Xiao Mao

13PUBLICATIONS
17CO-AUTHORS
Electrical energy transmission, networks and systemsNeurogeneticsGene mappingComputational complexity and computabilityNeonatology
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Publications (13)

|Mar 14, 2026
KCNJ4 variants disrupt inward-rectifier potassium channel function and cause refractory epilepsy.

Hu Pan, Deng Liu, Wuhen Xu

|Jul 18, 2025
Novel TMEM53 missense variant generated a new ubiquitination site and cause Craniotubular dysplasia, Ikegawa type.

Ying Peng, Zhengqing Wan, Kai Li

|Jun 16, 2025
Compound Heterozygous Loss-of-Function Variants in CCM2L in a Fetus With Tetralogy of Fallot.

Dandan Ling, Wanqin Xie, Xiao Mao

|Mar 17, 2025
Compound heterozygosity of a De novo 16q24.1 deletion and missense mutation in COX4I1 leads to developmental regression, intellectual disability, and seizures.

Zhen Liu, Mei He, Xuan Luo

|Apr 08, 2024
Compound heterozygous B3GALNT2 mutations in a fetus with encephalocele: A case report.

Dandan Ling, Wanqin Xie, Xiao Mao

|Nov 14, 2023
De novo variants in KCNJ3 are associated with early-onset epilepsy.

Juan Li, Shiyue Mei, Xiao Mao

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Frequent Collaborators

2 joint publications

Hua Wang

2 joint publications

Zhen Liu

2 joint publications

Wanqin Xie

2 joint publications

Dandan Ling