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Ali Gholipour

Publications and source records attributed to Ali Gholipour.

At least 19 recordsLinked to original sources

An MRI Atlas of the Human Fetal Brain: Reference and Segmentation Tools for Fetal Brain MRI Analysis

Characterizing in-utero brain development is essential for understanding typical and atypical neurodevelopment. Building on prior spatiotemporal fetal brain MRI atlases, we present the CRL-2025 fetal brain atlas, a spatiotemporal (4D) atlas of the developing fetal brain between 21 and 37 gestational weeks. This atlas is constructed from MRI scans of 159 fetuses with typically developing brains using a diffeomorphic deformable registration framework integrated with kernel regression on age. CRL-2025 uniquely includes detailed tissue segmentations, transient white matter compartments, and parcellation into 126 anatomical regions. It offers significantly enhanced anatomical details over the CRL-2017 atlas and is presented along with a re-release of the CRL diffusion MRI atlas featuring newly created tissue segmentation and labels. We release de-identified, processed subject-level fetal MRI datasets used to generate CRL-2025, providing input-output transparency and reproducibility. We also provide FetalSEG, a deep learning-based multiclass segmentation tool to facilitate automatic fetal brain MRI segmentation. The CRL-2025 atlas and its tools enable scalable fetal brain MRI segmentation, analysis, and neurodevelopmental research for the broader community.

q-bio.QM

Harmonization in Magnetic Resonance Imaging: A Survey of Acquisition, Image-level, and Feature-level Methods

Magnetic resonance imaging (MRI) has greatly advanced neuroscience research and clinical diagnostics. However, imaging data collected across different scanners, acquisition protocols, or imaging sites often exhibit substantial heterogeneity, known as batch effects or site effects. These non-biological sources of variability can obscure true biological signals, reduce reproducibility and statistical power, and severely impair the generalizability of learning-based models across datasets. Image harmonization is grounded in the central hypothesis that site-related biases can be eliminated or mitigated while preserving meaningful biological information, thereby improving data comparability and consistency. This review provides a comprehensive overview of key concepts, methodological advances, publicly available datasets, and evaluation metrics in the field of MRI harmonization. We systematically cover the full imaging pipeline and categorize harmonization approaches into prospective acquisition and reconstruction, retrospective image-level and feature-level methods, and traveling-subject-based techniques. By synthesizing existing methods and evidence, we revisit the central hypothesis of image harmonization and show that, although site invariance can be achieved with current techniques, further evaluation is required to verify the preservation of biological information. To this end, we summarize the remaining challenges and highlight key directions for future research, including the need for standardized validation benchmarks, improved evaluation strategies, and tighter integration of harmonization methods across the imaging pipeline.

eess.IV

Rapid, High-resolution and Distortion-free $R_{2}^{*}$ Mapping of Fetal Brain using Multi-echo Radial FLASH and Model-based Reconstruction

Purpose: To develop a rapid, high-resolution and distortion-free technique for simultaneous water-fat separation, $R_{2}^{*}$ and $B_{0}$ mapping of the fetal brain at 3T. Methods: A 2D multi-echo radial FLASH sequence with blip gradients is adapted for data acquisition during maternal free breathing. A calibrationless model-based reconstruction with sparsity constraints is developed to jointly estimate water, fat, $R_{2}^{*}$ and $B_{0}$ field maps directly from k-space. This approach was validated and compared to reference methods using numerical and NIST phantoms and data from nine fetuses between 26 and 36 weeks of gestation age. Results: Both numerical and experimental phantom studies confirm good accuracy and precision. In fetal studies, model-based reconstruction yields quantitative $R_{2}^{*}$ values in close agreement with those from a parallel imaging compressed sensing (PICS) technique using Graph Cut (intra-class correlation coefficient [ICC] = 0.9601), while providing enhanced image detail. Repeated scans confirm good reproducibility (ICC = 0.9213). Compared to multi-echo EPI, the proposed radial technique produces higher-resolution (1.1 $\times$ 1.1 $\times$ 3 mm$^{3}$ vs. 2-3 $\times$ 2-3 $\times$ 3 mm$^{3}$) $R_{2}^{*}$ maps with reduced distortion. Despite of differences in motion, resolution and distortion, $R_{2}^{*}$ values are comparable between the two acquisition strategies (ICC = 0.8049). Additionally, the proposed approach enables synthesis of high-resolution and distortion-free $R_{2}^{*}$-weighted images. Conclusion: This study demonstrates the feasibility of using multi-echo radial FLASH combined with calibrationless model-based reconstruction for motion-robust, distortion-free $R_{2}^{*}$ mapping of the fetal brain at 3T, achieving a nominal resolution of $1.1 \times 1.1 \times 3$ mm$^{3}$ within 2 seconds per slice.

physics.med-ph

A Unified Deep Learning Framework for Motion Correction in Medical Imaging

Deep learning has shown significant value in medical image registration for motion correction, however, current techniques are either limited by the type and range of motion they can handle, or require iterative inference and/or retraining for new imaging data. To address these limitations, we introduce UniMo, a Unified Motion Correction framework that leverages deep neural networks to correct for various types of motion in medical imaging. UniMo exploits an alternating optimization scheme for a unified loss function to train an integrated model of 1) an equivariant neural network for global rigid motion correction and 2) an encoder-decoder network to correct local deformations. It features a geometric deformation augmenter that 1) enhances the robustness of global motion correction by addressing any local deformations, and 2) generates augmented data to improve the training process. UniMo is a hybrid model that uses both image intensities and shapes to achieve robust performance amid image appearance variations, and, therefore, it generalizes well to various medical imaging modalities without a need for network retraining. We trained and tested UniMo to track motion in fetal magnetic resonance imaging. Then we tested the trained model, without retraining, on various image modalities from three public datasets, including MedMNIST, lung CT, and BraTS. The results show that UniMo surpassed existing motion correction methods in terms of accuracy, and, notably, it enabled one-time training on a single modality while maintaining high stability and adaptability for inference across multiple unseen imaging datasets. By offering a unified solution, UniMo marks a significant advantage in challenging applications with a mixture of bulk motion and local deformations. https://github.com/IntelligentImaging/UNIMO

eess.IV

Detailed delineation of the fetal brain in diffusion MRI via multi-task learning

Diffusion-weighted MRI is increasingly used to study the normal and abnormal development of fetal brain in-utero. Recent studies have shown that dMRI can offer invaluable insights into the neurodevelopmental processes in the fetal stage. However, because of the low data quality and rapid brain development, reliable analysis of fetal dMRI data requires dedicated computational methods that are currently unavailable. The lack of automated methods for fast, accurate, and reproducible data analysis has seriously limited our ability to tap the potential of fetal brain dMRI for medical and scientific applications. In this work, we developed and validated a unified computational framework to (1) segment the brain tissue into white matter, cortical/subcortical gray matter, and cerebrospinal fluid, (2) segment 31 distinct white matter tracts, and (3) parcellate the brain's cortex and delineate the deep gray nuclei and white matter structures into 96 anatomically meaningful regions. We utilized a set of manual, semi-automatic, and automatic approaches to annotate 97 fetal brains. Using these labels, we developed and validated a multi-task deep learning method to perform the three computations. Our evaluations show that the new method can accurately carry out all three tasks, achieving a mean Dice similarity coefficient of 0.865 on tissue segmentation, 0.825 on white matter tract segmentation, and 0.819 on parcellation. The proposed method can greatly advance the field of fetal neuroimaging as it can lead to substantial improvements in fetal brain tractography, tract-specific analysis, and structural connectivity assessment.

eess.IV

Ground-truth effects in learning-based fiber orientation distribution estimation in neonatal brains

Diffusion Magnetic Resonance Imaging (dMRI) is a non-invasive method for depicting brain microstructure in vivo. Fiber orientation distributions (FODs) are mathematical representations extensively used to map white matter fiber configurations. Recently, FOD estimation with deep neural networks has seen growing success, in particular, those of neonates estimated with fewer diffusion measurements. These methods are mostly trained on target FODs reconstructed with multi-shell multi-tissue constrained spherical deconvolution (MSMT-CSD), which might not be the ideal ground truth for developing brains. Here, we investigate this hypothesis by training a state-of-the-art model based on the U-Net architecture on both MSMT-CSD and single-shell three-tissue constrained spherical deconvolution (SS3T-CSD). Our results suggest that SS3T-CSD might be more suited for neonatal brains, given that the ratio between single and multiple fiber-estimated voxels with SS3T-CSD is more realistic compared to MSMT-CSD. Additionally, increasing the number of input gradient directions significantly improves performance with SS3T-CSD over MSMT-CSD. Finally, in an age domain-shift setting, SS3T-CSD maintains robust performance across age groups, indicating its potential for more accurate neonatal brain imaging.

eess.IV

Diffusion Tensor Estimation with Uncertainty Calibration

It is highly desirable to know how uncertain a model's predictions are, especially for models that are complex and hard to understand as in deep learning. Although there has been a growing interest in using deep learning methods in diffusion-weighted MRI, prior works have not addressed the issue of model uncertainty. Here, we propose a deep learning method to estimate the diffusion tensor and compute the estimation uncertainty. Data-dependent uncertainty is computed directly by the network and learned via loss attenuation. Model uncertainty is computed using Monte Carlo dropout. We also propose a new method for evaluating the quality of predicted uncertainties. We compare the new method with the standard least-squares tensor estimation and bootstrap-based uncertainty computation techniques. Our experiments show that when the number of measurements is small the deep learning method is more accurate and its uncertainty predictions are better calibrated than the standard methods. We show that the estimation uncertainties computed by the new method can highlight the model's biases, detect domain shift, and reflect the strength of noise in the measurements. Our study shows the importance and practical value of modeling prediction uncertainties in deep learning-based diffusion MRI analysis.

cs.LG

Cross-Age and Cross-Site Domain Shift Impacts on Deep Learning-Based White Matter Fiber Estimation in Newborn and Baby Brains

Deep learning models have shown great promise in estimating tissue microstructure from limited diffusion magnetic resonance imaging data. However, these models face domain shift challenges when test and train data are from different scanners and protocols, or when the models are applied to data with inherent variations such as the developing brains of infants and children scanned at various ages. Several techniques have been proposed to address some of these challenges, such as data harmonization or domain adaptation in the adult brain. However, those techniques remain unexplored for the estimation of fiber orientation distribution functions in the rapidly developing brains of infants. In this work, we extensively investigate the age effect and domain shift within and across two different cohorts of 201 newborns and 165 babies using the Method of Moments and fine-tuning strategies. Our results show that reduced variations in the microstructural development of babies in comparison to newborns directly impact the deep learning models' cross-age performance. We also demonstrate that a small number of target domain samples can significantly mitigate domain shift problems.

eess.IV

SpaER: Learning Spatio-temporal Equivariant Representations for Fetal Brain Motion Tracking

In this paper, we introduce SpaER, a pioneering method for fetal motion tracking that leverages equivariant filters and self-attention mechanisms to effectively learn spatio-temporal representations. Different from conventional approaches that statically estimate fetal brain motions from pairs of images, our method dynamically tracks the rigid movement patterns of the fetal head across temporal and spatial dimensions. Specifically, we first develop an equivariant neural network that efficiently learns rigid motion sequences through low-dimensional spatial representations of images. Subsequently, we learn spatio-temporal representations by incorporating time encoding and self-attention neural network layers. This approach allows for the capture of long-term dependencies of fetal brain motion and addresses alignment errors due to contrast changes and severe motion artifacts. Our model also provides a geometric deformation estimation that properly addresses image distortions among all time frames. To the best of our knowledge, our approach is the first to learn spatial-temporal representations via deep neural networks for fetal motion tracking without data augmentation. We validated our model using real fetal echo-planar images with simulated and real motions. Our method carries significant potential value in accurately measuring, tracking, and correcting fetal motion in fetal MRI sequences.

eess.IV

White matter tract crossing and bottleneck regions in the fetal brain

There is a growing interest in using diffusion MRI to study the white matter tracts and structural connectivity of the fetal brain. Recent progress in data acquisition and processing suggests that this imaging modality has a unique role in elucidating the normal and abnormal patterns of neurodevelopment in utero. However, there have been no efforts to quantify the prevalence of crossing tracts and bottleneck regions, important issues that have been extensively researched for adult brains. In this work, we determined the brain regions with crossing tracts and bottlenecks between 23 and 36 gestational weeks. We performed probabilistic tractography on 59 fetal brain scans and extracted a set of 51 distinct white tracts, which we grouped into 10 major tract bundle groups. We analyzed the results to determine the patterns of tract crossings and bottlenecks. Our results showed that 20-25% of the white matter voxels included two or three crossing tracts. Bottlenecks were more prevalent. Between 75-80% of the voxels were characterized as bottlenecks, with more than 40% of the voxels involving four or more tracts. The results of this study highlight the challenge of fetal brain tractography and structural connectivity assessment and call for innovative image acquisition and analysis methods to mitigate these problems.

q-bio.NC

HAITCH: A Framework for Distortion and Motion Correction in Fetal Multi-Shell Diffusion-Weighted MRI

Diffusion magnetic resonance imaging (dMRI) is pivotal for probing the microstructure of the rapidly-developing fetal brain. However, fetal motion during scans and its interaction with magnetic field inhomogeneities result in artifacts and data scattering across spatial and angular domains. The effects of those artifacts are more pronounced in high-angular resolution fetal dMRI, where signal-to-noise ratio is very low. Those effects lead to biased estimates and compromise the consistency and reliability of dMRI analysis. This work presents HAITCH, the first and the only publicly available tool to correct and reconstruct multi-shell high-angular resolution fetal dMRI data. HAITCH offers several technical advances that include a blip-reversed dual-echo acquisition for dynamic distortion correction, advanced motion correction for model-free and robust reconstruction, optimized multi-shell design for enhanced information capture and increased tolerance to motion, and outlier detection for improved reconstruction fidelity. The framework is open-source, flexible, and can be used to process any type of fetal dMRI data including single-echo or single-shell acquisitions, but is most effective when used with multi-shell multi-echo fetal dMRI data that cannot be processed with any of the existing tools. Validation experiments on real fetal dMRI scans demonstrate significant improvements and accurate correction across diverse fetal ages and motion levels. HAITCH successfully removes artifacts and reconstructs high-fidelity fetal dMRI data suitable for advanced diffusion modeling, including fiber orientation distribution function estimation. These advancements pave the way for more reliable analysis of the fetal brain microstructure and tractography under challenging imaging conditions.

physics.med-ph

Anatomically Constrained Tractography of the Fetal Brain

Diffusion-weighted Magnetic Resonance Imaging (dMRI) is increasingly used to study the fetal brain in utero. An important computation enabled by dMRI is streamline tractography, which has unique applications such as tract-specific analysis of the brain white matter and structural connectivity assessment. However, due to the low fetal dMRI data quality and the challenging nature of tractography, existing methods tend to produce highly inaccurate results. They generate many false streamlines while failing to reconstruct streamlines that constitute the major white matter tracts. In this paper, we advocate for anatomically constrained tractography based on an accurate segmentation of the fetal brain tissue directly in the dMRI space. We develop a deep learning method to compute the segmentation automatically. Experiments on independent test data show that this method can accurately segment the fetal brain tissue and drastically improve tractography results. It enables the reconstruction of highly curved tracts such as optic radiations. Importantly, our method infers the tissue segmentation and streamline propagation direction from a diffusion tensor fit to the dMRI data, making it applicable to routine fetal dMRI scans. The proposed method can lead to significant improvements in the accuracy and reproducibility of quantitative assessment of the fetal brain with dMRI.

cs.CV

Fetal-BET: Brain Extraction Tool for Fetal MRI

Fetal brain extraction is a necessary first step in most computational fetal brain MRI pipelines. However, it has been a very challenging task due to non-standard fetal head pose, fetal movements during examination, and vastly heterogeneous appearance of the developing fetal brain and the neighboring fetal and maternal anatomy across various sequences and scanning conditions. Development of a machine learning method to effectively address this task requires a large and rich labeled dataset that has not been previously available. As a result, there is currently no method for accurate fetal brain extraction on various fetal MRI sequences. In this work, we first built a large annotated dataset of approximately 72,000 2D fetal brain MRI images. Our dataset covers the three common MRI sequences including T2-weighted, diffusion-weighted, and functional MRI acquired with different scanners. Moreover, it includes normal and pathological brains. Using this dataset, we developed and validated deep learning methods, by exploiting the power of the U-Net style architectures, the attention mechanism, multi-contrast feature learning, and data augmentation for fast, accurate, and generalizable automatic fetal brain extraction. Our approach leverages the rich information from multi-contrast (multi-sequence) fetal MRI data, enabling precise delineation of the fetal brain structures. Evaluations on independent test data show that our method achieves accurate brain extraction on heterogeneous test data acquired with different scanners, on pathological brains, and at various gestational stages. This robustness underscores the potential utility of our deep learning model for fetal brain imaging and image analysis.

eess.IV

Characterizing normal perinatal development of the human brain structural connectivity

Early brain development is characterized by the formation of a highly organized structural connectome. The interconnected nature of this connectome underlies the brain's cognitive abilities and influences its response to diseases and environmental factors. Hence, quantitative assessment of structural connectivity in the perinatal stage is useful for studying normal and abnormal neurodevelopment. However, estimation of the connectome from diffusion MRI data involves complex computations. For the perinatal period, these computations are further challenged by the rapid brain development and imaging difficulties. Combined with high inter-subject variability, these factors make it difficult to chart the normal development of the structural connectome. As a result, there is a lack of reliable normative baselines of structural connectivity metrics at this critical stage in brain development. In this study, we developed a computational framework, based on spatio-temporal averaging, for determining such baselines. We used this framework to analyze the structural connectivity between 33 and 44 postmenstrual weeks using data from 166 subjects. Our results unveiled clear and strong trends in the development of structural connectivity in perinatal stage. Connection weighting based on fractional anisotropy and neurite density produced the most consistent results. We observed increases in global and local efficiency, a decrease in characteristic path length, and widespread strengthening of the connections within and across brain lobes and hemispheres. We also observed asymmetry patterns that were consistent between different connection weighting approaches. The new computational method and results are useful for assessing normal and abnormal development of the structural connectome early in life.

q-bio.NC

TBSS++: A novel computational method for Tract-Based Spatial Statistics

Diffusion-weighted magnetic resonance imaging (dMRI) is widely used to assess the brain white matter. One of the most common computations in dMRI involves cross-subject tract-specific analysis, whereby dMRI-derived biomarkers are compared between cohorts of subjects. The accuracy and reliability of these studies hinges on the ability to compare precisely the same white matter tracts across subjects. This is an intricate and error-prone computation. Existing computational methods such as Tract-Based Spatial Statistics (TBSS) suffer from a host of shortcomings and limitations that can seriously undermine the validity of the results. We present a new computational framework that overcomes the limitations of existing methods via (i) accurate segmentation of the tracts, and (ii) precise registration of data from different subjects/scans. The registration is based on fiber orientation distributions. To further improve the alignment of cross-subject data, we create detailed atlases of white matter tracts. These atlases serve as an unbiased reference space where the data from all subjects is registered for comparison. Extensive evaluations show that, compared with TBSS, our proposed framework offers significantly higher reproducibility and robustness to data perturbations. Our method promises a drastic improvement in accuracy and reproducibility of cross-subject dMRI studies that are routinely used in neuroscience and medical research.

eess.IV

Direct segmentation of brain white matter tracts in diffusion MRI

The brain white matter consists of a set of tracts that connect distinct regions of the brain. Segmentation of these tracts is often needed for clinical and research studies. Diffusion-weighted MRI offers unique contrast to delineate these tracts. However, existing segmentation methods rely on intermediate computations such as tractography or estimation of fiber orientation density. These intermediate computations, in turn, entail complex computations that can result in unnecessary errors. Moreover, these intermediate computations often require dense multi-shell measurements that are unavailable in many clinical and research applications. As a result, current methods suffer from low accuracy and poor generalizability. Here, we propose a new deep learning method that segments these tracts directly from the diffusion MRI data, thereby sidestepping the intermediate computation errors. Our experiments show that this method can achieve segmentation accuracy that is on par with the state of the art methods (mean Dice Similarity Coefficient of 0.826). Compared with the state of the art, our method offers far superior generalizability to undersampled data that are typical of clinical studies and to data obtained with different acquisition protocols. Moreover, we propose a new method for detecting inaccurate segmentations and show that it is more accurate than standard methods that are based on estimation uncertainty quantification. The new methods can serve many critically important clinical and scientific applications that require accurate and reliable non-invasive segmentation of white matter tracts.

eess.IV

3D Brainformer: 3D Fusion Transformer for Brain Tumor Segmentation

Magnetic resonance imaging (MRI) is critically important for brain mapping in both scientific research and clinical studies. Precise segmentation of brain tumors facilitates clinical diagnosis, evaluations, and surgical planning. Deep learning has recently emerged to improve brain tumor segmentation and achieved impressive results. Convolutional architectures are widely used to implement those neural networks. By the nature of limited receptive fields, however, those architectures are subject to representing long-range spatial dependencies of the voxel intensities in MRI images. Transformers have been leveraged recently to address the above limitations of convolutional networks. Unfortunately, the majority of current Transformers-based methods in segmentation are performed with 2D MRI slices, instead of 3D volumes. Moreover, it is difficult to incorporate the structures between layers because each head is calculated independently in the Multi-Head Self-Attention mechanism (MHSA). In this work, we proposed a 3D Transformer-based segmentation approach. We developed a Fusion-Head Self-Attention mechanism (FHSA) to combine each attention head through attention logic and weight mapping, for the exploration of the long-range spatial dependencies in 3D MRI images. We implemented a plug-and-play self-attention module, named the Infinite Deformable Fusion Transformer Module (IDFTM), to extract features on any deformable feature maps. We applied our approach to the task of brain tumor segmentation, and assessed it on the public BRATS datasets. The experimental results demonstrated that our proposed approach achieved superior performance, in comparison to several state-of-the-art segmentation methods.

eess.IV

Learning to segment fetal brain tissue from noisy annotations

Automatic fetal brain tissue segmentation can enhance the quantitative assessment of brain development at this critical stage. Deep learning methods represent the state of the art in medical image segmentation and have also achieved impressive results in brain segmentation. However, effective training of a deep learning model to perform this task requires a large number of training images to represent the rapid development of the transient fetal brain structures. On the other hand, manual multi-label segmentation of a large number of 3D images is prohibitive. To address this challenge, we segmented 272 training images, covering 19-39 gestational weeks, using an automatic multi-atlas segmentation strategy based on deformable registration and probabilistic atlas fusion, and manually corrected large errors in those segmentations. Since this process generated a large training dataset with noisy segmentations, we developed a novel label smoothing procedure and a loss function to train a deep learning model with smoothed noisy segmentations. Our proposed methods properly account for the uncertainty in tissue boundaries. We evaluated our method on 23 manually-segmented test images of a separate set of fetuses. Results show that our method achieves an average Dice similarity coefficient of 0.893 and 0.916 for the transient structures of younger and older fetuses, respectively. Our method generated results that were significantly more accurate than several state-of-the-art methods including nnU-Net that achieved the closest results to our method. Our trained model can serve as a valuable tool to enhance the accuracy and reproducibility of fetal brain analysis in MRI.

eess.IV