Wang B - Search Results

1

Mutations in Hnrnpa1 cause congenital heart defects.

Yu Z, Tang PL, Wang J, Bao S, Shieh JT, Leung AW, Zhang Z, Gao F, Wong SY, Hui AL, Gao Y, Dung N, Zhang ZG, Fan Y, Zhou X, Zhang Y, Wong DS, Sham PC, Azhar A, Kwok PY, Tam PP, Lian Q, Cheah KS, Wang B, Song YQ. Yu Z, et al. Among authors: wang j, wang b. JCI Insight. 2018 Jan 25;3(2):e98555. doi: 10.1172/jci.insight.98555. eCollection 2018 Jan 25. JCI Insight. 2018. PMID: 29367466 Free PMC article.

2

Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease.

Wang B, Zhou S, Yang Z, Xie YC, Wang J, Zhang P, Lv Z, Zheng C, Ma X. Wang B, et al. Among authors: wang j. J Neurol Sci. 2008 Jul 15;270(1-2):148-51. doi: 10.1016/j.jns.2008.02.021. Epub 2008 Apr 8. J Neurol Sci. 2008. PMID: 18396294

3

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: wang 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

4

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: wang 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

5

A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family.

Wang K, Wang B, Wang J, Zhou S, Yun B, Suo P, Cheng J, Ma X, Zhu S. Wang K, et al. Among authors: wang j, wang b. Mol Vis. 2009 Dec 16;15:2813-20. Mol Vis. 2009. PMID: 20019893 Free PMC article.

6

Wang B, Zhou S, Chen Q, Xie X, Huang G, Wang J, Zhoua S, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2011 Feb 3;146(3):415-6. doi: 10.1016/j.ijcard.2009.12.013. Epub 2010 Feb 24. Int J Cardiol. 2011. PMID: 20181399

7

Association between -238 but not -308 polymorphism of Tumor necrosis factor alpha (TNF-alpha)v and unexplained recurrent spontaneous abortion (URSA) in Chinese population.

Liu C, Wang J, Zhou S, Wang B, Ma X. Liu C, et al. Among authors: wang j, wang b. Reprod Biol Endocrinol. 2010 Sep 28;8:114. doi: 10.1186/1477-7827-8-114. Reprod Biol Endocrinol. 2010. PMID: 20920206 Free PMC article.

8

Evaluation of next-generation sequencing software in mapping and assembly.

Bao S, Jiang R, Kwan W, Wang B, Ma X, Song YQ. Bao S, et al. Among authors: wang b. J Hum Genet. 2011 Jun;56(6):406-14. doi: 10.1038/jhg.2011.43. Epub 2011 Apr 28. J Hum Genet. 2011. PMID: 21525877 Free article. Review.

9

Two novel mutations of the IRX4 gene in patients with congenital heart disease.

Cheng Z, Wang J, Su D, Pan H, Huang G, Li X, Li Z, Shen A, Xie X, Wang B, Ma X. Cheng Z, et al. Among authors: wang j, wang b. Hum Genet. 2011 Nov;130(5):657-62. doi: 10.1007/s00439-011-0996-7. Epub 2011 May 5. Hum Genet. 2011. PMID: 21544582

10

A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree.

Ding X, Wang B, Luo Y, Hu S, Zhou G, Zhou Z, Wang J, Ma X, Qi Y. Ding X, et al. Among authors: wang j, wang b. Mol Vis. 2011;17:1343-9. Epub 2011 May 20. Mol Vis. 2011. PMID: 21647269 Free PMC article.

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