# Véronique Frémeaux‐Bacchi

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/veronique-fremeaux-bacchi/

## Facts

| Field | Value |
| --- | --- |
| Citations | 33,298 |
| Field | Complement system in diseases |
| h-index | 94 |
| i10-index | 275 |
| Last Known Institution | Assistance Publique – Hôpitaux de Paris |
| OpenAlex ID | https://openalex.org/A5025683973 |
| ORCID iD | https://orcid.org/0000-0002-4865-8528 |
| Works | 553 |

## Researcher papers

Showing 12 of 15.

- [Genetics and Outcome of Atypical Hemolytic Uremic Syndrome](https://scholariq.org/papers/genetics-and-outcome-of-atypical-hemolytic-uremic-syndrome/)
- [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/)
- [C3 glomerulopathy: consensus report](https://scholariq.org/papers/c3-glomerulopathy-consensus-report/)
- [An international consensus approach to the management of atypical hemolytic uremic syndrome in children](https://scholariq.org/papers/an-international-consensus-approach-to-the-management-of-atypical-hemolytic/)
- [Haemolytic uraemic syndrome](https://scholariq.org/papers/haemolytic-uraemic-syndrome/)
- [Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies](https://scholariq.org/papers/use-of-eculizumab-for-atypical-haemolytic-uraemic-syndrome-and-c3/)
- [Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome](https://scholariq.org/papers/recessive-mutations-in-dgke-cause-atypical-hemolytic-uremic-syndrome/)
- [Endothelium structure and function in kidney health and disease](https://scholariq.org/papers/endothelium-structure-and-function-in-kidney-health-and-disease/)
- [Pregnancy-Associated Hemolytic Uremic Syndrome Revisited in the Era of Complement Gene Mutations](https://scholariq.org/papers/pregnancy-associated-hemolytic-uremic-syndrome-revisited-in-the-era-of/)
- [C3 glomerulopathy — understanding a rare complement-driven renal disease](https://scholariq.org/papers/c3-glomerulopathy-understanding-a-rare-complement-driven-renal-disease/)
- [C3 glomerulopathy: a new classification](https://scholariq.org/papers/c3-glomerulopathy-a-new-classification/)
- [Current Understanding of the Role of Complement in IgA Nephropathy](https://scholariq.org/papers/current-understanding-of-the-role-of-complement-in-iga-nephropathy/)

## 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/)
- [Blood groups and transfusion](https://scholariq.org/topics/blood-groups-and-transfusion/)
- [Coagulation, Bradykinin, Polyphosphates, and Angioedema](https://scholariq.org/topics/coagulation-bradykinin-polyphosphates-and-angioedema/)
- [Hemoglobinopathies and Related Disorders](https://scholariq.org/topics/hemoglobinopathies-and-related-disorders/)

## Researcher university

- [Assistance Publique – Hôpitaux de Paris](https://scholariq.org/institutions/assistance-publique-hopitaux-de-paris/)

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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.