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Ute Hamann

Name	Ute Hamann
Place	Heidelberg (Wirkungsort) Deutschland
Academic degree	Dr. med. (an der Medizinischen Fakultät der Universität Heidelberg) (1982) Prof. Dr.
Further information	Arbeitsgruppe Molekulargenetik des Mammakarzinoms, Deutsches Krebsforschungszentrum Heidelberg; Lehrbeauftragte Medizinische Fakultät Heidelberg
Record type	Person
GND-Identifier	1074024230
Record ID	1074024230
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 Native American ancestry and breast cancer risk in Colombian and Mexican women: ruling out potential confounding through ancestry-informative markers Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry Breast cancer risks associated with missense variants in breast cancer susceptibility genes 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 Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies? Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer Genome-wide DNA methylation profiling in peripheral blood of triple negative breast cancer patients Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients Genetic predisposition to ductal carcinoma in situ of the breast Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 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 Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus Genetic predisposition to ductal carcinoma in situ of the breast 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 in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk 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 7q21-rs6964587 and breast cancer risk: an extended case–control study by the Breast Cancer Association Consortium Frequenzen und Regulation von 2,4,6-trinitrophenyl-spezifischen [trinitrophenyl-spezifischen] zytotoxischen T-Vorläuferzellen

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Katalog der Deutschen Nationalbibliothek

Ute Hamann

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

Native American ancestry and breast cancer risk in Colombian and Mexican women: ruling out potential confounding through ancestry-informative markers

Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

Breast cancer risks associated with missense variants in breast cancer susceptibility genes

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

Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

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

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

Genome-wide DNA methylation profiling in peripheral blood of triple negative breast cancer patients

Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure

High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients

Genetic predisposition to ductal carcinoma in situ of the breast

Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2

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

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

Genetic predisposition to ductal carcinoma in situ of the breast

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 in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

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

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

7q21-rs6964587 and breast cancer risk: an extended case–control study by the Breast Cancer Association Consortium

Frequenzen und Regulation von 2,4,6-trinitrophenyl-spezifischen [trinitrophenyl-spezifischen] zytotoxischen T-Vorläuferzellen