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Author Details
Full Name
Katherine E Miller
Affiliation
College of Medicine, The Ohio State University
ORCID
Career Start Year
2017
Papers
38
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36631516
Single-nuclei transcriptomics enable detection of somatic variants in patient brain tissue.
Sci Rep
2023
37583388
Oncolytic virus-driven immune remodeling revealed in mouse medulloblastomas at single cell resolution.
Mol Ther Oncolytics
2023
35802027
Cerebral organoids containing an AUTS2 missense variant model microcephaly.
Brain
2023
35716171
Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case-based review.
Genes Chromosomes Cancer
2023
37013636
A novel transcriptional signature identifies T-cell infiltration in high-risk paediatric cancer.
Genome Med
2023
36583990
Manufacture and Characterization of Good Manufacturing Practice-Compliant SARS-COV-2 Cytotoxic T Lymphocytes.
J Infect Dis
2023
36871221
Single-cell RNA sequencing reveals immunosuppressive myeloid cell diversity during malignant progression in a murine model of glioma.
Cell Rep
2023
36827605
Correspondence comprehensive characterization of a brainstem aggregoma (light and heavy chain deposition disease).
Brain Pathol
2023
34610950
Characterization of the Genomic and Immunologic Diversity of Malignant Brain Tumors through Multisector Analysis.
Cancer Discov
2022
35617766
Pediatric CNS cancer genomics and immunogenomics.
Curr Opin Genet Dev
2022
35840846
ASO Visual Abstract: Patient-Specific Sarcoma Organoids for Personalized Translational Research: Unification of the Operating Room with Rare Cancer Research and Clinical Implications.
Ann Surg Oncol
2022
35788257
High early death rates, treatment resistance, and short survival of Black adolescents and young adults with AML.
Blood Adv
2022
35780216
Patient-Specific Sarcoma Organoids for Personalized Translational Research: Unification of the Operating Room with Rare Cancer Research and Clinical Implications.
Ann Surg Oncol
2022
35687047
Detection of brain somatic variation in epilepsy-associated developmental lesions.
Epilepsia
2022
35712307
Salivary miRNA Expression in Children With Persistent Post-concussive Symptoms.
Front Public Health
2022
36411471
Molecular and spatial heterogeneity of microglia in Rasmussen encephalitis.
Acta Neuropathol Commun
2022
35912263
Molecular Heterogeneity in Pediatric Malignant Rhabdoid Tumors in Patients With Multi-Organ Involvement.
Front Oncol
2022
35967098
An unusual case of atypical teratoid/rhabdoid tumor, initially diagnosed as atypical pituitary adenoma in a 13-year-old male patient.
Neurooncol Adv
2022
36191838
Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome-Based Resolution of Isoform Complexity.
J Mol Diagn
2022
35105718
Immune Activity and Response Differences of Oncolytic Viral Therapy in Recurrent Glioblastoma: Gene Expression Analyses of a Phase IB Study.
Clin Cancer Res
2022
33074854
YAP1-FAM118B Fusion Defines a Rare Subset of Childhood and Young Adulthood Meningiomas.
Am J Surg Pathol
2021
33827698
Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma.
Acta Neuropathol Commun
2021
33637608
Clinical response to dabrafenib plus trametinib in a pediatric ganglioglioma with <i>BRAF</i> p.T599dup mutation.
Cold Spring Harb Mol Case Stud
2021
34895332
Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal ependymomas.
Acta Neuropathol Commun
2021
34863095
Discovery of clinically relevant fusions in pediatric cancer.
BMC Genomics
2021
34667072
Maternal mosaicism for a missense variant in the <i>SMS</i> gene that causes Snyder-Robinson syndrome.
Cold Spring Harb Mol Case Stud
2021
34041825
Gastroblastoma with a novel EWSR1-CTBP1 fusion presenting in adolescence.
Genes Chromosomes Cancer
2021
34278266
Endogenous retrovirus envelope as a tumor-associated immunotherapeutic target in murine osteosarcoma.
iScience
2021
34048549
PTEN somatic mutations contribute to spectrum of cerebral overgrowth.
Brain
2021
32181236
The Financial Impact of Genetic Diseases in a Pediatric Accountable Care Organization.
Front Public Health
2020
32637635
Somatic <i>SLC35A2</i> mosaicism correlates with clinical findings in epilepsy brain tissue.
Neurol Genet
2020
30957677
Identification of Rare Variants Predisposing to Thyroid Cancer.
Thyroid
2019
31195167
Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma.
Eur J Med Genet
2019
29434027
Genome sequencing identifies somatic <i>BRAF</i> duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma.
Cold Spring Harb Mol Case Stud
2018
29515625
Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital.
Front Genet
2018
28535206
Clinical exome sequencing reports: current informatics practice and future opportunities.
J Am Med Inform Assoc
2017
29046692
A patient with van Maldergem syndrome with endocrine abnormalities, hypogonadotropic hypogonadism, and breast aplasia/hypoplasia.
Int J Pediatr Endocrinol
2017
28425983
Addressing a patient-controlled approach for genomic data sharing.
Genet Med
2017
1 - 38 of 38
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Daniel R Bou??
Nationwide Children's Hospital
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James Fitch
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Kristen Leraas
Nationwide Children's Hospital
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Anthony R Miller
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Tracy A Bedrosian
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Jonathan L Finlay
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Diana S Osorio
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