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759 results on '"Dörk, Thilo"'

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

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

4. Genome-wide association analyses of ovarian cancer patients undergoing primary debulking surgery identify candidate genes for residual disease

6. Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

7. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

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

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

10. Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

12. The impact of coding germline variants on contralateral breast cancer risk and survival

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

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

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

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

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

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

23. Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk

24. The association between weight at birth and breast cancer risk revisited using Mendelian randomisation

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

27. Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39

28. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

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

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

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

34. History of hypertension, heart disease, and diabetes and ovarian cancer patient survival : evidence from the ovarian cancer association consortium

38. Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

39. Association of two genomic variants with HPV type-specific risk of cervical cancer

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

41. Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study

43. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

44. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

45. Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

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

47. Two truncating variants in FANCC and breast cancer risk

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

49. Shared heritability and functional enrichment across six solid cancers

50. Polymorphisms of the hypothalamic–pituitary–adrenal axis may lead to an inadequate response to stress and contribute to sudden infant death syndrome.

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