Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Whole Exome Sequencing of Multiple Atypical Meningiomas in a Patient without History of Neurofibromatosis Type II: A Case Report.

The American journal of case reports - 28 May 2020

Lyu Jian, Quan Yu, Wang Ju-Bo, Gong Shou-Ping

Abstract excerpt

BACKGROUND The pathogenesis of sporadic multiple meningiomas in the patients without history of neurofibromatosis type II remains unclear. We report whole exome sequencing (WES) of 2 metachronous multiple meningiomas of the same patient. CASE REPORT A 39-year-old female had a 5-month history of headache and her magnetic resonance imaging (MRI) revealed a significantly enhanced intracranial space-occupying...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Exome Sequencing
Share to Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Meningeal Neoplasms

Share to Meningioma

Share to Mutation

Share to Neoplasm Recurrence, Local

Share to Neurofibromatosis 2

Source

Open in PubMed Open full text

Identifiers

PMID: 32461543
DOI: 10.12659/AJCR.923928
PMCID: PMC7286185

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Whole Exome Sequencing of Multiple Atypical Meningiomas in a Patient without History of Neurofibromatosis Type II: A Case Report.PMID 32461543Read ↗

Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodules.Semantic proximity Read ↗

Comprehensive genomic analysis reveals clonal origin and subtype-specific evolution in a case of sporadic multiple meningiomas.Semantic proximity Read ↗

Comprehensive genomic analysis of sporadic multiple meningiomas reveals clonal origin and histotype-specific evolution: a case reportSemantic proximity Read ↗

Exome sequencing on malignant meningiomas identified mutations in neurofibromatosis type 2 (NF2) and meningioma 1 (MN1) genes.Semantic proximity Read ↗

Genomic sequencing of meningiomas identifies oncogenic SMO and AKT1 mutations.Semantic proximity Read ↗

Meningioma genomics: a therapeutic challenge for cliniciansSemantic proximity Read ↗

Meningioma Genomics: Diagnostic, Prognostic, and Therapeutic ApplicationsSemantic proximity Read ↗

Next generation sequencing identifies novel potential actionable mutations for grade I meningioma treatment.Semantic proximity Read ↗

A new amplicon-based gene panel for next generation sequencing characterization of meningiomas.Semantic proximity Read ↗

Clinical potential of meningioma genomic insights: a practical review for neurosurgeons.Semantic proximity Read ↗

Life and death of molecular subclones in recurrent meningioma: A case study.Semantic proximity Read ↗

Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.