Zhang Q - Search Results

1

Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype.

Perrault I, Estrada-Cuzcano A, Lopez I, Kohl S, Li S, Testa F, Zekveld-Vroon R, Wang X, Pomares E, Andorf J, Aboussair N, Banfi S, Delphin N, den Hollander AI, Edelson C, Florijn R, Jean-Pierre M, Leowski C, Megarbane A, Villanueva C, Flores B, Munnich A, Ren H, Zobor D, Bergen A, Chen R, Cremers FP, Gonzalez-Duarte R, Koenekoop RK, Simonelli F, Stone E, Wissinger B, Zhang Q, Kaplan J, Rozet JM. Perrault I, et al. Among authors: zhang q. PLoS One. 2013;8(1):e51622. doi: 10.1371/journal.pone.0051622. Epub 2013 Jan 7. PLoS One. 2013. PMID: 23308101 Free PMC article.

2

Linkage analysis of two families with X-linked recessive congenital motor nystagmus.

Guo X, Li S, Jia X, Xiao X, Wang P, Zhang Q. Guo X, et al. Among authors: zhang q. J Hum Genet. 2006;51(1):76-80. doi: 10.1007/s10038-005-0316-y. Epub 2005 Oct 21. J Hum Genet. 2006. PMID: 16240070

3

CSNB1 in Chinese families associated with novel mutations in NYX.

Xiao X, Jia X, Guo X, Li S, Yang Z, Zhang Q. Xiao X, et al. Among authors: zhang q. J Hum Genet. 2006;51(7):634-40. doi: 10.1007/s10038-006-0406-5. Epub 2006 May 3. J Hum Genet. 2006. PMID: 16670814

4

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy.

Jia X, Li S, Xiao X, Guo X, Zhang Q. Jia X, et al. Among authors: zhang q. J Hum Genet. 2006;51(10):851-856. doi: 10.1007/s10038-006-0032-2. Epub 2006 Sep 14. J Hum Genet. 2006. PMID: 16972023

5

The 208delG mutation in FSCN2 does not associate with retinal degeneration in Chinese individuals.

Zhang Q, Li S, Xiao X, Jia X, Guo X. Zhang Q, et al. Invest Ophthalmol Vis Sci. 2007 Feb;48(2):530-3. doi: 10.1167/iovs.06-0669. Invest Ophthalmol Vis Sci. 2007. PMID: 17251446

6

FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus.

Zhang Q, Xiao X, Li S, Guo X. Zhang Q, et al. Mol Vis. 2007 Aug 3;13:1375-8. Mol Vis. 2007. PMID: 17768376

7

Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism.

Fang S, Guo X, Jia X, Xiao X, Li S, Zhang Q. Fang S, et al. Among authors: zhang q. Mol Vis. 2008;14:1974-82. Epub 2008 Oct 30. Mol Vis. 2008. PMID: 18978956 Free PMC article.

8

Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.

Yang Z, Xiao X, Li S, Zhang Q. Yang Z, et al. Among authors: zhang q. Mol Vis. 2009;15:312-8. Epub 2009 Feb 9. Mol Vis. 2009. PMID: 19204786 Free PMC article.

9

Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.

Yu D, Jia X, Zhang AM, Li S, Zou Y, Zhang Q, Yao YG. Yu D, et al. Among authors: zhang q, zhang am. PLoS One. 2010 Oct 18;5(10):e13426. doi: 10.1371/journal.pone.0013426. PLoS One. 2010. PMID: 20976138 Free PMC article.

10

mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population.

Jia X, Li S, Wang P, Guo X, Zhang Q. Jia X, et al. Among authors: zhang q. Biochem Biophys Res Commun. 2010 Dec 10;403(2):237-41. doi: 10.1016/j.bbrc.2010.11.017. Epub 2010 Nov 11. Biochem Biophys Res Commun. 2010. PMID: 21074518

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