# deCODE Genetics (Iceland)

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/decode-genetics-iceland/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 83.8 |
| Citations | 2,493,287 |
| City | Reykjavik |
| Country | IS |
| Description | deCODE Genetics (Iceland) is a research organisation in Reykjavik, IS. OpenAlex records 1,881 works and 2,493,287 citations for it. 530 researchers list it as their most recent affiliation. |
| Homepage | http://www.decode.com/ |
| OpenAlex ID | https://openalex.org/I1327191685 |
| Researchers | 530 |
| ROR ID | https://ror.org/04dzdm737 |
| Type | company |
| Wikidata ID | https://www.wikidata.org/wiki/Q493712 |
| Works | 1,881 |

## University papers

Showing 12 of 103.

- [Biological, clinical and population relevance of 95 loci for blood lipids](https://scholariq.org/papers/biological-clinical-and-population-relevance-of-95-loci-for-blood-lipids/)
- [Discovery and refinement of loci associated with lipid levels](https://scholariq.org/papers/discovery-and-refinement-of-loci-associated-with-lipid-levels/)
- [A reference panel of 64,976 haplotypes for genotype imputation](https://scholariq.org/papers/a-reference-panel-of-64-976-haplotypes-for-genotype-imputation/)
- [Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index](https://scholariq.org/papers/association-analyses-of-249-796-individuals-reveal-18-new-loci-associated-with/)
- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Variant of <i>TREM2</i> Associated with the Risk of Alzheimer's Disease](https://scholariq.org/papers/variant-of-i-trem2-i-associated-with-the-risk-of-alzheimer-s-disease/)
- [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/)
- [w2145813488](https://scholariq.org/papers/w2145813488/)
- [Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes](https://scholariq.org/papers/variant-of-transcription-factor-7-like-2-tcf7l2-gene-confers-risk-of-type-2/)
- [New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk](https://scholariq.org/papers/new-genetic-loci-implicated-in-fasting-glucose-homeostasis-and-their-impact-on/)
- [Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use](https://scholariq.org/papers/association-studies-of-up-to-1-2-million-individuals-yield-new-insights-into-the/)
- [Hundreds of variants clustered in genomic loci and biological pathways affect human height](https://scholariq.org/papers/hundreds-of-variants-clustered-in-genomic-loci-and-biological-pathways-affect/)

## University top topics

Showing 8 of 25.

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomics and Phylogenetic Studies](https://scholariq.org/topics/genomics-and-phylogenetic-studies/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Genetic Mapping and Diversity in Plants and Animals](https://scholariq.org/topics/genetic-mapping-and-diversity-in-plants-and-animals/)

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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.