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74 results on '"Dörk, Thilo"'

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2. Bone Marrow Failure and Immunodeficiency Associated with Human RAD50 Variants

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

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

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

7. Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility

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

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

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

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

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

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

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

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

18. Shared heritability and functional enrichment across six solid cancers

20. Identification of nine new susceptibility loci for endometrial cancer

21. Correction: Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

22. Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci

23. Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer

25. Patient survival and tumor characteristics associated with CHEK2:p.I157T – findings from the Breast Cancer Association Consortium

26. Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)

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

28. Candidate gene variants of the immune system and sudden infant death syndrome

29. Genetic predisposition to ductal carcinoma in situ of the breast

30. Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1

34. Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

36. Double heterozygotes among breast cancer patients analyzed for BRCA1, CHEK2, ATM, NBN/NBS1, and BLM germ-line mutations

37. Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe

39. Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom’s syndrome, is associated with breast cancer in Slavic populations

40. New mutations in the ATM gene and clinical data of 25 AT patients

41. Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer

44. Combined effects of single nucleotide polymorphisms TP53 R72P and MDM2 SNP309, and p53 expression on survival of breast cancer patients

45. TGFB1 gene polymorphism Leu10Pro (c.29T>C), prostate cancer incidence and quality of life in patients treated with brachytherapy

46. Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer risk

49. NBS1 variant I171V and breast cancer risk

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