A citation-based method for searching scientific literature

Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
Times Cited: 89







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



Times Cited
  Times     Co-cited
Similarity


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
165
15



From patients to partners: participant-centric initiatives in biomedical research.
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
157
12

Broad Consent for Research With Biological Samples: Workshop Conclusions.
Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M Fullerton, Hank Greely, Mats G Hansson, Sara Hull, Scott Kim,[...]. Am J Bioeth 2015
133
12

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
155
11

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
167
11

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
208
11

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
444
10


Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
90
10

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
227
10

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
296
10


Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
43
20

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
78
11

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
10


From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
215
8


Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
463
8

Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
121
8

Engaging the public on biobanks: outcomes of the BC biobank deliberation.
K C O'Doherty, M M Burgess. Public Health Genomics 2009
65
12

A review of the key issues associated with the commercialization of biobanks.
Timothy Caulfield, Sarah Burningham, Yann Joly, Zubin Master, Mahsa Shabani, Pascal Borry, Allan Becker, Michael Burgess, Kathryn Calder, Christine Critchley,[...]. J Law Biosci 2014
41
19


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
155
7

Research ethics. Research practice and participant preferences: the growing gulf.
S B Trinidad, S M Fullerton, E J Ludman, G P Jarvik, E B Larson, W Burke. Science 2011
66
10

Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
132
7

Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project.
Catherine A McCarty, Donna Chapman-Stone, Teresa Derfus, Philip F Giampietro, Norman Fost. Am J Med Genet A 2008
60
11


The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
101
7

Meeting the governance challenges of next-generation biorepository research.
Stephanie M Fullerton, Nicholas R Anderson, Greg Guzauskas, Dena Freeman, Kelly Fryer-Edwards. Sci Transl Med 2010
47
14

Biobanking: the foundation of personalized medicine.
Robert E Hewitt. Curr Opin Oncol 2011
161
7

Biobanking for better healthcare.
Peter H J Riegman, Manuel M Morente, Fay Betsou, Pasquale de Blasio, Peter Geary. Mol Oncol 2008
155
7

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
117
7


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
458
6

Connecting the public with biobank research: reciprocity matters.
Herbert Gottweis, George Gaskell, Johannes Starkbaum. Nat Rev Genet 2011
33
18

Biobank governance: heterogeneous modes of ordering and democratization.
Herbert Gottweis, Georg Lauss. J Community Genet 2012
20
30

Ethical norms and the international governance of genetic databases and biobanks: findings from an international study.
Alexander Morgan Capron, Alexandre Mauron, Bernice Simone Elger, Andrea Boggio, Agomoni Ganguli-Mitra, Nikola Biller-Andorno. Kennedy Inst Ethics J 2009
27
22

Power to the people: a wiki-governance model for biobanks.
Edward S Dove, Yann Joly, Bartha M Knoppers. Genome Biol 2012
24
25

Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
37
16

Study newsletters, community and ethics advisory boards, and focus group discussions provide ongoing feedback for a large biobank.
Catherine A McCarty, Ann Garber, Jonathan C Reeser, Norman C Fost. Am J Med Genet A 2011
32
18

Neglected ethical issues in biobank management: Results from a U.S. study.
R Jean Cadigan, Dragana Lassiter, Kaaren Haldeman, Ian Conlon, Erik Reavely, Gail E Henderson. Life Sci Soc Policy 2013
48
12

The Mayo Clinic Biobank: a building block for individualized medicine.
Janet E Olson, Euijung Ryu, Kiley J Johnson, Barbara A Koenig, Karen J Maschke, Jody A Morrisette, Mark Liebow, Paul Y Takahashi, Zachary S Fredericksen, Ruchi G Sharma,[...]. Mayo Clin Proc 2013
132
6

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
114
6

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
52
11


Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
76
7



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.