Author: Preben Bo Mortensen

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Preprints

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

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

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Common risk variants identified in autism spectrum disorder

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A Major Role for Common Genetic Variation in Anxiety Disorders

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

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

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

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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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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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Paternal-age-related de novo mutations and risk for five disorders

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

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

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

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The Anorexia Nervosa Genetics Initiative: Overview and Methods

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Spatial gene-by-environment mapping for schizophrenia reveals locale of upbringing effects beyond urban-rural differences

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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

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

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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.

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

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Meta-analysis of Scandinavian Schizophrenia Exomes

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