A citation-based method for searching scientific literature

Effy Vayena, Urs Gasser. PLoS Med 2016
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
475
19

Privacy Risks from Genomic Data-Sharing Beacons.
Suyash S Shringarpure, Carlos D Bustamante. Am J Hum Genet 2015
80
14


Public's attitudes on participation in a biobank for research: an Italian survey.
Corinna Porteri, Patrizio Pasqualetti, Elena Togni, Michael Parker. BMC Med Ethics 2014
33
14

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
145
14

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
95
14


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
171
14

Enterprising or altruistic selves? Making up research subjects in genetics research.
Richard Tutton, Barbara Prainsack. Sociol Health Illn 2011
21
9

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
451
9


Redefining genomic privacy: trust and empowerment.
Yaniv Erlich, James B Williams, David Glazer, Kenneth Yocum, Nita Farahany, Maynard Olson, Arvind Narayanan, Lincoln D Stein, Jan A Witkowski, Robert C Kain. PLoS Biol 2014
50
9

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
9

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
9



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
98
9

Balancing Benefits and Risks of Immortal Data: Participants' Views of Open Consent in the Personal Genome Project.
Oscar A Zarate, Julia Green Brody, Phil Brown, Mónica D Ramirez-Andreotta, Laura Perovich, Jacob Matz. Hastings Cent Rep 2016
14
14

Human Genome Project: Twenty-five years of big biology.
Eric D Green, James D Watson, Francis S Collins. Nature 2015
89
9

Willingness to donate blood samples for genetic research: a survey from a community in Singapore.
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
55
9

Toward a roadmap in global biobanking for health.
Jennifer R Harris, Paul Burton, Bartha Maria Knoppers, Klaus Lindpaintner, Marianna Bledsoe, Anthony J Brookes, Isabelle Budin-Ljøsne, Rex Chisholm, David Cox, Mylène Deschênes,[...]. Eur J Hum Genet 2012
84
9

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
56
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
54
9


Towards a data sharing culture: recommendations for leadership from academic health centers.
Heather A Piwowar, Michael J Becich, Howard Bilofsky, Rebecca S Crowley. PLoS Med 2008
63
9

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
9

Genetics. Genomic research and human subject privacy.
Zhen Lin, Art B Owen, Russ B Altman. Science 2004
181
9

The NCBI dbGaP database of genotypes and phenotypes.
Matthew D Mailman, Michael Feolo, Yumi Jin, Masato Kimura, Kimberly Tryka, Rinat Bagoutdinov, Luning Hao, Anne Kiang, Justin Paschall, Lon Phan,[...]. Nat Genet 2007
672
9

Found your DNA on the web: reconciling privacy and progress.
Amy Gutmann, James W Wagner. Hastings Cent Rep 2013
11
18


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
9

Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes.
Brian H Shirts, Angela Jacobson, Gail P Jarvik, Brian L Browning. Genet Med 2014
15
13

The First Amendment Right to Speak About the Human Genome.
Barbara J Evans. Univ Pa J Const Law 2014
13
15


The FDA and genomic tests--getting regulation right.
Barbara J Evans, Wylie Burke, Gail P Jarvik. N Engl J Med 2015
57
9

Ownership of medical information.
Mark A Hall, Kevin A Schulman. JAMA 2009
23
9


An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
281
9





Unpatients-why patients should own their medical data.
Leonard J Kish, Eric J Topol. Nat Biotechnol 2015
33
9

Broad data sharing in genetic research: views of institutional review board professionals.
Amy A Lemke, Maureen E Smith, Wendy A Wolf, Susan Brown Trinidad. IRB 2011
12
16

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
136
9

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
9


Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
159
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.