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Author: Shuyang Yao

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  • All-time downloads: 60,901 (rank: 546 out of 364,448)
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    • bioinformatics: 3,277 (rank: 2,880 (tie) out of 31,523)
    • genetics: 37,945 (rank: 98 out of 34,070)
    • genomics: 19,679 (rank: 428 out of 39,230)

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Preprints

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Local genetic effects on gene expression across 44 human tissues

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.

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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

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Using three-dimensional regulatory chromatin interactions from adult and fetal cortex to interpret genetic results for psychiatric disorders and cognitive traits

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Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Subtle stratification confounds estimates of heritability from rare variants

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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

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RICOPILI: Rapid Imputation for COnsortias PIpeLIne

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A method to exploit the structure of genetic ancestry space to enhance case-control studies

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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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