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Author Details
Full Name
Robert S Fulton
Affiliation
McDonnell Genome Institute, Washington University School of Medicine
ORCID
Career Start Year
1994
Papers
194
H Index
101
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36711871
Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.
medRxiv
2023
37910143
Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.
Cancer Res Commun
2023
37339484
Genomic landscape of TP53-mutated myeloid malignancies.
Blood Adv
2023
36711871
Genomic landscape of <i>TP53</i> -mutated myeloid malignancies.
medRxiv
2023
37079859
Persistent Molecular Disease in Adult Patients With AML Evaluated With Whole-Exome and Targeted Error-Corrected DNA Sequencing.
JCO Precis Oncol
2023
36947201
Utility of targeted gene sequencing to differentiate myeloid malignancies from other cytopenic conditions.
Blood Adv
2023
37910143
Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.
Cancer Res Commun
2023
36947201
Utility of targeted gene sequencing to differentiate myeloid malignancies from other cytopenic conditions.
Blood Adv
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
35019859
Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid Leukemia.
Blood Cancer Discov
2022
35395066
Recurrent switch 2 domain RAC2 mutations in intravascular large B-cell lymphoma.
Blood Adv
2022
35709710
Convergent Clonal Evolution of Signaling Gene Mutations Is a Hallmark of Myelodysplastic Syndrome Progression.
Blood Cancer Discov
2022
35962045
Author Correction: Comparative and demographic analysis of orang-utan genomes.
Nature
2022
35961988
Nine out of ten samples were mistakenly switched by The Orang-utan Genome Consortium.
Sci Data
2022
35444317
The Human Pangenome Project: a global resource to map genomic diversity.
Nature
2022
35568002
Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.
Cancer Genet
2022
36273232
Personalized ctDNA micro-panels can monitor and predict clinical outcomes for patients with triple-negative breast cancer.
Sci Rep
2022
35995947
Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer.
Nat Genet
2022
35864110
Author Correction: A general approach for detecting expressed mutations in AML cells using single cell RNA-sequencing.
Nat Commun
2022
35675516
IL-1β expression in bone marrow dendritic cells is induced by TLR2 agonists and regulates HSC function.
Blood
2022
35041928
Failure to Detect Mutations in U2AF1 due to Changes in the GRCh38 Reference Sequence.
J Mol Diagn
2022
35019859
Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid Leukemia.
Blood Cancer Discov
2022
34873300
Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells.
Leukemia
2022
35444317
The Human Pangenome Project: a global resource to map genomic diversity.
Nature
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
35395066
Recurrent switch 2 domain RAC2 mutations in intravascular large B-cell lymphoma.
Blood Adv
2022
35568002
Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.
Cancer Genet
2022
36273232
Personalized ctDNA micro-panels can monitor and predict clinical outcomes for patients with triple-negative breast cancer.
Sci Rep
2022
35995947
Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer.
Nat Genet
2022
35962045
Author Correction: Comparative and demographic analysis of orang-utan genomes.
Nature
2022
35961988
Nine out of ten samples were mistakenly switched by The Orang-utan Genome Consortium.
Sci Data
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
34873300
Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells.
Leukemia
2022
33098427
Rapid and Extraction-Free Detection of SARS-CoV-2 from Saliva by Colorimetric Reverse-Transcription Loop-Mediated Isothermal Amplification.
Clin Chem
2021
33704937
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.
N Engl J Med
2021
33963182
Co-evolution of tumor and immune cells during progression of multiple myeloma.
Nat Commun
2021
33785770
A domestic cat whole exome sequencing resource for trait discovery.
Sci Rep
2021
33098427
Rapid and Extraction-Free Detection of SARS-CoV-2 from Saliva by Colorimetric Reverse-Transcription Loop-Mediated Isothermal Amplification.
Clin Chem
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
34591593
Genomic Profiling of Lung Adenocarcinoma in Never-Smokers.
J Clin Oncol
2021
33785770
A domestic cat whole exome sequencing resource for trait discovery.
Sci Rep
2021
33704937
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.
N Engl J Med
2021
34591593
Genomic Profiling of Lung Adenocarcinoma in Never-Smokers.
J Clin Oncol
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
33963182
Co-evolution of tumor and immune cells during progression of multiple myeloma.
Nat Commun
2021
32532883
Precise breakpoint detection in a patient with 9p- syndrome.
Cold Spring Harb Mol Case Stud
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
1 - 50 of 388
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Kelly A Frazer
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Collaborators
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The Ohio State University
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Co-authored papers
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Co-authored papers
59
Catrina Fronick
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Co-authored papers
58
Christopher A Miller
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Co-authored papers
58
Lucinda Fulton
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Co-authored papers
55
Li Ding
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44
Matthew J Walter
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Co-authored papers
42
John F DiPersio
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Co-authored papers
39
Daniel C Link
Washington University School of Medicine
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37
Peter Westervelt
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34
Sharon E Heath
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Co-authored papers
34
Michelle O'Laughlin
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
32
David E Larson
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers
32
Daniel C Koboldt
Institute for Genomic Medicine, Nationwide Children's Hospital
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31
Timothy A Graubert
Massachusetts General Hospital
Co-authored papers
31
Tina Graves
McDonnell Genome Institute, Washington University
Co-authored papers
30
Vincent Magrini
The Ohio State University
Co-authored papers
28
Michael D McLellan
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers
25
Jacqueline E Payton
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Co-authored papers
21
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18
George M Weinstock
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