Name: Yingying Qin

Country: China

Affiliation:

Reproductive Medicine, Center of Shandong University

Email: Send an Email


Address:

157#,Jing Liu Road, Jinan Shandong, Province China

Research Interests:

reproductive endocrinology assisted reproductive technology premature ovarian insufficiency diminished ovarian reserve PCOS preimplantation genetic test

Biography:

Education And Employment: 

  • 1995-2000 School of Medicine, Qingdao University (Major in Medicine) 
  • Bachelor 2002-2007 School of Medicine, Shandong University (Major in Obstetrics and Gynecology) M.D.
  • Ph.D. 2006-2007 Baylor College of Medicine, USA International Scholar 
  • 2016-Present Center for Reproductive Medicine, Shandong University Professor, Chief Physician 

Publications:

  1. Genetics of primary ovarian insufficiency: new developments and opportunities. Hum Reprod Update 2015;21:787-808. 
  2. CSB-PGBD3 Mutations Cause Premature Ovarian Failure. PLoS Genet 2015;11:e1005419. 
  3. Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women. Maturitas 2014;77:64-67 
  4. Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure. Fertil Steril 2014;101:1104-1109 e1106. 
  5. Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF). Hum Mol Genet 2012;21:430-436. 
  6. ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature ovarian failure. Orphanet J Rare Dis 2012;7:5. 
  7. Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure. Fertil Steril NOTE 2009;91:1507-1509. 
  8. Analysis of LHX8 mutation in premature ovarian failure. Fertil Steril 2008;89:1012-1014. 
  9. Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure. Fertil Steril 2007;88:1465-1467. 
  10. NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet NOTE 2007;81:576-581. 
  11. Antimullerian hormone: correlation with age and androgenic and metabolic factors in women from birth to postmenopause. Fertil Steril 2016;105:481-485 e481. 
  12. Mutations in MSH5 in primary ovarian insufficiency. Hum Mol Genet 2017;26:1452-1457. 
  13. Identification of patients with primary ovarian insufficiency caused by autoimmunity. Reprod Biomed Online 2017;35:475-479. 
  14. Minichromosome maintenance complex component 8 mutations cause primary ovarian insufficiency. Fertil Steril 2016;106:1485-1489 e1482. 
  15. The screening of HELQ gene in Chinese patients with premature ovarian failure. Reprod Biomed Online 2015;31:573-576.