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



Robert Klitzman, Paul S Appelbaum, Wendy Chung. JAMA 2013
Times Cited: 61




List of shared articles



Times cited

Integrating Genomics into Psychiatric Practice: Ethical and Legal Challenges for Clinicians.
Eric T Ward, Kristin M Kostick, Gabriel Lázaro-Muñoz. Harv Rev Psychiatry 2019
4

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17

Improved ethical guidance for the return of results from psychiatric genomics research.
G Lázaro-Muñoz, M S Farrell, J J Crowley, D M Filmyer, R A Shaughnessy, R C Josiassen, P F Sullivan. Mol Psychiatry 2018
20

Which Results to Return: Subjective Judgments in Selecting Medically Actionable Genes.
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Anya E R Prince, R Jean Cadigan. Genet Test Mol Biomarkers 2017
14

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





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

The Advantages and Challenges of Testing Children for Heritable Predisposition to Cancer.
Chimene Kesserwan, Lainie Friedman Ross, Angela R Bradbury, Kim E Nichols. Am Soc Clin Oncol Educ Book 2016
14

Clinical exome performance for reporting secondary genetic findings.
Jason Y Park, Peter Clark, Eric Londin, Marialuisa Sponziello, Larry J Kricka, Paolo Fortina. Clin Chem 2015
24

Identification of Medically Actionable Secondary Findings in the 1000 Genomes.
Emily Olfson, Catherine E Cottrell, Nicholas O Davidson, Christina A Gurnett, Jonathan W Heusel, Nathan O Stitziel, Li-Shiun Chen, Sarah Hartz, Rakesh Nagarajan, Nancy L Saccone,[...]. PLoS One 2015
53

A protocol for the identification and validation of novel genetic causes of kidney disease.
Andrew Mallett, Chirag Patel, Barbara Maier, Julie McGaughran, Michael Gabbett, Minoru Takasato, Anne Cameron, Peter Trnka, Stephen I Alexander, Gopala Rangan,[...]. BMC Nephrol 2015
7

Management of Incidental Findings in Clinical Genomic Sequencing.
Joel B Krier, Robert C Green. Curr Protoc Hum Genet 2015
7

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