Corinne Antignac
Inserm(FR)Université Paris Cité(FR)Assistance Publique – Hôpitaux de Paris(FR)Institut des Maladies Génétiques Imagine(FR)
Publications by Year
Research Areas
Renal Diseases and Glomerulopathies, Renal and related cancers, Genetic and Kidney Cyst Diseases, Biomedical Research and Pathophysiology, Cell Adhesion Molecules Research
Most-Cited Works
- → NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome(2000)1,440 cited
- → Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination(2003)641 cited
- → A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis(1998)640 cited
- → X-linked Alport Syndrome(2000)581 cited
- → Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure(2001)530 cited
- → Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome(1994)511 cited