.
Michael K Paasche-Orlow, Holly A Taylor, Frederick L Brancati. N Engl J Med 2003
380
7

Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
167
7

Harvard Personal Genome Project: lessons from participatory public research.
Madeleine P Ball, Jason R Bobe, Michael F Chou, Tom Clegg, Preston W Estep, Jeantine E Lunshof, Ward Vandewege, Alexander Zaranek, George M Church. Genome Med 2014
47
7


Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
52
7

The emerging need for family-centric initiatives for obtaining consent in personal genome research.
Jusaku Minari, Harriet Teare, Colin Mitchell, Jane Kaye, Kazuto Kato. Genome Med 2014
12
16

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
7

National survey of British public's views on use of identifiable medical data by the National Cancer Registry.
Geraldine Barrett, Jackie A Cassell, Janet L Peacock, Michel P Coleman. BMJ 2006
80
7

Extracting information from hospital records: what patients think about consent.
Bruce Campbell, Helen Thomson, Jessica Slater, Colin Coward, Katrina Wyatt, Kieran Sweeney. Qual Saf Health Care 2007
20
10




Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper.
Charles Safran, Meryl Bloomrosen, W Edward Hammond, Steven Labkoff, Suzanne Markel-Fox, Paul C Tang, Don E Detmer, Expert Panel. J Am Med Inform Assoc 2007
296
7

The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
122
7


Medicine. Big data meets public health.
Muin J Khoury, John P A Ioannidis. Science 2014
139
7

Big data. The parable of Google Flu: traps in big data analysis.
David Lazer, Ryan Kennedy, Gary King, Alessandro Vespignani. Science 2014
530
7

Finding the missing link for big biomedical data.
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
164
7


The inevitable application of big data to health care.
Travis B Murdoch, Allan S Detsky. JAMA 2013
523
7


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.