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Author: Jakob Grove

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  • All-time downloads: 56,284 (rank: 571 out of 360,137)
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    • bioinformatics: 492 (rank: 18,314 (tie) out of 31,168)
    • genetics: 50,469 (rank: 65 out of 33,837)
    • genomics: 5,323 (rank: 3,096 out of 39,021)

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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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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Common risk variants identified in autism spectrum disorder

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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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Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

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ASD and ADHD have a similar burden of rare protein-truncating variants

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Genome-wide association study implicates CHRNA2 in cannabis use disorder

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The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

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Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD

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Social and non-social autism symptom and trait domains are genetically dissociable

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Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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The Anorexia Nervosa Genetics Initiative: Overview and Methods

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Estimating the functional impact of INDELs in transcription factor binding sites: a genome-wide landscape

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Genome-wide association study of school grades identifies a genetic overlap between language ability, psychopathology and creativity

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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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Identification of risk variants and characterization of the polygenic architecture of disruptive behavior disorders in the context of ADHD

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Meta-analysis of Scandinavian Schizophrenia Exomes

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Examining sex-differentiated genetic effects across neuropsychiatric and behavioral traits

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