Georgia Chenevix Trench


Ontology type: schema:Person     


Person Info

NAME

Georgia

SURNAME

Chenevix Trench

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-01 Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-12 Guidelines for whole genome bisulphite sequencing of intact and FFPET DNA on the Illumina HiSeq X Ten in EPIGENETICS & CHROMATIN
  • 2018-12 Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers in BREAST CANCER RESEARCH
  • 2018-12 Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer in SCIENTIFIC REPORTS
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2018-07 Characterization of a novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient in BREAST CANCER RESEARCH AND TREATMENT
  • 2018-04 Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study in BRITISH JOURNAL OF CANCER
  • 2018-01 Multidimensional phenotyping of breast cancer cell lines to guide preclinical research in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-12 Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study in BREAST CANCER RESEARCH
  • 2017-12 Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families in BREAST CANCER RESEARCH AND TREATMENT
  • 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
  • 2017-07 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes in NATURE GENETICS
  • 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
  • 2017-04 Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 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 Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab in GENETICS IN MEDICINE
  • 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 High content screening application for cell-type specific behaviour in heterogeneous primary breast epithelial subpopulations in BREAST CANCER RESEARCH
  • 2016-12 Genetic predisposition to ductal carcinoma in situ of the breast 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 rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk in SCIENTIFIC REPORTS
  • 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
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-07 Assessing the genetic architecture of epithelial ovarian cancer histological subtypes in HUMAN GENETICS
  • 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 Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer in NATURE GENETICS
  • 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 Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer in NATURE COMMUNICATIONS
  • 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 Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis in BMC MEDICINE
  • 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
  • 2015-08 Genome-wide significant risk associations for mucinous ovarian carcinoma in NATURE GENETICS
  • 2015-05 Paclitaxel sensitivity in relation to ABCB1 expression, efflux and single nucleotide polymorphisms in ovarian cancer in SCIENTIFIC REPORTS
  • 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 Evidence for a time-dependent association between FOLR1 expression and survival from ovarian carcinoma: implications for clinical testing. An Ovarian Tumour Tissue Analysis consortium study in BRITISH JOURNAL OF CANCER
  • 2014-12 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy in NATURE COMMUNICATIONS
  • 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 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 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2014-10 Meta-analysis of the global gene expression profile of triple-negative breast cancer identifies genes for the prognostication and treatment of aggressive breast cancer in ONCOGENESIS
  • 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
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