Neuropathology and Applied Neurobiology

Papers
(The TQCC of Neuropathology and Applied Neurobiology 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 2022-05-01 to 2026-05-01.)
ArticleCitations
Oral Abstracts62
Issue Information39
Intelligence quotient–genotype association in dystrophinopathies: A systematic review and meta‐analysis33
Neuropathological Characterisation of McLeod Syndrome With a Proposed New Grading System29
Editorial29
Role of Astrocytic and Microglial Phenotype in the Biology of Hippocampal Sclerosis27
Novel naturally occurring autoantibodies attenuate α‐synuclein pathology in a mouse model of Parkinson's disease26
Cortical Layer‐Specific Remodelling of Parvalbumin and Perineuronal Net Networks in Alcohol Use Disorder25
The Diagnostic Value of Confocal Laser Endomicroscopy in Brain Tumours When Performed by Blinded, Untrained Neuropathologists23
An autopsy case of late‐onset spinocerebellar atrophy type 1422
Neuronal infection is a major pathogenetic mechanism and cause of fatalities in human acute Nipah virus encephalitis21
19
Response letter: Complexities in pericyte markers18
Analysing cerebrospinal fluid with explainable deep learning: From diagnostics to insights18
Neuronal and astrocytic tetraploidy is increased in drug‐resistant epilepsy18
18
Synaptic gene expression changes in frontotemporal dementia due to the MAPT 10 + 16 mutation17
Anaplastic ganglioglioma—A diagnosis comprising several distinct tumour types16
Myostatin in idiopathic inflammatory myopathies: Serum assessment and disease activity16
Myopathology and Immune Profile of Granulomatous Myositis in Sarcoid Myopathy16
Author Index16
ACTA1 ‐Related Adult‐Onset Scapuloperoneal Myopathy With Cores and Rods16
Rapid bacterial identification from formalin‐fixed paraffin‐embedded neuropathology specimens using 16S rDNA nanopore sequencing16
Erratum16
A novel SREBF1::NACC1 gene fusion in an unclassifiable intracranial tumour16
Cover Image, Volume 50, Issue 315
Genetic inhibition of PDK1 robustly reduces plaque deposition and ameliorates gliosis in the 5×FAD mouse model of Alzheimer's disease15
124th Meeting of the British Neuropathological Society The View, Royal College of Surgeons of England, Lincoln's Inn Fields, London15
15
Perineuronal nets are phagocytosed by MMP‐9 expressing microglia and astrocytes in the SOD1 G93A ALS mouse model15
Application of Oral Mucosal Epithelial Cells in Noninvasive Pathological Diagnosis of Neuronal Intranuclear Inclusion Disease14
Issue Information14
14
A standardised protocol for blood and cerebrospinal fluid collection and processing for biomarker research in ataxia14
Evidence of neural crest cell origin of a DICER1 mutant CNS sarcoma in a child with DICER1 syndrome and NRAS‐mutant neurocutaneous melanosis13
Epigenetic age acceleration is associated with oligodendrocyte proportions in MSA and control brain tissue13
Phenotypic and epigenetic heterogeneity in FGFR2 ‐fused glial and glioneuronal tumours12
Adult‐onset Alexander disease with unusual inflammatory features and a novel GFAP mutation in two patients12
G Protein‐Coupled Receptor 32 Contributes to Inflammation Resolution and Neuronal Excitability Dysfunction in Patients With Focal Cortical Dysplasia IIb and Tuberous Sclerosis Complex12
m6A mRNA methylation in human brain is disrupted in Lewy body disorders11
RNA sequencing of peripheral blood in amyotrophic lateral sclerosis reveals distinct molecular subtypes: Considerations for biomarker discovery11
10
126th Meeting of the British Neuropathological Society The View, Royal College of Surgeons of England, Lincoln's Inn Fields, London10
WNT‐activated, MYC ‐amplified medulloblastoma displaying intratumoural heterogeneity10
Robust methylation‐based classification of brain tumours using nanopore sequencing10
Microglia induce an interferon‐stimulated gene expression profile in glioblastoma and increase glioblastoma resistance to temozolomide10
Is islet amyloid polypeptide indeed expressed in the human brain?10
TDP‐43 pathology and functional deficits in wild‐type and ALS/FTD mutant cyclin F mouse models10
Comprehensive analysis of intratumoural heterogeneity of somatic copy number alterations in diffuse glioma reveals clonality‐dependent prognostic patterns10
Hippocampal dentate granule cells in temporal lobe epilepsy: A morphometry and transcriptomic study10
The genomic landscape of dysembryoplastic neuroepithelial tumours and a comprehensive analysis of recurrent cases9
Intramuscular Nerve Bundles Reflect TDP‐43 Pathology in the Medulla and Spinal Cord of ALS Patients9
Evaluating Basigin as a Potential Biomarker of Blood–Brain Barrier Dysfunction in Cerebral Amyloid Angiopathy9
Interferon‐gamma contributes to disease progression in the Ndufs4 (−/−) model of Leigh syndrome9
Axonal response of mitochondria to demyelination and complex IV activity within demyelinated axons in experimental models of multiple sclerosis9
Fibroblast growth factor 9 (FGF9)‐mediated neurodegeneration: Implications for progressive multiple sclerosis?9
Issue Information8
Corrigendum8
Issue Information8
8
Muscle biopsy practices in the evaluation of neuromuscular disease: A systematic literature review7
Amino‐terminally elongated Aβ peptides are generated by the secreted metalloprotease ADAMTS4 and deposit in a subset of Alzheimer's disease brains7
Adult brain tumour research in 2024: Status, challenges and recommendations7
Nanopore sequencing identifies Borrelia miyamotoi as an unexpected cause of meningitis after B cell depletion7
7
Quantitative cellular changes in multiple system atrophy brains7
Pathological Characterisation of Posterior Cortical Atrophy in Comparison With Amnestic Alzheimer's Disease7
Atypical teratoid/rhabdoid tumour‐TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition7
GFAP expression in the brain during human postnatal development7
Letter to the editor6
Ageing‐related tau astrogliopathy severely affecting the substantia nigra6
Proteomic profiling of polyglucosan bodies associated with glycogenin‐1 deficiency in skeletal muscle6
A novel homozygous nonsense variant in COL12A1 causes myopathic Ehlers‐Danlos syndrome: A case report and literature review6
Unfolded protein response markers Grp78 and eIF2alpha are upregulated with increasing alpha‐synuclein levels in Lewy body disease6
Enhancing the Performance of a Blood‐Based Diagnostic Screening Tool for Dysferlinopathy: Optimising an Immunoassay Across Continents6
Cytoplasmic HDAC4 recovers synaptic function in the 3×Tg mouse model of Alzheimer's disease6
Regional redistribution of CB1 cannabinoid receptors in human foetal brains with Down's syndrome and their functional modifications in Ts65Dn +/+ mic6
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment6
Lipofuscin Accumulation in Dysmorphic Neurons in FCDIIa Focal Epilepsy: A Case Report and Literature Review6
Regulation of CNS pathology by Serpina3n/SERPINA3: The knowns and the puzzles6
0.62604188919067