Related references
Note: Only part of the references are listed.The genomic landscape across 474 surgically accessible epileptogenic human brain lesions
Javier A. Lopez-Rivera et al.
BRAIN (2023)
Heterogeneity and excitability of BRAFV600E-induced tumors is determined by Akt/mTOR-signaling state and Trp53-loss
Silvia Cases-Cunillera et al.
NEURO-ONCOLOGY (2022)
Integrated genotype-phenotype analysis of long-term epilepsy-associated ganglioglioma
Yujiao Wang et al.
BRAIN PATHOLOGY (2022)
Crystallographic landscape of SHP2 provides molecular insights for SHP2 targeted drug discovery
Yihui Song et al.
MEDICINAL RESEARCH REVIEWS (2022)
Glioblastoma hijacks neuronal mechanisms for brain invasion
Varun Venkataramani et al.
CELL (2022)
Detection of brain somatic variation in epilepsy-associated developmental lesions
Tracy A. Bedrosian et al.
EPILEPSIA (2022)
Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma
Calixto-Hope G. Lucas et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2022)
Neocortical development and epilepsy: insights from focal cortical dysplasia and brain tumours
Ingmar Blumcke et al.
LANCET NEUROLOGY (2021)
Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course
Annika K. Wefers et al.
ACTA NEUROPATHOLOGICA (2020)
Long-term epilepsy-associated tumors: transcriptional signatures reflect clinical course
Daniel Delev et al.
SCIENTIFIC REPORTS (2020)
Low-grade developmental and epilepsy associated brain tumors: a critical update 2020
Rutger Juriaan Slegers et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2020)
Low-Grade Gliomas in Patients with Noonan Syndrome: Case-Based Review of the Literature
Mariachiara Lodi et al.
DIAGNOSTICS (2020)
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay
Katja Kobow et al.
ACTA NEUROPATHOLOGICA (2020)
Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study
Herm J. Lamberink et al.
LANCET NEUROLOGY (2020)
Glutamatergic synaptic input to glioma cells drives brain tumour progression
Varun Venkataramani et al.
NATURE (2019)
Genomic Analysis of Dysembryoplastic Neuroepithelial Tumor Spectrum Reveals a Diversity of Molecular Alterations Dysregulating the MAPK and PI3K/mTOR Pathways
Lea F. Surrey et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2019)
Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype-phenotype analysis
I. Bluemcke et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2019)
DNA methylation-based classification of central nervous system tumours
David Capper et al.
NATURE (2018)
BRAF somatic mutation contributes to intrinsic epileptogenicity in pediatric brain tumors
Hyun Yong Koh et al.
NATURE MEDICINE (2018)
Preprocessing, normalization and integration of the Illumina HumanMethylationEPIC array with minfi
Jean-Philippe Fortin et al.
BIOINFORMATICS (2017)
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
I. Blumcke et al.
NEW ENGLAND JOURNAL OF MEDICINE (2017)
Noonan Syndrome, PTPN11 Mutations, and Brain Tumors. A Clinical Report and Review of the Literature
Aurore Siegfried et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2017)
Low-grade epilepsy-associated neuroepithelial tumours - the 2016 WHO classification
Ingmar Bluemcke et al.
NATURE REVIEWS NEUROLOGY (2016)
Brain tumour cells interconnect to a functional and resistant network
Matthias Osswald et al.
NATURE (2015)
Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays
Martin J. Aryee et al.
BIOINFORMATICS (2014)
Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11
Jin-Lan Chen et al.
MOLECULAR CYTOGENETICS (2014)
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray
Yi-an Chen et al.
EPIGENETICS (2013)
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo et al.
NATURE GENETICS (2011)
Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines
Alicia A. Romano et al.
PEDIATRICS (2010)
Control of CNS cell-fate decisions by SHP-2 and its dysregulation in Noonan syndrome
Andree S. Gauthier et al.
NEURON (2007)
Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia
T Niihori et al.
JOURNAL OF HUMAN GENETICS (2005)
Share Paper
