A citation-based method for searching scientific literature

Sharon E Plon, H Paul Cooper, Bethany Parks, Shweta U Dhar, P Adam Kelly, Armin D Weinberg, Stephanie Staggs, Tao Wang, Susan Hilsenbeck. Genet Med 2011
Times Cited: 77



Tom Walsh, Ming K Lee, Silvia Casadei, Anne M Thornton, Sunday M Stray, Christopher Pennil, Alex S Nord, Jessica B Mandell, Elizabeth M Swisher, Mary-Claire King. Proc Natl Acad Sci U S A 2010
Times Cited: 321




List of shared articles



Times cited

Breast Cancer Risk Assessment: Moving Beyond BRCA 1 and 2.
Jennifer Scalia-Wilbur, Bradley L Colins, Richard T Penson, Don S Dizon. Semin Radiat Oncol 2016
9

Advances in the diagnosis of hereditary kidney cancer: Initial results of a multigene panel test.
Kevin A Nguyen, Jamil S Syed, Carin R Espenschied, Holly LaDuca, Ansh M Bhagat, Alfredo Suarez-Sarmiento, Timothy K O'Rourke, Karina L Brierley, Erin W Hofstatter, Brian Shuch. Cancer 2017
20

ENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes.
Amanda B Spurdle, Sue Healey, Andrew Devereau, Frans B L Hogervorst, Alvaro N A Monteiro, Katherine L Nathanson, Paolo Radice, Dominique Stoppa-Lyonnet, Sean Tavtigian, Barbara Wappenschmidt,[...]. Hum Mutat 2012
177


Application of Panel-Based Tests for Inherited Risk of Cancer.
Payal D Shah, Katherine L Nathanson. Annu Rev Genomics Hum Genet 2017
21

Multiplex genetic testing for cancer susceptibility: out on the high wire without a net?
Susan M Domchek, Angela Bradbury, Judy E Garber, Kenneth Offit, Mark E Robson. J Clin Oncol 2013
155

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes.
J M Eggington, K R Bowles, K Moyes, S Manley, L Esterling, S Sizemore, E Rosenthal, A Theisen, J Saam, C Arnell,[...]. Clin Genet 2014
113