A citation-based method for searching scientific literature

Irene Jao, Francis Kombe, Salim Mwalukore, Susan Bull, Michael Parker, Dorcas Kamuya, Sassy Molyneux, Vicki Marsh. J Empir Res Hum Res Ethics 2015
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


Developing Ethical Practices for Public Health Research Data Sharing in South Africa: The Views and Experiences From a Diverse Sample of Research Stakeholders.
Spencer G Denny, Blessing Silaigwana, Douglas Wassenaar, Susan Bull, Michael Parker. J Empir Res Hum Res Ethics 2015
24
45

Perceived Benefits, Harms, and Views About How to Share Data Responsibly: A Qualitative Study of Experiences With and Attitudes Toward Data Sharing Among Research Staff and Community Representatives in Thailand.
Phaik Yeong Cheah, Decha Tangseefa, Aimatcha Somsaman, Tri Chunsuttiwat, François Nosten, Nicholas P J Day, Susan Bull, Michael Parker. J Empir Res Hum Res Ethics 2015
21
52

Sweat, Skepticism, and Uncharted Territory: A Qualitative Study of Opinions on Data Sharing Among Public Health Researchers and Research Participants in Mumbai, India.
Ketaki Hate, Sanna Meherally, Neena Shah More, Anuja Jayaraman, Susan Bull, Michael Parker, David Osrin. J Empir Res Hum Res Ethics 2015
17
64

Trust, Respect, and Reciprocity: Informing Culturally Appropriate Data-Sharing Practice in Vietnam.
Laura Merson, Tran Viet Phong, Le Nguyen Thanh Nhan, Nguyen Thanh Dung, Ta Thi Dieu Ngan, Nguyen Van Kinh, Michael Parker, Susan Bull. J Empir Res Hum Res Ethics 2015
18
55

Best Practices for Ethical Sharing of Individual-Level Health Research Data From Low- and Middle-Income Settings.
Susan Bull, Phaik Yeong Cheah, Spencer Denny, Irene Jao, Vicki Marsh, Laura Merson, Neena Shah More, Le Nguyen Thanh Nhan, David Osrin, Decha Tangseefa,[...]. J Empir Res Hum Res Ethics 2015
32
33


Sharing research data to improve public health.
Mark Walport, Paul Brest. Lancet 2011
122
33

Ethical data release in genome-wide association studies in developing countries.
Michael Parker, Susan J Bull, Jantina de Vries, Tsiri Agbenyega, Ogobara K Doumbo, Dominic P Kwiatkowski. PLoS Med 2009
45
29

Sharing health data: good intentions are not enough.
Elizabeth Pisani, Carla AbouZahr. Bull World Health Organ 2010
62
29



Ethical issues in human genomics research in developing countries.
Jantina de Vries, Susan J Bull, Ogobara Doumbo, Muntaser Ibrahim, Odile Mercereau-Puijalon, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2011
80
29

Data sharing: not as simple as it seems.
Neil Pearce, Allan H Smith. Environ Health 2011
29
25

Time for fair trade in research data.
Elizabeth Pisani, James Whitworth, Basia Zaba, Carla Abou-Zahr. Lancet 2010
22
27

Sharing health data: developing country perspectives.
Viroj Tangcharoensathien, Jirawan Boonperm, Pongpisut Jongudomsuk. Bull World Health Organ 2010
16
37

Preparing for responsible sharing of clinical trial data.
Michelle M Mello, Jeffrey K Francer, Marc Wilenzick, Patricia Teden, Barbara E Bierer, Mark Barnes. N Engl J Med 2013
94
25

Prepublication data sharing.
Ewan Birney, Thomas J Hudson, Eric D Green, Chris Gunter, Sean Eddy, Jane Rogers, Jennifer R Harris, S Dusko Ehrlich, Rolf Apweiler, Christopher P Austin,[...]. Nature 2009
154
25




Research Stakeholders' Views on Benefits and Challenges for Public Health Research Data Sharing in Kenya: The Importance of Trust and Social Relations.
Irene Jao, Francis Kombe, Salim Mwalukore, Susan Bull, Michael Parker, Dorcas Kamuya, Sassy Molyneux, Vicki Marsh. PLoS One 2015
13
46

Research capacity. Enabling the genomic revolution in Africa.
Charles Rotimi, Akin Abayomi, Alash'le Abimiku, Victoria May Adabayeri, Clement Adebamowo, Ezekiel Adebiyi, Adebowale D Ademola, Adebowale Adeyemo, Dwomoa Adu, Dissou Affolabi,[...]. Science 2014
213
25

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
25


Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience.
Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2012
65
20

Challenges in biobank governance in Sub-Saharan Africa.
Ciara Staunton, Keymanthri Moodley. BMC Med Ethics 2013
37
20

Ethical issues in genomic research on the African continent: experiences and challenges to ethics review committees.
Michèle Ramsay, Jantina de Vries, Himla Soodyall, Shane A Norris, Osman Sankoh. Hum Genomics 2014
33
20

Regulation of genomic and biobanking research in Africa: a content analysis of ethics guidelines, policies and procedures from 22 African countries.
Jantina de Vries, Syntia Nchangwi Munung, Alice Matimba, Sheryl McCurdy, Odile Ouwe Missi Oukem-Boyer, Ciara Staunton, Aminu Yakubu, Paulina Tindana. BMC Med Ethics 2017
32
20

Access to patient-level data from GlaxoSmithKline clinical trials.
Perry Nisen, Frank Rockhold. N Engl J Med 2013
87
16



Qualitative data analysis: the framework approach.
Joanna Smith, Jill Firth. Nurse Res 2011
395
16

Raw data from clinical trials: within reach?
Peter Doshi, Steven N Goodman, John P A Ioannidis. Trends Pharmacol Sci 2013
35
16

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
16

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
64
16


Part II: HIPAA and disclosure risk issues.
Virginia A de Wolf, Joan E Sieber, Philip M Steel, Alvan O Zarate. IRB 2006
4
75

Preparing individual patient data from clinical trials for sharing: the GlaxoSmithKline approach.
Sara Hughes, Karen Wells, Paul McSorley, Andrew Freeman. Pharm Stat 2014
14
21

Data sharing: reaching consensus.
Jimmy Whitworth. Bull World Health Organ 2010
10
30




Secure use of individual patient data from clinical trials.
Patrick Vallance, Iain Chalmers. Lancet 2013
13
23



Access to patient-level trial data--a boon to drug developers.
Hans-Georg Eichler, Frank Pétavy, Francesco Pignatti, Guido Rasi. N Engl J Med 2013
41
12

Sharing of clinical trial data among trialists: a cross sectional survey.
Vinay Rathi, Kristina Dzara, Cary P Gross, Iain Hrynaszkiewicz, Steven Joffe, Harlan M Krumholz, Kelly M Strait, Joseph S Ross. BMJ 2012
54
12

Sharing of research data.
Donald J Harris. Lancet 2011
3
100

Blueprint for a deliberative public forum on biobanking policy: were theoretical principles achievable in practice?
Caron Molster, Susannah Maxwell, Leanne Youngs, Gaenor Kyne, Fiona Hope, Hugh Dawkins, Peter O'Leary. Health Expect 2013
24
12



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.