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Author Details
Full Name
Christopher A Miller
Affiliation
Washington University School of Medicine
ORCID
Career Start Year
2009
Papers
117
H Index
51
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36055401
Combined Kdm6a and Trp53 Deficiency Drives the Development of Squamous Cell Skin Cancer in Mice.
J Invest Dermatol
2023
37910143
Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.
Cancer Res Commun
2023
37160317
Melanoma in a patient with DNMT3A overgrowth syndrome.
Cold Spring Harb Mol Case Stud
2023
37179276
Induction of cancer neoantigens facilitates development of clinically relevant models for the study of pancreatic cancer immunobiology.
Cancer Immunol Immunother
2023
37339484
Genomic landscape of TP53-mutated myeloid malignancies.
Blood Adv
2023
37400526
Genetic characterization of primary and metastatic high-grade serous ovarian cancer tumors reveals distinct features associated with survival.
Commun Biol
2023
37027480
Computational prediction of MHC anchor locations guides neoantigen identification and prioritization.
Sci Immunol
2023
36480766
Clonal Hematopoiesis and Risk of Incident Lung Cancer.
J Clin Oncol
2023
36711871
Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.
medRxiv
2023
34670359
Tumor suppressor function of <i>WT1</i> in acute promyelocytic leukemia.
Haematologica
2022
35709710
Convergent Clonal Evolution of Signaling Gene Mutations Is a Hallmark of Myelodysplastic Syndrome Progression.
Blood Cancer Discov
2022
35510362
Efficient Algorithms Unlock Understanding of Clonal Evolution in Cancer.
Blood Cancer Discov
2022
35429619
Recurrent transcriptional responses in AML and MDS patients treated with decitabine.
Exp Hematol
2022
35568002
Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.
Cancer Genet
2022
35864110
Author Correction: A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.
Nat Commun
2022
35041928
Failure to Detect Mutations in U2AF1 due to Changes in the GRCh38 Reference Sequence.
J Mol Diagn
2022
35313694
Somatic <i>Dnmt3a</i> inactivation leads to slow, canonical DNA methylation loss in murine hematopoietic cells.
iScience
2022
34873300
Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells.
Leukemia
2022
35236053
Decitabine salvage for <i>TP53</i>-mutated, relapsed/refractory acute myeloid leukemia after cytotoxic induction therapy.
Haematologica
2022
35019859
Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid Leukemia.
Blood Cancer Discov
2022
33388420
Enhanced Efficacy and Increased Long-Term Toxicity of CNS-Directed, AAV-Based Combination Therapy for Krabbe Disease.
Mol Ther
2021
33879241
Optimized polyepitope neoantigen DNA vaccines elicit neoantigen-specific immune responses in preclinical models and in clinical translation.
Genome Med
2021
33846253
Dnmt3a deficiency in the skin causes focal, canonical DNA hypomethylation and a cellular proliferation phenotype.
Proc Natl Acad Sci U S A
2021
33704937
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.
N Engl J Med
2021
34546980
U2af1 is a haplo-essential gene required for hematopoietic cancer cell survival in mice.
J Clin Invest
2021
34780480
Kdm6a deficiency restricted to mouse hematopoietic cells causes an age- and sex-dependent myelodysplastic syndrome-like phenotype.
PLoS One
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
34125173
Tumor suppressor function of Gata2 in acute promyelocytic leukemia.
Blood
2021
34341766
Bam-readcount - rapid generation of basepair-resolution sequence metrics.
ArXiv
2021
34315901
Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth Syndrome.
Nat Commun
2021
34255749
HPV transcript expression affects cervical cancer response to chemoradiation.
JCI Insight
2021
32369930
Unmasking Intra-tumoral Heterogeneity and Clonal Evolution in NF1-MPNST.
Genes (Basel)
2020
31907209
pVACtools: A Computational Toolkit to Identify and Visualize Cancer Neoantigens.
Cancer Immunol Res
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
32577507
The clonal evolution of metastatic colorectal cancer.
Sci Adv
2020
32868873
HPV-EM: an accurate HPV detection and genotyping EM algorithm.
Sci Rep
2020
32133512
Treatment of an aggressive orthotopic murine glioblastoma model with combination checkpoint blockade and a multivalent neoantigen vaccine.
Neuro Oncol
2020
32484854
Interleukin-15 superagonist (N-803) treatment of PML and JCV in a post-allogeneic hematopoietic stem cell transplant patient.
Blood Adv
2020
30467844
Exome analysis of treatment-related AML after APL suggests secondary evolution.
Br J Haematol
2019
31413257
A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.
Nat Commun
2019
30923101
Shared cell of origin in a patient with Erdheim-Chester disease and acute myeloid leukemia.
Haematologica
2019
30906654
Detection of neoantigen-specific T cells following a personalized vaccine in a patient with glioblastoma.
Oncoimmunology
2019
30553776
Smc3 is required for mouse embryonic and adult hematopoiesis.
Exp Hematol
2019
29092827
Somatic mutations and clonal hematopoiesis in congenital neutropenia.
Blood
2018
29891591
A case of acute myeloid leukemia with promyelocytic features characterized by expression of a novel <i>RARG</i>-<i>CPSF6</i> fusion.
Blood Adv
2018
30181556
The prognostic effects of somatic mutations in ER-positive breast cancer.
Nat Commun
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
29872146
Somatic mutations in benign breast disease tissue and risk of subsequent invasive breast cancer.
Br J Cancer
2018
30429476
Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer.
Nat Commun
2018
1 - 50 of 117
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Richard K Wilson
The Ohio State University
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The Ohio State University
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John F DiPersio
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Daniel C Link
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Catrina Fronick
McDonnell Genome Institute, Washington University in St. Louis School of Medicine
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Peter Westervelt
Washington University School of Medicine
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Sharon E Heath
Washington University School of Medicine.
Co-authored papers
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Li Ding
McDonnell Genome Institute, Washington University School of Medicine
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Malachi Griffith
Washington University
Co-authored papers
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Obi L Griffith
Washington University
Co-authored papers
23
Michelle O'Laughlin
McDonnell Genome Institute, Washington University School of Medicine
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Timothy A Graubert
Massachusetts General Hospital
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David E Larson
McDonnell Genome Institute, Washington University School of Medicine
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Michael D McLellan
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers
19
Lukas D Wartman
Washington University School of Medicine in St. Louis
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Joshua F McMichael
Washington University
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Vincent Magrini
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