# Naomichi Matsumoto

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/naomichi-matsumoto/

## Facts

| Field | Value |
| --- | --- |
| Citations | 39,479 |
| Field | Genomics and Rare Diseases |
| h-index | 86 |
| i10-index | 580 |
| Last Known Institution | Yokohama City University Hospital |
| OpenAlex ID | https://openalex.org/A5085467135 |
| ORCID iD | https://orcid.org/0000-0001-9846-6500 |
| Works | 1,388 |

## Researcher papers

- [Haploinsufficiency of NSD1 causes Sotos syndrome](https://scholariq.org/papers/haploinsufficiency-of-nsd1-causes-sotos-syndrome/)
- [Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome](https://scholariq.org/papers/mutations-affecting-components-of-the-swi-snf-complex-cause-coffin-siris/)
- [Spectrum of <i>MLL2</i> (<i>ALR</i>) mutations in 110 cases of Kabuki syndrome](https://scholariq.org/papers/spectrum-of-i-mll2-i-i-alr-i-mutations-in-110-cases-of-kabuki-syndrome/)
- [<i>MLL2</i> and <i>KDM6A</i> mutations in patients with Kabuki syndrome](https://scholariq.org/papers/i-mll2-i-and-i-kdm6a-i-mutations-in-patients-with-kabuki-syndrome/)

## Researcher topics

- [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/)
- [RNA regulation and disease](https://scholariq.org/topics/rna-regulation-and-disease/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [Yokohama City University Hospital](https://scholariq.org/institutions/yokohama-city-university-hospital/)

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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.