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Author: Farhad Hormozdiari

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    • bioinformatics: 1,340 (rank: 7,987 (tie) out of 31,489)
    • genetics: 24,364 (rank: 209 out of 34,165)
    • genomics: 4,288 (rank: 4,136 (tie) out of 39,299)

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Preprints

The GTEx Consortium atlas of genetic regulatory effects across human tissues

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Local genetic effects on gene expression across 44 human tissues

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Detecting genome-wide directional effects of transcription factor binding on polygenic disease risk

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Polygenicity of complex traits is explained by negative selection

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Widespread allelic heterogeneity in complex traits

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Exploiting the GTEx resources to decipher the mechanisms at GWAS loci

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Leveraging molecular QTL to understand the genetic architecture of diseases and complex traits

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Colocalization of GWAS and eQTL Signals Detects Target Genes

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Functionally-informed fine-mapping and polygenic localization of complex trait heritability

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Evaluating the informativeness of deep learning annotations for human complex diseases

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Leveraging allele-specific expression to refine fine-mapping for eQTL studies

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Selection on the FADS region in Europeans

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HapIso : An Accurate Method for the Haplotype-Specific Isoforms Reconstruction from Long Single-Molecule Reads

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Genes with high network connectivity are enriched for disease heritability

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The Multivariate Normal Distribution Framework for Analyzing Association Studies

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Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx

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Disease heritability enrichment of regulatory elements is concentrated in elements with ancient sequence age and conserved function across species

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Annotations capturing cell-type-specific TF binding explain a large fraction of disease heritability

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Identifying Causal Variants by Fine Mapping Across Multiple Studies

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Functional disease architectures reveal unique biological role of transposable elements

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