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9. Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2

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

11. Frequent somatic mutations of chromatin remodeling genes in metastatic cutaneous squamous cell carcinoma

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

15. Allele‐specific imbalance mapping identifies HDAC9 as a candidate gene for cutaneous squamous cell carcinoma

16. Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.

18. Sequence divergence of Mus spretus and Mus musculus across a skin cancer susceptibility locus.

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

21. Supplementary Table 2 from Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

22. Supplementary Table 1 from Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk

23. Supplementary Table 3 from Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

24. Supplementary Tables 1-9 from Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

25. Data from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

28. Supplementary Methods, Tables 1-3, Figure 1 from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

30. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

36. Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

40. The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium

42. KMT2D loss drives aggressive tumor phenotypes in cutaneous squamous cell carcinoma

44. Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer

46. Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

49. Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

50. ­­Differences in Somatic TP53 Mutation Type in Breast Tumors by Race and Receptor Status

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