# David M. Hougaard

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/david-m-hougaard/

## Facts

| Field | Value |
| --- | --- |
| Citations | 62,044 |
| Field | Genetic Associations and Epidemiology |
| h-index | 99 |
| i10-index | 382 |
| Last Known Institution | Statens Serum Institut |
| OpenAlex ID | https://openalex.org/A5081337637 |
| ORCID iD | https://orcid.org/0000-0001-5928-3517 |
| Works | 606 |

## Researcher papers

- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Common variants conferring risk of schizophrenia](https://scholariq.org/papers/common-variants-conferring-risk-of-schizophrenia/)
- [Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains](https://scholariq.org/papers/genome-wide-analyses-of-adhd-identify-27-risk-loci-refine-the-genetic/)
- [Rare coding variation provides insight into the genetic architecture and phenotypic context of autism](https://scholariq.org/papers/rare-coding-variation-provides-insight-into-the-genetic-architecture-and/)
- [A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations](https://scholariq.org/papers/a-genome-wide-association-study-identifies-cdhr3-as-a-susceptibility-locus-for/)
- [Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project](https://scholariq.org/papers/clinical-validation-of-cutoff-target-ranges-in-newborn-screening-of-metabolic/)
- [Genetic analyses identify widespread sex-differential participation bias](https://scholariq.org/papers/genetic-analyses-identify-widespread-sex-differential-participation-bias/)
- [Common variants at VRK2 and TCF4 conferring risk of schizophrenia](https://scholariq.org/papers/common-variants-at-vrk2-and-tcf4-conferring-risk-of-schizophrenia/)
- [Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women](https://scholariq.org/papers/genetic-predisposition-to-hypertension-is-associated-with-preeclampsia-in/)
- [Expanding the range of ZNF804A variants conferring risk of psychosis](https://scholariq.org/papers/expanding-the-range-of-znf804a-variants-conferring-risk-of-psychosis/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Birth, Development, and Health](https://scholariq.org/topics/birth-development-and-health/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)

## Researcher university

- [Statens Serum Institut](https://scholariq.org/institutions/statens-serum-institut/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.