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Johannes C. Paetzold

Publications and source records attributed to Johannes C. Paetzold.

At least 19 recordsLinked to original sources

MAdam: Metric-Aware Multi-Objective Adam

Multi-objective optimization (MOO) underlies many machine learning problems, yet MOO solvers across the loss-balancing, gradient-balancing, and Pareto-based families almost universally hand their reconciled directions to Adam~\citep{kingma2015adam}. We show this coupling introduces two systematic gaps between the solver's intent and the optimizer's execution. The first is a weighting mismatch: Adam's second-moment denominator entangles the time-varying preference vector with gradient statistics, marginalizing the preference into a history average and collapsing distinct Pareto trade-offs toward a near-uniform mixture. The second is a geometric mismatch: Adam's adaptive metric distorts the Euclidean geometry MOO solvers assume, turning aligned objectives into apparent conflicts. To resolve both jointly, we introduce MAdam (Metric-Aware Multi-Objective Adam), a drop-in wrapper that leaves both solver and optimizer unchanged. MAdam preconditions the reconciled direction by the preference-conditioned curvature of the scalarized objective; on this whitened input, Adam's second moment collapses to identity, so the realized update is governed by the preference-conditioned metric. Across multi-task learning, Pareto-front recovery, physics-informed neural networks, and medical imaging, MAdam improves over Adam in aggregate for every solver family. Our code is available at https://github.com/lfb-1/MAdam.

cs.LG↗

Optimization Encoders: Rethinking Second-Order Meta-Learning for Neural Fields

Conditional neural fields represent signals continuously, but their effectiveness depends on how the conditional latent representations are inferred from observed data. In meta-learning, this encoding occurs through gradient updates induced by the decoder, tying representation learning directly to decoder design. We formalize this connection by interpreting latent optimization as an optimization encoder, unifying the roles of second-order differentiation, latent parameterization, and task supervision. This concept enables second-order meta-learning for end-to-end training of the encoding procedure alongside the decoder, and clarifies which learning pathway first-order approximations discard. Guided by this view, we introduce Attentive Latent Fields (MetaLF), an equivariant transformer-based neural field that contextualizes a latent pointcloud through self-attention. These interactions shape both field predictions and the updates that construct their representation, allowing local observations to inform coherent non-local structure. Disentangling the inner encoding objective from outer task supervision unifies reconstruction, classification, and segmentation within an end-to-end meta-learning framework, using reconstruction-only latent adaptation at test time. Controlled experiments on polynomial fields link latent coordination to lower effective rank and stronger alignment with the underlying function space. Across image and 3D shape reconstruction, MetaLF improves fidelity within three to five gradient updates, while supporting semantic prediction across images, shapes, and volumes. Together, these findings position the optimization encoder perspective as a unified basis for designing neural fields around how representations are constructed, coordinated, and used.

cs.LG↗

Sparse cubical complexes for efficient topology-preservation in image data

Persistent homology (PH) is a frequently used tool for extracting and preserving topological information from image data, particularly in image segmentation, where preservation of topological structures is important. However, despite its general applicability across dimensionality, domains, and target structures, the runtime cost of PH-based methods often makes their practical use infeasible. In this work, we argue that this runtime cost is largely driven by processing information that is unimportant for downstream application (e.g. as optimization objective). We propose sparse cubical filtrations as an alternative foundation for PH computation, reducing subsequent computational costs by factors of up to 100 on real datasets. We show close agreement with the optimization signal of the dense counterpart and empirically evaluate our solution's effectiveness as an optimization objective in realistic training regimes where other PH-based objectives can practically not operate (i.e., 3D data with large patch sizes). We show how our solution improves topological accuracy by up to 80\% across six diverse datasets while maintaining pixel- and region-based accuracy.

cs.CV↗

MELD: Multi-Task Equilibrated Learning Detector for AI-Generated Text

Large language models are widely used in everyday writing, making reliable AI-generated text detection crucial for academic integrity, content moderation, and provenance tracking. Yet high AUROC on clean, in-distribution benchmarks is not sufficient. Practical detectors must resist adversarial rewrites, generalize to unseen generators and writing domains, and maintain low false-positive rates (FPR). A pooled AI-versus-human objective does not explicitly require the model to distinguish among generator families, so it may fail to learn the generator-specific structure needed for generalization and attribution. We introduce MELD (Multi-Task Equilibrated Learning Detector), which instead trains on class-balanced, family-specific AI-versus-human tasks while sharing a common representation of human writing. MELD produces detection, generator-family, rewrite-task, and token-level predictions in a single forward pass. Format normalization further makes its scores invariant to the modeled reformatting operations. MELD ranks first among open-source submissions in the public RAID leaderboard and matches or exceeds supervised baselines on five of six held-out evaluation pools. To evaluate transfer to unseen generators, we introduce MELD-eval, a held-out test pool built from four frontier chat models. Without further fine-tuning, MELD achieves 99.7% TPR at 1% FPR on MELD-eval and 98% TPR at the same FPR on a held-out generator whose family is absent from training. Finally, in a case study of 5.9 million scientific texts from 2016--2026, MELD's prediction scores remain stable through 2022 and increase from 2023 onward, coinciding with the widespread adoption of LLM-based writing tools. The model, MELD-eval pool, source code, and live demo are available.

cs.CL↗

A Multimodal 3D Foundation Model for Light Sheet Fluorescence Microscopy Enables Few-Shot Segmentation, Classification, and Deblurring

Light sheet fluorescence microscopy (LSM) enables high-resolution, three-dimensional (3D) imaging of biological specimens, providing rich volumetric data for studying cellular organization, pathology, and vascular networks. However, the size, dimensionality, and annotation burden of LSM data make supervised deep learning approaches costly and difficult to scale. Additionally, despite the abundance of unannotated LSM volumes, foundation models for this modality remain underexplored due to computational challenges and the complexity of volumetric representation learning. In this work, we introduce a 3D foundation model for LSM data, pretrained on a large curated collection of 3D images spanning multiple organisms, stains, and imaging protocols. We learn transferable volumetric representations by jointly optimizing for masked reconstruction and image-text alignment. The pretrained backbone drastically reduces the annotation burden, enabling efficient, few-shot adaptation for varied downstream tasks. We evaluate this approach on downstream segmentation, classification, and deblurring. Our results demonstrate consistent improvements over baselines, (1) when measured using standard evaluation metrics and (2) when rigorously assessed by domain experts. This highlights the potential of foundation model pretraining to reduce annotation requirements while improving performance across diverse LSM analysis tasks. Pretrained model weights and code for pretraining and finetuning are publicly available: https://github.com/AdinaScheinfeld/lsm_fm_public_repo.git.

cs.CV↗

Interpretable Retinal Disease Prediction Using Biology-Informed Heterogeneous Graph Representations

Interpretability is crucial for utilizing machine learning models as clinical decision support tools for medical diagnostics. However, most state-of-the-art image classifiers based on neural networks are not interpretable. As a result, clinicians often resort to known biomarkers to guide diagnosis, although biomarker-based classification often suffers from drastic information loss compared to raw medical images. This work proposes a method that preserves the rich imaging information while simultaneously enhancing the interpretability of predictions for diabetic retinopathy staging from optical coherence tomography angiography (OCTA) images. The core contribution of our method is a novel biology-informed heterogeneous graph representation that models retinal vessel segments, intercapillary areas, and the foveal avascular zone (FAZ) in a human-interpretable way. This graph representation allows us to frame diabetic retinopathy staging as a graph-level classification task, which we solve using an established, efficient graph neural network architecture. We compare our method against established methods, including classical biomarker-based classifiers, convolutional neural networks (CNNs), and vision transformers in predicting the clinically assigned DR stage based on color fundus photography images. We find stage agreement rates of our method and alternative vision model based classifiers saturating at AUC-ROC values of 84%. Crucially, we use our biology-informed graph to provide explanations of great detail. Our approach surpasses existing methods in precisely localizing and identifying abnormal vessels and non-perfusion areas. Our approach sets the stage for the interpretable identification of patients who require special attention due to their traceable microvascular changes, only observable using the details of OCTA images.

cs.CV↗

GeoPose: Patient-agnostic CTA-to-DSA registration through projection-space calibration

Aligning intraoperative biplanar digital subtraction angiography (DSA) to pre-procedural computed tomography angiography (CTA) requires rapid and accurate 3D-to-2D registration. Optimization-based methods are sensitive to initialization and may require hundreds of iterations, whereas learning-based approaches commonly rely on patient-specific training. We propose GeoPose, a population-trained framework that estimates the C-arm pose in a learned canonical frame and transfers it to the native frame of an unseen CTA through projection-space calibration and transform composition. A population-trained residual network refines the pose, followed optionally by low-budget image-driven optimization. GeoPose requires neither patient-specific adaptation nor explicit inter-volume preregistration. On 80 DSA observations from 20 held-out patients, optimization-free GeoPose achieved a carotid mean projected centerline distance (mPCD) of 5.8 mm and a clDice of 0.45, compared with 14.5 mm and 0.28 for the best-performing baseline, while requiring only 0.15 s. After 25 optimization iterations, GeoPose reached an mPCD of 4.6 mm and a clDice of 0.58 in approximately two seconds. Under the same budget, native-initialized optimization achieved 14.6 mm and 0.15, respectively. GeoPose thus provides rapid native-frame registration with fixed population-level weights and the geometric correspondence required for downstream biplanar 3D vascular reconstruction.

cs.CV↗

Unifying Active Learning and Semi-Supervised Learning for Medical Image Segmentation

In practical settings, medical image segmentation models are often developed with limited annotated data rather than fully labeled datasets. Training frequently begins in ultra-low labeled regimes where only a small number of volumes are annotated. In such scenarios, practitioners must simultaneously decide which cases to annotate and how to best use the remaining unlabeled data. Although active learning (AL) and semi-supervised learning (SSL) both target annotation scarcity, they are typically designed and optimized independently, resulting in objective mismatch and unstable training during early-stage "cold start" conditions. We propose RegAL, a unified active semi-supervised framework governed by a shared topology-aware Pareto optimization that couples sample acquisition with unlabeled data utilization. RegAL evaluates images along three complementary axes, voxel-wise uncertainty, feature diversity, and a novel topological consistency metric, to select anatomically informative edge cases for annotation. On the other hand, the same criteria are used to identify geometrically stable atlas candidates for diffeomorphic registration-guided augmentation to train a self-supervised Mean Teacher segmentation network. Across BraTS 2021, dHCP, and ProstateX, RegAL remains stable with few labeled volumes and consistently outperforms state-of-the-art AL, SSL, and active semi-supervised baselines across Dice and boundary-distance (ASD, HD95) metrics under extreme annotation scarcity.

cs.CV↗

Beyond scalar losses: calibrating segmentation models via gradient vector field surgery

Region-based loss functions, such as the Dice loss, have established themselves as the de facto standard for highly class- and region-imbalanced segmentation tasks. However, models trained using region-based loss functions are notoriously miscalibrated and typically yield over-confident predictions. In medical imaging applications, such as defining tumor resection margins, this miscalibration is hindering clinical adoption. In this work, we outline a novel gradient perspective on this overconfidence and show how it affects region-based loss functions. We propose a "surgery" on the gradient vector field as a simple, yet effective intervention to mitigate calibration issues. This surgery adds a factor to the loss's partial derivative, scaling the gradient's magnitude linearly with the prediction error. In empirical evaluations across 2D and 3D medical segmentation tasks, we demonstrate the effectiveness of this intervention while maintaining high prediction accuracy when used in conjunction with any region-based loss function.

cs.CV↗

The TopCoW Challenge -- Topology-Aware Circle of Willis Segmentation for CT and MR Angiography

The Circle of Willis (CoW) is an important network of arteries connecting major circulations of the brain. Its vascular architecture is believed to influence the risk, severity, and outcome of serious neurovascular diseases. However, characterizing the highly variable CoW anatomy remains a manual and time-consuming expert task. The CoW is commonly imaged by two non-invasive angiographic imaging modalities, magnetic resonance angiography (MRA) and computed tomography angiography (CTA), yet few datasets with annotated CoW anatomy exist, and there have been no established benchmarks for comparing CoW segmentation algorithms. We organized the TopCoW benchmark challenge alongside the release of an annotated CoW dataset with 125 paired MRA and CTA scans from the same patients. Voxel-level annotations for 13 vessel components were created using virtual reality technology and verified by clinical experts. Participants submitted algorithms for CoW segmentation and variant classification, which we evaluated on internal and external test sets comprising 226 scans from over five centers. The benchmark includes voxel-level segmentation, CoW component detection, CoW variant classification, and two clinical application tasks. We received submissions from over 250 participants across six continents. Top-performing teams achieved over 90% Dice scores for CoW segmentation, over 80% F1 scores for detecting key vessel components, and over 70% balanced accuracy in CoW variant classification across nearly all test sets. The best algorithms also supported clinically relevant downstream tasks by accurately classifying fetal-type posterior cerebral arteries and localizing aneurysms in relation to CoW anatomy. This benchmark demonstrated the utility of CoW segmentation algorithms for some downstream clinical applications with explainability.

cs.CV↗

VERITAS: A Multi-Agent Co-Scientist for Verifiable Image-Derived Hypothesis Testing

Scientific research based on multimodal clinical data (including medical imaging) requires coordinating clinical, radiological, programming, and biostatistical expertise, a fragmented process that bottlenecks discovery. We present VERITAS (Verifiable Epistemic Reasoning for Image-Derived Hypothesis Testing via Agentic Systems), a clinical co-scientist: a multi-agent system that autonomously tests natural-language hypotheses and produces a fully auditable evidence trail, tracing every conclusion through executable outputs from analysis plan to segmentation masks to statistical code to final verdict. Unlike prior AI-scientist systems, which mainly operate on tabular or text data, VERITAS grounds autonomous discovery directly in medical images. It decomposes the workflow into four phases handled by role-specialized agents, and introduces an epistemic evidence label framework that mechanically classifies outcomes as Supported, Refuted, Underpowered, or Invalid by jointly evaluating significance, effect direction, and study power. This distinction is critical in medical imaging, where non-significant results often reflect insufficient sample size rather than absent effects. We construct a tiered benchmark of 64 hypotheses spanning six complexity levels across cardiac and brain glioma MRI datasets. VERITAS reaches 81.4% verdict accuracy with frontier models and 71.2% with locally-hosted open-weight models (8-30B), outperforming all single-model baselines in both classes. It also produces the highest rate of independently verifiable statistical outputs (86.6%), so even its failures remain diagnosable through artifact inspection. Structured multi-agent decomposition thus substitutes for model scale while preserving the verifiability that scientific discovery demands. We release code, hypothesis bank, and evaluation pipeline at https://github.com/LucZot/veritas.

cs.MA↗

TG-OT: Topology-guided CCTA-IVUS registration via optimal transport matching

Registering coronary CT angiography (CCTA) and intravascular ultrasound (IVUS) enables comprehensive coronary analysis that neither modality can provide alone, yet their fusion remains challenging due to differences in imaging geometry, resolution, and artifact profiles. Existing methods depend on pre-computed lumen or vessel wall segmentations that are unreliable under IVUS acoustic shadowing from calcifications, limiting their clinical applicability. We propose TG-OT, a fully automatic CCTA-IVUS registration framework that eliminates this dependency by integrating trained feature detectors directly into the registration pipeline. Lightweight CNNs are trained to predict calcifications, bifurcations, and lumen radii on the topological $(θ, z)$ cylinder, encouraging topologically coherent detections without requiring explicit segmentation. Registration is formulated as an optimization over centerline warping parameters, driven by an unbalanced Sinkhorn optimal transport loss on the cylindrical geometry that provides spatially informative gradients even for spatially disjoint predictions, complemented by a lumen matching term. Evaluated on $N{=}47$ paired CCTA-IVUS cases in a 5-fold cross-validation setup, TG-OT achieves strong longitudinal ($\overline{\text{Dice}}_\text{ctl}{=}0.99$), rotational ($\overline{S}_c{=}0.96$), and lumen alignment ($\overline{\text{Dice}}_\text{L}{=}0.69$) without manual interaction or prior segmentation, marking a meaningful step toward clinical integration of automatic CCTA-IVUS fusion.

eess.IV↗

BackSplit: The Importance of Sub-dividing the Background in Biomedical Lesion Segmentation

Segmenting small lesions in medical images remains notoriously difficult. Most prior work tackles this challenge by either designing better architectures, loss functions, or data augmentation schemes; and collecting more labeled data. We take a different view, arguing that part of the problem lies in how the background is modeled. Common lesion segmentation collapses all non-lesion pixels into a single "background" class, ignoring the rich anatomical context in which lesions appear. In reality, the background is highly heterogeneous-composed of tissues, organs, and other structures that can now be labeled manually or inferred automatically using existing segmentation models. In this paper, we argue that training with fine-grained labels that sub-divide the background class, which we call BackSplit, is a simple yet powerful paradigm that can offer a significant performance boost without increasing inference costs. From an information theoretic standpoint, we prove that BackSplit increases the expected Fisher Information relative to conventional binary training, leading to tighter asymptotic bounds and more stable optimization. With extensive experiments across multiple datasets and architectures, we empirically show that BackSplit consistently boosts small-lesion segmentation performance, even when auxiliary labels are generated automatically using pretrained segmentation models. Additionally, we demonstrate that auxiliary labels derived from interactive segmentation frameworks exhibit the same beneficial effect, demonstrating its robustness, simplicity, and broad applicability.

cs.CV↗

Synthetic Vasculature and Pathology Enhance Vision-Language Model Reasoning

Vision-Language Models (VLMs) offer a promising path toward interpretable medical diagnosis by allowing users to ask about clinical explanations alongside predictions and across different modalities. However, training VLMs for detailed reasoning requires large-scale image-text datasets. In many specialized domains, for example in reading Optical Coherence Tomography Angiography (OCTA) images, such precise text with grounded description of pathologies is scarce or even non-existent. To overcome this bottleneck, we introduce Synthetic Vasculature Reasoning (SVR), a framework that controllably synthesizes images and corresponding text, specifically: realistic retinal vasculature with Diabetic Retinopathy (DR) features: capillary dropout, microaneurysms, neovascularization, and tortuosity, while automatically generating granular reasoning texts. Based on this we curate OCTA-100K-SVR, an OCTA image-reasoning dataset with 100,000 pairs. Our experiments show that a general-purpose VLM (Qwen3-VL-8b) trained on the dataset achieves a zero-shot balanced classification accuracy of 89.67% on real OCTA images, outperforming supervised baselines. Through human expert evaluation we also demonstrate that it significantly enhances explanation quality and pathology localization on clinical data.

cs.CV↗

The MICCAI Federated Tumor Segmentation (FeTS) Challenge 2024: Efficient and Robust Aggregation Methods for Federated Learning

We present the design and results of the MICCAI Federated Tumor Segmentation (FeTS) Challenge 2024, which focuses on federated learning (FL) for glioma sub-region segmentation in multi-parametric MRI and evaluates new weight aggregation methods aimed at improving robustness and efficiency. Six participating teams were evaluated using a standardized FL setup and a multi-institutional dataset derived from the BraTS glioma benchmark, consisting of 1,251 training cases, 219 validation cases, and 570 hidden test cases with segmentations for enhancing tumor (ET), tumor core (TC), and whole tumor (WT). Teams were ranked using a cumulative scoring system that considered both segmentation performance, measured by Dice Similarity Coefficient (DSC) and the 95th percentile Hausdorff Distance (HD95), and communication efficiency assessed through the convergence score. A PID-controller-based method achieved the top overall ranking, obtaining mean DSC values of 0.733, 0.761, and 0.751 for ET, TC, and WT, respectively, with corresponding HD95 values of 33.922 mm, 33.623 mm, and 32.309 mm, while also demonstrating the highest communication efficiency with a convergence score of 0.764. These findings advance the state of federated learning for medical imaging, surpassing top-performing methods from previous challenge iterations and highlighting PID controllers as effective mechanisms for stabilizing and optimizing weight aggregation in FL. The challenge code is available at https://github.com/FeTS-AI/Challenge.

cs.CV↗

Graph Conditioned Diffusion for Controllable Histopathology Image Generation

Recent advances in Diffusion Probabilistic Models (DPMs) have set new standards in high-quality image synthesis. Yet, controlled generation remains challenging, particularly in sensitive areas such as medical imaging. Medical images feature inherent structure such as consistent spatial arrangement, shape or texture, all of which are critical for diagnosis. However, existing DPMs operate in noisy latent spaces that lack semantic structure and strong priors, making it difficult to ensure meaningful control over generated content. To address this, we propose graph-based object-level representations for Graph-Conditioned-Diffusion. Our approach generates graph nodes corresponding to each major structure in the image, encapsulating their individual features and relationships. These graph representations are processed by a transformer module and integrated into a diffusion model via the text-conditioning mechanism, enabling fine-grained control over generation. We evaluate this approach using a real-world histopathology use case, demonstrating that our generated data can reliably substitute for annotated patient data in downstream segmentation tasks. The code is available here.

cs.CV↗

A Graph-Based Framework for Interpretable Whole Slide Image Analysis

The histopathological analysis of whole-slide images (WSIs) is fundamental to cancer diagnosis but is a time-consuming and expert-driven process. While deep learning methods show promising results, dominant patch-based methods artificially fragment tissue, ignore biological boundaries, and produce black-box predictions. We overcome these limitations with a novel framework that transforms gigapixel WSIs into biologically-informed graph representations and is interpretable by design. Our approach builds graph nodes from tissue regions that respect natural structures, not arbitrary grids. We introduce an adaptive graph coarsening technique, guided by learned embeddings, to efficiently merge homogeneous regions while preserving diagnostically critical details in heterogeneous areas. Each node is enriched with a compact, interpretable feature set capturing clinically-motivated priors. A graph attention network then performs diagnosis on this compact representation. We demonstrate strong performance on challenging cancer staging and survival prediction tasks. Crucially, our resource-efficient model ($>$13x fewer parameters and $>$300x less data) achieves results competitive with a massive foundation model, while offering full interpretability through feature attribution. Our code is publicly available at https://github.com/HistoGraph31/pix2pathology.

eess.IV↗

Fine-tuning Vision Language Models with Graph-based Knowledge for Explainable Medical Image Analysis

Accurate staging of Diabetic Retinopathy (DR) is essential for guiding timely interventions and preventing vision loss. However, current staging models are hardly interpretable, and most public datasets contain no clinical reasoning or interpretation beyond image-level labels. In this paper, we present a novel method that integrates graph representation learning with vision-language models (VLMs) to deliver explainable DR diagnosis. Our approach leverages optical coherence tomography angiography (OCTA) images by constructing biologically informed graphs that encode key retinal vascular features such as vessel morphology and spatial connectivity. A graph neural network (GNN) then performs DR staging while integrated gradients highlight critical nodes and edges and their individual features that drive the classification decisions. We collect this graph-based knowledge which attributes the model's prediction to physiological structures and their characteristics. We then transform it into textual descriptions for VLMs. We perform instruction-tuning with these textual descriptions and the corresponding image to train a student VLM. This final agent can classify the disease and explain its decision in a human interpretable way solely based on a single image input. Experimental evaluations on both proprietary and public datasets demonstrate that our method not only improves classification accuracy but also offers more clinically interpretable results. An expert study further demonstrates that our method provides more accurate diagnostic explanations and paves the way for precise localization of pathologies in OCTA images.

cs.CV↗