# Peter Nürnberg

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/peter-nurnberg/

## Facts

| Field | Value |
| --- | --- |
| Citations | 59,498 |
| Field | Genomics and Rare Diseases |
| h-index | 127 |
| i10-index | 541 |
| Last Known Institution | University of Cologne |
| OpenAlex ID | https://openalex.org/A5078248666 |
| ORCID iD | https://orcid.org/0000-0002-7228-428X |
| Works | 748 |

## Researcher papers

Showing 12 of 23.

- [Comprehensive genomic profiles of small cell lung cancer](https://scholariq.org/papers/comprehensive-genomic-profiles-of-small-cell-lung-cancer/)
- [Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer](https://scholariq.org/papers/integrative-genome-analyses-identify-key-somatic-driver-mutations-of-small-cell/)
- [Swarm Learning for decentralized and confidential clinical machine learning](https://scholariq.org/papers/swarm-learning-for-decentralized-and-confidential-clinical-machine-learning/)
- [The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4](https://scholariq.org/papers/the-centrosomal-protein-nephrocystin-6-is-mutated-in-joubert-syndrome-and/)
- [Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible](https://scholariq.org/papers/positional-cloning-uncovers-mutations-in-plce1-responsible-for-a-nephrotic/)
- [Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement](https://scholariq.org/papers/mutations-in-the-tight-junction-gene-claudin-19-cldn19-are-associated-with-renal/)
- [Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies](https://scholariq.org/papers/genome-wide-mega-analysis-identifies-16-loci-and-highlights-diverse-biological/)
- [Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome](https://scholariq.org/papers/recessive-mutations-in-dgke-cause-atypical-hemolytic-uremic-syndrome/)
- [Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes](https://scholariq.org/papers/mutations-in-grin2a-cause-idiopathic-focal-epilepsy-with-rolandic-spikes/)
- [COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness](https://scholariq.org/papers/coq6-mutations-in-human-patients-produce-nephrotic-syndrome-with-sensorineural/)
- [Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling](https://scholariq.org/papers/exome-capture-reveals-znf423-and-cep164-mutations-linking-renal-ciliopathies-to/)
- [Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors](https://scholariq.org/papers/integrative-genomic-profiling-of-large-cell-neuroendocrine-carcinomas-reveals/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)

## Researcher university

- [University of Cologne](https://scholariq.org/institutions/university-of-cologne/)

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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.