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Author: Eli A Stahl

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    • genomics: 7,044 (rank: 2,377 (tie) out of 42,763)
    • neuroscience: 570 (rank: 29,404 (tie) out of 67,824)

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Preprints

Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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Partitioning heritability by functional category using GWAS summary statistics

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Genomewide association study identifies 30 loci associated with bipolar disorder

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The PAGE Study: How Genetic Diversity Improves Our Understanding of the Architecture of Complex Traits

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Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Co-localization of Conditional eQTL and GWAS Signatures in Schizophrenia

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Genome-wide association study implicates CHRNA2 in cannabis use disorder

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Penetrance and pleiotropy of polygenic risk scores for schizophrenia in 106,160 patients across four healthcare systems

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

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Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development.

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Transcriptomic Imputation of Bipolar Disorder and Bipolar subtypes reveals 29 novel associated genes

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

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Integrative analysis of rare variants and pathway information shows convergent results between immune pathways, drug targets and epilepsy genes

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Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with signatures from post mortem adult brains

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Dynamic landscape and genetic regulation of RNA editing in schizophrenia

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Analysis of Genetically Regulated Gene Expression identifies a trauma type specific PTSD gene, SNRNP35

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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

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Characterization of single gene copy number variants in schizophrenia

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Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records

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mTADA: a framework for analyzing de novo mutations in multiple traits

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Rare protein coding variants implicate genes involved in risk of suicide death

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Genomic dissection of 43 serum urate-associated loci provides multiple insights into molecular mechanisms of urate control.

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