Jinying Luo (Jin-Fu Zhou, Jinfu Zhou)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 8

Top Topics

Duchenne Muscular Dystrophy

Dna Methylation

Preterm Infants

Polycyclic Aromatic Hydrocarbons

Top Venues

Orphanet journal of rare diseases

Molecular biology reports

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

This page only lists publications with an associated author ORCID identifier.

Publications

Jinfu Zhou, Guilin Li, Yinglin Zeng, Xiaolong Qiu, Peiran Zhao, Ting Huang, Xi Wang, Jinying Luo, Na Lin, Liangpu Xu
Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis. Orphanet journal of rare diseases 19 (1) (2024)
Jinfu Zhou, Guilin Li, Yinglin Zeng, Xiaolong Qiu, Peiran Zhao, Ting Huang, Xi Wang, Jinying Luo, Na Lin, Liangpu Xu
Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis. Orphanet journal of rare diseases 19 (1) (2024)
Jinfu Zhou, Guilin Li, Lin Deng, Peiran Zhao, Yinglin Zeng, Xiaolong Qiu, Jinying Luo, Liangpu Xu
Biochemical and molecular features of chinese patients with glutaric acidemia type 1 from Fujian Province, southeastern China. Orphanet journal of rare diseases 18 (1) (2023)
Jinying Luo, Sining Liao, Chenran Zhang, Jinying Luo, Guilin Li, Huangyuan Li
Expression profiling of N6-methyladenosine-modified mRNA in PC12 cells in response to unconjugated bilirubin. Molecular biology reports (2023)
Jinying Luo, Yinglin Zeng, Xiaolong Qiu, Qingying Lin, Weifeng Chen, Jinying Luo, Liangpu Xu
Characterization of phenylalanine hydroxylase gene variants and analysis of genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China. Molecular biology reports 49 (11) (2022)
Jinying Luo, Jinying Luo, Junyu Lin, Yinglin Zeng, Xiaolong Qiu, Wenbin Zhu, Guanghua Liu
Perinatal risk factors for congenital hypothyroidism: A retrospective cohort study performed at a tertiary hospital in China. Medicine 99 (26) (2020)
Jinying Luo, Jin-Ying Luo, Wen-Bin Zhu, Chang-Yi Yang, Ying-Lin Zeng, Xiao-Long Qiu
Association between genetic polymorphism of heme oxygenase 1 promoter and neonatal hyperbilirubinemia: a meta-analysis. 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 34 (1) (2019)
Jinying Luo, Chang-Yi Yang, Wen-Bin Zhu, Shuwei Chen, Yinglin Zeng, Jing Wang, Hong Zhao, Yao Chen, Feng Lin
Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study. BioMed research international 2018 (2018)