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Molecular Genetics & Genomic Medicine|May 9, 2019
The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association ConsortiumTomotaka Ugai, Roger L Milne, Hidemi Ito, et al.European Journal of Epidemiology|October 3, 2023
Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancerKatharina Wichert, Reiner Hoppe, Katja Ickstadt, et al.Ebiomedicine|October 21, 2019
Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestryYaohua Yang, Xiang Shu, Xiao-Ou Shu, et al.International Journal of Cancer|July 4, 2017
Gene-environment interactions involving functional variants: Results from the Breast Cancer Association ConsortiumMyrto Barrdahl, Anja Rudolph, John L Hopper, et al.Nature Genetics|April 19, 2011
Genome-wide association study identifies a common variant associated with risk of endometrial cancerAmanda B Spurdle, Deborah J Thompson, Shahana Ahmed, et al.Oncotarget|February 10, 2017
TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancerRainer Fagerholm, Sofia Khan, Marjanka K Schmidt, et al.International Journal of Epidemiology|January 10, 2018
Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association ConsortiumAnja Rudolph, Minsun Song, Mark N Brook, et al.Breast Cancer Research : BCR|April 13, 2022
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel lociHongjie Chen, Shaoqi Fan, Jennifer Stone, et al.Oncotarget|August 29, 2015
SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survivalMaral Jamshidi, Rainer Fagerholm, Sofia Khan, et al.Nature Genetics|August 17, 2023
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer riskNaomi Wilcox, Martine Dumont, Anna González-Neira, et al.Pageof 22