Rodrigue Rizk

CV
h-index8
7papers
13citations
Novelty56%
AI Score56

7 Papers

2.7LGFeb 17Code
AI-CARE: Carbon-Aware Reporting Evaluation Metric for AI Models

KC Santosh, Srikanth Baride, Rodrigue Rizk

As machine learning (ML) continues its rapid expansion, the environmental cost of model training and inference has become a critical societal concern. Existing benchmarks overwhelmingly focus on standard performance metrics such as accuracy, BLEU, or mAP, while largely ignoring energy consumption and carbon emissions. This single-objective evaluation paradigm is increasingly misaligned with the practical requirements of large-scale deployment, particularly in energy-constrained environments such as mobile devices, developing regions, and climate-aware enterprises. In this paper, we propose AI-CARE, an evaluation tool for reporting energy consumption, and carbon emissions of ML models. In addition, we introduce the carbon-performance tradeoff curve, an interpretable tool that visualizes the Pareto frontier between performance and carbon cost. We demonstrate, through theoretical analysis and empirical validation on representative ML workloads, that carbon-aware benchmarking changes the relative ranking of models and encourages architectures that are simultaneously accurate and environmentally responsible. Our proposal aims to shift the research community toward transparent, multi-objective evaluation and align ML progress with global sustainability goals. The tool and documentation are available at https://github.com/USD-AI-ResearchLab/ai-care.

8.6IVJul 22, 2025Code
MLRU++: Multiscale Lightweight Residual UNETR++ with Attention for Efficient 3D Medical Image Segmentation

Nand Kumar Yadav, Rodrigue Rizk, William CW Chen et al.

Accurate and efficient medical image segmentation is crucial but challenging due to anatomical variability and high computational demands on volumetric data. Recent hybrid CNN-Transformer architectures achieve state-of-the-art results but add significant complexity. In this paper, we propose MLRU++, a Multiscale Lightweight Residual UNETR++ architecture designed to balance segmentation accuracy and computational efficiency. It introduces two key innovations: a Lightweight Channel and Bottleneck Attention Module (LCBAM) that enhances contextual feature encoding with minimal overhead, and a Multiscale Bottleneck Block (M2B) in the decoder that captures fine-grained details via multi-resolution feature aggregation. Experiments on four publicly available benchmark datasets (Synapse, BTCV, ACDC, and Decathlon Lung) demonstrate that MLRU++ achieves state-of-the-art performance, with average Dice scores of 87.57% (Synapse), 93.00% (ACDC), and 81.12% (Lung). Compared to existing leading models, MLRU++ improves Dice scores by 5.38% and 2.12% on Synapse and ACDC, respectively, while significantly reducing parameter count and computational cost. Ablation studies evaluating LCBAM and M2B further confirm the effectiveness of the proposed architectural components. Results suggest that MLRU++ offers a practical and high-performing solution for 3D medical image segmentation tasks. Source code is available at: https://github.com/1027865/MLRUPP

3.6CLApr 2
Fragile Reasoning: A Mechanistic Analysis of LLM Sensitivity to Meaning-Preserving Perturbations

Shou-Tzu Han, Rodrigue Rizk, KC Santosh

Large language models demonstrate strong performance on mathematical reasoning benchmarks, yet remain surprisingly fragile to meaning-preserving surface perturbations. We systematically evaluate three open-weight LLMs, Mistral-7B, Llama-3-8B, and Qwen2.5-7B, on 677 GSM8K problems paired with semantically equivalent variants generated through name substitution and number format paraphrasing. All three models exhibit substantial answer-flip rates (28.8%-45.1%), with number paraphrasing consistently more disruptive than name swaps. To trace the mechanistic basis of these failures, we introduce the Mechanistic Perturbation Diagnostics (MPD) framework, combining logit lens analysis, activation patching, component ablation, and the Cascading Amplification Index (CAI) into a unified diagnostic pipeline. CAI, a novel metric quantifying layer-wise divergence amplification, outperforms first divergence layer as a failure predictor for two of three architectures (AUC up to 0.679). Logit lens reveals that flipped samples diverge from correct predictions at significantly earlier layers than stable samples. Activation patching reveals a stark architectural divide in failure localizability: Llama-3 failures are recoverable by patching at specific layers (43/60 samples), while Mistral and Qwen failures are broadly distributed (3/60 and 0/60). Based on these diagnostic signals, we propose a mechanistic failure taxonomy (localized, distributed, and entangled) and validate it through targeted repair experiments: steering vectors and layer fine-tuning recover 12.2% of localized failures (Llama-3) but only 7.2% of entangled (Qwen) and 5.2% of distributed (Mistral) failures.

5.7LGApr 27
Robust and Clinically Reliable EEG Biomarkers: A Cross Population Framework for Generalizable Parkinson's Disease Detection

Nicholas R. Rasmussen, Longwei Wang, Rodrigue Rizk et al.

Developing robust and clinically reliable EEG biomarkers requires evaluation frameworks that explicitly address cross population generalization in multi site settings such as Parkinsons disease (PD) detection. Models trained under i.i.d. assumptions often capture population specific artifacts rather than disease relevant neural structure, leading to poor generalization across clinical cohorts. EEG further amplifies this challenge due to low signal to noise ratio and heterogeneous acquisition conditions. We propose a population aware evaluation framework to assess the robustness and clinical reliability of EEG biomarkers under distribution shift. Using an n gram expansion strategy, we enumerate all cross population train test configurations across five independent cohorts, resulting in 75 directional evaluations. A nested cross validation design with integrated channel selection ensures prospective biomarker identification without population leakage. Results show that cross population transfer is asymmetric and that both accuracy and biomarker stability improve with increasing training population diversity, achieving up to 94.1% accuracy on held out cohorts. A theoretical analysis based on mixture risk optimization and hypothesis space contraction explains these trends, showing that multi population training promotes population robust representations. This work establishes a principled framework for learning robust, generalizable, and clinically reliable EEG biomarkers for multi site biomedical applications.

2.3SPDec 28, 2025
Channel Selected Stratified Nested Cross Validation for Clinically Relevant EEG Based Parkinsons Disease Detection

Nicholas R. Rasmussen, Rodrigue Rizk, Longwei Wang et al.

The early detection of Parkinsons disease remains a critical challenge in clinical neuroscience, with electroencephalography offering a noninvasive and scalable pathway toward population level screening. While machine learning has shown promise in this domain, many reported results suffer from methodological flaws, most notably patient level data leakage, inflating performance estimates and limiting clinical translation. To address these modeling pitfalls, we propose a unified evaluation framework grounded in nested cross validation and incorporating three complementary safeguards: (i) patient level stratification to eliminate subject overlap and ensure unbiased generalization, (ii) multi layered windowing to harmonize heterogeneous EEG recordings while preserving temporal dynamics, and (iii) inner loop channel selection to enable principled feature reduction without information leakage. Applied across three independent datasets with a heterogeneous number of channels, a convolutional neural network trained under this framework achieved 80.6% accuracy and demonstrated state of the art performance under held out population block testing, comparable to other methods in the literature. This performance underscores the necessity of nested cross validation as a safeguard against bias and as a principled means of selecting the most relevant information for patient level decisions, providing a reproducible foundation that can extend to other biomedical signal analysis domains.

3.6CVNov 5, 2025
I Detect What I Don't Know: Incremental Anomaly Learning with Stochastic Weight Averaging-Gaussian for Oracle-Free Medical Imaging

Nand Kumar Yadav, Rodrigue Rizk, William CW Chen et al.

Unknown anomaly detection in medical imaging remains a fundamental challenge due to the scarcity of labeled anomalies and the high cost of expert supervision. We introduce an unsupervised, oracle-free framework that incrementally expands a trusted set of normal samples without any anomaly labels. Starting from a small, verified seed of normal images, our method alternates between lightweight adapter updates and uncertainty-gated sample admission. A frozen pretrained vision backbone is augmented with tiny convolutional adapters, ensuring rapid domain adaptation with negligible computational overhead. Extracted embeddings are stored in a compact coreset enabling efficient k-nearest neighbor anomaly (k-NN) scoring. Safety during incremental expansion is enforced by dual probabilistic gates, a sample is admitted into the normal memory only if its distance to the existing coreset lies within a calibrated z-score threshold, and its SWAG-based epistemic uncertainty remains below a seed-calibrated bound. This mechanism prevents drift and false inclusions without relying on generative reconstruction or replay buffers. Empirically, our system steadily refines the notion of normality as unlabeled data arrive, producing substantial gains over baselines. On COVID-CXR, ROC-AUC improves from 0.9489 to 0.9982 (F1: 0.8048 to 0.9746); on Pneumonia CXR, ROC-AUC rises from 0.6834 to 0.8968; and on Brain MRI ND-5, ROC-AUC increases from 0.6041 to 0.7269 and PR-AUC from 0.7539 to 0.8211. These results highlight the effectiveness and efficiency of the proposed framework for real-world, label-scarce medical imaging applications.

14.4CVJul 14, 2025
Winsor-CAM: Human-Tunable Visual Explanations from Deep Networks via Layer-Wise Winsorization

Casey Wall, Longwei Wang, Rodrigue Rizk et al.

Interpreting the decision-making process of Convolutional Neural Networks (CNNs) is critical for deploying models in high-stakes domains. Gradient-weighted Class Activation Mapping (Grad-CAM) is a widely used method for visual explanations, yet it typically focuses on the final convolutional layer or naïvely averages across layers, strategies that can obscure important semantic cues or amplify irrelevant noise. We propose Winsor-CAM, a novel, human-tunable extension of Grad-CAM that generates robust and coherent saliency maps by aggregating information across all convolutional layers. To mitigate the influence of noisy or extreme attribution values, Winsor-CAM applies Winsorization, a percentile-based outlier attenuation technique. A user-controllable threshold allows for semantic-level tuning, enabling flexible exploration of model behavior across representational hierarchies. Evaluations on standard architectures (ResNet50, DenseNet121, VGG16, InceptionV3) using the PASCAL VOC 2012 dataset demonstrate that Winsor-CAM produces more interpretable heatmaps and achieves superior performance in localization metrics, including intersection-over-union and center-of-mass alignment, when compared to Grad-CAM and uniform layer-averaging baselines. Winsor-CAM advances the goal of trustworthy AI by offering interpretable, multi-layer insights with human-in-the-loop control.