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743 results on '"Burwinkel, B."'

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1. Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

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

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

4. FANCM missense variants and breast cancer risk

5. Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

6. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

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

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

11. Incorporating progesterone receptor expression into the PREDICT breast prognostic model

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

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

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

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

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

18. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

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

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

21. Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078)).

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

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

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

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

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

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

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

31. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

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

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

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

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

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

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

38. Two truncating variants in FANCC and breast cancer risk.

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

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

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

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

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

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

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

46. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.

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

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

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

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

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