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1. Making the Connection: How Membrane Contact Sites Have Changed Our View of Organelle Biology

2. Corrigendum to “Current and future diagnostic and treatment strategies for patients with invasive lobular breast cancer”: [Annals of Oncology 33 (2022) 769–785, (S092375342201167X), (10.1016/j.annonc.2022.05.006)]

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

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

5. Current and future diagnostic and treatment strategies for patients with invasive lobular breast cancer

6. 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?

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

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

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

10. 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

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

12. Vedolizumab for ulcerative colitis: Real world outcomes from a multicenter observational cohort of Australia and Oxford

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

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

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

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

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

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

23. A systematic review and meta-analysis of the association between poor oral health and substance abuse

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

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

26. Genomic Evolution of Breast Cancer Metastasis and Relapse

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

28. FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium.

29. Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

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

31. Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

32. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

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

34. FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

35. Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

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

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

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

39. Genome-wide association analysis identifies three new breast cancer susceptibility loci

40. Germline BRCA1 mutations increase prostate cancer risk.

41. Genome-wide association analysis identifies three new breast cancer susceptibility loci

42. Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

43. 11q13 is a susceptibility locus for hormone receptor positive breast cancer

44. Genome-wide association analysis identifies three new breast cancer susceptibility loci

45. Genome-wide association analysis identifies three new breast cancer susceptibility loci

46. Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

47. Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk.

48. Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

49. Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript

50. BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients.

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