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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.
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A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.
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Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
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Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.
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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.
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A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.
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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
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Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer.
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Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.
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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.
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Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.
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Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.
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Prediction of breast cancer risk based on profiling with common genetic variants.
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Association analysis identifies 65 new breast cancer risk loci.
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
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Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer.
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A common coding variant in CASP8 is associated with breast cancer risk.
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19p13.1 is a triple-negative-specific breast cancer susceptibility locus.
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Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.
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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.
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The contributions of breast density and common genetic variation to breast cancer risk.
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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
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Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.
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Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.
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Hanne Meijers-Heijboer, Ans van den Ouweland, Jan Klijn, Marijke Wasielewski, Anja de Snoo, Rogier Oldenburg, Antoinette Hollestelle, Mark Houben, Ellen Crepin, Monique van Veghel-Plandsoen,[...]. Nat Genet 2002
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METAL: fast and efficient meta-analysis of genomewide association scans.
Cristen J Willer, Yun Li, Gonçalo R Abecasis. Bioinformatics 2010
Cristen J Willer, Yun Li, Gonçalo R Abecasis. Bioinformatics 2010
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