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Human Genetics|August 14, 2012
Genome-wide association study of glioma and meta-analysisPreetha Rajaraman, Beatrice S Melin, Zhaoming Wang, et al.
Human Molecular Genetics|January 24, 2024
Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortiaHeather M Ochs-Balcom, Leah Preus, Zhaohui Du, et al.
Scientific Reports|April 14, 2022
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 womenXiaoliang Wang, Pooja Middha Kapoor, Paul L Auer, et al.
European Urology|May 20, 2023
Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational InsightsStella Koutros, Lambertus A Kiemeney, Parichoy Pal Choudhury, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Overlap of high-risk individuals across family history, genetic & non-genetic breast cancer risk models: Analysis of 180,398 women from European & Asian ancestriesPeh Joo Ho, Christine Kim Yan Loo, Meng Huang Goh, et al.
Cancers|November 13, 2025
Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 WomenPeh Joo Ho, Christine Kim Yan Loo, Ryan Jak Yang Lim, et al.
Communications Biology|January 19, 2022
Rare germline copy number variants (CNVs) and breast cancer riskJoe Dennis, Jonathan P Tyrer, Logan C Walker, et al.
Breast Cancer Research : BCR|December 29, 2024
Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk predictionKristia Yiangou, Nasim Mavaddat, Joe Dennis, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2024
Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk predictionKristia Yiangou, Nasim Mavaddat, Joe Dennis, et al.
Human Mutation|May 10, 2024
A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: application to <i>BRCA1</i> and <i>BRCA2</i>Maria Zanti, Denise G O'Mahony, Michael T Parsons, et al.
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