Author: Jonas Byberg-Grauholm

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Preprints

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

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

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  • Site-wide: 854
  • In genetics: 23
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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• Year to date:
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Common risk variants identified in autism spectrum disorder

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  • Site-wide: 1,124
  • In genetics: 31
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Genomewide association study identifies 30 loci associated with bipolar disorder

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  • Site-wide: 1,300
  • In genetics: 39
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  • Site-wide: 22,168
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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: 2,776
  • In genetic and genomic medicine: 12
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A Major Role for Common Genetic Variation in Anxiety Disorders

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  • Site-wide: 3,652
  • In genetics: 135
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Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

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  • Site-wide: 5,168
  • In psychiatry and clinical psychology: 20
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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

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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

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

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Genome-wide association study implicates CHRNA2 in cannabis use disorder

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  • Site-wide: 10,237
  • In genomics: 1,081
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  • Site-wide: 42,833

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • Site-wide: 12,952
  • In genomics: 1,359
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  • Site-wide: 93,060
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  • Site-wide: 136,900

A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

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  • Site-wide: 13,549
  • In genetics: 638
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Genome-wide Association Study of Anxiety and Stress-related Disorders in the iPSYCH Cohort

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  • Site-wide: 15,368
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  • Site-wide: 72,909
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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

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  • Site-wide: 17,963
  • In genetics: 854
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The genetic architecture of sporadic and recurrent miscarriage

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  • Site-wide: 18,102
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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: 19,007
  • In genomics: 1,883
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  • Site-wide: 34,364
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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

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  • Site-wide: 19,504
  • In genomics: 1,922
• Year to date:
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  • Site-wide: 42,903

Complex spatio-temporal distribution and genogeographic affinity of mitochondrial DNA haplogroups in 24,216 Danes

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  • Site-wide: 25,932
  • In genomics: 2,415
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The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

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  • In genetics: 1,520
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The female protective effect against autism spectrum disorder

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  • Site-wide: 37,230
  • In genetic and genomic medicine: 136
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Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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  • Site-wide: 41,842
  • In genetics: 1,930
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  • Site-wide: 124,322
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Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups.

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  • Site-wide: 61,121
  • In psychiatry and clinical psychology: 208
• Year to date:
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Meta-analysis of Scandinavian Schizophrenia Exomes

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  • Site-wide: 61,155
  • In genetics: 2,756
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  • Site-wide: 59,881

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

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  • Site-wide: 84,627
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  • Site-wide: 92,277
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  • Site-wide: 115,091

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

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  • Site-wide: 99,998
  • In epidemiology: 4,163
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  • Site-wide: 21,700
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Genome-wide association study of febrile seizures identifies seven new loci implicating fever response and neuronal excitability genes

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  • Site-wide: 123,642
  • In genetic and genomic medicine: 632
• Year to date:
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  • Site-wide: 46,081

Accounting for age-of-onset and family history improves power in genome-wide association studies

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  • Site-wide: 125,182
  • In bioinformatics: 10,030
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  • Site-wide: 22,728

Elevated DNA Methylation Gestational Age is associated with the Risk of Later Bipolar Disorder and Anorexia Nervosa in Twins

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  • Site-wide: 133,760
  • In epidemiology: 5,473
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  • Site-wide: 100,386
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Mendelian randomization study of spermine oxidase and cancer risk

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  • Site-wide: 135,473
  • In genetic and genomic medicine: 716
• Year to date:
  • Site-wide: 90,731
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  • Site-wide: 102,261

Polygenic heterogeneity across obsessive-compulsive disorder subgroups defined by a comorbid diagnosis

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  • Site-wide: 140,849
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• Year to date:
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