D grade · PMID 42016909
View analysis →Finding therapies hidden in 1,516 Parkinson’s papers.
Neurocompute scores biomedical literature, surfaces overlooked patterns, and turns Parkinson’s research into a living discovery terminal.
Ranked discovery teasers
D grade · PMID 42038539
View analysis →D grade · PMID 41976987
View analysis →D grade · PMID 41944949
View analysis →D grade · PMID 41996661
View analysis →D grade · PMID 41907062
View analysis →D grade · PMID 41961337
View analysis →D grade · PMID 42043421
View analysis →D grade · PMID 41957057
View analysis →D grade · PMID 41912064
View analysis →Database feed
All ranked Parkinson’s papers
The paper reports that DING, a phosphatase found in human brain and derived from St. John's wort, reduces Tau phosphorylation and increases neuronal survival in PC12 cells and correlates with lower phospho‑Tau in a small postmortem human cohort.
DING's neuroprotective, Tau‑dephosphorylating activity points to a potentially broad neuroprotective mechanism that could be explored for Parkinson's-related neurodegeneration, but the evidence is limited (small human sample, in vitro models) and it lacks direct data on alpha‑synuclein,…
The paper presents a high-accuracy (97.4%) deep-learning pipeline—using InceptionGAN augmentation, ConvNeXt and MaxViT feature extractors with Cross-Fusion Attention and hyperparameter optimization (Bayesian + genetic algorithms)—for classifying Alzheimer's and Parkinson's disease from brain MRI…
This work could improve MRI-based diagnosis and patient stratification for clinical studies, but it provides little actionable biological insight or direct therapeutic targets for Parkinson's disease drug discovery.
Small cross-sectional study of 20 Ghanaian PD patients found high rates of malnutrition (≈75%), sarcopenia (45%) and constipation (80%), low caloric/protein intake linked to lower BMI/body fat, thigh circumference inversely correlated with disease duration, and protein intake inversely correlated…
Identifies modifiable nutritional deficits and sarcopenia as actionable targets for symptomatic management and multidisciplinary interventions in PD—especially in resource-limited settings—though the small sample and lack of mechanistic data limit direct therapeutic-discovery impact.
In rotenone and 6-OHDA rat models of Parkinson's, systemic uridine (30 mg/kg for 28 days) reduced peripheral lymphocyte SDH and LDH hyperactivity and serum lipid peroxides, and this effect was abolished by the mitoKATP inhibitor 5-hydroxydecanoate, implicating mitoKATP-mediated mitochondrial…
Suggests a repurposable metabolite (uridine) that targets mitoKATP to modulate mitochondrial function and systemic oxidative biomarkers in PD models, providing a mechanistic, mitochondria-focused lead and peripheral biomarker strategy for translational follow-up despite lack of direct CNS…
Multimodal imaging of >300 PD-spectrum participants reveals stage-dependent corticostriatal reorganization: early hyperconnectivity between the posterior caudate and primary motor cortex peaking around ~50% putaminal dopamine loss, and progressive loss of posterior putamen–posterior cortical…
Provides stage-specific functional circuit biomarkers that can inform disease staging and the timing/targets for circuit-level interventions (e.g., neuromodulation) despite limited direct molecular or druggable targets.
Multicenter study of 108 idiopathic RBD patients found 40% discordance between striatal dopaminergic imaging and quantitative motor testing, with a motor-slowing/DAT-normal subgroup showing worse cognition and autonomic dysfunction, suggesting a more diffuse progression pattern.
Demonstrates that DaT-SPECT alone may miss clinically relevant prodromal phenotypes, supporting multimodal biomarker and phenotypic stratification to improve patient selection and outcome measures for Parkinson's therapeutic trials.
Case report plus systematic review (19 patients) describing SEZ6L2 autoimmunity as a rare cause of subacute cerebellar ataxia frequently accompanied by cognitive dysfunction and parkinsonism, with ~47% showing partial improvement after immunotherapy.
Identifies an antibody-associated, immunotherapy-responsive syndrome that can present with parkinsonism and cognitive decline, offering a diagnostic biomarker (SEZ6L2 antibodies) and a potential immunomodulatory treatment angle for a subset of PD-like presentations.
A broad, up-to-date review positioning glycolysis and cell type–specific metabolic reprogramming as a central pathological axis across neurodegenerative diseases and summarizing actionable targets (e.g., PFKFB3, ANLS, microglial glycolysis), multimodal measurement methods, and therapeutic…
For Parkinson’s research it highlights modifiable metabolic pathways and translational tools that could yield repurposable targets and biomarkers, albeit with limited PD-specific causal data and important cell type/stage complexities to address.
Postmortem analysis reveals alpha-synuclein inclusions in cerebellar oligodendrocytes, concurrent myelin rarefaction, and hypertrophy of dentate nucleus neurons in idiopathic Parkinson’s disease.
By implicating oligodendroglial alpha-synucleinopathy and impaired glial–neuronal metabolic coupling in cerebello–basal ganglia circuits, the study uncovers a novel, actionable mechanism with potential biomarker and therapeutic targets (oligodendrocytes/myelin and alpha-syn clearance) for PD.
Using human iPSC-derived microglia, the study shows IFNγ reprograms microglial metabolism and lipidome toward a resolving-like phenotype that partially counteracts α-synuclein PFF-driven harmful secretome effects on human dopaminergic neurons.
Identifies actionable immunometabolic and secretome-linked mechanisms (IFNγ signaling, TGM2, TGFβ1, glycolytic/tryptophan/phospholipid pathways) that can be targeted or used as biomarkers to modulate microglia-neuron interactions in α-synuclein-driven Parkinson's pathology.
Perspective proposing that hepatic stress—through bile acid–driven dysbiosis and mitochondrial antigen presentation—may expose mitochondrial antigens and elicit autoimmune responses that contribute to Parkinson's disease initiation and progression.
Highlights a testable liver–mitochondria–immune axis that connects metabolism, microbiome, and immune activation and suggests new biomarker and therapeutic avenues (e.g., bile-acid modulation, microbiome or liver-targeted immune interventions), though the idea remains speculative and requires…
A narrative review linking endocannabinoid system modulation to regulation of nitrosative stress and neuroinflammation, arguing that cannabinoid-based interventions may slow progression in neurodegenerative diseases including Parkinson's disease.
Useful for Parkinson's drug discovery as it highlights nitrosative stress and ECS-targeting (possible repurposing of cannabinoids) as multi-mechanism therapeutic avenues, but its review-level scope and limited PD-specific mechanistic or preclinical/clinical actionable data reduce immediate…
This study finds significant enrichment of likely pathogenic VPS13C variants in idiopathic REM sleep behavior disorder (iRBD), especially the iRBD-first α-synucleinopathy subtype, and links carriers to worse RBD symptoms, autonomic and REM EEG abnormalities, and faster conversion to overt…
By nominating VPS13C variants as a prodromal genetic marker that predicts phenotype severity and accelerated conversion, the work enables patient stratification for early intervention trials and supports functional follow-up of VPS13C-linked pathways (e.g., lysosomal/mitochondrial biology) for…
Real-world, open-label multicentre study of 50 advanced PD patients found subcutaneous foslevodopa/foscarbidopa infusion significantly improved motor function (UPDRS III), sleep and PDQ-8 quality-of-life scores with low dropout over 6–12 months across White and non-White cohorts.
Provides clinically actionable evidence for a non-oral continuous levodopa delivery that addresses gastroparesis-related fluctuations and is tolerable across racial groups, supporting broader translational adoption for symptomatic management in advanced PD.
A prospective cohort of Gaucher disease patients (22 baseline, 18 followed ~37 months) shows progressive subtle parkinsonism, increased non-motor symptoms including sleep disturbances, declining memory performance, high prevalence/progression of sensorineural hearing loss, and frequent multifocal…
Because GBA1-linked lysosomal dysfunction is a major Parkinson's risk pathway, these longitudinal clinical and sensory measures offer natural-history data and candidate biomarkers that can inform patient stratification, monitoring, and design of GBA-targeted or lysosome-focused therapeutic trials.
Post-hoc analysis of a 52-week phase 3 trial showed subcutaneous foslevodopa/foscarbidopa infusion reduced OFF time and increased ON time without dyskinesia similarly in patients with and without prior DBS, with overall comparable safety but a higher rate of severe treatment-emergent adverse events…
Provides strong translational value by supporting a non-surgical, continuous levodopa/carbidopa option for advanced PD regardless of DBS history, helping guide clinical decision-making and safety monitoring for post-DBS patients.
RNA-seq of striata from rotenone-treated rats revealed several hundred DEGs including altered Ddc and Angpt2 and dysregulation of circadian genes (Per3 down, Arntl up), pointing to disrupted dopamine synthesis and clock pathways.
Links rotenone-induced nigrostriatal injury to circadian-clock and angiopoietic/dopaminergic gene changes, offering candidate biomarkers/targets (Angpt2, Ddc, clock genes) for translational follow-up despite limited functional validation in this study.
This study validates the 35-item PRO-PD patient-reported outcome measure (four-factor structure) as reliable, remotely deployable, and sensitive to patient-perceived longitudinal change in Parkinson's symptoms across motor and non-motor domains.
A robust, remote-capable, patient-centered outcome measure like PRO-PD facilitates scalable clinical and lifestyle intervention studies, improving ability to detect meaningful symptom change and accelerating translational research and trial readiness in Parkinson's disease.
This small cross-sectional 16S study reports distinct gut and oral microbiota between symmetric and asymmetric PD—higher gut α-diversity and Desulfobacterota enrichment in symmetric PD versus more butyrate-producing bacteria in asymmetric PD, with associated predicted functional pathway differences.
The findings support gut–brain axis heterogeneity in PD and suggest microbiome-based biomarkers or stratification for targeted interventions, but the results are correlative, from a modest cohort and 16S-based predictions, so require larger mechanistic validation before therapeutic translation.
A narrative review summarizing epidemiology, classification, proposed pathophysiology, and clinical management of headaches in Parkinson's disease, noting prevalence (up to ~49%), types (tension-type, migraine), links to motor fluctuations and dopaminergic therapy, and evidence from cohorts and…
Although it does not advance core molecular targets for disease-modification, the paper highlights an underrecognized non-motor phenotype and mechanistic themes (nociceptive and neuroplastic pain, therapy-related effects) that can inform symptomatic management, patient stratification, and ancillary…