Michael Duyzend, M.D., Ph.D.
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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"Michael Duyzend"
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| Cacheiro P, Lawson S, Van den Veyver IB, et al. (2024) Lethal phenotypes in Mendelian disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101141 |
| Cacheiro P, Lawson S, Van den Veyver IB, et al. (2024) Lethal phenotypes in Mendelian disorders. Medrxiv : the Preprint Server For Health Sciences |
| Hudac CM, Bove J, Barber S, et al. (2020) Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers. Autism Research : Official Journal of the International Society For Autism Research |
| Guo H, Duyzend MH, Coe BP, et al. (2018) Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| 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 |
| 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 |
| Turner TN, Hormozdiari F, Duyzend MH, et al. (2015) Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA. American Journal of Human Genetics |
| 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 |
| Duyzend MH, Eichler EE. (2015) Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism". Biological Psychiatry. 77: 769-71 |