Mudge, Joann
National Center for Genome Resources
4 papers on CoChatORCID 0000-0002-2972-1640
Most cited papers
- Verified
Carrier testing for severe childhood recessive diseases by next-generation sequencing
Bell, C. J., Dinwiddie, D. L., Miller, N. A., Hateley, S. L., Ganusova, E. E., Mudge, J., Langley, R. J., Zhang, L., Lee, C. C., Schilkey, F. D., et al. (2011) · Science Translational Medicine
Genomics and Rare DiseasesPrenatal Screening and Diagnostics
Cited by 706
- Verified
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
Baranzini, S. E., Mudge, J., van Velkinburgh, J. C., Khankhanian, P., Khrebtukova, I., Miller, N. A., Zhang, L., Farmer, A. D., Bell, C. J., Kim, R. W., et al. (2010) · Nature
Multiple Sclerosis Research StudiesGenetic Associations and Epidemiology
Cited by 476
- Verified
Dense sampling of bird diversity increases power of comparative genomics
Feng, S., Stiller, J., Deng, Y., Armstrong, J., Fang, Q., Reeve, A. H., Xie, D., Chen, G., Guo, C., Faircloth, B. C., et al. (2020) · Nature
Genomics and Phylogenetic StudiesChromosomal and Genetic Variations
Cited by 459
- Verified
A highly annotated whole-genome sequence of a Korean individual
Kim, J.-I., Ju, Y. S., Park, H., Kim, S., Lee, S., Yi, J.-H., Mudge, J., Miller, N. A., Hong, D., Bell, C. J., et al. (2009) · Nature
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 330
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