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

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

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

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

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

6. 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

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

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

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

10. Polygenic risk scores for prediction of breast cancer and breast cancer subtypes

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

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

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

14. BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

15. Correspondence: SEMA4A variation and risk of colorectal cancer

16. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

17. Recurrent Coding Sequence Variation Explains only A Small Fraction of the Genetic Architecture of Colorectal Cancer

18. Fine-scale mapping of the 4q24 locus identifies & pr two Independent loci associated with breast cancer risk

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