A citation-based method for searching scientific literature

David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
Times Cited: 79







List of co-cited articles
427 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
199
25

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
137
17

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
107
17


Engaging the public on biobanks: outcomes of the BC biobank deliberation.
K C O'Doherty, M M Burgess. Public Health Genomics 2009
59
20

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
84
12



Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
83
11




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
11

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
153
10



The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
85
8

Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project.
Catherine A McCarty, Donna Chapman-Stone, Teresa Derfus, Philip F Giampietro, Norman Fost. Am J Med Genet A 2008
57
12

Biobanking: international norms.
Bartha Maria Knoppers. J Law Med Ethics 2005
50
14


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
99
8

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
47
14

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
190
8


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
37
18

Collection, storage and use of blood samples for future research: views of Egyptian patients expressed in a cross-sectional survey.
Alaa Abou-Zeid, Henry Silverman, Magdi Shehata, Mohamed Shams, Mervat Elshabrawy, Tamer Hifnawy, Safa Abdel Rahman, Bahiga Galal, Hany Sleem, Nabiel Mikhail,[...]. J Med Ethics 2010
24
29

Making policy decisions about population screening for breast cancer: the role of citizens' deliberation.
Charlotte Paul, Rachel Nicholls, Patricia Priest, Rob McGee. Health Policy 2008
40
15

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
195
7

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
502
7

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
420
7


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
144
7


Ethics and biobanks.
M G Hansson. Br J Cancer 2009
99
7

Deliberations about deliberative methods: issues in the design and evaluation of public participation processes.
Julia Abelson, Pierre-Gerlier Forest, John Eyles, Patricia Smith, Elisabeth Martin, Francois-Pierre Gauvin. Soc Sci Med 2003
269
7

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
425
7

Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
45
13

Reconsidering the value of consent in biobank research.
Judy Allen, Beverley McNamara. Bioethics 2011
40
15


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
125
7


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
94
7

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
51
11

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
139
7

Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks.
Elaine Gibson, Kevin Brazil, Michael D Coughlin, Claudia Emerson, Francois Fournier, Lisa Schwartz, Karen V Szala-Meneok, Karen M Weisbaum, Donald J Willison. BMC Med Ethics 2008
7
71

Public participation in health care priority setting: A scoping review.
Craig Mitton, Neale Smith, Stuart Peacock, Brian Evoy, Julia Abelson. Health Policy 2009
155
6

DNA data sharing: research participants' perspectives.
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
68
7

Assessing the public's views in research ethics controversies: deliberative democracy and bioethics as natural allies.
Scott Y H Kim, Ian F Wall, Aimee Stanczyk, Raymond De Vries. J Empir Res Hum Res Ethics 2009
40
12

Informed consent in a changing environment.
Mary Boulton, Michael Parker. Soc Sci Med 2007
23
21

The emergence of epidemiology in the genomics age.
Muin J Khoury, Robert Millikan, Julian Little, Marta Gwinn. Int J Epidemiol 2004
54
9


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.