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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: Ole Mors

  • ORCiD: http://orcid.org/0000-0002-5660-0393
  • Most recently observed institution: The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark; Psychosis Research Unit, Aarhus University Hospital, Risskov, Denmark,

Rankings

  • All-time downloads: 55,922 (rank: 220 out of 277,419)
  • Categories:
    • bioinformatics: 122 (rank: 23,115 (tie) out of 24,391)
    • epidemiology: 155 (rank: 6,863 (tie) out of 9,530)
    • genetics: 51,201 (rank: 57 out of 27,685)
    • genomics: 3,636 (rank: 3,815 (tie) out of 31,917)
    • neuroscience: 808 (rank: 12,079 (tie) out of 45,818)

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
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    • Site-wide: 559 out of 62,482
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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
  • Downloaded 8,726 times
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    • In genetics: 13 out of 3,548
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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

genetics more details view paper
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    • In genetics: 32 out of 3,548
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Common risk variants identified in autism spectrum disorder

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

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

genetics more details view paper
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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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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Minimal phenotyping yields GWAS hits of low specificity for major depression

genetics more details view paper
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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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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: 515 out of 3,548
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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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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
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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

genetics more details view paper
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    • In genetics: 929 out of 3,548
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Pharmacogenetics of antidepressant response: a polygenic approach

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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
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New insights on the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation

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
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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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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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Assessing 42 inflammatory markers in 321 control subjects and 887 major depressive disorder cases: BMI and other confounders and overall predictive ability for current depression

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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
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    • In genetics: 2,148 out of 3,548
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Genetic variation in the Major Histocompatibility Complex and association with depression

genetics more details view paper
  • Downloaded 282 times
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    • In genetics: 2,161 out of 3,548
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Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: meta-analysis of data from genome-wide association studies

genetics more details view paper
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    • Site-wide: 32,819 out of 62,482

Statin treatment and the risk of depression

epidemiology more details view paper
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Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders – findings from a Danish population-based study

bioinformatics more details view paper
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  • Since beginning of last month:
    • Site-wide: 30,185 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
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    • Site-wide: 5,020 out of 62,482

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