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



C Sue Richards, Sherri Bale, Daniel B Bellissimo, Soma Das, Wayne W Grody, Madhuri R Hegde, Elaine Lyon, Brian E Ward. Genet Med 2008
Times Cited: 512




List of shared articles



Times cited


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
14

Understanding and interpretation of a variant of uncertain significance (VUS) genetic test result by pediatric providers who do not specialize in genetics.
Chelsea Menke, Chinmayee B Nagaraj, Brian Dawson, Hua He, Sanjukta Tawde, Emily G Wakefield. J Genet Couns 2021
0

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
0

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
53

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