Molecular Neurodegeneration

Papers
(The H4-Index of Molecular Neurodegeneration is 52. 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 2021-08-01 to 2025-08-01.)
ArticleCitations
In Memoriam of John T. Trojanowski, MD, PhD 1946-2022372
Mutations in PSEN1 predispose inflammation in an astrocyte model of familial Alzheimer’s disease through disrupted regulated intramembrane proteolysis230
Regulation of the hippocampal translatome by Apoer2-ICD release221
Guidelines for bioinformatics of single-cell sequencing data analysis in Alzheimer’s disease: review, recommendation, implementation and application207
Emerging targets of α-synuclein spreading in α-synucleinopathies: a review of mechanistic pathways and interventions202
Tau interactome and RNA binding proteins in neurodegenerative diseases194
Mis-localization of endogenous TDP-43 leads to ALS-like early-stage metabolic dysfunction and progressive motor deficits181
TREM2 dependent and independent functions of microglia in Alzheimer’s disease169
Cautions on utilizing plasma GFAP level as a biomarker for reactive astrocytes in neurodegenerative diseases169
Inhibition of soluble epoxide hydrolase confers neuroprotection and restores microglial homeostasis in a tauopathy mouse model168
A genome-wide search for pleiotropy in more than 100,000 harmonized longitudinal cognitive domain scores154
Multimarker synaptic protein cerebrospinal fluid panels reflect TDP-43 pathology and cognitive performance in a pathological cohort of frontotemporal lobar degeneration151
Astrocytic autophagy plasticity modulates Aβ clearance and cognitive function in Alzheimer’s disease142
Border-associated macrophages promote cerebral amyloid angiopathy and cognitive impairment through vascular oxidative stress140
Circadian clocks, cognition, and Alzheimer’s disease: synaptic mechanisms, signaling effectors, and chronotherapeutics139
The Parkinson’s disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons134
Single-cell peripheral immunoprofiling of Lewy body and Parkinson’s disease in a multi-site cohort132
Sex dependent glial-specific changes in the chromatin accessibility landscape in late-onset Alzheimer’s disease brains123
Correction: Blood-brain barrier-associated pericytes internalize and clear aggregated amyloid-β42 by LRP1-dependent apolipoprotein E isoform-specific mechanism100
Immunotherapy against tau fragment diminishes AD pathology, improving synaptic function and cognition100
HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases98
Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement91
Unravelling cell type-specific responses to Parkinson’s Disease at single cell resolution90
The role of peripheral inflammatory insults in Alzheimer’s disease: a review and research roadmap89
Human VCP mutant ALS/FTD microglia display immune and lysosomal phenotypes independently of GPNMB87
The role of NURR1 in metabolic abnormalities of Parkinson’s disease85
Correction: Sodium oligomannate alters gut microbiota, reduces cerebral amyloidosis and reactive microglia in a sex-specific manner83
Alzheimer risk gene product Pyk2 suppresses tau phosphorylation and phenotypic effects of tauopathy79
BAX activation in mouse retinal ganglion cells occurs in two temporally and mechanistically distinct steps76
Combination therapy using GDNF and cell transplant in Parkinson’s disease73
In Memoriam of Edward H. Koo, MD 1954–202572
Repetitive transcranial magnetic stimulation alleviates motor impairment in Parkinson’s disease: association with peripheral inflammatory regulatory T-cells and SYT672
Clinical progression and genetic pathways in body-first and brain-first Parkinson’s disease72
Finding memo: versatile interactions of the VPS10p-Domain receptors in Alzheimer’s disease71
Selective reduction of astrocyte apoE3 and apoE4 strongly reduces Aβ accumulation and plaque-related pathology in a mouse model of amyloidosis71
α-Synuclein pathology disrupts mitochondrial function in dopaminergic and cholinergic neurons at-risk in Parkinson’s disease71
APOE targeting strategy in Alzheimer’s disease: lessons learned from protective variants70
Correction: The major TMEM106B dementia risk allele affects TMEM106B protein levels, fibril formation, and myelin lipid homeostasis in the ageing human hippocampus68
TMEM106B aggregation in neurodegenerative diseases: linking genetics to function67
Deficits in mitochondrial TCA cycle and OXPHOS precede rod photoreceptor degeneration during chronic HIF activation65
A perspective on Alzheimer’s disease: exploring the potential of terminal/paradoxical lucidity and psychedelics64
ASO-mediated knock-down of GPNMB in mutant-GRN and in Grn-deficient peripheral myeloid cells disrupts lysosomal function and immune responses62
Correction: HDGFL2 cryptic proteins report presence of TDP-43 pathology in neurodegenerative diseases60
Using mass spectrometry to validate mouse models of tauopathy58
Evidence suggesting that microglia make amyloid from neuronally expressed APP: a hypothesis55
Common features of neurodegenerative disease: exploring the brain-eye connection and beyond (part 2): the 2021 pre-symposium of the 15th international conference on Alzheimer’s and Parkinson’s disease55
Dementia with lewy bodies patients with high tau levels display unique proteome profiles55
The PKCι-β-arrestin2 axis disrupts SORLA retrograde trafficking, driving its degradation and amyloid pathology in Alzheimer’s disease54
Contribution of amyloid deposition from oligodendrocytes in a mouse model of Alzheimer’s disease53
RETRACTED ARTICLE: Aging exacerbates the brain inflammatory micro-environment contributing to α-synuclein pathology and functional deficits in a mouse model of DLB/PD53
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypes53
The transcription factor combination MEF2 and KLF7 promotes axonal sprouting in the injured spinal cord with functional improvement and regeneration-associated gene expression52
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