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Endocrine-Related Cancer|September 3, 2015
Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancerTracy A O'Mara, Dylan M Glubb, Jodie N Painter, et al.
Cancer Medicine|April 3, 2018
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analysesJodie N Painter, Tracy A O'Mara, Andrew P Morris, et al.
The Journal of Clinical Investigation|October 29, 2024
Immunological and molecular features of the tumor microenvironment of long-term survivors of ovarian cancerBrad H Nelson, Phineas Hamilton, Minh Tung Phung, et al.
JAMA|January 26, 2012
Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancerKelly L Bolton, Georgia Chenevix-Trench, Cindy Goh, et al.
Breast Cancer Research : BCR|January 4, 2011
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 studyRoger L Milne, Mia M Gaudet, Amanda B Spurdle, et al.
The Journal of Pathology|December 13, 2021
Validated biomarker assays confirm that ARID1A loss is confounded with MMR deficiency, CD8+ TIL infiltration, and provides no independent prognostic value in endometriosis-associated ovarian carcinomasKarolin Heinze, Tayyebeh M Nazeran, Sandra Lee, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 27, 2019
A combination of the immunohistochemical markers CK7 and SATB2 is highly sensitive and specific for distinguishing primary ovarian mucinous tumors from colorectal and appendiceal metastasesNicola S Meagher, Linyuan Wang, Peter F Rambau, et al.
Human Genetics|December 2, 2015
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 ConsortiumJieping Lei, Anja Rudolph, Kirsten B Moysich, et al.
Human Molecular Genetics|July 6, 2016
Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer riskJennifer B Permuth, Ailith Pirie, Y Ann Chen, et al.
Nature Genetics|February 13, 2007
A common coding variant in CASP8 is associated with breast cancer riskAngela Cox, Alison M Dunning, Montserrat Garcia-Closas, et al.
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