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Author Details

Dennis T Maglinte
2010
16
10
PMIDPaper TitleJournal TitlePublished Year
38008288An Exome Capture-Based RNA-Sequencing Assay for Genome-Wide Identification and Prioritization of Clinically Important Fusions in Pediatric Tumors.J Mol Diagn2024
35082777Persistence of SARS CoV-2 S1 Protein in CD16+ Monocytes in Post-Acute Sequelae of COVID-19 (PASC) up to 15 Months Post-Infection.Front Immunol2022
36115539Mitochondrial DNA haplogroup, genetic ancestry, and susceptibility to Ewing sarcoma.Mitochondrion2022
33866984Utility of viral whole-genome sequencing for institutional infection surveillance during the coronavirus disease 2019 (COVID-19) pandemic.Infect Control Hosp Epidemiol2022
35317603Implementation of a Streamlined SARS-CoV-2 Whole-Genome Sequencing Assay for Expeditious Surveillance during the Emergence of the Omicron Variant.J Clin Microbiol2022
33915337Increased viral variants in children and young adults with impaired humoral immunity and persistent SARS-CoV-2 infection: A consecutive case series.EBioMedicine2021
33688673Persistent SARS-CoV-2 infection and increasing viral variants in children and young adults with impaired humoral immunity.medRxiv2021
33619507Early pandemic molecular diversity of SARS-CoV-2 in children.medRxiv2021
34095334High Prevalence of SARS-CoV-2 Genetic Variation and D614G Mutation in Pediatric Patients With COVID-19.Open Forum Infect Dis2020
30755392A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants.Cold Spring Harb Mol Case Stud2019
30138724OncoKids: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.J Mol Diagn2018
28371217Inherited germline ATRX mutation in two brothers with ATR-X syndrome and osteosarcoma.Am J Med Genet A2017
28985730Clinical utility of the low-density Infinium QC genotyping Array in a genomics-based diagnostics laboratory.BMC Medical Genomics2017
27155049A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families.J Mol Diagn2016
26061751Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.N Engl J Med2015
20661424Epigenetic analysis of KSHV latent and lytic genomes.PLoS Pathog2010
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Center for Epigenetics, Van Andel Research Institute
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Children's Hospital Los Angeles
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Children's Hospital Los Angeles
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Van Andel Institute
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Center for Personalized Medicine, Children's Hospital Los Angeles
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Nationwide Children's Hospital
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The University of MD Anderson Cancer Center
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University of Texas MD Anderson Cancer Center
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Canada British Columbia Cancer Research Centre, University of British Columbia
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