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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 64,998 bioRxiv papers from 288,069 authors.

Author: Anders D. Børglum

  • Most recently observed institution: Center for Genomics and Personalized Medicine

Rankings

  • All-time downloads: 59,197 (rank: 212 out of 288,069)
  • Categories:
    • genetics: 55,839 (rank: 50 out of 28,649)
    • genomics: 2,899 (rank: 4,936 (tie) out of 32,817)
    • neuroscience: 459 (rank: 21,879 (tie) out of 47,947)

Downloads per author, site-wide

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

genetics more details view paper
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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

genetics more details view paper
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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

genetics more details view paper
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A major role for common genetic variation in anxiety disorders

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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

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

genomics more details view paper
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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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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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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A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

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Genome-wide association study implicates CHRNA2 in cannabis use disorder

genomics more details view paper
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A genome-wide association study for shared risk across major psychiatric disorders in a nation-wide birth cohort implicates fetal neurodevelopment as a key mediator

genetics more details view paper
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Genome-wide Association Study of Anxiety and Stress-related Disorders in the iPSYCH Cohort

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

genetics more details view paper
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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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Disentangling genetically confounded polygenic associations between Attention-Deficit/Hyperactivity Disorder, literacy and language

genetics more details view paper
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Genetic markers of ADHD-related variations in intracranial volume

genetics more details view paper
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Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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The neurobiology of BRD1 implicates sex-biased dysregulation of nuclear receptor signaling in mental disorders

neuroscience more details view paper
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Shared genetic background between children and adults with attention deficit/hyperactivity disorder

genetics more details view paper
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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

genetics more details view paper
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Exploring Genetic Variation That Influences Brain Methylation In Attention-Deficit/Hyperactivity Disorder

genetics more details view paper
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Identification of risk variants and characterization of the polygenic architecture of disruptive behavior disorders in the context of ADHD

genomics more details view paper
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Intellectual Disability-related genes increase ADHD risk and locomotor activity in Drosophila

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