| Rare variant phasing using paired tumor:normal sequence data. | 0 | 0.34 | 2019 |
| A loop-counting method for covariate-corrected low-rank biclustering of gene-expression and genome-wide association study data. | 0 | 0.34 | 2018 |
| Cell type discovery and representation in the era of high-content single cell phenotyping. | 1 | 0.63 | 2017 |
| Production of a Preliminary Quality Control Pipeline for Single Nuclei RNA-Seq and Its Application in the Analysis of Cell Type Diversity of Post-Mortem Human Brain Neocortex. | 0 | 0.34 | 2017 |
| The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. | 9 | 0.61 | 2016 |
| Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies | 1 | 0.37 | 2015 |
| An application and empirical comparison of statistical analysis methods for associating rare variants to a complex phenotype. | 0 | 0.34 | 2011 |
| The VA Hypertension Primary Care Longitudinal Cohort: Electronic medical records in the post-genomic era. | 1 | 0.35 | 2010 |
| A Covering Method For Detecting Genetic Associations Between Rare Variants And Common Phenotypes | 13 | 2.34 | 2010 |
| Prestige centrality-based functional outlier detection in gene expression analysis. | 2 | 0.39 | 2009 |
| Predicting functional regulatory polymorphisms. | 4 | 0.45 | 2008 |
| Accurate prediction of deleterious protein kinase polymorphisms. | 8 | 0.57 | 2007 |
