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LI Shanshan
- Graduate Supervisor, Associate Chief Physician
- Department: Osteoporosis and Bone Diseases
- Research Area: Endocrinology and Metabolism
- Research Interests: Clinical and Molecular Mechanisms of Metabolic Bone Diseases
- Contact: lissane0508@126.com
- MD from Shanghai Jiao Tong University School of Medicine, 2018
- Li S#, Shao R, Li S, Zhao J, Deng Q, Li P, Wei Z, Xu S, Chen L, Li B, Zou W, Zhang Z. A monoallelic variant in CCN2 causes an autosomal dominant spondyloepimetaphyseal dysplasia with low bone mass. Bone Res. 2024, 12(1):60.
- Li S#, Lyu S, Fu W, Hu Y, Yue H, Chen L, Zhang Z. Clinical and genetic profiles of 985 Chinese families with skeletal dysplasia. Chin Med J (Engl). 2023, 136(12):1485-1487.
- Xu Y, Zhang Z, Yue H, Li S#, Zhang Z. Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy. J Bone Miner Res. 2021, 36(8):1459-1468.
- Lv S, Zhao J, Xi L, Lin X, Wang C, Yue H, Gu J, Hu W, Fu W, Wei Z, Zhang H, Hu Y, Li S#, Zhang Z. Genetics Evaluation of Targeted Exome Sequencing in 223 Chinese Probands With Genetic Skeletal Dysplasias. Front Cell Dev Biol. 2021, 9:715042.
- Li SS#, He JW, Fu WZ, Liu YJ, Hu YQ, Zhang ZL. Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention. 2017, 32(8):1659-1666.
- 01/01/2020-12/31/2022
National Natural Science Foundation of China, ¥200, 000, 81900807
Pathogenic Mechanism of Familial Spondylometaphyseal Dysplasia Caused by Mutations in the Novel Disease Gene CTGF
Role: Principal Investigator - 01/01/2024-12/31/2027
National Natural Science Foundation of China, ¥650, 000, 82370888
Role and Mechanism of Osteoblast Lineage Dysfunction in the Pathogenesis of X-linked Dominant Hypophosphatemic Rickets/Osteomalacia
Role: Principal Investigator
