Dan-yan Zhuang

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017

Hua Tang, Zhidai Liu, Peng-hui Zhang, 2020, Human mutation.

[Clinical features and SLC6A8 gene mutations of cerebral creatine deficiency syndrome I: an analysis of two families].

Wen-Hao Zhou, Bing-bing Wu, Dan-yan Zhuang, 2020, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Molecular genotyping of G6PD mutations for neonates in Ningbo area

Dan-yan Zhuang, Qiaoli Yu, Haibo Li, 2021, Journal of clinical laboratory analysis.

Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China

Haiyan Qiu, Dan-yan Zhuang, Xiangchun Yang, 2021, Frontiers in Genetics.

Identification of Six Novel Variants of ACAD8 in Isobutyryl-CoA Dehydrogenase Deficiency With Increased C4 Carnitine Using Tandem Mass Spectrometry and NGS Sequencing

Li-Ming Zhou, Dan-yan Zhuang, Xiang Yang, 2022, Frontiers in Genetics.

Prenatal diagnosis to identify compound heterozygous variants in PKDCC that causes rhizomelic limb shortening with dysmorphic features in a fetus from China

Dan-yan Zhuang, Haibo Li, Lulu Yan, 2023, BMC Medical Genomics.

Random forest classifier improving phenylketonuria screening performance in two Chinese populations

Zongfu Cao, Xu Ma, Dan-yan Zhuang, 2022, Frontiers in Molecular Biosciences.

[Study on newborn screening for Duchenne muscular dystrophy and diagnostic strategy].

Zongfu Cao, Dan-yan Zhuang, Haibo Li, 2021, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.