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1. The Impact of COVID-19 on Cancer Screening: Challenges and Opportunities

2. Comparing the Diagnostic Yield of Germline Exome Versus Panel Sequencing in the Diverse Population of the Texas KidsCanSeq Pediatric Cancer Study

4. Genomic profiling of subcutaneous patient-derived xenografts reveals immune constraints on tumor evolution in childhood solid cancer

5. Comprehensive characterization of patient-derived xenograft models of pediatric leukemia

6. Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium

7. Families' experiences accessing care after genomic sequencing in the pediatric cancer context: "It's just been a big juggle".

9. Reaching high-risk underserved individuals for cancer genetic counseling by video-teleconferencing.

12. Use of risk-reducing surgeries in a prospective cohort of 1,499 BRCA1 and BRCA2 mutation carriers

13. Neonatal medical exposures and characteristics of low birth weight hepatoblastoma cases: A report from the Children's Oncology Group

14. Long-term risk of medical conditions associated with breast cancer treatment

15. Parental Tobacco and Alcohol Use and Risk of Hepatoblastoma in Offspring: A Report from the Children's Oncology Group

17. Activating mutation in MET oncogene in familial colorectal cancer

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

20. Circulating tumor DNA sequencing of pediatric solid and brain tumor patients: An institutional feasibility study

21. Defining function of wild-type and three patient-specific TP53 mutations in a zebrafish model of embryonal rhabdomyosarcoma

22. Frequency and spectrum of clinically significant molecular alterations detected by tumor gene panel testing for pediatric cancer patients in the Texas KidsCanSeq study.

24. Abstract 3572: Genomic profiling of subcutaneous patient derived xenograft models of solid childhood cancer

25. Supplementary Table S1: Exposures to avoid prior to metanephrine testing from Von Hippel–Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

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

27. 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 Figure 4 from Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

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

30. Supplementary Figure 1 from Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

31. Supplementary Figure 2 from Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

32. Data from Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

33. Supplementary Figure 1 from RASSF1A Polymorphism A133S Is Associated with Early Onset Breast Cancer in BRCA1/2 Mutation Carriers

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

35. 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

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

37. Data from RASSF1A Polymorphism A133S Is Associated with Early Onset Breast Cancer in BRCA1/2 Mutation Carriers

38. 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

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

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

41. Supplementary Figure 3 from Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

42. Supplementary Figure Legends 1-4 from Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

48. Defining function of wild-type and three patient-specific TP53 mutations in a zebrafish model of embryonal rhabdomyosarcoma.

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