Acta Neuropathologica

Papers
(The H4-Index of Acta Neuropathologica is 40. 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 2021-06-01 to 2025-06-01.)
ArticleCitations
Dysregulated coordination of MAPT exon 2 and exon 10 splicing underlies different tau pathologies in PSP and AD149
A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques138
Regulated cell death and its role in Alzheimer’s disease and amyotrophic lateral sclerosis133
Macrophages and endothelial cells in the neurovascular unit127
Co-registration of MALDI-MSI and histology demonstrates gangliosides co-localize with amyloid beta plaques in Alzheimer’s disease122
The proteomic landscape of glioblastoma recurrence reveals novel and targetable immunoregulatory drivers103
Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy102
Comprehensive assessment of TDP-43 neuropathology data in the National Alzheimer’s Coordinating Center database92
Capillary basement membrane reduplication in myositis patients with mild clinical features of systemic sclerosis supports the concept of ‘scleromyositis’92
Wolframin is a novel regulator of tau pathology and neurodegeneration87
Integrative multi-omics reveals two biologically distinct groups of pilocytic astrocytoma86
Metabologenomic characterization uncovers a clinically aggressive IDH mutant glioma subtype75
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility74
RNA methyltransferase NSun2 deficiency promotes neurodegeneration through epitranscriptomic regulation of tau phosphorylation74
Identification of high-performing antibodies for the reliable detection of Tau proteoforms by Western blotting and immunohistochemistry72
A familial missense variant in the Alzheimer’s disease gene SORL1 impairs its maturation and endosomal sorting69
Cryptic exon detection and transcriptomic changes revealed in single-nuclei RNA sequencing of C9ORF72 patients spanning the ALS-FTD spectrum63
BTK inhibition limits microglia-perpetuated CNS inflammation and promotes myelin repair62
RNA aptamer reveals nuclear TDP-43 pathology is an early aggregation event that coincides with STMN-2 cryptic splicing and precedes clinical manifestation in ALS62
Progranulin deficiency results in sex-dependent alterations in microglia in response to demyelination60
Cell-specific MAPT gene expression is preserved in neuronal and glial tau cytopathologies in progressive supranuclear palsy58
TDP-43 pathology in the retina of patients with frontotemporal lobar degeneration58
The Alzheimer’s disease GWAS risk alleles in the ABCA7 promoter and 5’ region reduce ABCA7 expression55
TBK1 haploinsufficiency in ALS and FTD compromises membrane trafficking54
TREM2 gene expression associations with Alzheimer’s disease neuropathology are region-specific: implications for cortical versus subcortical microglia54
Cross-platform transcriptional profiling identifies common and distinct molecular pathologies in Lewy body diseases54
Detection of blood–brain barrier disruption in brains of patients with COVID-19, but no evidence of brain penetration by SARS-CoV-252
Even heterozygous loss of CDKN2A/B greatly accelerates recurrence in aggressive meningioma52
Multi-level profiling unravels mitochondrial dysfunction in myotonic dystrophy type 251
Genetical and epigenetical profiling identifies two subgroups of pineal parenchymal tumors of intermediate differentiation (PPTID) with distinct molecular, histological and clinical characteristics51
Biomarkers for parkinsonian disorders in CNS-originating EVs: promise and challenges51
From metabolomics to proteomics: understanding the role of dopa decarboxylase in Parkinson’s disease. Scientific commentary on: “Comprehensive proteomics of CSF, plasma, and urine identify DDC and oth49
Tau seeding in chronic traumatic encephalopathy parallels disease severity48
Jorge Cervós-Navarro 1930–202147
Expanding the spectrum of amyloid-β plaque pathology: the Down syndrome associated ‘bird-nest plaque’45
Spinal astrocyte dysfunction drives motor neuron loss in late-onset spinal muscular atrophy45
Neuropathological associations of limbic-predominant age-related TDP-43 encephalopathy neuropathological change (LATE-NC) differ between the oldest-old and younger-old44
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy43
Clinicopathological and molecular characterization of three cases classified by DNA-methylation profiling as “Glioneuronal Tumors, NOS, Subtype A”42
Myeloid cell iron uptake pathways and paramagnetic rim formation in multiple sclerosis41
Clinical applicability of miR517a detection in liquid biopsies of ETMR patients40
PolyGA targets the ER stress-adaptive response by impairing GRP75 function at the MAM in C9ORF72-ALS/FTD40
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