Vincent Moriniere
Paris, France
Last Updated: 09/26/2026
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Found 31 publications
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
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
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
Targeted RNAseq from patients' urinary cells to validate pathogenic noncoding variants in autosomal dominant polycystic kidney disease genes: a proof of concept.
Journal: Kidney international
Published: February 28, 2024
Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence.
Journal: Kidney international reports
Published: September 28, 2023
VNtyper enables accurate alignment-free genotyping of MUC1 coding VNTR using short-read sequencing data in autosomal dominant tubulointerstitial kidney disease.
Journal: iScience
Published: March 03, 2023
The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies.
Journal: Kidney international
Published: November 15, 2022
Bi-allelic pathogenic variants in ITGA8 cause slowly progressive renal disease of unknown etiology.
Journal: Clinical genetics
Published: July 30, 2022
A wave of deep intronic mutations in X-linked Alport syndrome.
Journal: Kidney international
Published: July 05, 2022
Last Updated: 09/26/2026