Junyan Mao

Junyan Mao

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Junyan Mao

Fudan University

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

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

Representative Publications

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6 February 2025 in The Journal Of Prevention of Alzheimer's Disease
Verified
Journal Article
Open access
YLYue Ling
Yue Ling
YPYongsheng Pan
Yongsheng Pan
WLWei Li
Wei Li
JMJunyan Mao
Junyan Mao
BHBo Hong
Bo Hong
SXShifu Xiao
Shifu Xiao
Mild cognitive impairment (MCI) and preclinical MCI (e.g., subjective cognitive decline, SCD) are considered risk states of dementia, such as Alzheimer's Disease (AD). However, it is challenging to accurately predict conversion from normal cognition (NC) to MCI, which is important for early detection and intervention. Since neuropathological changes may have occurred in the brain many years before clinical AD, we sought to detect the subtle brain changes in the pre-MCI stage using a deep-learning method based on structural Magnetic Resonance Imaging (MRI). To discover early structural neuroimaging changes that differentiate between stable and progressive cognitive status, and to establish a predictive model for MCI conversion. We first created a unique deep-learning framework for pre-AD conversion prediction through the Alzheimer's Disease Neuroimaging Initiative-1 (ADNI-1) database (n = 845). Then, we tested the model on ADNI-2 (n = 321, followed 3 years) and our private study (n = 109), the China Longitudinal Aging Study (CLAS), to validate the rationality for pre-MCI conversion prediction. The CLAS is a 7-year community-based cohort study in Shanghai. Our framework consisted of two steps: 1) a single-ROI-based network (SRNet) for identifying informative regions in the brain, and 2) a multi-ROI-based network (MRNet) for pre-AD conversion prediction. We then utilized these "ROI-based deep learning" neural networks to create a composite score using advanced algorithm-building. We coined this score as the Progressive Index (PI), which serves as a metric for assessing the propensity of AD conversion. Ultimately, we employed the PI to gauge its predictive capability for MCI conversion in both ADNI-2 and CLAS datasets. We primarily utilized baseline T1-weighted MRI scans to identify the most discriminative brain regions and subsequently developed the PI in both training and validation datasets. We compared the PI across different cognitive groups and conducted logistic regression models along with their AUCs, adjusting for education level, gender, neuropsychological test scores, and the presence of comorbid conditions. We trained the SRNet and MRNet using 845 subjects from ADNI-1 with baseline MRI data, in which AD and progressive MCI (converting to AD within 3 years) patients were considered as positive samples, while NC and stable MCI (remaining stable for 3 years) subjects were considered as negative samples. The convolutional neural networks identified the top 10 regions of interest (ROIs) for distinguishing progressive from stable cases. These key brain regions included the hippocampus, amygdala, temporal lobe, insula, and anterior cerebellum. A total of 321 subjects from ADNI-2, including 209 NC (18 progressive NC (pNC), 113 stable NC (sNC), and 78 remaining NC (rNC)) and 112 SCD (11 pSCD, 5 sSCD, and 96 rSCD), as well as 109 subjects from CLAS, including 17 sNC, 16 pNC, 52 sSCD and 24 pSCD participated in the test set, separately. We found that the PI score effectively sorted all subjects by their stages (stable vs progressive). Furthermore, the PI score demonstrated excellent discrimination between the two outcomes in the CLAS data(p<0.001), even after controlling for age, gender, education level, depression symptoms, anxiety symptoms, somatic diseases, and baseline MoCA score. Better performance for prediction progression to MCI in CLAS was obtained when the PI score was combined with clinical measures (AUC=0.812; 95 %CI: 0.725-0.900). This study effectively predicted the progression to MCI among order individuals at normal cognition state by deep learning algorithm with MRI scans. Exploring the key brain alterations during the very early stages, specifically the transition from NC to MCI, based on deep learning methods holds significant potential for further research and contributes to a deeper understanding of disease mechanisms.


2 November 2026
Verified
Conference Paper
Open access
SXShuchang Xu
Shuchang Xu
MTMinglong Tang
Minglong Tang
JMJunyan Mao
Junyan Mao
XJXiaofu Jin
Xiaofu Jin
WZWazeer Zulfikar
Wazeer Zulfikar
PMPatricia Jeffrey Maes
Patricia Jeffrey Maes

23 September 2026 in Proceedings of the ACM on Human-Computer Interaction
Verified
Journal Article
Open access
YSYuling Sun
Yuling Sun
ZYZhennan Yi
Zhennan Yi
JMJunyan Mao
Junyan Mao
MTMinglong Tang
Minglong Tang
XMXiaojuan Ma
Xiaojuan Ma
NGNing Gu
Ning Gu
Reminiscence Therapy (RT), as a typical Non-pharmacological intervention (NPI), has become increasingly important in dementia care. While GenAI-powered tools have shown potential in enhancing RT, they often struggle with practical usability and effectiveness due to the complex and situated nature of real-world intervention processes. In this study, we conduct a three-stage, in-the-wild research, including a formative study with professional therapists, a therapist-involved iterative participatory design study, and an in-situ evaluation with key stakeholders, to explore how GenAI-powered tools can be effectively designed and used to support personalized, professional, and collaborative RT practices. Our findings reveal that while theory-driven tools can achieve technical and therapeutic effectiveness in the lab, the practical effectiveness is not solely determined by their theoretically grounded design, but emerges through role-stretched and negotiated use within distributed, multi-stakeholder care practices. Based on our findings, we propose a series of practical implications for future GenAI-powered intervention technologies.