A citation-based method for searching scientific literature

Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
Times Cited: 124







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



Times Cited
  Times     Co-cited
Similarity


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
91
25


Moving from trust to trustworthiness: Experiences of public engagement in the Scottish Health Informatics Programme.
Mhairi Aitken, Sarah Cunningham-Burley, Claudia Pagliari. Sci Public Policy 2016
30
33

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
213
9





Big health data: the need to earn public trust.
Tjeerd-Pieter van Staa, Ben Goldacre, Iain Buchan, Liam Smeeth. BMJ 2016
35
22

A case study of the Secure Anonymous Information Linkage (SAIL) Gateway: a privacy-protecting remote access system for health-related research and evaluation.
Kerina H Jones, David V Ford, Chris Jones, Rohan Dsilva, Simon Thompson, Caroline J Brooks, Martin L Heaven, Daniel S Thayer, Cynthia L McNerney, Ronan A Lyons. J Biomed Inform 2014
80
8

The other side of the coin: Harm due to the non-use of health-related data.
Kerina H Jones, Graeme Laurie, Leslie Stevens, Christine Dobbs, David V Ford, Nathan Lea. Int J Med Inform 2017
36
19

Consensus Statement on Public Involvement and Engagement with Data Intensive Health Research.
Mhairi Aitken, Mary P Tully, Carol Porteous, Simon Denegri, Sarah Cunningham-Burley, Natalie Banner, Corri Black, Michael Burgess, Lynsey Cross, Johannes Jm van Delden,[...]. Int J Popul Data Sci 2019
17
41

On moving targets and magic bullets: Can the UK lead the way with responsible data linkage for health research?
G Laurie, J Ainsworth, J Cunningham, C Dobbs, K H Jones, D Kalra, N C Lea, N Sethi. Int J Med Inform 2015
12
50

Big data analytics in healthcare: promise and potential.
Wullianallur Raghupathi, Viju Raghupathi. Health Inf Sci Syst 2014
474
6


Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
132
6

The care.data consensus? A qualitative analysis of opinions expressed on Twitter.
Rebecca Hays, Gavin Daker-White. BMC Public Health 2015
19
31

Our data, our society, our health: A vision for inclusive and transparent health data science in the United Kingdom and beyond.
Elizabeth Ford, Andy Boyd, Juliana K F Bowles, Alys Havard, Robert W Aldridge, Vasa Curcin, Michelle Greiver, Katie Harron, Vittal Katikireddi, Sarah E Rodgers,[...]. Learn Health Syst 2019
18
33

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 2019
20
30

Data Safe Havens and Trust: Toward a Common Understanding of Trusted Research Platforms for Governing Secure and Ethical Health Research.
Nathan Christopher Lea, Jacqueline Nicholls, Christine Dobbs, Nayha Sethi, James Cunningham, John Ainsworth, Martin Heaven, Trevor Peacock, Anthony Peacock, Kerina Jones,[...]. JMIR Med Inform 2016
18
27

From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
89
5

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
115
5

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
55
9

Regulation and the social licence for medical research.
Mary Dixon-Woods, Richard E Ashcroft. Med Health Care Philos 2008
30
16

Data Resource Profile: Clinical Practice Research Datalink (CPRD).
Emily Herrett, Arlene M Gallagher, Krishnan Bhaskaran, Harriet Forbes, Rohini Mathur, Tjeerd van Staa, Liam Smeeth. Int J Epidemiol 2015
5


National electronic health records and the digital disruption of moral orders.
Karin Garrety, Ian McLoughlin, Rob Wilson, Gregor Zelle, Mike Martin. Soc Sci Med 2014
14
35

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
121
5

The SAIL databank: linking multiple health and social care datasets.
Ronan A Lyons, Kerina H Jones, Gareth John, Caroline J Brooks, Jean-Philippe Verplancke, David V Ford, Ginevra Brown, Ken Leake. BMC Med Inform Decis Mak 2009
254
5

The SAIL Databank: building a national architecture for e-health research and evaluation.
David V Ford, Kerina H Jones, Jean-Philippe Verplancke, Ronan A Lyons, Gareth John, Ginevra Brown, Caroline J Brooks, Simon Thompson, Owen Bodger, Tony Couch,[...]. BMC Health Serv Res 2009
234
5

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
62
8

Investigating the Extent to Which Patients Should Control Access to Patient Records for Research: A Deliberative Process Using Citizens' Juries.
Mary P Tully, Kyle Bozentko, Sarah Clement, Amanda Hunn, Lamiece Hassan, Ruth Norris, Malcolm Oswald, Niels Peek. J Med Internet Res 2018
19
26


Finding the missing link for big biomedical data.
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
167
4

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
4

Views on health information sharing and privacy from primary care practices using electronic medical records.
Gihan Perera, Anne Holbrook, Lehana Thabane, Gary Foster, Donald J Willison. Int J Med Inform 2011
71
5

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
120
4


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

The inevitable application of big data to health care.
Travis B Murdoch, Allan S Detsky. JAMA 2013
534
4

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
138
4

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
36
11

The FAIR Guiding Principles for scientific data management and stewardship.
Mark D Wilkinson, Michel Dumontier, I Jsbrand Jan Aalbersberg, Gabrielle Appleton, Myles Axton, Arie Baak, Niklas Blomberg, Jan-Willem Boiten, Luiz Bonino da Silva Santos, Philip E Bourne,[...]. Sci Data 2016
4

Google DeepMind and healthcare in an age of algorithms.
Julia Powles, Hal Hodson. Health Technol (Berl) 2017
74
5


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
52
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
89
4

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
97
4

The role of administrative data in the big data revolution in social science research.
Roxanne Connelly, Christopher J Playford, Vernon Gayle, Chris Dibben. Soc Sci Res 2016
42
9

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
55
7


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.