# Han G. Brunner

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/han-g-brunner/

## Facts

| Field | Value |
| --- | --- |
| Citations | 50,712 |
| Field | Genomics and Rare Diseases |
| h-index | 104 |
| i10-index | 344 |
| Last Known Institution | Radboud University Nijmegen |
| OpenAlex ID | https://openalex.org/A5030485933 |
| ORCID iD | https://orcid.org/0000-0001-9274-8865 |
| Works | 498 |

## Researcher papers

- [The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data](https://scholariq.org/papers/the-enigma-consortium-large-scale-collaborative-analyses-of-neuroimaging-and/)
- [International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases](https://scholariq.org/papers/international-cooperation-to-enable-the-diagnosis-of-all-rare-genetic-diseases/)
- [CEP152 is a genome maintenance protein disrupted in Seckel syndrome](https://scholariq.org/papers/cep152-is-a-genome-maintenance-protein-disrupted-in-seckel-syndrome/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Cardiomyopathy and Myosin Studies](https://scholariq.org/topics/cardiomyopathy-and-myosin-studies/)

## Researcher university

- [Radboud University Nijmegen](https://scholariq.org/institutions/radboud-university-nijmegen/)

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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.