Bradley Coe, Ph.D.

Affiliations: 
Genome Sciences University of Washington, Seattle, Seattle, WA 
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"Bradley Coe"
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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
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
Coe BP, Stessman HAF, Sulovari A, et al. (2019) Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity. Nature Genetics. 51: 106-116
Guo H, Wang T, Wu H, et al. (2018) Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model. Molecular Autism. 9: 64
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
Jansen S, Hoischen A, Coe BP, et al. (2017) A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. European Journal of Human Genetics : Ejhg
Wilfert AB, Sulovari A, Turner TN, et al. (2017) Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications. Genome Medicine. 9: 101
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