Yang Q - Search Results

1

A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia.

Huang C, Yang Q, Ke T, Wang H, Wang X, Shen J, Tu X, Tian J, Liu JY, Wang QK, Liu M. Huang C, et al. Among authors: yang q. J Hum Genet. 2006;51(12):1133-1137. doi: 10.1007/s10038-006-0071-8. Epub 2006 Oct 26. J Hum Genet. 2006. PMID: 17066260

2

The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family.

Ke T, Nie SW, Yang QB, Liu JP, Zhou LN, Ren X, Liu JY, Wang Q, Liu MG. Ke T, et al. Among authors: yang qb. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Oct;23(5):481-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 17029191

3

Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.

Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK. Liu M, et al. Among authors: yang q, yang j. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3461-6. doi: 10.1167/iovs.05-1438. Invest Ophthalmol Vis Sci. 2006. PMID: 16877416

4

A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families.

Wang X, Xiao F, Yang Q, Liang B, Tang Z, Jiang L, Zhu Q, Chang W, Jiang J, Jiang C, Ren X, Liu JY, Wang QK, Liu M. Wang X, et al. Among authors: yang q. Am J Med Genet A. 2006 Sep 1;140A(17):1846-53. doi: 10.1002/ajmg.a.31372. Am J Med Genet A. 2006. PMID: 16892395

5

The R1947X mutation of NF1 causing autosomal dominant neurofibromatosis type 1 in a Chinese family.

Yang Q, Huang C, Yang X, Feng Y, Wang Q, Liu M. Yang Q, et al. Among authors: yang x. J Genet Genomics. 2008 Feb;35(2):73-6. doi: 10.1016/S1673-8527(08)60011-9. J Genet Genomics. 2008. PMID: 18407053

6

[NF1 mutation analysis in a Chinese family with neuro- fibromatosis type].

Huang YH, Yang QB, Deng YH, Yu NW, Wang Q, Liu MG. Huang YH, et al. Among authors: yang qb. Yi Chuan. 2008 Mar;30(3):309-12. doi: 10.3724/sp.j.1005.2008.00309. Yi Chuan. 2008. PMID: 18331998 Chinese.

7

Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.

Wang P, Yang Q, Wu X, Yang Y, Shi L, Wang C, Wu G, Xia Y, Yang B, Zhang R, Xu C, Cheng X, Li S, Zhao Y, Fu F, Liao Y, Fang F, Chen Q, Tu X, Wang QK. Wang P, et al. Among authors: yang q, yang b, yang y. Biochem Biophys Res Commun. 2010 Jul 16;398(1):98-104. doi: 10.1016/j.bbrc.2010.06.042. Epub 2010 Jun 15. Biochem Biophys Res Commun. 2010. PMID: 20558140 Free PMC article.

8

Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndrome.

Yang Q, Li L, Yang R, Shen GQ, Chen Q, Foldvary-Schaefer N, Ondo WG, Wang QK. Yang Q, et al. Among authors: yang r. Mov Disord. 2011 Feb 15;26(3):516-9. doi: 10.1002/mds.23459. Epub 2011 Jan 24. Mov Disord. 2011. PMID: 21264940 Free PMC article.

9

Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population.

Yang Q, Li L, Chen Q, Foldvary-Schaefer N, Ondo WG, Wang QK. Yang Q, et al. Sleep Med. 2011 Sep;12(8):800-4. doi: 10.1016/j.sleep.2011.06.006. Sleep Med. 2011. PMID: 21925394 Free PMC article.

10

Digital Quantitative Detection for Heterogeneous Protein and mRNA Expression Patterns in Circulating Tumor Cells.

Li H, Li J, Zhang Z, Yang Q, Du H, Dong Q, Guo Z, Yao J, Li S, Li D, Pang N, Li C, Zhang W, Zhou L. Li H, et al. Among authors: yang q. Adv Sci (Weinh). 2024 Nov 18:e2410120. doi: 10.1002/advs.202410120. Online ahead of print. Adv Sci (Weinh). 2024. PMID: 39556692

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