Osnat Penn, Ph.D.

Affiliations: 
Genome Sciences University of Washington, Seattle, Seattle, WA 
Google:
"Osnat Penn"
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Chow J, Jensen M, Amini H, et al. (2019) Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders. Genome Medicine. 11: 65
Dougherty ML, Underwood JG, Nelson BJ, et al. (2018) Transcriptional fates of human-specific segmental duplications in brain. Genome Research
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
Hormozdiari F, Penn O, Borenstein E, et al. (2015) The discovery of integrated gene networks for autism and related disorders. Genome Research. 25: 142-54
Bernier R, Golzio C, Xiong B, et al. (2014) Disruptive CHD8 mutations define a subtype of autism early in development. Cell. 158: 263-76
See more...