# Christian Becker

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/christian-becker/

## Facts

| Field | Value |
| --- | --- |
| Citations | 17,184 |
| Field | Genetic Associations and Epidemiology |
| h-index | 59 |
| i10-index | 86 |
| Last Known Institution | University of Cologne |
| OpenAlex ID | https://openalex.org/A5104167195 |
| ORCID iD | https://orcid.org/0009-0002-2964-4486 |
| Works | 121 |

## Researcher papers

- [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/)
- [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/)
- [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/)
- [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/)
- [Loss of Nephrocystin-3 Function Can Cause Embryonic Lethality, Meckel-Gruber-like Syndrome, Situs Inversus, and Renal-Hepatic-Pancreatic Dysplasia](https://scholariq.org/papers/loss-of-nephrocystin-3-function-can-cause-embryonic-lethality-meckel-gruber-like/)
- [Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis](https://scholariq.org/papers/loss-of-glis2-causes-nephronophthisis-in-humans-and-mice-by-increased-apoptosis/)
- [LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome](https://scholariq.org/papers/lrp4-mutations-alter-wnt-catenin-signaling-and-cause-limb-and-kidney/)
- [A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations](https://scholariq.org/papers/a-systematic-approach-to-mapping-recessive-disease-genes-in-individuals-from/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Biochemical Analysis and Sensing Techniques](https://scholariq.org/topics/biochemical-analysis-and-sensing-techniques/)
- [Neurobiology and Insect Physiology Research](https://scholariq.org/topics/neurobiology-and-insect-physiology-research/)
- [Olfactory and Sensory Function Studies](https://scholariq.org/topics/olfactory-and-sensory-function-studies/)
- [Genomics and Phylogenetic Studies](https://scholariq.org/topics/genomics-and-phylogenetic-studies/)

## 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.