Stefan Eriksson, Gert Helgesson. Eur J Hum Genet 2005
Times Cited: 65
Times Cited: 65
Times Cited
Times Co-cited
Similarity
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
33
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
20
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
20
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
20
The social and ethical issues of post-genomic human biobanks.
Anne Cambon-Thomsen. Nat Rev Genet 2004
Anne Cambon-Thomsen. Nat Rev Genet 2004
16
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
15
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
15
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
13
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
13
Ethical, legal, and social implications of biobanks for genetics research.
Susanne B Haga, Laura M Beskow. Adv Genet 2008
Susanne B Haga, Laura M Beskow. Adv Genet 2008
13
Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
13
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
12
The right to withdraw consent to research on biobank samples.
Gert Helgesson, Linus Johnsson. Med Health Care Philos 2005
Gert Helgesson, Linus Johnsson. Med Health Care Philos 2005
42
20
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
13
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
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
12
Informed consent in biobank research: a deliberative approach to the debate.
David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
12
Coding and consent: moral challenges of the database project in Iceland.
Vilhjalmur Arnason. Bioethics 2004
Vilhjalmur Arnason. Bioethics 2004
10
'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
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
10
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
9
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
20
Human genetic research, DNA banking and consent: a question of 'form'?
M Deschênes, G Cardinal, B M Knoppers, K C Glass. Clin Genet 2001
M Deschênes, G Cardinal, B M Knoppers, K C Glass. Clin Genet 2001
10
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
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
9
Solidarity and equity: new ethical frameworks for genetic databases.
R Chadwick, K Berg. Nat Rev Genet 2001
R Chadwick, K Berg. Nat Rev Genet 2001
9
Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion.
David Kaufman, Gail Geller, Lisa Leroy, Juli Murphy, Joan Scott, Kathy Hudson. Am J Med Genet C Semin Med Genet 2008
David Kaufman, Gail Geller, Lisa Leroy, Juli Murphy, Joan Scott, Kathy Hudson. Am J Med Genet C Semin Med Genet 2008
10
The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
9
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
9
Obtaining consent for future research with induced pluripotent cells: opportunities and challenges.
Katriina Aalto-Setälä, Bruce R Conklin, Bernard Lo. PLoS Biol 2009
Katriina Aalto-Setälä, Bruce R Conklin, Bernard Lo. PLoS Biol 2009
12
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
7
An empirical survey on biobanking of human genetic material and data in six EU countries.
Isabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, Jenny Duchier, Brigitte Jansen, Jürgen Simon, Paula Lobato De Faria, Anna Perez-Lezaun, Bert Visser, Garrath D Williams,[...]. Eur J Hum Genet 2003
Isabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, Jenny Duchier, Brigitte Jansen, Jürgen Simon, Paula Lobato De Faria, Anna Perez-Lezaun, Bert Visser, Garrath D Williams,[...]. Eur J Hum Genet 2003
7
Ethical issues in tissue banking for research: a brief review of existing organizational policies.
Keith Bauer, Sara Taub, Kayhan Parsi. Theor Med Bioeth 2004
Keith Bauer, Sara Taub, Kayhan Parsi. Theor Med Bioeth 2004
13
Securing our genetic health: engendering trust in UK Biobank.
Alan Petersen. Sociol Health Illn 2005
Alan Petersen. Sociol Health Illn 2005
14
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
12
Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issues, ownership, return of benefits. A professional perspective.
Béatrice Godard, Jörg Schmidtke, Jean-Jacques Cassiman, Ségolène Aymé. Eur J Hum Genet 2003
Béatrice Godard, Jörg Schmidtke, Jean-Jacques Cassiman, Ségolène Aymé. Eur J Hum Genet 2003
7
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
7
From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
7
National population-based biobanks for genetic research.
Helen Swede, Carol L Stone, Alyssa R Norwood. Genet Med 2007
Helen Swede, Carol L Stone, Alyssa R Norwood. Genet Med 2007
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.