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Author Details

Calixto-Hope G Lucas
University of California San Francisco
2014
48
14
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36227281Hypermitotic meningiomas harbor DNA methylation subgroups with distinct biological and clinical features.Neuro Oncol2023
36227281Hypermitotic meningiomas harbor DNA methylation subgroups with distinct biological and clinical features.Neuro Oncol2023
37711972Radiotherapy and radiosurgery for meningiomas.Neurooncol Adv2023
37686092Management and Molecular Characterization of Intraventricular Glioblastoma: A Single-Institution Case Series.Int J Mol Sci2023
36840626Clinical, histological, and molecular features of gliomas in adults with neurofibromatosis type 1.Neuro Oncol2023
36897259Molecular profiling identifies at least 3 distinct types of posttransplant lymphoproliferative disorder involving the CNS.Blood Adv2023
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
36993679Merlin<sup>S13</sup> phosphorylation controls meningioma Wnt signaling and magnetic resonance imaging features.Res Sq2023
37503127NOTCH3 drives meningioma tumorigenesis and resistance to radiotherapy.bioRxiv2023
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
37711972Radiotherapy and radiosurgery for meningiomas.Neurooncol Adv2023
37503127NOTCH3 drives meningioma tumorigenesis and resistance to radiotherapy.bioRxiv2023
37686092Management and Molecular Characterization of Intraventricular Glioblastoma: A Single-Institution Case Series.Int J Mol Sci2023
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
36993679Merlin<sup>S13</sup> phosphorylation controls meningioma Wnt signaling and magnetic resonance imaging features.Res Sq2023
37436963Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs.Neuro Oncol2023
36723772Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas.Acta Neuropathol2023
36840626Clinical, histological, and molecular features of gliomas in adults with neurofibromatosis type 1.Neuro Oncol2023
36897259Molecular profiling identifies at least 3 distinct types of posttransplant lymphoproliferative disorder involving the CNS.Blood Adv2023
34825267EWSR1-BEND2 fusion defines an epigenetically distinct subtype of astroblastoma.Acta Neuropathol2022
35395677Prospective genomically guided identification of "early/evolving" and "undersampled" IDH-wildtype glioblastoma leads to improved clinical outcomes.Neuro Oncol2022
35587280Recurrent ACVR1 mutations in posterior fossa ependymoma.Acta Neuropathol2022
35703914Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma.J Neuropathol Exp Neurol2022
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
35667693Giant cell myositis associated with metastatic thymoma and granulomatous hypercalcaemia.BMJ Case Rep2022
36382111A case (report) for mechanistic validation of meningioma molecular therapies.Neurooncol Adv2022
36315366Radiotherapy for meningiomas.J Neurooncol2022
35534562Meningioma DNA methylation groups identify biological drivers and therapeutic vulnerabilities.Nat Genet2022
35061986Resection with intraoperative cesium-131 brachytherapy as salvage therapy for recurrent brain tumors.J Neurosurg2022
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
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
35587280Recurrent ACVR1 mutations in posterior fossa ependymoma.Acta Neuropathol2022
35703914Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma.J Neuropathol Exp Neurol2022
35667693Giant cell myositis associated with metastatic thymoma and granulomatous hypercalcaemia.BMJ Case Rep2022
35534562Meningioma DNA methylation groups identify biological drivers and therapeutic vulnerabilities.Nat Genet2022
35759011Intratumor and informatic heterogeneity influence meningioma molecular classification.Acta Neuropathol2022
35395677Prospective genomically guided identification of "early/evolving" and "undersampled" IDH-wildtype glioblastoma leads to improved clinical outcomes.Neuro Oncol2022
36315366Radiotherapy for meningiomas.J Neurooncol2022
36382111A case (report) for mechanistic validation of meningioma molecular therapies.Neurooncol Adv2022
35945463Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1.Acta Neuropathol2022
35157770A genetically distinct pediatric subtype of primary CNS large B-cell lymphoma is associated with favorable clinical outcome.Blood Adv2022
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
35061986Resection with intraoperative cesium-131 brachytherapy as salvage therapy for recurrent brain tumors.J Neurosurg2022
33147331Targeted Next-Generation Sequencing Identifies Molecular and Genetic Events in Dedifferentiated Chondrosarcoma.Arch Pathol Lab Med2021
34128073Sarcomatous Meningioma: Diagnostic Pitfalls and the Utility of Molecular Testing.J Neuropathol Exp Neurol2021
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Collaborators

Arie Perry
University of California san francisco
Co-authored papers 24
David A Solomon
University of California san francisco
Co-authored papers 23
David R Raleigh
University of California san francisco
Co-authored papers 22
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Feinberg School of Medicine, Northwestern University
Co-authored papers 17
Nancy Ann Oberheim Bush
University of California san francisco
Co-authored papers 13
Michael W McDermott
University of California san francisco
Co-authored papers 12
Joanna J Phillips
University of California san francisco
Co-authored papers 11
Harish N Vasudevan
University of California San Francisco
Co-authored papers 11
Javier E Villanueva-Meyer
University of California san francisco
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Mitchel S Berger
University of California san francisco
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Abrar Choudhury
University of California San Francisco
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William C Chen
University of California San Francisco
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Kanish Mirchia
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Steve E Braunstein
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Penny K Sneed
University of California San Francisco
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Lauren Boreta
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Siyuan John Liu
University of California San Francisco.
Co-authored papers 4
Jacob S Young
Co-authored papers 3
Kyounghee Seo
University of California san francisco
Co-authored papers 3
Matthew S Susko
University of California San Francisco
Co-authored papers 3
Craig Horbinski
Co-authored papers 3
Samuel H Cheshier
Co-authored papers 3
Joseph F Costello
University of California san francisco
Co-authored papers 3
Sabine Mueller
University Children's Hospital Zurich
Co-authored papers 3
Zied Abdullaev
Co-authored papers 2
Felix Sahm
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 2
Haley K Perlow
Co-authored papers 2
Release 1.2