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1. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (vol 5, 4999, 2014)

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

3. Meeting abstracts from the Annual Conference on Hereditary Cancers 2016

4. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

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

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

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

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

9. Identification of novel genetic markers of breast cancer survival

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

11. Assessing associations between the AURKAHMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

12. Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2

13. Identification of novel genetic markers of breast cancer survival

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

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

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

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

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

19. Refined histopathological predictors of BRCA1\ud and BRCA2 mutation status: a large-scale analysis\ud of breast cancer characteristics from the BCAC,\ud CIMBA, and ENIGMA consortia

20. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

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

22. Genetic Predisposition to In Situ and Invasive Lobular\ud Carcinoma of the Breast

23. A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

24. MicroRNA related polymorphisms and breast cancer risk

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

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

27. Identification of novel genetic markers of breast cancer survival

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

29. Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

30. Assessing associations between the AURKAHMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

31. Candidate genetic modifiers for breast and ovarian cancer risk inBRCA1andBRCA2 mutation carriers

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

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

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

35. FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

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

37. DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

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

39. Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

40. MicroRNA related polymorphisms and breast cancer risk

41. Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

42. Refined histopathological predictors of BRCA1 and BRCA2 mutation status: A large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

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

44. Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

45. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

46. Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

47. MicroRNA Related Polymorphisms and Breast Cancer Risk

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

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

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

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