Assessing Interactions between the Association of Common Genetic Variant at 1p11 (rs11249433) and Hormone Receptor Status with Breast Cancer Risk

Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry

(2012) Dezheng Huo et al.   CARCINOGENESIS

The global breast cancer burden

(2012) John R Benson et al.   Future Oncology

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

(2011) Aiko Sueta et al.   BREAST CANCER RESEARCH AND TREATMENT

Replication of Breast Cancer GWAS Susceptibility Loci in the Women's Health Initiative African American SHARe Study

(2011) C. M. Hutter et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

Common Breast Cancer Susceptibility Loci Are Associated with Triple-Negative Breast Cancer

(2011) K. N. Stevens et al.   CANCER RESEARCH

Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans

(2011) Fang Chen et al.   HUMAN MOLECULAR GENETICS

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

(2011) Antonis C Antoniou et al.   HUMAN MOLECULAR GENETICS

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium†

(2011) Jonine D. Figueroa et al.   HUMAN MOLECULAR GENETICS

Interactions Between Genetic Variants and Breast Cancer Risk Factors in the Breast and Prostate Cancer Cohort Consortium

(2011) D. Campa et al.   JNCI-Journal of the National Cancer Institute

Genetic Variants at 1p11.2 and Breast Cancer Risk: A Two-Stage Study in Chinese Women

(2011) Yue Jiang et al.   PLoS One

A combined analysis of genome-wide association studies in breast cancer

(2010) Jingmei Li et al.   BREAST CANCER RESEARCH AND TREATMENT

Evaluation of Breast Cancer Susceptibility Loci in Chinese Women

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

Association Between 9p21 Genomic Markers and Heart Disease

(2010) Glenn E. Palomaki et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutations

(2010) Yi-Ping Fu et al.   Molecular Cancer

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

(2010) Clare Turnbull et al.   NATURE GENETICS

Novel Breast Cancer Risk Alleles and Interaction with Ionizing Radiation among U.S. Radiologic Technologists

(2010) Parveen Bhatti et al.   RADIATION RESEARCH

Breast Cancer in Developing Countries: Opportunities for Improved Survival

(2010) Lawrence N. Shulman et al.   Journal of Oncology

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

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

(2009) Shahana Ahmed et al.   NATURE GENETICS

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

(2009) L. A. Hindorff et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Notch Signaling Regulates Mammary Stem Cell Function and Luminal Cell-Fate Commitment

(2008) Toula Bouras et al.   Cell Stem Cell

“Westernizing” Women's Risks? Breast Cancer in Lower-Income Countries

(2008) Peggy Porter   NEW ENGLAND JOURNAL OF MEDICINE