Search

Your search keyword '"Johnson, Nichola"' showing total 35 results

Search Constraints

Start Over You searched for: Author "Johnson, Nichola" Remove constraint Author: "Johnson, Nichola" Topic single nucleotide Remove constraint Topic: single nucleotide
35 results on '"Johnson, Nichola"'

Search Results

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

2. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

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

4. Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent.

5. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.

6. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

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

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

9. Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk.

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

11. Prediction of breast cancer risk based on profiling with common genetic variants.

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

13. Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

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

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

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

17. Unbiased analysis of potential targets of breast cancer susceptibility loci by Capture Hi-C

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

19. A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium.

20. Genetic predisposition to in situ and invasive lobular carcinoma of the breast.

21. A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium

22. Identification of New Genetic Susceptibility Loci for Breast Cancer Through Consideration of Gene‐Environment Interactions

23. Large-scale genotyping identifies 41 new loci associated with breast cancer risk

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

25. Genome-wide association studies identify four ER negative-specific breast cancer risk loci.

26. A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication

27. 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

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

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

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

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

32. Association of ESR1 gene tagging SNPs with breast cancer risk

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

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

35. Common non-synonymous snps associated with breast cancer susceptibility: findings from the breast cancer association consortium

Catalog

Books, media, physical & digital resources