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Kong Xiangyin
Kong Xiangyin
Unknown affiliation
Verified email at sibs.ac.cn
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Year
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
S Xiao, C Yu, X Chou, W Yuan, Y Wang, L Bu, G Fu, M Qian, J Yang, ...
Nature genetics 27 (2), 201-204, 2001
4492001
Predicting drug-target interaction networks based on functional groups and biological features
Z He, J Zhang, XH Shi, LL Hu, X Kong, YD Cai, KC Chou
PloS one 5 (3), e9603, 2010
3682010
Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract
L Bu, Y Jin, Y Shi, R Chu, A Ban, H Eiberg, L Andres, H Jiang, G Zheng, ...
Nature genetics 31 (3), 276-278, 2002
3552002
miR-124 is frequently down-regulated in medulloblastoma and is a negative regulator of SLC16A1
KKW Li, JC Pang, AK Ching, CK Wong, X Kong, Y Wang, L Zhou, Z Chen, ...
Human pathology 40 (9), 1234-1243, 2009
2182009
Analysis and prediction of the metabolic stability of proteins based on their sequential features, subcellular locations and interaction networks
T Huang, XH Shi, P Wang, Z He, KY Feng, LL Hu, X Kong, YX Li, YD Cai, ...
PloS one 5 (6), e10972, 2010
1842010
Genes that escape X-inactivation in humans have high intraspecific variability in expression, are associated with mental impairment but are not slow evolving
Y Zhang, A Castillo-Morales, M Jiang, Y Zhu, L Hu, AO Urrutia, X Kong, ...
Molecular biology and evolution 30 (12), 2588-2601, 2013
1432013
Triphalangeal thumb–polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer
M Sun, F Ma, X Zeng, Q Liu, XL Zhao, FX Wu, GP Wu, ZF Zhang, B Gu, ...
Journal of medical genetics 45 (9), 589-595, 2008
1352008
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2
X Liu, D Han, J Li, B Han, X Ouyang, J Cheng, X Li, Z Jin, Y Wang, ...
The American Journal of Human Genetics 86 (1), 65-71, 2010
1282010
Epigenetic activation of TWIST1 by MTDH promotes cancer stem–like cell traits in breast cancer
Y Liang, J Hu, J Li, Y Liu, J Yu, X Zhuang, L Mu, X Kong, D Hong, Q Yang, ...
Cancer research 75 (17), 3672-3680, 2015
1132015
Alternative promoters influence alternative splicing at the genomic level
D Xin, L Hu, X Kong
PloS one 3 (6), e2377, 2008
992008
A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family
C Yu, X Meng, S Zhang, G Zhao, L Hu, X Kong
Genomics 82 (5), 575-579, 2003
962003
A new locus for hereditary gingival fibromatosis (GINGF2) maps to 5q13–q22
S Xiao, L Bu, L Zhu, G Zheng, M Yang, M Qian, L Hu, J Liu, G Zhao, ...
Genomics 74 (2), 180-185, 2001
962001
Genome-wide interaction-based association analysis identified multiple new susceptibility loci for common diseases
Y Liu, H Xu, S Chen, X Chen, Z Zhang, Z Zhu, X Qin, L Hu, J Zhu, ...
PLoS genetics 7 (3), e1001338, 2011
942011
Prediction of deleterious non-synonymous SNPs based on protein interaction network and hybrid properties
T Huang, P Wang, ZQ Ye, H Xu, Z He, KY Feng, LL Hu, WR Cui, K Wang, ...
PLoS One 5 (7), e11900, 2010
942010
Prediction and analysis of cell-penetrating peptides using pseudo-amino acid composition and random forest models
L Chen, C Chu, T Huang, X Kong, YD Cai
Amino acids 47, 1485-1493, 2015
912015
Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay
Z Zhang, D Xin, P Wang, L Zhou, L Hu, X Kong, LD Hurst
BMC biology 7, 1-13, 2009
872009
Identification of drug-drug interactions using chemical interactions
L Chen, C Chu, YH Zhang, M Zheng, LC Zhu, X Kong, T Huang
Current Bioinformatics 12 (6), 526-534, 2017
842017
Removal of Hsf4 leads to cataract development in mice through down-regulation of γS-crystallin and Bfsp expression
X Shi, B Cui, Z Wang, L Weng, Z Xu, J Ma, G Xu, X Kong, L Hu
BMC Molecular Biology 10, 1-14, 2009
842009
Analysis and prediction of drug–drug interaction by minimum redundancy maximum relevance and incremental feature selection
L Liu, L Chen, YH Zhang, L Wei, S Cheng, X Kong, M Zheng, T Huang, ...
Journal of Biomolecular Structure and Dynamics 35 (2), 312-329, 2017
822017
CYLD mutation causes multiple familial trichoepithelioma in three Chinese families
G Zheng, L Hu, W Huang, K Chen, X Zhang, S Yang, J Sun, Y Jiang, ...
Human mutation 23 (4), 400-400, 2004
822004
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