Wei Wang

发表

De novo mutations in histone modifying genes in congenital heart disease

Murim Choi, Hongyu Zhao, Alexander E. Lopez, 2013, Nature.

Simultaneous set-wise testing under dependence, with applications to genome-wide association studies

Wenguang Sun, Zhi Wei, Wei Wang, 2010 .

SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data

H. Hakonarson, P. Hu, Zhi Wei, 2011, Nucleic acids research.

Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing

H. Hakonarson, W. Johnson, T. Jiang, 2013, Genome Medicine.

Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease.

H. Hakonarson, Cecilia Kim, K. Van Steen, 2013, American journal of human genetics.

Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications.

Ying Liu, Wei Wang, Mark Yandell, 2011, Discovery medicine.

Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy

Larry N. Singh, G. Dreyfuss, Zhi Wei, 2013, Proceedings of the National Academy of Sciences.

A change-point model for identifying 3′UTR switching by next-generation RNA sequencing

Hongzhe Li, Zhi Wei, Wei Wang, 2014, Bioinform..

The SLE Transcriptome Exhibits Evidence of Chronic Endotoxin Exposure and Has Widespread Dysregulation of Non-Coding and Coding RNAs

Angela M. Yu, Zhe Zhang, M. Petri, 2014, PloS one.

Minor introns are embedded molecular switches regulated by highly unstable U6atac snRNA

G. Dreyfuss, Zhi Wei, K. Dittmar, 2013, eLife.

Toward more accurate variant calling for “personal genomes”

W. Johnson, T. Jiang, Zhi Wei, 2013 .

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

Joseph T. Glessner, Debra K. Shivers, J. Glessner, 2016, BMC Medical Genetics.

An empirical Bayes testing procedure for detecting variants in analysis of next generation sequencing data

Zhi Wei, Wei Wang, Zhigen Zhao, 2013, 1401.2278.

Collapsing singletons may boost signal for associating rare variants in sequencing study

Zhi Wei, Wei Wang, 2014, BMC Proceedings.