A citation-based method for searching scientific literature

Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
Times Cited: 67







List of co-cited articles
277 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
191
32


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
132
20

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
76
19



From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat. Rev. Genet. 2008
187
14



Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat. Rev. Genet. 2005
102
11

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
122
11

The debate over research on stored biological samples: what do sources think?
Dave Wendler, Ezekiel Emanuel. Arch. Intern. Med. 2002
121
11

Research with stored biological samples: what do research participants want?
Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, Susan G Hilsenbeck, Franklin G Miller, Ezekiel J Emanuel, David Wendler. Arch. Intern. Med. 2005
74
11

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
76
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
88
11

The social and ethical issues of post-genomic human biobanks.
Anne Cambon-Thomsen. Nat. Rev. Genet. 2004
103
10


Genebanks: a comparison of eight proposed international genetic databases.
Melissa A Austin, Sarah Harding, Courtney McElroy. Community Genet 2003
52
13


Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
43
16

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N. Engl. J. Med. 2003
79
10


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
156
10


Biobanking: international norms.
Bartha Maria Knoppers. J Law Med Ethics 2005
48
12

Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol. 2008
139
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
394
8

The consent problem within DNA biobanks.
Darren Shickle. Stud Hist Philos Biol Biomed Sci 2006
38
15

The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur. J. Hum. Genet. 2006
163
8

Cancer patients' attitudes toward future research uses of stored human biological materials.
Paul R Helft, Victoria L Champion, Rachael Eckles, Cynthia S Johnson, Eric M Meslin. J Empir Res Hum Res Ethics 2007
33
18

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
190
8


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
107
8

Human genetic research, DNA banking and consent: a question of 'form'?
M Deschênes, G Cardinal, B M Knoppers, K C Glass. Clin. Genet. 2001
43
11

An empirical survey on biobanking of human genetic material and data in six EU countries.
Isabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, Jenny Duchier, Brigitte Jansen, Jürgen Simon, Paula Lobato De Faria, Anna Perez-Lezaun, Bert Visser, Garrath D Williams,[...]. Eur. J. Hum. Genet. 2003
62
8

Informed consent and biobanks.
Ellen Wright Clayton. J Law Med Ethics 2005
50
10

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
60
8




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
55
9

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
51
9

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
36
13

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.
Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V Pearson, Dietrich A Stephan, Stanley F Nelson, David W Craig. PLoS Genet. 2008
395
7

Ethics and biobanks.
M G Hansson. Br. J. Cancer 2009
93
7

Reconsidering the value of consent in biobank research.
Judy Allen, Beverley McNamara. Bioethics 2011
38
13

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
104
7

Power to the people: a wiki-governance model for biobanks.
Edward S Dove, Yann Joly, Bartha M Knoppers. Genome Biol. 2012
19
26

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
76
7

Involving study populations in the review of genetic research.
R R Sharp, M W Foster. J Law Med Ethics 2000
60
6


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.