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231 results on '"Bolla, MK"'

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

2. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

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

4. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

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

6. Association analysis identifies 65 new breast cancer risk loci

7. Rare, protein-truncating variants in $\textit{ATM}$, $\textit{CHEK2}$ and $\textit{PALB2}$, but not $\textit{XRCC2}$, are associated with increased breast cancer risks

8. Bromodomain protein 4 discriminates tissue-specific super-enhancers containing disease-specific susceptibility loci in prostate and breast cancer

9. PALB2, CHEK2 and ATM rare variants and cancer risk: Data from COGS

10. rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

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

12. Fine-mapping of the 1p11.2 breast cancer susceptibility locus

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

14. Five endometrial cancer risk loci identified through genome-wide association analysis

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

16. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

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

18. RAD51B in familial breast cancer

19. Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21

20. Genetic predisposition to ductal carcinoma in situ of the breast

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

22. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

23. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

24. Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair EDITORIAL COMMENT

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

26. Identification of novel genetic markers of breast cancer survival

27. Refined histopathological predictors of BRCA1 and BRCA2 mutation status: A large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

28. MicroRNA related polymorphisms and breast cancer risk

29. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

30. FGF receptor genes and breast cancer susceptibility: Results from the Breast Cancer Association Consortium

33. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

34. Gene-environment interactions involving functional variants: Results from the Breast Cancer Association Consortium

35. Association analysis identifies 65 new breast cancer risk loci

36. rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

37. Prediction of breast cancer risk based on common genetic variants in women of East Asian ancestry

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

39. Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

40. TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer

41. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

42. Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21

43. DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

44. Childhood, adolescent and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers.

45. Polygenic risk scores stratify breast cancer risk among women with benign breast disease.

46. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset.

47. Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification.

48. Germline copy number variants and endometrial cancer risk.

49. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

50. Disentangling the relationships of body mass index and circulating sex hormone concentrations in mammographic density using Mendelian randomization.

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