# Kāri Stefánsson

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/kari-stefansson/

## Facts

| Field | Value |
| --- | --- |
| Citations | 212,276 |
| Field | Genetic Associations and Epidemiology |
| h-index | 221 |
| i10-index | 767 |
| Last Known Institution | deCODE Genetics (Iceland) |
| OpenAlex ID | https://openalex.org/A5018239255 |
| ORCID iD | https://orcid.org/0000-0003-1676-864X |
| Works | 1,144 |

## Researcher papers

Showing 12 of 38.

- [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/)
- [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/)
- [Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease](https://scholariq.org/papers/large-scale-meta-analysis-of-genome-wide-association-data-identifies-six-new/)
- [Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes](https://scholariq.org/papers/meta-analysis-of-genome-wide-association-data-and-large-scale-replication/)
- [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/)
- [A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction](https://scholariq.org/papers/a-common-variant-on-chromosome-9p21-affects-the-risk-of-myocardial-infarction/)
- [A mega-analysis of genome-wide association studies for major depressive disorder](https://scholariq.org/papers/a-mega-analysis-of-genome-wide-association-studies-for-major-depressive-disorder/)
- [Humoral Immune Response to SARS-CoV-2 in Iceland](https://scholariq.org/papers/humoral-immune-response-to-sars-cov-2-in-iceland/)
- [Variants conferring risk of atrial fibrillation on chromosome 4q25](https://scholariq.org/papers/variants-conferring-risk-of-atrial-fibrillation-on-chromosome-4q25/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Nutrition, Genetics, and Disease](https://scholariq.org/topics/nutrition-genetics-and-disease/)

## Researcher university

- [deCODE Genetics (Iceland)](https://scholariq.org/institutions/decode-genetics-iceland/)

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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.