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Author Details

Arie Perry
University of California san francisco
1984
441
93
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36227281Hypermitotic meningiomas harbor DNA methylation subgroups with distinct biological and clinical features.Neuro Oncol2023
35657335Low-risk meningioma: Initial outcomes from NRG Oncology/RTOG 0539.Neuro Oncol2023
36227281Hypermitotic meningiomas harbor DNA methylation subgroups with distinct biological and clinical features.Neuro Oncol2023
35678633Molecular characterization of metachronous atypical teratoid rhabdoid tumors occurring in a young man 15 years apart.Pediatr Blood Cancer2023
36437415Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.Acta Neuropathol2023
36897259Molecular profiling identifies at least 3 distinct types of posttransplant lymphoproliferative disorder involving the CNS.Blood Adv2023
36826690Sarcomatous Transformation of a Medically Treated Lactotroph Pituitary Neuroendocrine Tumor?Endocr Pathol2023
37268858Multilineage Pituitary Neuroendocrine Tumors (PitNETs) Expressing PIT1 and SF1.Endocr Pathol2023
37436963Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs.Neuro Oncol2023
36993741Targeted gene expression profiling predicts meningioma outcomes and radiotherapy responses.Res Sq2023
36543154Cauda Equina Neuroendocrine Tumors: Distinct Epithelial Neuroendocrine Neoplasms of Spinal Origin.Am J Surg Pathol2023
36786841Correction to: Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.Acta Neuropathol2023
37503127NOTCH3 drives meningioma tumorigenesis and resistance to radiotherapy.bioRxiv2023
37487571Cavernous sinus hemangioma: Histopathological spectrum of 8 cases.J Neuropathol Exp Neurol2023
37546798Meningeal solitary fibrous tumor cell states phenocopy cerebral vascular development and homeostasis.Res Sq2023
37292686Spatial genomic, biochemical, and cellular mechanisms drive meningioma heterogeneity and evolution.Res Sq2023
36723772Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas.Acta Neuropathol2023
37487571Cavernous sinus hemangioma: Histopathological spectrum of 8 cases.J Neuropathol Exp Neurol2023
37546798Meningeal solitary fibrous tumor cell states phenocopy cerebral vascular development and homeostasis.Res Sq2023
37503127NOTCH3 drives meningioma tumorigenesis and resistance to radiotherapy.bioRxiv2023
35678633Molecular characterization of metachronous atypical teratoid rhabdoid tumors occurring in a young man 15 years apart.Pediatr Blood Cancer2023
35657335Low-risk meningioma: Initial outcomes from NRG Oncology/RTOG 0539.Neuro Oncol2023
37292686Spatial genomic, biochemical, and cellular mechanisms drive meningioma heterogeneity and evolution.Res Sq2023
36993741Targeted gene expression profiling predicts meningioma outcomes and radiotherapy responses.Res Sq2023
37436963Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs.Neuro Oncol2023
37268858Multilineage Pituitary Neuroendocrine Tumors (PitNETs) Expressing PIT1 and SF1.Endocr Pathol2023
36723772Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas.Acta Neuropathol2023
36786841Correction to: Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.Acta Neuropathol2023
36543154Cauda Equina Neuroendocrine Tumors: Distinct Epithelial Neuroendocrine Neoplasms of Spinal Origin.Am J Surg Pathol2023
36437415Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.Acta Neuropathol2023
36826690Sarcomatous Transformation of a Medically Treated Lactotroph Pituitary Neuroendocrine Tumor?Endocr Pathol2023
36897259Molecular profiling identifies at least 3 distinct types of posttransplant lymphoproliferative disorder involving the CNS.Blood Adv2023
34821426Intracranial mesenchymal tumors with FET-CREB fusion are composed of at least two epigenetic subgroups distinct from meningioma and extracranial sarcomas.Brain Pathol2022
35395677Prospective genomically guided identification of "early/evolving" and "undersampled" IDH-wildtype glioblastoma leads to improved clinical outcomes.Neuro Oncol2022
35703914Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma.J Neuropathol Exp Neurol2022
35511927CXCL14 Promotes a Robust Brain Tumor-Associated Immune Response in Glioma.Clin Cancer Res2022
35759011Intratumor and informatic heterogeneity influence meningioma molecular classification.Acta Neuropathol2022
35945463Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1.Acta Neuropathol2022
35689747Immature PIT1-Lineage Pituitary Neuroendocrine Tumor: a 17-Year-Old Male with Pathogenic AIP Mutation.Endocr Pathol2022
36130567NTRK3 gene fusion in an adult ganglioglioma: illustrative case.J Neurosurg Case Lessons2022
36201019Molecular and clinicopathologic characteristics of gliomas with EP300::BCOR fusions.Acta Neuropathol2022
35475853Orbital Rosai-Dorfman Disease Presenting as Optic Neuritis.J Neuroophthalmol2022
35534562Meningioma DNA methylation groups identify biological drivers and therapeutic vulnerabilities.Nat Genet2022
35291028Overview of the 2022 WHO Classification of Pituitary Tumors.Endocr Pathol2022
34910220Activating NTRK2 and ALK receptor tyrosine kinase fusions extend the molecular spectrum of pleomorphic xanthoastrocytomas of early childhood: a diagnostic overlap with infant-type hemispheric glioma.Acta Neuropathol2022
35213084Molecular neuropathology of brain-invasive meningiomas.Brain Pathol2022
35175291Molecular Biomarker Testing for the Diagnosis of Diffuse Gliomas.Arch Pathol Lab Med2022
35157770A genetically distinct pediatric subtype of primary CNS large B-cell lymphoma is associated with favorable clinical outcome.Blood Adv2022
34825267EWSR1-BEND2 fusion defines an epigenetically distinct subtype of astroblastoma.Acta Neuropathol2022
34821426Intracranial mesenchymal tumors with FET-CREB fusion are composed of at least two epigenetic subgroups distinct from meningioma and extracranial sarcomas.Brain Pathol2022
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Collaborators

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Co-authored papers 71
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Co-authored papers 26
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 24
Heinrich Heine University
Co-authored papers 24
University of California San Francisco
Co-authored papers 24
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Mayo Clinic
Co-authored papers 22
University of California san francisco
Co-authored papers 21
Institute of Pathology, University Hospital Heidelberg
Co-authored papers 20
Co-authored papers 20
National Cancer Institute
Co-authored papers 20
St. Jude Children's Research Hospital
Co-authored papers 19
University of California san francisco
Co-authored papers 18
Co-authored papers 18
University of California san francisco
Co-authored papers 18
Co-authored papers 18
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 17
Co-authored papers 17
University of California Los Angeles
Co-authored papers 16
Feinberg School of Medicine, Northwestern University
Co-authored papers 16
University of California san francisco
Co-authored papers 15
University of California san francisco
Co-authored papers 15
Charite University Medicine Berlin
Co-authored papers 15
University Children's Hospital Zurich
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