CoCites: A citation-based method for searching scientific literature

BRCA1 and BRCA2: different roles in a common pathway of genome protection.

Rohini Roy, Jarin Chun, Simon N Powell. Nat Rev Cancer 2011
Times Cited: 791

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector, Karl Voelkerding, Heidi L Rehm. Genet Med 2015
Times Cited: 11756

List of shared articles

Times cited

Gastric cancer genetic predisposition and clinical presentations: Established heritable causes and potential candidate genes.
José Garcia-Pelaez, Rita Barbosa-Matos, Celina São José, Sónia Sousa, Irene Gullo, Nicoline Hoogerbrugge, Fátima Carneiro, Carla Oliveira. Eur J Med Genet 2022

Characterization of Synonymous BRCA1:c.132C>T as a Pathogenic Variant.
Jun Li, Ping Wang, Cuiyun Zhang, Sile Han, Han Xiao, Zhiyuan Liu, Xiaoyan Wang, Weiling Liu, Bing Wei, Jie Ma,[...]. Front Oncol 2022

Sequencing of BRCA1/2-alterations using NGS-based technology: annotation as a challenge.
Silvana Ebner, Ria Winkelmann, Saskia Martin, Jens Köllermann, Peter J Wild, Melanie Demes. Oncotarget 2022

The functional impact of BRCA1 BRCT domain variants using multiplexed DNA double-strand break repair assays.
Aleksandra I Adamovich, Mariame Diabate, Tapahsama Banerjee, Gregory Nagy, Nahum Smith, Kathryn Duncan, Erika Mendoza Mendoza, Gisselle Prida, Michael A Freitas, Lea M Starita,[...]. Am J Hum Genet 2022

Identification of deleterious variants of uncertain significance in BRCA2 BRC4 repeat through molecular dynamics simulations.
Siddharth Sinha, Zixin Qin, Benjamin Tam, San Ming Wang. Brief Funct Genomics 2022