A citation-based method for searching scientific literature

Fida K Dankar, Marton Gergely, Samar K Dankar. Comput Struct Biotechnol J 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity



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
81
22

Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials.
Adam Nishimura, Jantey Carey, Patricia J Erwin, Jon C Tilburt, M Hassan Murad, Jennifer B McCormick. BMC Med Ethics 2013
232
22

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
135
22

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
211
22

The patient perspective in health care networks.
Kasper Raus, Eric Mortier, Kristof Eeckloo. BMC Med Ethics 2018
4
25

The Use of Samples Originating From Doping Control Procedures for Research Purposes: A Qualitative Study.
Thijs Devriendt, Amicia Phillips, Mahsa Shabani, Pascal Borry. J Empir Res Hum Res Ethics 2019
1
100

A qualitative study of Institutional Ethics Committees: Members' understanding of research guidelines, privacy, and challenges to privacy protection.
Nagendra N Mishra, Triptish Bhatia, Vishwajit L Nimgaonkar, Smita N Deshpande, Lisa S Parker. Indian J Med Ethics 2018
3
33


Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
32
11

Challenges of web-based personal genomic data sharing.
Mahsa Shabani, Pascal Borry. Life Sci Soc Policy 2015
12
11

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
113
11


Privacy in the Genomic Era.
Muhammad Naveed, Erman Ayday, Ellen W Clayton, Jacques Fellay, Carl A Gunter, Jean-Pierre Hubaux, Bradley A Malin, Xiaofeng Wang. ACM Comput Surv 2015
54
11


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
119
11

Genetics. Genomic research and human subject privacy.
Zhen Lin, Art B Owen, Russ B Altman. Science 2004
179
11

Data privacy in the age of personal genomics.
Dennis Grishin, Kamal Obbad, George M Church. Nat Biotechnol 2019
11
11

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
178
11

A risk-based framework for biomedical data sharing.
Fida K Dankar, Radja Badji. J Biomed Inform 2017
5
20


The cost-effectiveness of returning incidental findings from next-generation genomic sequencing.
Caroline S Bennette, Carlos J Gallego, Wylie Burke, Gail P Jarvik, David L Veenstra. Genet Med 2015
66
11

Biomedical data privacy: problems, perspectives, and recent advances.
Bradley A Malin, Khaled El Emam, Christine M O'Keefe. J Am Med Inform Assoc 2013
49
11

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
27
11

Blockchain technology for improving clinical research quality.
Mehdi Benchoufi, Philippe Ravaud. Trials 2017
39
11



Don't just invite us to the table: authentic community engagement.
Sharon F Terry. Genet Test Mol Biomarkers 2013
8
12


Inclusion of Indigenous Australians in biobanks: a step to reducing inequity in health care.
Imogen Elsum, Callum McEwan, Emma E Kowal, Yvonne Cadet-James, Margaret Kelaher, Lynn Woodward. Med J Aust 2019
2
50

Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach.
Menno Mostert, Annelien L Bredenoord, Monique C I H Biesaart, Johannes J M van Delden. Eur J Hum Genet 2016
35
11


Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
46
11

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
92
11

Sharing health-related data: a privacy test?
Stephanie Om Dyke, Edward S Dove, Bartha M Knoppers. NPJ Genom Med 2016
21
11

The personal genome project.
G M Church. Mol Syst Biol 2005
122
11

An Exploration of Useful Telemedicine-Based Resources for Clinical Research.
Brian E Bunnell, Gina Sprague, Suparna Qanungo, Michelle Nichols, Kathryn Magruder, Steven Lauzon, Jihad S Obeid, Leslie A Lenert, Brandon M Welch. Telemed J E Health 2020
8
12

A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent.
Stephanie A Kraft, Melissa Constantine, David Magnus, Kathryn M Porter, Sandra Soo-Jin Lee, Michael Green, Nancy E Kass, Benjamin S Wilfond, Mildred K Cho. Clin Trials 2017
25
11

Assessing the quality of reports of randomized clinical trials: is blinding necessary?
A R Jadad, R A Moore, D Carroll, C Jenkinson, D J Reynolds, D J Gavaghan, H J McQuay. Control Clin Trials 1996
11

Informed consent: how much and what do patients understand?
Matthew E Falagas, Ioanna P Korbila, Konstantina P Giannopoulou, Barbara K Kondilis, George Peppas. Am J Surg 2009
168
11


Formative Evaluation of Participant Experience With Mobile eConsent in the App-Mediated Parkinson mPower Study: A Mixed Methods Study.
Megan Doerr, Amy Maguire Truong, Brian M Bot, John Wilbanks, Christine Suver, Lara M Mangravite. JMIR Mhealth Uhealth 2017
34
11

Evaluation of a prototype interactive consent program for pediatric clinical trials: a pilot study.
Alan R Tait, Terri Voepel-Lewis, Maureen McGonegal, Robert Levine. J Am Med Inform Assoc 2012
15
11

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
23
11

The Acceptability of Online Consent in a Self-Test Serosurvey of Responders to the 2014-2016 West African Ebola Outbreak.
Catherine R McGowan, Catherine F Houlihan, Patricia Kingori, Judith R Glynn. Public Health Ethics 2017
2
50


Evaluation of a REDCap-based Workflow for Supporting Federal Guidance for Electronic Informed Consent.
Cindy Chen, Scott P Turner, Evan T Sholle, Scott W Brown, Vanessa L I Blau, Julianna P Brouwer, Alicia N Lewis, Curtis L Cole, David M Nanus, Manish A Shah,[...]. AMIA Jt Summits Transl Sci Proc 2019
6
16


A rural community's involvement in the design and usability testing of a computer-based informed consent process for the Personalized Medicine Research Project.
Andrea N Mahnke, Joseph M Plasek, David G Hoffman, Nathan S Partridge, Wendy S Foth, Carol J Waudby, Luke V Rasmussen, Valerie D McManus, Catherine A McCarty. Am J Med Genet A 2014
12
11

A Digital Decision Support Tool to Enhance Decisional Capacity for Clinical Trial Consent: Design and Development.
Robert D Furberg, Alexa M Ortiz, Rebecca R Moultrie, Melissa Raspa, Anne C Wheeler, Lauren A McCormack, Donald B Bailey. JMIR Res Protoc 2018
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.