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Author Details
Full Name
Sean Davis
Affiliation
Johns Hopkins School of Medicine, National Cancer Institute, Princeton University, University of Colorado Anschutz Medical Campus, University of Pittsburgh, University of Washington
ORCID
0000-0002-8991-6458
Career Start Year
1974
Papers
114
H Index
54
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37745420
<i>bamSliceR</i>: cross-cohort variant and allelic bias analysis for rare variants and rare diseases.
bioRxiv
2023
34717047
Infantile-onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotype.
Epilepsia Open
2022
35760813
GenomicSuperSignature facilitates interpretation of RNA-seq experiments through robust, efficient comparison to public databases.
Nat Commun
2022
35143491
Ten simple rules for large-scale data processing.
PLoS Comput Biol
2022
32026945
Toward a gold standard for benchmarking gene set enrichment analysis.
Brief Bioinform
2021
32823322
From Patient Engagement to Precision Oncology: Leveraging Informatics to Advance Cancer Care.
Yearb Med Inform
2020
31949145
Melanoblast transcriptome analysis reveals pathways promoting melanoma metastasis.
Nat Commun
2020
30828438
restfulSE: A semantically rich interface for cloud-scale genomics with Bioconductor.
F1000Res
2019
31249680
BiocPkgTools: Toolkit for mining the <i>Bioconductor</i> package ecosystem.
F1000Res
2019
29489755
Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.
Nature
2018
30473781
Orchestrating a community-developed computational workshop and accompanying training materials.
F1000Res
2018
29092936
Software for the Integration of Multiomics Experiments in Bioconductor.
Cancer Res
2017
28114280
RARRES2 functions as a tumor suppressor by promoting β-catenin phosphorylation/degradation and inhibiting p38 phosphorylation in adrenocortical carcinoma.
Oncogene
2017
28407484
Autoreactive T Cells and Chronic Fungal Infection Drive Esophageal Carcinogenesis.
Cell Host Microbe
2017
28935813
ASXL3 Is a Novel Pluripotency Factor in Human Respiratory Epithelial Cells and a Potential Therapeutic Target in Small Cell Lung Cancer.
Cancer Res
2017
28975082
Resources for Interpreting Variants in Precision Genomic Oncology Applications.
Front Oncol
2017
27005934
caOmicsV: an R package for visualizing multidimensional cancer genomic data.
BMC Bioinformatics
2016
26463000
Public data and open source tools for multi-assay genomic investigation of disease.
Brief Bioinform
2016
27694491
Upregulation of IFN-Inducible and Damage-Response Pathways in Chronic Graft-versus-Host Disease.
J Immunol
2016
27626441
On the Selective Packaging of Genomic RNA by HIV-1.
Viruses
2016
27132513
TNF-α modulates genome-wide redistribution of οNp63α/TAp73 and NF-κB cREL interactive binding on TP53 and AP-1 motifs to promote an oncogenic gene program in squamous cancer.
Oncogene
2016
26962861
Whole Genome Sequencing of Newly Established Pancreatic Cancer Lines Identifies Novel Somatic Mutation (c.2587G>A) in Axon Guidance Receptor Plexin A1 as Enhancer of Proliferation and Invasion.
PLoS One
2016
27087319
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
Am J Hum Genet
2016
25488748
miR30a inhibits LOX expression and anaplastic thyroid cancer progression.
Cancer Res
2015
26084801
A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.
Cancer Discov
2015
25944801
Inhibition of Survivin with YM155 Induces Durable Tumor Response in Anaplastic Thyroid Cancer.
Clin Cancer Res
2015
25940539
Dual inhibition of HDAC and EGFR signaling with CUDC-101 induces potent suppression of tumor growth and metastasis in anaplastic thyroid cancer.
Oncotarget
2015
25633503
Orchestrating high-throughput genomic analysis with Bioconductor.
Nat Methods
2015
25629959
Antagonistic cross-regulation between Sox9 and Sox10 controls an anti-tumorigenic program in melanoma.
PLoS Genet
2015
25686607
Super-enhancers delineate disease-associated regulatory nodes in T cells.
Nature
2015
25764003
Characterization of genomic alterations in radiation-associated breast cancer among childhood cancer survivors, using comparative genomic hybridization (CGH) arrays.
PLoS One
2015
25773928
Integrated analysis of DNA methylation, immunohistochemistry and mRNA expression, data identifies a methylation expression index (MEI) robustly associated with survival of ER-positive breast cancer patients.
Breast Cancer Res Treat
2015
24241536
High prevalence of MAP2K1 mutations in variant and IGHV4-34-expressing hairy-cell leukemias.
Nat Genet
2014
25032700
NCI-60 whole exome sequencing and pharmacological CellMiner analyses.
PLoS One
2014
25030697
Lineage of origin in rhabdomyosarcoma informs pharmacological response.
Genes Dev
2014
24292683
Downregulation of IGFBP2 is associated with resistance to IGF1R therapy in rhabdomyosarcoma.
Oncogene
2014
24423287
Genome-wide methylation patterns in papillary thyroid cancer are distinct based on histological subtype and tumor genotype.
J Clin Endocrinol Metab
2014
22935230
Harnessing genomics to identify environmental determinants of heritable disease.
Mutat Res
2013
24274149
Rb1 loss modifies but does not initiate alveolar rhabdomyosarcoma.
Skelet Muscle
2013
24247619
Prohibitin expression is associated with high grade breast cancer but is not a driver of amplification at 17q21.33.
Pathology
2013
24267888
A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway.
Cell
2013
23856246
The exomes of the NCI-60 panel: a genomic resource for cancer biology and systems pharmacology.
Cancer Res
2013
23901115
Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma.
Proc Natl Acad Sci U S A
2013
23940108
Oncogenic ETS fusions deregulate E2F3 target genes in Ewing sarcoma and prostate cancer.
Genome Res
2013
23937229
RCircos: an R package for Circos 2D track plots.
BMC Bioinformatics
2013
23577124
Whole genome and transcriptome sequencing of a B3 thymoma.
PLoS One
2013
23193258
NCBI GEO: archive for functional genomics data sets--update.
Nucleic Acids Res
2013
23271725
Chromothripsis and focal copy number alterations determine poor outcome in malignant melanoma.
Cancer Res
2013
23323543
SRAdb: query and use public next-generation sequencing data from within R.
BMC Bioinformatics
2013
21765476
CHEK2 genomic and proteomic analyses reveal genetic inactivation or endogenous activation across the 60 cell lines of the US National Cancer Institute.
Oncogene
2012
1 - 50 of 114
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row(s) 1 - 30 of 30
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Center for Cancer Research, National Cancer Institute, National Institutes of Health
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Center for Cancer Research, National Cancer Institute
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Graduate School of Public Health and Health Policy, City University of New York
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National Institute of Child Health and Development
Co-authored papers
5
Electron Kebebew
Stanford University School of Medicine
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Yuelin J Zhu
National Cancer Institute, National Institutes of Health
Co-authored papers
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Glenn Merlino
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William C Reinhold
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