# Fabian Grubert

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/fabian-grubert/

## Facts

| Field | Value |
| --- | --- |
| Citations | 46,534 |
| Field | Genomics and Chromatin Dynamics |
| h-index | 32 |
| i10-index | 36 |
| Last Known Institution | Stanford University |
| OpenAlex ID | https://openalex.org/A5072640628 |
| Works | 43 |

## Researcher papers

- [Architecture of the human regulatory network derived from ENCODE data](https://scholariq.org/papers/architecture-of-the-human-regulatory-network-derived-from-encode-data/)
- [Mapping copy number variation by population-scale genome sequencing](https://scholariq.org/papers/mapping-copy-number-variation-by-population-scale-genome-sequencing/)
- [Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy](https://scholariq.org/papers/mutations-in-dnmt1-cause-autosomal-dominant-cerebellar-ataxia-deafness-and/)

## Researcher topics

- [Genomics and Chromatin Dynamics](https://scholariq.org/topics/genomics-and-chromatin-dynamics/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [RNA Research and Splicing](https://scholariq.org/topics/rna-research-and-splicing/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [Stanford University](https://scholariq.org/institutions/stanford-university/)

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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.
