# Peter F. Zipfel

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

## Facts

| Field | Value |
| --- | --- |
| Citations | 31,267 |
| Field | Complement system in diseases |
| h-index | 99 |
| i10-index | 337 |
| Last Known Institution | National Center for Complementary and Integrative Health |
| OpenAlex ID | https://openalex.org/A5067381987 |
| ORCID iD | 0000-0002-6149-2411 |
| Works | 926 |

## Researcher papers

Showing 12 of 14.

- [Complement regulators and inhibitory proteins](https://scholariq.org/papers/complement-regulators-and-inhibitory-proteins/)
- [Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype](https://scholariq.org/papers/relative-role-of-genetic-complement-abnormalities-in-sporadic-and-familial-ahus/)
- [Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference](https://scholariq.org/papers/atypical-hemolytic-uremic-syndrome-and-c3-glomerulopathy-conclusions-from-a/)
- [Complement factor H binds malondialdehyde epitopes and protects from oxidative stress](https://scholariq.org/papers/complement-factor-h-binds-malondialdehyde-epitopes-and-protects-from-oxidative/)
- [C3 glomerulopathy — understanding a rare complement-driven renal disease](https://scholariq.org/papers/c3-glomerulopathy-understanding-a-rare-complement-driven-renal-disease/)
- [Membranoproliferative Glomerulonephritis Type II (Dense Deposit Disease)](https://scholariq.org/papers/membranoproliferative-glomerulonephritis-type-ii-dense-deposit-disease/)
- [Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency](https://scholariq.org/papers/factor-h-autoantibodies-in-atypical-hemolytic-uremic-syndrome-correlate-with/)
- [Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome](https://scholariq.org/papers/mutations-in-factor-h-reduce-binding-affinity-to-c3b-and-heparin-and-surface/)
- [Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome](https://scholariq.org/papers/deletion-of-complement-factor-h-related-genes-cfhr1-and-cfhr3-is-associated-with/)
- [ApoE attenuates unresolvable inflammation by complex formation with activated C1q](https://scholariq.org/papers/apoe-attenuates-unresolvable-inflammation-by-complex-formation-with-activated/)
- [Atypical aHUS: State of the art](https://scholariq.org/papers/atypical-ahus-state-of-the-art/)
- [Factor H family proteins: on complement, microbes and human diseases](https://scholariq.org/papers/factor-h-family-proteins-on-complement-microbes-and-human-diseases/)

## Researcher topics

- [Complement system in diseases](https://scholariq.org/topics/complement-system-in-diseases/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Vector-borne infectious diseases](https://scholariq.org/topics/vector-borne-infectious-diseases/)
- [Blood groups and transfusion](https://scholariq.org/topics/blood-groups-and-transfusion/)
- [Antifungal resistance and susceptibility](https://scholariq.org/topics/antifungal-resistance-and-susceptibility/)

## Researcher university

- [National Center for Complementary and Integrative Health](https://scholariq.org/institutions/national-center-for-complementary-and-integrative-health/)

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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.