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

3. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

4. Shared heritability and functional enrichment across six solid cancers

5. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4)

6. Risk of Ovarian Cancer and the NF-? B Pathway: Genetic Association with IL1A and TNFSF10

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

8. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

9. A Kallikrein 15 (KLK15) single nucleotide polymorphism located close to a novel exon shows evidence of association with poor ovarian cancer survival

10. Evidence for a time-dependent association between FOLR1 expression and survival from ovarian carcinoma:implications for clinical testing. An Ovarian Tumour Tissue Analysis consortium study

11. The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population

12. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers : Implications for risk prediction

13. Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium

14. Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis

15. Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer

19. Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survival

20. Preface

21. Evidence for a time-dependent association between FOLR1 expression and survival from ovarian carcinoma: implications for clinical testing. An Ovarian Tumour Tissue Analysis consortium study.

22. Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

23. Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

25. Cell cycle genes and ovarian cancer susceptibility: a tagSNP analysis.

26. Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer.

27. Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.

28. Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations.

29. Ovarian carcinoma in situ with germline BRCA1 mutation and loss of heterozygosity at BRCA1 and TP53.

30. Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

31. Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium

32. Variation in NF- B Signaling Pathways and Survival in Invasive Epithelial Ovarian Cancer

33. Perception and recognition memory in monkeys following lesions of area TE and perirhinal cortex.

34. Analysis of Over 10,000 Cases Finds No Association between Previously Reported Candidate Polymorphisms and Ovarian Cancer Outcome

35. Obesity and risk of ovarian cancer subtypes: evidence from the Ovarian Cancer Association Consortium

36. Risk of Ovarian Cancer and the NF- B Pathway: Genetic Association with IL1A and TNFSF10

37. The Role of KRAS rs61764370 in Invasive Epithelial Ovarian Cancer: Implications for Clinical Testing

38. Prostate Cancer Susceptibility Polymorphism rs2660753 Is Not Associated with Invasive Ovarian Cancer

39. LIN28B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer

40. MicroRNA Processing and Binding Site Polymorphisms Are Not Replicated in the Ovarian Cancer Association Consortium

41. Genetic Variation in TYMS in the One-Carbon Transfer Pathway Is Associated with Ovarian Carcinoma Types in the Ovarian Cancer Association Consortium

42. Single Nucleotide Polymorphisms in the TP53 Region and Susceptibility to Invasive Epithelial Ovarian Cancer

43. Dissociation between the effects of damage to perirhinal cortex and area TE.

44. Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility 'hot-spot'

46. Next generation sequencing approaches to identify novel susceptibility genes for epithelial ovarian cancer

47. Functional analysis of low-moderate risk susceptibility genes emerging from pathway based approaches and genome wide association studies in epithelial ovarian cancer

48. Prognostic gene expression signature for high-grade serous ovarian cancer.

49. Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the Ovarian Cancer Association Consortium pooled analysis.

50. BRCA1 promoter deletions in young women with breast cancer and a strong family history: a population-based study.

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