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Author Details
Full Name
Christopher DeBoever
Affiliation
Stanford University
ORCID
Career Start Year
2010
Papers
23
H Index
15
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37235597
Assessing the potential of polygenic scores to strengthen medical risk prediction models of COVID-19.
PLoS One
2023
36042219
Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy.
Nat Commun
2022
33989816
γδ T Cells Control Gut Pathology in a Chronic Inflammatory Model of Colorectal Cancer.
Cell Mol Gastroenterol Hepatol
2021
34822764
Bayesian model comparison for rare-variant association studies.
Am J Hum Genet
2021
32522985
Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats.
Nat Commun
2020
32275883
Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases.
Am J Hum Genet
2020
30520965
Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics.
Bioinformatics
2019
31492854
Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology.
Nat Commun
2019
31570892
Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits.
Nat Genet
2019
29691392
Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study.
Nat Commun
2018
28874753
Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancer.
Nat Commun
2017
28388430
Large-Scale Profiling Reveals the Influence of Genetic Variation on Gene Expression in Human Induced Pluripotent Stem Cells.
Cell Stem Cell
2017
28410642
iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types.
Stem Cell Reports
2017
28188128
Interaction Landscape of Inherited Polymorphisms with Somatic Events in Cancer.
Cancer Discov
2017
29074555
Efficient Prioritization of Multiple Causal eQTL Variants via Sparse Polygenic Modeling.
Genetics
2017
27492256
Distinct splicing signatures affect converged pathways in myelodysplastic syndrome patients carrying mutations in different splicing regulators.
RNA
2016
27815263
High-level ROR1 associates with accelerated disease progression in chronic lymphocytic leukemia.
Blood
2016
25768983
Transcriptome sequencing reveals potential mechanism of cryptic 3' splice site selection in SF3B1-mutated cancers.
PLoS Comput Biol
2015
25860294
Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell development.
Blood Cancer J
2015
26015570
Systematic transcriptome analysis reveals tumor-specific isoforms for ovarian cancer diagnosis and therapy.
Proc Natl Acad Sci U S A
2015
24909518
MiningABs: mining associated biomarkers across multi-connected gene expression datasets.
BMC Bioinformatics
2014
24023918
Whole transcriptome sequencing enables discovery and analysis of viruses in archived primary central nervous system lymphomas.
PLoS One
2013
20843365
Context dependent substitution biases vary within the human genome.
BMC Bioinformatics
2010
1 - 23 of 23
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