Cargando…
Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?
BACKGROUND: Breast cancer risk for BRCA1 and BRCA2 pathogenic mutation carriers is modified by risk factors that cluster in families, including genetic modifiers of risk. We considered genetic modifiers of risk for carriers of high-risk mutations in other breast cancer susceptibility genes. METHODS:...
Autores principales: | Nguyen-Dumont, Tú, Teo, Zhi L., Hammet, Fleur, Roberge, Alexis, Mahmoodi, Maryam, Tsimiklis, Helen, Park, Daniel J., Pope, Bernard J., Lonie, Andrew, Kapuscinski, Miroslav K., Mahmood, Khalid, Goldgar, David E., Giles, Graham G., Winship, Ingrid, Hopper, John L., Southey, Melissa C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806316/ https://www.ncbi.nlm.nih.gov/pubmed/29422015 http://dx.doi.org/10.1186/s12885-018-4028-z |
Ejemplares similares
-
Expanded genetic analysis of a PALB2 c.3113G>A mutation carrying multiple-case breast cancer family via exome sequencing
por: Teo, ZL, et al.
Publicado: (2012) -
Population-Based Estimates of the Age-Specific Cumulative Risk of Breast Cancer for Pathogenic Variants in CHEK2: Findings from the Australian Breast Cancer Family Registry
por: Nguyen-Dumont, Tú, et al.
Publicado: (2021) -
Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2
por: Nguyen-Dumont, Tú, et al.
Publicado: (2013) -
Identification of new breast cancer predisposition genes via whole exome sequencing
por: Southey, MC, et al.
Publicado: (2012) -
FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets
por: Pope, Bernard J, et al.
Publicado: (2013)