A citation-based method for searching scientific literature

Rihab Yassin, Nicole Lockhart, Mariana González del Riego, Karen Pitt, Jeffrey W Thomas, Linda Weiss, Carolyn Compton. Cancer Epidemiol Biomarkers Prev 2010
Times Cited: 33







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



Times Cited
  Times     Co-cited
Similarity


The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
24

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
49
21



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
174
15

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
15

Genetic research and biobanks.
Don Chalmers. Methods Mol Biol 2011
12
41

Biobanking for better healthcare.
Peter H J Riegman, Manuel M Morente, Fay Betsou, Pasquale de Blasio, Peter Geary. Mol Oncol 2008
156
15

Key elements of access policies for biorepositories associated with population science research.
Shannon M Lemrow, Graham A Colditz, Jimmie B Vaught, Patricia Hartge. Cancer Epidemiol Biomarkers Prev 2007
13
38

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
54
15

The evolution of biobanking best practices.
Jim Vaught, Nicole C Lockhart. Clin Chim Acta 2012
66
15

Stewardship practices of U.S. biobanks.
Gail E Henderson, Teresa P Edwards, R Jean Cadigan, Arlene M Davis, Catherine Zimmer, Ian Conlon, Bryan J Weiner. Sci Transl Med 2013
29
17

'Access arrangements' for biobanks: a fine line between facilitating and hindering collaboration.
S Fortin, S Pathmasiri, R Grintuch, M Deschênes. Public Health Genomics 2011
27
18

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
128
15

Biobanking past, present and future: responsibilities and benefits.
Yvonne G De Souza, John S Greenspan. AIDS 2013
116
15

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
28
14


Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
56
12

Developing a simplified consent form for biobanking.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. PLoS One 2010
60
12

Development of a large-scale de-identified DNA biobank to enable personalized medicine.
D M Roden, J M Pulley, M A Basford, G R Bernard, E W Clayton, J R Balser, D R Masys. Clin Pharmacol Ther 2008
544
12

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
105
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
156
12

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
96
12

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
12

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
204
12

International approaches to advancing biospecimen science.
Helen M Moore, Carolyn C Compton, Joseph Alper, Jimmie B Vaught. Cancer Epidemiol Biomarkers Prev 2011
46
12

Biological sample collection and processing for molecular epidemiological studies.
Nina T Holland, Martyn T Smith, Brenda Eskenazi, Maria Bastaki. Mutat Res 2003
160
12

Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
86
12

Personal medicine--the new banking crisis.
Christopher Thomas Scott, Timothy Caulfield, Emily Borgelt, Judy Illes. Nat Biotechnol 2012
57
12

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
105
12

An NCI perspective on creating sustainable biospecimen resources.
Jimmie Vaught, Joyce Rogers, Kimberly Myers, Mark David Lim, Nicole Lockhart, Helen Moore, Sherilyn Sawyer, Jeffrey L Furman, Carolyn Compton. J Natl Cancer Inst Monogr 2011
78
12

"That's a good question": university researchers' views on ownership and retention of human genetic specimens.
R Jean Cadigan, Michele M Easter, Allison W Dobson, Arlene M Davis, Barbra B Rothschild, Catherine Zimmer, Rene Sterling, Gail Henderson. Genet Med 2011
12
33

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
43
12

International Charter of principles for sharing bio-specimens and data.
Deborah Mascalzoni, Edward S Dove, Yaffa Rubinstein, Hugh J S Dawkins, Anna Kole, Pauline McCormack, Simon Woods, Olaf Riess, Franz Schaefer, Hanns Lochmüller,[...]. Eur J Hum Genet 2015
74
12

Towards a data sharing Code of Conduct for international genomic research.
Bartha Maria Knoppers, Jennifer R Harris, Anne Marie Tassé, Isabelle Budin-Ljøsne, Jane Kaye, Mylène Deschênes, Ma'n H Zawati. Genome Med 2011
65
12

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
122
12

Biospecimen "ownership": point.
Roberta B Ness. Cancer Epidemiol Biomarkers Prev 2007
11
27

Ownership and use of tissue specimens for research.
Rina Hakimian, David Korn. JAMA 2004
49
9

Genetic research on stored tissue samples from minors: a systematic review of the ethical literature.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. Am J Med Genet A 2009
34
9

Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study.
Philippe A Melas, Louise K Sjöholm, Tord Forsner, Maigun Edhborg, Niklas Juth, Yvonne Forsell, Catharina Lavebratt. J Med Ethics 2010
47
9





Research ethics. Children and population biobanks.
David Gurwitz, Isabel Fortier, Jeantine E Lunshof, Bartha Maria Knoppers. Science 2009
57
9



Principles of human subjects protections applied in an opt-out, de-identified biobank.
Jill Pulley, Ellen Clayton, Gordon R Bernard, Dan M Roden, Daniel R Masys. Clin Transl Sci 2010
144
9

Ethics and medical research in children.
Andrew J Davidson, Mike O'Brien. Paediatr Anaesth 2009
32
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.