A citation-based method for searching scientific literature

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: 324



Sharon E Plon, Diana M Eccles, Douglas Easton, William D Foulkes, Maurizio Genuardi, Marc S Greenblatt, Frans B L Hogervorst, Nicoline Hoogerbrugge, Amanda B Spurdle, Sean V Tavtigian. Hum Mutat 2008
Times Cited: 542




List of shared articles



Times cited

Germline testing for homologous recombination repair genes-opportunities and challenges.
Steffen Hirsch, Laura Gieldon, Christian Sutter, Nicola Dikow, Christian P Schaaf. Genes Chromosomes Cancer 2021
2

Genomic profiling in oncology clinical practice.
N Rodríguez, D Viñal, J Rodríguez-Cobos, J De Castro, G Domínguez. Clin Transl Oncol 2020
2

Male Breast Cancer: Results of the Application of Multigene Panel Testing to an Italian Cohort of Patients.
Gianluca Tedaldi, Michela Tebaldi, Valentina Zampiga, Ilaria Cangini, Francesca Pirini, Elisa Ferracci, Rita Danesi, Valentina Arcangeli, Mila Ravegnani, Giovanni Martinelli,[...]. Diagnostics (Basel) 2020
4

Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families.
Anna Coppa, Arianna Nicolussi, Sonia D'Inzeo, Carlo Capalbo, Francesca Belardinilli, Valeria Colicchia, Marialaura Petroni, Massimo Zani, Sergio Ferraro, Christian Rinaldi,[...]. Cancer Med 2018
16

Accurate classification of BRCA1 variants with saturation genome editing.
Gregory M Findlay, Riza M Daza, Beth Martin, Melissa D Zhang, Anh P Leith, Molly Gasperini, Joseph D Janizek, Xingfan Huang, Lea M Starita, Jay Shendure. Nature 2018
218

Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group.
Sarah M Nielsen, Diana M Eccles, Iris L Romero, Fahd Al-Mulla, Judith Balmaña, Michela Biancolella, Rien Bslok, Maria Adelaide Caligo, Mariarosaria Calvello, Gabriele Lorenzo Capone,[...]. JCO Precis Oncol 2018
12

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas.
Rodrigo A Toledo, Nelly Burnichon, Alberto Cascon, Diana E Benn, Jean-Pierre Bayley, Jenny Welander, Carli M Tops, Helen Firth, Trish Dwight, Tonino Ercolino,[...]. Nat Rev Endocrinol 2017
113

Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
Gianluca Tedaldi, Michela Tebaldi, Valentina Zampiga, Rita Danesi, Valentina Arcangeli, Mila Ravegnani, Ilaria Cangini, Francesca Pirini, Elisabetta Petracci, Andrea Rocca,[...]. Oncotarget 2017
42