Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium

The Korean Hereditary Breast Cancer (KOHBRA) Study: Protocols and Interim Report

(2011) Sang Ah Han et al.   CLINICAL ONCOLOGY

Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study

(2011) Olivia Fletcher et al.   JNCI-Journal of the National Cancer Institute

Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence

(2011) Ben Zhang et al.   LANCET ONCOLOGY

Role of ferritin alterations in human breast cancer cells

(2010) Svitlana I. Shpyleva 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

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

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

(2010) Antonis C Antoniou et al.   NATURE GENETICS

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

(2010) Clare Turnbull et al.   NATURE 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

Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

(2010) Mia M. Gaudet et al.   PLoS Genetics

Screening and association testing of common coding variation in steroid hormone receptor co-activator and co-repressor genes in relation to breast cancer risk: the Multiethnic Cohort

(2009) Christopher A Haiman et al.   BMC CANCER

Chemokine Receptors as Targets for Cancer Therapy

(2009) Xuesong Wu et al.   CURRENT PHARMACEUTICAL DESIGN

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits

(2009) Yoon Shin Cho et al.   NATURE GENETICS

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

Association of genetic polymorphisms of ER-α and the estradiol-synthesizing enzyme genes CYP17 and CYP19 with breast cancer risk in Chinese women

(2008) Lina Zhang et al.   BREAST CANCER RESEARCH AND TREATMENT

Serum organochlorines and breast cancer risk in Japanese women: a case–control study

(2008) Hiroaki Itoh et al.   CANCER CAUSES & CONTROL

Genetic variants of BLM interact with RAD51 to increase breast cancer susceptibility

(2008) Shian-ling Ding et al.   CARCINOGENESIS

A tandem repeat of human telomerase reverse transcriptase (hTERT) and risk of breast cancer development and metastasis in Chinese women

(2008) Y. Wang et al.   CARCINOGENESIS

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

(2008) J. Liang et al.   CARCINOGENESIS

Cellular FLICE-Like Inhibitory Protein (C-FLIP): A Novel Target for Cancer Therapy

(2008) Ahmad Safa et al.   CURRENT CANCER DRUG TARGETS

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

(2008) Simon N Stacey et al.   NATURE GENETICS

FLIP and the death effector domain family

(2008) J W Yu et al.   ONCOGENE

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