A citation-based method for searching scientific literature

Jihoon Kim, Hyeoneui Kim, Elizabeth Bell, Tyler Bath, Paulina Paul, Anh Pham, Xiaoqian Jiang, Kai Zheng, Lucila Ohno-Machado. JAMA Netw Open 2019
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


Clinical Trial Participants' Views of the Risks and Benefits of Data Sharing.
Michelle M Mello, Van Lieou, Steven N Goodman. N Engl J Med 2018
82
14

Comparison of consumers' views on electronic data sharing for healthcare and research.
Katherine K Kim, Jill G Joseph, Lucila Ohno-Machado. J Am Med Inform Assoc 2015
59
14


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
29
14

Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative Study.
Karen Spencer, Caroline Sanders, Edgar A Whitley, David Lund, Jane Kaye, William Gregory Dixon. J Med Internet Res 2016
76
14

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
58
14

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
95
14

Patients, privacy and trust: patients' willingness to allow researchers to access their medical records.
Laura J Damschroder, Joy L Pritts, Michael A Neblo, Rosemarie J Kalarickal, John W Creswell, Rodney A Hayward. Soc Sci Med 2007
104
14


"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research.
Sandra S-J Lee, Mildred K Cho, Stephanie A Kraft, Nina Varsava, Katie Gillespie, Kelly E Ormond, Benjamin S Wilfond, David Magnus. Genet Med 2019
37
10

Research Use of Electronic Health Records: Patients' Views on Alternative Approaches to Permission.
Catherine M Hammack-Aviran, Kathleen M Brelsford, Kevin C McKenna, Ross D Graham, Zachary M Lampron, Laura M Beskow. AJOB Empir Bioeth 2020
5
60

Sharing my health data: a survey of data sharing preferences of healthy individuals.
Elizabeth A Bell, Lucila Ohno-Machado, M Adela Grando. AMIA Annu Symp Proc 2014
24
12

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
37
7


Public preferences about secondary uses of electronic health information.
David Grande, Nandita Mitra, Anand Shah, Fei Wan, David A Asch. JAMA Intern Med 2013
93
7


Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia.
Richard Milne, Katherine I Morley, Heidi Howard, Emilia Niemiec, Dianne Nicol, Christine Critchley, Barbara Prainsack, Danya Vears, James Smith, Claire Steed,[...]. Hum Genet 2019
28
7

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods.
Anna Middleton, Emilia Niemiec, Barbara Prainsack, Jason Bobe, Lauren Farley, Claire Steed, James Smith, Paul Bevan, Natasha Bonhomme, Erika Kleiderman,[...]. Per Med 2018
18
11

Transparency and choice in learning healthcare systems.
Jeffrey R Botkin. Learn Health Syst 2017
6
33

Standard Versus Simplified Consent Materials for Biobank Participation: Differences in Patient Knowledge and Trial Accrual.
Sarah B Garrett, Marie Murphy, James Wiley, Daniel Dohan. J Empir Res Hum Res Ethics 2017
11
18

A systematic literature review of individuals' perspectives on privacy and genetic information in the United States.
Ellen W Clayton, Colin M Halverson, Nila A Sathe, Bradley A Malin. PLoS One 2018
45
7

Patient Preferences for Use of Archived Biospecimens from Oncology Trials When Adequacy of Informed Consent Is Unclear.
Jeffrey Peppercorn, Eric Campbell, Steve Isakoff, Nora K Horick, Julia Rabin, Katharine Quain, Lecia V Sequist, Aditya Bardia, Deborah Collyar, Fay Hlubocky,[...]. Oncologist 2020
4
50

Routes for breaching and protecting genetic privacy.
Yaniv Erlich, Arvind Narayanan. Nat Rev Genet 2014
149
7


Using Electronic Health Records for Population Health Research: A Review of Methods and Applications.
Joan A Casey, Brian S Schwartz, Walter F Stewart, Nancy E Adler. Annu Rev Public Health 2016
205
7

Does an interactive trust-enhanced electronic consent improve patient experiences when asked to share their health records for research? A randomized trial.
Christopher A Harle, Elizabeth H Golembiewski, Kiarash P Rahmanian, Babette Brumback, Janice L Krieger, Kenneth W Goodman, Arch G Mainous, Ray E Moseley. J Am Med Inform Assoc 2019
11
18

Patients' attitudes towards sharing their health information.
Richard Whiddett, Inga Hunter, Judith Engelbrecht, Jocelyn Handy. Int J Med Inform 2006
130
7


Patients' consent preferences for research uses of information in electronic medical records: interview and survey data.
Donald J Willison, Karim Keshavjee, Kalpana Nair, Charlie Goldsmith, Anne M Holbrook. BMJ 2003
87
7

Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?
Donald J Willison, Valerie Steeves, Cathy Charles, Lisa Schwartz, Jennifer Ranford, Gina Agarwal, Ji Cheng, Lehana Thabane. BMC Med Ethics 2009
50
7

Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
Anna Middleton, Richard Milne, Mohamed A Almarri, Shamim Anwer, Jerome Atutornu, Elena E Baranova, Paul Bevan, Maria Cerezo, Yali Cong, Christine Critchley,[...]. Am J Hum Genet 2020
19
10

Sharing data for future research-engaging participants' views about data governance beyond the original project: a DIRECT Study.
Nisha Shah, Victoria Coathup, Harriet Teare, Ian Forgie, Giuseppe Nicola Giordano, Tue Haldor Hansen, Lenka Groeneveld, Michelle Hudson, Ewan Pearson, Hartmut Ruetten,[...]. Genet Med 2019
16
12

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
110
7

Patients' and public views and attitudes towards the sharing of health data for research: a narrative review of the empirical evidence.
Shona Kalkman, Johannes van Delden, Amitava Banerjee, Benoît Tyl, Menno Mostert, Ghislaine van Thiel. J Med Ethics 2022
31
7


Mental health professionals' perceptions on patients control of data sharing.
Julia Ivanova, Adela Grando, Anita Murcko, Michael Saks, Mary Jo Whitfield, Christy Dye, Darwyn Chern. Health Informatics J 2020
4
50


Data Sharing: An Ethical and Scientific Imperative.
Howard Bauchner, Robert M Golub, Phil B Fontanarosa. JAMA 2016
65
3


Public attitudes about health information technology, and its relationship to health care quality, costs, and privacy.
Daniel S Gaylin, Adil Moiduddin, Shamis Mohamoud, Katie Lundeen, Jennifer A Kelly. Health Serv Res 2011
34
3


Humanizing Artificial Intelligence.
Sonoo Thadaney Israni, Abraham Verghese. JAMA 2019
27
3



Implementing Machine Learning in Health Care - Addressing Ethical Challenges.
Danton S Char, Nigam H Shah, David Magnus. N Engl J Med 2018
288
3

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
3

Family perspectives on integrated child health information systems.
Terry Marie Hastings. J Public Health Manag Pract 2004
3
33


The limitations of "vulnerability" as a protection for human research participants.
Carol Levine, Ruth Faden, Christine Grady, Dale Hammerschmidt, Lisa Eckenwiler, Jeremy Sugarman. Am J Bioeth 2004
147
3



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.