Bradley Coe, Ph.D.
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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"Bradley Coe"
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Publications
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| Cingoz S, Soydemir D, Oner TO, et al. (2022) Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations. European Journal of Medical Genetics. 104497 |
| Fanjul-Fernández M, Brown NJ, Hickey P, et al. (2021) A family study implicates GBE1 in the etiology of autism spectrum disorder. Human Mutation |
| Wilfert AB, Turner TN, Murali SC, et al. (2021) Recent ultra-rare inherited variants implicate new autism candidate risk genes. Nature Genetics |
| Wang T, Hoekzema K, Vecchio D, et al. (2020) Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature Communications. 11: 5398 |
| Wang T, Hoekzema K, Vecchio D, et al. (2020) Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature Communications. 11: 4932 |
| Sadler B, Haller G, Antunes L, et al. (2020) Rare and duplications containing in clubfoot. Journal of Medical Genetics |
| Li YR, Glessner JT, Coe BP, et al. (2020) Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations. Nature Communications. 11: 255 |
| Tilghman JM, Ling AY, Turner TN, et al. (2019) Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease. The New England Journal of Medicine. 380: 1421-1432 |
| Maggiolini FAM, Cantsilieris S, D'Addabbo P, et al. (2019) Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus. Plos Genetics. 15: e1008075 |
| Ang CE, Ma Q, Wapinski OL, et al. (2019) The novel lncRNA is pro-neurogenic and mutated in human neurodevelopmental disorders. Elife. 8 |