DAVID MICHAEL HOUGAARD
Statens Serum Institut
Affiliation Statens Serum Institut Top Publications Biological insights from 108 schizophrenia-associated genetic loci (2014) – 8,206 citations Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) – 3,347 citations Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) – 2,921 citations Identification of common genetic risk ... <a title="DAVID MICHAEL HOUGAARD" class="read-more" href="https://journalsworld.com/researchers/david-michael-hougaard/" aria-label="Read more about DAVID MICHAEL HOUGAARD">Read more</a>
Read biography ↓Biography, research & contributions
Affiliation
Statens Serum Institut
Top Publications
- Biological insights from 108 schizophrenia-associated genetic loci (2014) - 8,206 citations
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) - 3,347 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) - 2,921 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) - 2,739 citations
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) - 2,358 citations
At a glance
- Full name
- DAVID MICHAEL HOUGAARD
- ORCID
- 0000-0001-5928-3517
- OpenAlex ID
- https://openalex.org/A5081337637
Research interests
- Genetic Associations and Epidemiology, Schizophrenia research and treatment, Autism Spectrum Disorder Research, Metabolism and Genetic Disorders, Genomics and Rare Diseases
Research topics
Education
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Selected research & further reading
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See the source-linked reading and original works in the research guide above.
Citation & publication trends
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Source: OpenAlex · Retrieved 2026-10-07. Metrics are database-specific and are not a scientific ranking.
Most-cited linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- 8,206OpenAlex citations
- 3,347OpenAlex citations
- 2,921OpenAlex citations
- Identification of common genetic risk variants for autism spectrum disorder ↗2019 · Nature Genetics2,739OpenAlex citations
- 2,358OpenAlex citations
Recent linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- Identification of common genetic risk variants for autism spectrum disorder ↗2019 · Nature Genetics
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Awards & honors
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Career timeline
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Co-authors
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Sign in to claim this profileSources & data information
Editorial review: 2026-10-07 · Last data update: 2026-10-07 23:09:35
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