Jing Chen

Association between IFNGR1 gene polymorphisms and tuberculosis susceptibility: A meta-analysis

X. Yuan, Ying Wang, Liwei Cheng, 2022, Frontiers in Public Health.

Case report: 17α− hydroxylase deficiency due to a hotspot variant and a novel compound heterozygous variant in the CYP17A1 gene of five Chinese patients

Qiang Zhang, X. Fu, Jing Chen, 2022, Frontiers in Pediatrics.

Associations between ERAP1 polymorphisms and ankylosing spondylitis susceptibility in HLA-B27 positive population: a Meta-analysis and bioinformatics analysis

N. Hu, Yanyan Bai, Jing Chen, 2022, Nucleosides, nucleotides & nucleic acids.

PKD2 gene variants in Chinese patients with autosomal dominant polycystic kidney disease

C. Mei, Z. Mao, Lijun Sun, 2021, Clinical Genetics.

The G41D mutation in SOD1-related amyotrophic lateral sclerosis exhibits phenotypic heterogeneity among individuals

Xiuli Li, Hongjing Liu, Xinhong Feng, 2022, Medicine.