MD from Shanghai Jiao Tong University School of Medicine, 2018
Master of Medicine from Shanghai Jiao Tong University School of Medicine, 2007 (7-year Undergraduate and Master's Program)
Associate chief physician, Department of Osteoporosis and Bone Diseases, Shanghai Sixth People's Hospital
Jiemei Gu, Hao Zhang, Qingyun Xue et al. Denosumab biosimilar (LY06006) in Chinese postmenopausal osteoporotic women: A randomized, double-blind, placebo-controlled, multicenter phase III study. Journal of Orthopaedic Translation. 29;38:117-125. 2022. doi: 10.1016/j.jot.2022.06.007.
Jiemei Gu, Hua Yue, Chun Wang et al. Vitamin D pathway gene variation rs3740165 is associated with serological uric acid levels in healthy Chinese women. Frontiers in Endocrinology. 13;13:1059964. 2022. doi: 10.3389/fendo.2022.1059964.
Hao Zhang, Jie-Mei Gu, Ai-Jun Chao et al. A phase III randomized, double-blind, placebo-controlled trial of the denosumab biosimilar QL1206 in postmenopausal Chinese women with osteoporosis and high fracture risk. Acta Pharmacologica Sinica. 44(2):446-453. 2023. doi: 10.1038/s41401-022-00954-y.
Jiemei Gu, Chun Wang, Hao Zhang, et al. No association between the vitamin D pathway gene polymorphisms and bone biomarkers response to calcium and low dose calcitriol supplementation in postmenopausal Chinese women: a one-year prospective study. BIOMARKERS. 23(7):664-669.2018. doi: 10.1080/1354750X.2018.1474259.
Gu J, Wang C, Zhang H,et al. Targeted resequencing of phosphorus metabolism related genes in 86 patients with hypophosphatemic rickets/osteomalacia. Int J Mol Med. 42(3):1603-1614.2018. doi: 10.3892/ijmm.2018.3730.
Gu JM, Wang L, Lin H, et al. The efficacy and safety of weekly 35-mg risedronate dosing regimen for Chinese postmenopausal women with osteoporosis or osteopenia: 1-year data. Acta Pharmacol Sin. 36(7):841-6.2015. doi: 10.1038/aps.2015.30.
Jie-Mei Gu, Yao-Hua Ke, Hua Yue et al. A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family. Bone. 52(1):9-16. 2013. doi: 10.1016/j.bone.2012.09.012.
Gu JM, Hu YQ, Zhang H, et al. A mutation in NOTCH2 gene in a Chinese patient with Hajdu-Cheney syndrome. Joint Bone Spine. 80(5):548-9.2013. doi: 10.1016/j.jbspin.2013.02.008.
Gu JM, Zhang ZL, Zhang H et al. Thirteen Chinese patients with sporadic Paget's disease of bone: clinical features, SQSTM1 mutation identification, and functional analysis. J Bone Miner Metab. 30(5):525-33. 2012. doi: 10.1007/s00774-012-0352-6.
Gu JM, Xiao WJ, He JW, et al. Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families. Acta Pharmacol Sin . 30(12):1634-42.2009. doi: 10.1038/aps.2009.169.