A citation-based method for searching scientific literature

Dianne Nicol, Christine Critchley, Rebekah McWhirter, Tess Whitton. Soc Sci Med 2016
Times Cited: 32







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



Times Cited
  Times     Co-cited
Similarity



Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
104
31

We're not in it for the money-lay people's moral intuitions on commercial use of 'their' biobank.
Kristin Solum Steinsbekk, Lars Oystein Ursin, John-Arne Skolbekken, Berge Solberg. Med Health Care Philos 2013
28
32

Predicting intention to biobank: a national survey.
Christine R Critchley, Dianne Nicol, Margaret F A Otlowski, Mark J A Stranger. Eur J Public Health 2012
46
25

Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
179
25

Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
57
25

Public and biobank participant attitudes toward genetic research participation and data sharing.
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
175
21


A review of the key issues associated with the commercialization of biobanks.
Timothy Caulfield, Sarah Burningham, Yann Joly, Zubin Master, Mahsa Shabani, Pascal Borry, Allan Becker, Michael Burgess, Kathryn Calder, Christine Critchley,[...]. J Law Biosci 2014
47
21

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
27
25

Identifying public expectations of genetic biobanks.
Christine Critchley, Dianne Nicol, Rebekah McWhirter. Public Underst Sci 2017
17
35


Attitudes of publics who are unwilling to donate DNA data for research.
Anna Middleton, Richard Milne, Adrian Thorogood, Erika Kleiderman, Emilia Niemiec, Barbara Prainsack, Lauren Farley, Paul Bevan, Claire Steed, James Smith,[...]. Eur J Med Genet 2019
27
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
146
15

Factors influencing public participation in biobanking.
Mamoun Ahram, Areej Othman, Manal Shahrouri, Ebtihal Mustafa. Eur J Hum Genet 2014
43
15

Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature.
Alma Husedzinovic, Dominik Ose, Christoph Schickhardt, Stefan Fröhling, Eva C Winkler. Eur J Hum Genet 2015
30
16

Encouraging Participation And Transparency In Biobank Research.
Kayte Spector-Bagdady, Raymond G De Vries, Michele G Gornick, Andrew G Shuman, Sharon Kardia, Jodyn Platt. Health Aff (Millwood) 2018
18
27

Broad consent for biobanks is best - provided it is also deep.
Rasmus Bjerregaard Mikkelsen, Mickey Gjerris, Gunhild Waldemar, Peter Sandøe. BMC Med Ethics 2019
20
25

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
17
29

Biobanking past, present and future: responsibilities and benefits.
Yvonne G De Souza, John S Greenspan. AIDS 2013
121
12

Trends in ethical and legal frameworks for the use of human biobanks.
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
157
12

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
12

Public's attitudes on participation in a biobank for research: an Italian survey.
Corinna Porteri, Patrizio Pasqualetti, Elena Togni, Michael Parker. BMC Med Ethics 2014
35
12

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
92
12

Ethics of Research Biobanks: Islamic Perspectives.
Ghiath Alahmad, Kris Dierickx. Biopreserv Biobank 2018
8
50

'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
22

Cohort Profile: LifeLines, a three-generation cohort study and biobank.
Salome Scholtens, Nynke Smidt, Morris A Swertz, Stephan J L Bakker, Aafje Dotinga, Judith M Vonk, Freerk van Dijk, Sander K R van Zon, Cisca Wijmenga, Bruce H R Wolffenbuttel,[...]. Int J Epidemiol 2015
351
12

Potential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?
J L Ridgeway, L C Han, J E Olson, K A Lackore, B A Koenig, T J Beebe, J Y Ziegenfuss. Public Health Genomics 2013
32
12

Modernizing Research Regulations Is Not Enough: It's Time to Think Outside the Regulatory Box.
Suzanne M Rivera, Kyle B Brothers, R Jean Cadigan, Heather L Harrell, Mark A Rothstein, Richard R Sharp, Aaron J Goldenberg. Am J Bioeth 2017
6
66

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
230
12

Trust in Centralized Large-Scale Data Repository: A Qualitative Analysis.
Reinder Broekstra, Judith Aris-Meijer, Els Maeckelberghe, Ronald Stolk, Sabine Otten. J Empir Res Hum Res Ethics 2020
6
66


Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V Campbell, Calvin W L Ho, Kazuto Kato, Jusaku Minari, Chih-Hsing Ho, Colin Mitchell,[...]. BMC Med Ethics 2016
58
9

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
12

The role of race and trust in tissue/blood donation for genetic research.
Jada Bussey-Jones, Joanne Garrett, Gail Henderson, Mairead Moloney, Connie Blumenthal, Giselle Corbie-Smith. Genet Med 2010
79
9


Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
50
9

Tackling community concerns about commercialisation and genetic research: a modest interdisciplinary proposal.
Gillian Haddow, Graeme Laurie, Sarah Cunningham-Burley, Kathryn G Hunter. Soc Sci Med 2007
56
9

The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
134
9

Biobank attributes associated with higher patient participation: a randomized study.
Angèle Gayet-Ageron, Sandrine Rudaz, Thomas Perneger. Eur J Hum Genet 2016
8
37

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
137
9

Research on stored biological samples: views of African American and White American cancer patients.
Rebecca D Pentz, Laurent Billot, David Wendler. Am J Med Genet A 2006
65
9

Biobanking for research: a survey of patient population attitudes and understanding.
Alanna Kulchak Rahm, Michelle Wrenn, Nikki M Carroll, Heather Spencer Feigelson. J Community Genet 2013
58
9

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
10


Ethics and biobanks.
M G Hansson. Br J Cancer 2009
107
9

Attitudes toward medical and genetic confidentiality in the Saudi research biobank: An exploratory survey.
Ghiath Alahmad, Tamer Hifnawy, Badaruddin Abbasi, Kris Dierickx. Int J Med Inform 2016
9
33

Sustainability in biobanking.
Daniel Simeon-Dubach, Marianne K Henderson. Biopreserv Biobank 2014
29
10

Targeting Future Customers: An Introductory Biobanking Course for Undergraduate Students of Life Sciences.
Ahmed Samir Abdelhafiz, Merhan Ahmed Fouda, Shaimaa Ibrahim El-Jaafary, Maysa Ibrahim Farghly, Mazen Salem, Ahmed Tammam, Hala Gabr. Biopreserv Biobank 2017
10
30



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.