A citation-based method for searching scientific literature

Neil C Manson. J Med Ethics 2019
Times Cited: 11







List of co-cited articles
17 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
221
36

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
96
27

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
66
27

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
41
18

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
230
18

Trust Me, I'm a Doctor: Examining Changes in How Privacy Concerns Affect Patient Withholding Behavior.
Daniel M Walker, Tyler Johnson, Eric W Ford, Timothy R Huerta. J Med Internet Res 2017
18
18


Public attitudes toward health information exchange: perceived benefits and concerns.
Linda Dimitropoulos, Vaishali Patel, Scott A Scheffler, Steve Posnack. Am J Manag Care 2011
53
18

Patient perspectives of medical confidentiality: a review of the literature.
Pamela Sankar, Susan Mora, Jon F Merz, Nora L Jones. J Gen Intern Med 2003
48
18

Understanding the patient privacy perspective on health information exchange: A systematic review.
Nelson Shen, Thérèse Bernier, Lydia Sequeira, John Strauss, Michelle Pannor Silver, Abigail Carter-Langford, David Wiljer. Int J Med Inform 2019
19
18

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
122
18

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
27
18

Authority and the Future of Consent in Population-Level Biomedical Research.
Mark Sheehan, Rachel Thompson, Jon Fistein, Jim Davies, Michael Dunn, Michael Parker, Julian Savulescu, Kerrie Woods. Public Health Ethics 2019
8
25


We don't need unilateral DNRs: taking informed non-dissent one step further.
Diego Real de Asúa, Katarina Lee, Peter Koch, Inmaculada de Melo-Martín, Trevor Bibler. J Med Ethics 2019
2
50

Informed consent for functional MRI research on comatose patients following severe brain injury: balancing the social benefits of research against patient autonomy.
Tommaso Bruni, Mackenzie Graham, Loretta Norton, Teneille Gofton, Adrian M Owen, Charles Weijer. J Med Ethics 2019
4
25

Obesity, equity and choice.
Timothy M Wilkinson. J Med Ethics 2019
4
25

Equity and preventive regulations.
Elizabeth Fenton. J Med Ethics 2019
1
100


Public preferences about secondary uses of electronic health information.
David Grande, Nandita Mitra, Anand Shah, Fei Wan, David A Asch. JAMA Intern Med 2013
89
9

Adoption, non-adoption, and abandonment of a personal electronic health record: case study of HealthSpace.
Trisha Greenhalgh, Susan Hinder, Katja Stramer, Tanja Bratan, Jill Russell. BMJ 2010
163
9


Purposeful Sampling for Qualitative Data Collection and Analysis in Mixed Method Implementation Research.
Lawrence A Palinkas, Sarah M Horwitz, Carla A Green, Jennifer P Wisdom, Naihua Duan, Kimberly Hoagwood. Adm Policy Ment Health 2015
9


Legal Barriers to the Growth of Health Information Exchange-Boulders or Pebbles?
Michelle M Mello, Julia Adler-Milstein, Karen L Ding, Lucia Savage. Milbank Q 2018
26
9


The Impact of Mental Illness Stigma on Seeking and Participating in Mental Health Care.
Patrick W Corrigan, Benjamin G Druss, Deborah A Perlick. Psychol Sci Public Interest 2014
380
9


A piece of my mind. Let's show patients their mental health records.
Michael W Kahn, Sigall K Bell, Jan Walker, Tom Delbanco. JAMA 2014
40
9


Measuring interoperable EHR adoption and maturity: a Canadian example.
Bobby Gheorghiu, Simon Hagens. BMC Med Inform Decis Mak 2016
17
9

Behavioral Health Information Technology: From Chaos To Clarity.
Piper A Ranallo, Amy M Kilbourne, Angela S Whatley, Harold Alan Pincus. Health Aff (Millwood) 2016
18
9

A Web-Based Patient Portal for Mental Health Care: Benefits Evaluation.
Sarah Kipping, Melanie I Stuckey, Alexandra Hernandez, Tan Nguyen, Sanaz Riahi. J Med Internet Res 2016
44
9


What is an adequate sample size? Operationalising data saturation for theory-based interview studies.
Jill J Francis, Marie Johnston, Clare Robertson, Liz Glidewell, Vikki Entwistle, Martin P Eccles, Jeremy M Grimshaw. Psychol Health 2010
741
9

Qualitative evaluation of health information exchange efforts.
Joan S Ash, Kenneth P Guappone. J Biomed Inform 2007
27
9

The HITECH Era and the Path Forward.
Vindell Washington, Karen DeSalvo, Farzad Mostashari, David Blumenthal. N Engl J Med 2017
44
9



The value of connected health information: perceptions of electronic health record users in Canada.
Sukirtha Tharmalingam, Simon Hagens, Jennifer Zelmer. BMC Med Inform Decis Mak 2016
19
9



Perceptions of predisposing, enabling, and reinforcing factors influencing the use of a continuity of care document in special needs PLWH.
Michelle Odlum, Peter Gordon, Eli Camhi, Rebecca Schnall, Paul Teixeira, Suzanne Bakken. J Health Care Poor Underserved 2012
7
14





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.