Brain Pathology

Papers
(The TQCC of Brain Pathology is 6. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
Variable histopathology features of neuronal dyslamination in the cerebral neocortex adjacent to epilepsy‐associated vascular malformations suggest complex pathogenesis of focal cortical dysplasia ILA137
A 29‐year‐old man with a right intracranial mass95
A 71‐year‐old female with an intrasellar mass90
Society News79
Issue Information77
Issue Information67
62
Acknowledgement to Reviewer60
Peripheral blood‐derived immune cell counts as prognostic indicators and their relationship with DNA methylation subclasses in glioblastoma patients57
A 53‐year‐old female with suprasellar mass44
Left dural‐based mass in a 62‐year‐old female43
Issue Information42
Exploiting nanopore sequencing for characterization and grading of IDH‐mutant gliomas41
A 53‐year‐old man with a 16‐year history of asymmetrical proximal muscle weakness, facial muscle weakness, and scapular winging40
A diffuse glioma with oligodendroglial‐like cells and extensive calcifications38
A tribute to John Q. Trojanowski (1946–2022), neuropathologist extraordinaire33
Society News29
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Recent data and developments in myositis28
An 82‐year‐old man with a right frontal lobe rim‐enhancing lesion26
The post‐stroke young adult brain has limited capacity to re‐express the gene expression patterns seen during early postnatal brain development25
Astrocyte‐derived Interleukin‐31 causes poor prognosis in elderly patients with intracerebral hemorrhage25
Multiple intra‐axial lesions in a 57‐year‐old male with a history of B‐cell chronic lymphocytic leukemia25
SPI1 activates TGF‐β1/PI3K/Akt signaling through transcriptional upregulation of FKBP12 to support the mesenchymal phenotype of glioma stem cells24
MET fusions and splicing variants is a strong adverse prognostic factor in astrocytoma, isocitrate dehydrogenase mutant24
Inactivation of the CB2 receptor accelerated the neuropathological deterioration in TDP‐43 transgenic mice, a model of amyotrophic lateral sclerosis23
Fetal growth restriction adversely impacts trajectory of hippocampal neurodevelopment and function23
Neuropathological stage‐dependent proteome mapping of the olfactory tract in Alzheimer's disease: From early olfactory‐related omics signatures to computational repurposing of drug candidat23
Design and application of a customizable relational DataBase to assess clinicopathological correlations and concomitant pathology in neurodegenerative diseases22
Protective role of Angiogenin in muscle regeneration in amyotrophic lateral sclerosis: Diagnostic and therapeutic implications21
Reply to letter by Melmed et al.20
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Upper motor neuron‐predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological study20
Assessment of Ki‐67 and mitoses in pituitary neuroendocrine tumours—Consistency counts20
Histamine in murine narcolepsy: What do genetic and immune models tell us?18
A 7‐year‐old female with hypotonia and scoliosis18
Issue Information18
Deep learning‐based segmentation in MRI‐(immuno)histological examination of myelin and axonal damage in normal‐appearing white matter and white matter hyperintensities18
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Nicorandil treatment improves survival and spatial learning in aged granulin knockout mice17
Pathologic TDP‐43 downregulates myelin gene expression in the monkey brain17
Issue Information17
Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination, and nodal/paranodal pathology are characteristic of multiple system atrophy17
Hypothesis review: Alzheimer's overture guidelines16
Neuropathological and cerebrospinal fluid correlates of choroid plexus inflammation in progressive multiple sclerosis15
IDH‐mutant brainstem gliomas in adolescent and young adult patients: Report of three cases and review of the literature15
Studying the imaging features and infarction mechanism of vertebrobasilar dolichoectasia with high‐resolution magnetic resonance imaging15
Accumulation of misfolded SOD1 outlines distinct patterns of motor neuron pathology and death during disease progression in a SOD1G93A mouse model of amyotrophic later15
A 4‐year‐old boy with a ventricular mass15
Association of CD2AP neuronal deposits with Braak neurofibrillary stage in Alzheimer’s disease14
Inorganic phosphate exporter heterozygosity in mice leads to brain vascular calcification, microangiopathy, and microgliosis14
Poly‐GA immunohistochemistry is a reliable tool for detecting C9orf72 hexanucleotide repeat expansions14
A new amplicon‐based gene panel for next generation sequencing characterization of meningiomas14
Alpha‐synuclein‐associated changes in PINK1‐PRKN‐mediated mitophagy are disease context dependent14
Multiple intracranial hemorrhages in a postmenopausal female13
Oligodendrocyte progenitor cells' fate after neonatal asphyxia—Puzzling implications for the development of hypoxic–ischemic encephalopathy13
Histopathological patterns in atypical teratoid/rhabdoid tumors are related to molecular subgroup13
Distribution of ubiquilin 2 and TDP‐43 aggregates throughout the CNS in UBQLN2 p.T487I‐linked amyotrophic lateral sclerosis and frontotemporal dement12
Herpes simplex virus‐1 infection alters microtubule‐associated protein Tau splicing and promotes Tau pathology in neural models of Alzheimer's disease12
Postmortem quantitative MRI disentangles histological lesion types in multiple sclerosis12
Pathological tau signatures and nuclear alterations in neurons, astrocytes and microglia in Alzheimer's disease, progressive supranuclear palsy, and dementia with Lewy bodies12
Tumor‐associated astrocytes promote tumor progression of Sonic Hedgehog medulloblastoma by secreting lipocalin‐212
TDP‐43 and tau concurrence in the entorhinal subfields in primary age‐related tauopathy and preclinical Alzheimer's disease11
Pathological changes within the cerebral vasculature in Alzheimer’s disease: New perspectives11
Multiple system atrophy with hippocampal pathology11
Human amygdala involvement in Alzheimer's disease revealed by stereological and dia‐PASEF analysis11
Posterior pituitary tumors and other rare entities involving the pituitary gland11
Huntingtin CAG repeats in neuropathologically confirmed tauopathies: Novel insights11
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Introduction to the mini‐symposium “molecular neuropathology of meningioma”10
Infective myositis10
A 57‐year‐old woman with falls, slurred speech, and abnormal MRI signal in the pons, middle cerebellar peduncles, and cerebellum10
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Correction to “A 4‐year‐old boy with a ventricular mass”9
Lack of classical astroblastoma features in pediatric MN1::BEND2‐fused brain tumors9
Axonal injury following mild traumatic brain injury is exacerbated by repetitive insult and is linked to the delayed attenuation of NeuN expression without concomitant neuronal death in the mouse9
Society News9
Perivascular phosphorylated TDP‐43 inclusions are associated with Alzheimer's disease pathology and loss of CD146 and Aquaporin‐49
Nanoarchitecture of CaV2.1 channels and GABAB receptors in the mouse hippocampus: Impact of APP/PS1 pathology9
Altered immune response is associated with sex difference in vulnerability to Alzheimer's disease in human prefrontal cortex8
Acknowledgement to Reviewers8
Single‐nucleus RNA sequencing unveils critical regulators in various hippocampal neurons for anti‐N‐methyl‐D‐aspartate receptor encephalitis8
A 64‐year‐old woman with frontal lobe lesion and drug‐resistant epilepsy8
Subcortical plaques and inflammation reflect cortical and meningeal pathologies in progressive multiple sclerosis8
Impact of α‐synuclein spreading on the nigrostriatal dopaminergic pathway depends on the onset of the pathology8
Evidence of beta amyloid independent small vessel disease in familial Alzheimer's disease8
Announcing the Asian Oceanian Society of Neuropathology guidelines for Adapting Diagnostic Approaches for Practical Taxonomy in Resource‐Restrained Regions (AOSNP‐ADAPTR)8
Motor neuron involvement expands the neuropathological phenotype of late‐onset ataxia in RFC1 mutation (CANVAS)8
An 11‐year‐old boy with a posterior fossa tumor8
Enhanced Creutzfeldt‐Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease7
Brain‐derived textiloma post glioblastoma resection and application of oxidized regenerated cellulose: A pilot, bedside‐to‐bench, translational study7
Society News7
Society News7
Corrigendum7
Felice Giangaspero—A man of style and substance7
Progress in stratified stroke characterization—associated with better diagnosis, accurate prognosis and improved treatment strategies7
Dendritic spine loss in epileptogenic Type II focal cortical dysplasia: Role of enhanced classical complement pathway activation7
Meeting report of the 20th International Congress of Neuropathology (ICN) 2023 in Berlin7
Society News7
A 24‐year‐old woman with a recurrent intracranial mass6
72‐year‐old man with right homonymous hemianopia and gait instability6
Information theory approaches to improve glioma diagnostic workflows in surgical neuropathology6
AtypicalTDP‐43 protein expression in anALSpedigree carrying a p.Y374Xtruncation mutation inTARDBP6
Society News6
Plasma mid‐regional pro‐adrenomedullin: A biomarker of the ischemic penumbra in hyperacute stroke6
Distribution of ferritin complex in the adult brain and altered composition in neuroferritinopathy due to a novel variant in the ferritin heavy chain gene FTH1 (c.409_410del; p.6
Diverse changes in microglia morphology and axonal pathology during the course of 1 year after mild traumatic brain injury in pigs6
A vade mecum for crossing the second translational “valley of death” in brain tumor classification6
A 76‐year‐old male with multiple enhancing brain lesions6
RNA‐sequencing highlights differential regulated pathways involved in cell cycle and inflammation in orbitofacial neurofibromas6
IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS‐associated amyotrophic lateral sclerosis6
Targeting the interaction of GABAB receptors with CaMKII with an interfering peptide restores receptor expression after cerebral ischemia and inhibits progressive neuronal death in mouse br6
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