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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| Rohm D, Black JB, McCutcheon SR, et al. (2024) Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing. Biorxiv : the Preprint Server For Biology |
| Nuttle X, Burt ND, Currall B, et al. (2023) Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries. Cell Reports Methods. 100672 |
| Giannuzzi G, Chatron N, Mannik K, et al. (2023) Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts. Npj Genomic Medicine. 8: 9 |
| Liao C, Moyses-Oliveira M, De Esch CEF, et al. (2023) Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies. Cell Genomics. 3: 100277 |
| Tai DJC, Razaz P, Erdin S, et al. (2022) Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models. American Journal of Human Genetics |
| Collins RL, Glessner JT, Porcu E, et al. (2022) A cross-disorder dosage sensitivity map of the human genome. Cell |
| Giannuzzi G, Chatron N, Mannik K, et al. (2022) Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts. Npj Genomic Medicine. 7: 38 |
| 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 |