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1. Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

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

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

4. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

5. The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

6. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021)

7. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

8. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

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

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

11. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

12. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

13. Shared heritability and functional enrichment across six solid cancers

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

15. Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

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

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

18. A transcriptome-wide association study among 97,898 women to identify candidate susceptibility genes for epithelial ovarian cancer risk

19. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

20. Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

21. Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

22. Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

23. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

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

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

26. Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

27. Male breast cancer in BRCA1 and BRCA2 mutation carriers: Pathology data from the Consortium of Investigators of Modifiers of BRCA1/2

28. Identification of six new susceptibility loci for invasive epithelial ovarian cancer

29. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

30. Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers

31. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

32. Partial Restoration of Degraded DNA from Archival Paraffin-Embedded Tissues

33. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

34. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

35. Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

36. Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

37. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

38. Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

39. Exploring the link between MORF4L1 and risk of breast cancer

40. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

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

42. Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

43. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

44. BRCA2 Polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers

45. HLA gene polymorphism is a modifier of age-related breast cancer penetrance in carriers of BRCA1 pathogenic alleles.

46. The Spectrum of Disease-Associated Alleles in Countries with a Predominantly Slavic Population.

47. Pathways and targeting avenues of BRAF in non-small cell lung cancer.

48. Agnostic Administration of Targeted Anticancer Drugs: Looking for a Balance between Hype and Caution.

49. Structural implications of amyloidogenic rare variants Ser282Leu and Gln356Arg identified in h-BRCA1.

50. Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk.

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