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W81xwh-10-1-0341

Funded outputs count: 42
Funder award ID: W81XWH-10-1-0341
OpenAlex ID: G459917499
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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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 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 · 14
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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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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 · 88
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
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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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
2021 · Anna Morra, Maria Escala-Garcia, et al. · Breast Cancer Research · 22
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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.
2021 · Morra, Anna, Escala-Garcia, Maria, et al. · Apollo (University of Cambridge)
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Mendelian randomisation study of smoking exposure in relation to breast cancer risk
2021 · Hanla A. Park, Sonja Neumeyer, et al. · British Journal of Cancer · 22
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Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?
2021 · JooYong Park, Ji-Yeob Choi, et al. · Cancers · 9
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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
2021 · Juliette Coignard, Michael Lush, et al. · Nature Communications · 40
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CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers
2021 · NBCS Collaborators, Nichola Johnson, et al. · British Journal of Cancer · 9
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
2020 · de Kort, Wim L. A. M., Wildiers, Hans, et al. · Kölner Universitäts PublikationsServer (Universität zu Köln) · 7
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Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
2020 · Jingjing Liu, Wendy J. C. Prager - van der Smissen, et al. · Scientific Reports · 6
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A Mendelian randomization analysis of circulating lipid traits and breast cancer risk
2019 · Alicia Beeghly-Fadiel, Nikhil K Khankari, et al. · International Journal of Epidemiology · 88
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Two truncating variants in FANCC and breast cancer risk
2019 · Thilo Dörk, Paolo Peterlongo, et al. · Scientific Reports · 9
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Genome-wide association study of germline variants and breast cancer-specific mortality
2019 · NBCS Collaborators, Maria Escala-Garcia, et al. · British Journal of Cancer · 62
Shared heritability and functional enrichment across six solid cancers
2019 · Xia Jiang, Hilary K. Finucane, et al. · Nature Communications · 110
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
2018 · NBCS Collaborators, Lang Wu, et al. · Nature Genetics · 216
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
2018 · The Profile Study, Fredrick R. Schumacher, et al. · Nature Genetics · 902
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