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CA148112

Funded outputs count: 91
Funder award ID: CA148112
OpenAlex ID: G3918072604
Circulating Inflammatory Markers and Mammographic Density Phenotypes: a Mendelian Randomization Analysis
2026 · Austin Hammermeister Suger, Tabitha A. Harrison, et al. · medRxiv
PRANA: A Deep Learning Method for Adapting Polygenic Risk Scores to Diverse Ethnic Groups
2026 · Hagai Levi, Qin Wang, et al. · medRxiv
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Differences in overall survival for invasive epithelial ovarian cancer by race and ethnicity: results from the Ovarian Cancer Association Consortium
2026 · Nicola S. Meagher, Kami K. White, et al. · British Journal of Cancer
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Genomic risk model to implement precision prostate cancer screening in clinical care: the ProGRESS study
2026 · Jason L. Vassy, Anna M. Dornisch, et al. · Nature Cancer · 8
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
2025 · Daniel R. Barnes, Jonathan P. Tyrer, et al. · npj Genomic Medicine · 1
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Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
2025 · Barnes, Daniel R, Tyrer, Jonathan P, et al. · eScholarship (California Digital Library)
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GWAS meta-analysis identifies five susceptibility loci for endometrial cancer
2025 · Dhanya Ramachandran, Xuemin Wang, et al. · EBioMedicine · 4
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Lessons learned from a candidate gene study investigating aromatase inhibitor treatment outcome in breast cancer
2025 · Reiner Hoppe, Stefan Winter, et al. · npj Breast Cancer · 1
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Phenome-wide Mendelian randomisation analysis of 378,142 cases reveals risk factors for eight common cancers
2024 · Molly Went, Amit Sud, et al. · Nature Communications · 28
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Genome-wide association analyses of ovarian cancer patients undergoing primary debulking surgery identify candidate genes for residual disease
2024 · Dhanya Ramachandran, Jonathan P. Tyrer, et al. · npj Genomic Medicine · 5
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Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer
2023 · Katharina Wichert, Reiner Hoppe, et al. · European Journal of Epidemiology · 8
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A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2
2023 · Maria Zanti, Denise G. O'Mahony, et al. · Human Mutation · 6
Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
2023 · Hagai Levi, Shai Carmi, et al. · Journal of Medical Genetics · 4
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Association of the CHEK2 c. 1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival
2023 · Anna Morra, Maartje A. C. Schreurs, et al. · Cancer Medicine · 11
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Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
2023 · Stefanie H. Mueller, Alvina G. Lai, et al. · Genome Medicine · 15
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Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival
2023 · Josephine M.N. Lopes Cardozo, Irene L. Andrulis, et al. · Journal of Clinical Oncology · 29
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Lifestyle and personal factors associated with having macroscopic residual disease after ovarian cancer primary cytoreductive surgery
2022 · Minh Tung Phung, Penelope M. Webb, et al. · Gynecologic Oncology · 2
Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci
2022 · Amber A DeVries, Joe Dennis, et al. · JNCI Journal of the National Cancer Institute · 13
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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
2022 · Christopher Hakkaart, John F. Pearson, et al. · Communications Biology · 14
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CA-125 Levels Are Predictive of Survival in Low-Grade Serous Ovarian Cancer—A Multicenter Analysis
2022 · Christoph Wohlmuth, Vladimir Djedovic, et al. · Cancers · 13
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Assessing the causal role of epigenetic clocks in the development of multiple cancers: a Mendelian randomization study
2022 · Fernanda Morales-Berstein, Daniel L McCartney, et al. · eLife · 86
Body Shape Phenotypes And Breast Cancer Risk: A Mendelian Randomization Analysis.
2022 · Laia Peruchet Noray, Niki Dimou, et al. · Research Square
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Rare germline copy number variants (CNVs) and breast cancer risk
2022 · Joe Dennis, Jonathan P. Tyrer, et al. · Communications Biology · 15
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Common variants in breast cancer risk loci predispose to distinct tumor subtypes
2022 · Thomas U. Ahearn, Haoyu Zhang, et al. · Breast Cancer Research · 33
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High Prediagnosis Inflammation-Related Risk Score Associated with Decreased Ovarian Cancer Survival
2021 · Katharine K. Brieger, Minh Tung Phung, et al. · Cancer Epidemiology Biomarkers & Prevention · 9
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