# Klaus Warnatz

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/klaus-warnatz/

## Facts

| Field | Value |
| --- | --- |
| Citations | 24,868 |
| Field | Immunodeficiency and Autoimmune Disorders |
| h-index | 75 |
| i10-index | 223 |
| Last Known Institution | University of Freiburg |
| OpenAlex ID | https://openalex.org/A5032056056 |
| ORCID iD | https://orcid.org/0000-0002-1172-865X |
| Works | 398 |

## Researcher papers

- [International Consensus Document (ICON): Common Variable Immunodeficiency Disorders](https://scholariq.org/papers/international-consensus-document-icon-common-variable-immunodeficiency-disorders/)
- [Clinical picture and treatment of 2212 patients with common variable immunodeficiency](https://scholariq.org/papers/clinical-picture-and-treatment-of-2212-patients-with-common-variable/)
- [The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity](https://scholariq.org/papers/the-european-society-for-immunodeficiencies-esid-registry-working-definitions/)
- [Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects](https://scholariq.org/papers/phenotype-penetrance-and-treatment-of-133-cytotoxic-t-lymphocyte-antigen-4/)
- [Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies](https://scholariq.org/papers/monogenic-mutations-differentially-affect-the-quantity-and-quality-of-t/)
- [Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects](https://scholariq.org/papers/deficiency-of-caspase-recruitment-domain-family-member-11-card11-causes-profound/)
- [The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiency](https://scholariq.org/papers/the-card11-bcl10-malt1-cbm-signalosome-complex-stepping-into-the-limelight-of/)
- [Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations](https://scholariq.org/papers/characterization-of-the-clinical-and-immunologic-phenotype-and-management-of-157/)

## Researcher topics

- [Immunodeficiency and Autoimmune Disorders](https://scholariq.org/topics/immunodeficiency-and-autoimmune-disorders/)
- [Immune Cell Function and Interaction](https://scholariq.org/topics/immune-cell-function-and-interaction/)
- [T-cell and B-cell Immunology](https://scholariq.org/topics/t-cell-and-b-cell-immunology/)
- [Blood disorders and treatments](https://scholariq.org/topics/blood-disorders-and-treatments/)
- [Cystic Fibrosis Research Advances](https://scholariq.org/topics/cystic-fibrosis-research-advances/)

## Researcher university

- [University of Freiburg](https://scholariq.org/institutions/university-of-freiburg/)

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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.