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List of works by David M Hougaard

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Common variants conferring risk of schizophrenia

scientific article
Genome-wide association analysis identifies 13 new risk loci for schizophrenia

scientific article published in October 2013
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

scientific article published on 26 April 2018
Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

scientific article published on 26 February 2018
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

scientific article published on 26 November 2018
Identification of common genetic risk variants for autism spectrum disorder

scientific article published on 25 February 2019
Genome-wide association study identifies 30 loci associated with bipolar disorder.

scientific article
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

scientific article published on 2 December 2012
Neonatal vitamin D status and risk of schizophrenia: a population-based case-control study

scientific article published on September 2010
Genome-wide associations for birth weight and correlations with adult disease

scientific article
Common variants at VRK2 and TCF4 conferring risk of schizophrenia

scientific article published on 26 July 2011
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

scientific article published on 15 May 2017
Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.

scientific article published on July 2015
An epigenetic clock for gestational age at birth based on blood methylation data

scientific article
The utility of neonatal dried blood spots for the assessment of neonatal vitamin D status.

scientific article published on May 2010
Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk

scientific article published on 14 September 2011
A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

scientific article published on 28 January 2019
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

scientific article published on 2 December 2017
Elevated polygenic burden for autism is associated with differential DNA methylation at birth

scientific article published on 28 March 2018
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

scientific article published on 01 May 2019
Vitamin D status during pregnancy and the risk of subsequent postpartum depression: a case-control study

scientific article
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

scientific article published on 08 October 2019
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study

scientific article published on 07 June 2018
Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study

scientific article
Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

article
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

scientific article
The association between neonatal vitamin D status and risk of schizophrenia

scientific article published in Scientific Reports
Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia

scientific article published on 19 April 2016
Genome-wide association study implicates CHRNA2 in cannabis use disorder

scientific article published on 17 June 2019
Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

scholarly article published 3 June 2017
Anthropometry in Klinefelter Syndrome - Multifactorial Influences Due to CAG Length, Testosterone Treatment and Possibly Intrauterine Hypogonadism

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

scientific article
Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

scientific article
Few differences in cytokines between patients newly diagnosed with type 1 diabetes and their healthy siblings

Short QTc interval in males with klinefelter syndrome-influence of CAG repeat length, body composition, and testosterone replacement therapy.

scientific article published on 23 January 2015
Neonatal Levels of Inflammatory Markers and Later Risk of Schizophrenia

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

scientific article published on 25 November 2019
A major role for common genetic variation in anxiety disorders

scientific article published on 20 November 2019
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article
Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy

scientific article published on 9 December 2016
Association of the polygenic risk score for schizophrenia with mortality and suicidal behavior - A Danish population-based study.

scientific article published on 06 December 2016
Common risk variants identified in autism spectrum disorder

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

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

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
Exploring Cuba's population structure and demographic history using genome-wide data

scientific article published on 30 July 2018
Levels of adiponectin and leptin at onset of type 1 diabetes have changed over time in children and adolescents

Foetal oestrogens and autism

scientific article published on 29 July 2019

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