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1. A Likelihood Ratio Approach for Utilizing Case‐Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

3. Incorporating progesterone receptor expression into the PREDICT breast prognostic model

4. PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

5. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

6. PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

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

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

9. 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

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

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

12. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

15. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association ConsortiumBreast Cancer Risk Factors and Survival By Tumor Subtype

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

17. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

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

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

20. The impact of coding germline variants on contralateral breast cancer risk and survival

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

22. I'm Not Crying, You're Crying: An Evaluation of the Impact of Emotional Text on Negation Comprehension

23. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

24. Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

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

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

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

29. Adherence to and optimization of guidelines for Risk of Recurrence/Prosigna testing using a machine learning model: a Swedish multicenter study

30. PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1

31. BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

32. Genetic modifiers of CHEK2*1100delC-associated breast cancer risk

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

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

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

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

37. Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

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

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

40. An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression

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

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

43. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.

44. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

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

46. RAD51B in Familial Breast Cancer.

47. The impact of circulating protein levels identified by affinity proteomics on short-term, overall breast cancer risk

48. The association between weight at birth and breast cancer risk revisited using Mendelian randomisation

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

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

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