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126 results on '"Beesley, Jonathan"'

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

2. 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

3. Identification of a Locus Near ULK1 Associated With Progression-Free Survival in Ovarian Cancer

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

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

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

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

8. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

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

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

11. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

12. Association analysis identifies 65 new breast cancer risk loci

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

14. Fine‐scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

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

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

17. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

18. Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer

19. Evidence of a genetic link between endometriosis and ovarian cancer

20. Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.

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

22. Genome-wide significant risk associations for mucinous ovarian carcinoma

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

24. Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

25. Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

26. Identification of six new susceptibility loci for invasive epithelial ovarian cancer.

27. Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1

28. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.

29. Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk.

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

31. ABCA transporter gene expression and poor outcome in epithelial ovarian cancer.

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

33. ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: A comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas

34. Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.

35. Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers

36. 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

37. Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC).

38. Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2.

39. 7q21-rs6964587 and breast cancer risk: an extended case–control study by the Breast Cancer Association Consortium

40. Association Between a Germline OCA2 Polymorphism at Chromosome 15q13.1 and Estrogen Receptor–Negative Breast Cancer Survival

41. Risk of Estrogen Receptor–Positive and –Negative Breast Cancer and Single–Nucleotide Polymorphism 2q35-rs13387042

42. Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study

43. The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

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

45. Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab

46. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

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

48. Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

49. Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers

50. Xenobiotic-Metabolizing Gene Polymorphisms and Ovarian Cancer Risk

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