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Hwihun Jeong

Hwihun Jeong contributes to research discovery and scholarly infrastructure.

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Published work

3 published item(s)

preprint2026arXiv

A Target-Free Harmonization Method for MRI

In MRI, variations in scan parameters, sequence, or hardware can lead to discrepancies in image appearance, even for the same subject. These inconsistencies, known as domain shifts, can hinder image analysis and degrade the performance of deep learning models trained on data from specific target domains. MRI image harmonization aims to address these issues by aligning source domain images to the target domain images while preserving biological information such as anatomical structures. However, most existing harmonization approaches require access to both source and target domain data in training or test time. This dependence induces data sharing between institutions, raising concerns about patient privacy and substantially limiting the harmonization approaches that can be practically deployed in clinical settings. To overcome these limitations, we introduce TgtFreeHarmony, the harmonization framework tailored for target-free scenarios, eliminating the need for target domain data and any data sharing, enabling privacy-preserving harmonization directly within the source institution. Our approach estimates the target domain style by searching the manifold of MRI domain style constructed via a disentanglement-based generator using Bayesian optimization guided by the performance of a downstream task model, which is trained on target domain data. We evaluated our method on the brain tissue segmentation task across multiple institutes and demonstrated that it effectively harmonizes source images into target images, leading to improved downstream task performance. By enabling harmonization without any access to target-domain data, TgtFreeHarmony establishes a new direction of harmonization preserving data privacy that can be realistically deployed within clinical environments.

preprint2026arXiv

Longitudinal QSM: Enhancing consistency of multiple time point susceptibility maps via simultaneous reconstruction

Quantitative susceptibility mapping (QSM) has been increasingly applied in longitudinal studies of neurodegenerative diseases and aging to assess temporal alterations in brain iron and myelin. The accuracy of such investigations depends on the repeatability and sensitivity of measurements. However, the ill-posed nature of the QSM processing steps makes the reconstruction vulnerable to background field changes, head orientation changes, noise, and imperfect registration, which compromise repeatability and sensitivity and hinder reliable detection of true changes. To address these limitations, we propose Longitudinal QSM, a simultaneous reconstruction framework that jointly estimates susceptibility maps across time points while enforcing spatial sparsity of temporal changes. The method was evaluated through simulations and in-vivo experiments and compared with conventional reconstruction methods. Longitudinal QSM consistently reduced inter-scan variability and accurately recovered simulated lesion changes. Application to stroke patient and multiple sclerosis patient data further demonstrated that the framework stabilizes non-lesion variability while preserving lesion-related temporal changes. This approach offers a promising tool for monitoring subtle temporal changes in brain iron and myelin in various neurodegenerative diseases as well as throughout aging and development.

preprint2020arXiv

A geometric approach to separate the effects of magnetic susceptibility and chemical shift/exchange in a phantom with isotropic magnetic susceptibility

Purpose: To separate the effects of magnetic susceptibility and chemical shift/exchange in a phantom with isotropic magnetic susceptibility. To generate a chemical shift/exchange-corrected quantitative susceptibility mapping (QSM) result. Theory and Methods: Magnetic susceptibility and chemical shift/exchange are the properties of a material. Both are known to induce the resonance frequency shift in MRI. In current QSM, the susceptibility is reconstructed from the frequency shift, ignoring the contribution of the chemical shift/exchange. In this work, a simple geometric approach, which averages the frequency shift maps from three orthogonal B0 directions to generate a chemical shift/exchange map, is developed using the fact that the average nullifies the (isotropic) susceptibility effects. The resulting chemical shift/exchange map is subtracted from the total frequency shift, producing a frequency shift map solely from susceptibility. Finally, this frequency shift map is reconstructed to a susceptibility map using a QSM algorithm. The proposed method is validated in numerical simulations and applied to phantom experiments with olive oil, bovine serum albumin, ferritin, and iron oxide solutions. Results: Both simulations and experiments confirm that the method successfully separates the contributions of the susceptibility and chemical shift/exchange, reporting the susceptibility and chemical shift/exchange of olive oil (susceptibility: 0.62 ppm, chemical shift: -3.60 ppm), bovine serum albumin (susceptibility: -0.059 ppm, chemical shift: 0.008 ppm), ferritin (susceptibility: 0.125 ppm, chemical shift: -0.005 ppm), and iron oxide (susceptibility: 0.30 ppm, chemical shift: -0.039 ppm) solutions. Conclusion: The proposed method successfully separates the susceptibility and chemical shift/exchange in phantoms with isotropic magnetic susceptibility.