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3. NTHL1 is a recessive cancer susceptibility gene

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

6. Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

7. RAD51B in Familial Breast Cancer.

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

9. Posaconazole‐ibrutinib interaction cannot be avoided by staggered dosing: How to optimize ibrutinib dose during posaconazole treatment

11. Genome-wide association study of germline variants and breast cancer-specific mortality

13. Posaconazole‐ibrutinib interaction cannot be avoided by staggered dosing: How to optimize ibrutinib dose during posaconazole treatment.

14. Ticagrelor Increases Exposure to the Breast Cancer Resistance Protein Substrate Rosuvastatin.

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

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

19. Association analysis identifies 65 new breast cancer risk loci

22. High miR-30 Expression Associates with Improved Breast Cancer Patient Survival and Treatment Outcome

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

24. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

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

26. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

27. The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

28. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

29. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

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

31. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

32. Implementation of CYP2D6copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

33. Recurrent moderate‐risk mutations in Finnish breast and ovarian cancer patients

34. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

35. Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

36. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

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

38. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

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

40. RAD51B in Familial Breast Cancer

41. FANCMc.5101C>T mutation associates with breast cancer survival and treatment outcome

42. RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families

44. FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome.

45. RAD51B in Familial Breast Cancer

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

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

48. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

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

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

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