Cargando…
Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases
Not all familial ovarian cancer (OC) cases are explained by pathogenic germline variants in known risk genes. A candidate gene approach involving DNA repair pathway genes was applied to identify rare recurring pathogenic variants in familial OC cases not associated with known OC risk genes from a po...
Autores principales: | Alenezi, Wejdan M., Fierheller, Caitlin T., Serruya, Corinne, Revil, Timothée, Oros, Kathleen K., Subramanian, Deepak N., Bruce, Jeffrey, Spiegelman, Dan, Pugh, Trevor, Campbell, Ian G., Mes-Masson, Anne-Marie, Provencher, Diane, Foulkes, William D., Haffaf, Zaki El, Rouleau, Guy, Bouchard, Luigi, Greenwood, Celia M. T., Ragoussis, Jiannis, Tonin, Patricia N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030840/ https://www.ncbi.nlm.nih.gov/pubmed/36969007 http://dx.doi.org/10.3389/fonc.2023.1111191 |
Ejemplares similares
-
Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic BRCA1 and BRCA2 Variants
por: Alenezi, Wejdan M., et al.
Publicado: (2022) -
Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene
por: Fierheller, Caitlin T., et al.
Publicado: (2023) -
The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population
por: Alenezi, Wejdan M., et al.
Publicado: (2022) -
A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
por: Fierheller, Caitlin T., et al.
Publicado: (2021) -
The Genetic Analyses of French Canadians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families
por: Fierheller, Caitlin T., et al.
Publicado: (2021)