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Author Details
Full Name
Dennis T Maglinte
Affiliation
ORCID
Career Start Year
2010
Papers
16
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
38008288
An Exome Capture-Based RNA-Sequencing Assay for Genome-Wide Identification and Prioritization of Clinically Important Fusions in Pediatric Tumors.
J Mol Diagn
2024
35082777
Persistence of SARS CoV-2 S1 Protein in CD16+ Monocytes in Post-Acute Sequelae of COVID-19 (PASC) up to 15 Months Post-Infection.
Front Immunol
2022
36115539
Mitochondrial DNA haplogroup, genetic ancestry, and susceptibility to Ewing sarcoma.
Mitochondrion
2022
33866984
Utility of viral whole-genome sequencing for institutional infection surveillance during the coronavirus disease 2019 (COVID-19) pandemic.
Infect Control Hosp Epidemiol
2022
35317603
Implementation of a Streamlined SARS-CoV-2 Whole-Genome Sequencing Assay for Expeditious Surveillance during the Emergence of the Omicron Variant.
J Clin Microbiol
2022
33915337
Increased viral variants in children and young adults with impaired humoral immunity and persistent SARS-CoV-2 infection: A consecutive case series.
EBioMedicine
2021
33688673
Persistent SARS-CoV-2 infection and increasing viral variants in children and young adults with impaired humoral immunity.
medRxiv
2021
33619507
Early pandemic molecular diversity of SARS-CoV-2 in children.
medRxiv
2021
34095334
High Prevalence of SARS-CoV-2 Genetic Variation and D614G Mutation in Pediatric Patients With COVID-19.
Open Forum Infect Dis
2020
30755392
A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants.
Cold Spring Harb Mol Case Stud
2019
30138724
OncoKids: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.
J Mol Diagn
2018
28371217
Inherited germline ATRX mutation in two brothers with ATR-X syndrome and osteosarcoma.
Am J Med Genet A
2017
28985730
Clinical utility of the low-density Infinium QC genotyping Array in a genomics-based diagnostics laboratory.
BMC Medical Genomics
2017
27155049
A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families.
J Mol Diagn
2016
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
20661424
Epigenetic analysis of KSHV latent and lytic genomes.
PLoS Pathog
2010
1 - 16 of 16
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