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1. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

2. Assessing the impact of MRI based diagnostics on pre-treatment disease classification and prognostic model performance in men diagnosed with new prostate cancer from an unscreened population

3. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

4. KLK3 SNP–SNP interactions for prediction of prostate cancer aggressiveness

5. Polygenic hazard score is associated with prostate cancer in multi-ethnic populations

6. European polygenic risk score for prediction of breast cancer shows similar performance in Asian women

7. Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants

9. Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestryResearch in context

10. Publisher Correction: Shared heritability and functional enrichment across six solid cancers

11. Association analyses identify 31 new risk loci for colorectal cancer susceptibility

12. Shared heritability and functional enrichment across six solid cancers

13. Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

14. Prediction models for prostate cancer to be used in the primary care setting: a systematic review

15. Germline variation at 8q24 and prostate cancer risk in men of European ancestry

16. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

17. Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

18. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

19. Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

20. Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

21. Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

22. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

23. Responses to provision of personalised cancer risk information: a qualitative interview study with members of the public

24. Notes to the Plays

25. Introduction

28. Appendix

29. Preface

31. Contents

33. Notes

34. Title, Copyright

35. Bibliography

39. From Bad to Worse

40. Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study

41. Appraising the role of previously reported risk factors in epithelial ovarian cancer risk: A Mendelian randomization analysis.

42. The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association Consortium

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

44. Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

45. Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis.

46. Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.

47. Association between Prostinogen (KLK15) genetic variants and prostate cancer risk and aggressiveness in Australia and a meta-analysis of GWAS data.

48. Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers.

49. Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies.

50. iHELP: Personalised Health Monitoring and Decision Support Based on Artificial Intelligence and Holistic Health Records.

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