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1. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

3. A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

4. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

5. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.

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

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

8. Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

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

10. Functionalization of single-walled carbon nanotubes and their binding to cancer cells

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

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

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

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

15. 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).

16. Breast cancer risk factors and survival by tumor subtype: Pooled analyses from the breast cancer association consortium.

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

18. Genetic insights into biological mechanisms governing human ovarian ageing.

19. 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)).

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

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

22. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.

23. Genetic insights into biological mechanisms governing human ovarian ageing

24. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium

25. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

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

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

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

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

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

31. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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