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52 results on '"Relling, Mary V."'

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1. Investigation of inherited noncoding genetic variation impacting the pharmacogenomics of childhood acute lymphoblastic leukemia treatment

3. Rituximab administration in pediatric patients with newly diagnosed acute lymphoblastic leukemia

4. Correction: Outstanding outcomes with two low intensity regimens in children with low-risk B-ALL: a report from COG AALL0932

5. Pharmacotypes across the genomic landscape of pediatric acute lymphoblastic leukemia and impact on treatment response

6. The genomic landscape of pediatric acute lymphoblastic leukemia

7. Epigenomic profiling of glucocorticoid responses identifies cis-regulatory disruptions impacting steroid resistance in childhood acute lymphoblastic leukemia

8. Noncoding genetic variation in GATA3 increases acute lymphoblastic leukemia risk through local and global changes in chromatin conformation

9. Pharmacodynamics of cerebrospinal fluid asparagine after asparaginase

10. Profiling chromatin accessibility in pediatric acute lymphoblastic leukemia identifies subtype-specific chromatin landscapes and gene regulatory networks

11. Network-based systems pharmacology reveals heterogeneity in LCK and BCL2 signaling and therapeutic sensitivity of T-cell acute lymphoblastic leukemia

12. Integrative genomic analyses reveal mechanisms of glucocorticoid resistance in acute lymphoblastic leukemia

13. Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk

14. PAX5-driven subtypes of B-progenitor acute lymphoblastic leukemia

15. Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies

16. Multiplex assessment of protein variant abundance by massively parallel sequencing

17. The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia

19. NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity

21. Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children

22. NALP3 inflammasome upregulation and CASP1 cleavage of the glucocorticoid receptor cause glucocorticoid resistance in leukemia cells

23. Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia

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

25. Erratum to: Between-course targeting of methotrexate exposure using pharmacokinetically guided dosage adjustments

26. Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse

27. Between-course targeting of methotrexate exposure using pharmacokinetically guided dosage adjustments

28. Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells

29. Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia

30. Germline genomic variants associated with childhood acute lymphoblastic leukemia

31. BCR–ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros

33. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

37. Polymorphisms in the MLL breakpoint cluster region (BCR)

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