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

2. Comparison of the ABC and ACMG systems for variant classification

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

4. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

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

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

9. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association ConsortiumBreast Cancer Risk Factors and Survival By Tumor Subtype

10. Global prevalence, cascade of care, and prophylaxis coverage of hepatitis B in 2022: a modelling study

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

12. Global change in hepatitis C virus prevalence and cascade of care between 2015 and 2020: a modelling study

14. Male Infertility associated with a Novel PRKAR1A Mutation in Carney Complex.

15. Global Presence and Penetrance of CSF1R-Related Disorder.

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

17. Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21

20. Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction

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

24. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

26. Influence of OASL gene polymorphisms on host response to interferon therapy in chronic hepatitis C virus patients

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

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

30. Publisher Correction: Shared heritability and functional enrichment across six solid cancers

31. Two truncating variants in FANCC and breast cancer risk

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

33. Shared heritability and functional enrichment across six solid cancers

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

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

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

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

39. Comparative proteomics analysis of human FFPE testicular tissues reveals new candidate biomarkers for distinction among azoospermia types and subtypes

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

42. Association analysis identifies 65 new breast cancer risk loci

43. Alström Syndrome with Early Vision and Hearing Impairement

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

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

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

48. Molecular Diagnostics of ß-Thalassemia

50. Genetic Variation of The BRCA1 and BRCA2 Genes in Macedonian Patients

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