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

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

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

7. Evaluation of vitamin D biosynthesis and pathway target genes reveals UGT2A1/2 and EGFR polymorphisms associated with epithelial ovarian cancer in African American Women

8. Shared heritability and functional enrichment across six solid cancers

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

10. PREDICTING RISK OF OVARIAN MALIGNANCY IMPROVED SCREENING AND EARLY DETECTION FEASIBILITY STUDY (PROMISE-FS)

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

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

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

14. Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

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

16. Abstract 4246: Comparison of pathology versus IHC-based ovarian carcinoma histology assignment using gene expression, DNA methylation, and clinical outcome data

17. 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

18. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

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

20. COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

22. Genome-wide association study for ovarian cancer susceptibility using pooled DNA.

23. Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

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

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

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

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

29. Association of KRAS SNP rs61764370 with risk of invasive epithelial ovarian cancer: Implications for clinical testing

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

35. Preface

36. O-58 The UK MARIBS study of MRI breast screening: progress on genetic and density projects

37. 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.

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

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

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

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

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

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

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

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

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

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

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