A citation-based method for searching scientific literature

Paul R Helft, Victoria L Champion, Rachael Eckles, Cynthia S Johnson, Eric M Meslin. J Empir Res Hum Res Ethics 2007
Times Cited: 40







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



Times Cited
  Times     Co-cited
Similarity


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
65
45

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
37

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
116
30



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
22

Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
138
22



Obtaining 'fresh' consent for genetic research with biological samples archived 10 years ago.
Eric Vermeulen, Marjanka K Schmidt, Neil K Aaronson, Marianne Kuenen, Flora E van Leeuwen. Eur J Cancer 2009
27
29

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
140
20

Patients' views on identifiability of samples and informed consent for genetic research.
Sara Chandros Hull, Richard R Sharp, Jeffrey R Botkin, Mark Brown, Mark Hughes, Jeremy Sugarman, Debra Schwinn, Pamela Sankar, Dragana Bolcic-Jankovic, Brian R Clarridge,[...]. Am J Bioeth 2008
81
17

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
176
17

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
182
17



DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
70
15

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
232
15

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
15

Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
86
15

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
107
15


Formative research on perceptions of biobanking: what community members think.
John S Luque, Gwendolyn P Quinn, Francisco A Montel-Ishino, Mariana Arevalo, Shalanda A Bynum, Shalewa Noel-Thomas, Kristen J Wells, Clement K Gwede, Cathy D Meade. J Cancer Educ 2012
67
15

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
75
12



Ownership and uses of human tissue: what are the opinions of surgical in-patients?
R J Bryant, R F Harrison, R D Start, A S A Chetwood, A M Chesshire, M W R Reed, S S Cross. J Clin Pathol 2008
23
21


Cancer patient perceptions on the ethical and legal issues related to biobanking.
Zubin Master, Jaime O Claudio, Christen Rachul, Jean C Y Wang, Mark D Minden, Timothy Caulfield. BMC Med Genomics 2013
35
14

Two large-scale surveys on community attitudes toward an opt-out biobank.
Kyle B Brothers, Daniel R Morrison, Ellen W Clayton. Am J Med Genet A 2011
52
12

Public preferences regarding informed consent models for participation in population-based genomic research.
Jodyn Platt, Juli Bollinger, Rachel Dvoskin, Sharon L R Kardia, David Kaufman. Genet Med 2014
55
12

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
95
12


Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
56
10

TuBaFrost 3: regulatory and ethical issues on the exchange of residual tissue for research across Europe.
E-B van Veen, P H J Riegman, W N M Dinjens, K H Lam, M H A Oomen, A Spatz, R Mager, C Ratcliffe, K Knox, D Kerr,[...]. Eur J Cancer 2006
46
10


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
10

Patients' views on residual blood use for research purposes.
N Hamajima, K Tajima, H Oya, T Kato, K Okuma, H Kaneda, S Moritaka, T Kato. Jpn J Cancer Res 1998
10
40


Consent to using human tissue.
Peter Furness. BMJ 2003
19
21

One-time general consent for research on biological samples: opt out system for patients is optimal and endorsed in many countries.
Jan Willem W Coebergh, Evert-Ben van Veen, Jan P Vandenbroucke, Paul van Diest, Wolter Oosterhuis. BMJ 2006
13
30

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
158
10

Opt-out plus, the patients' choice: preferences of cancer patients concerning information and consent regimen for future research with biological samples archived in the context of treatment.
E Vermeulen, M K Schmidt, N K Aaronson, M Kuenen, P van der Valk, C Sietses, P van den Tol, F E van Leeuwen. J Clin Pathol 2009
26
15



The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
10

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
97
10

Patients' attitudes to informed consent for genomic research with donated samples.
J Ignacio Valle-Mansilla, Miguel Ruiz-Canela, Daniel P Sulmasy. Cancer Invest 2010
14
28

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
107
10

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
107
10


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.