M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
Times Cited: 47
Times Cited: 47
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
51
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
48
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
44
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
34
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
31
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
25
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
25
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
23
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
23
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
23
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
23
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
19
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
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
14
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
14
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
14
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
14
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
"What are they going to do with the information?" Latino/Latina and African American perspectives on the Human Genome Project.
Amy Schulz, Cleopatra Caldwell, Sarah Foster. Health Educ Behav 2003
Amy Schulz, Cleopatra Caldwell, Sarah Foster. Health Educ Behav 2003
16
ASHG report. Statement on informed consent for genetic research. The American Society of Human Genetics.
. Am J Hum Genet 1996
. Am J Hum Genet 1996
12
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
12
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
12
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
12
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
12
Ethical issues in genetic research: disclosure and informed consent.
P R Reilly, M F Boshar, S H Holtzman. Nat Genet 1997
P R Reilly, M F Boshar, S H Holtzman. Nat Genet 1997
10
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
23
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
10
Racial differences in factors that influence the willingness to participate in medical research studies.
Vickie L Shavers, Charles F Lynch, Leon F Burmeister. Ann Epidemiol 2002
Vickie L Shavers, Charles F Lynch, Leon F Burmeister. Ann Epidemiol 2002
8
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
40
Awareness and motivation of Japanese donors of blood for research.
T Nakayama, K Muto, N Yoshiike, T Yokoyama. Am J Public Health 1999
T Nakayama, K Muto, N Yoshiike, T Yokoyama. Am J Public Health 1999
40
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
8
The experience of Spain's early modern soldiers: combat, welfare and violence.
L White. War Hist 2002
L White. War Hist 2002
26
Patients' consent preferences for research uses of information in electronic medical records: interview and survey data.
Donald J Willison, Karim Keshavjee, Kalpana Nair, Charlie Goldsmith, Anne M Holbrook. BMJ 2003
Donald J Willison, Karim Keshavjee, Kalpana Nair, Charlie Goldsmith, Anne M Holbrook. BMJ 2003
8
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
8
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
8
Employees' perspectives on ethically important aspects of genetic research participation: a pilot study.
Laura Weiss Roberts, Teddy D Warner, Cynthia M A Geppert, Melinda Rogers, Katherine A Green Hammond. Compr Psychiatry 2005
Laura Weiss Roberts, Teddy D Warner, Cynthia M A Geppert, Melinda Rogers, Katherine A Green Hammond. Compr Psychiatry 2005
23
Privacy in genetics research.
B P Fuller, M J Kahn, P A Barr, L Biesecker, E Crowley, J Garber, M K Mansoura, P Murphy, J Murray, J Phillips,[...]. Science 1999
B P Fuller, M J Kahn, P A Barr, L Biesecker, E Crowley, J Garber, M K Mansoura, P Murphy, J Murray, J Phillips,[...]. Science 1999
8
Strategies for consulting with the community: the cases of four large-scale genetic databases.
B Godard, J Marshall, C Laberge, B M Knoppers. Sci Eng Ethics 2004
B Godard, J Marshall, C Laberge, B M Knoppers. Sci Eng Ethics 2004
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
8
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
8
Native Hawaiian preferences for informed consent and disclosure of results from genetic research.
Megan Fong, Kathryn L Braun, R Mei-Ling Chang. J Cancer Educ 2006
Megan Fong, Kathryn L Braun, R Mei-Ling Chang. J Cancer Educ 2006
19
Informed consent and subject motivation to participate in a large, population-based genomics study: the Marshfield Clinic Personalized Medicine Research Project.
Catherine A McCarty, Anuradha Nair, Diane M Austin, Philip F Giampietro. Community Genet 2007
Catherine A McCarty, Anuradha Nair, Diane M Austin, Philip F Giampietro. Community Genet 2007
8
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
8
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
8
Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
8
Biobank Recruitment: Motivations for Nonparticipation.
Katrina A B Goddard, K Sabina Smith, Chuhe Chen, Carmit McMullen, Cheryl Johnson. Biopreserv Biobank 2009
Katrina A B Goddard, K Sabina Smith, Chuhe Chen, Carmit McMullen, Cheryl Johnson. Biopreserv Biobank 2009
13
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.