# Karola Rehnström

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/karola-rehnstrom/

## Facts

| Field | Value |
| --- | --- |
| Citations | 20,279 |
| Field | Genetic Associations and Epidemiology |
| h-index | 44 |
| i10-index | 62 |
| OpenAlex ID | https://openalex.org/A5037520665 |
| Works | 79 |

## Researcher papers

- [Synaptic, transcriptional and chromatin genes disrupted in autism](https://scholariq.org/papers/synaptic-transcriptional-and-chromatin-genes-disrupted-in-autism/)
- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters](https://scholariq.org/papers/lineage-specific-genome-architecture-links-enhancers-and-non-coding-disease/)
- [Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension](https://scholariq.org/papers/phenotypic-characterization-of-i-eif2ak4-i-mutation-carriers-in-a-large-cohort/)

## 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/)
- [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/)

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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.