Yi Wang

发表

Hormonal changes throughout puberty in congenital hypogonadotropic hypogonadism and Pump indication

C. Gong, B. Cao, Jiajia Chen, 2020 .

Fulminant Type 1 Diabetes in Children: A Multicenter Study in China

Qiao-zhi Yang, C. Gong, Yu-Wen Cheng, 2017, Journal of diabetes research.

Correlation Analysis of Genotypes and Phenotypes in Chinese Male Pediatric Patients With Congenital Hypogonadotropic Hypogonadism

C. Gong, Yi Wang, M. Qin, 2022, Frontiers in Endocrinology.

Glucagon Secretion in Response to Hypoglycemia in Patients with Congenital Hyperinsulinism

C. Gong, C. Su, Yi Wang, 2014 .

Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature

Zhihong Wu, Hengqiang Zhao, N. Wu, 2021, Frontiers in Cell and Developmental Biology.

Clinical and genetic features of 64 young male paediatric patients with congenital hypogonadotropic hypogonadism

Y. Liu, C. Gong, Yuanyuan Tian, 2017, Clinical endocrinology.

Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients

Zhihong Wu, Hengqiang Zhao, N. Wu, 2021, Frontiers in Endocrinology.

SOX2 heterozygous mutation causes multiple extra-ocular phenotypes in boys

C. Gong, Xiaoya Ren, Yi Wang, 2020 .

Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants.

Yiping Shen, Jian Wang, C. Gong, 2017, Clinica chimica acta; international journal of clinical chemistry.

Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature.

J. Lupski, Zhihong Wu, Shuyang Zhang, 2021, Journal of genetics and genomics = Yi chuan xue bao.

Influence of initial insulin dosage on blood glucose dynamics of children and adolescents with newly diagnosed type 1 diabetes mellitus

Di Wu, C. Gong, Liya Wei, 2017, Pediatric diabetes.

The Clinical and Genetic Characteristics of Chinese Male Pediatric Patients With Congenital Hypogonadotropic Hypogonadism

C. Gong, Yi Wang, Beibei Zhang, 2021 .

New insights into 5α-reductase type 2 deficiency based on a multi-centre study: regional distribution and genotype–phenotype profiling of SRD5A2 in 190 Chinese patients

C. Gong, Shaoke Chen, F. Luo, 2019, Journal of Medical Genetics.

Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study

C. Gong, Shaoke Chen, Ge-li Liu, 2022, Journal of personalized medicine.

AR mutations in 28 patients with androgen insensitivity syndrome (Prader grade 0–3)

C. Gong, Yi Wang, M. Qin, 2017, Science China Life Sciences.