Buckingham, Kati J
University of Washington
2 papers on CoChatORCID 0009-0003-0627-0554
Most cited papers
- Verified
Exome sequencing identifies the cause of a mendelian disorder
Ng, S. B., Buckingham, K. J., Lee, C., Bigham, A. W., Tabor, H. K., Dent, K. M., Huff, C. D., Shannon, P. T., Jabs, E. W., Nickerson, D. A., et al. (2010) · Nature Genetics
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 1,957
- Verified
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
Chong, J. X., Buckingham, K. J., Jhangiani, S. N., Boehm, C., Sobreira, N., Smith, J. D., Harrell, T. M., McMillin, M. J., Wiszniewski, W., Gambin, T., et al. (2015) · The American Journal of Human Genetics
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 643
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