arXiv subjects

Dina Zemlyanker

Publications and source records attributed to Dina Zemlyanker.

6 recordsLinked to original sources

arXiv2026

Improving Neuropathological Reconstruction Fidelity via AI Slice Imputation

Neuropathological analyses benefit from spatially precise volumetric reconstructions that enhance anatomical delineation and improve morphometric accuracy. Our prior work has shown the feasibility of reconstructing 3D brain volumes from 2D dissection photographs. However these outputs sometimes exhibit coarse, overly smooth reconstructions of structures, especially under high anisotropy (i.e., reconstructions from thick slabs). Here, we introduce a computationally efficient super-resolution step that imputes slices to generate anatomically consistent isotropic volumes from anisotropic 3D reconstructions of dissection photographs. By training on domain-randomized synthetic data, we ensure that our method generalizes across dissection protocols and remains robust to large slab thicknesses. The imputed volumes yield improved automated segmentations, achieving higher Dice scores, particularly in cortical and white matter regions. Validation on surface reconstruction and atlas registration tasks demonstrates more accurate cortical surfaces and MRI registration. By enhancing the resolution and anatomical fidelity of photograph-based reconstructions, our approach strengthens the bridge between neuropathology and neuroimaging. Our method is publicly available at https://surfer.nmr.mgh.harvard.edu/fswiki/mri_3d_photo_recon

cs.CV↗

arXiv2025

Deep generative priors for 3D brain analysis

Diffusion models have recently emerged as powerful generative models in medical imaging. However, it remains a major challenge to combine these data-driven models with domain knowledge to guide brain imaging problems. In neuroimaging, Bayesian inverse problems have long provided a successful framework for inference tasks, where incorporating domain knowledge of the imaging process enables robust performance without requiring extensive training data. However, the anatomical modeling component of these approaches typically relies on classical mathematical priors that often fail to capture the complex structure of brain anatomy. In this work, we present the first general-purpose application of diffusion models as priors for solving a wide range of medical imaging inverse problems. Our approach leverages a score-based diffusion prior trained extensively on diverse brain MRI data, paired with flexible forward models that capture common image processing tasks such as super-resolution, bias field correction, inpainting, and combinations thereof. We further demonstrate how our framework can refine outputs from existing deep learning methods to improve anatomical fidelity. Experiments on heterogeneous clinical and research MRI data show that our method achieves state-of-the-art performance producing consistent, high-quality solutions without requiring paired training datasets. These results highlight the potential of diffusion priors as versatile tools for brain MRI analysis.

cs.CV↗

arXiv2025

Reference-Free 3D Reconstruction of Brain Dissection Slabs via Learned Atlas Coordinates

Correlation of neuropathology with MRI has the potential to transfer microscopic signatures of pathology to in vivo scans. There is increasing interest in building these correlations from 3D reconstructed stacks of slab photographs, which are routinely taken during dissection at brain banks. These photographs bypass the need for ex vivo MRI, which is not widely accessible. However, existing methods either require a corresponding 3D reference (e.g., an ex vivo MRI scans, or a brain surface acquired with a structured light scanner) or a full stack of brain slabs, which severely limits applicability. Here we propose RefFree, a 3D reconstruction method for dissection photographs that does not require an external reference. RefFree coherently reconstructs a 3D volume for an arbitrary set of slabs (including a single slab) using predicted 3D coordinates in the standard atlas space (MNI) as guidance. To support RefFree's pipeline, we train an atlas coordinate prediction network that estimates the coordinate map from a 2D photograph, using synthetic photographs generated from digitally sliced 3D MRI data with randomized appearance for enhanced generalization. As a by-product, RefFree can propagate information (e.g., anatomical labels) from atlas space to one single photograph even without reconstruction. Experiments on simulated and real data show that, when all slabs are available, RefFree achieves performance comparable to existing classical methods but at substantially higher speed. Moreover, RefFree yields accurate reconstruction and registration for partial stacks or even a single slab. Our code is available at https://github.com/lintian-a/reffree.

eess.IV↗

arXiv2025

Learning to Upscale 3D Segmentations in Neuroimaging

Obtaining high-resolution (HR) segmentations from coarse annotations is a pervasive challenge in computer vision. Applications include inferring pixel-level segmentations from token-level labels in vision transformers, upsampling coarse masks to full resolution, and transferring annotations from legacy low-resolution (LR) datasets to modern HR imagery. These challenges are especially acute in 3D neuroimaging, where manual labeling is costly and resolutions continually increase. We propose a scalable framework that generalizes across resolutions and domains by regressing signed distance maps, enabling smooth, boundary-aware supervision. Crucially, our model predicts one class at a time, which substantially reduces memory usage during training and inference (critical for large 3D volumes) and naturally supports generalization to unseen classes. Generalization is further improved through training on synthetic, domain-randomized data. We validate our approach on ultra-high-resolution (UHR) human brain MRI (~100 μm), where most existing methods operate at 1 mm resolution. Our framework effectively upsamples such standard-resolution segmentations to UHR detail. Results on synthetic and real data demonstrate superior scalability and generalization compared to conventional segmentation methods. Code is available at: https://github.com/HuXiaoling/Learn2Upscale.

cs.CV↗

arXiv2025

Automated Segmentation of Coronal Brain Tissue Slabs for 3D Neuropathology

Advances in image registration and machine learning have recently enabled volumetric analysis of postmortem brain tissue from conventional photographs of coronal slabs, which are routinely collected in brain banks and neuropathology laboratories worldwide. One caveat of this methodology is the requirement of segmentation of the tissue from photographs, which currently requires costly manual intervention. In this article, we present a deep learning model to automate this process. The automatic segmentation tool relies on a U-Net architecture that was trained with a combination of 1,414 manually segmented images of both fixed and fresh tissue, from specimens with varying diagnoses, photographed at two different sites. Automated model predictions on a subset of photographs not seen in training were analyzed to estimate performance compared to manual labels, including both inter- and intra-rater variability. Our model achieved a median Dice score over 0.98, mean surface distance under 0.4mm, and 95\% Hausdorff distance under 1.60mm, which approaches inter-/intra-rater levels. Our tool is publicly available at surfer.nmr.mgh.harvard.edu/fswiki/PhotoTools.

cs.CV↗

arXiv2025

From Low Field to High Value: Robust Cortical Mapping from Low-Field MRI

Three-dimensional reconstruction of cortical surfaces from MRI for morphometric analysis is fundamental for understanding brain structure. While high-field MRI (HF-MRI) is standard in research and clinical settings, its limited availability hinders widespread use. Low-field MRI (LF-MRI), particularly portable systems, offers a cost-effective and accessible alternative. However, existing cortical surface analysis tools are optimized for high-resolution HF-MRI and struggle with the lower signal-to-noise ratio and resolution of LF-MRI. In this work, we present a machine learning method for 3D reconstruction and analysis of portable LF-MRI across a range of contrasts and resolutions. Our method works "out of the box" without retraining. It uses a 3D U-Net trained on synthetic LF-MRI to predict signed distance functions of cortical surfaces, followed by geometric processing to ensure topological accuracy. We evaluate our method using paired HF/LF-MRI scans of the same subjects, showing that LF-MRI surface reconstruction accuracy depends on acquisition parameters, including contrast type (T1 vs T2), orientation (axial vs isotropic), and resolution. A 3mm isotropic T2-weighted scan acquired in under 4 minutes, yields strong agreement with HF-derived surfaces: surface area correlates at r=0.96, cortical parcellations reach Dice=0.98, and gray matter volume achieves r=0.93. Cortical thickness remains more challenging with correlations up to r=0.70, reflecting the difficulty of sub-mm precision with 3mm voxels. We further validate our method on challenging postmortem LF-MRI, demonstrating its robustness. Our method represents a step toward enabling cortical surface analysis on portable LF-MRI. Code is available at https://surfer.nmr.mgh.harvard.edu/fswiki/ReconAny

cs.CV↗