Author: Jonas Bybjerg-Grauholm

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Preprints

Genome-wide by environment interaction study of stressful life events and hospital-treated depression in the iPSYCH2012 sample

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

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Common risk variants identified in autism spectrum disorder

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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A Major Role for Common Genetic Variation in Anxiety Disorders

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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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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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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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Genome-wide Association Study of Anxiety and Stress-related Disorders in the iPSYCH Cohort

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The genetic architecture of sporadic and recurrent miscarriage

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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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Genome-wide association study of school grades identifies a genetic overlap between language ability, psychopathology and creativity

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

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The female protective effect against autism spectrum disorder

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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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Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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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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Meta-analysis of Scandinavian Schizophrenia Exomes

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

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

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

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

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Mendelian randomization study of spermine oxidase and cancer risk

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  • In genetic and genomic medicine: 775
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Polygenic heterogeneity across obsessive-compulsive disorder subgroups defined by a comorbid diagnosis

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Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention deficit hyperactivity disorder

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