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

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A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry (2012) 6.34

Genetic architectures of psychiatric disorders: the emerging picture and its implications. Nat Rev Genet (2012) 5.99

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A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nat Genet (2011) 3.37

Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat Genet (2012) 3.20

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nat Genet (2015) 3.02

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Genome-wide association study identifies a common variant associated with risk of endometrial cancer. Nat Genet (2011) 1.84

19p13.1 is a triple-negative-specific breast cancer susceptibility locus. Cancer Res (2012) 1.81

Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. Nat Genet (2011) 1.77

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Common breast cancer susceptibility loci are associated with triple-negative breast cancer. Cancer Res (2011) 1.65

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Genetic susceptibility to triple-negative breast cancer. Cancer Res (2013) 1.48

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Fine-mapping of breast cancer susceptibility loci characterizes genetic risk in African Americans. Hum Mol Genet (2011) 1.45

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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. Breast Cancer Res (2012) 1.38

A common deletion in the APOBEC3 genes and breast cancer risk. J Natl Cancer Inst (2013) 1.36

ESR1 is co-expressed with closely adjacent uncharacterised genes spanning a breast cancer susceptibility locus at 6q25.1. PLoS Genet (2011) 1.28

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11q13 is a susceptibility locus for hormone receptor positive breast cancer. Hum Mutat (2012) 1.26

Genetic variants associated with breast size also influence breast cancer risk. BMC Med Genet (2012) 1.26

Novel genetic markers of breast cancer survival identified by a genome-wide association study. Cancer Res (2012) 1.24

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Evaluation of polygenic risk scores for predicting breast and prostate cancer risk. Genet Epidemiol (2011) 1.23

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium. Hum Mol Genet (2014) 1.22

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2. Breast Cancer Res (2011) 1.22

Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers. PLoS One (2011) 1.20

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Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer. Hum Mol Genet (2011) 1.17

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Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Cancer Epidemiol Biomarkers Prev (2012) 1.17

Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. Nat Commun (2014) 1.16

A dynamic model for genome-wide association studies. Hum Genet (2011) 1.15

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC). PLoS One (2012) 1.13

TGF-β signaling pathway and breast cancer susceptibility. Cancer Epidemiol Biomarkers Prev (2011) 1.13

Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status. J Med Genet (2012) 1.13

The contributions of breast density and common genetic variation to breast cancer risk. J Natl Cancer Inst (2015) 1.11

Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas. Hum Mol Genet (2012) 1.11

A genome-wide association study of breast cancer in women of African ancestry. Hum Genet (2012) 1.11

Evaluating genome-wide association study-identified breast cancer risk variants in African-American women. PLoS One (2013) 1.10

Genetic susceptibility loci for subtypes of breast cancer in an African American population. Cancer Epidemiol Biomarkers Prev (2012) 1.10

Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles. PLoS One (2013) 1.10

Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk. Nat Genet (2012) 1.10

Comprehensive functional annotation of seventy-one breast cancer risk Loci. PLoS One (2013) 1.10

Rare allelic forms of PRDM9 associated with childhood leukemogenesis. Genome Res (2012) 1.09

Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility. Hum Genet (2011) 1.08

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ANRIL: molecular mechanisms and implications in human health. Int J Mol Sci (2013) 1.07

Identification of inherited genetic variations influencing prognosis in early-onset breast cancer. Cancer Res (2013) 1.06

The non-protein coding breast cancer susceptibility locus Mcs5a acts in a non-mammary cell-autonomous fashion through the immune system and modulates T-cell homeostasis and functions. Breast Cancer Res (2011) 1.05

Genome-wide "pleiotropy scan" identifies HNF1A region as a novel pancreatic cancer susceptibility locus. Cancer Res (2011) 1.05

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk. Hum Mol Genet (2014) 1.05

Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women. Breast Cancer Res (2012) 1.05

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A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. Cancer Epidemiol Biomarkers Prev (2014) 1.03

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Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians. Breast Cancer Res Treat (2012) 1.01

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Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. Am J Hum Genet (2015) 1.00

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium. Hum Mol Genet (2013) 1.00

Telomere length and genetic variation in telomere maintenance genes in relation to ovarian cancer risk. Cancer Epidemiol Biomarkers Prev (2012) 1.00

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Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Nat Commun (2014) 1.00

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet (2008) 30.20

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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet (2007) 22.96

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Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet (2009) 7.30

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New common variants affecting susceptibility to basal cell carcinoma. Nat Genet (2009) 4.15

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Multiple newly identified loci associated with prostate cancer susceptibility. Nat Genet (2008) 15.43

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