Farhad Hormozdiari, B.S.
Affiliations: | University of Washington, Seattle, Seattle, WA |
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"Farhad Hormozdiari"
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| LaPierre N, Taraszka K, Huang H, et al. (2021) Identifying causal variants by fine mapping across multiple studies. Plos Genetics. 17: e1009733 |
| Alipanahi B, Hormozdiari F, Behsaz B, et al. (2021) Large-scale machine learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology. American Journal of Human Genetics |
| Barbeira AN, Bonazzola R, Gamazon ER, et al. (2021) Exploiting the GTEx resources to decipher the mechanisms at GWAS loci. Genome Biology. 22: 49 |
| Weissbrod O, Hormozdiari F, Benner C, et al. (2020) Functionally informed fine-mapping and polygenic localization of complex trait heritability. Nature Genetics. 52: 1355-1363 |
| Dey KK, van de Geijn B, Kim SS, et al. (2020) Evaluating the informativeness of deep learning annotations for human complex diseases. Nature Communications. 11: 4703 |
| Gay NR, Gloudemans M, Antonio ML, et al. (2020) Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx. Genome Biology. 21: 233 |
| Zou J, Hormozdiari F, Jew B, et al. (2019) Leveraging allelic imbalance to refine fine-mapping for eQTL studies. Plos Genetics. 15: e1008481 |
| van de Geijn B, Finucane H, Gazal S, et al. (2019) Annotations capturing cell-type-specific TF binding explain a large fraction of disease heritability. Human Molecular Genetics |
| Hormozdiari F, van de Geijn B, Nasser J, et al. (2019) Functional disease architectures reveal unique biological role of transposable elements. Nature Communications. 10: 4054 |
| O'Connor LJ, Schoech AP, Hormozdiari F, et al. (2019) Extreme Polygenicity of Complex Traits Is Explained by Negative Selection. American Journal of Human Genetics |