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B072
Molekulargenetik des Mammakarzinoms Also known as:B072 Molekulargenetik des Mammakarzinoms; B072 Molekulargenetik des Mammarzinoms| ID | I:(DE-He78)B072-20160331 |
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Journal Article
The contribution of rare germline variants to the immune landscape of breast cancer.
Genome medicine nn, nn (2026) [10.1186/s13073-026-01662-6]
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A multi-ancestry genome-wide study of tamoxifen metabolism and breast cancer recurrence.
npj Breast cancer 12, 71 (2026) [10.1038/s41523-026-00931-2]
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Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer.
The breast 85, 104619 (2026) [10.1016/j.breast.2025.104619]
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Compartment-specific tumor-infiltrating immune cells and prognosis in breast cancer
iScience 29(2), 114759 (2026) [10.1016/j.isci.2026.114759]
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Journal Article (Erratum/Correction)
Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
Nature Communications 16(1), 8237 (2025) [10.1038/s41467-025-63507-x]
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Genetic landscape of Pakistani familial breast cancer patients using multigene panel testing.
International journal of cancer 157(10), 2081-2091 (2025) [10.1002/ijc.70070]
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Journal Article
Establishing the First Genetic Variant Registry for Breast and Ovarian Cancer in Colombia: Insights and Implications.
Diseases 13(7), 222 (2025) [10.3390/diseases13070222]
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Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification.
Nature Communications 16(1), 4852 (2025) [10.1038/s41467-025-59979-6]
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Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer.
npj Genomic Medicine 10(1), 73 (2025) [10.1038/s41525-025-00529-w]
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Journal Article
Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women.
Cancers 17(21), 3561 (2025) [10.3390/cancers17213561]
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