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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

2. Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

3. Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer

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

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

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

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

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

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

12. Residential Greenness and Cardiovascular Disease Incidence, Readmission, and Mortality.

13. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

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

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

16. Association Between Road Traffic Noise and Incidence of Diabetes Mellitus and Hypertension in Toronto, Canada: A Population‐Based Cohort Study

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

19. Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis.

20. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.

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

25. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

26. Breast Cancer

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

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

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

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

32. Ambient Fine Particulate Matter and Mortality among Survivors of Myocardial Infarction: Population-Based Cohort Study

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

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

35. Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

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

37. Ambient PM2.5, O3, and NO2 Exposures and Associations with Mortality over 16 Years of Follow-Up in the Canadian Census Health and Environment Cohort (CanCHEC)

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

39. Within- and between-city contrasts in nitrogen dioxide and mortality in 10 Canadian cities; a subset of the Canadian Census Health and Environment Cohort (CanCHEC)

40. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

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

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

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

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

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