User profiles for David M. Hougaard

David Hougaard

Director Department for Congenital Disorders, Statens Serum Institut
Verified email at ssi.dk
Cited by 59640

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

…, JJ Hottenga, DM Hougaard, M Hu, CL Hyde, M Ising… - Nature …, 2018 - nature.com
Major depressive disorder (MDD) is a common illness accompanied by considerable
morbidity, mortality, costs, and heightened risk of suicide. We conducted a genome-wide …

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

…, K Stefansson, M Nordentoft, DM Hougaard… - Nature …, 2019 - nature.com
Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral
disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute …

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

…, V Golimbet, J Grove, DM Hougaard, M Mattheisen… - Nature …, 2018 - nature.com
Schizophrenia is a debilitating psychiatric condition often associated with poor quality of life
and decreased life expectancy. Lack of progress in improving treatment outcomes has been …

Identification of common genetic risk variants for autism spectrum disorder

…, DH Geschwind, M Nordentoft, DM Hougaard… - Nature …, 2019 - nature.com
Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of
neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic variants …

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

…, ML Hamshere, P Holmans, DM Hougaard… - Nature …, 2013 - nature.com
Schizophrenia is an idiopathic mental disorder with a heritable component and a substantial
public health impact. We conducted a multi-stage genome-wide association study (GWAS) …

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

…, X He, GE Herman, I Hertz-Picciotto, DM Hougaard… - Cell, 2020 - cell.com
We present the largest exome sequencing study of autism spectrum disorder (ASD) to date (n
= 35,584 total samples, 11,986 with ASD). Using an enhanced analytical framework to …

[PDF][PDF] Modeling linkage disequilibrium increases accuracy of polygenic risk scores

…, MV Hollegaard, DM Hougaard, M Ikeda… - The american journal of …, 2015 - cell.com
Polygenic risk scores have shown great promise in predicting complex disease risk and will
become more accurate as training sample sizes increase. The standard approach for …

Rare coding variants in ten genes confer substantial risk for schizophrenia

…, E Hämäläinen, HO Heyne, M Holi, DM Hougaard… - Nature, 2022 - nature.com
Rare coding variation has historically provided the most direct connections between gene
function and disease pathogenesis. By meta-analysing the whole exomes of 24,248 …

[PDF][PDF] Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

…, CA Hartman, Z Hawi, A Hervás, DM Hougaard… - Cell, 2019 - cell.com
Genetic influences on psychiatric disorders transcend diagnostic boundaries, suggesting
substantial pleiotropy of contributing loci. However, the nature and mechanisms of these …

[PDF][PDF] Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

…, MV Hollegaard, DM Hougaard, M Ikeda… - The American Journal of …, 2014 - cell.com
Regulatory and coding variants are known to be enriched with associations identified by
genome-wide association studies (GWASs) of complex disease, but their contributions to trait …