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Bioinformatics (Oxford, England)|April 6, 2021
Customized de novo mutation detection for any variant calling pipeline: SynthDNMAojie Lian, James Guevara, Kun Xia, et al.
Frontiers in Immunology|May 14, 2026
Microglia in autism spectrum disorder: heterogeneity, immunometabolism, and synapse-related pathwaysAojie Lian, Mei He, Hong Zhang, et al.
Functional & Integrative Genomics|July 8, 2026
Integrative functional genomics maps synaptic and developmental-regulatory autism risk-gene sets across human cortexAojie Lian, Qiong Wang, Mei He, et al.
Molecular Medicine Reports|May 12, 2018
Identification of a VHL gene mutation in a Chinese family with Von Hippel‑Lindau syndromeZhengwen He, Lu Xia, Zhiyong Deng, et al.
Mitochondrion|March 11, 2023
A comprehensive perspective of Huntington's disease and mitochondrial dysfunctionYinghong Dai, Haonan Wang, Aojie Lian, et al.
Brain & Development|February 14, 2025
Effects of sulforaphane on ABC and SRS scales in patients with autism spectrum disorder: a meta-analysisJialing Guo, Yichao Wang, Weijun He, et al.
Medicine|January 5, 2019
A novel variation of SERPINC1 caused deep venous thrombosis in a Chinese family: A case reportYu Peng, Tun Wang, Yu Zheng, et al.
NPJ Parkinson'S Disease|January 3, 2024
Risk factors associated with age at onset of Parkinson's disease in the UK BiobankYuanfeng Huang, Qian Chen, Zheng Wang, et al.
Plos Computational Biology|June 15, 2019
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genomeKymberleigh A Pagel, Danny Antaki, AoJie Lian, et al.
Frontiers in Molecular Neuroscience|March 13, 2023
<i>De novo</i> variants in <i>MAST4</i> related to neurodevelopmental disorders with developmental delay and infantile spasms: Genotype-phenotype associationXi Zhang, Neng Xiao, Yang Cao, et al.
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