A citation-based method for searching scientific literature

E A Whitley, N Kanellopoulou, J Kaye. Public Health Genomics 2012
Times Cited: 26







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



Times Cited
  Times     Co-cited
Similarity


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
120
26

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
213
26

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
64
23

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
469
23

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
159
19

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
39
19


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
19

Researchers' opinions towards the communication of results of biobank research: a survey study.
Tineke M Meulenkamp, Sjef J K Gevers, Jasper A Bovenberg, Ellen M A Smets. Eur J Hum Genet 2012
12
41

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
15

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
229
15

Personal privacy, public benefits, and biobanks: a conjoint analysis of policy priorities and public perceptions.
Daryl Pullman, Holly Etchegary, Katherine Gallagher, Kathleen Hodgkinson, Montgomery Keough, David Morgan, Catherine Street. Genet Med 2012
35
15

A solidarity-based approach to the governance of research biobanks.
Barbara Prainsack, Alena Buyx. Med Law Rev 2013
39
15

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
81
15

Power to the people: a wiki-governance model for biobanks.
Edward S Dove, Yann Joly, Bartha M Knoppers. Genome Biol 2012
24
12


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
11


Challenges in creating an opt-in biobank with a registrar-based consent process and a commercial EHR.
Keith Marsolo, Jeremy Corsmo, Michael G Barnes, Carrie Pollick, Jamie Chalfin, Jeremy Nix, Christopher Smith, Rajesh Ganta. J Am Med Inform Assoc 2012
18
16

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
11

Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European countries.
Elena Salvaterra, Roberto Giorda, Maria T Bassi, Renato Borgatti, Lisbeth E Knudsen, Andrea Martinuzzi, Maria Nobile, Uberto Pozzoli, Gian P Ramelli, Gianl L Reni,[...]. Biopreserv Biobank 2012
15
20

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
463
11

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
Catherine A McCarty, Rex L Chisholm, Christopher G Chute, Iftikhar J Kullo, Gail P Jarvik, Eric B Larson, Rongling Li, Daniel R Masys, Marylyn D Ritchie, Dan M Roden,[...]. BMC Med Genomics 2011
446
11

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
11

Biobanking for research: a survey of patient population attitudes and understanding.
Alanna Kulchak Rahm, Michelle Wrenn, Nikki M Carroll, Heather Spencer Feigelson. J Community Genet 2013
54
11

Assessing the need for a standardized cancer HUman Biobank (caHUB): findings from a national survey with cancer researchers.
Holly A Massett, Nancy L Atkinson, Deanne Weber, Renate Myles, Colleen Ryan, Meredith Grady, Carolyn Compton. J Natl Cancer Inst Monogr 2011
40
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
448
11

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
92
11

Testing an online, dynamic consent portal for large population biobank research.
Daniel B Thiel, Jodyn Platt, Tevah Platt, Susan B King, Nicole Fisher, Robert Shelton, Sharon L R Kardia. Public Health Genomics 2015
25
12

Research ethics: Treat donors as partners in biobank research.
Krishanu Saha, J Benjamin Hurlbut. Nature 2011
27
7

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
53
7

DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
69
7

Ethical endgames: broad consent for narrow interests; open consent for closed minds.
Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm. Camb Q Healthc Ethics 2011
18
11

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
7

Written informed consent and selection bias in observational studies using medical records: systematic review.
Michelle E Kho, Mark Duffett, Donald J Willison, Deborah J Cook, Melissa C Brouwers. BMJ 2009
121
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
83
7

The policies of ethics committees in the management of biobanks used for research: an Italian survey.
Corinna Porteri, Elena Togni, Patrizio Pasqualetti. Eur J Hum Genet 2014
4
50


New models for large prospective studies: is there a better way?
Teri A Manolio, Brenda K Weis, Catherine C Cowie, Robert N Hoover, Kathy Hudson, Barnett S Kramer, Chris Berg, Rory Collins, Wendy Ewart, J Michael Gaziano,[...]. Am J Epidemiol 2012
72
7

Genetics. Genomic research and human subject privacy.
Zhen Lin, Art B Owen, Russ B Altman. Science 2004
179
7

Ethics. Identifiability in genomic research.
William W Lowrance, Francis S Collins. Science 2007
112
7


For what am I participating? The need for communication after receiving consent from biobanking project participants: experience in Japan.
Maiko Watanabe, Yusuke Inoue, Chiungfang Chang, Hyunsoo Hong, Izumi Kobayashi, Satoshi Suzuki, Kaori Muto. J Hum Genet 2011
18
11

The privacy-reciprocity connection in biobanking: comparing German with UK strategies.
A Hobbs, J Starkbaum, U Gottweis, H E Wichmann, H Gottweis. Public Health Genomics 2012
26
7

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
169
7

Biobank research: who benefits from individual consent?
Joanna Stjernschantz Forsberg, Mats G Hansson, Stefan Eriksson. BMJ 2011
18
11

Dynamic consent in the digital age of biology: online initiatives and regulatory considerations.
Richman Wee, Mark Henaghan, Ingrid Winship. J Prim Health Care 2013
10
20

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
61
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.