Shiguo Chen

Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family

Sheng Lin, Lichun Xie, Yongheng Duan, 2017, Genetics and molecular biology.

A Novel Potentially Causative Variant of NDUFAF7 Revealed by Mutation Screening in a Chinese Family With Pathologic Myopia.

Sheng Lin, Yongheng Duan, Kaifeng Zheng, 2017, Investigative ophthalmology & visual science.

Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency in the Shenzhen Population

Kaifeng Zheng, Shiguo Chen, Shan Duan, 2021, Human Heredity.

Novel association between a transient receptor potential cation channel subfamily M member 5 expression quantitative trait locus rs35197079 and decreased susceptibility of gestational diabetes mellitus in a Chinese population

Shiguo Chen, Linghua Zhang, Shan Duan, 2021, Journal of diabetes investigation.

Assessment of the association between the polymorphism rs1256031 of the estrogen receptor β gene and GDM susceptibility

Sheng Lin, Kaifeng Zheng, Shiguo Chen, 2020, Nagoya journal of medical science.

The association between the rs4987105 of 5-lipoxygenase (ALOX5) gene and gestational glucose metabolism in Chinese population

Sheng Lin, Shiguo Chen, Shan Duan, 2020, BMC Research Notes.