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

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

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

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

5. 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?

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

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

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

9. 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

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

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

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

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

14. Erratum: Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature communications (2019) 10 1 (431))

15. Subsequent Event Risk in Individuals With Established Coronary Heart Disease

16. Shared heritability and functional enrichment across six solid cancers

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

18. Polygenic risk scores for prediction of breast cancer and breast cancer subtypes

19. The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

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

21. The BRCA2 c.68‐7T > A variant is not pathogenic:a model for clinical calibration of spliceogenicity

22. Body mass index and breast cancer survival:a Mendelian randomization analysis

23. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

24. Genetic modifiers of CHEK2∗1100delC-associated breast cancer risk

25. Newborn genome-wide DNA methylation in association with pregnancy anxiety reveals a potential role for GABBR1

26. Body mass index and breast cancer survival

27. PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1

28. Reproductive profiles and risk of breast cancer subtypes

29. TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer

30. PHIP:a novel candidate breast cancer susceptibility locus on 6q14.1

31. PALB2, CHEK2 and ATM rare variants and cancer risk:data from COGS

32. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

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

34. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

35. BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

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

37. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

38. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

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

40. Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1

41. Prediction of breast cancer risk based on profiling with common genetic variants

42. A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients

43. Identification of novel genetic markers of breast cancer survival

44. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

45. Common germline polymorphisms associated with breast cancer-specific survival

46. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

47. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

48. Fine-scale mapping of the 4q24 locus identifies & pr two Independent loci associated with breast cancer risk

49. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

50. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

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