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Author: Preben Bo Mortensen

  • ORCiD: http://orcid.org/0000-0002-5230-9865
  • Most recently observed institution: The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; National Centre for Register-based Research (NCRR) & Centre for Integrated Register-Based Research, CIRRAU, Aarhus University, Aarhus Denmark,

Rankings

  • All-time downloads: 42,982 (rank: 327 out of 278,042)
  • Categories:
    • epidemiology: 469 (rank: 2,422 (tie) out of 9,528)
    • genetics: 40,639 (rank: 81 out of 27,703)
    • genomics: 1,874 (rank: 7,282 (tie) out of 31,942)

Downloads per author, site-wide

Preprints

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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    • In genetics: 13 out of 3,561
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    • Site-wide: 2,278 out of 62,660
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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
  • Downloaded 6,234 times
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    • Site-wide: 266 out of 62,660
    • In genetics: 29 out of 3,561
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    • Site-wide: 107 out of 62,660
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    • Site-wide: 170 out of 62,660

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
  • Downloaded 6,099 times
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    • In genetics: 32 out of 3,561
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    • Site-wide: 289 out of 62,660
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    • Site-wide: 2,018 out of 62,660

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 3,561
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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 3,561
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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

genetics more details view paper
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    • In genetics: 236 out of 3,561
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A major role for common genetic variation in anxiety disorders

genetics more details view paper
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    • In genetics: 239 out of 3,561
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

genetics more details view paper
  • Downloaded 1,540 times
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    • In genetics: 302 out of 3,561
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ASD and ADHD have a similar burden of rare protein-truncating variants

genetics more details view paper
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A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

genetics more details view paper
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    • In genetics: 517 out of 3,561
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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: 1,090 out of 4,312
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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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    • In genetics: 553 out of 3,561
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Mitochondrial DNA SNPs associated with Schizophrenia exhibit Highly Variable Inter-allelic Haplogroup Affiliation and Nuclear Genogeographic Affinity: Bi-Genomic Linkage Disequilibrium raises Major Concerns for Link to Disease

genomics more details view paper
  • Downloaded 765 times
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Paternal-age-related de novo mutations and risk for five disorders

genetics more details view paper
  • Downloaded 725 times
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    • In genetics: 818 out of 3,561
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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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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: 1,329 out of 3,561
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The Anorexia Nervosa Genetics Initiative: Overview and Methods

genetics more details view paper
  • Downloaded 471 times
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Spatial gene-by-environment mapping for schizophrenia reveals locale of upbringing effects beyond urban-rural differences

epidemiology more details view paper
  • Downloaded 469 times
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    • In epidemiology: 274 out of 1,556
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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
  • Downloaded 395 times
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    • In genetics: 1,645 out of 3,561
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    • Site-wide: 29,025 out of 62,660

Exploring contributors to variability in estimates of SNP-heritability and genetic correlations from the iPSYCH case-cohort and published meta-studies of major psychiatric disorders.

genetics more details view paper
  • Downloaded 284 times
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    • In genetics: 2,148 out of 3,561
  • Year to date:
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  • Since beginning of last month:
    • Site-wide: 35,664 out of 62,660

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: 4,187 out of 4,312
  • Year to date:
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  • Since beginning of last month:
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