# F. Kyle Satterstrom

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/f-kyle-satterstrom/

## Facts

| Field | Value |
| --- | --- |
| Citations | 18,019 |
| Field | Autism Spectrum Disorder Research |
| h-index | 39 |
| i10-index | 62 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5039331408 |
| ORCID iD | https://orcid.org/0000-0001-6187-7680 |
| Works | 113 |

## Researcher papers

- [Identification of common genetic risk variants for autism spectrum disorder](https://scholariq.org/papers/identification-of-common-genetic-risk-variants-for-autism-spectrum-disorder/)
- [Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism](https://scholariq.org/papers/large-scale-exome-sequencing-study-implicates-both-developmental-and-functional/)
- [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/)
- [Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders](https://scholariq.org/papers/genomic-relationships-novel-loci-and-pleiotropic-mechanisms-across-eight/)
- [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/)
- [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/)

## Researcher topics

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

## Researcher university

- [Broad Institute](https://scholariq.org/institutions/broad-institute/)

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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.