Author: Jakob Grove

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Preprints

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

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  • Site-wide: 665
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  • Site-wide: 7,010
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  • Site-wide: 7,010

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

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  • Site-wide: 739
  • In genetics: 22
• Year to date:
  • Site-wide: 4,158
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  • Site-wide: 4,158

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

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  • Site-wide: 812
  • In genetics: 25
• Year to date:
  • Site-wide: 22,421
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Common risk variants identified in autism spectrum disorder

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  • Site-wide: 1,050
  • In genetics: 34
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  • Site-wide: 2,128
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Genomewide association study identifies 30 loci associated with bipolar disorder

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  • Site-wide: 1,126
  • In genetics: 38
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  • Site-wide: 14,646
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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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  • Site-wide: 4,088
  • In genetic and genomic medicine: 11
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  • Site-wide: 873
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

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  • Site-wide: 5,428
  • In genetics: 261
• Year to date:
  • Site-wide: 62,861
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Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa

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  • Site-wide: 6,517
  • In genomics: 745
• Year to date:
  • Site-wide: 21,779
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ASD and ADHD have a similar burden of rare protein-truncating variants

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  • Site-wide: 8,720
  • In genetics: 433
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

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  • Site-wide: 9,150
  • In genetics: 452
• Year to date:
  • Site-wide: 84,153
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  • Site-wide: 84,153

Genome-wide association study implicates CHRNA2 in cannabis use disorder

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  • Site-wide: 9,450
  • In genomics: 1,059
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  • Site-wide: 22,449
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  • Site-wide: 22,449

Genome-wide association study of over 40,000 bipolar disorder cases provides novel biological insights

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  • Site-wide: 10,112
  • In psychiatry and clinical psychology: 32
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  • Site-wide: 2,461
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  • Site-wide: 2,461

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 11,245
  • In genomics: 1,252
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  • Site-wide: 55,712
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  • Site-wide: 55,712

Genetic Architecture of 11 Major Psychiatric Disorders at Biobehavioral, Functional Genomic, and Molecular Genetic Levels of Analysis

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  • Site-wide: 11,786
  • In genetic and genomic medicine: 39
• Year to date:
  • Site-wide: 2,053
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Genome-wide association study of school grades identifies a genetic overlap between language ability, psychopathology and creativity

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  • Site-wide: 17,582
  • In genomics: 1,828
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  • Site-wide: 15,372
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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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  • Site-wide: 23,078
  • In genetics: 1,149
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  • Site-wide: 3,168
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Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD

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  • Site-wide: 26,551
  • In genetics: 1,327
• Year to date:
  • Site-wide: 70,976
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  • Site-wide: 70,976

The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

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  • Site-wide: 28,444
  • In genetics: 1,421
• Year to date:
  • Site-wide: 47,951
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Social and non-social autism symptom and trait domains are genetically dissociable

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  • Site-wide: 29,116
  • In genetics: 1,448
• Year to date:
  • Site-wide: 31,651
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  • Site-wide: 31,651

Examining sex-differentiated genetic effects across neuropsychiatric and behavioral traits

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  • Site-wide: 33,654
  • In genetics: 1,655
• Year to date:
  • Site-wide: 18,588
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Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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  • Site-wide: 36,733
  • In genetics: 1,799
• Year to date:
  • Site-wide: 85,830
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  • Site-wide: 85,830

Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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  • Site-wide: 37,057
  • In genetics: 1,809
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The Anorexia Nervosa Genetics Initiative: Overview and Methods

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  • Site-wide: 37,837
  • In genetics: 1,850
• Year to date:
  • Site-wide: 83,867
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  • Site-wide: 83,867

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

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  • Site-wide: 42,981
  • In genomics: 3,538
• Year to date:
  • Site-wide: 36,413
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  • Site-wide: 36,413

Estimating the functional impact of INDELs in transcription factor binding sites: a genome-wide landscape

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  • Site-wide: 44,640
  • In bioinformatics: 4,753
• Year to date:
  • Site-wide: 84,774
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  • Site-wide: 84,774

Meta-analysis of Scandinavian Schizophrenia Exomes

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  • Site-wide: 57,319
  • In genetics: 2,705
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  • Site-wide: 36,752
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  • Site-wide: 36,752

Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction

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  • Site-wide: 57,342
  • In genetics: 2,709
• Year to date:
  • Site-wide: 27,662
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  • Site-wide: 27,662

Polygenic prediction of school performance in children with and without psychiatric disorders

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  • Site-wide: 77,937
  • In genetics: 3,609
• Year to date:
  • Site-wide: 57,398
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  • Site-wide: 57,398

Maternal health around pregnancy and autism risk: a population-based study.

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  • Site-wide: 95,773
  • In psychiatry and clinical psychology: 348
• Year to date:
  • Site-wide: 102,261
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  • Site-wide: 102,261

The iPSYCH2015 Case-Cohort sample: updated directions for unravelling genetic and environmental architectures of severe mental disorders

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  • Site-wide: 117,195
  • In epidemiology: 4,735
• Year to date:
  • Site-wide: 20,178
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  • Site-wide: 20,178

Genome-wide association study of febrile seizures identifies seven new loci implicating fever response and neuronal excitability genes

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  • Site-wide: 119,267
  • In genetic and genomic medicine: 542
• Year to date:
  • Site-wide: 53,613
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  • Site-wide: 53,613