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: 130

List of shared articles

Times cited

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

Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities.
Chiara Di Resta, Silvia Galbiati, Paola Carrera, Maurizio Ferrari. EJIFCC 2018

Ethical considerations surrounding germline next-generation sequencing of children with cancer.
Liza-Marie Johnson, Kayla V Hamilton, Jessica M Valdez, Esther Knapp, Justin N Baker, Kim E Nichols. Expert Rev Mol Diagn 2017

Exome sequencing explained: a practical guide to its clinical application.
Eleanor G Seaby, Reuben J Pengelly, Sarah Ennis. Brief Funct Genomics 2016

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

The translational potential of research on the ethical, legal, and social implications of genomics.
Wylie Burke, Paul Appelbaum, Lauren Dame, Patricia Marshall, Nancy Press, Reed Pyeritz, Richard Sharp, Eric Juengst. Genet Med 2015

Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.
J A Anderson, R Z Hayeems, C Shuman, M J Szego, N Monfared, S Bowdin, R Zlotnik Shaul, M S Meyn. Clin Genet 2015

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

Towards a European consensus for reporting incidental findings during clinical NGS testing.
Jayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, Conny van Ravenswaaij-Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon-Thomsen, Philippos Patsalis, Joris Vermeesch,[...]. Eur J Hum Genet 2015

Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Marcia Van Riper, Rebecca L Walker, Eric T Juengst. Am J Bioeth 2015

Good laboratory practice for clinical next-generation sequencing informatics pipelines.
Amy S Gargis, Lisa Kalman, David P Bick, Cristina da Silva, David P Dimmock, Birgit H Funke, Sivakumar Gowrisankar, Madhuri R Hegde, Shashikant Kulkarni, Christopher E Mason,[...]. Nat Biotechnol 2015

Genomics in the clinic: ethical and policy challenges in clinical next-generation sequencing programs at early adopter USA institutions.
Lauren C Milner, Nanibaa' A Garrison, Mildred K Cho, Russ B Altman, Louanne Hudgins, Stephen J Galli, Henry J Lowe, Iris Schrijver, David C Magnus. Per Med 2015

Genomic test validation for incidental findings.
Jason Y Park, Paolo Fortina, Larry J Kricka. Clin Chem 2014

Cancer genomics and inherited risk.
Zsofia K Stadler, Kasmintan A Schrader, Joseph Vijai, Mark E Robson, Kenneth Offit. J Clin Oncol 2014

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

Grappling with genomic incidental findings in the clinical realm.
Sara Chandros Hull, Benjamin E Berkman. Chest 2014