Liu Y - Search Results

1

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.

Lu C, Wu W, Liu F, Yang K, Li J, Liu Y, Wang R, Si N, Gao P, Liu Y, Zhang S, Zhang X. Lu C, et al. Among authors: liu y, liu f. J Transl Med. 2018 Aug 30;16(1):241. doi: 10.1186/s12967-018-1605-5. J Transl Med. 2018. PMID: 30165862 Free PMC article.

2

Novel TRPM6 mutations in familial hypomagnesemia with secondary hypocalcemia.

Zhao Z, Pei Y, Huang X, Liu Y, Yang W, Sun J, Si N, Xing X, Li M, Wang O, Jiang Y, Zhang X, Xia W. Zhao Z, et al. Among authors: liu y. Am J Nephrol. 2013;37(6):541-8. doi: 10.1159/000350886. Epub 2013 May 16. Am J Nephrol. 2013. PMID: 23689795

3

[Identification of a pathogenic microduplication in a Chinese split-hand/split-foot malformation family].

Liu Y, Huang Y, Yang W, Zhang X. Liu Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):276-9. doi: 10.3760/cma.j.issn.1003-9406.2014.03.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928001 Chinese.

4

Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria.

Lu C, Liu J, Liu F, Liu Y, Ma D, Zhang X. Lu C, et al. Among authors: liu j, liu y, liu f. J Dermatol Sci. 2014 Dec;76(3):255-8. doi: 10.1016/j.jdermsci.2014.08.015. Epub 2014 Sep 11. J Dermatol Sci. 2014. PMID: 25288164 No abstract available.

5

Characterization of gene mutations and phenotypes of cystic fibrosis in Chinese patients.

Liu Y, Wang L, Tian X, Xu KF, Xu W, Li X, Yue C, Zhang P, Xiao Y, Zhang X. Liu Y, et al. Respirology. 2015 Feb;20(2):312-8. doi: 10.1111/resp.12452. Epub 2015 Jan 8. Respirology. 2015. PMID: 25580864

6

p.G970D is the most frequent CFTR mutation in Chinese patients with cystic fibrosis.

Tian X, Liu Y, Yang J, Wang H, Liu T, Xu W, Li X, Zhu Y, Xu KF, Zhang X. Tian X, et al. Among authors: liu y, liu t. Hum Genome Var. 2016 Jan 7;3:15063. doi: 10.1038/hgv.2015.63. eCollection 2016. Hum Genome Var. 2016. PMID: 27081564 Free PMC article.

7

RNF213 as the major susceptibility gene for Chinese patients with moyamoya disease and its clinical relevance.

Zhang Q, Liu Y, Zhang D, Wang R, Zhang Y, Wang S, Yu L, Lu C, Liu F, Zhou J, Zhang X, Zhao J. Zhang Q, et al. Among authors: liu y, liu f. J Neurosurg. 2017 Apr;126(4):1106-1113. doi: 10.3171/2016.2.JNS152173. Epub 2016 Apr 29. J Neurosurg. 2017. PMID: 27128593

8

The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.

Zhang Q, Liu Y, Yu L, Duan R, Ma Y, Ge P, Zhang D, Zhang Y, Wang R, Wang S, Zhao Y, Cao Y, Liu X, Deng X, Zhao J, Zhang X. Zhang Q, et al. Among authors: liu y, liu x. World Neurosurg. 2017 Mar;99:701-708.e1. doi: 10.1016/j.wneu.2016.12.119. Epub 2017 Jan 5. World Neurosurg. 2017. PMID: 28063898 Review.

9

Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome.

Liu Y, Xu Z, Feng R, Zhan Y, Wang J, Li G, Li X, Zhang W, Hu X, Tian X, Xu KF, Zhang X. Liu Y, et al. Orphanet J Rare Dis. 2017 May 30;12(1):104. doi: 10.1186/s13023-017-0656-7. Orphanet J Rare Dis. 2017. PMID: 28558743 Free PMC article.

10

A novel homozygous complex deletion in CFTR caused cystic fibrosis in a Chinese patient.

Liu K, Liu Y, Li X, Xu KF, Tian X, Zhang X. Liu K, et al. Among authors: liu y. Mol Genet Genomics. 2017 Oct;292(5):1083-1089. doi: 10.1007/s00438-017-1334-0. Epub 2017 Jun 15. Mol Genet Genomics. 2017. PMID: 28620757

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