Auflistung nach Autor "Brauch, Hiltrud"

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11q13 is a susceptibility locus for hormone receptor positive breast cancer

Justenhoven, Christina; Brauch, Hiltrud (2012)
19p13.1 Is a Triple-Negative-Specific Breast Cancer Susceptibility Locus

Brauch, Hiltrud (2012)
9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

Brauch, Hiltrud; Justenhoven, Christina (2012)
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Brauch, Hiltrud (2021)
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

Brauch, Hiltrud; Brenner, Hermann (2023)
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

Brauch, Hiltrud (2014)
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11

Brauch, Hiltrud; Justenhoven, Christina (2012)
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Brauch, Hiltrud; Brucker, Sara (2020)
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Brauch, Hiltrud; Lo, Wing-Yee; Brucker, Sara (2018)
Age- and Tumor Subtype Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

Brauch, Hiltrud; Lo, Wing-Yee; Justenhoven, Christina (2016)
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression

Brauch, Hiltrud (2016)
Association analysis identifies 65 new breast cancer risk loci

Brauch, Hiltrud; Brucker, Sara; Lo, Wing-Yee (2017)
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21

Brauch, Hiltrud (2016)
Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

Brauch, Hiltrud (2016)
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

Hoppe, Reiner; Brauch, Hiltrud (2021)
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival

Brauch, Hiltrud; Hoppe, Reiner (2023)
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

Brauch, Hiltrud; Brucker, Sara (2019)
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

Brauch, Hiltrud (2017)
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

Brauch, Hiltrud (2016)
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

Brauch, Hiltrud; Brucker, Sara (2020)

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Auflistung nach Autor "Brauch, Hiltrud"

Auflistung nach Autor "Brauch, Hiltrud"

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