A citation-based method for searching scientific literature

Wendy Lipworth, Rowena Forsyth, Ian Kerridge. Sociol Health Illn 2011
Times Cited: 36







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



Times Cited
  Times     Co-cited
Similarity


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
25


Why do participants enroll in population biobank studies? A systematic literature review.
Hélène Nobile, Eric Vermeulen, Kristof Thys, Manuela M Bergmann, Pascal Borry. Expert Rev Mol Diagn 2013
31
19

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
165
13

Neglected ethical issues in biobank management: Results from a U.S. study.
R Jean Cadigan, Dragana Lassiter, Kaaren Haldeman, Ian Conlon, Erik Reavely, Gail E Henderson. Life Sci Soc Policy 2013
48
13

Hypothetical and factual willingness to participate in biobank research.
Linus Johnsson, Gert Helgesson, Thorunn Rafnar, Ingibjorg Halldorsdottir, Kee-Seng Chia, Stefan Eriksson, Mats G Hansson. Eur J Hum Genet 2010
59
13

Connecting the public with biobank research: reciprocity matters.
Herbert Gottweis, George Gaskell, Johannes Starkbaum. Nat Rev Genet 2011
35
14


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
51
13

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
169
11


Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study.
Samantha A Streicher, Saskia C Sanderson, Ethylin Wang Jabs, Michael Diefenbach, Meg Smirnoff, Inga Peter, Carol R Horowitz, Barbara Brenner, Lynne D Richardson. J Community Genet 2011
59
11

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
155
11

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
49
11

The privacy-reciprocity connection in biobanking: comparing German with UK strategies.
A Hobbs, J Starkbaum, U Gottweis, H E Wichmann, H Gottweis. Public Health Genomics 2012
26
15

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
11

Biobanking: the foundation of personalized medicine.
Robert E Hewitt. Curr Opin Oncol 2011
161
11



Gift relationships in genetics research.
Richard Tutton. Sci Cult (Lond) 2002
28
14

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
11

An empirical reappraisal of public trust in biobanking research: rethinking restrictive consent requirements.
Wendy Lipworth, Bronwen Morrell, Rob Irvine, Ian Kerridge. J Law Med 2009
21
19

Informed consent in biobank research: a deliberative approach to the debate.
David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
83
11


Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
105
11

Biosamples as gifts? How participants in biobanking projects talk about donation.
Louise Locock, Anne-Marie R Boylan. Health Expect 2016
12
33


Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
201
8

Attitudes and perceptions of patients towards methods of establishing a DNA biobank.
Jill M Pulley, Margaret M Brace, Gordon R Bernard, Dan R Masys. Cell Tissue Bank 2008
74
8


Assessing the understanding of biobank participants.
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
104
8

Attitudes and beliefs of African Americans toward participation in medical research.
G Corbie-Smith, S B Thomas, M V Williams, S Moody-Ayers. J Gen Intern Med 1999
689
8


Communication of biobanks' research results: what do (potential) participants want?
Tineke M Meulenkamp, Sjef K Gevers, Jasper A Bovenberg, Gerard H Koppelman, Astrid van Hylckama Vlieg, Ellen M A Smets. Am J Med Genet A 2010
63
8

Biobanks and the phantom public.
Herbert Gottweis, Haidan Chen, Johannes Starkbaum. Hum Genet 2011
25
12

Closure of population biobanks and direct-to-consumer genetic testing companies.
Ma'n H Zawati, Pascal Borry, Heidi Carmen Howard. Hum Genet 2011
24
12

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
53
8

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
8

Toward a roadmap in global biobanking for health.
Jennifer R Harris, Paul Burton, Bartha Maria Knoppers, Klaus Lindpaintner, Marianna Bledsoe, Anthony J Brookes, Isabelle Budin-Ljøsne, Rex Chisholm, David Cox, Mylène Deschênes,[...]. Eur J Hum Genet 2012
80
8

Cancer as rubbish: donation of tumor tissue for research.
Bronwen Morrell, Wendy Lipworth, Renata Axler, Ian Kerridge, Miles Little. Qual Health Res 2011
16
18

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
8

A trial of consent procedures for future research with clinically derived biological samples.
E Vermeulen, M K Schmidt, N K Aaronson, M Kuenen, M-J Baas-Vrancken Peeters, H van der Poel, S Horenblas, H Boot, V J Verwaal, A Cats,[...]. Br J Cancer 2009
29
10

Cancer patient perceptions about biobanking and preferred timing of consent.
Kathryn L Braun, Joann U Tsark, Amy Powers, Kristen Croom, Robert Kim, Francine C Gachupin, Paul Morris. Biopreserv Biobank 2014
22
13

From patients to partners: participant-centric initiatives in biomedical research.
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
159
8



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
41
8

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
81
8


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
229
8


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.