# Corinne Antignac

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/corinne-antignac/

## Facts

| Field | Value |
| --- | --- |
| Citations | 31,170 |
| Field | Renal Diseases and Glomerulopathies |
| h-index | 106 |
| i10-index | 254 |
| Last Known Institution | Inserm |
| OpenAlex ID | https://openalex.org/A5067853725 |
| ORCID iD | 0000-0002-9934-4940 |
| Works | 427 |

## Researcher papers

Showing 12 of 21.

- [NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome](https://scholariq.org/papers/nphs2-encoding-the-glomerular-protein-podocin-is-mutated-in-autosomal-recessive/)
- [Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination](https://scholariq.org/papers/mutations-in-invs-encoding-inversin-cause-nephronophthisis-type-2-linking-renal/)
- [A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis](https://scholariq.org/papers/a-novel-gene-encoding-an-integral-membrane-protein-is-mutated-in-nephropathic/)
- [X-linked Alport Syndrome](https://scholariq.org/papers/x-linked-alport-syndrome-2/)
- [Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure](https://scholariq.org/papers/mutation-of-bsnd-causes-bartter-syndrome-with-sensorineural-deafness-and-kidney/)
- [Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome](https://scholariq.org/papers/identification-of-mutations-in-the-3-iv-and-4-iv-collagen-genes-in-autosomal/)
- [The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome](https://scholariq.org/papers/the-ciliary-gene-rpgrip1l-is-mutated-in-cerebello-oculo-renal-syndrome-joubert/)
- [X-Linked Alport Syndrome](https://scholariq.org/papers/x-linked-alport-syndrome/)
- [Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations](https://scholariq.org/papers/structure-of-the-gene-for-congenital-nephrotic-syndrome-of-the-finnish-type/)
- [Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling](https://scholariq.org/papers/exome-capture-reveals-znf423-and-cep164-mutations-linking-renal-ciliopathies-to/)
- [Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis](https://scholariq.org/papers/mutations-in-a-novel-gene-nphp3-cause-adolescent-nephronophthisis-tapeto-retinal/)
- [ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption](https://scholariq.org/papers/adck4-mutations-promote-steroid-resistant-nephrotic-syndrome-through-coq10/)

## Researcher topics

- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)
- [Biomedical Research and Pathophysiology](https://scholariq.org/topics/biomedical-research-and-pathophysiology/)
- [Cell Adhesion Molecules Research](https://scholariq.org/topics/cell-adhesion-molecules-research/)

## Researcher university

- [Inserm](https://scholariq.org/institutions/inserm/)

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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.