Neurology explores the intricate workings of the brain and nervous system, tackling everything from memory and movement to complex conditions like epilepsy and Alzheimer's. This field seeks to understand how our minds function and what happens when that delicate machinery falters, aiming to improve lives through better diagnosis and treatment.

At Gist.Science, we make the latest research from medRxiv accessible to everyone. We process every new preprint in this category, offering both straightforward plain-language explanations and detailed technical summaries so you can grasp the science at your own pace. Below are the latest papers in neurology, ready for you to explore.

🧠 neurology

Development of a Core Outcome Set for Mild Cognitive Impairment (MCI-COS): Recommendations from a multistakeholder Delphi consensus study

This paper presents the development of a ten-item Core Outcome Set for Mild Cognitive Impairment (MCI-COS) through a multistakeholder Delphi consensus process, aiming to standardize and prioritize patient-relevant outcomes in future research and clinical practice.

Gabb, V. G., Harding, S., McNair, A., Clayton, J., Barrett-Muir, W., Richardson, A., Dooley, J., Webb, J., Lemke, T., Co (…)2026-07-14
🧠 neurology

Gut-related Immune Activation in Parkinson's Disease with Asian LRRK2 Risk Variants: Associations with Systemic Inflammation and Clinical Severity

This study reveals that while gut permeability markers LBP and sCD14 do not differ based on Asian LRRK2 risk variants in Parkinson's disease, they are significantly associated with systemic inflammation and clinical severity, identifying LBP as a key marker of inflammatory burden in PD patients.

Toh, T. S., Ding, H. X., Khairul Anuar, A. N., Zulhaimi, N. S., Hor, J. W., Pang, Y. C., Kong, I. X., Zulkefli, J., Tay (…)2026-07-14
🧠 neurology

geneXplore: An Interactive Browser for X Chromosome-Wide Association Study Results

The paper introduces geneXplore, a freely accessible interactive web browser that addresses the lack of dedicated tools for X chromosome-wide association studies by providing systematic exploration of summary statistics across 1,944 phenotypes with specific support for distinguishing random X-inactivation, escape from X-inactivation, and sex-stratified analyses.

Cook, N., Boulais-Richard, J., Zeng, Y., Yang, C., Budde, J., Taliun, D., Gagliano Taliun, S. A., Cruchaga, C., Belloy (…)2026-07-14
🧠 neurology

Transdiagnostic quantitative assessment of dementias using in vivo MRI and data-driven disease progression modelling: a case study in Alzheimer's disease and dementia with Lewy bodies

This study demonstrates that a data-driven transdiagnostic approach using single-visit MRI can identify three distinct brain atrophy subtypes across Alzheimer's disease and dementia with Lewy bodies, offering a promising tool for in vivo biological staging and subtyping despite imperfect alignment with clinical diagnoses.

Castro Leal, G., Konuri, A., Young, A. L., Zebarjadi, N., Samantaray, T., Habich, A., Castellanos-Perilla, N., Camila Go (…)2026-07-11
🧠 neurology

Identifying Blood Proteomic Markers of Parkinson's Disease Dementia Using High-Throughput Approaches

Using high-throughput SomaScan assays on large cohorts, this study identified specific blood proteins associated with synaptic plasticity and lysosomal function that predict the progression to dementia in Parkinson's disease years before clinical symptoms appear, with Mendelian Randomisation suggesting a causal link between the Nogo receptor RTN4R and Lewy body dementia.

Real, R., Ravazio, R., Nodehi, A., Ben-Shlomo, Y., Williams, N., Barros, R. C., Grosset, D., Hu, M., Winchester, L., Mor (…)2026-07-10
🧠 neurology

Accelerometry-Derived REM Sleep Behavior Disorder Predicts Future Parkinson's Disease in the UK Biobank

This study demonstrates that applying a machine learning classifier to wrist accelerometry data in the UK Biobank effectively identifies individuals with REM sleep behavior disorder who have a significantly elevated, dose-dependent risk of developing Parkinson's disease, offering a scalable and superior alternative to questionnaire-based screening for prodromal risk enrichment.

Mejia, G. R., Brink-Kjaer, A., Liu, L., Zhou, L., Gunter, K., Ryu, K. H., Wickramaratne, S. D., Parekh, A., Gan-Or, Z. (…)2026-07-06
🧠 neurology

Hemispheric Asymmetry Features and Interpretable Machine Learning for Focal Cortical Dysplasia Classification in Drug-Resistant Epilepsy

This study demonstrates that an interpretable, L1-regularized logistic regression model utilizing hemispheric asymmetry features from structural MRI can achieve statistically significant accuracy in detecting focal cortical dysplasia, offering a transparent and anatomically grounded alternative to complex deep learning approaches for presurgical epilepsy evaluation.

Iraqui, A., Dang, H.2026-07-06
🧠 neurology

Developing a Specialized Dravet Syndrome Ontology for Rare Disease Informatics and AI Applications

This paper presents the development and validation of a specialized Dravet Syndrome ontology, created through expert-guided expansion of an existing epilepsy framework, which serves as a durable infrastructure for data harmonization, knowledge representation, and AI-driven translational informatics in rare disease research.

Golnari, P., Prantzalos, K., Upadhyaya, D. P., Buchhalter, J., Sahoo, S. S.2026-07-04