Cargando…

Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

BACKGROUND: Previous gene-environment interaction studies of breast cancer risk have provided sparse evidence of interactions. Using the largest available dataset to date, we performed a comprehensive assessment of potential effect modification of 205 common susceptibility variants by 13 established...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kapoor, Pooja Middha, Lindström, Sara, Behrens, Sabine, Wang, Xiaoliang, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Dunning, Alison M, Pharoah, Paul D P, Schmidt, Marjanka K, Kraft, Peter, García-Closas, Montserrat, Easton, Douglas F, Milne, Roger L, Chang-Claude, Jenny
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2020
Materias:	Genetics and Environment
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426027/ https://www.ncbi.nlm.nih.gov/pubmed/31605532 http://dx.doi.org/10.1093/ije/dyz193

Ejemplares similares

The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association Consortium
por: Ugai, Tomotaka, et al.
Publicado: (2019)

Gene–environment interactions involving functional variants: Results from the Breast Cancer Association Consortium
por: Barrdahl, Myrto, et al.
Publicado: (2017)

Commentary: No multiplicative GXE interactions for breast cancer risk: Have we reached a verdict or is the jury still out?
por: Terry, Mary Beth
Publicado: (2020)

High‐throughput automated scoring of Ki67 in breast cancer tissue microarrays from the Breast Cancer Association Consortium
por: Abubakar, Mustapha, et al.
Publicado: (2016)

Patient survival and tumor characteristics associated with CHEK2:p.I157T – findings from the Breast Cancer Association Consortium
por: Muranen, Taru A., et al.
Publicado: (2016)

Association between Common Variation in 120 Candidate Genes and Breast Cancer Risk
por: Pharoah, Paul D. P, et al.
Publicado: (2007)

Prediction of breast cancer risk based on common genetic variants in women of East Asian ancestry
por: Wen, Wanqing, et al.
Publicado: (2016)

The search for low-penetrance breast cancer genes
por: Ponder, BAJ, et al.
Publicado: (2005)

E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium
por: Horne, Hisani N., et al.
Publicado: (2018)

BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
por: Lee, Andrew, et al.
Publicado: (2019)

Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
por: Kirchhoff, Tomas, et al.
Publicado: (2012)

Breast cancer risk factors and their effects on survival: a Mendelian randomisation study
por: Escala-Garcia, Maria, et al.
Publicado: (2020)

Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
por: Wilcox, Naomi, et al.
Publicado: (2023)

Breast cancer susceptibility after BRCA1/2: finding the genes and potential practical applications
por: Ponder, BAJ, et al.
Publicado: (2006)

Correction: BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors
por: Lee, Andrew, et al.
Publicado: (2019)

Interactions between genes involved in the antioxidant defence system and breast cancer risk
por: Oestergaard, M Z, et al.
Publicado: (2006)

Is explantation of silicone breast implants useful in patients with complaints?
por: de Boer, M., et al.
Publicado: (2016)

Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks
por: Decker, Brennan, et al.
Publicado: (2017)

Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium
por: Howat, William J, et al.
Publicado: (2014)

Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
por: Wilcox, Naomi, et al.
Publicado: (2023)

Risk of congenital anomalies in relation to the uptake of trihalomethane from drinking water during pregnancy
por: Grazuleviciene, Regina, et al.
Publicado: (2013)

Familial risks of breast cancer
por: Easton, Douglas F
Publicado: (2002)

Risk factors for persistence of lower respiratory symptoms among community members exposed to the 2001 World Trade Center terrorist attacks
por: Jordan, Hannah T, et al.
Publicado: (2017)

Gene–environment interaction and risk of breast cancer
por: Rudolph, Anja, et al.
Publicado: (2016)

FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
por: Agarwal, D, et al.
Publicado: (2014)

Chromatin interactome mapping at 139 independent breast cancer risk signals
por: Beesley, Jonathan, et al.
Publicado: (2020)

miR-205 in Breast Cancer: State of the Art
por: Plantamura, Ilaria, et al.
Publicado: (2020)

Heterogeneity of luminal breast cancer characterised by immunohistochemical expression of basal markers
por: Sung, Hyuna, et al.
Publicado: (2016)

No association between a polymorphism in the steroid metabolism gene CYP17 and risk of breast cancer.
por: Dunning, A. M., et al.
Publicado: (1998)

Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk
por: Vachon, Celine M., et al.
Publicado: (2019)

Breast cancer risks associated with missense variants in breast cancer susceptibility genes
por: Dorling, Leila, et al.
Publicado: (2022)

Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey
por: Brédart, Anne, et al.
Publicado: (2018)

Genetic modifiers of CHEK2*1100delC associated breast cancer risk
por: Muranen, Taru A., et al.
Publicado: (2016)

Polygenic risk scores for prediction of breast cancer risk in Asian populations
por: Ho, Weang-Kee, et al.
Publicado: (2022)

Prediction and clinical utility of a contralateral breast cancer risk model
por: Giardiello, Daniele, et al.
Publicado: (2019)

Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium
por: Lei, Jieping, et al.
Publicado: (2015)

MiR-205 Dysregulations in Breast Cancer: The Complexity and Opportunities
por: Xiao, Yajuan, et al.
Publicado: (2019)

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
por: Mavaddat, Nasim, et al.
Publicado: (2019)

Combination of a 15-SNP Polygenic Risk Score and Classical Risk Factors for the Prediction of Breast Cancer Risk in Cypriot Women
por: Yiangou, Kristia, et al.
Publicado: (2021)

Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study
por: Milne, Roger L, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_faegoeph36veno3qmsdhee4llb