M G Hansson. Br J Cancer 2009
Times Cited: 107
Times Cited: 107
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
27
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
24
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
16
Ethical aspects of human biobanks: a systematic review.
Danijela Budimir, Ozren Polasek, Ana Marusić, Ivana Kolcić, Tatijana Zemunik, Vesna Boraska, Ana Jeroncić, Mladen Boban, Harry Campbell, Igor Rudan. Croat Med J 2011
Danijela Budimir, Ozren Polasek, Ana Marusić, Ivana Kolcić, Tatijana Zemunik, Vesna Boraska, Ana Jeroncić, Mladen Boban, Harry Campbell, Igor Rudan. Croat Med J 2011
26
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
13
The social and ethical issues of post-genomic human biobanks.
Anne Cambon-Thomsen. Nat Rev Genet 2004
Anne Cambon-Thomsen. Nat Rev Genet 2004
13
Banking together. A unified model of informed consent for biobanking.
Elena Salvaterra, Lucilla Lecchi, Silvia Giovanelli, Barbara Butti, Maria Teresa Bardella, Pier Alberto Bertazzi, Silvano Bosari, Guido Coggi, Domenico A Coviello, Faustina Lalatta,[...]. EMBO Rep 2008
Elena Salvaterra, Lucilla Lecchi, Silvia Giovanelli, Barbara Butti, Maria Teresa Bardella, Pier Alberto Bertazzi, Silvano Bosari, Guido Coggi, Domenico A Coviello, Faustina Lalatta,[...]. EMBO Rep 2008
19
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
16
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
18
The Havasupai Indian tribe case--lessons for research involving stored biologic samples.
Michelle M Mello, Leslie E Wolf. N Engl J Med 2010
Michelle M Mello, Leslie E Wolf. N Engl J Med 2010
11
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
11
Biobanking for better healthcare.
Peter H J Riegman, Manuel M Morente, Fay Betsou, Pasquale de Blasio, Peter Geary. Mol Oncol 2008
Peter H J Riegman, Manuel M Morente, Fay Betsou, Pasquale de Blasio, Peter Geary. Mol Oncol 2008
10
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
10
Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
10
"Broad" consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose.
Carlo Petrini. Soc Sci Med 2010
Carlo Petrini. Soc Sci Med 2010
14
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
10
Biobanking past, present and future: responsibilities and benefits.
Yvonne G De Souza, John S Greenspan. AIDS 2013
Yvonne G De Souza, John S Greenspan. AIDS 2013
10
Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results.
Joanna Stjernschantz Forsberg, Mats G Hansson, Stefan Eriksson. Eur J Hum Genet 2009
Joanna Stjernschantz Forsberg, Mats G Hansson, Stefan Eriksson. Eur J Hum Genet 2009
15
Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
9
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
8
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
8
Engaging the public on biobanks: outcomes of the BC biobank deliberation.
K C O'Doherty, M M Burgess. Public Health Genomics 2009
K C O'Doherty, M M Burgess. Public Health Genomics 2009
11
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
8
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
7
Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study.
Linus Johnsson, Mats G Hansson, Stefan Eriksson, Gert Helgesson. BMJ 2008
Linus Johnsson, Mats G Hansson, Stefan Eriksson, Gert Helgesson. BMJ 2008
15
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
16
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
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
7
Potential harms, anonymization, and the right to withdraw consent to biobank research.
Stefan Eriksson, Gert Helgesson. Eur J Hum Genet 2005
Stefan Eriksson, Gert Helgesson. Eur J Hum Genet 2005
10
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
10
Research ethics. Children and population biobanks.
David Gurwitz, Isabel Fortier, Jeantine E Lunshof, Bartha Maria Knoppers. Science 2009
David Gurwitz, Isabel Fortier, Jeantine E Lunshof, Bartha Maria Knoppers. Science 2009
11
Developing a simplified consent form for biobanking.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. PLoS One 2010
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. PLoS One 2010
11
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
7
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
7
Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
7
Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
12
The UK Biobank sample handling and storage validation studies.
Tim C Peakman, Paul Elliott. Int J Epidemiol 2008
Tim C Peakman, Paul Elliott. Int J Epidemiol 2008
6
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
6
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
6
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
7
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
7
Coding and consent: moral challenges of the database project in Iceland.
Vilhjalmur Arnason. Bioethics 2004
Vilhjalmur Arnason. Bioethics 2004
7
Integrating biobanks: addressing the practical and ethical issues to deliver a valuable tool for cancer research.
R William G Watson, Elaine W Kay, David Smith. Nat Rev Cancer 2010
R William G Watson, Elaine W Kay, David Smith. Nat Rev Cancer 2010
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
6
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.