Follow
Can Yang
Title
Cited by
Cited by
Year
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
7522012
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
5862010
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
2032014
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
2022009
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
1962010
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
1862011
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
1822013
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
1772014
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
1672016
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
1492017
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
1192014
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
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
932015
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
882020
Comments on 'An empirical comparison of several recent epistatic interaction detection methods'.
X Wan, C Yang, W Yu
Bioinformatics, 2011
872011
Improving genetic risk prediction by leveraging pleiotropy
C Li, C Yang, J Gelernter, H Zhao
Human genetics 133, 639-650, 2014
822014
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
742021
On high-dimensional misspecified mixed model analysis in genome-wide association study
J Jiang, C Li, D Paul, C Yang, H Zhao
702016
Deep generative learning via schrödinger bridge
G Wang, Y Jiao, Q Xu, Y Wang, C Yang
International conference on machine learning, 10794-10804, 2021
672021
Identifying main effects and epistatic interactions from large-scale SNP data via adaptive group Lasso
C Yang, X Wan, Q Yang, H Xue, W Yu
BMC bioinformatics 11, 1-11, 2010
592010
The system can't perform the operation now. Try again later.
Articles 1–20