# Denise Horn

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/denise-horn/

## Facts

| Field | Value |
| --- | --- |
| Citations | 18,175 |
| Field | Congenital limb and hand anomalies |
| h-index | 62 |
| i10-index | 162 |
| Last Known Institution | Humboldt-Universität zu Berlin |
| OpenAlex ID | https://openalex.org/A5049735533 |
| ORCID iD | https://orcid.org/0000-0003-0870-8911 |
| Works | 364 |

## Researcher papers

- [Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study](https://scholariq.org/papers/range-of-genetic-mutations-associated-with-severe-non-syndromic-sporadic/)
- [Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients](https://scholariq.org/papers/coffin-siris-syndrome-and-the-baf-complex-genotype-phenotype-study-in-63/)
- [GestaltMatcher facilitates rare disease matching using facial phenotype descriptors](https://scholariq.org/papers/gestaltmatcher-facilitates-rare-disease-matching-using-facial-phenotype/)

## Researcher topics

- [Congenital limb and hand anomalies](https://scholariq.org/topics/congenital-limb-and-hand-anomalies/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Researcher university

- [Humboldt-Universität zu Berlin](https://scholariq.org/institutions/humboldt-universitat-zu-berlin/)

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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.