A citation-based method for searching scientific literature

Judy Allen, Beverley McNamara. Bioethics 2011
Times Cited: 47







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



Times Cited
  Times     Co-cited
Similarity


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
36

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
115
23

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
105
21

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
174
19

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
96
19

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
19

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
105
14




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
171
14

Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
56
14

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
14


Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study.
Linus Johnsson, Mats G Hansson, Stefan Eriksson, Gert Helgesson. BMJ 2008
45
13

Tumour banks: well-guarded treasures in the interest of patients.
J Wolter Oosterhuis, Jan Willem Coebergh, Evert-Ben van Veen. Nat Rev Cancer 2003
115
12

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
12

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
12





DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
69
12

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
221
12

The ethics of research using biobanks: reason to question the importance attributed to informed consent.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
70
10

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
217
10

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
156
10


Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
138
10



Cancer as rubbish: donation of tumor tissue for research.
Bronwen Morrell, Wendy Lipworth, Renata Axler, Ian Kerridge, Miles Little. Qual Health Res 2011
16
31

Consent for biobanking: assessing the understanding and views of cancer patients.
Julien Mancini, Isabelle Pellegrini, Frédéric Viret, Norbert Vey, Lise-Marie Daufresne, Christian Chabannon, Claire Julian-Reynier. J Natl Cancer Inst 2011
21
23


Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
66
10

Why might people donate tissue for cancer research? Insights from organ/tissue/blood donation and clinical research.
Renata E Axler, Rob Irvine, Wendy Lipworth, Bronwen Morrell, Ian H Kerridge. Pathobiology 2008
21
23

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
161
10

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
54
10

A solidarity-based approach to the governance of research biobanks.
Barbara Prainsack, Alena Buyx. Med Law Rev 2013
40
12

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
92
10

Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
128
10


High rate of consent to bank biologic samples for future research: the Eastern Cooperative Oncology Group experience.
Thomas Malone, Paul J Catalano, Peter J O'Dwyer, Bruce Giantonio. J Natl Cancer Inst 2002
57
8

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
469
8

Alternative consent models for biobanks: the new Spanish law on biomedical research.
Antonio Casado da Rocha, José Antonio Seoane. Bioethics 2008
13
30

Development of a large-scale de-identified DNA biobank to enable personalized medicine.
D M Roden, J M Pulley, M A Basford, G R Bernard, E W Clayton, J R Balser, D R Masys. Clin Pharmacol Ther 2008
544
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
30
13

Principles of human subjects protections applied in an opt-out, de-identified biobank.
Jill Pulley, Ellen Clayton, Gordon R Bernard, Dan M Roden, Daniel R Masys. Clin Transl Sci 2010
144
8

Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study.
Philippe A Melas, Louise K Sjöholm, Tord Forsner, Maigun Edhborg, Niklas Juth, Yvonne Forsell, Catharina Lavebratt. J Med Ethics 2010
47
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.