Han B - Search Results

1

A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.

Du W, Han MK, Wang DY, Han B, Zong L, Lan L, Yang J, Shen Q, Xie LY, Yu L, Guan J, Wang QJ. Du W, et al. Among authors: han b, han mk. Chin Med J (Engl). 2017 Jan 5;130(1):88-92. doi: 10.4103/0366-6999.196565. Chin Med J (Engl). 2017. PMID: 28051029 Free PMC article.

2

Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss.

Zhao Y, Zhao F, Zong L, Zhang P, Guan L, Zhang J, Wang D, Wang J, Chai W, Lan L, Li Q, Han B, Yang L, Jin X, Yang W, Hu X, Wang X, Li N, Li Y, Petit C, Wang J, Wang HY, Wang Q. Zhao Y, et al. Among authors: han b. PLoS One. 2013 Jul 30;8(7):e69549. doi: 10.1371/journal.pone.0069549. Print 2013. PLoS One. 2013. PMID: 23936043 Free PMC article.

3

[Clinical analysis of sudden sensorineural hearing loss in patients with different ages].

Wang DY, Hou ZQ, Liu Y, Gao Y, Li Q, Lan L, Zhao FF, Han B, Wang QJ. Wang DY, et al. Among authors: han b. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 May;48(5):385-8. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24016562 Chinese.

4

A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family.

Zhao Y, Wang D, Zong L, Zhao F, Guan L, Zhang P, Shi W, Lan L, Wang H, Li Q, Han B, Yang L, Jin X, Wang J, Wang J, Wang Q. Zhao Y, et al. Among authors: han b. PLoS One. 2014 May 14;9(5):e97064. doi: 10.1371/journal.pone.0097064. eCollection 2014. PLoS One. 2014. PMID: 24827932 Free PMC article.

5

Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han.

Li Q, Ji Y, Han B, Zong L, Lan L, Zhao Y, Wang H, Wang D, Wang Q. Li Q, et al. Among authors: han b. Chin Med J (Engl). 2014;127(18):3233-7. Chin Med J (Engl). 2014. PMID: 25266519

6

Identification of a novel mutation of PJVK in the Chinese non-syndromic hearing loss population with low prevalence of the PJVK mutations.

Zhang QJ, Lan L, Li N, Qi Y, Zong L, Shi W, Yu L, Wang H, Yang J, Xie LY, Zhao F, Wang DY, Han B, Wang QJ. Zhang QJ, et al. Among authors: han b. Acta Otolaryngol. 2015 Mar;135(3):211-6. doi: 10.3109/00016489.2014.985799. Epub 2015 Jan 28. Acta Otolaryngol. 2015. PMID: 25631766

7

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans.

Guan J, Wang D, Cao W, Zhao Y, Du R, Yuan H, Liu Q, Lan L, Zong L, Yang J, Yin Z, Han B, Zhang F, Wang Q. Guan J, et al. Among authors: han b. J Hum Genet. 2016 Nov;61(11):917-922. doi: 10.1038/jhg.2016.86. Epub 2016 Jul 7. J Hum Genet. 2016. PMID: 27383657 Free PMC article.

8

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11.

Li L, Yuan H, Wang H, Guan J, Lan L, Wang D, Zong L, Liu Q, Han B, Huang D, Wang Q. Li L, et al. Among authors: han b. Acta Otolaryngol. 2018 May;138(5):463-470. doi: 10.1080/00016489.2017.1397743. Epub 2018 Feb 5. Acta Otolaryngol. 2018. PMID: 29400105

9

Phenotype and genotype analysis of a Chinese family with prelingual X-linked hereditary hearing impairment.

Han B, Cheng J, Yang SZ, Cao JY, Shen WD, Ji F, Kang DY, Zhang X, Dai P, Yuan HJ. Han B, et al. Chin Med J (Engl). 2009 Apr 5;122(7):830-3. Chin Med J (Engl). 2009. PMID: 19493398

10

Unilateral auditory neuropathy spectrum disorder.

Zhang QJ, Lan L, Shi W, Wang DY, Qi Y, Zong L, Li Q, Wang H, Ding HN, Li N, Han B, Wang QJ. Zhang QJ, et al. Among authors: han b. Acta Otolaryngol. 2012 Jan;132(1):72-9. doi: 10.3109/00016489.2011.629630. Epub 2011 Nov 10. Acta Otolaryngol. 2012. PMID: 22073929

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