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Author Details
Full Name
Georgia Chenevix-Trench
Affiliation
QIMR Berghofer Medical Research Institute
ORCID
Career Start Year
1959
Papers
513
H Index
91
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36929942
Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions.
J Natl Cancer Inst
2023
36707629
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women.
Eur J Hum Genet
2023
36929942
Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions.
J Natl Cancer Inst
2023
37168552
Multi-trait genome-wide association study identifies a novel endometrial cancer risk locus that associates with testosterone levels.
iScience
2023
36991492
CRISPR screens identify gene targets at breast cancer risk loci.
Genome Biol
2023
37503126
Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
medRxiv
2023
37503126
Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
medRxiv
2023
36991492
CRISPR screens identify gene targets at breast cancer risk loci.
Genome Biol
2023
37168552
Multi-trait genome-wide association study identifies a novel endometrial cancer risk locus that associates with testosterone levels.
iScience
2023
36707629
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women.
Eur J Hum Genet
2023
34320204
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores.
J Natl Cancer Inst
2022
36041172
Coffee consumption and risk of endometrial cancer: a pooled analysis of individual participant data in the Epidemiology of Endometrial Cancer Consortium (E2C2).
Am J Clin Nutr
2022
35585550
Breast cancer risks associated with missense variants in breast cancer susceptibility genes.
Genome Med
2022
35585550
Breast cancer risks associated with missense variants in breast cancer susceptibility genes.
Genome Med
2022
35501337
Epigenome erosion and SOX10 drive neural crest phenotypic mimicry in triple-negative breast cancer.
NPJ Breast Cancer
2022
36210504
Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci.
J Natl Cancer Inst
2022
36205748
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
2022
36205748
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
2022
33567813
Methotrexate-related central neurotoxicity: clinical characteristics, risk factors and genome-wide association study in children treated for acute lymphoblastic leukemia.
Haematologica
2022
34320204
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores.
J Natl Cancer Inst
2022
35042965
Rare germline copy number variants (CNVs) and breast cancer risk.
Commun Biol
2022
34906479
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
2022
35077220
Cancer Risks Associated With <i>BRCA1</i> and <i>BRCA2</i> Pathogenic Variants.
J Clin Oncol
2022
35263119
TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members.
J Clin Oncol
2022
35084436
Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes.
JAMA Oncol
2022
35585550
Breast cancer risks associated with missense variants in breast cancer susceptibility genes.
Genome Med
2022
35585550
Breast cancer risks associated with missense variants in breast cancer susceptibility genes.
Genome Med
2022
35501337
Epigenome erosion and SOX10 drive neural crest phenotypic mimicry in triple-negative breast cancer.
NPJ Breast Cancer
2022
36210504
Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci.
J Natl Cancer Inst
2022
36041172
Coffee consumption and risk of endometrial cancer: a pooled analysis of individual participant data in the Epidemiology of Endometrial Cancer Consortium (E2C2).
Am J Clin Nutr
2022
36205748
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
2022
36205748
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
2022
33567813
Methotrexate-related central neurotoxicity: clinical characteristics, risk factors and genome-wide association study in children treated for acute lymphoblastic leukemia.
Haematologica
2022
35042965
Rare germline copy number variants (CNVs) and breast cancer risk.
Commun Biol
2022
34906479
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
2022
35084436
Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes.
JAMA Oncol
2022
35263119
TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members.
J Clin Oncol
2022
35077220
Cancer Risks Associated With <i>BRCA1</i> and <i>BRCA2</i> Pathogenic Variants.
J Clin Oncol
2022
32546565
Population-based targeted sequencing of 54 candidate genes identifies <i>PALB2</i> as a susceptibility gene for high-grade serous ovarian cancer.
J Med Genet
2021
32359158
Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.
J Natl Cancer Inst
2021
33471991
Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.
N Engl J Med
2021
33471991
Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.
N Engl J Med
2021
34162658
Identification of a Locus Near <i>ULK1</i> Associated With Progression-Free Survival in Ovarian Cancer.
Cancer Epidemiol Biomarkers Prev
2021
33529165
RNF168 regulates R-loop resolution and genomic stability in BRCA1/2-deficient tumors.
J Clin Invest
2021
33990587
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Nat Commun
2021
34146516
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element.
Am J Hum Genet
2021
34341517
Mendelian randomisation study of smoking exposure in relation to breast cancer risk.
Br J Cancer
2021
32546565
Population-based targeted sequencing of 54 candidate genes identifies <i>PALB2</i> as a susceptibility gene for high-grade serous ovarian cancer.
J Med Genet
2021
32976626
Evaluating the role of alcohol consumption in breast and ovarian cancer susceptibility using population-based cohort studies and two-sample Mendelian randomization analyses.
Int J Cancer
2021
32851660
Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer.
Int J Cancer
2021
1 - 50 of 1,026
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143
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Co-authored papers
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Hoda Anton-Culver
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Alison M Dunning
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Xiaoqing Chen
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105
Susan J Ramus
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Jolanta Lissowska
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