Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, Susan G Hilsenbeck, Franklin G Miller, Ezekiel J Emanuel, David Wendler. Arch Intern Med 2005
Times Cited: 81
Times Cited: 81
Times Cited
Times Co-cited
Similarity
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
43
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
33
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
41
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
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
40
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
27
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
28
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
25
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
34
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
36
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
37
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
18
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
24
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
18
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
25
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
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
13
Consent for genetic research in a general population: an update on the National Health and Nutrition Examination Survey experience.
Geraldine M McQuillan, Qiyuan Pan, Kathryn S Porter. Genet Med 2006
Geraldine M McQuillan, Qiyuan Pan, Kathryn S Porter. Genet Med 2006
16
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
14
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
32
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
17
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
12
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
12
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
20
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
12
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
12
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
22
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
32
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
Kyle B Brothers, Daniel R Morrison, Ellen W Clayton. Am J Med Genet A 2011
17
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, participation in, and withdrawal from a population based cohort study involving genetic analysis.
K Matsui, Y Kita, H Ueshima. J Med Ethics 2005
K Matsui, Y Kita, H Ueshima. J Med Ethics 2005
18
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
N Hamajima, K Tajima, H Oya, T Kato, K Okuma, H Kaneda, S Moritaka, T Kato. Jpn J Cancer Res 1998
80
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
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
9
Consent in crisis: the need to reconceptualize consent to tissue banking research.
W Lipworth, R Ankeny, I Kerridge. Intern Med J 2006
W Lipworth, R Ankeny, I Kerridge. Intern Med J 2006
53
DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 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
9
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
Eric Vermeulen, Marjanka K Schmidt, Neil K Aaronson, Marianne Kuenen, Flora E van Leeuwen. Eur J Cancer 2009
29
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
28
Racial differences in enrolment in a cancer genetics registry.
Patricia G Moorman, Celette Sugg Skinner, James P Evans, Beth Newman, James R Sorenson, Brian Calingaert, Lisa Susswein, T Sydnee Crankshaw, Cathrine Hoyo, Joellen M Schildkraut. Cancer Epidemiol Biomarkers Prev 2004
Patricia G Moorman, Celette Sugg Skinner, James P Evans, Beth Newman, James R Sorenson, Brian Calingaert, Lisa Susswein, T Sydnee Crankshaw, Cathrine Hoyo, Joellen M Schildkraut. Cancer Epidemiol Biomarkers Prev 2004
10
Public willingness to participate in and public opinions about genetic variation research: a review of the literature.
Rene Sterling, Gail E Henderson, Giselle Corbie-Smith. Am J Public Health 2006
Rene Sterling, Gail E Henderson, Giselle Corbie-Smith. Am J Public Health 2006
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
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
8
DNA data sharing: research participants' perspectives.
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
9
Research and stored tissues. Persons as sources, samples as persons?
B M Knoppers, C M Laberge. JAMA 1995
B M Knoppers, C M Laberge. JAMA 1995
15
Attitudes and beliefs of African Americans toward participation in medical research.
G Corbie-Smith, S B Thomas, M V Williams, S Moody-Ayers. J Gen Intern Med 1999
G Corbie-Smith, S B Thomas, M V Williams, S Moody-Ayers. J Gen Intern Med 1999
7
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
7
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
7
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
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.