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16 results on '"Beckmann, M. W. (Matthias W.)"'

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1. Rare germline copy number variants (CNVs) and breast cancer risk

2. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

3. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

4. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

5. 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

6. CYP3A7*1C allele:linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

7. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

8. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

9. Shared heritability and functional enrichment across six solid cancers

10. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

11. Polygenic risk scores for prediction of breast cancer and breast cancer subtypes

12. Genome-wide association study of germline variants and breast cancer-specific mortality

13. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

14. The BRCA2 c.68‐7T > A variant is not pathogenic:a model for clinical calibration of spliceogenicity

15. PHIP:a novel candidate breast cancer susceptibility locus on 6q14.1

16. PALB2, CHEK2 and ATM rare variants and cancer risk:data from COGS

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