A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population

Common Genetic Variants Associated with Breast Cancer in Korean Women and Differential Susceptibility According to Intrinsic Subtype

(2011) W. Han et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

Breast and cervical cancer in 187 countries between 1980 and 2010: a systematic analysis

(2011) Mohammad H Forouzanfar et al.   LANCET

Evaluation of Breast Cancer Susceptibility Loci in Chinese Women

(2010) J. Long et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women

(2010) Jill S. Barnholtz-Sloan et al.   CARCINOGENESIS

Incidence of Breast Cancer and Its Subtypes in Relation to Individual and Multiple Low-Penetrance Genetic Susceptibility Loci

(2010) Gillian K. Reeves et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Cancer Incidence and Incidence Rates in Japan in 2005: Based on Data from 12 Population-based Cancer Registries in the Monitoring of Cancer Incidence in Japan (MCIJ) Project

(2010) T. Matsuda et al.   JAPANESE JOURNAL OF CLINICAL ONCOLOGY

Genetic and Clinical Predictors for Breast Cancer Risk Assessment and Stratification Among Chinese Women

(2010) Wei Zheng et al.   JNCI-Journal of the National Cancer Institute

Breast cancer prevention based on gene-environment interaction

(2010) Minkyo Song et al.   MOLECULAR CARCINOGENESIS

Genetic susceptibility to breast cancer

(2010) Nasim Mavaddat et al.   Molecular Oncology

Genome-wide association study identifies five new breast cancer susceptibility loci

(2010) Clare Turnbull et al.   NATURE GENETICS

Performance of Common Genetic Variants in Breast-Cancer Risk Models

(2010) Sholom Wacholder et al.   NEW ENGLAND JOURNAL OF MEDICINE

Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus

(2010) Simon N. Stacey et al.   PLoS Genetics

Identification of a Functional Genetic Variant at 16q12.1 for Breast Cancer Risk: Results from the Asia Breast Cancer Consortium

(2010) Jirong Long et al.   PLoS Genetics

FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation

(2009) Miriam S. Udler et al.   HUMAN MOLECULAR GENETICS

FGFR2intronic polymorphisms interact with reproductive risk factors of breast cancer: Results of a case control study in Japan

(2009) Takakazu Kawase et al.   INTERNATIONAL JOURNAL OF CANCER

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)

(2009) Gilles Thomas et al.   NATURE GENETICS

Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1

(2009) Wei Zheng et al.   NATURE GENETICS

Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2

(2009) Shahana Ahmed et al.   NATURE GENETICS

Human genetic variation and its contribution to complex traits

(2009) Kelly A. Frazer et al.   NATURE REVIEWS GENETICS

Proportion of Invasive Breast Cancer Attributable to Risk Factors Modifiable after Menopause

(2008) B. L. Sprague et al.   AMERICAN JOURNAL OF EPIDEMIOLOGY

Genetic variants in fibroblast growth factor receptor 2 (FGFR2) contribute to susceptibility of breast cancer in Chinese women

(2008) J. Liang et al.   CARCINOGENESIS

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

(2008) Simon N Stacey et al.   NATURE GENETICS

Polygenes, Risk Prediction, and Targeted Prevention of Breast Cancer

(2008) Paul D.P. Pharoah et al.   NEW ENGLAND JOURNAL OF MEDICINE

Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33

(2008) B. Gold et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics

(2008) Montserrat Garcia-Closas et al.   PLoS Genetics