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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 62,933 bioRxiv papers from 279,142 authors.

Author: Marie Bækvad-Hansen

  • Most recently observed institution: The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; Center for Neonatal Screening, Department for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark,

Rankings

  • All-time downloads: 29,320 (rank: 600 out of 279,142)
  • Categories:
    • genetics: 28,273 (rank: 138 out of 27,802)
    • genomics: 1,047 (rank: 12,129 (tie) out of 31,956)

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Preprints

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

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No bioRxiv download data for this paper yet.

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

genetics more details view paper
  • Downloaded 8,867 times
  • Download rankings, all-time:
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    • In genetics: 11 out of 3,563
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    • Site-wide: 569 out of 62,933
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    • Site-wide: 1,856 out of 62,933

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

genetics more details view paper
  • Downloaded 8,726 times
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    • Site-wide: 9,438 out of 62,933

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
  • Downloaded 6,099 times
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A major role for common genetic variation in anxiety disorders

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  • Downloaded 1,829 times
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ASD and ADHD have a similar burden of rare protein-truncating variants

genetics more details view paper
  • Downloaded 1,174 times
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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

genetics more details view paper
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    • Site-wide: 3,206 out of 62,933

Genome-wide association study implicates CHRNA2 in cannabis use disorder

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

genetics more details view paper
  • Downloaded 486 times
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    • In genetics: 1,339 out of 3,563
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