A citation-based method for searching scientific literature

Christopher A Cassa, Sarah K Savage, Patrick L Taylor, Robert C Green, Amy L McGuire, Kenneth D Mandl. Genome Res 2012
Times Cited: 70

List of shared articles

Times cited

A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.
Eliseos J Mucaki, Natasha G Caminsky, Ami M Perri, Ruipeng Lu, Alain Laederach, Matthew Halvorsen, Joan H M Knoll, Peter K Rogan. BMC Med Genomics 2016

How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples.
Sumit Middha, Noralane M Lindor, Shannon K McDonnell, Janet E Olson, Kiley J Johnson, Eric D Wieben, Gianrico Farrugia, James R Cerhan, Stephen N Thibodeau. Front Genet 2015

Views of genetics health professionals on the return of genomic results.
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014

Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014

Self-guided management of exome and whole-genome sequencing results: changing the results return model.
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet Med 2013