Related references
Note: Only part of the references are listed.Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis
Abigail K. Suwala et al.
ACTA NEUROPATHOLOGICA (2021)
Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
Thomas Bonduelle et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2021)
Neuropathology of the 21st century for the Latin American epilepsy community
Jose Eduardo Peixoto-Santos et al.
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY (2021)
Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial
Ingmar Bluemcke et al.
EPILEPSIA (2021)
Toward a refined genotype-phenotype classification scheme for the international consensus classification of Focal Cortical Dysplasia
Ingmar Blumcke et al.
BRAIN PATHOLOGY (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)
DNA Methylation Profiling Identifies Distinct Clusters in Angiosarcomas
Marije E. Weidema et al.
CLINICAL CANCER RESEARCH (2020)
Diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear clusters (DGONC) - a molecularly defined glioneuronal CNS tumour class displaying recurrent monosomy 14
M. Y. Deng et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (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)
Clinical Relevance of BRAF V600E Mutation Status in Brain Tumors with a Focus on a Novel Management Algorithm
Adam Kowalewski et al.
TARGETED ONCOLOGY (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)
International consensus recommendations on the diagnostic work-up for malformations of cortical development
Renske Oegema et al.
NATURE REVIEWS NEUROLOGY (2020)
Advances in Targeted Therapies for Pediatric Brain Tumors
Timothy Mueller et al.
CURRENT TREATMENT OPTIONS IN NEUROLOGY (2020)
Fastai: A Layered API for Deep Learning
Jeremy Howard et al.
INFORMATION (2020)
Age-related MR characteristics in mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE)
Till Hartlieb et al.
EPILEPSY & BEHAVIOR (2019)
Methylation array profiling of adult brain tumours: diagnostic outcomes in a large, single centre
Zane Jaunmuktane et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2019)
Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasia
Katja Kobow et al.
EPILEPSIA (2019)
Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1
Philipp Sievers et al.
ACTA NEUROPATHOLOGICA (2019)
Dissecting the genetic basis of focal cortical dysplasia: a large cohort study
Sara Baldassari et al.
ACTA NEUROPATHOLOGICA (2019)
Machine learning analysis of DNA methylation profiles distinguishes primary lung squamous cell carcinomas from head and neck metastases
Philipp Jurmeister et al.
SCIENCE TRANSLATIONAL MEDICINE (2019)
Papillary glioneuronal tumor (PGNT) exhibits a characteristic methylation profile and fusions involving PRKCA
Yanghao Hou et al.
ACTA NEUROPATHOLOGICA (2019)
DNA methylation-based reclassification of olfactory neuroblastoma
David Capper et al.
ACTA NEUROPATHOLOGICA (2018)
Second-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia-associated epilepsy
Theo Ribierre et al.
JOURNAL OF CLINICAL INVESTIGATION (2018)
DNA methylation-based classification of central nervous system tumours
David Capper et al.
NATURE (2018)
Review: The international consensus classification of Focal Cortical Dysplasia - a critical update 2018
I. M. Najm et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2018)
Polymorphous low-grade neuroepithelial tumor of the young (PLNTY): an epileptogenic neoplasm with oligodendroglioma-like components, aberrant CD34 expression, and genetic alterations involving the MAP kinase pathway
Jason T. Huse et al.
ACTA NEUROPATHOLOGICA (2017)
Preprocessing, normalization and integration of the Illumina HumanMethylationEPIC array with minfi
Jean-Philippe Fortin et al.
BIOINFORMATICS (2017)
Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological Entity
Johannes Schurr et al.
BRAIN PATHOLOGY (2017)
DNA methylation-based classification and grading system for meningioma: a multicentre, retrospective analysis
Felix Sahm et al.
LANCET ONCOLOGY (2017)
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
I. Blumcke et al.
NEW ENGLAND JOURNAL OF MEDICINE (2017)
Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias
Alissa M. D'Gama et al.
CELL REPORTS (2017)
Epigenetic control of epilepsy target genes contributes to a cellular memory of epileptogenesis in cultured rat hippocampal neurons
K. Kiese et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2017)
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly
Diana Alcantara et al.
BRAIN (2017)
International recommendation for a comprehensive neuropathologic workup of epilepsy surgery brain tissue: A consensus Task Force report from the ILAE Commission on Diagnostic Methods
Ingmar Bluemcke et al.
EPILEPSIA (2016)
Low-grade epilepsy-associated neuroepithelial tumours - the 2016 WHO classification
Ingmar Bluemcke et al.
NATURE REVIEWS NEUROLOGY (2016)
Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism
Ghayda M. Mirzaa et al.
JAMA NEUROLOGY (2016)
Etiology matters - Genomic DNA Methylation Patterns in Three Rat Models of Acquired Epilepsy
Konrad J. Debski et al.
SCIENTIFIC REPORTS (2016)
Familial Focal Epilepsy with Focal Cortical Dysplasia Due to DEPDC5 Mutations
Stephanie Baulac et al.
ANNALS OF NEUROLOGY (2015)
Mammalian Target of Rapamycin Pathway Mutations Cause Hemimegalencephaly and Focal Cortical Dysplasia
Alissa M. D'Gama et al.
ANNALS OF NEUROLOGY (2015)
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia
Laura A. Jansen et al.
BRAIN (2015)
limma powers differential expression analyses for RNA-sequencing and microarray studies
Matthew E. Ritchie et al.
NUCLEIC ACIDS RESEARCH (2015)
A tree of the human brain
Sten Linnarsson
SCIENCE (2015)
Somatic mutation in single human neurons tracks developmental and transcriptional history
Michael A. Lodato et al.
SCIENCE (2015)
Malformations of cortical development: clinical features and genetic causes
Renzo Guerrini et al.
LANCET NEUROLOGY (2014)
Deep sequencing reveals increased DNA methylation in chronic rat epilepsy
Katja Kobow et al.
ACTA NEUROPATHOLOGICA (2013)
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray
Yi-an Chen et al.
EPIGENETICS (2013)
International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods
Ingmar Bluemcke et al.
EPILEPSIA (2013)
Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias
Roland Coras et al.
EPILEPSIA (2012)
The emerging role of DNA methylation in epileptogenesis
Katja Kobow et al.
EPILEPSIA (2012)
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly
Jeong Ho Lee et al.
NATURE GENETICS (2012)
The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission
Ingmar Bluemcke et al.
EPILEPSIA (2011)
An international consensus classification for focal cortical dysplasias
Ingmar Bluemcke et al.
LANCET NEUROLOGY (2011)
Interobserver and intraobserver reproducibility in focal cortical dysplasia (malformations of cortical development)
Wendy A. Chamberlain et al.
EPILEPSIA (2009)
IDH1 and IDH2 Mutations in Gliomas
Hai Yan et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
MGMT gene silencing and benefit from temozolomide in glioblastoma
ME Hegi et al.
NEW ENGLAND JOURNAL OF MEDICINE (2005)