Author: David M Hougaard

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Preprints

Preterm birth, stillbirth, and early neonatal mortality during the Danish COVID-19 lockdown

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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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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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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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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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  • In genomics: 1,077
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  • Site-wide: 31,113
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

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  • Site-wide: 122,900
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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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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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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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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The genetic architecture of sporadic and recurrent miscarriage

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

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The female protective effect against autism spectrum disorder

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Untargeted metabolomic study of autism in newborn screening samples: a pilot study

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

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Gestational-age-dependent development of the neonatal metabolome

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

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

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

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Mendelian randomization study of spermine oxidase and cancer risk

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Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

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

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