Osnat Penn, Ph.D.
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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Publications
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| Chow J, Jensen M, Amini H, et al. (2019) Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders. Genome Medicine. 11: 65 |
| Hodge RD, Bakken TE, Miller JA, et al. (2019) Conserved cell types with divergent features in human versus mouse cortex. Nature |
| Dougherty ML, Underwood JG, Nelson BJ, et al. (2018) Transcriptional fates of human-specific segmental duplications in brain. Genome Research |
| Xue AY, Di Pizio A, Levit A, et al. (2018) Independent Evolution of Strychnine Recognition by Bitter Taste Receptor Subtypes. Frontiers in Molecular Biosciences. 5: 9 |
| 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 |
| Stessman HA, Willemsen MH, Fenckova M, et al. (2016) Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders. American Journal of Human Genetics. 98: 541-552 |
| Bar-Rogovsky H, Stern A, Penn O, et al. (2015) Assessing the prediction fidelity of ancestral reconstruction by a library approach. Protein Engineering, Design & Selection : Peds. 28: 507-18 |