Zhilei Zhang

Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Wei Cheng, Yun Sun, Yanyun Wang, 2014 .

Neonatal Screening and Genotype-Phenotype Correlation of 21-Hydroxylase Deficiency in the Chinese Population

Yun Sun, Yanyun Wang, T. Jiang, 2021, Frontiers in Genetics.

A joint method for the screening of pharmacological chaperones for phenylalanine hydroxylase.

Tao Jiang, Zhengfeng Xu, Yun Sun, 2021, Organic & biomolecular chemistry.

Current attitudes and preconceptions on newborn genetic screening in the Chinese reproductive-aged population

Tao Jiang, Yun Sun, Yanyun Wang, 2022, Orphanet Journal of Rare Diseases.

Molecular characterization of coxsackievirus B5 from the sputum of pneumonia children patients of Kunming, Southwest China

Li Tan, Y. Pan, Lingmei Yan, 2023, Virology Journal.

Two cases of hand, foot, and mouth disease caused by enterovirus A71 after vaccination.

Lingmei Yan, Xiaodang Wang, Qiangming Sun, 2021, International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases.

Combined genetic screening and traditional biochemical screening to optimize newborn screening systems.

Tao Jiang, Yun Sun, Yanyun Wang, 2022, Clinica chimica acta; international journal of clinical chemistry.

Analysis of five cases of hypermethioninemia diagnosed by neonatal screening

Yun Sun, Yanyun Wang, T. Jiang, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

Neonatal screening and genotype-phenotype correlation of hyperphenylalaninemia in the Chinese population

Tao Jiang, Yun Sun, Yanyun Wang, 2021, Orphanet Journal of Rare Diseases.

Newborn genetic screening is highly effective for high-risk infants: A single-centre study in China

Zhilei Zhang, Yahong Li, Xianwei Guan, 2023, Journal of global health.

Utility, benefits, and risks of newborn genetic screening carrier reports for families

Zhilei Zhang, Yahong Li, Xianwei Guan, 2024, Journal of global health.

Creatine Kinase-MM/Proto-oncogene Tyrosine-Protein Kinase Receptor as a Sensitive Indicator for Duchenne Muscular Dystrophy Carriers.

Zhengfeng Xu, D. Hong, D. Ma, 2024, Molecular Neurobiology.