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1. FANCM missense variants and breast cancer risk

2. Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

3. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

4. Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

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

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

7. Breast cancer risk genes - Association analysis in more than 113,000 women.

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

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

10. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

11. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

12. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.

13. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

14. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

15. Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

16. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

17. Shared heritability and functional enrichment across six solid cancers.

18. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4).

19. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.

20. Erratum: Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature communications (2019) 10 1 (431))

21. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

22. PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1

23. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

24. Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

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

26. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

27. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

28. Age-And tumor subtype-specific breast cancer risk estimates for CHEK2∗1100delC Carriers

29. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

30. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

31. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

32. MicroRNA related polymorphisms and breast cancer risk

33. Prediction of breast cancer risk based on profiling with common genetic variants

34. Fine-scale mapping of the 4q24 locus identifies & pr two Independent loci associated with breast cancer risk

35. Large-scale genotyping identifies 41 new loci associated with breast cancer risk

36. Comparison of 6q25 Breast Cancer Hits from Asian and\ud European Genome Wide Association Studies in the\ud Breast Cancer Association Consortium (BCAC)

37. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

38. MicroRNA related polymorphisms and breast cancer risk

39. 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: Evidence from the Breast Cancer Association Consortium

40. Comparison of 6q25 breast cancer hits from Asian and European genome wide association studies in the Breast Cancer Association consortium (BCAC)

41. Breast cancer risk and 6q22.33: Combined results from breast cancer association consortium and consortium of investigators on modifiers of brca1/2

42. Genome-wide association analysis identifies three new breast cancer susceptibility loci

43. Confirmation of 5p12 as a susceptibility locus for progesterone-receptor- positive, lower grade breast cancer

44. Missense Variants in ATM in 26,101 Breast Cancer Cases and 29,842 Controls

45. Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers.

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