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88 results on '"Jakimovska M"'

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1. Cystic fibrosis mutation spectrum in north macedonia: A step toward personalized therapy

2. Clinical Relevance of CHEK2 And NBN Mutations in the Macedonian Population

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

31. The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

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

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

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

35. Polygenic risk scores for prediction of breast cancer and breast cancer subtypes

37. The impact of antenatal care on the neonatal outcome

40. Circulating serum sVCAM-1 concentration in advanced ovarian cancer patients: correlation with concentration in ascites

41. Laparoscopic injury of the obturator nerve during fertility-sparing procedure for cervical cancer

42. Life-threatening bleeding after pelvic lymphadenectomy for cervical cancer: endovascular management of ruptured false aneurysm of the external iliac artery

43. Ovarian sclerosing stromal tumor mimicking malignancy: case series and literature review.

44. An implementation of the learning curve cumulative summation test to evaluate a practicum for endometrial cancer ultrasound staging.

45. A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: application to BRCA1 and BRCA2 .

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

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

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

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

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