PubRank

Xiangyin Kong

Author PubWeight™ 57.95‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract. Nat Genet 2002 2.21
2 Genes that escape X-inactivation in humans have high intraspecific variability in expression, are associated with mental impairment but are not slow evolving. Mol Biol Evol 2013 1.61
3 Analysis and prediction of the metabolic stability of proteins based on their sequential features, subcellular locations and interaction networks. PLoS One 2010 1.51
4 Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases. PLoS Genet 2011 1.46
5 Predicting drug-target interaction networks based on functional groups and biological features. PLoS One 2010 1.39
6 Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2. Am J Hum Genet 2010 1.34
7 miR-124 is frequently down-regulated in medulloblastoma and is a negative regulator of SLC16A1. Hum Pathol 2009 1.28
8 A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family. Genomics 2003 1.22
9 Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus. Mol Vis 2008 1.17
10 Prediction of deleterious non-synonymous SNPs based on protein interaction network and hybrid properties. PLoS One 2010 1.15
11 A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract. Mol Vis 2003 1.13
12 Alternative promoters influence alternative splicing at the genomic level. PLoS One 2008 1.11
13 Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay. BMC Biol 2009 1.11
14 Activation of paternally expressed imprinted genes in newly derived germline-competent mouse parthenogenetic embryonic stem cell lines. Cell Res 2007 1.07
15 Removal of Hsf4 leads to cataract development in mice through down-regulation of gamma S-crystallin and Bfsp expression. BMC Mol Biol 2009 1.04
16 Analysis and prediction of translation rate based on sequence and functional features of the mRNA. PLoS One 2011 1.04
17 The gamma S-crystallin gene is mutated in autosomal recessive cataract in mouse. Genomics 2002 1.03
18 A novel computational approach to predict transcription factor DNA binding preference. J Proteome Res 2009 1.00
19 The impact of nucleosome positioning on the organization of replication origins in eukaryotes. Biochem Biophys Res Commun 2009 1.00
20 CYLD mutation causes multiple familial trichoepithelioma in three Chinese families. Hum Mutat 2004 0.99
21 Mutation screening of HSF4 in 150 age-related cataract patients. Mol Vis 2008 0.99
22 Evidence that the nonsense-mediated mRNA decay pathway participates in X chromosome dosage compensation in mammals. Biochem Biophys Res Commun 2009 0.98
23 Dosage compensation on the active X chromosome minimizes transcriptional noise of X-linked genes in mammals. Genome Biol 2009 0.97
24 Computational analysis of HIV-1 resistance based on gene expression profiles and the virus-host interaction network. PLoS One 2011 0.96
25 Evidence for common short natural trans sense-antisense pairing between transcripts from protein coding genes. Genome Biol 2008 0.94
26 Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation. Am J Hum Genet 2009 0.94
27 Molecular analysis of PinX1 in medulloblastomas. Int J Cancer 2004 0.93
28 Refinement of the locus for non-syndromic sensorineural deafness (DFN2). J Genet 2004 0.92
29 Association of IL4R gene polymorphisms with asthma in Chinese populations. Hum Mutat 2007 0.91
30 Epigenetic inactivation of DLC-1 in supratentorial primitive neuroectodermal tumor. Hum Pathol 2005 0.91
31 A single C to T transition in intron 5 of LMBR1 gene is associated with triphalangeal thumb-polysyndactyly syndrome in a Chinese family. Biochem Biophys Res Commun 2007 0.90
32 Systematic analysis of human lysine acetylation proteins and accurate prediction of human lysine acetylation through bi-relative adapted binomial score Bayes feature representation. Mol Biosyst 2012 0.90
33 Predicting transcriptional activity of multiple site p53 mutants based on hybrid properties. PLoS One 2011 0.90
34 Novel mutations in the IRF6 gene for Van der Woude syndrome. Hum Genet 2003 0.89
35 Novel association strategy with copy number variation for identifying new risk Loci of human diseases. PLoS One 2010 0.88
36 Identifying protein complexes using hybrid properties. J Proteome Res 2009 0.88
37 Hypomethylation in the promoter region of POMC gene correlates with ectopic overexpression in thymic carcinoids. J Endocrinol 2005 0.88
38 A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15. Hum Genet 2006 0.88
39 Dysfunctions associated with methylation, microRNA expression and gene expression in lung cancer. PLoS One 2012 0.87
40 Length of the ORF, position of the first AUG and the Kozak motif are important factors in potential dual-coding transcripts. Cell Res 2010 0.86
41 Evidence for OTUD-6B participation in B lymphocytes cell cycle after cytokine stimulation. PLoS One 2011 0.86
42 Nonsense-mediated decay targets have multiple sequence-related features that can inhibit translation. Mol Syst Biol 2010 0.86
43 Identification of vimentin as a novel target of HSF4 in lens development and cataract by proteomic analysis. Invest Ophthalmol Vis Sci 2009 0.85
44 Divergence of exonic splicing elements after gene duplication and the impact on gene structures. Genome Biol 2009 0.85
45 A novel locus for disseminated superficial porokeratosis maps to chromosome 18p11.3. J Invest Dermatol 2004 0.84
46 Identification of a new target region by loss of heterozygosity at 5p15.33 in sporadic gastric carcinomas: genotype and phenotype related. Cancer Lett 2005 0.83
47 Prediction of nucleosome positioning based on transcription factor binding sites. PLoS One 2010 0.83
48 Predicting protein subcellular locations with feature selection and analysis. Protein Pept Lett 2010 0.83
49 The inhibition of CMV promoter by heat shock factor 4b is regulated by Daxx. Int J Biochem Cell Biol 2010 0.83
50 SKAP2, a novel target of HSF4b, associates with NCK2/F-actin at membrane ruffles and regulates actin reorganization in lens cell. J Cell Mol Med 2011 0.82
51 Stearoyl-CoA desaturase 1 deficiency protects mice from immune-mediated liver injury. Lab Invest 2008 0.82
52 Screening of Kozak-motif-located SNPs and analysis of their association with human diseases. Biochem Biophys Res Commun 2010 0.81
53 Prediction and analysis of cell-penetrating peptides using pseudo-amino acid composition and random forest models. Amino Acids 2015 0.81
54 A computational method for the identification of new candidate carcinogenic and non-carcinogenic chemicals. Mol Biosyst 2015 0.77
55 Genes that Escape X-Inactivation in Humans Have High Intraspecific Variability in Expression, Are Associated with Mental Impairment but Are Not Slow Evolving. Mol Biol Evol 2015 0.77
56 Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study. Sci Rep 2013 0.77
57 MicroRNA or NMD: why have two RNA silencing systems? J Genet Genomics 2013 0.76
58 Linkage analysis suggests a locus of ichthyosis vulgaris on 1q22. J Hum Genet 2003 0.76
59 Alterations to proteins in the lens of hereditary Crygs-mutated cataractous mice. Mol Vis 2010 0.75
60 De novo structure variations of the Y chromosome in a 47,XXY female with ovarian failure: a case report. Cytogenet Genome Res 2014 0.75
61 A study of the ultrastructure and gene location of hereditary gingival fibromatosis. Zhonghua Kou Qiang Yi Xue Za Zhi 2002 0.75
62 Prediction of bioactive compound pathways using chemical interaction and structural information. Comb Chem High Throughput Screen 2016 0.75