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G

Georgia Chenevix-Trench

qimr berghofer
H指数:115
被引数:7.0万

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Clarifying risk-factor associations with quantitative breast tumor features: a pooled analysis of 24 studies

阐明风险因素与定量乳腺肿瘤特征的关系:24项研究的合并分析

2026-07-240
PRE
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer

398,238名女性的全基因组关联研究揭示了七个与高级别浆液性卵巢癌相关的位点

2025-11-200
OAAI
Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women

基于家族史、多基因风险评分和传统风险模型的乳腺癌高风险分类阈值重叠:一项针对180,398名女性的研究

2025-11-030
OAAI
Polygenic risk score for breast cancer risk prediction in Asian BRCA1 and BRCA2 pathogenic variants carriers

亚洲BRCA1和BRCA2致病性变异携带者乳腺癌风险的polygenic risk score多基因风险评分

2025-09-300
OA
Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction

欧洲血统人群的多基因得分分布差异: 对乳腺癌风险预测的影响

2024-12-290
OAAI
Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

乳腺癌易感基因种系致病变异的共同观察: BRIDGES测序数据集的分析结果

2024-09-013
PRE
Understanding the genetic complexity of puberty timing across the allele frequency spectrum

了解等位基因频谱中青春期时间的遗传复杂性

2024-07-013
OAAI
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

整合多组学分析以确定卵巢癌风险区域的遗传和功能机制

2024-06-016
PRE
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

欧洲血统女性乳腺癌风险的全基因组基因-环境相互作用研究

2023-08-093
OAAI
CRISPR screens identify gene targets at breast cancer risk loci

CRISPR筛选确定乳腺癌风险位点的基因靶标

2023-03-2910
OAAI
The impact of coding germline variants on contralateral breast cancer risk and survival
2023-03-0112
OAAI
Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

拷贝数变异是已知和新的风险位点的卵巢癌风险等位基因

2022-10-106
OAAI
Epigenome erosion and SOX10 drive neural crest phenotypic mimicry in triple-negative breast cancer
2022-05-0211
OAAI
Rare germline copy number variants (CNVs) and breast cancer risk

罕见种系拷贝数变异 (CNVs) 与乳腺癌风险

2022-01-1813
OAAI
Common variants in breast cancer risk loci predispose to distinct tumor subtypes

乳腺癌风险位点的常见变异易患不同的肿瘤亚型

2022-01-0417
OAAI
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants

携带BRCA1和BRCA2致病错义变异体的女性与携带蛋白截断变异体的女性相比,患乳腺癌和卵巢癌的风险

2022-01-0117
OAAI
Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

原发性乳腺癌诊断中存在远处转移的乳腺癌患者的种系变异和乳腺癌生存率

2021-10-052
OAAI
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

基于313变异的多基因风险评分对具有杂合BRCA1或BRCA2致病变异的欧洲血统女性对侧乳腺癌风险预测的预测能力

2021-09-0120
OAAI