A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
29

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
22

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
22




False hopes and best data: consent to research and the therapeutic misconception.
P S Appelbaum, L H Roth, C W Lidz, P Benson, W Winslade. Hastings Cent Rep 1987
560
16




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
69
11


Attitudes to bioethical issues: a case study of a screening project.
U Gustafsson Stolt, P E Liss, T Svensson, J Ludvigsson. Soc Sci Med 2002
20
30


Empirical data about women's attitudes toward a biobank focused on pregnancy outcomes.
Josh W Joseph, Alon B Neidich, Carole Ober, Lainie Friedman Ross. Am J Med Genet A 2008
28
21


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

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
11

Beyond "misunderstanding": written information and decisions about taking part in a genetic epidemiology study.
Mary Dixon-Woods, Richard E Ashcroft, Clare J Jackson, Martin D Tobin, Joelle Kivits, Paul R Burton, Nilesh J Samani. Soc Sci Med 2007
85
11


Gift relationships in genetics research.
Richard Tutton. Sci Cult (Lond) 2002
28
21


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

Reconsidering the value of consent in biobank research.
Judy Allen, Beverley McNamara. Bioethics 2011
46
13

Governing UK Biobank: the importance of ensuring public trust.
Richard Tutton, Jane Kaye, Klaus Hoeyer. Trends Biotechnol 2004
31
16

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
9

Empty ethics: the problem with informed consent.
Oonagh Corrigan. Sociol Health Illn 2003
160
9


Issues of consent and feedback in a genetic epidemiological study of women with breast cancer.
M P M Richards, M Ponder, P Pharoah, S Everest, J Mackay. J Med Ethics 2003
43
11

Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
184
9



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
9

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
81
9

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
9

Genebanks: a comparison of eight proposed international genetic databases.
Melissa A Austin, Sarah Harding, Courtney McElroy. Community Genet 2003
54
7


Consent for genetic research in a general population: the NHANES experience.
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
125
7


Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
84
7


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

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
44
9


Trust, The fragile foundation of contemporary biomedical research.
N E Kass, J Sugarman, R Faden, M Schoch-Spana. Hastings Cent Rep 1996
169
7


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
55
7



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
66
7


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.