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Author Details

Michael D McLellan
McDonnell Genome Institute, Washington University in St. Louis
2003
68
50
PMIDPaper TitleJournal TitlePublished Year
35241842Stem cell architecture drives myelodysplastic syndrome progression and predicts response to venetoclax-based therapy.Nat Med2022
35484266Author Correction: Stem cell architecture drives myelodysplastic syndrome progression and predicts response to venetoclax-based therapy.Nat Med2022
35241842Stem cell architecture drives myelodysplastic syndrome progression and predicts response to venetoclax-based therapy.Nat Med2022
35484266Author Correction: Stem cell architecture drives myelodysplastic syndrome progression and predicts response to venetoclax-based therapy.Nat Med2022
34255749HPV transcript expression affects cervical cancer response to chemoradiation.JCI Insight2021
33879241Optimized polyepitope neoantigen DNA vaccines elicit neoantigen-specific immune responses in preclinical models and in clinical translation.Genome Med2021
34255749HPV transcript expression affects cervical cancer response to chemoradiation.JCI Insight2021
33879241Optimized polyepitope neoantigen DNA vaccines elicit neoantigen-specific immune responses in preclinical models and in clinical translation.Genome Med2021
32868873HPV-EM: an accurate HPV detection and genotyping EM algorithm.Sci Rep2020
32868873HPV-EM: an accurate HPV detection and genotyping EM algorithm.Sci Rep2020
29507395Pan-cancer analysis of somatic mutations across 21 neuroendocrine tumor types.Cell Res2018
29625052Pathogenic Germline Variants in 10,389 Adult Cancers.Cell2018
29438696The Integrated Genomic Landscape of Thymic Epithelial Tumors.Cancer Cell2018
29596782Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.Cell Syst2018
29507395Pan-cancer analysis of somatic mutations across 21 neuroendocrine tumor types.Cell Res2018
29438696The Integrated Genomic Landscape of Thymic Epithelial Tumors.Cancer Cell2018
29625052Pathogenic Germline Variants in 10,389 Adult Cancers.Cell2018
29596782Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.Cell Syst2018
28582538BreakPoint Surveyor: a pipeline for structural variant visualization.Bioinformatics2017
28348404Proteogenomic integration reveals therapeutic targets in breast cancer xenografts.Nat Commun2017
28582538BreakPoint Surveyor: a pipeline for structural variant visualization.Bioinformatics2017
28619968Breast Cancer Neoantigens Can Induce CD8<sup>+</sup> T-Cell Responses and Antitumor Immunity.Cancer Immunol Res2017
28747753Corrigendum: Protein-structure-guided discovery of functional mutations across 19 cancer types.Nat Genet2017
28440318Corrigendum: Proteogenomic integration reveals therapeutic targets in breast cancer xenografts.Nat Commun2017
29423104Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer.Oncotarget2017
28440318Corrigendum: Proteogenomic integration reveals therapeutic targets in breast cancer xenografts.Nat Commun2017
28348404Proteogenomic integration reveals therapeutic targets in breast cancer xenografts.Nat Commun2017
29423104Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer.Oncotarget2017
28619968Breast Cancer Neoantigens Can Induce CD8<sup>+</sup> T-Cell Responses and Antitumor Immunity.Cancer Immunol Res2017
28747753Corrigendum: Protein-structure-guided discovery of functional mutations across 19 cancer types.Nat Genet2017
27251275Proteogenomics connects somatic mutations to signalling in breast cancer.Nature2016
27251275Proteogenomics connects somatic mutations to signalling in breast cancer.Nature2016
27294619Protein-structure-guided discovery of functional mutations across 19 cancer types.Nat Genet2016
26657142Systematic discovery of complex insertions and deletions in human cancers.Nat Med2016
26631509An Analysis of the Sensitivity of Proteogenomic Mapping of Somatic Mutations and Novel Splicing Events in Cancer.Mol Cell Proteomics2016
26631509An Analysis of the Sensitivity of Proteogenomic Mapping of Somatic Mutations and Novel Splicing Events in Cancer.Mol Cell Proteomics2016
26657142Systematic discovery of complex insertions and deletions in human cancers.Nat Med2016
27294619Protein-structure-guided discovery of functional mutations across 19 cancer types.Nat Genet2016
25252869Clonal evolution revealed by whole genome sequencing in a case of primary myelofibrosis transformed to secondary acute myeloid leukemia.Leukemia2015
25501392Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes.Nat Genet2015
26158448Genome Modeling System: A Knowledge Management Platform for Genomics.PLoS Comput Biol2015
26451490Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer.Cell2015
26689913Patterns and functional implications of rare germline variants across 12 cancer types.Nat Commun2015
25252869Clonal evolution revealed by whole genome sequencing in a case of primary myelofibrosis transformed to secondary acute myeloid leukemia.Leukemia2015
26451490Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer.Cell2015
26689913Patterns and functional implications of rare germline variants across 12 cancer types.Nat Commun2015
26158448Genome Modeling System: A Knowledge Management Platform for Genomics.PLoS Comput Biol2015
25501392Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes.Nat Genet2015
24497850Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.PLoS Genet2014
25326804Age-related mutations associated with clonal hematopoietic expansion and malignancies.Nat Med2014
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Collaborators

Li Ding
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 46
Richard K Wilson
The Ohio State University
Co-authored papers 39
Elaine R Mardis
The Ohio State University
Co-authored papers 37
Timothy J Ley
Washington University School of Medicine
Co-authored papers 28
Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 25
Michael C Wendl
Washington University in St Louis
Co-authored papers 20
Daniel C Koboldt
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 20
Ken Chen
University of Texas MD Anderson Cancer Center
Co-authored papers 19
Christopher A Miller
Washington University School of Medicine
Co-authored papers 19
Timothy A Graubert
Massachusetts General Hospital
Co-authored papers 19
David E Larson
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 19
John F DiPersio
Washington University School of Medicine
Co-authored papers 18
Matthew J Walter
Washington University School of Medicine in St. Louis
Co-authored papers 18
Lucinda Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 17
Daniel C Link
Washington University School of Medicine
Co-authored papers 16
Cyriac Kandoth
University of California los angeles
Co-authored papers 15
Mark A Watson
Washington University School of Medicine
Co-authored papers 14
Sharon E Heath
Washington University School of Medicine.
Co-authored papers 14
Joshua F McMichael
Washington University
Co-authored papers 14
Qunyuan Zhang
Co-authored papers 14
Beifang Niu
Co-authored papers 13
Peter Westervelt
Washington University School of Medicine
Co-authored papers 13
Jacqueline E Payton
Washington University School of Medicine.
Co-authored papers 11
Vincent Magrini
The Ohio State University
Co-authored papers 11
Charles Lu
Co-authored papers 11
Rakesh Nagarajan
Current or past members of the College of American Pathologists
Co-authored papers 9
Matthew A Wyczalkowski
Washington University in St Louis
Co-authored papers 9
Rhonda E Ries
Clinical Research Division, Fred Hutchinson Cancer Research Center
Co-authored papers 9
Kai Ye
Co-authored papers 9
Matthew J Ellis
Co-authored papers 8
Release 1.2