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

2. PI-07: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES

3. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

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

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

6. MicroRNA related polymorphisms and breast cancer risk

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

8. FGF receptor genes and breast cancer susceptibility: Results from the Breast Cancer Association Consortium

9. Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

10. Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel

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

12. Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer

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

14. A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

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

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

17. P1481: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES

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

19. A Genome-Wide Gene-Based Gene-Environment Interaction Study of Breast Cancer in More than 90,000 Women

20. Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women

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

22. Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci

23. Rare germline copy number variants (CNVs) and breast cancer risk

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

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

26. Rare germline copy number variants (CNVs) and breast cancer risk

27. 149P Associations between the 313-SNP polygenic risk score and breast cancer risk in women from Crete

28. P135: THE CLINGEN HEMOGLOBINOPATHY VARIANT CURATION EXPERT PANEL

29. Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals

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

31. Elective cancer surgery in COVID-19–Free surgical pathways during the SARS-cov-2 pandemic: An international, multicenter, comparative cohort study

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

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

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

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

36. Combined Associations of a Polygenic Risk Score and Classical Risk Factors with Breast Cancer Risk.

37. 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.

38. Gene-environment interactions relevant to estrogen and risk of breast cancer: Can gene-environment interactions be detected only among candidate snps from genome-wide association studies?.

39. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis.

40. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

41. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

42. 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

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

44. Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

45. Gene-environment interactions relevant to estrogen and risk of breast cancer:can gene-environment interactions be detected only among candidate SNPs from genome-wide association studies?

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

47. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

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

49. 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

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