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19 results on '"Schmidt, M. K. (Marjanka K.)"'

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1. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

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

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

4. 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?

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

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

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

8. 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

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

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

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

12. Shared heritability and functional enrichment across six solid cancers

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

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

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

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

17. Body mass index and breast cancer survival:a Mendelian randomization analysis

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

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

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