A citation-based method for searching scientific literature

Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng, Kelly A Frazer, Bruce Korf, David H Ledbetter, James R Lupski, Clay Marsh, David Mrazek, Michael F Murray, Peter H O'Donnell, Daniel J Rader, Mary V Relling, Alan R Shuldiner, David Valle, Richard Weinshilboum, Eric D Green, Geoffrey S Ginsburg. Genet Med 2013
Times Cited: 323

List of shared articles

Times cited

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.
Dean A Regier, Stuart J Peacock, Reka Pataky, Kimberly van der Hoek, Gail P Jarvik, Jeffrey Hoch, David Veenstra. CMAJ 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

The unintended implications of blurring the line between research and clinical care in a genomic age.
Benjamin E Berkman, Sara Chandros Hull, Lisa Eckstein. Per Med 2014

Do physicians think genomic medicine will be useful for patient care?
Sridharan Raghavan, Jason L Vassy. Per Med 2014

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

Massively parallel sequencing: the new frontier of hematologic genomics.
Jill M Johnsen, Deborah A Nickerson, Alex P Reiner. Blood 2013

Ethical, legal, and social implications of incorporating genomic information into electronic health records.
Ribhi Hazin, Kyle B Brothers, Bradley A Malin, Barbara A Koenig, Saskia C Sanderson, Mark A Rothstein, Marc S Williams, Ellen W Clayton, Iftikhar J Kullo. Genet Med 2013