Layer, Ryan M.
University of Colorado Boulder
3 papers on CoChatORCID 0000-0002-5823-3232
Most cited papers
- Verified
A complete reference genome improves analysis of human genetic variation
Aganezov, S., Yan, S. M., Soto, D. C., Kirsche, M., Zarate, S., Avdeyev, P., Taylor, D. J., Shafin, K., Shumate, A., Xiao, C., et al. (2022) · Science
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 441
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Mapping and characterization of structural variation in 17,795 human genomes
Genomics, N. C. F. C. D., Abel, H. J., Larson, D. E., Regier, A. A., Chiang, C., Das, I., Kanchi, K. L., Layer, R. M., Neale, B. M., Salerno, W. J., et al. (2020) · Nature
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 310
- Verified
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Werling, D. M., Brand, H., An, J.-Y., Stone, M. R., Zhu, L., Glessner, J. T., Collins, R. L., Dong, S., Layer, R. M., Markenscoff-Papadimitriou, E., et al. (2018) · Nature Genetics
Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology
Cited by 293
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