Author details

Full Name

Deanne Taylor

Affiliation

ORCID

Career Start Year

1999

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35074468	Betacoronavirus-specific alternate splicing.	Genomics	2022
36246576	Host transcriptional responses in nasal swabs identify potential SARS-CoV-2 infection in PCR negative patients.	iScience	2022
35484100	Targeting CD123 in blastic plasmacytoid dendritic cell neoplasm using allogeneic anti-CD123 CAR T cells.	Nat Commun	2022
35664076	The interplay between lncRNAs, RNA-binding proteins and viral genome during SARS-CoV-2 infection reveals strong connections with regulatory events involved in RNA metabolism and immune response.	Theranostics	2022
34984927	Differentiating children with sepsis with and without acute respiratory distress syndrome using proteomics.	Am J Physiol Lung Cell Mol Physiol	2022
35233572	TARGETED DOWN REGULATION OF CORE MITOCHONDRIAL GENES DURING SARS-COV-2 INFECTION.	bioRxiv	2022
35233546	System-wide transcriptome damage and tissue identity loss in COVID-19 patients.	Cell Rep Med	2022
35151364	Gene-Interaction-Sensitive enrichment analysis in congenital heart disease.	BioData Min	2022
35015683	Modulation of CD22 Protein Expression in Childhood Leukemia by Pervasive Splicing Aberrations: Implications for CD22-Directed Immunotherapies.		2022
35015563	Fusion Oncogenes Are Associated With Increased Metastatic Capacity and Persistent Disease in Pediatric Thyroid Cancers.	J Clin Oncol	2022
34822785	Fundamental Biological Features of Spaceflight: Advancing the Field to Enable Deep-Space Exploration.	Cell	2021
34230929	Betacoronavirus-specific alternate splicing.	bioRxiv	2021
34115127	International Analysis of Electronic Health Records of Children and Youth Hospitalized With COVID-19 Infection in 6 Countries.	JAMA Netw Open	2021
33948587	The Great Deceiver: miR-2392's Hidden Role in Driving SARS-CoV-2 Infection.	bioRxiv	2021
33731876	Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders.	Genet Med	2021
33621495	Prolonged, Controlled Daytime versus Delayed Eating Impacts Weight and Metabolism.	Curr Biol	2021
34000298	An interdomain helix in IRE1Î± mediates the conformational change required for the sensor's activation.	Journal of Biological Chemistry	2021
33925651	Common Variation in Cytoskeletal Genes is Associated with Conotruncal Heart Defects.	Genes (Basel)	2021
33758858	Systemic Tissue and Cellular Disruption from SARS-CoV-2 Infection revealed in COVID-19 Autopsies and Spatial Omics Tissue Maps.	bioRxiv	2021
34356046	Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.	Genes (Basel)	2021
33259790	Prolonged, Controlled Daytime versus Delayed Eating Impacts Weight and Metabolism.	Curr Biol	2021
34624208	Role of miR-2392 in driving SARS-CoV-2 infection.	Cell Rep	2021
33119584	A transcriptome-based classifier to determine molecular subtypes in medulloblastoma.	PLoS Comput Biol	2020
31591467	Retention of CD19 intron 2 contributes to CART-19 resistance in leukemias with subclonal frameshift mutations in CD19.	Leukemia	2020
32120377	Derivation of a metabolic signature associated with bacterial meningitis in infants.	Pediatr Res	2020
32045996	NASA GeneLab Platform Utilized for Biological Response to Space Radiation in Animal Models.	Cancers (Basel)	2020
31988426	Author Correction: Multi-omics analysis of multiple missions to space reveal a theme of lipid dysregulation in mouse liver.	Sci Rep	2020
32214318	Ten simple rules for providing effective bioinformatics research support.	PLoS Comput Biol	2020
31758088	Correction: Transient stabilization, rather than inhibition, of MYC amplifies extrinsic apoptosis and therapeutic responses in refractory B-cell lymphoma.	Leukemia	2020
32750314	XACT-Seq Comprehensively Defines the Promoter-Position and Promoter-Sequence Determinants for Initial-Transcription Pausing.	Molecular Cell	2020
33242417	Comprehensive Multi-omics Analysis Reveals Mitochondrial Stress as a Central Biological Hub for Spaceflight Impact.	Cell	2020
33242416	Fundamental Biological Features of Spaceflight: Advancing the Field to Enable Deep-Space Exploration.	Cell	2020
33188371	Guidelines for reporting single-cell RNA-seq experiments.	Nat Biotechnol	2020
32516339	Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects.	PLoS One	2020
33336201	A New Era for Space Life Science: International Standards for Space Omics Processing.	Patterns (N Y)	2020
31296308	A comparison of survival analysis methods for cancer gene expression RNA-Sequencing data.	Cancer Genet	2019
31844325	Multi-omics analysis of multiple missions to space reveal a theme of lipid dysregulation in mouse liver.	Sci Rep	2019
30517739	Aberrant splicing in B-cell acute lymphoblastic leukemia.	Nucleic Acids Res	2019
31141530	The association of elevated maternal genetic risk scores for hypertension, type 2 diabetes and obesity and having a child with a congenital heart defect.	PLoS ONE	2019
31222980	Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status.	Birth Defects Res	2019
30914792	Transient stabilization, rather than inhibition, of MYC amplifies extrinsic apoptosis and therapeutic responses in refractory B-cell lymphoma.	Leukemia	2019
30729789	Limits of Spatial Resolution of Phase Encoding Dimensions in MRI of Metals.	Journal of Physical Chemistry Letters	2019
31316053	Sphingosine-1-phosphate receptor 3 in the medial prefrontal cortex promotes stress resilience by reducing inflammatory processes.	Nature Communications	2019
31314787	Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects.	PLoS One	2019
29681497	CapZyme-Seq Comprehensively Defines Promoter-Sequence Determinants for RNA 5' Capping with NAD<sup/>.	Molecular Cell	2018
30357359	Aberrant splicing in B-cell acute lymphoblastic leukemia.	Nucleic Acids Res	2018
29186554	Preclinical validation of a targeted next generation sequencing-based comprehensive chromosome screening methodology in human blastocysts.	Molecular Human Reproduction	2018
29309924	Aggressive triple negative breast cancers have unique molecular signature on the basis of mitochondrial genetic and functional defects.	Biochim Biophys Acta Mol Basis Dis	2018
28560097	<i>pathVar:</i> a new method for pathway-based interpretation of gene expression variability.	PeerJ	2017
28468790	Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.	Circ Cardiovasc Genet	2017