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Can Yang
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Moving object detection by detecting contiguous outliers in the low-rank representation
X Zhou, C Yang, W Yu
IEEE transactions on pattern analysis and machine intelligence 35 (3), 597-610, 2012
7602012
BOOST: A fast approach to detecting gene-gene interactions in genome-wide case-control studies
X Wan, C Yang, Q Yang, H Xue, X Fan, NLS Tang, W Yu
The American Journal of Human Genetics 87 (3), 325-340, 2010
5972010
GPA: a statistical approach to prioritizing GWAS results by integrating pleiotropy and annotation
D Chung, C Yang, C Li, J Gelernter, H Zhao
PLoS genetics 10 (11), e1004787, 2014
2102014
SNPHarvester: a filtering-based approach for detecting epistatic interactions in genome-wide association studies
C Yang, Z He, X Wan, Q Yang, H Xue, W Yu
Bioinformatics 25 (4), 504-511, 2009
2032009
Predictive rule inference for epistatic interaction detection in genome-wide association studies
X Wan, C Yang, Q Yang, H Xue, NLS Tang, W Yu
Bioinformatics 26 (1), 30-37, 2010
1982010
GBOOST: a GPU-based tool for detecting gene–gene interactions in genome–wide case control studies
LS Yung, C Yang, X Wan, W Yu
Bioinformatics 27 (9), 1309-1310, 2011
1912011
Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder
P Xie, HR Kranzler, C Yang, H Zhao, LA Farrer, J Gelernter
Biological psychiatry 74 (9), 656-663, 2013
1842013
Low-rank modeling and its applications in image analysis
X Zhou, C Yang, H Zhao, W Yu
ACM Computing Surveys (CSUR) 47 (2), 1-33, 2014
1822014
Total variation regularized tensor RPCA for background subtraction from compressive measurements
W Cao, Y Wang, J Sun, D Meng, C Yang, A Cichocki, Z Xu
IEEE Transactions on Image Processing 25 (9), 4075-4090, 2016
1742016
Leveraging functional annotations in genetic risk prediction for human complex diseases
Y Hu, Q Lu, R Powles, X Yao, C Yang, F Fang, X Xu, H Zhao
PLoS computational biology 13 (6), e1005589, 2017
1602017
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ...
Genome biology 15, 1-18, 2014
1232014
Testing and controlling for horizontal pleiotropy with probabilistic Mendelian randomization in transcriptome-wide association studies
Z Yuan, H Zhu, P Zeng, S Yang, S Sun, C Yang, J Liu, X Zhou
Nature communications 11 (1), 3861, 2020
992020
Pervasive pleiotropy between psychiatric disorders and immune disorders revealed by integrative analysis of multiple GWAS
Q Wang, C Yang, J Gelernter, H Zhao
Human genetics 134, 1195-1209, 2015
942015
MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study
X Wan, C Yang, Q Yang, H Xue, NLS Tang, W Yu
BMC bioinformatics 10, 1-15, 2009
942009
Comments on 'An empirical comparison of several recent epistatic interaction detection methods'.
X Wan, C Yang, W Yu
Bioinformatics, 2011
882011
Deep generative learning via schrödinger bridge
G Wang, Y Jiao, Q Xu, Y Wang, C Yang
International conference on machine learning, 10794-10804, 2021
842021
A unified framework for cross-population trait prediction by leveraging the genetic correlation of polygenic traits
M Cai, J Xiao, S Zhang, X Wan, H Zhao, G Chen, C Yang
The American Journal of Human Genetics 108 (4), 632-655, 2021
842021
Bayesian weighted Mendelian randomization for causal inference based on summary statistics
J Zhao, J Ming, X Hu, G Chen, J Liu, C Yang
Bioinformatics 36 (5), 1501-1508, 2020
842020
Improving genetic risk prediction by leveraging pleiotropy
C Li, C Yang, J Gelernter, H Zhao
Human genetics 133, 639-650, 2014
832014
On high-dimensional misspecified mixed model analysis in genome-wide association study
J Jiang, C Li, D Paul, C Yang, H Zhao
732016
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Articles 1–20