A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity




Google Search as an Additional Source in Systematic Reviews.
Jan Piasecki, Marcin Waligora, Vilius Dranseika. Sci Eng Ethics 2018
16
100

Public attitudes regarding the use of electronic health information and residual clinical tissues for research.
Jeffrey R Botkin, Erin Rothwell, Rebecca Anderson, Louisa A Stark, Joyce Mitchell. J Community Genet 2014
21
100

The Academic Viewpoint on Patient Data Ownership in the Context of Big Data: Scoping Review.
Martin Mirchev, Iskra Mircheva, Albena Kerekovska. J Med Internet Res 2020
2
100

Assessing and Minimizing Re-identification Risk in Research Data Derived from Health Care Records.
Gregory E Simon, Susan M Shortreed, R Yates Coley, Robert B Penfold, Rebecca C Rossom, Beth E Waitzfelder, Katherine Sanchez, Frances L Lynch. EGEMS (Wash DC) 2019
7
100

Willingness to share personal health record data for care improvement and public health: a survey of experienced personal health record users.
Elissa R Weitzman, Skyler Kelemen, Liljana Kaci, Kenneth D Mandl. BMC Med Inform Decis Mak 2012
42
100

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
45
100

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
281
100

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
59
100

The importance of purpose: moving beyond consent in the societal use of personal health information.
David Grande, Nandita Mitra, Anand Shah, Fei Wan, David A Asch. Ann Intern Med 2014
21
100



Sharing medical data for health research: the early personal health record experience.
Elissa R Weitzman, Liljana Kaci, Kenneth D Mandl. J Med Internet Res 2010
54
100


Emerging ethical issues regarding digital health data. On the World Medical Association Draft Declaration on Ethical Considerations Regarding Health Databases and Biobanks.
Christine Aicardi, Lorenzo Del Savio, Edward S Dove, Federica Lucivero, Niccolo Tempini, Barbara Prainsack. Croat Med J 2016
10
100


The Role of Google Scholar in Evidence Reviews and Its Applicability to Grey Literature Searching.
Neal Robert Haddaway, Alexandra Mary Collins, Deborah Coughlin, Stuart Kirk. PLoS One 2015
254
100

Unpatients-why patients should own their medical data.
Leonard J Kish, Eric J Topol. Nat Biotechnol 2015
33
100


A solidarity-based approach to the governance of research biobanks.
Barbara Prainsack, Alena Buyx. Med Law Rev 2013
40
100

Anonymising and sharing individual patient data.
Khaled El Emam, Sam Rodgers, Bradley Malin. BMJ 2015
69
100



Alternatives to project-specific consent for access to personal information for health research: insights from a public dialogue.
Donald J Willison, Marilyn Swinton, Lisa Schwartz, Julia Abelson, Cathy Charles, David Northrup, Ji Cheng, Lehana Thabane. BMC Med Ethics 2008
33
100

An ethics framework for public health.
N E Kass. Am J Public Health 2001
387
100

Trustworthy reuse of health data: a transnational perspective.
A Geissbuhler, C Safran, I Buchan, R Bellazzi, S Labkoff, K Eilenberg, A Leese, C Richardson, J Mantas, P Murray,[...]. Int J Med Inform 2013
37
100

Patient Perspectives on the Ethical Implementation of a Rapid Learning System for Oncology Care.
Rochelle D Jones, Aaron N Sabolch, Erin Aakhus, Rebecca A Spence, Angela R Bradbury, Reshma Jagsi. J Oncol Pract 2017
15
100

Justice, health, and healthcare.
N Daniels. Am J Bioeth 2001
122
100

Ownership of medical information.
Mark A Hall, Kevin A Schulman. JAMA 2009
23
100

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
23
100

The spectrum of ethical issues in a Learning Health Care System: a systematic qualitative review.
Stuart McLennan, Hannes Kahrass, Susanne Wieschowski, Daniel Strech, Holger Langhof. Int J Qual Health Care 2018
14
100

The full spectrum of ethical issues in dementia care: systematic qualitative review.
Daniel Strech, Marcel Mertz, Hannes Knüppel, Gerald Neitzke, Martina Schmidhuber. Br J Psychiatry 2013
36
100

Ethical issues in public health surveillance: a systematic qualitative review.
Corinna Klingler, Diego Steven Silva, Christopher Schuermann, Andreas Alois Reis, Abha Saxena, Daniel Strech. BMC Public Health 2017
25
100

Public responses to the sharing and linkage of health data for research purposes: a systematic review and thematic synthesis of qualitative studies.
Mhairi Aitken, Jenna de St Jorre, Claudia Pagliari, Ruth Jepson, Sarah Cunningham-Burley. BMC Med Ethics 2016
97
100

The Effect of the General Data Protection Regulation on Medical Research.
John Mark Michael Rumbold, Barbara Pierscionek. J Med Internet Res 2017
44
100



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
48
100

Use of electronic patient records for research: views of patients and staff in general practice.
Fiona Stevenson, Nigel Lloyd, Louise Harrington, Paul Wallace. Fam Pract 2013
23
100


Patients' consent preferences regarding the use of their health information for research purposes: a qualitative study.
Kalpana Nair, Donald Willison, Anne Holbrook, Karim Keshavjee. J Health Serv Res Policy 2004
30
100

Data Sharing and Embedded Research.
Gregory E Simon, Gloria Coronado, Lynn L DeBar, Laura M Dember, Beverly B Green, Susan S Huang, Jeffrey G Jarvik, Vincent Mor, Joakim Ramsberg, Edward J Septimus,[...]. Ann Intern Med 2017
14
100

A systematic review of re-identification attacks on health data.
Khaled El Emam, Elizabeth Jonker, Luk Arbuckle, Bradley Malin. PLoS One 2011
109
100


Learning to Regulate Learning Healthcare Systems.
Jan Piasecki, Vilius Dranseika. Camb Q Healthc Ethics 2019
3
100

HIPAA and Protecting Health Information in the 21st Century.
I Glenn Cohen, Michelle M Mello. JAMA 2018
38
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
100


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.