Author details

Full Name

Brian Harding

Affiliation

ORCID

Career Start Year

1982

Papers

113

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35484145	Molecular and functional heterogeneity in dorsal and ventral oligodendrocyte progenitor cells of the mouse forebrain in response to DNA damage.	Nat Commun	2022
34111619	Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy.	Pediatr Neurol	2021
33970744	Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsy.	J Neurogenet	2021
32619987	The utility of brain biopsy in pediatric cryptogenic neurological disease.	Journal of Neurosurgery: Pediatrics	2020
32106287	The Neuropathology of MIRAGE Syndrome.	J Neuropathol Exp Neurol	2020
29804288	CDKN2A/B Loss Is Associated with Anaplastic Transformation in a Case of NTRK2 Fusion-positive Pilocytic Astrocytoma.	Neuropathol Appl Neurobiol	2019
31685033	BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester disease.	Acta Neuropathol Commun	2019
31617914	Genomic Analysis of Dysembryoplastic Neuroepithelial Tumor Spectrum Reveals a Diversity of Molecular Alterations Dysregulating the MAPK and PI3K/mTOR Pathways.	J Neuropathol Exp Neurol	2019
29746611	Adult Human Hippocampus: No New Neurons in Sight.	Cerebral Cortex	2018
29767381	Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activation.	Acta Neuropathol	2018
29530960	Clinical Reasoning: A 12-year-old girl with headache and change in mental status.	Neurology	2018
27886392	Deregulated expression of EZH2 in congenital brainstem disconnection.	Neuropathol Appl Neurobiol	2017
28987191	Developmental and perinatal brain diseases.	Handbook of Clinical Neurology	2017
26331236	Pontine tegmental cap dysplasia: neuropathological confirmation of a rare clinical/radiological syndrome.	Neuropathol Appl Neurobiol	2016
26894208	Degos disease mimicking primary vasculitis of the CNS.	Neurol Neuroimmunol Neuroinflamm	2016
26735972	A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease.	PLoS One	2016
27453579	Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons.	Am J Hum Genet	2016
25040262	Chromosome band 7q34 deletions resulting in KIAA1549-BRAF and FAM131B-BRAF fusions in pediatric low-grade Gliomas.	Brain Pathol	2015
25470343	Spectrum of neuropathophysiology in spinal muscular atrophy type I.	J Neuropathol Exp Neurol	2015
26339958	Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy.	J Neurosurg Pediatr	2015
26070982	Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73.	Brain	2015
24767714	Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors.	Cancer Genet	2014
24333734	Epigenetic genome-wide analysis identifies BEX1 as a candidate tumour suppressor gene in paediatric intracranial ependymoma.	Cancer Letters	2014
24365052	Imaging findings of patients with metastatic neuroblastoma to the brain.	Acad Radiol	2014
23835274	Brain tumor presenting as somnambulism in an adolescent.	Pediatr Neurol	2013
22135027	Role of routine neuropathological examination for determining cause of death in sudden unexpected deaths in infancy (SUDI).	J Clin Pathol	2012
21955927	Distinctive multicystic hemispheric lesions suggesting a novel variant of infantile astrocytoma.	Clin Neuropathol	2011
20052518	Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation.	Journal of Neuro-Oncology	2010
20811463	Cortical malformations: unfolding polymicrogyria.	Nature Reviews Neurology	2010
20352236	Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell.	Acta Neuropathol	2010
19659957	Is CSF cytology a useful diagnostic procedure in staging paediatric CNS tumours?	Cytopathology	2009
19523942	Astrocytoma derived short-term cell cultures retain molecular signatures characteristic of the tumour in situ.	Experimental Cell Research	2009
18663750	Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13.	Genes Chromosomes and Cancer	2008
17847070	Quantification of normal range of inflammatory changes in morphologically normal pediatric muscle.	Muscle Nerve	2008
18670637	Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytoma.	Neoplasia	2008
18093223	Peritoneal dissemination of a malignant glioma.	Cytopathology	2008
18000912	Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.	Am J Med Genet A	2007
17907237	International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trials.	Arthritis Rheum	2007
17984686	An investigation of the expression of G1-phase cell cycle proteins in focal cortical dysplasia type IIB.	J Neuropathol Exp Neurol	2007
17441989	Pathological tau tangles localize to focal cortical dysplasia in older patients.	Epilepsia	2007
16409553	Vascular colocalization of P-glycoprotein, multidrug-resistance associated protein 1, breast cancer resistance protein and major vault protein in human epileptogenic pathologies.	Neuropathol Appl Neurobiol	2006
16417544	Hippocampal sclerosis in children with lesional epilepsy is influenced by age at seizure onset.	Epilepsia	2006
16281906	Mcm2 labelling of balloon cells in focal cortical dysplasia.	Neuropathol Appl Neurobiol	2005
16151726	Cortical neuronal densities and lamination in focal cortical dysplasia.	Acta Neuropathol	2005
16047140	Spontaneous regression of residual low-grade cerebellar pilocytic astrocytomas in children.	Pediatric Radiology	2005
16174309	Psychopathology in children with epilepsy before and after temporal lobe resection.	Developmental Medicine and Child Neurology	2005
16393166	Taylor-type focal cortical dysplasia in infants: some MRI lesions almost disappear with maturation of myelination.	Epilepsia	2005
14570817	Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity.	Brain	2004
15249610	Germline and mosaic mutations of FLN1 in men with periventricular heterotopia.	Neurology	2004
15349877	Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats.	Ann Neurol	2004