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2. Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

3. FANCM missense variants and breast cancer risk

4. Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: A combined case-control study

5. Impact of parental cancer on IQ, stress resilience, and physical fitness in young men

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

8. PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in similar to 200,000 patients (vol 24, 69, 2022)

9. PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

11. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

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

15. A genome-wide gene-based gene-environment interaction study of breast cancer in more than 90,000 women.

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

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

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

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

20. Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

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

22. Breast cancer risks associated with missense variants in breast cancer susceptibility genes.

23. Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies

24. PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in similar to 200,000 patients

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

26. PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in similar to 200,000 patients (vol 24, 69, 2022)

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

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

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

32. Technological readiness and implementation of genomic‐driven precision medicine for complex diseases

35. CYP3A7*1C allele:linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

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

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

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

39. 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).

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

41. Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer.

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

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

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

45. 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)).

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

47. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.

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

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

50. 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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