A citation-based method for searching scientific literature

Laurent Castéra, Valentin Harter, Etienne Muller, Sophie Krieger, Nicolas Goardon, Agathe Ricou, Antoine Rousselin, Germain Paimparay, Angelina Legros, Olivia Bruet, Céline Quesnelle, Florian Domin, Chankannira San, Baptiste Brault, Robin Fouillet, Caroline Abadie, Odile Béra, Pascaline Berthet, Thierry Frébourg, Dominique Vaur. Genet Med 2018
Times Cited: 33



Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
Times Cited: 4661




List of shared articles



Times cited

HRness in Breast and Ovarian Cancers.
Elizabeth Santana Dos Santos, François Lallemand, Ambre Petitalot, Sandrine M Caputo, Etienne Rouleau. Int J Mol Sci 2020
5

Literature Review of BARD1 as a Cancer Predisposing Gene with a Focus on Breast and Ovarian Cancers.
Wejdan M Alenezi, Caitlin T Fierheller, Neil Recio, Patricia N Tonin. Genes (Basel) 2020
5

Non-Coding Variants in BRCA1 and BRCA2 Genes: Potential Impact on Breast and Ovarian Cancer Predisposition.
Elizabeth Santana Dos Santos, François Lallemand, Leslie Burke, Dominique Stoppa-Lyonnet, Melissa Brown, Sandrine M Caputo, Etienne Rouleau. Cancers (Basel) 2018
7

Comprehensive Functional Characterization and Clinical Interpretation of 20 Splice-Site Variants of the RAD51C Gene.
Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, Elena Bueno-Martínez, Patricia Llovet, Beatriz Díez-Gómez, María José Caloca, Pedro Pérez-Segura, Eugenia Fraile-Bethencourt, Marta Colmena, Sara Carvalho,[...]. Cancers (Basel) 2020
2

Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients.
Elisabeth Jarhelle, Hilde Monica Frostad Riise Stensland, Geir Åsmund Myge Hansen, Siri Skarsfjord, Christoffer Jonsrud, Monica Ingebrigtsen, Nina Strømsvik, Marijke Van Ghelue. Sci Rep 2019
4

BARD1 is A Low/Moderate Breast Cancer Risk Gene: Evidence Based on An Association Study of the Central European p.Q564X Recurrent Mutation.
Malwina Suszynska, Wojciech Kluzniak, Dominika Wokolorczyk, Anna Jakubowska, Tomasz Huzarski, Jacek Gronwald, Tadeusz Debniak, Marek Szwiec, Magdalena Ratajska, Katarzyna Klonowska,[...]. Cancers (Basel) 2019
14

FANCM regulates repair pathway choice at stalled replication forks.
Arvind Panday, Nicholas A Willis, Rajula Elango, Francesca Menghi, Erin E Duffey, Edison T Liu, Ralph Scully. Mol Cell 2021
0