M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
Times Cited: 57
Times Cited: 57
Times Cited
Times Co-cited
Similarity
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
50
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
49
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
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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
29
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
28
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
23
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
24
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
17
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
24
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
15
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
15
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
15
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
15
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
14
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
27
Factors influencing public participation in biobanking.
Mamoun Ahram, Areej Othman, Manal Shahrouri, Ebtihal Mustafa. Eur J Hum Genet 2014
Mamoun Ahram, Areej Othman, Manal Shahrouri, Ebtihal Mustafa. Eur J Hum Genet 2014
18
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
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
12
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
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
14
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
Hypothetical and factual willingness to participate in biobank research.
Linus Johnsson, Gert Helgesson, Thorunn Rafnar, Ingibjorg Halldorsdottir, Kee-Seng Chia, Stefan Eriksson, Mats G Hansson. Eur J Hum Genet 2010
Linus Johnsson, Gert Helgesson, Thorunn Rafnar, Ingibjorg Halldorsdottir, Kee-Seng Chia, Stefan Eriksson, Mats G Hansson. Eur J Hum Genet 2010
12
Biobanking for research: a survey of patient population attitudes and understanding.
Alanna Kulchak Rahm, Michelle Wrenn, Nikki M Carroll, Heather Spencer Feigelson. J Community Genet 2013
Alanna Kulchak Rahm, Michelle Wrenn, Nikki M Carroll, Heather Spencer Feigelson. J Community Genet 2013
12
Public's attitudes on participation in a biobank for research: an Italian survey.
Corinna Porteri, Patrizio Pasqualetti, Elena Togni, Michael Parker. BMC Med Ethics 2014
Corinna Porteri, Patrizio Pasqualetti, Elena Togni, Michael Parker. BMC Med Ethics 2014
20
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
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
10
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
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
10
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
Public attitudes regarding willingness to participate in medical research studies.
J M Trauth, D Musa, L Siminoff, I K Jewell, E Ricci. J Health Soc Policy 2000
J M Trauth, D Musa, L Siminoff, I K Jewell, E Ricci. J Health Soc Policy 2000
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
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
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
8
Factors that influence characteristics of genetic biobanks.
Jennifer E Sanner, Lorraine Frazier. J Nurs Scholarsh 2007
Jennifer E Sanner, Lorraine Frazier. J Nurs Scholarsh 2007
15
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
8
Racial and ethnic disparity in participation in DNA collection at the Atlanta site of the National Birth Defects Prevention Study.
Krista S Crider, Jennita Reefhuis, Alison Woomert, Margaret A Honein. Am J Epidemiol 2006
Krista S Crider, Jennita Reefhuis, Alison Woomert, Margaret A Honein. Am J Epidemiol 2006
16
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
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
8
Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
8
Engaging diverse populations about biospecimen donation for cancer research.
Julie H T Dang, Elisa M Rodriguez, John S Luque, Deborah O Erwin, Cathy D Meade, Moon S Chen. J Community Genet 2014
Julie H T Dang, Elisa M Rodriguez, John S Luque, Deborah O Erwin, Cathy D Meade, Moon S Chen. J Community Genet 2014
8
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
8
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
7
Using a telephone survey to acquire genetic and behavioral data related to cigarette smoking in "made-anonymous" and "registry" samples.
Lynn T Kozlowski, George P Vogler, David J Vandenbergh, Andrew A Strasser, Richard J O'Connor, Berwood A Yost. Am J Epidemiol 2002
Lynn T Kozlowski, George P Vogler, David J Vandenbergh, Andrew A Strasser, Richard J O'Connor, Berwood A Yost. Am J Epidemiol 2002
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
16
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
7
Personal characteristics of older primary care patients who provide a buccal swab for apolipoprotein E testing and banking of genetic material: the spectrum study.
Hillary R Bogner, Marsha N Wittink, Jon F Merz, Joseph B Straton, Peter F Cronholm, Peter V Rabins, Joseph J Gallo. Community Genet 2004
Hillary R Bogner, Marsha N Wittink, Jon F Merz, Joseph B Straton, Peter F Cronholm, Peter V Rabins, Joseph J Gallo. Community Genet 2004
10
Warranted concerns, warranted outlooks: a focus group study of public understandings of genetic research.
Benjamin R Bates, John A Lynch, Jennifer L Bevan, Celeste M Condit. Soc Sci Med 2005
Benjamin R Bates, John A Lynch, Jennifer L Bevan, Celeste M Condit. Soc Sci Med 2005
7
Attitudes of urban American Indians and Alaska Natives regarding participation in research.
Dedra Buchwald, Veronica Mendoza-Jenkins, Calvin Croy, Helen McGough, Marjorie Bezdek, Paul Spicer. J Gen Intern Med 2006
Dedra Buchwald, Veronica Mendoza-Jenkins, Calvin Croy, Helen McGough, Marjorie Bezdek, Paul Spicer. J Gen Intern Med 2006
9
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
9
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
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.