Xander Nuttle, Ph.D.

Affiliations: 
Genome Sciences University of Washington, Seattle, Seattle, WA 
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"Xander Nuttle"
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Publications

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Giannuzzi G, Schmidt PJ, Porcu E, et al. (2019) The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals. American Journal of Human Genetics
Fiddes IT, Lodewijk GA, Mooring M, et al. (2018) Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis. Cell. 173: 1356-1369.e22
Wallace AS, Hudac CM, Steinman KJ, et al. (2018) Longitudinal report of child with de novo 16p11.2 triplication. Clinical Case Reports. 6: 147-154
Dennis MY, Harshman L, Nelson BJ, et al. (2017) The evolution and population diversity of human-specific segmental duplications. Nature Ecology & Evolution. 1: 69
Dennis MY, Harshman L, Nelson BJ, et al. (2017) The evolution and population diversity of human-specific segmental duplications. Nature Ecology & Evolution. 1
Dougherty ML, Nuttle X, Penn O, et al. (2017) The birth of a human-specific neural gene by incomplete duplication and gene fusion. Genome Biology. 18: 49
Nuttle X, Giannuzzi G, Duyzend MH, et al. (2016) Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility. Nature
Duyzend MH, Nuttle X, Coe BP, et al. (2015) Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV. American Journal of Human Genetics
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
Nuttle X, Huddleston J, O'Roak BJ, et al. (2013) Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions. Nature Methods. 10: 903-9
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