邱贵兴，1942年生，籍贯江苏无锡，骨科学家，中国工程院院士，北京协和医院教授，主任医师，博士生导师。1960年考入中国协和医科大学医疗系专业（八年制）。1979年在中国协和医科大学攻读硕士学位，从事临床医学研究。1988年升为副主任医师。1993年升为主任医师。

长期从事骨科医教研管工作，研究方向涵盖我国转化医学发展战略研究、慢性脊柱退行性疾病及畸形的早期干预及规范化诊疗、骨关节疾病的病因学研究与临床诊疗、骨生物材料的研发与临床转化、脊柱畸形的分型与分子遗传学研究等。

天美麻花星空

1. Liu L#, Sun L#, Chen Y#, Wang M#, Yu C, Huang Y, Zhao S, Du H, Chen S, Fan X, Tian W, Wu Z; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study group, Qiu G*, Zhang TJ*, Wu N*. Delineation of dual molecular diagnosis in patients with skeletal deformity. Orphanet journal of rare diseases2022, 17(1):139.

2. Wu D#, Chang X#, Tian J, Kang L, Wu Y, Liu J, Wu X, Huang Y, Gao B, Wang H*, Qiu G*, Wu Z*. Bone mesenchymal stem cells stimulation by magnetic nanoparticles and a static magnetic field: release of exosomal miR-1260a improves osteogenesis and angiogenesis. J Nanobiotechnology 2021, 19(1):209.

3. Wu XD#, Huang W, Qiu GX*. Denosumab for the Prevention of Falls in Older People: We Need More Evidence. Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research. 2020, 35(8):1609-1610.

4. Liu J#, Wu N#*, Yang N#, Takeda K#, Chen W#, Li W, Du R, Liu S, Zhou Y, Zhang L, Liu Z, Zuo Y, Zhao S, Blank R, Pehlivan D, Dong S, Zhang J, Shen J, Si N, Wang Y, Liu G, Li S, Zhao Y, Zhao H, Chen Y, Zhao Y, Song X, Hu J, Lin M, Tian Y, Yuan B, Yu K, Niu Y, Yu B, Li X, Chen J, Yan Z, Zhu Q, Meng X, Chen X, Su J, Zhao X, Wang X, Ming Y, Li X, Raggio C L, Zhang B, Weng X, Zhang S, Zhang X, Watanabe K, Matsumoto M, Jin L, Shen Y, Sobreira N L, Posey J E, Giampietro P F, Valle D, Liu P, Wu Z, Ikegawa S, Lupski J R, Zhang F, Qiu G*. TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. Genetics in medicine: official journal of the American College of Medical Genetics 2019, 21(7): 1548-1558.

5. Liu G#, Liu S#, Lin M#, Li X, Chen W, Zuo Y, Liu J, Niu Y, Zhao S, Long B, Wu Z, Wu N*, Qiu G*. Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population. Journal of cellular and molecular medicine 2018, 22(3):1964-1971.

6. Xu Q#, Wu N#, Cui L, Wu Z, Qiu G*. Filamin B: The next hotspot in skeletal research? J Genet Genomics. 2017 , 44(7):335-342.

7. Chen J#, Liu J#, Zhou Y#, Liu S, Liu G, Zuo Y, Wu Z, Wu N*, Qiu G*. Molecular therapeutic strategies for FGFR3 gene-related skeletal dysplasia. Journal of molecular medicine (Berlin, Germany) 2017, 95(12): 1303-1313.

8. Zhu Q#, Wu N#, Liu G, Zhou Y, Liu S, Chen J, Liu J, Zuo Y, Liu Z, Chen W, Chen Y, Chen J, Lin M, Zhao Y, Yang Y, Wang S, Yang X, Ma Y, Wang J, Chen X, Zhang J, Shen J, Wu Z*, Qiu G*. Comparative analysis of serum proteome in congenital scoliosis patients with TBX6 haploinsufficiency - a first report pointing to lipid metabolism. Journal of cellular and molecular medicine 2017, 22(1): 533-545.

9. Wu N#, Ming X#, Xiao J#, Wu Z#, Chen X#, Shinawi M, Shen Y, Yu G, Liu J, Xie H, Gucev Z S, Liu S, Yang N, Al-Kateb H, Chen J, Zhang J, Hauser N, Zhang T, Tasic V, Liu P, Su X, Pan X, Liu C, Wang L, Shen J, Shen J, Chen Y, Zhang T, Zhang J, Choy K W, Wang J, Wang Q, Li S, Zhou W, Guo J, Wang Y, Zhang C, Zhao H, An Y, Zhao Y, Wang J, Liu Z, Zuo Y, Tian Y, Weng X, Sutton V R, Wang H, Ming Y, Kulkarni S, Zhong T P, Giampietro P F, Dunwoodie S L, Cheung S W, Zhang X, Jin L, Lupski J R, Qiu G*, Zhang F*. TBX6 null variants and a common hypomorphic allele in congenital scoliosis. The New England journal of medicine 2015, 372(4): 341-350.

10. Qiu G#*, Zhang J, Wang Y, Xu H, Zhang J, Weng X, Lin J, Zhao Y, Shen J, Yang X, Luk KD, Lu D, Lu WW. A new operative classification of idiopathic scoliosis: a peking union medical college method. Spine (Phila Pa 1976) 2005, 30(12):1419-26.