Yuya Aoto - Publications

Clinical and Genetic Insights Into Isolated Proteinuria With CUBN Variants.

Journal: Kidney international reports

Published: December 12, 2025

Clinical use of the VNtyper-Kestrel pipeline for MUC1 variant detection in autosomal-dominant tubulointerstitial kidney disease.

Journal: Clinical and experimental nephrology

Published: March 04, 2025

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

Journal: Kidney international reports

Published: September 08, 2024

COL4A5 Intronic Variants at Third to Fifth Nucleotides Cause Alport Syndrome.

Journal: Kidney international reports

Published: July 26, 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

Management of children with obesity at local hospital and impact of COVID-19 pandemic.

Journal: Frontiers in pediatrics

Published: May 25, 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

Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritis.

Journal: Pediatric nephrology (Berlin, Germany)

Published: March 16, 2023

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

Journal: Clinical and experimental nephrology

Published: January 26, 2023

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

Clinical and pathological investigation of oligomeganephronia.

Journal: Pediatric nephrology (Berlin, Germany)

Published: April 01, 2022

Detecting pathogenic deep intronic variants in Gitelman syndrome.

Journal: American journal of medical genetics. Part A

Published: January 28, 2022