A citation-based method for searching scientific literature

Amy L McGuire, Steven Joffe, Barbara A Koenig, Barbara B Biesecker, Laurence B McCullough, Jennifer S Blumenthal-Barby, Timothy Caulfield, Sharon F Terry, Robert C Green. Science 2013
Times Cited: 128



Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
Times Cited: 122




List of shared articles



Times cited

Personal genomic screening: How best to facilitate preparedness of future clients.
Jane Fleming, Bronwyn Terrill, Marie Dziadek, Edwin P Kirk, Tony Roscioli, Kristine Barlow-Stewart. Eur J Med Genet 2019
1

Effect of Public Deliberation on Attitudes toward Return of Secondary Results in Genomic Sequencing.
Michele C Gornick, Aaron M Scherer, Erica J Sutton, Kerry A Ryan, Nicole L Exe, Ming Li, Wendy R Uhlmann, Scott Y H Kim, J Scott Roberts, Raymond G De Vries. J Genet Couns 2017
13

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
71

Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.
Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
12

Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium.
Michael D Linderman, Daiva E Nielsen, Robert C Green. J Pers Med 2016
30

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Robert C Green, Katrina A B Goddard, Gail P Jarvik, Laura M Amendola, Paul S Appelbaum, Jonathan S Berg, Barbara A Bernhardt, Leslie G Biesecker, Sawona Biswas, Carrie L Blout,[...]. Am J Hum Genet 2016
97

Research participants in NGS studies want to know about incidental findings.
Anne Marie Jelsig, Niels Qvist, Klaus Brusgaard, Lilian Bomme Ousager. Eur J Hum Genet 2015
21



Patients' views on incidental findings from clinical exome sequencing.
Kristin E Clift, Colin M E Halverson, Alexander S Fiksdal, Ashok Kumbamu, Richard R Sharp, Jennifer B McCormick. Appl Transl Genom 2015
57

Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
Brooke L Levenseller, Danielle J Soucier, Victoria A Miller, Diana Harris, Laura Conway, Barbara A Bernhardt. J Genet Couns 2014
53

Whole genome sequencing as a diagnostic test: challenges and opportunities.
Caitlin C Chrystoja, Eleftherios P Diamandis. Clin Chem 2014
45

Managing incidental genomic findings in clinical trials: fulfillment of the principle of justice.
Rafael Dal-RĂ©, Nicholas Katsanis, Sara Katsanis, Lisa S Parker, Carmen Ayuso. PLoS Med 2014
10