Jie Xie

Prognostic relevance and therapeutic implications of centromere protein F expression in patients with esophageal squamous cell carcinoma.

Yang Mi, J. Gao, Jie Xie, 2013, Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus.

Identification of a novel SUOX pathogenic variants as the cause of isolated sulfite oxidase deficiency in a Chinese pedigree

Weiying Jiang, Jie Xie, Hualei Luo, 2021, Molecular genetics & genomic medicine.

Novel recessive PDZD7 biallelic mutations associated with hereditary hearing loss in a Chinese pedigree.

Weiying Jiang, Jie Xie, Hualei Luo, 2019, Gene.

Mutation analysis and pathogenicity identification of Mucopolysaccharidosis type IVA in 8 south China families.

M. Du, Weiying Jiang, Chunmiao Guo, 2019, Gene.

Cx32 mediates norepinephrine‐promoted EGFR‐TKI resistance in a gap junction‐independent manner in non‐small‐cell lung cancer

H. Ge, L. Tao, Jie Xie, 2019, Journal of cellular physiology.

Case report: exome sequencing achieved a definite diagnosis in a Chinese family with muscle atrophy

Hui Jiang, Chunmiao Guo, Jing-xin Pan, 2021, BMC Neurology.

Two novel mutations in the PPIB gene cause a rare pedigree of osteogenesis imperfecta type IX.

Wei Zhang, Weiying Jiang, Z. Fang, 2017, Clinica chimica acta; international journal of clinical chemistry.