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

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, Fergus J Couch, David E Goldgar. Hum Mutat 2012
Times Cited: 177

List of shared articles

Times cited

Understanding of BRCA VUS genetic results by breast cancer specialists.
B K Eccles, E Copson, T Maishman, J E Abraham, D M Eccles. BMC Cancer 2015

Classification and Clinical Management of Variants of Uncertain Significance in High Penetrance Cancer Predisposition Genes.
Setareh Moghadasi, Diana M Eccles, Peter Devilee, Maaike P G Vreeswijk, Christi J van Asperen. Hum Mutat 2016

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

Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.
Giovana T Torrezan, Fernanda G Dos Santos R de Almeida, Márcia C P Figueiredo, Bruna D de Figueiredo Barros, Cláudia A A de Paula, Renan Valieris, Jorge E S de Souza, Rodrigo F Ramalho, Felipe C C da Silva, Elisa N Ferreira,[...]. Front Genet 2018

Comprehensive analysis and ACMG-based classification of CHEK2 variants in hereditary cancer patients.
Gardenia Vargas-Parra, Jesús Del Valle, Paula Rofes, Mireia Gausachs, Agostina Stradella, José M Moreno-Cabrera, Angela Velasco, Eva Tornero, Mireia Menéndez, Xavier Muñoz,[...]. Hum Mutat 2020

Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?
Jae Yeon Cheon, Jessica Mozersky, Robert Cook-Deegan. Genome Med 2014