Meina Gao

Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency

Dan-dan Ruan, Jie-wei Luo, Yan-ping Zhang, 2023, Thrombosis Journal.

AARS2-Related Leukodystrophy: a Case Report and Literature Review

T. Peng, Yanyan Zhang, Jie Li, 2022, The Cerebellum.

Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis

Dan-dan Ruan, Jie-wei Luo, Yan-ping Zhang, 2023, Pediatric Rheumatology.

Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case report.

Dan-dan Ruan, Jian-Hui Zhang, Jie-wei Luo, 2024, Annals of hematology.

A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia.

Dan-dan Ruan, Jie-wei Luo, Xin-fu Lin, 2024, Clinica chimica acta; international journal of clinical chemistry.