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Simon Winther Albertsen

Publications and source records attributed to Simon Winther Albertsen.

2 recordsLinked to original sources

CATCH: Counterfactual Anatomical Tissue Inpainting with Conditional Haar Diffusion

BraTS local synthesis replaces masked regions in T1-weighted brain MRI with plausible tumor-free tissue while preserving observed anatomy. We present CATCH, conditional 3D diffusion in an invertible Haar-wavelet domain. Its denoiser receives noisy target coefficients, voided-image coefficients, and a signed mask; tumor-excluded wavelet reconstruction and a hole-focused loss guide training, and hard compositing preserves observed voxels. We compare fixed masks, tumor-component augmentation, and a weighted mixture of tumor-derived, irregular-blob, and ellipsoidal masks. Of 25 development cases, five prespecified cases select each arm's checkpoint and all 25 of their trajectory aggregations; a separate 75-case internal set compares the frozen pipelines and selects a weighted mixture for organizer evaluation. Five-trajectory averaging yielded internal SSIM/PSNR/MSE (mean$\pm$SD) of $0.80\pm0.13$, $19.18\pm1.80$dB, and $0.010\pm0.005$. As the sole officially evaluated pipeline, weighted mixture yielded $0.772\pm0.119$, $20.89\pm3.27$dB, and $0.0098\pm0.0054$ on the 219-case BraTS 2026 validation set. Against compute-matched random augmentation internally, it improved SSIM by 0.019 (95% bootstrap CI: 0.013-0.025), PSNR by 0.95dB, and MSE by 0.003; all three paired comparisons remained significant after Holm correction. Results favor the complete weighted-mixture policy within CATCH; absent official fixed- and random-pipeline scores and a directly comparable external baseline limit broader conclusions.

cs.CV↗

RARE-UNet: Resolution-Aligned Routing Entry for Adaptive Medical Image Segmentation

Accurate segmentation is crucial for clinical applications, but existing models often assume fixed, high-resolution inputs and degrade significantly when faced with lower-resolution data in real-world scenarios. To address this limitation, we propose RARE-UNet, a resolution-aware multi-scale segmentation architecture that dynamically adapts its inference path to the spatial resolution of the input. Central to our design are multi-scale blocks integrated at multiple encoder depths, a resolution-aware routing mechanism, and consistency-driven training that aligns multi-resolution features with full-resolution representations. We evaluate RARE-UNet on two benchmark brain imaging tasks for hippocampus and tumor segmentation. Compared to standard UNet, its multi-resolution augmented variant, and nnUNet, our model achieves the highest average Dice scores of 0.84 and 0.65 across resolution, while maintaining consistent performance and significantly reduced inference time at lower resolutions. These results highlight the effectiveness and scalability of our architecture in achieving resolution-robust segmentation. The codes are available at: https://github.com/simonsejse/RARE-UNet.

eess.IV↗