PubRank

Xiangtian Zhou

Author PubWeight™ 54.95‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 MicroRNA-34a inhibits uveal melanoma cell proliferation and migration through downregulation of c-Met. Invest Ophthalmol Vis Sci 2008 1.80
2 Deletion of G protein-coupled receptor 48 leads to ocular anterior segment dysgenesis (ASD) through down-regulation of Pitx2. Proc Natl Acad Sci U S A 2008 1.53
3 Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families. Ophthalmology 2010 1.44
4 The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation. Invest Ophthalmol Vis Sci 2006 1.23
5 Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. Am J Hum Genet 2011 1.23
6 Involvement of PI3K/Akt signaling pathway in hepatocyte growth factor-induced migration of uveal melanoma cells. Invest Ophthalmol Vis Sci 2008 1.22
7 Gene therapy following subretinal AAV5 vector delivery is not affected by a previous intravitreal AAV5 vector administration in the partner eye. Mol Vis 2009 1.16
8 Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis. Invest Ophthalmol Vis Sci 2011 1.16
9 Axial myopia induced by a monocularly-deprived facemask in guinea pigs: A non-invasive and effective model. Exp Eye Res 2005 1.13
10 A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population. Hum Mol Genet 2011 1.09
11 Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse. Exp Eye Res 2010 1.07
12 Exome sequencing reveals CCDC111 mutation associated with high myopia. Hum Genet 2013 1.07
13 Toll-like receptors (TLRs) expression and function in response to inactivate hyphae of Fusarium solani in immortalized human corneal epithelial cells. Mol Vis 2007 1.05
14 The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family. Gene 2006 1.04
15 Axial myopia induced by hyperopic defocus in guinea pigs: A detailed assessment on susceptibility and recovery. Exp Eye Res 2009 1.01
16 Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation. Ophthalmology 2009 1.00
17 Biomechanical properties of the cornea in high myopia. Vision Res 2008 0.99
18 Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family. Mitochondrion 2006 0.99
19 Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy. Biochem Biophys Res Commun 2005 0.96
20 Inhibition of experimental myopia by a dopamine agonist: different effectiveness between form deprivation and hyperopic defocus in guinea pigs. Mol Vis 2011 0.95
21 Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation. Biochem Biophys Res Commun 2005 0.94
22 A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population. Hum Mol Genet 2013 0.92
23 Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation. Biochem Biophys Res Commun 2009 0.91
24 The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss. Biochem Biophys Res Commun 2007 0.90
25 The presence of m1 to m5 receptors in human sclera: evidence of the sclera as a potential site of action for muscarinic receptor antagonists. Curr Eye Res 2006 0.90
26 Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation. J Genet Genomics 2008 0.89
27 A comparative transcriptomic analysis of uveal melanoma and normal uveal melanocyte. PLoS One 2011 0.88
28 Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population. Mol Vis 2010 0.88
29 Developmental expression of three small GTPases in the mouse eye. Mol Vis 2007 0.88
30 Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation. Mol Genet Metab 2010 0.87
31 cAMP level modulates scleral collagen remodeling, a critical step in the development of myopia. PLoS One 2013 0.86
32 Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families. Biochem Biophys Res Commun 2010 0.85
33 Deciphering gene expression program of MAP3K1 in mouse eyelid morphogenesis. Dev Biol 2012 0.85
34 Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation. Biochem Biophys Res Commun 2009 0.84
35 The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation. Mitochondrion 2011 0.83
36 The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy. Biochem Biophys Res Commun 2007 0.83
37 Spontaneous axial myopia and emmetropization in a strain of wild-type guinea pig (Cavia porcellus). Invest Ophthalmol Vis Sci 2008 0.82
38 Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation. Mol Genet Metab 2010 0.82
39 The role of cGMP in ocular growth and the development of form-deprivation myopia in guinea pigs. Invest Ophthalmol Vis Sci 2013 0.81
40 Expression of melanin-related genes in cultured adult human retinal pigment epithelium and uveal melanoma cells. Mol Vis 2007 0.81
41 Feasibility of two-dimensional gel electrophoresis used for proteomic analysis of human scleral fibroblasts. Curr Eye Res 2007 0.81
42 Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families. Biochem Biophys Res Commun 2006 0.81
43 Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy. Invest Ophthalmol Vis Sci 2014 0.80
44 Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation. Biochim Biophys Acta 2009 0.80
45 Spontaneous high myopia in one eye will affect the development of form deprivation myopia in the fellow eye. Curr Eye Res 2011 0.79
46 The FGF2 gene in a myopia animal model and human subjects. Mol Vis 2012 0.79
47 Disruption of emmetropization and high susceptibility to deprivation myopia in albino guinea pigs. Invest Ophthalmol Vis Sci 2011 0.79
48 Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families. Mitochondrion 2013 0.78
49 On the compensation of horizontal coma aberrations in young human eyes. Ophthalmic Physiol Opt 2008 0.78
50 Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Nat Commun 2016 0.78
51 Development of the human superior colliculus and the retinocollicular projection. Exp Eye Res 2005 0.78
52 Association study of 15q14 and 15q25 with high myopia in the Han Chinese population. BMC Genet 2014 0.77
53 Association analysis of retinoic acid receptor beta (RARbeta) gene with high myopia in Chinese subjects. Mol Vis 2010 0.77
54 Mechanism of pH-sensitive polymer-assisted protein refolding and its application in TGF-beta1 and KGF-2. Biotechnol Prog 2009 0.77
55 The effect of temporal and spatial stimuli on the refractive status of guinea pigs following natural emmetropization. Invest Ophthalmol Vis Sci 2013 0.77
56 Central vagal sensory and motor connections: human embryonic and fetal development. Auton Neurosci 2004 0.77
57 Development of the human nucleus of the solitary tract: a cyto- and chemoarchitectural study. Auton Neurosci 2006 0.76
58 Assessment of exonic single nucleotide polymorphisms in the adenosine A2A receptor gene to high myopia susceptibility in Chinese subjects. Mol Vis 2011 0.76
59 Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families. Invest Ophthalmol Vis Sci 2010 0.76
60 [Intestinal microbiota and enterohepatic diseases]. Zhonghua Gan Zang Bing Za Zhi 2014 0.75
61 [A preliminary study on development of human visual system in fetus by DiI-tracing]. Zhonghua Yan Ke Za Zhi 2002 0.75
62 Development of the human dorsal nucleus of the vagus. Early Hum Dev 2007 0.75
63 [How to inhibit the incidence rate of myopia]. Zhonghua Yi Xue Za Zhi 2014 0.75
64 Effects of muscarinic receptor modulators on ocular biometry of guinea pigs. Ophthalmic Physiol Opt 2014 0.75