Corinne Antignac
Paris, 75015, France
Last Updated: 09/26/2026
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Found 109 publications
Podocin oligomers regulate the ordering of nephrin chains, providing the molecular basis of NPHS2 interallelic interactions.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 14, 2026
From dysphagia to kidney disease: Alport syndrome with leiomyomatosis.
Journal: Kidney international
Published: February 22, 2026
Exome Sequencing in a Large Cohort with Ciliopathy-Related Kidney Disease.
Journal: Clinical journal of the American Society of Nephrology : CJASN
Published: July 03, 2025
Genetic screening in kidney transplant candidates.
Journal: Clinical kidney journal
Published: March 26, 2025
Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.
Journal: Pediatric nephrology (Berlin, Germany)
Published: February 20, 2025
Using VNtyper from Whole Exome Sequencing Data to Detect Pathogenic Variants in the MUC1 Gene.
Journal: Journal of the American Society of Nephrology : JASN
Published: December 09, 2024
Organoids, organs-on-chips, complex in vitro model: Definitions, applications, validation, ethics.
Journal: Therapie
Published: October 11, 2024
Diagnosis, management and treatment of the Alport syndrome - 2024 guideline on behalf of ERKNet, ERA and ESPN.
Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: September 30, 2024
Phenotypic Heterogeneity of ADTKD-MUC1 Diagnosed Using VNtyper, a Novel Genetic Technique.
Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation
Published: July 16, 2024
Last Updated: 09/26/2026