Junhai Zhang

Dr. Junhai Zhang

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

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

Representative Publications

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8 September 2018 in Journal of Magnetic Resonance Imaging
Verified
Journal Article
Closed access
PDF file
YRYan Ren
Yan Ren
XZXi Zhang
Xi Zhang
WRWenting Rui
Wenting Rui
HPHaopeng Pang
Haopeng Pang
TQTianming Qiu
Tianming Qiu
XFXiaoyuan Feng
Xiaoyuan Feng

1 July 2019 in Journal of Affective Disorders
Verified
Journal Article
Closed access
WGWenqing Gong
Wenqing Gong
SZShanshan Zhang
Shanshan Zhang
YZYing Zong
Ying Zong
Shi Dong YunShi Dong Yun
Shi Dong Yun
ZRZhonggan Ren
Zhonggan Ren
QLQiong Liu
Qiong Liu

16 January 2019 in Journal of Magnetic Resonance Imaging
Verified
Journal Article
Closed access
PDF file
HPHaopeng Pang
Haopeng Pang
XDXuefei Dang
Xuefei Dang
YRYan Ren
Yan Ren
DZDongxiao Zhuang
Dongxiao Zhuang
TQTianming Qiu
Tianming Qiu
XFXiaoyuan Feng
Xiaoyuan Feng

1 January 2019 in European Journal of Radiology
Verified
Journal Article
Closed access
WRWenting Rui
Wenting Rui
YWYue Wu
Yue Wu
ZMZengyi Ma
Zengyi Ma
YWYongfei Wang
Yongfei Wang
YWYin Wang
Yin Wang
ZYZhenwei Yao
Zhenwei Yao

21 June 2023 in Nanoscale Advances
Verified
Journal Article
Open access
PDF file
QZQi Zhang
Qi Zhang
SWShiman Wu
Shiman Wu
YLYajie Li
Yajie Li
MLMao Lai
Mao Lai
QLQing Li
Qing Li
JZJunhai Zhang
Junhai Zhang
By targeting the enriched vascular endothelial growth factor receptor (VEGFR) in endometriosis, we develop an MRI contrast agent, NaGdF 4 @PEG@bevacizumab–Cy5.5 nanoparticles (NPBCNs) to detect endometriosis in MRI and fluorescence imaging.

3 March 2021 in Journal of Computer Assisted Tomography
Verified
Journal Article
Closed access
QZQi Zhang
Qi Zhang
DWDongdong Wang
Dongdong Wang
SWShiman Wu
Shiman Wu
YRYan Ren
Yan Ren
YLYajie Bm Li
Yajie Bm Li
XFXiaoyuan Feng
Xiaoyuan Feng
Purpose: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common familial arteriopathy characterized by recurrent lacunar stroke, migraine, and depression. The mechanism of cognitive dysfunction in CADASIL is still uncertain. The aim of this study was to use tract-based spatial statistics (TBSS) to map voxelwise the spatial distribution of brain microstructural change revealed by DTI-derived indices in patients with CADASIL to further study the underlying neuropsychopathological mechanism of CADASIL. Method: Twelve patients with CADASIL and 11 age-, sex-matched healthy controls underwent magnetic resonance imaging at 3 T. Then we evaluated DTI-derived indices (fractional anisotropy [FA], mode of anisotropy [MO], mean diffusivity [MD], axial diffusivity [AD] and radial diffusivity [RD]) of brain white matter (WM) between CADASIL patients and healthy subjects through TBSS. Results: Compared with healthy controls, patients with CADASIL showed extensive decreased FA, MO and increased RD, AD, and MD throughout the entire brain (mainly the WM of the temporal poles, inferior and superior longitudinal fasciculus, inferior fronto-occipital fasciculus, corpus callosum, uncinate fasciculus, internal capsule, external capsule, corona radiata, thalamic radiation, and cingulum). Furthermore, these WM microstructural alterations were significantly correlated with cognitive scores and Scheltens scores. Decreased FA values and MO values were positively correlated with Montreal Cognitive Assessment scores in CADASIL patients. Increased AD, RD, and MD values were significantly negatively correlated with Montreal Cognitive Assessment scores. Conclusions: Widespread WM abnormalities were clearly shown in CADASIL by using TBSS. Severity of microstructural changes correlates significantly with extension of T2 hyperintensity. Moreover, WM microstructural damage and cognitive impairment were significantly correlated. This study indicated that WM tract damage plays an important role in cognitive impairment in CADASIL.