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303 results on '"Dork T."'

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1. FANCM missense variants and breast cancer risk

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

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

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

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

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

7. Cross-Cancer Genome-Wide Association Study of Endometrial Cancer and Epithelial Ovarian Cancer Identifies Genetic Risk Regions Associated with Risk of Both Cancers.

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

9. Polygenic risk modeling for prediction of epithelial ovarian cancer risk (vol 30, pg 349, 2021)

10. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

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

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

13. Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

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

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

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

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

18. 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).

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

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

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

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

23. 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)).

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

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

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

27. 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.

28. 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?.

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

30. Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer

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

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

33. 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

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

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

36. Mendelian randomisation study of smoking exposure in relation to 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. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

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

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

41. Two truncating variants in FANCC and breast cancer risk.

42. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.

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

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

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

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

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

48. Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria

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