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Health-f2-2009-223175

Funded outputs count: 69
Funder award ID: HEALTH-F2-2009-223175
OpenAlex ID: G3714974232
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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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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Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women
2024 · Figueroa, J., Lee, D.G., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis
2024 · Castelao, J.E., Geisler, J., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Combined Associations of a Polygenic Risk Score and Classical Risk Factors with Breast Cancer Risk
2024 · Mavaddat, N., Schoemaker, M.J., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
2024 · Koutros, S., Janni, W., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
2024 · Manoukian, S., Ramachandran, D., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
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Leisure time television watching, computer use and risks of breast, colorectal and prostate cancer: A Mendelian randomisation analysis
2023 · Nikos Papadimitriou, Nabila Kazmi, et al. · Cancer Medicine · 3
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Investigation of common genetic risk factors between thyroid traits and breast cancer
2023 · Elise A Lucotte, Yazdan Asgari, et al. · Human Molecular Genetics · 6
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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
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
2023 · Pooja Middha, Xiaoliang Wang, et al. · Breast Cancer Research · 13
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GCPBayes pipeline: a tool for exploring pleiotropy at the gene level
2023 · Yazdan Asgari, Pierre-Emmanuel Sugier, et al. · NAR Genomics and Bioinformatics · 2
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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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Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2
2023 · Denise G. O’Mahony, Susan J. Ramus, et al. · British Journal of Cancer · 21
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Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions
2023 · Sara Lindström, Lu Wang, et al. · JNCI Journal of the National Cancer Institute · 31
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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 · 28
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 · 12
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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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Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study
2022 · Suzanne C Dixon-Suen, Sarah J Lewis, et al. · British Journal of Sports Medicine · 87
Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women
2022 · Xiaoliang Wang, Pooja Middha Kapoor, et al. · Scientific Reports · 6
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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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Polygenic risk modeling for prediction of epithelial ovarian cancer risk
2022 · Eileen O. Dareng, Jonathan P. Tyrer, et al. · European Journal of Human Genetics · 73
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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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Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis
2021 · Maria Escala-Garcia, Sander Canisius, et al. · Scientific Reports · 5
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