Asa Kettis-Lindblad, Lena Ring, Eva Viberth, Mats G Hansson. Scand J Public Health 2007
Times Cited: 42
Times Cited: 42
Times Cited
Times Co-cited
Similarity
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Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
40
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
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
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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
Asa Kettis-Lindblad, Lena Ring, Eva Viberth, Mats G Hansson. Eur J Public Health 2006
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
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
28
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
26
Donors perceptions of consent to and feedback from biobank research: time to acknowledge diversity?
K Hoeyer. Public Health Genomics 2010
K Hoeyer. Public Health Genomics 2010
21
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
21
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
19
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
19
The social and ethical issues of post-genomic human biobanks.
Anne Cambon-Thomsen. Nat Rev Genet 2004
Anne Cambon-Thomsen. Nat Rev Genet 2004
19
Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
16
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
24
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
16
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
16
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
16
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
25
A study of public opinion on the use of tissue samples from living subjects for clinical research.
M L Goodson, B G Vernon. J Clin Pathol 2004
M L Goodson, B G Vernon. J Clin Pathol 2004
14
Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
14
'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
14
Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework.
Bernice S Elger, Arthur L Caplan. EMBO Rep 2006
Bernice S Elger, Arthur L Caplan. EMBO Rep 2006
14
The ethics of research biobanking: a critical review of the literature.
Klaus Hoeyer. Biotechnol Genet Eng Rev 2008
Klaus Hoeyer. Biotechnol Genet Eng Rev 2008
14
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
11
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
11
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
11
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
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
11
The uneasy ethical and legal underpinnings of large-scale genomic biobanks.
Henry T Greely. Annu Rev Genomics Hum Genet 2007
Henry T Greely. Annu Rev Genomics Hum Genet 2007
11
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
Linus Johnsson, Mats G Hansson, Stefan Eriksson, Gert Helgesson. BMJ 2008
11
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
11
Ethical framework for previously collected biobank samples.
Gert Helgesson, Joakim Dillner, Joyce Carlson, Claus R Bartram, Mats G Hansson. Nat Biotechnol 2007
Gert Helgesson, Joakim Dillner, Joyce Carlson, Claus R Bartram, Mats G Hansson. Nat Biotechnol 2007
11
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
11
"Broad" consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose.
Carlo Petrini. Soc Sci Med 2010
Carlo Petrini. Soc Sci Med 2010
11
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
11
Research understanding, attitude and awareness towards biobanking: a survey among Italian twin participants to a genetic epidemiological study.
Virgilia Toccaceli, Corrado Fagnani, Lorenza Nisticò, Cristina D'Ippolito, Lorenzo Giannantonio, Sonia Brescianini, Maria Antonietta Stazi. BMC Med Ethics 2009
Virgilia Toccaceli, Corrado Fagnani, Lorenza Nisticò, Cristina D'Ippolito, Lorenzo Giannantonio, Sonia Brescianini, Maria Antonietta Stazi. BMC Med Ethics 2009
26
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
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
11
National survey of British public's views on use of identifiable medical data by the National Cancer Registry.
Geraldine Barrett, Jackie A Cassell, Janet L Peacock, Michel P Coleman. BMJ 2006
Geraldine Barrett, Jackie A Cassell, Janet L Peacock, Michel P Coleman. BMJ 2006
9
Coding and consent: moral challenges of the database project in Iceland.
Vilhjalmur Arnason. Bioethics 2004
Vilhjalmur Arnason. Bioethics 2004
9
22
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
9
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
9
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
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
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
9
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
11
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
Paul R Helft, Victoria L Champion, Rachael Eckles, Cynthia S Johnson, Eric M Meslin. J Empir Res Hum Res Ethics 2007
10
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
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.