# Matthew Solomonson

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/matthew-solomonson/

## Facts

| Field | Value |
| --- | --- |
| Citations | 24,508 |
| Field | Genomics and Rare Diseases |
| h-index | 41 |
| i10-index | 50 |
| Last Known Institution | Broad Institute |
| OpenAlex ID | https://openalex.org/A5066806865 |
| ORCID iD | https://orcid.org/0000-0002-5344-9026 |
| Works | 70 |

## Researcher papers

- [Mapping the human genetic architecture of COVID-19](https://scholariq.org/papers/mapping-the-human-genetic-architecture-of-covid-19/)
- [The ExAC browser: displaying reference data information from over 60 000 exomes](https://scholariq.org/papers/the-exac-browser-displaying-reference-data-information-from-over-60-000-exomes/)
- [Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals](https://scholariq.org/papers/ultra-rare-genetic-variation-in-the-epilepsies-a-whole-exome-sequencing-study-of/)
- [A first update on mapping the human genetic architecture of COVID-19](https://scholariq.org/papers/a-first-update-on-mapping-the-human-genetic-architecture-of-covid-19/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Phylogenetic Studies](https://scholariq.org/topics/genomics-and-phylogenetic-studies/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## 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.