Farhad Hormozdiari, B.S.

Affiliations: 
University of Washington, Seattle, Seattle, WA 
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"Farhad Hormozdiari"

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Evan Eichler research assistant 2010-2010 Simon Fraser
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Publications

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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
Hasin-Brumshtein Y, Khan AH, Hormozdiari F, et al. (2016) Hypothalamic transcriptomes of 99 mouse strains reveal trans eQTL hotspots, splicing QTLs and novel non-coding genes. Elife. 5
Hormozdiari F, Kang EY, Bilow M, et al. (2016) Imputing Phenotypes for Genome-wide Association Studies. American Journal of Human Genetics
Freedman AH, Schweizer RM, Ortega-Del Vecchyo D, et al. (2016) Demographically-Based Evaluation of Genomic Regions under Selection in Domestic Dogs. Plos Genetics. 12: e1005851
Mangul S, Taegyun Yang H, Hormozdiari F, et al. (2016) HapIso: An accurate method for the haplotype-specific isoforms reconstruction from long single-molecule reads Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 9683: 80-92
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
Sudmant PH, Rausch T, Gardner EJ, et al. (2015) An integrated map of structural variation in 2,504 human genomes. Nature. 526: 75-81
Sudmant PH, Mallick S, Nelson BJ, et al. (2015) Global diversity, population stratification, and selection of human copy number variation. Science (New York, N.Y.)
Hormozdiari F, Kichaev G, Yang WY, et al. (2015) Identification of causal genes for complex traits. Bioinformatics (Oxford, England). 31: i206-i213
Kloosterman WP, Francioli LC, Hormozdiari F, et al. (2015) Characteristics of de novo structural changes in the human genome. Genome Research. 25: 792-801
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