Cargando…
Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab
PURPOSE: This study examined the utility of sets of Single Nucleotide Polymorphisms (SNPs) in familial but non-BRCA-associated breast cancer (BC). METHODS: We derived a polygenic risk score (PRS) based on 24 known BC risk SNPs for 4,365 women from the BCFR and kConFab familial BC cohorts. We compare...
Autores principales: | Li, Hongyan, Feng, Bingjian, Miron, Alexander, Chen, Xiaoqing, Beesley, Jonathan, Bimeh, Emmanuella, Barrowdale, Daniel, John, Esther M., Daly, Mary B., Andrulis, Irene L., Buys, Saundra S., Kraft, Peter, Thorne, Heather, Chenevix-Trench, Georgia, Southey, Melissa, Antoniou, Antonis C., James, Paul A., Terry, Mary Beth, Phillips, Kelly-Anne, Hopper, John L., Mitchell, Gillian, Goldgar, David E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107177/ https://www.ncbi.nlm.nih.gov/pubmed/27171545 http://dx.doi.org/10.1038/gim.2016.43 |
Ejemplares similares
-
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
por: Mann, Graham J, et al.
Publicado: (2006) -
kConFab: a unique Australasian research initiative for familial breast cancer
por: Sambrook, J
Publicado: (2000) -
The kConFab experience – 14 years of biobanking
por: Thorne, H, et al.
Publicado: (2012) -
Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer
por: Barnes, D R, et al.
Publicado: (2013) -
Rare variants in the ATM gene and risk of breast cancer
por: Goldgar, David E, et al.
Publicado: (2011)