M L Goodson, B G Vernon. J Clin Pathol 2004
Times Cited: 41
Times Cited: 41
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
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
46
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
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
39
Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?
Asa Kettis-Lindblad, Lena Ring, Eva Viberth, Mats G Hansson. Eur J Public Health 2006
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39
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
Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, Susan G Hilsenbeck, Franklin G Miller, Ezekiel J Emanuel, David Wendler. Arch Intern Med 2005
36
Why surgical patients do not donate tissue for commercial research: review of records.
Alison L Jack, Christopher Womack. BMJ 2003
Alison L Jack, Christopher Womack. BMJ 2003
36
The debate over research on stored biological samples: what do sources think?
Dave Wendler, Ezekiel Emanuel. Arch Intern Med 2002
Dave Wendler, Ezekiel Emanuel. Arch Intern Med 2002
34
Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
29
Consent for genetic research in a general population: the NHANES experience.
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
26
Informed consent for genetic research on blood stored for more than a decade: a population based study.
Birgitta Stegmayr, Kjell Asplund. BMJ 2002
Birgitta Stegmayr, Kjell Asplund. BMJ 2002
26
Willingness to donate blood samples for genetic research: a survey from a community in Singapore.
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
24
Consent to the use of stored DNA for genetics research: a survey of attitudes in the Jewish population.
M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
19
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
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
19
Views of female breast cancer patients who donated biologic samples regarding storage and use of samples for genetic research.
K A Kaphingst, J M Janoff, L N Harris, K M Emmons. Clin Genet 2006
K A Kaphingst, J M Janoff, L N Harris, K M Emmons. Clin Genet 2006
17
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
Jill M Pulley, Margaret M Brace, Gordon R Bernard, Dan R Masys. Cell Tissue Bank 2008
17
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
Rebecca D Pentz, Laurent Billot, David Wendler. Am J Med Genet A 2006
17
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
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
22
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
Thomas Malone, Paul J Catalano, Peter J O'Dwyer, Bruce Giantonio. J Natl Cancer Inst 2002
14
No consent should be needed for using leftover body material for scientific purposes. For.
Paul J van Diest. BMJ 2002
Paul J van Diest. BMJ 2002
14
Ethical issues in tissue banking for research: a brief review of existing organizational policies.
Keith Bauer, Sara Taub, Kayhan Parsi. Theor Med Bioeth 2004
Keith Bauer, Sara Taub, Kayhan Parsi. Theor Med Bioeth 2004
16
Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: a population-based study.
Asa Kettis-Lindblad, Lena Ring, Eva Viberth, Mats G Hansson. Scand J Public Health 2007
Asa Kettis-Lindblad, Lena Ring, Eva Viberth, Mats G Hansson. Scand J Public Health 2007
14
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
Gillian Haddow, Graeme Laurie, Sarah Cunningham-Burley, Kathryn G Hunter. Soc Sci Med 2007
14
Human tissue samples and ethics--attitudes of the general public in Sweden to biobank research.
Tore Nilstun, Göran Hermerén. Med Health Care Philos 2006
Tore Nilstun, Göran Hermerén. Med Health Care Philos 2006
20
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
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
14
Ownership and uses of human tissue: does the Nuffield bioethics report accord with opinion of surgical inpatients?
R D Start, W Brown, R J Bryant, M W Reed, S S Cross, G Kent, J C Underwood. BMJ 1996
R D Start, W Brown, R J Bryant, M W Reed, S S Cross, G Kent, J C Underwood. BMJ 1996
20
Attitudes of the Japanese public and doctors towards use of archived information and samples without informed consent: preliminary findings based on focus group interviews.
Atsushi Asai, Motoki Ohnishi, Etsuyo Nishigaki, Miho Sekimoto, Shunichi Fukuhara, Tsuguya Fukui. BMC Med Ethics 2002
Atsushi Asai, Motoki Ohnishi, Etsuyo Nishigaki, Miho Sekimoto, Shunichi Fukuhara, Tsuguya Fukui. BMC Med Ethics 2002
20
'Science is really needed--that's all I know': informed consent and the non-verbal practices of collecting blood for genetic research in northern Sweden.
Klaus Hoeyer. New Genet Soc 2003
Klaus Hoeyer. New Genet Soc 2003
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
David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
12
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
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
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
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
21
Public attitudes to the storage of blood left over from routine general practice tests and its use in research.
Shaun Treweek, Alex Doney, David Leiman. J Health Serv Res Policy 2009
Shaun Treweek, Alex Doney, David Leiman. J Health Serv Res Policy 2009
14
Informed consent for genetic research on stored tissue samples.
E W Clayton, K K Steinberg, M J Khoury, E Thomson, L Andrews, M J Kahn, L M Kopelman, J O Weiss. JAMA 1995
E W Clayton, K K Steinberg, M J Khoury, E Thomson, L Andrews, M J Kahn, L M Kopelman, J O Weiss. JAMA 1995
9
Informed consent for research on stored blood and tissue samples: a survey of institutional review board practices.
Mary Terrell White, Jennifer Gamm. Account Res 2002
Mary Terrell White, Jennifer Gamm. Account Res 2002
19
Family attitudes to research using samples taken at coroner's postmortem examinations: review of records.
Christopher Womack, Alison L Jack. BMJ 2003
Christopher Womack, Alison L Jack. BMJ 2003
22
Ethical issues in tissue banking for research: the prospects and pitfalls of setting international standards.
Karen J Maschke, Thomas H Murray. Theor Med Bioeth 2004
Karen J Maschke, Thomas H Murray. Theor Med Bioeth 2004
19
Human tissue research in the genomic era of medicine: balancing individual and societal interests.
T T Ashburn, S K Wilson, B I Eisenstein. Arch Intern Med 2000
T T Ashburn, S K Wilson, B I Eisenstein. Arch Intern Med 2000
10
No consent should be needed for using leftover body material for scientific purposes. Against.
Julian Savulescu. BMJ 2002
Julian Savulescu. BMJ 2002
26
Obtaining explicit consent for the use of archival tissue samples: practical issues.
P N Furness, M L Nicholson. J Med Ethics 2004
P N Furness, M L Nicholson. J Med Ethics 2004
13
Community engagement in genetic research: results of the first public consultation for the Quebec CARTaGENE project.
Béatrice Godard, Jennifer Marshall, Claude Laberge. Community Genet 2007
Béatrice Godard, Jennifer Marshall, Claude Laberge. Community Genet 2007
9
Ethical and legal issues in research involving human subjects: do you want a piece of me?
M B Kapp. J Clin Pathol 2006
M B Kapp. J Clin Pathol 2006
10
Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
9
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
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
9
9
Ethical and legal issues in the procurement, storage and use of DNA.
M J McQueen. Clin Chem Lab Med 1998
M J McQueen. Clin Chem Lab Med 1998
27
Breaking the stalemate: a prospective regulatory framework for unforseen research uses of human tissue samples and health information.
H T Greely. Wake Forest Law Rev 1999
H T Greely. Wake Forest Law Rev 1999
9
The experience of Spain's early modern soldiers: combat, welfare and violence.
L White. War Hist 2002
L White. War Hist 2002
20
7
Potential harms, anonymization, and the right to withdraw consent to biobank research.
Stefan Eriksson, Gert Helgesson. Eur J Hum Genet 2005
Stefan Eriksson, Gert Helgesson. Eur J Hum Genet 2005
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.