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1. Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

2. Correction: Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

3. Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

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

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

6. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

7. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

11. Supplementary Table 2 from Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

12. Supplementary Table 3 from Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

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

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

15. Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 gene

16. Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

19. Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium

20. Identification of a DMBT1 Polymorphism Associated with Increased Breast Cancer Risk and Decreased Promoter Activity

24. Nuclear receptor coregulator SNP discovery and impact on breast cancer risk

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

26. Additional file 4: Table S5. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

27. Additional file 2: Table S3. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

28. Additional file 6: Table S6. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

29. Additional file 7: Table S7. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

30. Additional file 3: Table S4. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

31. Additional file 5: Table S2. of Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

32. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

33. Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

34. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

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

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

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

39. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

40. Identification of six new susceptibility loci for invasive epithelial ovarian cancer

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

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

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

44. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

45. MicroRNA Related Polymorphisms and Breast Cancer Risk

46. Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

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

48. 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

49. Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1

50. Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus:Putative Functional Variants Differentially Bind FOXA1 and E2F1

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