# Bodo Grimbacher

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/bodo-grimbacher/

## Facts

| Field | Value |
| --- | --- |
| Citations | 37,863 |
| Field | Immunodeficiency and Autoimmune Disorders |
| h-index | 98 |
| i10-index | 315 |
| Last Known Institution | University of Freiburg |
| OpenAlex ID | https://openalex.org/A5070228992 |
| ORCID iD | https://orcid.org/0000-0002-6897-6806 |
| Works | 1,951 |

## Researcher papers

Showing 12 of 15.

- [Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans](https://scholariq.org/papers/mutations-in-tnfrsf13b-encoding-taci-are-associated-with-common-variable/)
- [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/)
- [Thalassemia Syndromes](https://scholariq.org/papers/thalassemia-syndromes/)
- [Loss of Interleukin-10 Signaling and Infantile Inflammatory Bowel Disease: Implications for Diagnosis and Therapy](https://scholariq.org/papers/loss-of-interleukin-10-signaling-and-infantile-inflammatory-bowel-disease/)
- [Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study](https://scholariq.org/papers/clinical-spectrum-and-features-of-activated-phosphoinositide-3-kinase-syndrome-a/)
- [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/)
- [The phenotype of human STK4 deficiency](https://scholariq.org/papers/the-phenotype-of-human-stk4-deficiency/)
- [DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients](https://scholariq.org/papers/dock8-deficiency-clinical-and-immunological-phenotype-and-treatment-options-a/)
- [The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency](https://scholariq.org/papers/the-extended-phenotype-of-lps-responsive-beige-like-anchor-protein-lrba/)
- [The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency](https://scholariq.org/papers/the-extended-clinical-phenotype-of-64-patients-with-dedicator-of-cytokinesis-8/)
- [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/)

## Researcher topics

- [Immunodeficiency and Autoimmune Disorders](https://scholariq.org/topics/immunodeficiency-and-autoimmune-disorders/)
- [Blood disorders and treatments](https://scholariq.org/topics/blood-disorders-and-treatments/)
- [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/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)

## 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.