# Anders D. Børglum

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/anders-d-b-rglum/

## Facts

| Field | Value |
| --- | --- |
| Citations | 67,935 |
| Field | Genetic Associations and Epidemiology |
| h-index | 104 |
| i10-index | 365 |
| Last Known Institution | Aarhus University |
| OpenAlex ID | https://openalex.org/A5035161779 |
| ORCID iD | https://orcid.org/0000-0001-8627-7219 |
| Works | 701 |

## Researcher papers

Showing 12 of 15.

- [Biological insights from 108 schizophrenia-associated genetic loci](https://scholariq.org/papers/biological-insights-from-108-schizophrenia-associated-genetic-loci/)
- [Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder](https://scholariq.org/papers/discovery-of-the-first-genome-wide-significant-risk-loci-for-attention-deficit/)
- [Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection](https://scholariq.org/papers/common-schizophrenia-alleles-are-enriched-in-mutation-intolerant-genes-and-in/)
- [Common variants conferring risk of schizophrenia](https://scholariq.org/papers/common-variants-conferring-risk-of-schizophrenia/)
- [Genome-wide association analysis identifies 13 new risk loci for schizophrenia](https://scholariq.org/papers/genome-wide-association-analysis-identifies-13-new-risk-loci-for-schizophrenia/)
- [Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes](https://scholariq.org/papers/genomic-dissection-of-bipolar-disorder-and-schizophrenia-including-28/)
- [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/)
- [Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases](https://scholariq.org/papers/partitioning-heritability-of-regulatory-and-cell-type-specific-variants-across/)
- [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/)
- [Association between Mental Disorders and Subsequent Medical Conditions](https://scholariq.org/papers/association-between-mental-disorders-and-subsequent-medical-conditions/)
- [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/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Attention Deficit Hyperactivity Disorder](https://scholariq.org/topics/attention-deficit-hyperactivity-disorder/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)

## Researcher university

- [Aarhus University](https://scholariq.org/institutions/aarhus-university/)

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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.