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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 62,482 bioRxiv papers from 277,419 authors.

Author: Jakob Grove

  • ORCiD: http://orcid.org/0000-0003-2284-5744
  • Most recently observed institution: Department of Biomedicine, Aarhus University, Denmark; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; Center for Genomics and Personalized Medicine & Bioinformatics Research Centre, Aarhus University, Denmark

Rankings

  • All-time downloads: 47,699 (rank: 286 out of 277,419)
  • Categories:
    • bioinformatics: 440 (rank: 14,624 (tie) out of 24,391)
    • genetics: 43,240 (rank: 75 out of 27,685)
    • genomics: 4,019 (rank: 3,375 (tie) out of 31,917)

Downloads per author, site-wide

Preprints

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

genetics more details view paper
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    • In genetics: 11 out of 3,548
  • Year to date:
    • Site-wide: 559 out of 62,482
  • Since beginning of last month:
    • Site-wide: 1,660 out of 62,482

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: 137 out of 62,482
    • In genetics: 13 out of 3,548
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    • Site-wide: 2,274 out of 62,482
  • Since beginning of last month:
    • Site-wide: 8,448 out of 62,482

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

genetics more details view paper
  • Downloaded 6,234 times
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    • In genetics: 29 out of 3,548
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    • Site-wide: 107 out of 62,482
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    • Site-wide: 165 out of 62,482

Genomewide association study identifies 30 loci associated with bipolar disorder

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  • Downloaded 6,099 times
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    • In genetics: 32 out of 3,548
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    • Site-wide: 288 out of 62,482
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    • Site-wide: 1,957 out of 62,482

Common risk variants identified in autism spectrum disorder

genetics more details view paper
  • Downloaded 5,933 times
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    • In genetics: 37 out of 3,548
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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
  • Downloaded 2,198 times
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    • In genetics: 181 out of 3,548
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Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa

genomics more details view paper
  • Downloaded 1,634 times
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    • In genomics: 608 out of 4,297
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

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  • Downloaded 1,540 times
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    • In genetics: 301 out of 3,548
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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  • Downloaded 1,174 times
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Genome-wide association study implicates CHRNA2 in cannabis use disorder

genomics more details view paper
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    • In genomics: 1,088 out of 4,297
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The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

genetics more details view paper
  • Downloaded 617 times
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    • Site-wide: 39,811 out of 62,482

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

genetics more details view paper
  • Downloaded 497 times
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    • In genetics: 1,288 out of 3,548
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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: 1,327 out of 3,548
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The Anorexia Nervosa Genetics Initiative: Overview and Methods

genetics more details view paper
  • Downloaded 471 times
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    • In genetics: 1,380 out of 3,548
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  • Since beginning of last month:
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Estimating the functional impact of INDELs in transcription factor binding sites: a genome-wide landscape

bioinformatics more details view paper
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    • Site-wide: 49,565 out of 62,482

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

genetics more details view paper
  • Downloaded 398 times
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    • In genetics: 1,622 out of 3,548
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    • Site-wide: 3,471 out of 62,482

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

genomics more details view paper
  • Downloaded 72 times
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    • In genomics: 4,186 out of 4,297
  • Year to date:
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