Diffusion-weighted MRI (dMRI) is increasingly used to study the normal and abnormal development of fetal brain in-utero. It offers invaluable insights into the neurodevelopmental processes in the fetal stage. However, 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, 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. 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. Further validation on independent external data shows generalizability of the proposed method. The new method can help advance the field of fetal neuroimaging as it can lead to substantial improvements in fetal brain tractography, tract-specific analysis, and structural connectivity assessment.

The interpretation and analysis of Magnetic resonance imaging (MRI) benefit from high spatial resolution. Unfortunately, direct acquisition of high spatial resolution MRI is time-consuming and costly, which increases the potential for motion artifact, and suffers from reduced signal-to-noise ratio (SNR). Super-resolution reconstruction (SRR) is one of the most widely used methods in MRI since it allows for the trade-off between high spatial resolution, high SNR, and reduced scan times. Deep learning has emerged for improved SRR as compared to conventional methods. However, current deep learning-based SRR methods require large-scale training datasets of high-resolution images, which are practically difficult to obtain at a suitable SNR. We sought to develop a methodology that allows for dataset-free deep learning-based SRR, through which to construct images with higher spatial resolution and of higher SNR than can be practically obtained by direct Fourier encoding. We developed a dataset-free learning method that leverages a generative neural network trained for each specific scan or set of scans, which in turn, allows for SRR tailored to the individual patient. With the SRR from three short duration scans, we achieved high quality brain MRI at an isotropic spatial resolution of 0.125 cubic mm with six minutes of imaging time for T2 contrast and an average increase of 7.2 dB (34.2%) in SNR to these short duration scans. Motion compensation was achieved by aligning the three short duration scans together. We assessed our technique on simulated MRI data and clinical data acquired from 15 subjects. Extensive experimental results demonstrate that our approach achieved superior results to state-of-the-art methods, while in parallel, performed at reduced cost as scans delivered with direct high-resolution acquisition.