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1. Multi-modal AI for comprehensive breast cancer prognostication

2. Reproductive factors and mammographic density within the International Consortium of Mammographic Density: A cross-sectional study

5. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

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

7. Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

9. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

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

13. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

14. Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families

15. Presentation of Breast Cancer and Impact of Patient Navigation on Timeliness of Diagnosis and Treatment and on Adherence to Treatment Recommendations in a Multicenter Network in Malaysia

16. The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.

17. Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

18. Relevance of the MHC region for breast cancer susceptibility in Asians

19. Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

20. Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women

21. Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk

22. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

23. Overlap of high-risk individuals predicted by family history, and genetic and non-genetic breast cancer risk prediction models: implications for risk stratification

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

25. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

26. The association of age at menarche and adult height with mammographic density in the International Consortium of Mammographic Density

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

28. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.

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

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

31. Association of ESR1 germline variants with TP53 somatic variants in breast tumors in a genome-wide study

32. Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families

33. Evaluating genetic variants associated with breast cancer risk in high and moderate-penetrance genes in Asians

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

35. Gene expression signature for predicting homologous recombination deficiency in triple-negative breast cancer.

36. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

37. Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.

38. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

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

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

41. Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk

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

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. Clustering of HR+/HER2- breast cancer in an Asian cohort is driven by immune phenotypes

47. Association ofESR1germline variants withTP53somatic variants in breast tumors in a genome-wide study

48. Germline breast cancer susceptibility genes, tumor characteristics, and survival

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

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