Author

Lingli Zhang

Shanghai Jiao Tong University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Same name, identified by ORCID

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:database / resource· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:imaging· 1 Research Focus:spatial domain detection· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Edmund T. RollsiD· 1 shared Fei LiiD· 1 shared Fēi LiiD· 1 shared Jianfeng FengiD· 1 shared Jiaying ZhangiD· 1 shared Jincheng WangiD· 1 shared Jinyu WuiD· 1 shared Juehua YuiD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperNeuroscience

Edmund T. RollsORCID

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2 papers

Recent·Most cited

Abnormal white matter development during early childhood in autism and developmental disability

Yuqi Liu, Jiaying Zhang, Edmund T. Rolls, Yuan Dai, Shujie Geng, Linhong Deng, Zilin Chen, Yue Zhang, Minyi Tao, Lingli Zhang, Tai Ren, Jianfeng Feng, Miao Cao, Fēi Li

This study examines white matter development in children with autism, developmental delay/intellectual disorder, and typical development, identifying delayed growth patterns and their clinical associations.

bioRxiv · Nov 15, 2023 · PreprintNeuroscience

De novo variants in Chinese ASD trios reveal genetic basis underlying autism without developmental delay and intellectual disabilities

Jincheng Wang, Juehua Yu, Mengdi Wang, Lingli Zhang, Kan Yang, Xiujuan Du, Jinyu Wu, Xiaoqun Wang, Fei Li, Zilong Qiu

This study identifies de novo variants in Chinese ASD trios, finding that ASD without DD/ID has fewer disruptive variants and novel risk genes not in existing databases.

bioRxiv · Sep 30, 2021 · PreprintNeuroscience