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Author Details

Jacqueline E Payton
Washington University School of Medicine.
2001
69
33
PMIDPaper TitleJournal TitlePublished Year
36711871Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.medRxiv2023
37339484Genomic landscape of TP53-mutated myeloid malignancies.Blood Adv2023
35019859Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid Leukemia.Blood Cancer Discov2022
35709710Convergent Clonal Evolution of Signaling Gene Mutations Is a Hallmark of Myelodysplastic Syndrome Progression.Blood Cancer Discov2022
35895896Proteomic and phosphoproteomic landscapes of acute myeloid leukemia.Blood2022
34873300Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells.Leukemia2022
34157105Determining subpopulation methylation profiles from bisulfite sequencing data of heterogeneous samples using DXM.Nucleic Acids Res2021
33704937Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.N Engl J Med2021
34644581Nuclear-localized human respiratory syncytial virus NS1 protein modulates host gene transcription.Cell Rep2021
34461601Loss of synergistic transcriptional feedback loops drives diverse B-cell cancers.EBioMedicine2021
34845035Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypes.Proc Natl Acad Sci U S A2021
34019588Epigenomic regulation of human T-cell leukemia virus by chromatin-insulator CTCF.PLoS Pathog2021
32571842BCALM (AC099524.1) Is a Human B Lymphocyte-Specific Long Noncoding RNA That Modulates B Cell Receptor-Mediated Calcium Signaling.J Immunol2020
33304977Validation and interpretation of IGH and TCR clonality testing by Ion Torrent S5 NGS for diagnosis and disease monitoring in B and T cell cancers.Pract Lab Med2020
30342313Epigenetic dynamics in normal and malignant B cells: die a hero or live to become a villain.Curr Opin Immunol2019
31644907RAG-Mediated DNA Breaks Attenuate PU.1 Activity in Early B Cells through Activation of a SPIC-BCLAF1 Complex.Cell Rep2019
31358475Novel cell adhesion/migration pathways are predictive markers of HDAC inhibitor resistance in cutaneous T cell lymphoma.EBioMedicine2019
30767760PLAIDOH: a novel method for functional prediction of long non-coding RNAs identifies cancer-specific LncRNA activities.BMC Genomics2019
30380364Immune Escape of Relapsed AML Cells after Allogeneic Transplantation.N Engl J Med2018
31080942Genotify: Fast, lightweight gene lookup and summarization.J Open Source Softw2018
27268204Targeted epigenetic repression of a lymphoma oncogene by sequence-specific histone modifiers induces apoptosis in DLBCL.Leuk Lymphoma2017
28362262A type I IFN-dependent DNA damage response regulates the genetic program and inflammasome activation in macrophages.Elife2017
28329684cis-Regulatory Circuits Regulating NEK6 Kinase Overexpression in Transformed B Cells Are Super-Enhancer Independent.Cell Rep2017
28378425Follicular lymphoma: State-of-the-art ICML workshop in Lugano 2015.Hematol Oncol2017
28215704CpG Island Hypermethylation Mediated by DNMT3A Is a Consequence of AML Progression.Cell2017
26834123Maternal T-Cell Engraftment Interferes With Human Leukocyte Antigen Typing in Severe Combined Immunodeficiency.Am J Clin Pathol2016
27183590NKG2D-NKG2D Ligand Interaction Inhibits the Outgrowth of Naturally Arising Low-Grade B Cell Lymphoma In Vivo.J Immunol2016
27156452Distinct Gene Regulatory Pathways for Human Innate versus Adaptive Lymphoid Cells.Cell2016
27181063Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia.Exp Hematol2016
26888867Mapping of Variable DNA Methylation Across Multiple Cell Types Defines a Dynamic Regulatory Landscape of the Human Genome.G3 (Bethesda)2016
26834154RAG-mediated DNA double-strand breaks activate a cell type-specific checkpoint to inhibit pre-B cell receptor signals.J Exp Med2016
25607463Enhancer sequence variants and transcription-factor deregulation synergize to construct pathogenic regulatory circuits in B-cell lymphoma.Immunity2015
26604030Short-Circuiting Gene Regulatory Networks: Origins of B Cell Lymphoma.Trends Genet2015
26305651Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia.JAMA2015
24211365Validation of a next-generation sequencing assay for clinical molecular oncology.J Mol Diagn2014
25435138HCoDES reveals chromosomal DNA end structures with single-nucleotide resolution.Mol Cell2014
23159595Detection of FLT3 internal tandem duplication in targeted, short-read-length, next-generation sequencing data.J Mol Diagn2013
23634996Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.N Engl J Med2013
23700471Quantitative label-free proteomics for discovery of biomarkers in cerebrospinal fluid: assessment of technical and inter-individual variation.PLoS One2013
23387820An integrated approach to characterize transcription factor and microRNA regulatory networks involved in Schwann cell response to peripheral nerve injury.BMC Genomics2013
22235101Pathway-specific analysis of gene expression data identifies the PI3K/Akt pathway as a novel therapeutic target in cervical cancer.Clin Cancer Res2012
22817890The origin and evolution of mutations in acute myeloid leukemia.Cell2012
22237025Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing.Nature2012
20646217Genome-wide polymorphism analysis demonstrates a monoclonal origin of pilocytic astrocytoma.Neuropathol Appl Neurobiol2011
21745356Identification of transcriptional regulatory networks specific to pilocytic astrocytoma.BMC Med Genomics2011
21325289Array-based comparative genomic hybridization identifies CDK4 and FOXM1 alterations as independent predictors of survival in malignant peripheral nerve sheath tumor.Clin Cancer Res2011
21436584Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression.J Clin Invest2011
21505136Use of whole-genome sequencing to diagnose a cryptic fusion oncogene.JAMA2011
21505135Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML.JAMA2011
21173135The changing spectrum of DNA-based specimen provenance testing in surgical pathology.Am J Clin Pathol2011
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Collaborators

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Washington University School of Medicine
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Washington University School of Medicine
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Washington University School of Medicine.
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Washington University School of Medicine in St. Louis
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Massachusetts General Hospital
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The Ohio State University
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Co-authored papers 14
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Washington University School of Medicine
Co-authored papers 13
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Co-authored papers 11
McDonnell Genome Institute, Washington University in St. Louis
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McDonnell Genome Institute, Washington University in St. Louis School of Medicine
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McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 10
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 9
Centene Center for Health Transformation, Centene Corporation
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McDonnell Genome Institute, Washington University School of Medicine
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University of Texas MD Anderson Cancer Center
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Institute for Genomic Medicine, Nationwide Children's Hospital
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St. Jude Children's Research Hospital
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Washington University School of Medicine in St. Louis
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McDonnell Genome Institute, Washington University School of Medicine
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The Ohio State University
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Harvard T.H. Chan School of Public Health
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