Thomas L. Casavant
Affiliations: | Electrical and Computer Engineering | University of Iowa, Iowa City, IA |
Area:
Bioinformatics Biology, GeneticsGoogle:
"Thomas Casavant"
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Publications
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| Walls WD, Moteki H, Thomas TR, et al. (2020) A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Human Genetics |
| Tollefson MR, Litman JM, Qi G, et al. (2019) Structural Insights into Hearing Loss Genetics from Polarizable Protein Repacking. Biophysical Journal |
| Azaiez H, Booth KT, Ephraim SS, et al. (2018) Genomic Landscape and Mutational Signatures of Deafness-Associated Genes. American Journal of Human Genetics |
| Monson ET, de Klerk K, Gaynor SC, et al. (2016) Whole-gene sequencing investigation of SAT1 in attempted suicide. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics |
| Goodman CW, Major HJ, Walls WD, et al. (2015) CNV-ROC: A cost effective, computer-aided analytical performance evaluator of chromosomal microarrays. Journal of Biomedical Informatics. 54: 106-13 |
| Shearer AE, Eppsteiner RW, Booth KT, et al. (2014) Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants. American Journal of Human Genetics. 95: 445-53 |
| Shearer AE, Black-Ziegelbein EA, Hildebrand MS, et al. (2013) Advancing genetic testing for deafness with genomic technology. Journal of Medical Genetics. 50: 627-34 |
| Nannapaneni K, Ben-Shahar Y, Keen HL, et al. (2013) Computational identification of operon-like transcriptional loci in eukaryotes. Computers in Biology and Medicine. 43: 738-43 |
| Wagner AH, Taylor KR, DeLuca AP, et al. (2013) Prioritization of retinal disease genes: an integrative approach. Human Mutation. 34: 853-9 |
| Wagner AH, Anand VN, Wang WH, et al. (2013) Exon-level expression profiling of ocular tissues. Experimental Eye Research. 111: 105-11 |