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Times Cited: 202
Times Cited: 202
Times Cited
Times Co-cited
Similarity
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
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The debate over research on stored biological samples: what do sources think?
Dave Wendler, Ezekiel Emanuel. Arch Intern Med 2002
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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
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Research and stored tissues. Persons as sources, samples as persons?
B M Knoppers, C M Laberge. JAMA 1995
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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
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ASHG report. Statement on informed consent for genetic research. The American Society of Human Genetics.
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Human genetic research, DNA banking and consent: a question of 'form'?
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Recommended policies for uses of human tissue in research, education, and quality control. Ad Hoc Committee on Stored Tissue, College of American Pathologists.
W Grizzle, W W Grody, W W Noll, M E Sobel, S A Stass, T Trainer, H Travers, V Weedn, K Woodruff. Arch Pathol Lab Med 1999
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Privacy in genetics research.
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17
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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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
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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
8
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
10
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
9
Patients' views on identifiability of samples and informed consent for genetic research.
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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
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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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Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.
Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V Pearson, Dietrich A Stephan, Stanley F Nelson, David W Craig. PLoS Genet 2008
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The uneasy ethical and legal underpinnings of large-scale genomic biobanks.
Henry T Greely. Annu Rev Genomics Hum Genet 2007
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Use of human tissues in research: clarifying clinician and researcher roles and information flows.
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J F Merz, P Sankar, S E Taube, V Livolsi. J Investig Med 1997
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The role of community review in evaluating the risks of human genetic variation research.
M W Foster, R R Sharp, W L Freeman, M Chino, D Bernsten, T H Carter. Am J Hum Genet 1999
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Group identity and human diversity: keeping biology straight from culture.
E T Juengst. Am J Hum Genet 1998
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Human tissue research in the genomic era of medicine: balancing individual and societal interests.
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Why surgical patients do not donate tissue for commercial research: review of records.
Alison L Jack, Christopher Womack. BMJ 2003
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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
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Disclosing individual genetic results to research participants.
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BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.
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Pharmacogenomics: translating functional genomics into rational therapeutics.
W E Evans, M V Relling. Science 1999
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Control of DNA samples and information.
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Principles, organization, and operation of a DNA bank for clinical trials: a Department of Veterans Affairs cooperative study.
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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
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Informed consent, participation in, and withdrawal from a population based cohort study involving genetic analysis.
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Genetics. Genomic research and human subject privacy.
Zhen Lin, Art B Owen, Russ B Altman. Science 2004
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Disclosing individual results of clinical research: implications of respect for participants.
David I Shalowitz, Franklin G Miller. JAMA 2005
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ACMG statement. Statement on storage and use of genetic materials. American College of Medical Genetics Storage of Genetics Materials Committee.
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The sequence of the human genome.
J C Venter, M D Adams, E W Myers, P W Li, R J Mural, G G Sutton, H O Smith, M Yandell, C A Evans, R A Holt,[...]. Science 2001
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Initial sequencing and analysis of the human genome.
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Involving study populations in the review of genetic research.
R R Sharp, M W Foster. J Law Med Ethics 2000
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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.