Karyn Steinberg, Ph.D.
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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"Karyn Steinberg"
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| Locke AE, Steinberg KM, Chiang CWK, et al. (2019) Exome sequencing of Finnish isolates enhances rare-variant association power. Nature |
| Huddleston J, Chaisson MJP, Steinberg KM, et al. (2018) Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data. Genome Research. 28: 144 |
| Schneider VA, Graves-Lindsay T, Howe K, et al. (2017) Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly. Genome Research |
| Church DM, Schneider VA, Steinberg KM, et al. (2015) Extending reference assembly models. Genome Biology. 16: 13 |
| Watson CT, Steinberg KM, Graves TA, et al. (2015) Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity. Genes and Immunity. 16: 24-34 |
| Steinberg KM, Schneider VA, Graves-Lindsay TA, et al. (2014) Single haplotype assembly of the human genome from a hydatidiform mole. Genome Research. 24: 2066-76 |
| Antonacci F, Dennis MY, Huddleston J, et al. (2014) Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability. Nature Genetics. 46: 1293-302 |
| Koboldt DC, Steinberg KM, Larson DE, et al. (2013) The next-generation sequencing revolution and its impact on genomics. Cell. 155: 27-38 |
| Watson CT, Steinberg KM, Huddleston J, et al. (2013) Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation. American Journal of Human Genetics. 92: 530-46 |
| Mueller M, Barros P, Witherden AS, et al. (2013) Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus. American Journal of Human Genetics. 92: 28-40 |