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Author Details

Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
1994
194
101
PMIDPaper TitleJournal TitlePublished Year
36711871Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.medRxiv2023
37910143Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.Cancer Res Commun2023
37339484Genomic landscape of TP53-mutated myeloid malignancies.Blood Adv2023
36711871Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.medRxiv2023
37079859Persistent Molecular Disease in Adult Patients With AML Evaluated With Whole-Exome and Targeted Error-Corrected DNA Sequencing.JCO Precis Oncol2023
36947201Utility of targeted gene sequencing to differentiate myeloid malignancies from other cytopenic conditions.Blood Adv2023
37910143Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.Cancer Res Commun2023
36947201Utility of targeted gene sequencing to differentiate myeloid malignancies from other cytopenic conditions.Blood Adv2023
37079859Persistent Molecular Disease in Adult Patients With AML Evaluated With Whole-Exome and Targeted Error-Corrected DNA Sequencing.JCO Precis Oncol2023
37339484Genomic landscape of TP53-mutated myeloid malignancies.Blood Adv2023
35019859Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid Leukemia.Blood Cancer Discov2022
35395066Recurrent switch 2 domain RAC2 mutations in intravascular large B-cell lymphoma.Blood Adv2022
35709710Convergent Clonal Evolution of Signaling Gene Mutations Is a Hallmark of Myelodysplastic Syndrome Progression.Blood Cancer Discov2022
35962045Author Correction: Comparative and demographic analysis of orang-utan genomes.Nature2022
35961988Nine out of ten samples were mistakenly switched by The Orang-utan Genome Consortium.Sci Data2022
35444317The Human Pangenome Project: a global resource to map genomic diversity.Nature2022
35568002Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.Cancer Genet2022
36273232Personalized ctDNA micro-panels can monitor and predict clinical outcomes for patients with triple-negative breast cancer.Sci Rep2022
35995947Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer.Nat Genet2022
35864110Author Correction: A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.Nat Commun2022
35675516IL-1β expression in bone marrow dendritic cells is induced by TLR2 agonists and regulates HSC function.Blood2022
35041928Failure to Detect Mutations in U2AF1 due to Changes in the GRCh38 Reference Sequence.J Mol Diagn2022
35019859Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid Leukemia.Blood Cancer Discov2022
34873300Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells.Leukemia2022
35444317The Human Pangenome Project: a global resource to map genomic diversity.Nature2022
35709710Convergent Clonal Evolution of Signaling Gene Mutations Is a Hallmark of Myelodysplastic Syndrome Progression.Blood Cancer Discov2022
35675516IL-1β expression in bone marrow dendritic cells is induced by TLR2 agonists and regulates HSC function.Blood2022
35395066Recurrent switch 2 domain RAC2 mutations in intravascular large B-cell lymphoma.Blood Adv2022
35568002Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.Cancer Genet2022
36273232Personalized ctDNA micro-panels can monitor and predict clinical outcomes for patients with triple-negative breast cancer.Sci Rep2022
35995947Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer.Nat Genet2022
35962045Author Correction: Comparative and demographic analysis of orang-utan genomes.Nature2022
35961988Nine out of ten samples were mistakenly switched by The Orang-utan Genome Consortium.Sci Data2022
35864110Author Correction: A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.Nat Commun2022
35041928Failure to Detect Mutations in U2AF1 due to Changes in the GRCh38 Reference Sequence.J Mol Diagn2022
34873300Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells.Leukemia2022
33098427Rapid and Extraction-Free Detection of SARS-CoV-2 from Saliva by Colorimetric Reverse-Transcription Loop-Mediated Isothermal Amplification.Clin Chem2021
33704937Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.N Engl J Med2021
33963182Co-evolution of tumor and immune cells during progression of multiple myeloma.Nat Commun2021
33785770A domestic cat whole exome sequencing resource for trait discovery.Sci Rep2021
33098427Rapid and Extraction-Free Detection of SARS-CoV-2 from Saliva by Colorimetric Reverse-Transcription Loop-Mediated Isothermal Amplification.Clin Chem2021
34845035Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypes.Proc Natl Acad Sci U S A2021
34591593Genomic Profiling of Lung Adenocarcinoma in Never-Smokers.J Clin Oncol2021
33785770A domestic cat whole exome sequencing resource for trait discovery.Sci Rep2021
33704937Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.N Engl J Med2021
34591593Genomic Profiling of Lung Adenocarcinoma in Never-Smokers.J Clin Oncol2021
34845035Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypes.Proc Natl Acad Sci U S A2021
33963182Co-evolution of tumor and immune cells during progression of multiple myeloma.Nat Commun2021
32532883Precise breakpoint detection in a patient with 9p- syndrome.Cold Spring Harb Mol Case Stud2020
31996479Remethylation 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 A2020
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Collaborators

The Ohio State University
Co-authored papers 121
The Ohio State University
Co-authored papers 92
Washington University School of Medicine
Co-authored papers 59
McDonnell Genome Institute, Washington University in St. Louis School of Medicine
Co-authored papers 58
Washington University School of Medicine
Co-authored papers 58
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 55
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 44
Washington University School of Medicine in St. Louis
Co-authored papers 42
Washington University School of Medicine
Co-authored papers 39
Washington University School of Medicine
Co-authored papers 37
Washington University School of Medicine
Co-authored papers 34
Washington University School of Medicine.
Co-authored papers 34
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 32
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 32
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 31
Massachusetts General Hospital
Co-authored papers 31
McDonnell Genome Institute, Washington University
Co-authored papers 30
The Ohio State University
Co-authored papers 28
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers 25
Washington University School of Medicine.
Co-authored papers 21
Washington University
Co-authored papers 18
Co-authored papers 18
The Genome Center at Washington University, Washington University School of Medicine
Co-authored papers 18
Washington University in St Louis
Co-authored papers 17
Institute of Informatics and Data Sciences, University of Missouri
Co-authored papers 17
Washington University School of Medicine.
Co-authored papers 16
University of Washington
Co-authored papers 16
Washington University
Co-authored papers 16
St. Jude Children's Research Hospital
Co-authored papers 16
Harvard T.H. Chan School of Public Health
Co-authored papers 16