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33 results on '"Tamimi R.M."'

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

2. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

3. Breast cancer risk factors and survival by tumor subtype: Pooled analyses from the breast cancer association consortium.

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

5. Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078)).

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

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

8. Combined Associations of a Polygenic Risk Score and Classical Risk Factors with Breast Cancer Risk.

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

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

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

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

14. Two truncating variants in FANCC and breast cancer risk.

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

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

17. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.

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

20. Two truncating variants in FANCC and breast cancer risk

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

22. PAM50 molecular intrinsic subtypes in the nurses' health Study cohorts

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

24. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.

25. Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk.

27. Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

29. Birth weight, breast cancer susceptibility loci, and breast cancer risk

30. Birth weight and mammographic density among postmenopausal women in Sweden

31. HM32 Cognitive coping in young women with breast cancer

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