AUTHOR=Glentis Stavros , Dimopoulos Alexandros C. , Rouskas Konstantinos , Ntritsos George , Evangelou Evangelos , Narod Steven A. , Mes-Masson Anne-Marie , Foulkes William D. , Rivera Barbara , Tonin Patricia N. , Ragoussis Jiannis , Dimas Antigone S. TITLE=Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer JOURNAL=Frontiers in Genetics VOLUME=10 YEAR=2019 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2019.01005 DOI=10.3389/fgene.2019.01005 ISSN=1664-8021 ABSTRACT=
Approximately 10% of breast cancer (BC) cases are hereditary BC (HBC), with HBC most commonly encountered in the context of hereditary breast and ovarian cancer (HBOC) syndrome. Although thousands of loss-of-function (LoF) alleles in over 20 genes have been associated with HBC susceptibility, the genetic etiology of approximately 50% of cases remains unexplained, even when polygenic risk models are considered. We focused on one of the least-studied European populations and applied whole-exome sequencing (WES) to 52 individuals from 17 Greek HBOC families, in which at least one patient was negative for known HBC risk variants. Initial screening revealed pathogenic variants in known cancer genes, including