Soo‐Hwang Teo

Adapting the BOADICEA breast and ovarian cancer risk models for the ethnically diverse UK population

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

The tumor microenvironment of 14,837 breast cancers is associated with clinical outcome independently of genomic subtypes

Genome-wide association study of Asian women identifies putative mammographic density-associated loci

Reproductive factors and mammographic density within the International Consortium of Mammographic Density: A cross-sectional study

Evaluation of Multiple Breast Cancer Polygenic Risk Score Panels in Women of Latin American Heritage

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

Analysis of variants in untranslated and promoter regions and breast cancer risk using whole genome sequencing data

Detecting Homologous Recombination Deficiency for Breast Cancer Through Integrative Analysis of Genomic Data

Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry

Evaluating Approaches for Constructing Polygenic Risk Scores for Prostate Cancer in Men of African and European Ancestry

Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

Genome- and transcriptome-wide association studies of 386,000 Asian and European-ancestry women provide new insights into breast cancer genetics

The association of age at menarche and adult height with mammographic density in the International Consortium of Mammographic Density

Predicting the Likelihood of Carrying a <i>BRCA1</i> or <i>BRCA2</i> Mutation in Asian Patients With Breast Cancer

Incorporating progesterone receptor expression into the PREDICT breast prognostic model

Exome sequencing identifies novel susceptibility genes and defines the contribution of coding variants to breast cancer risk

Polygenic risk scores for prediction of breast cancer risk in Asian populations

Germline <scp> <i>APOBEC3B</i> </scp> deletion increases somatic hypermutation in Asian breast cancer that is associated with Her2 subtype, <scp> <i>PIK3CA</i> </scp> mutations and immune activation

Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

Polygenic Risk Scores for Prediction of Breast Cancer in Korean women

European polygenic risk score for prediction of breast cancer shows similar performance in Asian women

Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants

Characterization of the Cancer Spectrum in Men With Germline<i>BRCA1</i>and<i>BRCA2</i>Pathogenic Variants

Health system strengthening: Integration of breast cancer care for improved outcomes

Epidemiological and ES cell‐based functional evaluation of <i>BRCA2</i> variants identified in families with breast cancer

Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women

Measurement challenge: protocol for international case–control comparison of mammographic measures that predict breast cancer risk