Yan J - Search Results

1

Lack of an association between CYP1A1 gene Ile462Val polymorphism and polycystic ovary syndrome in Chinese.

Wang B, Wang J, Liu J, Ni F, Yan J, Zhou S, Mu Y, Cao Y, Ma X. Wang B, et al. Among authors: yan j. Endocrine. 2009 Aug;36(1):16-9. doi: 10.1007/s12020-009-9205-z. Epub 2009 Jun 9. Endocrine. 2009. PMID: 19507064

2

Lack of association between interleukin-1a gene (IL-1a) C (-889) T variant and polycystic ovary syndrome in Chinese women.

Wang B, Zhou S, Wang J, Liu J, Ni F, Liu C, Yan J, Mu Y, Cao Y, Ma X. Wang B, et al. Among authors: yan j. Endocrine. 2009 Apr;35(2):198-203. doi: 10.1007/s12020-009-9152-8. Epub 2009 Feb 4. Endocrine. 2009. PMID: 19191034

3

Interleukin 1 beta (IL-1β) promoter C [-511] T polymorphism but not C [+3953] T polymorphism is associated with polycystic ovary syndrome.

Mu Y, Liu J, Wang B, Wen Q, Wang J, Yan J, Zhou S, Ma X, Cao Y. Mu Y, et al. Among authors: yan j. Endocrine. 2010 Feb;37(1):71-5. doi: 10.1007/s12020-009-9268-x. Epub 2009 Nov 10. Endocrine. 2010. PMID: 20963558

4

Identification of novel missense mutations of GDF9 in Chinese women with polycystic ovary syndrome.

Wang B, Zhou S, Wang J, Liu J, Ni F, Yan J, Mu Y, Cao Y, Ma X. Wang B, et al. Among authors: yan j. Reprod Biomed Online. 2010 Sep;21(3):344-8. doi: 10.1016/j.rbmo.2010.04.013. Epub 2010 Apr 24. Reprod Biomed Online. 2010. PMID: 20705511

5

Teratocarcinoma-derived growth factor 1 (TDGF1) sequence variants in patients with congenital heart defect.

Wang B, Yan J, Peng Z, Wang J, Liu S, Xie X, Ma X. Wang B, et al. Among authors: yan j. Int J Cardiol. 2011 Jan 21;146(2):225-7. doi: 10.1016/j.ijcard.2009.08.046. Epub 2009 Oct 24. Int J Cardiol. 2011. PMID: 19853938

6

Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

Wang B, Yan J, Mi R, Zhou S, Xie X, Wang J, Ma X. Wang B, et al. Among authors: yan j. Int J Cardiol. 2010 Nov 5;145(1):83-5. doi: 10.1016/j.ijcard.2009.05.030. Epub 2009 Jun 13. Int J Cardiol. 2010. PMID: 19525021

7

CFC1 mutations in Chinese children with congenital heart disease.

Wang B, Wang J, Liu S, Han X, Xie X, Tao Y, Yan J, Ma X. Wang B, et al. Among authors: yan j. Int J Cardiol. 2011 Jan 7;146(1):86-8. doi: 10.1016/j.ijcard.2009.07.034. Epub 2009 Oct 23. Int J Cardiol. 2011. PMID: 19853937

8

Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect.

Wang B, Li L, Xie X, Wang J, Yan J, Mu Y, Ma X. Wang B, et al. Among authors: yan j. Int J Cardiol. 2010 Nov 19;145(2):224-226. doi: 10.1016/j.ijcard.2009.05.067. Epub 2009 Jul 19. Int J Cardiol. 2010. PMID: 19619907

9

A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family.

He X, Gu F, Wang Y, Yan J, Zhang M, Huang S, Ma X. He X, et al. Among authors: yan j. Mol Vis. 2008 Jan 11;14:56-60. Mol Vis. 2008. PMID: 18246032 Free PMC article.

10

Two novel HAND1 mutations in Chinese patients with ventricular septal defect.

Cheng Z, Lib L, Li Z, Liu M, Yan J, Wang B, Ma X. Cheng Z, et al. Among authors: yan j. Clin Chim Acta. 2012 Apr 11;413(7-8):675-7. doi: 10.1016/j.cca.2011.10.014. Epub 2011 Oct 18. Clin Chim Acta. 2012. PMID: 22032825

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

19,403 results

Search Page

Filters