Skip to Main Content

Author Details

Christopher DeBoever
Stanford University
2010
23
15
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37235597Assessing the potential of polygenic scores to strengthen medical risk prediction models of COVID-19.PLoS One2023
36042219Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy.Nat Commun2022
33989816γδ T Cells Control Gut Pathology in a Chronic Inflammatory Model of Colorectal Cancer.Cell Mol Gastroenterol Hepatol2021
34822764Bayesian model comparison for rare-variant association studies.Am J Hum Genet2021
32522985Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats.Nat Commun2020
32275883Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases.Am J Hum Genet2020
30520965Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics.Bioinformatics2019
31492854Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology.Nat Commun2019
31570892Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits.Nat Genet2019
29691392Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study.Nat Commun2018
28874753Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancer.Nat Commun2017
28388430Large-Scale Profiling Reveals the Influence of Genetic Variation on Gene Expression in Human Induced Pluripotent Stem Cells.Cell Stem Cell2017
28410642iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types.Stem Cell Reports2017
28188128Interaction Landscape of Inherited Polymorphisms with Somatic Events in Cancer.Cancer Discov2017
29074555Efficient Prioritization of Multiple Causal eQTL Variants via Sparse Polygenic Modeling.Genetics2017
27492256Distinct splicing signatures affect converged pathways in myelodysplastic syndrome patients carrying mutations in different splicing regulators.RNA2016
27815263High-level ROR1 associates with accelerated disease progression in chronic lymphocytic leukemia.Blood2016
25768983Transcriptome sequencing reveals potential mechanism of cryptic 3' splice site selection in SF3B1-mutated cancers.PLoS Comput Biol2015
25860294Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell development.Blood Cancer J2015
26015570Systematic transcriptome analysis reveals tumor-specific isoforms for ovarian cancer diagnosis and therapy.Proc Natl Acad Sci U S A2015
24909518MiningABs: mining associated biomarkers across multi-connected gene expression datasets.BMC Bioinformatics2014
24023918Whole transcriptome sequencing enables discovery and analysis of viruses in archived primary central nervous system lymphomas.PLoS One2013
20843365Context dependent substitution biases vary within the human genome.BMC Bioinformatics2010
  • 1 - 23 of 23

Recommended Authors

Icahn School of Medicine at Mount Sinai
Career Start Year 2013
Number of shared co-authors 0
University of Texas Health Science Center at Houston
Career Start Year 2012
Number of shared co-authors 6
Aerospace Center Hospital
Career Start Year 2011
Number of shared co-authors 0
Broad Institute of MIT and Harvard
Career Start Year 2010
Number of shared co-authors 9
University of California san francisco
Career Start Year 2010
Number of shared co-authors 2
Vanderbilt University Medical Center
Career Start Year 2009
Number of shared co-authors 6
Regeneron Pharmaceuticals, Inc.
Career Start Year 2007
Number of shared co-authors 6
National Cancer Institute, 9609 Medical Center Drive
Career Start Year 2007
Number of shared co-authors 6
Children's Cancer Institute, Lowy Cancer Research Centre
Career Start Year 2006
Number of shared co-authors 2
The Center for Functional Cancer Epigenetics, Dana Farber Cancer Institute
Career Start Year 2006
Number of shared co-authors 3
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year 2006
Number of shared co-authors 2
Sanford School of Medicine, University of South Dakota
Career Start Year 2005
Number of shared co-authors 0
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 5
University of Southern California
Career Start Year 2004
Number of shared co-authors 4
Knight Cancer Institute, Oregon Health & Science University
Career Start Year 2004
Number of shared co-authors 1
University of California San Diego Health System
Career Start Year 2004
Number of shared co-authors 10
Genentech Inc.
Career Start Year 2004
Number of shared co-authors 4
Boston Children's Hospital, Seoul National University, Seoul National University Hospital
Career Start Year 2003
Number of shared co-authors 1
Meyer Cancer Center
Career Start Year 2002
Number of shared co-authors 0
Columbia University
Career Start Year 2002
Number of shared co-authors 3
University of Texas M.D. Anderson Cancer Center
Career Start Year 2001
Number of shared co-authors 2
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 4
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 17
Mayo Clinic
Career Start Year 2000
Number of shared co-authors 0
St. Jude Children's Research Hospital
Career Start Year 1999
Number of shared co-authors 0
Mayo Clinic
Career Start Year 1999
Number of shared co-authors 0
Icahn School of Medicine at Mount Sinai
Career Start Year 1998
Number of shared co-authors 9
QIMR Berghofer Medical Research Institute
Career Start Year 1996
Number of shared co-authors 4
Frederick National Laboratory for Cancer Research
Career Start Year 1994
Number of shared co-authors 0
Mayo Clinic
Career Start Year 1991
Number of shared co-authors 0

Collaborators

University of California, USA Institute for Genomic Medicine
Co-authored papers 12
Department of Pediatrics and Rady's Children's Hospital, University of California
Co-authored papers 6
USA Broad Institute of MIT and Harvard
Co-authored papers 6
Stanford University School of Medicine
Co-authored papers 5
Institute for Genomic Medicine, University of California San Diego
Co-authored papers 5
Stanford University School of Medicine.
Co-authored papers 4
Stanford University
Co-authored papers 3
University of California
Co-authored papers 3
University of California San Diego
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3
University of California San Diego
Co-authored papers 3
Stanford University
Co-authored papers 2
University of California
Co-authored papers 2
Stanford University School of Medicine
Co-authored papers 2
Takeda California Inc.
Co-authored papers 2
Massachusetts General Hospital
Co-authored papers 2
University of California
Co-authored papers 2
University of California
Co-authored papers 2
University of California San Diego
Co-authored papers 1
Illumina Inc.
Co-authored papers 1
Co-authored papers 1
University of California San Diego
Co-authored papers 1
Co-authored papers 1
University of Oxford
Co-authored papers 1
Moores Cancer Center, University of California San Diego
Co-authored papers 1
Stanford University
Co-authored papers 1
University of California San Diego
Co-authored papers 1
Stanford University
Co-authored papers 1
Moores Cancer Center, University of California San Diego
Co-authored papers 1