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Author: Douglas Ruderfer

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  • All-time downloads: 36,364 (rank: 723 out of 334,426)
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    • genetics: 8,946 (rank: 1,387 out of 32,426)
    • genomics: 27,418 (rank: 233 out of 36,847)

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Preprints

Analysis of protein-coding genetic variation in 60,706 humans

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

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The ExAC Browser: Displaying reference data information from over 60,000 exomes

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

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Functional annotation of rare structural variation in the human brain

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

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Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide

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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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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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Genetic risk for major depressive disorder and loneliness in gender-specific associations with coronary artery disease

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

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