A citation-based method for searching scientific literature

David Wendler. Hastings Cent Rep 2013
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


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
107
63

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
76
45

A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur. J. Hum. Genet. 2013
46
27

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
156
18

Public attitudes regarding the use of electronic health information and residual clinical tissues for research.
Jeffrey R Botkin, Erin Rothwell, Rebecca Anderson, Louisa A Stark, Joyce Mitchell.  2014
17
18

Respecting donors to biobank research.
Tom Tomlinson. Hastings Cent Rep 2013
15
18

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
191
18

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
128
18

Assessing the quality of democratic deliberation: a case study of public deliberation on the ethics of surrogate consent for research.
Raymond De Vries, Aimee Stanczyk, Ian F Wall, Rebecca Uhlmann, Laura J Damschroder, Scott Y Kim. Soc Sci Med 2010
30
18

Implementing a public deliberative forum.
Kieran O'Doherty, François-Pierre Gauvin, Colleen Grogan, Will Friedman. Hastings Cent Rep 2012
12
18

DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
67
18

Deliberative Discussion Focus Groups.
Erin Rothwell, Rebecca Anderson, Jeffrey R Botkin. Qual Health Res 2016
15
18

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
76
18

Genetics. No longer de-identified.
Amy L McGuire, Richard A Gibbs. Science 2006
105
18

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
48
18


Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am. J. Hum. Genet. 2017
56
18

Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
Laura M Beskow, Carrie B Dombeck, Cole P Thompson, J Kemp Watson-Ormond, Kevin P Weinfurt. Genet. Med. 2015
35
18

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
23
18


Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
93
9


Phylogenetic relationships of dengue-2 viruses.
J A Lewis, G J Chang, R S Lanciotti, R M Kinney, L W Mayer, D W Trent. Virology 1993
105
9

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
130
9

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
74
9


Biobanking: shifting the analogy from consent to surrogacy.
Ann M Mongoven, Stephanie Solomon. Genet. Med. 2012
8
12




Advocacy groups as research organizations: the PXE International example.
Sharon F Terry, Patrick F Terry, Katherine A Rauen, Jouni Uitto, Lionel G Bercovitch. Nat. Rev. Genet. 2007
87
9

Dynamic consent in the digital age of biology: online initiatives and regulatory considerations.
Richman Wee, Mark Henaghan, Ingrid Winship. J Prim Health Care 2013
4
25

The prevalence of hepatitis C virus infection in the United States, 1988 through 1994.
M J Alter, D Kruszon-Moran, O V Nainan, G M McQuillan, F Gao, L A Moyer, R A Kaslow, H S Margolis. N. Engl. J. Med. 1999
9

Two large-scale surveys on community attitudes toward an opt-out biobank.
Kyle B Brothers, Daniel R Morrison, Ellen W Clayton. Am. J. Med. Genet. A 2011
44
9

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
55
9


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
122
9

Biobanks containing clinical specimens: defining characteristics, policies, and practices.
Teresa Edwards, R Jean Cadigan, James P Evans, Gail E Henderson. Clin. Biochem. 2014
17
9

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
88
9

Long-term mortality after transfusion-associated non-A, non-B hepatitis. The National Heart, Lung, and Blood Institute Study Group.
L B Seeff, Z Buskell-Bales, E C Wright, S J Durako, H J Alter, F L Iber, F B Hollinger, G Gitnick, R G Knodell, R P Perrillo. N. Engl. J. Med. 1992
457
9



Parental Perspectives on a Pediatric Human Non-Subjects Biobank.
Kyle B Brothers, Ellen Wright Clayton.  2012
18
9

Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke.  2012
32
9

Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur. J. Hum. Genet. 2013
45
9

Genomic databases access agreements: legal validity and possible sanctions.
Yann Joly, Nik Zeps, Bartha M Knoppers. Hum. Genet. 2011
18
9

Community engagement in biobanking: Experiences from the eMERGE Network.
Amy A Lemke, Joel T Wu, Carol Waudby, Jill Pulley, Carol P Somkin, Susan Brown Trinidad.  2010
27
9

Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
45
9

Towards an understanding of British public attitudes concerning human cloning.
Richard Shepherd, Julie Barnett, Helen Cooper, Adrian Coyle, Jo Moran-Ellis, Victoria Senior, Chris Walton. Soc Sci Med 2007
13
9

Autoantibodies predate the onset of systemic lupus erythematosus in northern Sweden.
Catharina Eriksson, Heidi Kokkonen, Martin Johansson, Göran Hallmans, Göran Wadell, Solbritt Rantapää-Dahlqvist. Arthritis Res. Ther. 2011
97
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.