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1. Perceptions of Multicancer Detection Tests Among Primary Care Physicians and Laypersons: A Qualitative Study.

2. Primary care physicians and laypersons' perceptions of multicancer detection clinical trial designs.

3. Resource requirements to accelerate clinical applications of next-generation sequencing and radiomics: workshop commentary and review.

4. BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2.

5. Lexicon for blood‐based early detection and screening: BLOODPAC consensus document.

6. Cancer screening with multicancer detection tests: A translational science review.

7. Genetic variation in insulin-like growth factor signaling genes and breast cancer risk among BRCA1 and BRCA2 carriers

9. Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

10. Table A1: ICD-9-CM Neoplasm Terms for Lung Cancer from Impact of Broadening Trial Eligibility Criteria for Patients with Advanced Non–Small Cell Lung Cancer: Real-World Analysis of Select ASCO-Friends Recommendations

11. Supplementary Tables S1-S3 from The FDA Oncology Center of Excellence Scientific Collaborative: Charting a Course for Applied Regulatory Science Research in Oncology

12. Supplementary Tables 1-4 from Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

13. Data from Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

14. Supplementary Table 1 from Genetic Variation in IGF2 and HTRA1 and Breast Cancer Risk among BRCA1 and BRCA2 Carriers

15. Data from Modification of Ovarian Cancer Risk by BRCA1/2-Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers

16. Supplementary Table 4 from Modification of Ovarian Cancer Risk by BRCA1/2-Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers

17. Supplementary Table 2 from Modification of Ovarian Cancer Risk by BRCA1/2-Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers

18. Supplementary Table 2: Revised 7-14-09 from Modification of Ovarian Cancer Risk by BRCA1/2-Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers

19. Supplementary Table 3 from Modification of Ovarian Cancer Risk by BRCA1/2-Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers

20. Supplementary Table 1 from Modification of Ovarian Cancer Risk by BRCA1/2-Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers

21. Case Studies for Overcoming Challenges in Using Big Data in Cancer

22. Challenges to Using Big Data in Cancer

23. Impact of family history assessment on communication with family members and health care providers: A report from the Family Healthware™ Impact Trial (FHITr)

24. Evidence synthesis and guideline development in genomic medicine: current status and future prospects

28. Encoding laboratory testing data: case studies of the national implementation of HHS requirements and related standards in five laboratories

33. List of Contributors

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

42. Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality

45. The FDA Oncology Center of Excellence Scientific Collaborative: Charting a Course for Applied Regulatory Science Research in Oncology

49. Advances in counselling and surveillance of patients at risk for pancreatic cancer

50. Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer

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