Jinfu Zhou

Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian

Jing Wang, Hua Li, Wenbin Zhu, 2018, Medicine.

Clinical characteristics and risk factors of twin pregnancies with single fetal malformation: a multi-center analysis in Southeastern China

Jinying Luo, Qiuping Liao, Q. Han, 2019 .

N6-methyladenosine(m6A) demethylase FTO regulates cellular apoptosis following cobalt-induced oxidative stress.

Siying Wu, Huangyuan Li, Qianqian Su, 2021, Environmental pollution.

Perinatal risk factors for congenital hypothyroidism

Wenbin Zhu, Jinying Luo, Guanghua Liu, 2020, Medicine.

[Risk factors of 125 cases of neonatal congenital hypothyroidism during perinatal period].

Jing Wang, Wenbin Zhu, Jinying Luo, 2015, Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi.

A novel dual oxidase maturation factor 2 gene mutation for congenital hypothyroidism.

L. Lan, Jing Wang, Liyong Yang, 2013, International journal of molecular medicine.

Meta-analyses of maternal exposure to atmospheric particulate matter and risk of congenital anomalies in offspring

Siying Wu, Huangyuan Li, Qianqian Su, 2021, Environmental Science and Pollution Research.

Peripheral blood level of 17-hydroxyprogesterone in neonates and influencing factors

Jing Wang, Wenbin Zhu, Yueqing Su, 2015 .

Clinical Analysis of Eleven Cases of Spontaneous Umbilical Cord Vascular Rupture During Pregnancy

Jinying Luo, Jianying Yan, Jinfu Zhou, 2021 .

Cobalt induces neurodegeneration through FTO-triggered autophagy impairment by targeting TSC1 in an m6A-YTHDF2-dependent manner.

Yu Zhang, Siying Wu, Huangyuan Li, 2023, Journal of hazardous materials.

Characterization of phenylalanine hydroxylase gene variants and analysis of genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China

Liangpu Xu, Jinying Luo, Jinfu Zhou, 2022, Molecular Biology Reports.

Characterization of PAH Gene Mutations and Analysis of Genotype-Phenotype Correlation in Patients with Phenylalanine Hydroxylase Deficiency from Fujian Province, Southeastern China

Liangpu Xu, Jinying Luo, Jinfu Zhou, 2021 .

Association between genetic polymorphism of heme oxygenase 1 promoter and neonatal hyperbilirubinemia: a meta-analysis

Wenbin Zhu, Jinying Luo, Chang-Yi Yang, 2021, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study

Jing Wang, Wenbin Zhu, Changyi Yang, 2018, BioMed research international.

Biochemical and molecular features of chinese patients with glutaric acidemia type 1 from Fujian Province, southeastern China

Liangpu Xu, Jinying Luo, Guilin Li, 2023, Orphanet Journal of Rare Diseases.

Expression profiling of N6-methyladenosine-modified mRNA in PC12 cells in response to unconjugated bilirubin

Huangyuan Li, Chenran Zhang, Jinying Luo, 2023, Molecular Biology Reports.

The interplay between lncRNA NR_030777 and SF3B3 in neuronal damage caused by paraquat.

Yu Zhang, Siying Wu, Huangyuan Li, 2023, Ecotoxicology and environmental safety.