Acta Neuropathologica

Papers
(The H4-Index of Acta Neuropathologica is 41. 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 2021-11-01 to 2025-11-01.)
ArticleCitations
Regulated cell death and its role in Alzheimer’s disease and amyotrophic lateral sclerosis173
Co-registration of MALDI-MSI and histology demonstrates gangliosides co-localize with amyloid beta plaques in Alzheimer’s disease168
Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy160
A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques159
The proteomic landscape of glioblastoma recurrence reveals novel and targetable immunoregulatory drivers149
Macrophages and endothelial cells in the neurovascular unit120
Dysregulated coordination of MAPT exon 2 and exon 10 splicing underlies different tau pathologies in PSP and AD109
Comprehensive assessment of TDP-43 neuropathology data in the National Alzheimer’s Coordinating Center database106
Wolframin is a novel regulator of tau pathology and neurodegeneration103
Integrative multi-omics reveals two biologically distinct groups of pilocytic astrocytoma102
BTK inhibition limits microglia-perpetuated CNS inflammation and promotes myelin repair93
Identification of high-performing antibodies for the reliable detection of Tau proteoforms by Western blotting and immunohistochemistry71
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility71
A familial missense variant in the Alzheimer’s disease gene SORL1 impairs its maturation and endosomal sorting70
RNA methyltransferase NSun2 deficiency promotes neurodegeneration through epitranscriptomic regulation of tau phosphorylation69
Metabologenomic characterization uncovers a clinically aggressive IDH mutant glioma subtype69
RNA aptamer reveals nuclear TDP-43 pathology is an early aggregation event that coincides with STMN-2 cryptic splicing and precedes clinical manifestation in ALS68
Cryptic exon detection and transcriptomic changes revealed in single-nuclei RNA sequencing of C9ORF72 patients spanning the ALS-FTD spectrum67
Genetical and epigenetical profiling identifies two subgroups of pineal parenchymal tumors of intermediate differentiation (PPTID) with distinct molecular, histological and clinical characteristics63
Multi-level profiling unravels mitochondrial dysfunction in myotonic dystrophy type 255
Even heterozygous loss of CDKN2A/B greatly accelerates recurrence in aggressive meningioma55
The Alzheimer’s disease GWAS risk alleles in the ABCA7 promoter and 5’ region reduce ABCA7 expression54
Detection of blood–brain barrier disruption in brains of patients with COVID-19, but no evidence of brain penetration by SARS-CoV-254
Progranulin deficiency results in sex-dependent alterations in microglia in response to demyelination53
Biomarkers for parkinsonian disorders in CNS-originating EVs: promise and challenges51
TDP-43 pathology in the retina of patients with frontotemporal lobar degeneration49
Jorge Cervós-Navarro 1930–202148
TREM2 gene expression associations with Alzheimer’s disease neuropathology are region-specific: implications for cortical versus subcortical microglia48
Cell-specific MAPT gene expression is preserved in neuronal and glial tau cytopathologies in progressive supranuclear palsy48
Clinical applicability of miR517a detection in liquid biopsies of ETMR patients47
Expanding the spectrum of amyloid-β plaque pathology: the Down syndrome associated ‘bird-nest plaque’47
PolyGA targets the ER stress-adaptive response by impairing GRP75 function at the MAM in C9ORF72-ALS/FTD46
Neuropathological associations of limbic-predominant age-related TDP-43 encephalopathy neuropathological change (LATE-NC) differ between the oldest-old and younger-old45
Landscape of brain myeloid cell transcriptome along the spatiotemporal progression of Alzheimer’s disease reveals distinct sequential responses to Aβ and tau45
Myeloid cell iron uptake pathways and paramagnetic rim formation in multiple sclerosis45
Spinal astrocyte dysfunction drives motor neuron loss in late-onset spinal muscular atrophy44
Clinicopathological and molecular characterization of three cases classified by DNA-methylation profiling as “Glioneuronal Tumors, NOS, Subtype A”44
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 oth44
Phosphatidylinositol-3,4,5-trisphosphate interacts with alpha-synuclein and initiates its aggregation and formation of Parkinson’s disease-related fibril polymorphism43
Correction to: MET receptor serves as a promising target in melanoma brain metastases42
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy42
A CHCHD6–APP axis connects amyloid and mitochondrial pathology in Alzheimer’s disease41
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations41
Neuropathologic scales of cerebrovascular disease associated with diffusion changes on MRI41
Xenografted human iPSC-derived neurons with the familial Alzheimer’s disease APPV717I mutation reveal dysregulated transcriptome signatures linked to synaptic function and implicate LINGO2 as a diseas41
Rapid-CNS2: rapid comprehensive adaptive nanopore-sequencing of CNS tumors, a proof-of-concept study41
CSF p-tau205: a biomarker of tau pathology in Alzheimer’s disease41
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