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Hiltrud Brauch

Ärztin

Name	Hiltrud Brauch
Place	Bochum (Wirkungsort) Deutschland
Gender	weiblich
Academic degree	Prof. Dr.
Profession	Ärztin (characteristic profession)
Related	Ruhr-Universität Bochum. Institut für Prävention und Arbeitsmedizin
Record type	Person
GND-Identifier	1120622271
Record ID	1120622271
Involved in show all A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers Two truncating variants in FANCC and breast cancer risk Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry Common variants in breast cancer risk loci predispose to distinct tumor subtypes Epigenetic quantification of circulating immune cells in peripheral blood of triple-negative breast cancer patients 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 Mendelian randomisation study of smoking exposure in relation to breast cancer risk Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer Identification of nine new susceptibility loci for endometrial cancer A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study Predicting Triple-Negative Breast Cancer Subtype Using Multiple Single Nucleotide Polymorphisms for Breast Cancer Risk and Several Variable Selection Methods Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry Genetic predisposition to ductal carcinoma in situ of the breast 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 Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk Genetic predisposition to ductal carcinoma in situ of the breast Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer RAD51B in Familial Breast Cancer Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study Association of CYP2D6metabolizer status with mammographic density change in response to tamoxifen treatment A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication Evidence of Gene–Environment Interactions between Common Breast Cancer Susceptibility Loci and Established Environmental Risk Factors The UGT1A6_19_GG genotype is a breast cancer risk factor Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development Association of genetic variation in mitotic kinases with breast cancer risk No evidence that GATA3 rs570613 SNP modifies breast cancer risk The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study

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Katalog der Deutschen Nationalbibliothek

Hiltrud Brauch

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Two truncating variants in FANCC and breast cancer risk

Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer

A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Epigenetic quantification of circulating immune cells in peripheral blood of triple-negative breast cancer patients

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

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Identification of nine new susceptibility loci for endometrial cancer

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study

Predicting Triple-Negative Breast Cancer Subtype Using Multiple Single Nucleotide Polymorphisms for Breast Cancer Risk and Several Variable Selection Methods

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

Genetic predisposition to ductal carcinoma in situ of the breast

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

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2

Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus

Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

Genetic predisposition to ductal carcinoma in situ of the breast

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

RAD51B in Familial Breast Cancer

Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

Association of CYP2D6metabolizer status with mammographic density change in response to tamoxifen treatment

A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication

Evidence of Gene–Environment Interactions between Common Breast Cancer Susceptibility Loci and Established Environmental Risk Factors

The UGT1A6_19_GG genotype is a breast cancer risk factor

Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study

Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development

Association of genetic variation in mitotic kinases with breast cancer risk

No evidence that GATA3 rs570613 SNP modifies breast cancer risk

The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study