Jia Guo

Jia Guo

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 September 2023 in Scientific Reports
Verified
Journal Article
Open access
PDF file
JZJunhao Zhang
Junhao Zhang
VRVishwanatha M. Rao
Vishwanatha M. Rao
YTYe Tian
Ye Tian
YYYanting Yang
Yanting Yang
NANicolas Acosta
Nicolas Acosta
JGJia Guo
Jia Guo
Schizophrenia is a chronic neuropsychiatric disorder that causes distinct structural alterations within the brain. We hypothesize that deep learning applied to a structural neuroimaging dataset could detect disease-related alteration and improve classification and diagnostic accuracy. We tested this hypothesis using a single, widely available, and conventional T1-weighted MRI scan, from which we extracted the 3D whole-brain structure using standard post-processing methods. A deep learning model was then developed, optimized, and evaluated on three open datasets with T1-weighted MRI scans of patients with schizophrenia. Our proposed model outperformed the benchmark model, which was also trained with structural MR images using a 3D CNN architecture. Our model is capable of almost perfectly (area under the ROC curve = 0.987) distinguishing schizophrenia patients from healthy controls on unseen structural MRI scans. Regional analysis localized subcortical regions and ventricles as the most predictive brain regions. Subcortical structures serve a pivotal role in cognitive, affective, and social functions in humans, and structural abnormalities of these regions have been associated with schizophrenia. Our finding corroborates that schizophrenia is associated with widespread alterations in subcortical brain structure and the subcortical structural information provides prominent features in diagnostic classification. Together, these results further demonstrate the potential of deep learning to improve schizophrenia diagnosis and identify its structural neuroimaging signatures from a single, standard T1-weighted brain MRI.

8 June 2023
Verified
Book Chapter
Closed access
PDF file
JYJee Seok Yoon
Jee Seok Yoon
CZChenghao Zhang
Chenghao Zhang
HSHeung-Il Suk
Heung-Il Suk
JGJia Guo
Jia Guo
XLXiaoxiao Li
Xiaoxiao Li

29 July 2020 in PLOS ONE
Verified
Journal Article
Open access
PDF file
XFXinyang Feng
Xinyang Feng
JGJia Guo
Jia Guo
HSHannah C. Sigmon
Hannah C. Sigmon
RSRichard P. Sloan
Richard P. Sloan
ABAdam M. Brickman
Adam M. Brickman
FIFor The Alzheimer’s Disease Neuroimaging Initiative
For The Alzheimer’s Disease Neuroimaging Initiative
‘Normal aging’ in the brain refers to age-related changes that occur independent of disease, in particular Alzheimer’s disease. A major barrier to mapping normal brain aging has been the difficulty in excluding the earliest preclinical stages of Alzheimer’s disease. Here, before addressing this issue we first imaged a mouse model and learn that the best MRI measure of dendritic spine loss, a known pathophysiological driver of normal aging, is one that relies on the combined use of functional and structural MRI. In the primary study, we then deployed the combined functional-structural MRI measure to investigate over 100 cognitively-normal people from 20–72 years of age. Next, to cover the tail end of aging, in secondary analyses we investigated structural MRI acquired from cognitively-normal people, 60–84 years of age, who were Alzheimer’s-free via biomarkers. Collectively, the results from the primary functional-structural study, and the secondary structural studies revealed that the dentate gyrus is a hippocampal region differentially affected by aging, and that the entorhinal cortex is a region most resistant to aging. Across the cortex, the primary functional-structural study revealed and that the inferior frontal gyrus is differentially affected by aging, however, the secondary structural studies implicated other frontal cortex regions. Together, the results clarify how normal aging may affect the brain and has possible mechanistic and therapeutic implications.

13 September 2022 in Journal of Clinical Medicine
Verified
Journal Article
Open access
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YGYingwei Guo
Yingwei Guo
Yang YingjianYang Yingjian
Yang Yingjian
FCFengqiu Cao
Fengqiu Cao
MWMingming Wang
Mingming Wang
Yu LuoYu Luo
Yu Luo
YKYan Kang
Yan Kang
Background: The ability to accurately detect ischemic stroke and predict its neurological recovery is of great clinical value. This study intended to evaluate the performance of whole-brain dynamic radiomics features (DRF) for ischemic stroke detection, neurological impairment assessment, and outcome prediction. Methods: The supervised feature selection (Lasso) and unsupervised feature-selection methods (five-feature dimension-reduction algorithms) were used to generate four experimental groups with DRF in different combinations. Ten machine learning models were used to evaluate their performance by ten-fold cross-validation. Results: In experimental group_A, the best AUCs (0.873 for stroke detection, 0.795 for NIHSS assessment, and 0.818 for outcome prediction) were obtained by outstanding DRF selected by Lasso, and the performance of significant DRF was better than the five-feature dimension-reduction algorithms. The selected outstanding dimension-reduction DRF in experimental group_C obtained a better AUC than dimension-reduction DRF in experimental group_A but were inferior to the outstanding DRF in experimental group_A. When combining the outstanding DRF with each dimension-reduction DRF (experimental group_B), the performance can be improved in ischemic stroke detection (best AUC = 0.899) and NIHSS assessment (best AUC = 0.835) but failed in outcome prediction (best AUC = 0.806). The performance can be further improved when combining outstanding DRF with outstanding dimension-reduction DRF (experimental group_D), achieving the highest AUC scores in all three evaluation items (0.925 for stroke detection, 0.853 for NIHSS assessment, and 0.828 for outcome prediction). By the method in this study, comparing the best AUC of Ft-test in experimental group_A and the best_AUC in experimental group_D, the AUC in stroke detection increased by 19.4% (from 0.731 to 0.925), the AUC in NIHSS assessment increased by 20.1% (from 0.652 to 0.853), and the AUC in prognosis prediction increased by 14.9% (from 0.679 to 0.828). This study provided a potential clinical tool for detailed clinical diagnosis and outcome prediction before treatment.

21 December 2021 in Magnetic Resonance in Medicine
Verified
Journal Article
Closed access
PDF file
DMDavid J. Ma
David J. Ma
HLHortense A‐M. Le
Hortense A‐M. Le
YYYuming Ye
Yuming Ye
ALAndrew F. Laine
Andrew F. Laine
JLJeffery A. Lieberman
Jeffery A. Lieberman
JGJia Guo
Jia Guo

21 November 2022 in Frontiers in Neuroimaging
Verified
Journal Article
Open access
VRVishwanatha M. Rao
Vishwanatha M. Rao
ZWZihan Wan
Zihan Wan
SASoroush Arabshahi
Soroush Arabshahi
DMDavid J. Ma
David J. Ma
PLPin-Yu Lee
Pin-Yu Lee
JGJia Guo
Jia Guo
Brain tissue segmentation has demonstrated great utility in quantifying MRI data by serving as a precursor to further post-processing analysis. However, manual segmentation is highly labor-intensive, and automated approaches, including convolutional neural networks (CNNs), have struggled to generalize well due to properties inherent to MRI acquisition, leaving a great need for an effective segmentation tool. This study introduces a novel CNN-Transformer hybrid architecture designed to improve brain tissue segmentation by taking advantage of the increased performance and generality conferred by Transformers for 3D medical image segmentation tasks. We first demonstrate the superior performance of our model on various T1w MRI datasets. Then, we rigorously validate our model's generality applied across four multi-site T1w MRI datasets, covering different vendors, field strengths, scan parameters, and neuropsychiatric conditions. Finally, we highlight the reliability of our model on test-retest scans taken in different time points. In all situations, our model achieved the greatest generality and reliability compared to the benchmarks. As such, our method is inherently robust and can serve as a valuable tool for brain related T1w MRI studies. The code for the TABS network is available at: https://github.com/raovish6/TABS.