Fereydoun Hormozdiari, Ph.D.

Affiliations: 
Genome Sciences University of Washington, Seattle, Seattle, WA 
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"Fereydoun Hormozdiari"
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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
Ricketts C, Seidman D, Popic V, et al. (2019) Meltos: Multi-Sample Tumor Phylogeny Reconstruction for Structural Variants. Bioinformatics (Oxford, England)
Chaisson MJP, Sanders AD, Zhao X, et al. (2019) Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nature Communications. 10: 1784
Soylev A, Le T, Amini H, et al. (2019) Discovery of tandem and interspersed segmental duplications using high throughput sequencing. Bioinformatics (Oxford, England)
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
Kronenberg ZN, Fiddes IT, Gordon D, et al. (2018) High-resolution comparative analysis of great ape genomes. Science (New York, N.Y.). 360
Turner TN, Coe BP, Dickel DE, et al. (2017) Genomic Patterns of De Novo Mutation in Simplex Autism. Cell
Soylev A, Kockan C, Hormozdiari F, et al. (2017) Toolkit for automated and rapid discovery of structural variants. Methods (San Diego, Calif.)
Stessman HA, Xiong B, Coe BP, et al. (2017) Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. Nature Genetics
Hehir-Kwa JY, Marschall T, Kloosterman WP, et al. (2016) A high-quality human reference panel reveals the complexity and distribution of genomic structural variants. Nature Communications. 7: 12989
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