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1. Genomic profiles and clinical presentation of chordoma

3. Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies

4. Impact of Transcript (p16/p14ARF) Alteration on Cancer Risk in CDKN2A Germline Pathogenic Variant Carriers.

5. A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

6. DNA methylation age in paired tumor and adjacent normal breast tissue in Chinese women with breast cancer

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

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

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

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

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

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

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

19. Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival

23. Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer

24. Supplementary Table 3 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

25. Supplementary Table 1 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

26. FIGURE 2 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

27. Supplementary Figure 3 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

28. FIGURE 3 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

29. FIGURE 1 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

30. Supplementary Figure 5 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

31. Data from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

32. Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

33. Supplementary Figure 1 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

34. Supplementary Table 2 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

35. FIGURE 4 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

36. Supplementary Figure 2 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

37. Supplementary Figure 4 from Population-specific Mutation Patterns in Breast Tumors from African American, European American, and Kenyan Patients

39. Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1–Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome

42. Genome-wide association study of germline variants and breast cancer-specific mortality

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

45. Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families

46. Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies.

47. Immune gene expression profiling reveals heterogeneity in luminal breast tumors

48. Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

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

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