A citation-based method for searching scientific literature

Thomas Ploug, Søren Holm. Bioethics 2016
Times Cited: 34







List of co-cited articles
79 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
208
38


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
26


In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
39
17

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
17


An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
266
17

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
64
17

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
17

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
17

Informed consent and routinisation.
Thomas Ploug, Soren Holm. J Med Ethics 2013
21
23



Research on medical records without informed consent.
Franklin G Miller. J Law Med Ethics 2008
32
9

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


Factors affecting willingness to share electronic health data among California consumers.
Katherine K Kim, Pamela Sankar, Machelle D Wilson, Sarah C Haynes. BMC Med Ethics 2017
24
12


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
54
8

Facilitating the ethical use of health data for the benefit of society: electronic health records, consent and the duty of easy rescue.
Sebastian Porsdam Mann, Julian Savulescu, Barbara J Sahakian. Philos Trans A Math Phys Eng Sci 2016
26
11

Patient Perspectives on the Learning Health System: The Importance of Trust and Shared Decision Making.
Maureen Kelley, Cyan James, Stephanie Alessi Kraft, Diane Korngiebel, Isabelle Wijangco, Emily Rosenthal, Steven Joffe, Mildred K Cho, Benjamin Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2015
50
8

Alternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?
Donald J Willison, Lisa Schwartz, Julia Abelson, Cathy Charles, Marilyn Swinton, David Northrup, Lehana Thabane. J Am Med Inform Assoc 2007
62
8

Estimating the success of re-identifications in incomplete datasets using generative models.
Luc Rocher, Julien M Hendrickx, Yves-Alexandre de Montjoye. Nat Commun 2019
71
8

Ethics and informed consent for comparative effectiveness research with prospective electronic clinical data.
Ruth Faden, Nancy Kass, Danielle Whicher, Walter Stewart, Sean Tunis. Med Care 2013
47
8

Patients' attitudes towards sharing their health information.
Richard Whiddett, Inga Hunter, Judith Engelbrecht, Jocelyn Handy. Int J Med Inform 2006
121
8

Patient and Physician Views about Protocolized Dialysis Treatment in Randomized Trials and Clinical Care.
Ashley Kraybill, Laura M Dember, Steven Joffe, Jason Karlawish, Susan S Ellenberg, Vanessa Madden, Scott D Halpern. AJOB Empir Bioeth 2016
12
25

Informed consent within a learning health system: A scoping review.
Annabelle Cumyn, Adrien Barton, Roxanne Dault, Anne-Marie Cloutier, Rosalie Jalbert, Jean-François Ethier. Learn Health Syst 2019
7
42

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
5

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

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
11

Written informed consent and selection bias in observational studies using medical records: systematic review.
Michelle E Kho, Mark Duffett, Donald J Willison, Deborah J Cook, Melissa C Brouwers. BMJ 2009
119
5

Does consent bias research?
Mark A Rothstein, Abigail B Shoben. Am J Bioeth 2013
27
7



Impracticability of informed consent in the Registry of the Canadian Stroke Network.
Jack V Tu, Donald J Willison, Frank L Silver, Jiming Fang, Janice A Richards, Andreas Laupacis, Moira K Kapral. N Engl J Med 2004
291
5

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





The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
122
5

Reframing Consent for Clinical Research: A Function-Based Approach.
Neal W Dickert, Nir Eyal, Sara F Goldkind, Christine Grady, Steven Joffe, Bernard Lo, Franklin G Miller, Rebecca D Pentz, Robert Silbergleit, Kevin P Weinfurt,[...]. Am J Bioeth 2017
57
5



Ethical approval for national studies in Ireland: an illustration of current challenges.
M Smith, F Doyle, H M McGee, D De La Harpe. Ir J Med Sci 2004
9
22

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
35
5

Informed Consent.
Christine Grady, Steven R Cummings, Michael C Rowbotham, Michael V McConnell, Euan A Ashley, Gagandeep Kang. N Engl J Med 2017
84
5

Ethical challenges of big data in public health.
Effy Vayena, Marcel Salathé, Lawrence C Madoff, John S Brownstein. PLoS Comput Biol 2015
98
5

Patient and public attitudes towards informed consent models and levels of awareness of Electronic Health Records in the UK.
Fiona Riordan, Chrysanthi Papoutsi, Julie E Reed, Cicely Marston, Derek Bell, Azeem Majeed. Int J Med Inform 2015
43
5


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.