| De novo mutations in histone-modifying genes in congenital heart disease S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ... Nature 498 (7453), 220-223, 2013 | 980 | 2013 |
| Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing J O'Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu, P Bodily, L Tian, ... Genome medicine 5, 1-18, 2013 | 551 | 2013 |
| SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data Z Wei, W Wang, P Hu, GJ Lyon, H Hakonarson Nucleic acids research 39 (19), e132-e132, 2011 | 326 | 2011 |
| Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease Z Wei, W Wang, J Bradfield, J Li, C Cardinale, E Frackelton, C Kim, ... The American Journal of Human Genetics 92 (6), 1008-1012, 2013 | 214 | 2013 |
| Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy Z Zhang, AM Pinto, L Wan, W Wang, MG Berg, I Oliva, LN Singh, ... Proceedings of the National Academy of Sciences 110 (48), 19348-19353, 2013 | 195 | 2013 |
| The SLE transcriptome exhibits evidence of chronic endotoxin exposure and has widespread dysregulation of non-coding and coding RNAs L Shi, Z Zhang, AM Yu, W Wang, Z Wei, E Akhter, K Maurer, PC Reis, ... PloS one 9 (5), e93846, 2014 | 151 | 2014 |
| Minor introns are embedded molecular switches regulated by highly unstable U6atac snRNA I Younis, K Dittmar, W Wang, SW Foley, MG Berg, KY Hu, Z Wei, L Wan, ... Elife 2, e00780, 2013 | 102 | 2013 |
| Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications GJ Lyon, T Jiang, R Van Wijk, W Wang, PM Bodily, J Xing, L Tian, ... Discovery medicine 12 (62), 41, 2011 | 80 | 2011 |
| A change-point model for identifying 3′ UTR switching by next-generation RNA sequencing W Wang, Z Wei, H Li Bioinformatics 30 (15), 2162-2170, 2014 | 49 | 2014 |
| Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility TH Finkel, J Li, Z Wei, W Wang, H Zhang, EM Behrens, EL Reuschel, ... BMC medical genetics 17, 1-9, 2016 | 23 | 2016 |
| An empirical Bayes testing procedure for detecting variants in analysis of next generation sequencing data Z Zhao, W Wang, Z Wei The Annals of Applied Statistics, 2229-2248, 2013 | 20 | 2013 |
| SNVerGUI: a desktop tool for variant analysis of next-generation sequencing data W Wang, W Hu, F Hou, P Hu, Z Wei Journal of medical genetics 49 (12), 753-755, 2012 | 20 | 2012 |
| Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing. Genome Med. 2013; 5: 28 J O’Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu, P Bodily, L Tian, ... BioMed Central Full Text, 0 | 14 | |
| Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing. Genome Med J O’Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu, P Bodily, LF Tian, ... BioMed Central Ltd 5, 28, 2013 | 10 | 2013 |
| Collapsing singletons may boost signal for associating rare variants in sequencing study W Wang, Z Wei BMC proceedings 8, 1-4, 2014 | 3 | 2014 |
| Simultaneous set-wise testing under dependence, with applications to genome-wide association studies W Sun, W Wang, Z Wei Statistics and its Interface 3 (4), 501-511, 2010 | 3 | 2010 |
