Guo-li Wang

Mechanisms of tumor necrosis factor-alpha-induced leaks in intestine epithelial barrier.

Li-Wen Wu, F. Yin, F. He, 2012, Cytokine.

Diagnosis of intellectual disability/global developmental delay via genetic analysis in a central region of China

Li-Wen Wu, F. Yin, F. He, 2019, Chinese medical journal.

Leukodystrophy associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFAF1 gene

F. Yin, F. He, Jing Peng, 2016, Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis.

A Retrospective Analysis of Pathological and Clinical Diagnoses: Report of 240 Pediatric Autopsies

F. Yin, Jing Peng, Xiaolu Deng, 2012, Fetal and pediatric pathology.

The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review

F. He, Jing Peng, Li-fen Yang, 2022, Frontiers in Molecular Neuroscience.

Characterization, using comparative proteomics, of differentially expressed proteins in the hippocampus of the mesial temporal lobe of epileptic rats following treatment with valproate

F. Yin, Jing Peng, Liwen Wu, 2010, Amino Acids.

Genotype-phenotype correlations of STXBP1 pathogenic variants and the treatment choices for STXBP1-related disorders in China

F. Yin, F. He, Jing Peng, 2023, BMC Medical Genomics.

Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders.

Kuokuo Li, Hui Guo, Senwei Tan, 2023, Gene.