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Author Details

Vincent Magrini
The Ohio State University
1997
107
46
PMIDPaper TitleJournal TitlePublished Year
35716171Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case-based review.Genes Chromosomes Cancer2023
35149534Expanding the clinical phenotype of <i>FGFR1</i> internal tandem duplication.Cold Spring Harb Mol Case Stud2022
35857488Leveraging gene therapy to achieve long-term continuous or controllable expression of biotherapeutics.Sci Adv2022
35568002Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.Cancer Genet2022
35687047Detection of brain somatic variation in epilepsy-associated developmental lesions.Epilepsia2022
35962045Author Correction: Comparative and demographic analysis of orang-utan genomes.Nature2022
36191838Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome-Based Resolution of Isoform Complexity.J Mol Diagn2022
35045382A deletion in the N gene of SARS-CoV-2 may reduce test sensitivity for detection of SARS-CoV-2.Diagn Microbiol Infect Dis2022
34859533Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly.Hum Mutat2022
33074854YAP1-FAM118B Fusion Defines a Rare Subset of Childhood and Young Adulthood Meningiomas.Am J Surg Pathol2021
33827698Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma.Acta Neuropathol Commun2021
33893698Novel morphologic findings in PLAG1-rearranged soft tissue tumors.Genes Chromosomes Cancer2021
34895332Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas.Acta Neuropathol Commun2021
34863095Discovery of clinically relevant fusions in pediatric cancer.BMC Genomics2021
34716204Somatic variation as an incidental finding in the pediatric next-generation sequencing era.Cold Spring Harb Mol Case Stud2021
34041825Gastroblastoma with a novel EWSR1-CTBP1 fusion presenting in adolescence.Genes Chromosomes Cancer2021
34040190Somatic PIK3R1 variation as a cause of vascular malformations and overgrowth.Genet Med2021
34048549PTEN somatic mutations contribute to spectrum of cerebral overgrowth.Brain2021
33465168A novel sialic acid-binding adhesin present in multiple species contributes to the pathogenesis of Infective endocarditis.PLoS Pathog2021
32371413Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience.Cold Spring Harb Mol Case Stud2020
31949013<i>De novo</i> primary central nervous system pure erythroid leukemia/sarcoma with t(1;16)(p31;q24) <i>NFIA/CBFA2T3</i> translocation.Haematologica2020
31915069Correction to: Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma.Acta Neuropathol Commun2020
33028644Infantile fibrosarcoma-like tumor driven by novel <i>RBPMS-MET</i> fusion consolidated with cabozantinib.Cold Spring Harb Mol Case Stud2020
32637635Somatic <i>SLC35A2</i> mosaicism correlates with clinical findings in epilepsy brain tissue.Neurol Genet2020
30661756Characterizing the Major Structural Variant Alleles of the Human Genome.Cell2019
31685621Immunological ignorance is an enabling feature of the oligo-clonal T cell response to melanoma neoantigens.Proc Natl Acad Sci U S A2019
31271967Samovar: Single-Sample Mosaic Single-Nucleotide Variant Calling with Linked Reads.iScience2019
31308084Streptococcus oralis subsp. <i>dentisani</i> Produces Monolateral Serine-Rich Repeat Protein Fibrils, One of Which Contributes to Saliva Binding via Sialic Acid.Infect Immun2019
31195167Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma.Eur J Med Genet2019
30764877Comprehensive gene expression meta-analysis identifies signature genes that distinguish microglia from peripheral monocytes/macrophages in health and glioma.Acta Neuropathol Commun2019
29434027Genome sequencing identifies somatic <i>BRAF</i> duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma.Cold Spring Harb Mol Case Stud2018
30181556The prognostic effects of somatic mutations in ER-positive breast cancer.Nat Commun2018
30429476Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer.Nat Commun2018
29495964Improving eukaryotic genome annotation using single molecule mRNA sequencing.BMC Genomics2018
27002534Compartmentalization of functions and predicted miRNA regulation among contiguous regions of the nematode intestine.RNA Biol2017
28396521Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.Genome Res2017
28508897Whole genome analysis of a schistosomiasis-transmitting freshwater snail.Nat Commun2017
28832025Corrigendum: Whole genome analysis of a schistosomiasis-transmitting freshwater snail.Nat Commun2017
28760689Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes.Exp Hematol2017
27029710A genomic case study of mixed fibrolamellar hepatocellular carcinoma.Ann Oncol2016
26595813PML-RARA requires DNA methyltransferase 3A to initiate acute promyelocytic leukemia.J Clin Invest2016
26499396Identification of a novel fusion transcript between human relaxin-1 (RLN1) and human relaxin-2 (RLN2) in prostate cancer.Mol Cell Endocrinol2016
27148581A common founding clone with TP53 and PTEN mutations gives rise to a concurrent germ cell tumor and acute megakaryoblastic leukemia.Cold Spring Harb Mol Case Stud2016
27181063Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia.Exp Hematol2016
27058228A genomic analysis of Philadelphia chromosome-negative AML arising in patients with CML.Blood Cancer J2016
25258010RNA-sequencing reveals oligodendrocyte and neuronal transcripts in microglia relevant to central nervous system disease.Glia2015
26439490The Dynamic Genome and Transcriptome of the Human Fungal Pathogen Blastomyces and Close Relative Emmonsia.PLoS Genet2015
26305651Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia.JAMA2015
26645048Optimizing cancer genome sequencing and analysis.Cell Syst2015
26585233RNA Sequencing of Tumor-Associated Microglia Reveals Ccl5 as a Stromal Chemokine Critical for Neurofibromatosis-1 Glioma Growth.Neoplasia2015
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Collaborators

Elaine R Mardis
The Ohio State University
Co-authored papers 75
Richard K Wilson
The Ohio State University
Co-authored papers 59
Sean McGrath
Harvard T.H. Chan School of Public Health
Co-authored papers 32
Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 28
Daniel C Koboldt
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 23
Malachi Griffith
Washington University
Co-authored papers 19
Catherine E Cottrell
Nationwide Children's Hospital
Co-authored papers 19
Timothy J Ley
Washington University School of Medicine
Co-authored papers 18
Peter White
The Ohio State University
Co-authored papers 17
Catrina Fronick
McDonnell Genome Institute, Washington University in St. Louis School of Medicine
Co-authored papers 16
Christopher A Miller
Washington University School of Medicine
Co-authored papers 16
Lucinda Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 16
David E Larson
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 16
Obi L Griffith
Washington University
Co-authored papers 16
Jason Walker
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 16
Li Ding
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 14
Kathleen M Schieffer
Nationwide Children's Hospital
Co-authored papers 14
Benjamin J Kelly
Nationwide Children's Hospital
Co-authored papers 14
Daniel C Link
Washington University School of Medicine
Co-authored papers 13
Michelle O'Laughlin
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 12
Katherine E Miller
College of Medicine, The Ohio State University
Co-authored papers 12
Jasreet Hundal
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 12
Anthony R Miller
Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 11
Timothy A Graubert
Massachusetts General Hospital
Co-authored papers 11
Michael D McLellan
McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers 11
James Fitch
The Institute for Genomic Medicine, Nationwide Children's Hospital
Co-authored papers 11
Matthew J Walter
Washington University School of Medicine in St. Louis
Co-authored papers 11
John F DiPersio
Washington University School of Medicine
Co-authored papers 11
Tamara L Lamprecht
St. Jude Children's Research Hospital
Co-authored papers 10
Peter Westervelt
Washington University School of Medicine
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Release 1.2