Andrew Itsara, M.D., Ph.D.
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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"Andrew Itsara"Parents
Sign in to add mentor| Evan Eichler | grad student | 2007-2011 | University of Washington | |
| (Detection and Characterization of Human Copy-Number Variation.) | ||||
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Publications
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| Sivakumaran TA, Igo RP, Kidd JM, et al. (2018) Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration. Plos One. 13: e0209943 |
| Amendola LM, Dorschner MO, Robertson PD, et al. (2015) Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Research. 25: 305-15 |
| Nuttle X, Itsara A, Shendure J, et al. (2014) Resolving genomic disorder-associated breakpoints within segmental DNA duplications using massively parallel sequencing. Nature Protocols. 9: 1496-513 |
| Itsara A, Vissers LE, Steinberg KM, et al. (2012) Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing. American Journal of Human Genetics. 90: 599-613 |
| Sivakumaran TA, Igo RP, Kidd JM, et al. (2011) A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. Plos One. 6: e25598 |
| Itsara A, Wu H, Smith JD, et al. (2010) De novo rates and selection of large copy number variation. Genome Research. 20: 1469-81 |
| Girirajan S, Rosenfeld JA, Cooper GM, et al. (2010) A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nature Genetics. 42: 203-9 |
| Itsara A, Cooper GM, Baker C, et al. (2009) Population analysis of large copy number variants and hotspots of human genetic disease. American Journal of Human Genetics. 84: 148-61 |
| Mefford HC, Sharp AJ, Baker C, et al. (2008) Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. The New England Journal of Medicine. 359: 1685-99 |
| Sharp AJ, Itsara A, Cheng Z, et al. (2007) Optimal design of oligonucleotide microarrays for measurement of DNA copy-number. Human Molecular Genetics. 16: 2770-9 |