A citation-based method for searching scientific literature

Gaia Barazzetti, Francesca Bosisio, Daria Koutaissoff, Brenda Spencer. Eur J Hum Genet 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


A three-goal model for patients with multimorbidity: A qualitative approach.
Neeltje P Vermunt, Mirjam Harmsen, Glyn Elwyn, Gert P Westert, Jako S Burgers, Marcel G Olde Rikkert, Marjan J Faber. Health Expect 2018
31
66

Evaluating the consent preferences of UK research volunteers for genetic and clinical studies.
Susan E Kelly, Timothy D Spector, Lynn F Cherkas, Barbara Prainsack, Juliette M Harris. PLoS One 2015
25
66

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
122
33

Primary care physicians' views about gatekeeping in clinical research recruitment: A qualitative study.
Marilys Guillemin, Rosalind McDougall, Dominique Martin, Nina Hallowell, Alison Brookes, Lynn Gillam. AJOB Empir Bioeth 2017
10
33

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, Susannah Green, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2011
97
33



Pilot study: does the white coat influence research participation?
Jon F Merz, Timothy R Rebbeck, Pamela Sankar, Emma A Meagher. IRB 2002
1
100


Factors influencing public participation in biobanking.
Mamoun Ahram, Areej Othman, Manal Shahrouri, Ebtihal Mustafa. Eur J Hum Genet 2014
39
33

Governing UK Biobank: the importance of ensuring public trust.
Richard Tutton, Jane Kaye, Klaus Hoeyer. Trends Biotechnol 2004
31
33



Strategies to support recruitment of patients with life-limiting illness for research: the Palliative Care Research Cooperative Group.
Laura C Hanson, Janet Bull, Kathryn Wessell, Lisa Massie, Rachael E Bennett, Jean S Kutner, Noreen M Aziz, Amy Abernethy. J Pain Symptom Manage 2014
38
33

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
41
33



Medical decision-making capacity: knowledge, attitudes, and assessment practices of physicians in Switzerland.
Helena Hermann, Manuel Trachsel, Christine Mitchell, Nikola Biller-Andorno. Swiss Med Wkly 2014
11
33


Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
230
33

Consent and research governance in biobanks: evidence from focus groups with medical researchers.
E A Whitley, N Kanellopoulou, J Kaye. Public Health Genomics 2012
27
33

A template for broad consent in biobank research. Results and explanation of an evidence and consensus-based development process.
D Strech, S Bein, M Brumhard, W Eisenmenger, C Glinicke, T Herbst, R Jahns, S von Kielmansegg, G Schmidt, J Taupitz,[...]. Eur J Med Genet 2016
29
33

Shared decision making: a model for clinical practice.
Glyn Elwyn, Dominick Frosch, Richard Thomson, Natalie Joseph-Williams, Amy Lloyd, Paul Kinnersley, Emma Cording, Dave Tomson, Carole Dodd, Stephen Rollnick,[...]. J Gen Intern Med 2012
33

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
66
33

Some limits of informed consent.
O O'Neill. J Med Ethics 2003
218
33

Clinician gate-keeping in clinical research is not ethically defensible: an analysis.
Kerith Sharkey, Julian Savulescu, Sanchia Aranda, Penelope Schofield. J Med Ethics 2010
34
33


A three-talk model for shared decision making: multistage consultation process.
Glyn Elwyn, Marie Anne Durand, Julia Song, Johanna Aarts, Paul J Barr, Zackary Berger, Nan Cochran, Dominick Frosch, Dariusz Galasiński, Pål Gulbrandsen,[...]. BMJ 2017
224
33


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
91
33

Inequalities in global health inequalities research: A 50-year bibliometric analysis (1966-2015).
Lucinda Cash-Gibson, Diego F Rojas-Gualdrón, Juan M Pericàs, Joan Benach. PLoS One 2018
49
33


A qualitative study exploring stakeholder perspectives on the use of biological samples for future unspecified research in Malawi.
Limbanazo Matandika, Ruby Tionenji Ngóngóla, Khama Mita, Lucinda Manda-Taylor, Kate Gooding, Daniel Mwale, Francis Masiye, Joseph Mfutso-Bengo. BMC Med Ethics 2020
2
50

Development of a Biobank from a Legacy Collection in Universitas Gadjah Mada, Indonesia: Proposed Approach for Centralized Biobank Development in Low-Resource Institutions.
Jajah Fachiroh, Ery Kus Dwianingsih, Amirah Ellyza Wahdi, F Linda Tri Pramatasari, Sunandar Hariyanto, Nenes Pastiwi, Junaedy Yunus, Maimuna Mendy, Bart Scheerder, Lutfan Lazuardi. Biopreserv Biobank 2019
4
33


Practical Approach to Biobanking in Zimbabwe: Establishment of an Inclusive Stakeholder Framework.
Alice Matimba, Gunnel Tybring, Jekoniya Chitereka, Rutendo Zinyama-Gutsire, Collet Dandara, Eva Bürén, Milcah Dhoro, Collen Masimirembwa. Biopreserv Biobank 2016
3
33

Priorities for research on equity and health: towards an equity-focused health research agenda.
Piroska Östlin, Ted Schrecker, Ritu Sadana, Josiane Bonnefoy, Lucy Gilson, Clyde Hertzman, Michael P Kelly, Tord Kjellstrom, Ronald Labonté, Olle Lundberg,[...]. PLoS Med 2011
68
33

Broad consent for biobanks is best - provided it is also deep.
Rasmus Bjerregaard Mikkelsen, Mickey Gjerris, Gunhild Waldemar, Peter Sandøe. BMC Med Ethics 2019
14
33

A call for global governance of biobanks.
Haidan Chen, Tikki Pang. Bull World Health Organ 2015
21
33


Advancing good governance in data sharing and biobanking - international aspects.
Buddhika Fernando, Mandella King, Athula Sumathipala. Wellcome Open Res 2019
8
33

Informed Consent in Biomedical Research.
Fida K Dankar, Marton Gergely, Samar K Dankar. Comput Struct Biotechnol J 2019
10
33

Overview on health research ethics in Egypt and North Africa.
Diaa Marzouk, Wafaa Abd El Aal, Azza Saleh, Hany Sleem, Meriem Khyatti, Loubna Mazini, Kari Hemminki, Wagida A Anwar. Eur J Public Health 2014
11
33


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
215
33

Institutional Approaches to Research Integrity in Ghana.
Amos K Laar, Barbara K Redman, Kyle Ferguson, Arthur Caplan. Sci Eng Ethics 2020
2
50



Sprinting research and spot jogging regulation: the state of bioethics in Cameroon.
Godfrey B Tangwa, Nchangwi Syntia Munung. Camb Q Healthc Ethics 2011
2
50

Identifying structures, processes, resources and needs of research ethics committees in Egypt.
Hany Sleem, Samer S El-Kamary, Henry J Silverman. BMC Med Ethics 2010
31
33


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.