Life sciences · Preprint
arXiv · November 6, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Preprint.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Multi-label retinal screening requires capturing co-occurring pathologies and clinical context, yet standard multimodal fusion remains opaque. We propose a dual-hub heterogeneous graph neural network (GNN) that couples spatial fundus features and structured clinical covariates through cross-modal message passing while providing inherent interpretability. Rather than relying on post-hoc saliency approximations, our architecture exposes multi-level decision pathways during forward aggregation: spatially biased self-attention captures lesion-level patch interactions, while modality-specific graph attention coefficients explicitly quantify the contribution of visual regions and clinical risk factors to each disease node. Evaluated on the BRSET dataset (16,266 photographs from 8,524 patients), the proposed model achieves 76.1% Macro-AUPRC across seven conditions, matching or exceeding image-only (75.9%) and ResNet-50+MLP fusion (75.9%) baselines, with largest contextual gains in macular edema (+3.5%) and diabetic retinopathy (+2.1%). Codebase is available at: https://github.com/proshanto-c/ca-mlc-refactor.