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Author Details
Full Name
David H Spencer
Affiliation
Washington University School of Medicine.
ORCID
Career Start Year
2000
Papers
55
H Index
30
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36351182
Evaluation of Breast Implant-Associated Anaplastic Large Cell Lymphoma With Whole Exome and Genome Sequencing.
Aesthet Surg J
2023
37079859
Persistent Molecular Disease in Adult Patients With AML Evaluated With Whole-Exome and Targeted Error-Corrected DNA Sequencing.
JCO Precis Oncol
2023
37339484
Genomic landscape of TP53-mutated myeloid malignancies.
Blood Adv
2023
36711871
Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.
medRxiv
2023
36797416
KDM6B protects T-ALL cells from NOTCH1-induced oncogenic stress.
Leukemia
2023
34115842
Heterozygous variants of CLPB are a cause of severe congenital neutropenia.
Blood
2022
35709710
Convergent Clonal Evolution of Signaling Gene Mutations Is a Hallmark of Myelodysplastic Syndrome Progression.
Blood Cancer Discov
2022
35650442
Clonal dynamics of haematopoiesis across the human lifespan.
Nature
2022
35471774
Clinical whole-genome sequencing in cancer diagnosis.
Hum Mutat
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
35196021
Hematopoietic cell transplantation donor-derived memory-like NK cells functionally persist after transfer into patients with leukemia.
Sci Transl Med
2022
34670359
Tumor suppressor function of <i>WT1</i> in acute promyelocytic leukemia.
Haematologica
2022
34788385
DNMT3A overgrowth syndrome is associated with the development of hematopoietic malignancies in children and young adults.
Blood
2022
32398790
Contribution of CTCF binding to transcriptional activity at the HOXA locus in NPM1-mutant AML cells.
Leukemia
2021
33704937
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.
N Engl J Med
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
34036230
Impact of a 40-Gene Targeted Panel Test on Physician Decision Making for Patients With Acute Myeloid Leukemia.
JCO Precis Oncol
2021
32818246
Deletions in BCP-ALL result in a TAD more FLT3.
Blood
2020
31996479
Remethylation of <i>Dnmt3a</i><sup>-/-</sup> hematopoietic cells is associated with partial correction of gene dysregulation and reduced myeloid skewing.
Proc Natl Acad Sci U S A
2020
31685621
Immunological ignorance is an enabling feature of the oligo-clonal T cell response to melanoma neoantigens.
Proc Natl Acad Sci U S A
2019
31812712
Inflammatory cytokines promote clonal hematopoiesis with specific mutations in ulcerative colitis patients.
Exp Hematol
2019
29365324
Expression profiling of snoRNAs in normal hematopoiesis and AML.
Blood Adv
2018
29967526
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizures.
Pediatr Res
2018
29634818
Sequencing of Tumor DNA to Guide Cancer Risk Assessment and Therapy.
JAMA
2018
29618788
DNMT3A<sup>R882</sup>-associated hypomethylation patterns are maintained in primary AML xenografts, but not in the DNMT3A<sup>R882C</sup> OCI-AML3 leukemia cell line.
Blood Cancer J
2018
28760689
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes.
Exp Hematol
2017
28138153
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer.
Nat Genet
2017
28215704
CpG Island Hypermethylation Mediated by DNMT3A Is a Consequence of AML Progression.
Cell
2017
25345567
Clinical next-generation sequencing in patients with non-small cell lung cancer.
Cancer
2015
26386089
Occult Specimen Contamination in Routine Clinical Next-Generation Sequencing Testing.
Am J Clin Pathol
2015
26305651
Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia.
JAMA
2015
25995208
Remarkably Divergent Regions Punctuate the Genome Assembly of the Caenorhabditis elegans Hawaiian Strain CB4856.
Genetics
2015
25600023
Epigenomic analysis of the HOX gene loci reveals mechanisms that may control canonical expression patterns in AML and normal hematopoietic cells.
Leukemia
2015
24211364
Performance of common analysis methods for detecting low-frequency single nucleotide variants in targeted next-generation sequence data.
J Mol Diagn
2014
24613412
Functional heterogeneity of genetically defined subclones in acute myeloid leukemia.
Cancer Cell
2014
24656771
The R882H DNMT3A mutation associated with AML dominantly inhibits wild-type DNMT3A by blocking its ability to form active tetramers.
Cancer Cell
2014
24211365
Validation of a next-generation sequencing assay for clinical molecular oncology.
J Mol Diagn
2014
23297133
Genomic impact of transient low-dose decitabine treatment on primary AML cells.
Blood
2013
24303327
Clinical genomicist workstation.
AMIA Jt Summits Transl Sci Proc
2013
23634996
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.
N Engl J Med
2013
23810758
Comparison of clinical targeted next-generation sequence data from formalin-fixed and fresh-frozen tissue specimens.
J Mol Diagn
2013
23159595
Detection of FLT3 internal tandem duplication in targeted, short-read-length, next-generation sequencing data.
J Mol Diagn
2013
21059826
Red cell transfusion decreases hemoglobin A1c in patients with diabetes.
Clin Chem
2011
22031306
Validation and implementation of the GeneXpert MRSA/SA blood culture assay in a pediatric setting.
Am J Clin Pathol
2011
21885623
Direct-to-consumer genetic testing: reliable or risky?
Clin Chem
2011
19409521
IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.
Am J Hum Genet
2009
17493132
Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients.
Mol Microbiol
2007
17033972
Detecting disease-causing mutations in the human genome by haplotype matching.
Am J Hum Genet
2006
15743962
Evidence for diversifying selection at the pyoverdine locus of Pseudomonas aeruginosa.
J Bacteriol
2005
1 - 50 of 55
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row(s) 1 - 30 of 30
Collaborators
Timothy J Ley
Washington University School of Medicine
Co-authored papers
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McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
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Christopher A Miller
Washington University School of Medicine
Co-authored papers
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Washington University School of Medicine
Co-authored papers
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Co-authored papers
11
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Washington University School of Medicine.
Co-authored papers
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McDonnell Genome Institute, Washington University in St. Louis School of Medicine
Co-authored papers
10
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Washington University School of Medicine.
Co-authored papers
10
Peter Westervelt
Washington University School of Medicine
Co-authored papers
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Washington University School of Medicine in St. Louis
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The Ohio State University
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8
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Washington University School of Medicine in St. Louis
Co-authored papers
7
Shashikant Kulkarni
Centene Center for Health Transformation, Centene Corporation
Co-authored papers
7
Michelle O'Laughlin
McDonnell Genome Institute, Washington University School of Medicine
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7
Tamara L Lamprecht
St. Jude Children's Research Hospital
Co-authored papers
7
Malachi Griffith
Washington University
Co-authored papers
7
Obi L Griffith
Washington University
Co-authored papers
6
Elaine R Mardis
The Ohio State University
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Jeffery M Klco
St. Jude Children's Research Hospital
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Vincent Magrini
The Ohio State University
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