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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.
American Journal of Human Genetics|June 13, 2023
Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestryBurcu F Darst, Jiayi Shen, Ravi K Madduri, et al.
Nature Communications|December 10, 2021
Meta-analyses identify DNA methylation associated with kidney function and damagePascal Schlosser, Adrienne Tin, Pamela R Matias-Garcia, et al.
Journal of the American College of Cardiology|August 7, 2013
Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization studyMichael V Holmes, Tabassome Simon, Holly J Exeter, et al.
Human Mutation|February 21, 2018
The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicityMara Colombo, Irene Lòpez-Perolio, Huong D Meeks, 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.
The New England Journal of Medicine|March 31, 2025
Global Effect of Cardiovascular Risk Factors on Lifetime Estimates, Christina Magnussen, Jesus Alegre-Diaz, 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.
Ebiomedicine|May 20, 2023
Dissecting the genetic heterogeneity of gastric cancerTimo Hess, Carlo Maj, Jan Gehlen, 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.
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