A citation-based method for searching scientific literature


List of co-cited articles
64 articles co-cited >1



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
230
55

Informed consent and biobanks.
Ellen Wright Clayton. J Law Med Ethics 2005
58
44


Human genetic banking: altruism, benefit and consent.
Garrath Williams, Doris Schroeder. New Genet Soc 2004
25
44

Human genetic research, DNA banking and consent: a question of 'form'?
M Deschênes, G Cardinal, B M Knoppers, K C Glass. Clin Genet 2001
57
33


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
60
33

Ethical and policy issues in pediatric genetics.
Lainie Friedman Ross. Am J Med Genet C Semin Med Genet 2008
12
33

The consent problem within DNA biobanks.
Darren Shickle. Stud Hist Philos Biol Biomed Sci 2006
39
33


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
105
33

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
33


A human rights approach to an international code of conduct for genomic and clinical data sharing.
Bartha M Knoppers, Jennifer R Harris, Isabelle Budin-Ljøsne, Edward S Dove. Hum Genet 2014
48
33

Integration of DNA sample collection into a multi-site birth defects case-control study.
Sonja A Rasmussen, Edward J Lammer, Gary M Shaw, Richard H Finnell, Robert E McGehee, Margaret Gallagher, Paul A Romitti, Jeffrey C Murray. Teratology 2002
47
22

Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for Genetic Services.
B L Therrell, W H Hannon, K A Pass, F Lorey, C Brokopp, J Eckman, M Glass, R Heidenreich, S Kinney, S Kling,[...]. Biochem Mol Med 1996
96
22



Biobanking: international norms.
Bartha Maria Knoppers. J Law Med Ethics 2005
63
22


DNA testing, banking, and genetic privacy.
Patricia A Roche, George J Annas. N Engl J Med 2006
20
22

Population-based retrieval of newborn dried blood spots for researching paediatric cancer susceptibility genes.
Judith Klotz, Patricia Bryant, Homer B Wilcox, Mary Dillon, Bruce Wolf, Jerald Fagliano. Paediatr Perinat Epidemiol 2006
11
22




Minors and informed consent: a comparative approach.
Loes Stultiëns, Tom Goffin, Pascal Borry, Kris Dierickx, Herman Nys. Eur J Health Law 2007
36
22

Children's consent to research participation: social context and personal experience invalidate fixed cutoff rules.
Richard Ashcroft, Trudy Goodenough, Emma Williamson, Julie Kent. Am J Bioeth 2003
17
22

Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.
Ebony B Bookman, Aleisha A Langehorne, John H Eckfeldt, Kathleen C Glass, Gail P Jarvik, Michael Klag, Greg Koski, Arno Motulsky, Benjamin Wilfond, Teri A Manolio,[...]. Am J Med Genet A 2006
159
22

Biological sample collections from minors for genetic research: a systematic review of guidelines and position papers.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. Eur J Hum Genet 2009
33
22

Empirical data about women's attitudes towards a hypothetical pediatric biobank.
Alon B Neidich, Josh W Joseph, Carole Ober, Lainie Friedman Ross. Am J Med Genet A 2008
45
22

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
83
22

Alternative consent models for biobanks: the new Spanish law on biomedical research.
Antonio Casado da Rocha, José Antonio Seoane. Bioethics 2008
13
22

An empirical study of tissue banking in Australia: navigating regulatory and ethical challenges.
Georgina Clark, Wendy Lipworth, Bokey Les, J M Little, Ian H Kerridge. J Law Med 2006
4
50

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
81
22


Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
86
22


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
69
22

Governing UK Biobank: the importance of ensuring public trust.
Richard Tutton, Jane Kaye, Klaus Hoeyer. Trends Biotechnol 2004
31
22


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
138
22




Sample, data use and protection in biobanking in Europe: legal issues.
Eleni Zika, Tobias Schulte In den Bäumen, Jane Kaye, Angela Brand, Dolores Ibarreta. Pharmacogenomics 2008
24
22

Biobanking for Europe.
Martin Yuille, Gert-Jan van Ommen, Christian Bréchot, Anne Cambon-Thomsen, Georges Dagher, Ulf Landegren, Jan-Eric Litton, Markus Pasterk, Leena Peltonen, Mike Taussig,[...]. Brief Bioinform 2008
127
22

A legal framework for biobanking: the German experience.
Jürgen Simon, Rainer Paslack, Jürgen Robienski, David N Cooper, Jürgen W Goebel, Michael Krawczak. Eur J Hum Genet 2007
11
22

The regulation of biobanks in Spain.
Herman Nys, Geraldine Fobelets. Rev Derecho Genoma Hum 2008
5
40

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
184
22

National population-based biobanks for genetic research.
Helen Swede, Carol L Stone, Alyssa R Norwood. Genet Med 2007
51
22


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.