A citation-based method for searching scientific literature

Karen J Maschke. Nat Biotechnol 2005
Times Cited: 35







List of co-cited articles
133 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
232
34



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
158
22


Biobanking: international norms.
Bartha Maria Knoppers. J Law Med Ethics 2005
63
20


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
140
17

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
185
17




Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
137
14

Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
56
14

The consent problem within DNA biobanks.
Darren Shickle. Stud Hist Philos Biol Biomed Sci 2006
39
14




National population-based biobanks for genetic research.
Helen Swede, Carol L Stone, Alyssa R Norwood. Genet Med 2007
52
14

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
71
11

Genetics. Genomic research and human subject privacy.
Zhen Lin, Art B Owen, Russ B Altman. Science 2004
183
11

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
11

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
11


Genebanks: a comparison of eight proposed international genetic databases.
Melissa A Austin, Sarah Harding, Courtney McElroy. Community Genet 2003
55
11


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
202
11


DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
70
11


Informed consent and biobanks.
Ellen Wright Clayton. J Law Med Ethics 2005
58
11

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
11

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
65
11

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
219
11




The Babel of genetic data terminology.
Bartha Maria Knoppers, Madelaine Saginur. Nat Biotechnol 2005
41
8

Tumour banks: well-guarded treasures in the interest of patients.
J Wolter Oosterhuis, Jan Willem Coebergh, Evert-Ben van Veen. Nat Rev Cancer 2003
115
8



When two tribes go to war.
Rex Dalton. Nature 2004
46
8

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
223
8




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
162
8


Obligations in offering to disclose genetic research results.
Conrad V Fernandez, Charles Weijer. Am J Bioeth 2006
28
10

Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
75
8


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.