# Håkon Håkonarson

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/hakon-hakonarson/

## Facts

| Field | Value |
| --- | --- |
| Citations | 158,589 |
| Field | Genetic Associations and Epidemiology |
| h-index | 177 |
| i10-index | 817 |
| Last Known Institution | Children's Hospital of Philadelphia |
| OpenAlex ID | https://openalex.org/A5088244425 |
| ORCID iD | https://orcid.org/0000-0003-2814-7461 |
| Works | 1,475 |

## Researcher papers

Showing 12 of 29.

- [ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data](https://scholariq.org/papers/annovar-functional-annotation-of-genetic-variants-from-high-throughput/)
- [An improved framework for confound regression and filtering for control of motion artifact in the preprocessing of resting-state functional connectivity data](https://scholariq.org/papers/an-improved-framework-for-confound-regression-and-filtering-for-control-of/)
- [Functional impact of global rare copy number variation in autism spectrum disorders](https://scholariq.org/papers/functional-impact-of-global-rare-copy-number-variation-in-autism-spectrum/)
- [PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data](https://scholariq.org/papers/penncnv-an-integrated-hidden-markov-model-designed-for-high-resolution-copy/)
- [Autism genome-wide copy number variation reveals ubiquitin and neuronal genes](https://scholariq.org/papers/autism-genome-wide-copy-number-variation-reveals-ubiquitin-and-neuronal-genes/)
- [Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa](https://scholariq.org/papers/genome-wide-association-study-identifies-eight-risk-loci-and-implicates-metabo/)
- [Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders](https://scholariq.org/papers/convergence-of-genes-and-cellular-pathways-dysregulated-in-autism-spectrum/)
- [Common genetic variants on 5p14.1 associate with autism spectrum disorders](https://scholariq.org/papers/common-genetic-variants-on-5p14-1-associate-with-autism-spectrum-disorders/)
- [The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke](https://scholariq.org/papers/the-gene-encoding-5-lipoxygenase-activating-protein-confers-risk-of-myocardial/)
- [A genome-wide scan for common alleles affecting risk for autism](https://scholariq.org/papers/a-genome-wide-scan-for-common-alleles-affecting-risk-for-autism/)
- [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/)
- [Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies](https://scholariq.org/papers/genome-wide-mega-analysis-identifies-16-loci-and-highlights-diverse-biological/)

## 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/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Asthma and respiratory diseases](https://scholariq.org/topics/asthma-and-respiratory-diseases/)

## Researcher university

- [Children's Hospital of Philadelphia](https://scholariq.org/institutions/children-s-hospital-of-philadelphia/)

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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.