S. Cui

Risk of gestational diabetes recurrence and the development of type 2 diabetes among women with a history of gestational diabetes and risk factors: a study among 18 clinical centers in China

L. Feng, Cuilin Zhang, Huixia Yang, 2022, Chinese medical journal.

Genetic examination for fetuses with increased nuchal translucency by exome sequencing

Yingying Li, S. Cui, Y. Zhi, 2022, The journal of obstetrics and gynaecology research.

Risk Factors for Macrosomia in Multipara: A Multi-Center Retrospective Study

Y. Li, Rui-Yan Shan, Yumei Wei, 2022, Children.

An intractable epilepsy phenotype of ASNS novel mutation in two patients with asparagine synthase deficiency.

Changlian Zhu, Y. Li, L. Xia, 2022, Clinica chimica acta; international journal of clinical chemistry.

Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy

Yaqing Guo, Erfeng Yuan, Yuan Tian, 2020, Human Genomics.

Identification of a novel splicing mutation in the SLC25A13 gene from a patient with NICCD: a case report

Yaqing Guo, Linlin Zhang, Wenli Shi, 2019, BMC Pediatrics.

Pathogenic/likely pathogenic copy number variations and regions of homozygosity in fetal central nervous system malformations

S. Cui, Y. Zhi, Ling Liu, 2022, Archives of Gynecology and Obstetrics.

Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication

Yangyang Yuan, Erfeng Yuan, S. Cui, 2023, European Journal of Medical Research.