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Author: Danielle Posthuma

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    • genetics: 64,219 (rank: 43 out of 33,967)
    • genomics: 7,572 (rank: 1,958 out of 39,128)
    • neuroscience: 1,450 (rank: 10,144 (tie) out of 60,770)

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Preprints

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

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Genome-wide association analysis of lifetime cannabis use (N=184,765) identifies new risk loci, genetic overlap with mental health, and a causal influence of schizophrenia on cannabis use

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The genetic architecture of the human cerebral cortex

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimers disease risk

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Genome-wide Analysis of Insomnia (N=1,331,010) Identifies Novel Loci and Functional Pathways

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GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

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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 association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

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GWAS of brain volume on 54,407 individuals and cross-trait analysis with intelligence identifies shared genomic loci and genes

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A global view of pleiotropy and genetic architecture in complex traits

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FUMA: Functional mapping and annotation of genetic associations

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GWAS Meta-Analysis of Neuroticism (N=449,484) Identifies Novel Genetic Loci and Pathways

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

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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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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Exploring the genetic correlations of antisocial behavior and life history traits

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Functional consequences of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals

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An epigenome-wide association study of educational attainment (n = 10,767)

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Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

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The more the merrier? Multivariate approaches to genome-wide association analysis

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Genetic association study of psychotic experiences in UK Biobank

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Planar cell polarity pathway and development of the human visual cortex

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Lipid associated polygenic enrichment in Alzheimer's disease

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Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

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Quantitative proteomic alterations of human iPSC-based neuronal development indicate early onset of Rett syndrome.

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Genetic correlates of evolutionary adaptations in cognitive functional brain networks and their relationship to human cognitive functioning and disease

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