# Rolph Pfundt

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/rolph-pfundt/

## Facts

| Field | Value |
| --- | --- |
| Citations | 21,426 |
| Field | Genomics and Rare Diseases |
| h-index | 80 |
| i10-index | 248 |
| OpenAlex ID | https://openalex.org/A5016312541 |
| ORCID iD | https://orcid.org/0000-0002-0584-4398 |
| Works | 378 |

## Researcher papers

- [Evidence for 28 genetic disorders discovered by combining healthcare and research data](https://scholariq.org/papers/evidence-for-28-genetic-disorders-discovered-by-combining-healthcare-and/)

## 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/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)

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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.