Ute Hamann


Ontology type: schema:Person     


Person Info

NAME

Ute

SURNAME

Hamann

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2017-12 Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure in BMC GENOMICS
  • 2017-12 Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients in SCIENTIFIC REPORTS
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-05 Genetic modifiers of CHEK2*1100delC-associated breast cancer risk in GENETICS IN MEDICINE
  • 2017-01 Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-01 Contribution of BRCA1 large genomic rearrangements to early-onset and familial breast/ovarian cancer in Pakistan in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-12 Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2016-12 Genetic predisposition to ductal carcinoma in situ of the breast in BREAST CANCER RESEARCH
  • 2016-12 High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients in BMC CANCER
  • 2016-12 A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-10 Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) in SCIENTIFIC REPORTS
  • 2016-05 Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-05 Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry in CANCER CAUSES & CONTROL
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2016-01 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 in HUMAN GENETICS
  • 2015-12 A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients in BMC CANCER
  • 2015-12 Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy in BREAST CANCER RESEARCH
  • 2015-12 Inbreeding and homozygosity in breast cancer survival in SCIENTIFIC REPORTS
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-12 Common germline polymorphisms associated with breast cancer-specific survival in BREAST CANCER RESEARCH
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-07 Absence of the FANCM c.5101C>T mutation in BRCA1/2-negative triple-negative breast cancer patients from Pakistan in BREAST CANCER RESEARCH AND TREATMENT
  • 2015-04 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer in NATURE GENETICS
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2014-12 Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2014-12 Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia in BREAST CANCER RESEARCH
  • 2014-12 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy in NATURE COMMUNICATIONS
  • 2014-12 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2014-10 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche in NATURE
  • 2014-06 Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study in BREAST CANCER RESEARCH
  • 2014-06 Practical investigation of the performance of robust logistic regression to predict the genetic risk of hypertension in BMC PROCEEDINGS
  • 2014-06 Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-02 FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium in BRITISH JOURNAL OF CANCER
  • 2014-02 CYP2D6 Genotype and Adjuvant Tamoxifen: Meta‐Analysis of Heterogeneous Study Populations in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2013-12 Constitutional CHEK2mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan in BMC CANCER
  • 2013-04 Confirmation of the reduction of hormone replacement therapy-related breast cancer risk for carriers of the HSD17B1_937_G variant in BREAST CANCER RESEARCH AND TREATMENT
  • 2013-04 Large-scale genotyping identifies 41 new loci associated with breast cancer risk in NATURE GENETICS
  • 2013-04 Genome-wide association studies identify four ER negative–specific breast cancer risk loci in NATURE GENETICS
  • 2013-04 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2012-11 Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-06 Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients in FAMILIAL CANCER
  • 2012-02 Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers in BREAST CANCER RESEARCH
  • Affiliations

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