INDEX >> Academics >> Faculty & Interests >> Gong Yaoqin
 

Gong Yaoqin, PhD

Director of the Institute of Medical Genetics
School of Medicine, Shandong University

Director of the Key Lab of Experimental Teratology, Ministry of Education, China

Professor of Medical Genetics

BS (biology) Huazhong Normal University

MS (medical genetics) Shandong Medical University

PhD (Human Anatomy, Histology and Embryology) Shandong University

1994-1995 studying in Medical School of Harvard University

 


Selected Publications:

  1. Kutz WE, Gong YQ, Warman ML*. WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice. MOLECULAR AND CELLULAR BIOLOGY. 2005, 25 (1): 414-421
  2. Rhee DK, Marcelino J, Baker MA, Gong YQ, Smits P, Lefebvre V,Jay GD, Stewart M, Wang HW, Warman ML, Carpten JD*.The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth. JOURNAL OF CLINICAL INVESTIGATION. 2005,115 (3): 622-631
  3. Xiyu zhang, Qiji liu, Bingxi chen, Chenhong guo, Jiangxia li, Guimin Gao, Yishou guo and Yaoqin Gong*. A locus for nonspecific X-linked mental reatardation mapped to a 22.3 cM region of Xp11.3-q22.3. Am J Med Genet. 2004,129A:286-289
  4. Lu Y, Guo C, Liu Q, Zhang X, Cheng L, Li J, Chen B, Gao G, Zhou H, Guo Y, Li Y, Gong Y*. A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads. Am J Med Genet. 2003;120A(3):345-349.
  5. Gong Yaoqin*, LI Jiangxia, LIU Qiji, CHEN Bingxi, GUO Chenhong, GAO Guimin. Application of homozygos itymapping to the fine mapping of the osteoporosis-pseudogl ioma syndrome locus. Chin J Med Genet. 2003,20(1):53-55
  6. Liu Qiji, Gong Yaoqin*, Guo Chenhong, Chen Bingxi, Li Jiangxia, Guo Yishou. Linkage analysis of X-linked nuclear protein gene in Smith-Fineman-Myers syndrome. Chinese Journal of Medical Genetics, 2002£¬ 19£¨1£©£º22-25
  7. Liu Qiji, Gong Yaoqin*, Guo Chenhong, Chen Bingxi, Li Jiangxia, Guo Yishou. Polymorphic loci and polymorphism analysis of short tandem repeats within XNP gene. Acta Genetica Sinica. 2002, 29(3): 201-5
  8. Liu Qiji, Gong Yaoqin*, Chen Bingxi, Guo Chenhong, Li Jiangxia, Guo Yishou. Linkage analysis and mutation detection of GRIA3 in Smith-Fineman-Myers syndrome. Acta Genetica Sinica£¬2001£¬28£¨11£©£º985-990
  9. Gong YQ, Slee RB, Fukai N, Rawadi G, Roman-Roman S, Reginato AM, Wang HW, Cundy T,¡­Olsen BR, Warman ML*. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell, 2001, 107:513-523.
  10. Liang Xiaoyuan, Gong Yaoqin*, Liu Qiji, Li Jiangxia, Chen Bingxi, Guo Chenhong. The construction of rapid amplification of cDNA ends cDNA libraries from human fetal bone and joint. Chinese Journal of Medical Genetics, 2001£¬18£¨1£©£º24-27
  11. Gong Yaoqin*, Wei Jianjun, Shao Changshun, Guo Yishou, Chen Bingxi, Guo Chenhong, Matt Warman. Mapping the gene responsible for Smith-Fineman-Myers syndrome to Xq25. Chinese Journal of Medical Genetics, 1999£¬16£¨5£©£º277-280
  12. Yaoqin Gong, David Chitayat, Bronyn Kerr, Taiping Chen, Riyana Babul-Hirji, Adatiya pal, Michael Reiss, and Matthew L Warman*. Brachydactyly type B: Clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation. Am J Hum Genet , 1999£¬64: 570-577
  13. Yaoqin Gong, Deborah Karkow, Jose Marcelino, Douglas Wilkin, David Chitayat, Riyana Babul-Hirji, Louanne Hudgins, Cor W Cremers, Frans P M Cremers, Han G Brunner, Kent Reinker, David L Rimoin, Daniel H Cohn, Frances R Goodman, William Reardon, Michael Patton, Clair A Francomano , Matthew L Warman. Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. Nature Genetics, 21, 1999 March, 302-304
  14. Gong Yaoqin*, Chen Bingxi, Guo Chenhong, Liu Xiaojun, Zou Yaqun. Isolation and analysis of YAC end using reverse PCR. Chinese Journal of Medical Genetics, 1999£»16£¨1£©£º44-46

 


Operated by Institute of Medical Genetics Shandong University