To develop an integrative radiopathomic model based on deep learning to predict overall survival (OS) in locally advanced nasopharyngeal carcinoma (LANPC) patients. A cohort of 343 LANPC patients with pretreatment MRI and whole slide image (WSI) were randomly divided into training (n = 202), validation (n = 91), and external test (n = 50) sets. For WSIs, a self-attention mechanism was employed to assess the significance of different patches for the prognostic task, aggregating them into a WSI-level representation. For MRI, a multilayer perceptron was used to encode the extracted radiomic features, resulting in an MRI-level representation. These were combined in a multimodal fusion model to produce prognostic predictions. Model performances were evaluated using the concordance index (C-index), and Kaplan-Meier curves were employed for risk stratification. To enhance model interpretability, attention-based and Integrated Gradients techniques were applied to explain how WSIs and MRI features contribute to prognosis predictions. The radiopathomics model achieved high predictive accuracy in predicting the OS, with a C-index of 0.755 (95 % CI: 0.673-0.838) and 0.744 (95 % CI: 0.623-0.808) in the training and validation sets, respectively, outperforming single-modality models (radiomic signature: 0.636, 95 % CI: 0.584-0.688; deep pathomic signature: 0.736, 95 % CI: 0.684-0.810). In the external test, similar findings were observed for the predictive performance of the radiopathomics, radiomic signature, and deep pathomic signature, with their C-indices being 0.735, 0.626, and 0.660 respectively. The radiopathomics model effectively stratified patients into high- and low-risk groups (P < 0.001). Additionally, attention heatmaps revealed that high-attention regions corresponded with tumor areas in both risk groups. n: The radiopathomics model holds promise for predicting clinical outcomes in LANPC patients, offering a potential tool for improving clinical decision-making.

Mesh reconstruction is a cornerstone process across various applications, including in-silico trials, digital twins, surgical planning, and navigation. Recent advancements in deep learning have notably enhanced mesh reconstruction speeds. Yet, traditional methods predominantly rely on deforming a standardised template mesh for individual subjects, which overlooks the unique anatomical variations between them, and may compromise the fidelity of the reconstructions. In this paper, we propose an adaptive-template-based mesh reconstruction network (ATMRN), which generates adaptive templates from the given images for the subsequent deformation, moving beyond the constraints of a singular, fixed template. Our approach, validated on cortical magnetic resonance (MR) images from the OASIS dataset, sets a new benchmark in voxel-to-cortex mesh reconstruction, achieving an average symmetric surface distance of 0.267mm across four cortical structures. Our proposed method is generic and can be easily transferred to other image modalities and anatomical structures.

Magnetic Resonance Imaging (MRI) is highly susceptible to motion artifacts due to the extended acquisition times required for k-space sampling. These artifacts can compromise diagnostic utility, particularly for dynamic imaging. We propose a novel alternating minimization framework that leverages a bespoke diffusion model to jointly reconstruct and correct non-rigid motion-corrupted k-space data. The diffusion model uses a coarse-to-fine denoising strategy to capture large overall motion and reconstruct the lower frequencies of the image first, providing a better inductive bias for motion estimation than that of standard diffusion models. We demonstrate the performance of our approach on both real-world cine cardiac MRI datasets and complex simulated rigid and non-rigid deformations, even when each motion state is undersampled by a factor of 64x. Additionally, our method is agnostic to sampling patterns, anatomical variations, and MRI scanning protocols, as long as some low frequency components are sampled during each motion state.

A brain tumor is an abnormal growth in the brain that disrupts its functionality and poses a significant threat to human life by damaging neurons. Early detection and classification of brain tumors are crucial to prevent complications and maintain good health. Recent advancements in deep learning techniques have shown immense potential in image classification and segmentation for tumor identification and classification. In this study, we present a platform, BrainView, for detection, and segmentation of brain tumors from Magnetic Resonance Images (MRI) using deep learning. We utilized EfficientNetB7 pre-trained model to design our proposed DeepBrainNet classification model for analyzing brain MRI images to classify its type. We also proposed a EfficinetNetB7 based image segmentation model, called the EffB7-UNet, for tumor localization. Experimental results show significantly high classification (99.96%) and segmentation (92.734%) accuracies for our proposed models. Finally, we discuss the contours of a cloud application for BrainView using Flask and Flutter to help researchers and clinicians use our machine learning models online for research purposes.

This study centers around the competition between Convolutional Neural Networks (CNNs) with large convolutional kernels and Vision Transformers in the domain of computer vision, delving deeply into the issues pertaining to parameters and computational complexity that stem from the utilization of large convolutional kernels. Even though the size of the convolutional kernels has been extended up to 51×51, the enhancement of performance has hit a plateau, and moreover, striped convolution incurs a performance degradation. Enlightened by the hierarchical visual processing mechanism inherent in humans, this research innovatively incorporates a shared parameter mechanism for large convolutional kernels. It synergizes the expansion of the receptive field enabled by large convolutional kernels with the extraction of fine-grained features facilitated by small convolutional kernels. To address the surging number of parameters, a meticulously designed parameter sharing mechanism is employed, featuring fine-grained processing in the central region of the convolutional kernel and wide-ranging parameter sharing in the periphery. This not only curtails the parameter count and mitigates the model complexity but also sustains the model's capacity to capture extensive spatial relationships. Additionally, in light of the problems of spatial feature information loss and augmented memory access during the 1×1 convolutional channel compression phase, this study further puts forward a dynamic channel sampling approach, which markedly elevates the accuracy of tumor subregion segmentation. To authenticate the efficacy of the proposed methodology, a comprehensive evaluation has been conducted on three brain tumor segmentation datasets, namely BraTs2020, BraTs2024, and Medical Segmentation Decathlon Brain 2018. The experimental results evince that the proposed model surpasses the current mainstream ConvNet and Transformer architectures across all performance metrics, proffering novel research perspectives and technical stratagems for the realm of medical image segmentation.

Surface-based cortical analysis is valuable for a variety of neuroimaging tasks, such as spatial normalization, parcellation, and gray matter (GM) thickness estimation. However, most tools for estimating cortical surfaces work exclusively on scans with at least 1 mm isotropic resolution and are tuned to a specific magnetic resonance (MR) contrast, often T1-weighted (T1w). This precludes application using most clinical MR scans, which are very heterogeneous in terms of contrast and resolution. Here, we use synthetic domain-randomized data to train the first neural network for explicit estimation of cortical surfaces from scans of any contrast and resolution, without retraining. Our method deforms a template mesh to the white matter (WM) surface, which guarantees topological correctness. This mesh is further deformed to estimate the GM surface. We compare our method to recon-all-clinical (RAC), an implicit surface reconstruction method which is currently the only other tool capable of processing heterogeneous clinical MR scans, on ADNI and a large clinical dataset (n=1,332). We show a approximately 50 % reduction in cortical thickness error (from 0.50 to 0.24 mm) with respect to RAC and better recovery of the aging-related cortical thinning patterns detected by FreeSurfer on high-resolution T1w scans. Our method enables fast and accurate surface reconstruction of clinical scans, allowing studies (1) with sample sizes far beyond what is feasible in a research setting, and (2) of clinical populations that are difficult to enroll in research studies. The code is publicly available at https://github.com/simnibs/brainnet.

In many real-world applications, deployed models encounter inputs that differ from the data seen during training. Out-of-distribution detection identifies whether an input stems from an unseen distribution, while open-world recognition flags such inputs to ensure the system remains robust as ever-emerging, previously $unknown$ categories appear and must be addressed without retraining. Foundation and vision-language models are pre-trained on large and diverse datasets with the expectation of broad generalization across domains, including medical imaging. However, benchmarking these models on test sets with only a few common outlier types silently collapses the evaluation back to a closed-set problem, masking failures on rare or truly novel conditions encountered in clinical use. We therefore present $NOVA$, a challenging, real-life $evaluation-only$ benchmark of $\sim$900 brain MRI scans that span 281 rare pathologies and heterogeneous acquisition protocols. Each case includes rich clinical narratives and double-blinded expert bounding-box annotations. Together, these enable joint assessment of anomaly localisation, visual captioning, and diagnostic reasoning. Because NOVA is never used for training, it serves as an $extreme$ stress-test of out-of-distribution generalisation: models must bridge a distribution gap both in sample appearance and in semantic space. Baseline results with leading vision-language models (GPT-4o, Gemini 2.0 Flash, and Qwen2.5-VL-72B) reveal substantial performance drops across all tasks, establishing NOVA as a rigorous testbed for advancing models that can detect, localize, and reason about truly unknown anomalies.

Brain-to-image decoding has been recently propelled by the progress in generative AI models and the availability of large ultra-high field functional Magnetic Resonance Imaging (fMRI). However, current approaches depend on complicated multi-stage pipelines and preprocessing steps that typically collapse the temporal dimension of brain recordings, thereby limiting time-resolved brain decoders. Here, we introduce Dynadiff (Dynamic Neural Activity Diffusion for Image Reconstruction), a new single-stage diffusion model designed for reconstructing images from dynamically evolving fMRI recordings. Our approach offers three main contributions. First, Dynadiff simplifies training as compared to existing approaches. Second, our model outperforms state-of-the-art models on time-resolved fMRI signals, especially on high-level semantic image reconstruction metrics, while remaining competitive on preprocessed fMRI data that collapse time. Third, this approach allows a precise characterization of the evolution of image representations in brain activity. Overall, this work lays the foundation for time-resolved brain-to-image decoding.

Platinum resistance of high-grade serous ovarian cancer (HGSOC) cannot currently be recognized by specific molecular biomarkers. We aimed to compare the predictive capacity of various models integrating MRI habitat, whole slide images (WSIs), and clinical parameters to predict platinum sensitivity in HGSOC patients. A retrospective study involving 998 eligible patients from four hospitals was conducted. MRI habitats were clustered using K-means algorithm on multi-parametric MRI. Following feature extraction and selection, a Habitat model was developed. Vision Transformer (ViT) and multi-instance learning were trained to derive the patch-level prediction and WSI-level prediction on hematoxylin and eosin (H&E)-stained WSIs, respectively, forming a Pathology model. Logistic regression (LR) was used to create a Clinic model. A multi-modal model integrating Clinic, Habitat, and Pathology (CHP) was constructed using Multi-Head Attention (MHA) and compared with the unimodal models and Ensemble multi-modal models. The area under the curve (AUC) and integrated discrimination improvement (IDI) value were used to assess model performance and gains. In the internal validation cohort and the external test cohort, the Habitat model showed the highest AUCs (0.722 and 0.685) compared to the Clinic model (0.683 and 0.681) and the Pathology model (0.533 and 0.565), respectively. The AUCs (0.789 and 0.807) of the multi-modal model interating CHP based on MHA were highest than those of any unimodal models and Ensemble multi-modal models, with positive IDI values. MRI-based habitat imaging showed potentials to predict platinum sensitivity in HGSOC patients. Multi-modal integration of CHP based on MHA was helpful to improve prediction performance.

Deep learning (DL) reconstruction has been successful in realizing otherwise impracticable acceleration factors and improving image quality in conventional MRI field strengths; however, there has been limited application to ultra-high field MRI.The objective of this study was to evaluate the performance of a prototype DL-based image reconstruction technique in 7T MRI of the brain utilizing MP2RAGE and SPACE acquisitions, in comparison to reconstructions in conventional compressed sensing (CS) and controlled aliasing in parallel imaging (CAIPIRINHA) techniques. This retrospective study involved 60 patients who underwent 7T brain MRI between June 2024 and October 2024, comprised of 30 patients with MP2RAGE data and 30 patients with SPACE FLAIR data. Each set of raw data was reconstructed with DL-based reconstruction and conventional reconstruction. Image quality was independently assessed by two neuroradiologists using a 5-point Likert scale, which included overall image quality, artifacts, sharpness, structural conspicuity, and noise level. Inter-observer agreement was determined using top-box analysis. Contrast-to-noise ratio (CNR) and noise levels were quantitatively evaluated and compared using the Wilcoxon signed-rank test. DL-based reconstruction resulted in a significant increase in overall image quality and a reduction in subjective noise level for both MP2RAGE and SPACE FLAIR data (all P<0.001), with no significant differences in image artifacts (all P>0.05). When compared to standard reconstruction, the implementation of DL-based reconstruction yielded an increase in CNR of 49.5% [95% CI 33.0-59.0%] for MP2RAGE data and 90.6% [95% CI 73.2-117.7%] for SPACE FLAIR data, along with a decrease in noise of 33.5% [95% CI 23.0-38.0%] for MP2RAGE data and 47.5% [95% CI 41.9-52.6%] for SPACE FLAIR data. DL-based reconstruction of 7T MRI significantly enhanced image quality compared to conventional reconstruction without introducing image artifacts. The achievable high acceleration factors have the potential to substantially improve image quality and resolution in 7T MRI. CAIPIRINHA = Controlled Aliasing In Parallel Imaging Results IN Higher Acceleration; CNR = contrast-to-noise ratio; CS = compressed sensing; DL = deep learning; MNI = Montreal Neurological Institute; MP2RAGE = Magnetization-Prepared 2 Rapid Acquisition Gradient Echoes; SPACE = Sampling Perfection with Application-Optimized Contrasts using Different Flip Angle Evolutions.