# Nakagawanosato Hospital for the Disabled

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/nakagawanosato-hospital-for-the-disabled/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 49 |
| Citations | 1,352 |
| City | Saitama |
| Country | JP |
| Description | Nakagawanosato Hospital for the Disabled is a research organisation in Saitama, JP. OpenAlex records 33 works and 1,352 citations for it. |
| OpenAlex ID | https://openalex.org/I4210161874 |
| ROR ID | https://ror.org/02x1vjb06 |
| Type | healthcare |
| Works | 33 |

## University 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/)
- [ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms](https://scholariq.org/papers/itpkc-functional-polymorphism-associated-with-kawasaki-disease-susceptibility/)
- [A genome-wide association study identifies three new risk loci for Kawasaki disease](https://scholariq.org/papers/a-genome-wide-association-study-identifies-three-new-risk-loci-for-kawasaki/)
- [Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia](https://scholariq.org/papers/gain-of-function-mutations-in-trpv4-cause-autosomal-dominant-brachyolmia/)
- [Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III](https://scholariq.org/papers/genotypic-and-phenotypic-spectrum-in-tricho-rhino-phalangeal-syndrome-types-i/)
- [Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST](https://scholariq.org/papers/silver-russell-syndrome-in-a-girl-born-after-in-vitro-fertilization-partial/)
- [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/)
- [Serotonin Transporter Gene Variation Is a Risk Factor for Sudden Infant Death Syndrome in the Japanese Population](https://scholariq.org/papers/serotonin-transporter-gene-variation-is-a-risk-factor-for-sudden-infant-death/)
- [Decline of CSF orexin (hypocretin) levels in Prader–Willi syndrome](https://scholariq.org/papers/decline-of-csf-orexin-hypocretin-levels-in-prader-willi-syndrome/)

## University researchers

- [Toshiro Nagai](https://scholariq.org/researchers/toshiro-nagai/)

## University top topics

Showing 8 of 25.

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- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Dementia and Cognitive Impairment Research](https://scholariq.org/topics/dementia-and-cognitive-impairment-research/)

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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.