Parents
Sign in to add mentor| Ross C. Hardison | grad student | 2010-2015 | Penn State (Cell Biology Tree) |
| Marylyn D. Ritchie | post-doc |
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Publications
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| Singhal P, Guare L, Morse C, et al. (2023) DETECT: Feature extraction method for disease trajectory modeling in electronic health records. Amia Joint Summits On Translational Science Proceedings. Amia Joint Summits On Translational Science. 2023: 487-496 |
| Nam Y, Jung SH, Yun JS, et al. (2022) Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data. Bioinformatics (Oxford, England) |
| Humphrey J, Venkatesh S, Hasan R, et al. (2022) Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes. Nature Neuroscience |
| Wagner J, Olson ND, Harris L, et al. (2022) Benchmarking challenging small variants with linked and long reads. Cell Genomics. 2 |
| Byrska-Bishop M, Evani US, Zhao X, et al. (2022) High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios. Cell. 185: 3426-3440.e19 |
| Sahajpal NS, Jill Lai CY, Hastie A, et al. (2022) Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19. Iscience. 103760 |
| Foox J, Tighe SW, Nicolet CM, et al. (2021) Author Correction: Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nature Biotechnology |
| Foox J, Tighe SW, Nicolet CM, et al. (2021) Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nature Biotechnology. 39: 1129-1140 |
| Wilfert AB, Turner TN, Murali SC, et al. (2021) Recent ultra-rare inherited variants implicate new autism candidate risk genes. Nature Genetics |
| Padhi EM, Hayeck TJ, Cheng Z, et al. (2021) Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human Genomics. 15: 44 |