Arrow Research search

Author name cluster

Sukrit Gupta

Possible papers associated with this exact author name in Arrow. This page groups case-insensitive exact name matches and is not a full identity disambiguation profile.

3 papers
1 author row

Possible papers

3

JBHI Journal 2026 Journal Article

Encoding and Decoding of Brain Dynamic Functional Connectivity for ADHD Diagnosis

  • Deepank Girish
  • Yi Hao Chan
  • Sukrit Gupta
  • Jing Xia
  • Jagath C. Rajapakse

Recent studies have demonstrated strong associations between the changes in dynamic functional connectivity (FC) and both behavioral and cognitive functions. The sliding window technique is the most widely used method for evaluating dynamic FC; however, it faces two key challenges: distributional shifts across windows and high dimensionality, as FC is computed across windows of the entire time series. To address these issues, we propose BRAINMAP (Bi-level Representation using Attention for INterpretability with Mamba-Aided Prediction) to model the dynamic FC of the brain. BRAINMAP employs the Optimal Transport technique to correct distributional shifts across sliding windows and leverages Graph Neural Networks (GNNs) in conjunction with a hybrid approach that integrates an attention mechanism and the Mamba block to effectively capture spatiotemporal features for functional MR images. Finally, we introduce a novel Top-K sliding window feature selection algorithm to induce sparsity in dynamic FC. We conducted an extensive evaluation of our model for diagnosing Attention Deficit Hyperactivity Disorder (ADHD) using three resting-state fMRI datasets: ADHD-200, UCLA, and CNI-TLC, which comprise a total of 447 subjects with ADHD and 845 typically developing controls. Our architecture outperformed existing state-of-the-art dynamic FC models in ADHD detection, achieving improvements ranging from 3% to 12% across the three datasets. We demonstrate that our proposed model produces robust biomarkers, most notably the connection between the dorsal attention network and the visual network. Using an association study, we further establish the clinical relevance of the identified biomarkers.

YNIMG Journal 2025 Journal Article

Discovering robust biomarkers of psychiatric disorders from resting-state functional MRI via graph neural networks: A systematic review

  • Yi Hao Chan
  • Deepank Girish
  • Sukrit Gupta
  • Jing Xia
  • Chockalingam Kasi
  • Yinan He
  • Conghao Wang
  • Jagath C. Rajapakse

Graph neural networks (GNN) have emerged as a popular tool for modeling functional magnetic resonance imaging (fMRI) datasets. Many recent studies have reported significant improvements in disorder classification performance via more sophisticated GNN designs and highlighted salient features that could be potential biomarkers of the disorder. However, existing methods of evaluating their robustness are often limited to cross-referencing with existing literature, which is a subjective and inconsistent process. In this review, we provide an overview of how GNN and model explainability techniques (specifically, feature attributors) have been applied to fMRI datasets for disorder prediction tasks, with an emphasis on evaluating the robustness of potential biomarkers produced by these feature attributors for psychiatric disorders. Then, 65 studies using GNNs that reported potential fMRI biomarkers for psychiatric disorders (attention-deficit hyperactivity disorder, autism spectrum disorder, major depressive disorder, schizophrenia) published before 9 October 2024 were identified from 2 online databases (Scopus, PubMed). We found that while most studies have performant models, salient features highlighted in these studies (as determined by feature attribution scores) vary greatly across studies on the same disorder. Reproducibility of biomarkers is only limited to a small subset at the level of regions and few transdiagnostic biomarkers were identified. To address these issues, we suggest establishing new standards that are based on objective evaluation metrics to determine the robustness of these potential biomarkers. We further highlight gaps in the existing literature and put together a prediction-attribution-evaluation framework that could set the foundations for future research on discovering robust biomarkers of psychiatric disorders via GNNs.

YNICL Journal 2020 Journal Article

Ambivert degree identifies crucial brain functional hubs and improves detection of Alzheimer’s Disease and Autism Spectrum Disorder

  • Sukrit Gupta
  • Jagath C. Rajapakse
  • Roy E. Welsch

Functional modules in the human brain support its drive for specialization whereas brain hubs act as focal points for information integration. Brain hubs are brain regions that have a large number of both within and between module connections. We argue that weak connections in brain functional networks lead to misclassification of brain regions as hubs. In order to resolve this, we propose a new measure called ambivert degree that considers the node's degree as well as connection weights in order to identify nodes with both high degree and high connection weights as hubs. Using resting-state functional MRI scans from the Human Connectome Project, we show that ambivert degree identifies brain hubs that are not only crucial but also invariable across subjects. We hypothesize that nodal measures based on ambivert degree can be effectively used to classify patients from healthy controls for diseases that are known to have widespread hub disruption. Using patient data for Alzheimer's Disease and Autism Spectrum Disorder, we show that the hubs in the patient and healthy groups are very different for both the diseases and deep feedforward neural networks trained on nodal hub features lead to a significantly higher classification accuracy with significantly fewer trainable weights compared to using functional connectivity features. Thus, the ambivert degree improves identification of crucial brain hubs in healthy subjects and can be used as a diagnostic feature to detect neurological diseases characterized by hub disruption.

v2026.09.13