Eri Okada - Publications

Renal Prognostic Identification in Patients With Autosomal Dominant Polycystic Kidney Disease by Whole Genome Sequencing: A Prospective, Observational Study.

Journal: Kidney medicine

Published: September 22, 2025

Initial Suspicion of Autosomal Dominant Polycystic Kidney Disease Resulted in a Diagnosis of Autosomal Dominant Tubulointerstitial Kidney Disease Caused by a UMOD Mutation.

Journal: Internal medicine (Tokyo, Japan)

Published: June 18, 2025

Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort.

Journal: Clinical and experimental nephrology

Published: December 11, 2024

Comprehensive Splice Pattern Analysis for Previously Reported OCRL Splicing Variants and Their Phenotypic Contributions.

Journal: Kidney international reports

Published: September 08, 2024

Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: April 21, 2024

Evaluation of pathogenicity of WT1 intron variants by in vitro splicing analysis.

Journal: Clinical and experimental nephrology

Published: December 07, 2023

Renal Hemodynamic and Functional Changes in Patients with ADPKD.

Journal: Kidney360

Published: June 10, 2023

Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866.

Journal: Kidney international reports

Published: May 14, 2023

All reported non-canonical splice site variants in GLA cause aberrant splicing.

Journal: Clinical and experimental nephrology

Published: January 26, 2023

Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease.

Journal: Kidney international reports

Published: December 06, 2022

Aberrant splicing caused by exonic single nucleotide variants positioned 2nd or 3rd to the last nucleotide in the COL4A5 gene.

Journal: Clinical and experimental nephrology

Published: July 27, 2022

Polydactyly-derived allogeneic chondrocyte cell-sheet transplantation with high tibial osteotomy as regenerative therapy for knee osteoarthritis.

Journal: NPJ Regenerative medicine

Published: November 04, 2021