MaoQiang Tian

5PUBLICATIONS
1CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Genetically modified animals
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Publications (5)

|Sep 20, 2026
CSNK2B-associated epilepsy: family report and literature review.

|Jun 27, 2024
ADGRL1 variants: From developmental and epileptic encephalopathy to genetic epilepsy with febrile seizures plus.

Wenting Lei, Yurong Xiong, Yongyuan Shi

|Dec 13, 2022
Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability.

Mao-Qiang Tian, Xiao-Rong Liu, Si-Mei Lin

|Oct 26, 2022
Phenotypic expansion of KCNH1-associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub-regional locations.

Mao-Qiang Tian, Ren-Ke Li, Fan Yang

|Apr 26, 2022
Damaging novel mutations in PIGN cause developmental epileptic-dyskinetic encephalopathy: a case report.

Maoqiang Tian, Jing Chen, Juan Li

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Frequent Collaborators

1 joint publications

Wei-Ping Liao