A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity



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
238
54


Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
97
45

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
45

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
128
36

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
42
36


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
150
27


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
165
18

Research on medical records without informed consent.
Franklin G Miller. J Law Med Ethics 2008
33
18

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
18

Routinisation of informed consent in online health care systems.
Thomas Ploug, Søren Holm. Int J Med Inform 2015
8
25


Informed consent and routinisation.
Thomas Ploug, Soren Holm. J Med Ethics 2013
22
18


Does consent bias research?
Mark A Rothstein, Abigail B Shoben. Am J Bioeth 2013
28
18

Implementation of Electronic Consent at a Biobank: An Opportunity for Precision Medicine Research.
Natalie T Boutin, Kathleen Mathieu, Alison G Hoffnagle, Nicole L Allen, Victor M Castro, Megan Morash, P Pearl O'Rourke, Elizabeth L Hohmann, Neil Herring, Lynn Bry,[...]. J Pers Med 2016
34
18

Testing an online, dynamic consent portal for large population biobank research.
Daniel B Thiel, Jodyn Platt, Tevah Platt, Susan B King, Nicole Fisher, Robert Shelton, Sharon L R Kardia. Public Health Genomics 2015
29
18


Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. AJOB Prim Res 2012
36
18

Hypothetical and factual willingness to participate in biobank research.
Linus Johnsson, Gert Helgesson, Thorunn Rafnar, Ingibjorg Halldorsdottir, Kee-Seng Chia, Stefan Eriksson, Mats G Hansson. Eur J Hum Genet 2010
59
18


The stigmatization dilemma in public health policy--the case of MRSA in Denmark.
Thomas Ploug, Søren Holm, Mickey Gjerris. BMC Public Health 2015
10
20


Biobanking past, present and future: responsibilities and benefits.
Yvonne G De Souza, John S Greenspan. AIDS 2013
121
18

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
66
18

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
81
9


Bringing the Common Rule into the 21st Century.
Kathy L Hudson, Francis S Collins. N Engl J Med 2015
46
9

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
9



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
320
9



Saudi views on consenting for research on medical records and leftover tissue samples.
Mohammad M Al-Qadire, Muhammad M Hammami, Hunida M Abdulhameed, Eman A Al Gaai. BMC Med Ethics 2010
14
9


Genome sequencing in research requires a new approach to consent.
Isabelle Budin-Ljøsne, Heidi Beate Bentzen, Jan Helge Solbakk, Ola Myklebost. Tidsskr Nor Laegeforen 2015
2
50

Informed consent in the genomics era.
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
56
9

A dynamic model of patient consent to sharing of medical record data.
William G Dixon, Karen Spencer, Hawys Williams, Caroline Sanders, David Lund, Edgar A Whitley, Jane Kaye. BMJ 2014
10
10


Pediatric data sharing in genomic research: attitudes and preferences of parents.
Matthew D Burstein, Jill Oliver Robinson, Susan G Hilsenbeck, Amy L McGuire, Ching C Lau. Pediatrics 2014
22
9

Power to the people: a wiki-governance model for biobanks.
Edward S Dove, Yann Joly, Bartha M Knoppers. Genome Biol 2012
24
9

Glad you asked: participants' opinions of re-consent for dbGap data submission.
Evette J Ludman, Stephanie M Fullerton, Leslie Spangler, Susan Brown Trinidad, Monica M Fujii, Gail P Jarvik, Eric B Larson, Wylie Burke. J Empir Res Hum Res Ethics 2010
85
9

Development and pilot testing of a video-assisted informed consent process.
Susan C Sonne, Jeannette O Andrews, Stephanie M Gentilin, Stephanie Oppenheimer, Jihad Obeid, Kathleen Brady, Sharon Wolf, Randal Davis, Kathryn Magruder. Contemp Clin Trials 2013
31
9

Genotype-driven recruitment: a strategy whose time has come?
Isabelle Budin-Ljøsne, Kaitlin J Soye, Anne Marie Tassé, Bartha Maria Knoppers, Jennifer R Harris. BMC Med Genomics 2013
11
9

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
25
9

Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
Laura M Beskow, Carrie B Dombeck, Cole P Thompson, J Kemp Watson-Ormond, Kevin P Weinfurt. Genet Med 2015
42
9


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.