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1. Diagnostic classification of childhood cancer using multiscale transcriptomics

2. The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations

10. DNA hypermethylation within TERT promoter upregulates TERT expression in cancer

12. A curious case of growth failure and hypercalcemia: Answers

13. Data from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

14. Supplementary Table 3 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

15. Supplementary Table 4 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

16. Supplementary Table 1 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

17. Supplementary Figure 1 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

18. Supplementary Table 2 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

19. 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

20. Supplementary Figure 3 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

21. Supplementary Figure 2 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

22. Supplementary Figure 4 from Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

23. DICER1 RNase IIIb domain mutations trigger widespread miRNA dysregulation and MAPK activation in pediatric thyroid cancer

26. Late-onset tumors in rhabdoid tumor predisposition syndrome type-1 (RTPS1) and implications for surveillance

28. The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations

33. Contributors

34. Methylation of the TERT promoter and risk stratification of childhood brain tumours: an integrative genomic and molecular study

38. Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes

40. Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma

41. Treatment of Pediatric Adrenocortical Carcinoma With Surgery, Retroperitoneal Lymph Node Dissection, and Chemotherapy: The Children's Oncology Group ARAR0332 Protocol

43. Predicting Malignancy in Pediatric Thyroid Nodules:Early Experience with Machine Learning for Clinical Decision Support

50. A family of rhomboid-like genes: Drosophila rhomboid-1 and roughoid/rhomboid-2 cooperate to activate EGF receptor signaling

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