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1. Genome disorder and breast cancer susceptibility

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

4. Correction: Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

5. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

6. Additional file 2: Table S2. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

8. Additional file 10: Figure S2. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

9. Additional file 8: Table S8. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

10. Additional file 5: Table S4. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

11. Additional file 1: Table S1. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

12. Additional file 3: Table S3. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

13. Additional file 7: Table S7. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

14. Additional file 9: Figure S1. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

15. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

16. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

17. A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

18. Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk

22. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

27. Additional file 6: Table S5. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

28. Additional file 6: Table S5. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

29. Additional file 2: Table S2. of A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

30. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus

31. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

32. Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?

33. Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

34. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.

35. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

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