Ashwini Kumar Pandey

The paper derives lifespan trajectories of resting state bipolar EEG power from a large sample, finding age-related decreases followed by divergent patterns and sex-specific inter-frequency correlations.

This study uses EEGViT, a transformer-based model, to classify Alcohol Use Disorder from raw resting-state EEG data, achieving 56% accuracy with sex- and age-stratified results.

The paper analyzes resting state EEG power trajectories across age and sex in a large sample, finding age-related decreases and sex-specific reversals in certain frequency bands.

This study investigates phase-amplitude coupling (PAC) differences in frontomedial brain regions between individuals with alcohol use disorder (AUD) and controls, identifying significant clusters associated with AUD.

This study estimates brain age in individuals with alcohol use disorder (AUD) and finds accelerated brain aging associated with impaired neurocognition and impulsivity.

The paper examines neural activity in the reward network during win and loss outcomes in a gambling task and links these activations to behavioral and cognitive traits.

The paper analyzes EEG coherence development in adolescents and young adults using tensorial analysis of covariance matrices, revealing non-linear patterns and sex differences in neural connectivity.

The paper predicts brain age in individuals with and at risk for alcohol use disorder using morphological brain features and finds accelerated brain aging in both groups.

The paper examines how genetic variants in the cholinergic system affect theta band event-related oscillations, finding age and sex-dependent variations in these associations.

This study uses machine learning to predict alcohol-related memory problems in older adults by integrating multi-domain features including brain connectivity, polygenic risk, and lifestyle factors.

The paper integrates GWAS data with multi-omics datasets to identify novel genes for alcohol use disorder and link them to neurodegenerative diseases.

This paper conducts a multivariate GWAS of AUDIT items to correct biases and identify novel genetic associations between alcohol consumption, misuse, and health outcomes.