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Author Details
Full Name
Matthew J Walter
Affiliation
Washington University School of Medicine in St. Louis
ORCID
Career Start Year
1994
Papers
103
H Index
44
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36711871
Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.
medRxiv
2023
37597685
Phase I-II Trial of Early Azacitidine after Matched Unrelated Donor Hematopoietic Cell Transplantation.
Transplant Cell Ther
2023
38090662
Progressive, edematous plaques, mild pancytopenia, and inflammation.
JAAD Case Rep
2023
36947201
Utility of targeted gene sequencing to differentiate myeloid malignancies from other cytopenic conditions.
Blood Adv
2023
37042968
Statin use in myelodysplastic syndromes is associated with a better survival and decreased progression to leukemia.
Blood Adv
2023
37339484
Genomic landscape of TP53-mutated myeloid malignancies.
Blood Adv
2023
37369199
A functional link between lariat debranching enzyme and the intron-binding complex is defective in non-photosensitive trichothiodystrophy.
Mol Cell
2023
36480766
Clonal Hematopoiesis and Risk of Incident Lung Cancer.
J Clin Oncol
2023
36922625
Impact of U2AF1 mutations on circular RNA expression in myelodysplastic neoplasms.
Leukemia
2023
36853803
Increased clonal hematopoiesis involving DNA damage response genes in patients undergoing lung transplantation.
JCI Insight
2023
35019859
Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid Leukemia.
Blood Cancer Discov
2022
35709710
Convergent Clonal Evolution of Signaling Gene Mutations Is a Hallmark of Myelodysplastic Syndrome Progression.
Blood Cancer Discov
2022
35675516
IL-1β expression in bone marrow dendritic cells is induced by TLR2 agonists and regulates HSC function.
Blood
2022
35367529
Toll-like receptor and cytokine expression throughout the bone marrow differs between patients with low- and high-risk myelodysplastic syndromes.
Exp Hematol
2022
36130297
Genomic profiling for clinical decision making in myeloid neoplasms and acute leukemia.
Blood
2022
35895896
Proteomic and phosphoproteomic landscapes of acute myeloid leukemia.
Blood
2022
35041928
Failure to Detect Mutations in U2AF1 due to Changes in the GRCh38 Reference Sequence.
J Mol Diagn
2022
34873300
Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells.
Leukemia
2022
33288274
Corrigendum to "Haploinsufficiency of multiple del(5q) genes induce B cell abnormalities in mice" [Leuk. Res. 96C (2020) 106428].
Leuk Res
2021
33704937
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.
N Engl J Med
2021
33689684
A synthetic small molecule stalls pre-mRNA splicing by promoting an early-stage U2AF2-RNA complex.
Cell Chem Biol
2021
34469727
Mutant U2AF1-induced alternative splicing of H2afy (macroH2A1) regulates B-lymphopoiesis in mice.
Cell Rep
2021
34546980
U2af1 is a haplo-essential gene required for hematopoietic cancer cell survival in mice.
J Clin Invest
2021
34845035
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypes.
Proc Natl Acad Sci U S A
2021
34215620
Nonsense-Mediated RNA Decay Is a Unique Vulnerability of Cancer Cells Harboring <i>SF3B1</i> or <i>U2AF1</i> Mutations.
Cancer Res
2021
34341766
Bam-readcount - rapid generation of basepair-resolution sequence metrics.
ArXiv
2021
32347921
SF3B1-mutant MDS as a distinct disease subtype: a proposal from the International Working Group for the Prognosis of MDS.
Blood
2020
32739655
Haploinsufficiency of multiple del(5q) genes induce B cell abnormalities in mice.
Leuk Res
2020
32430504
Genetics of progression from MDS to secondary leukemia.
Blood
2020
30635634
TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups.
Leukemia
2019
31011167
U2AF1 mutations induce oncogenic IRAK4 isoforms and activate innate immune pathways in myeloid malignancies.
Nat Cell Biol
2019
31111762
The National MDS Natural History Study: design of an integrated data and sample biorepository to promote research studies in myelodysplastic syndromes.
Leuk Lymphoma
2019
30846499
Myelodysplastic syndrome-associated spliceosome gene mutations enhance innate immune signaling.
Haematologica
2019
29515031
Subclones dominate at MDS progression following allogeneic hematopoietic cell transplant.
JCI Insight
2018
30054334
Spliceosome Mutations Induce R Loop-Associated Sensitivity to ATR Inhibition in Myelodysplastic Syndromes.
Cancer Res
2018
30207916
Mutation Clearance after Transplantation for Myelodysplastic Syndrome.
N Engl J Med
2018
29959414
Discriminating a common somatic ASXL1 mutation (c.1934dup; p.G646Wfs*12) from artifact in myeloid malignancies using NGS.
Leukemia
2018
30632131
Identifying Molecular Markers of Relapse in Myelodysplastic Syndrome.
Oncology (Williston Park)
2018
30575467
Mutation Clearance after Transplantation for Myelodysplastic Syndrome.
N Engl J Med
2018
30380364
Immune Escape of Relapsed AML Cells after Allogeneic Transplantation.
N Engl J Med
2018
29617666
Systematic Analysis of Splice-Site-Creating Mutations in Cancer.
Cell Rep
2018
29386642
Cellular stressors contribute to the expansion of hematopoietic clones of varying leukemic potential.
Nat Commun
2018
29358180
Loss of Toll-like receptor 2 results in accelerated leukemogenesis in the <i>NUP98-HOXD13</i> mouse model of MDS.
Blood
2018
29661788
Germ line tissues for optimal detection of somatic variants in myelodysplastic syndromes.
Blood
2018
27940478
Splicing factor gene mutations in hematologic malignancies.
Blood
2017
28082444
Mutational landscape and response are conserved in peripheral blood of AML and MDS patients during decitabine therapy.
Blood
2017
28215704
CpG Island Hypermethylation Mediated by DNMT3A Is a Consequence of AML Progression.
Cell
2017
28178280
Knockdown of HSPA9 induces TP53-dependent apoptosis in human hematopoietic progenitor cells.
PLoS One
2017
27740633
Dynamic changes in the clonal structure of MDS and AML in response to epigenetic therapy.
Leukemia
2017
28057668
Antecedent CHIP in CML?
Blood
2017
1 - 50 of 103
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Co-authored papers
43
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Co-authored papers
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Co-authored papers
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42
Peter Westervelt
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Co-authored papers
38
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35
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Washington University School of Medicine.
Co-authored papers
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Richard K Wilson
The Ohio State University
Co-authored papers
34
Elaine R Mardis
The Ohio State University
Co-authored papers
26
Michelle O'Laughlin
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
22
Jacqueline E Payton
Washington University School of Medicine.
Co-authored papers
21
Catrina Fronick
McDonnell Genome Institute, Washington University in St. Louis School of Medicine
Co-authored papers
20
Li Ding
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
20
Michael D McLellan
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers
18
Vincent Magrini
The Ohio State University
Co-authored papers
11
Daniel C Koboldt
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers
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David E Larson
McDonnell Genome Institute, Washington University School of Medicine
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David H Spencer
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