Ming J. Ye

Kobe, Japan

Last Updated: 09/26/2026

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Found 22 publications

Identification of Genetic Variants in Status Epilepticus Associated With Fever.

Identification of Genetic Variants in Status Epilepticus Associated With Fever.

Journal: Brain and behavior

Published: June 04, 2024

End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapy.

End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapy.

Journal: Human genome variation

Published: December 26, 2023

Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population.

Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population.

Journal: Journal of human genetics

Published: October 27, 2021

Ultra-Sensitive Isopropanol Biochemical Gas Sensor (Bio-Sniffer) for Monitoring of Human Volatiles.

Ultra-Sensitive Isopropanol Biochemical Gas Sensor (Bio-Sniffer) for Monitoring of Human Volatiles.

Journal: Sensors (Basel, Switzerland)

Published: October 01, 2020

A woman with a dual genetic diagnosis of autosomal dominant tubulointerstitial kidney disease and KBG syndrome.

A woman with a dual genetic diagnosis of autosomal dominant tubulointerstitial kidney disease and KBG syndrome.

Journal: CEN case reports

Published: May 26, 2020

Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome.

Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome.

Journal: Kidney international

Published: February 18, 2020

Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations.

Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations.

Journal: CEN case reports

Published: January 05, 2020

Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5.

Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5.

Journal: Nature communications

Published: May 05, 2019

A girl with CLOVES syndrome with a recurrent PIK3CA somatic mutation and pancreatic steatosis.

A girl with CLOVES syndrome with a recurrent PIK3CA somatic mutation and pancreatic steatosis.

Journal: Human genome variation

Published: February 16, 2019

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.

Journal: Molecular genetics & genomic medicine

Published: December 11, 2018

Effects of oral health instructions on glycemic control and oral health status of periodontitis patients with type 2 diabetes mellitus: A preliminary observation.

Effects of oral health instructions on glycemic control and oral health status of periodontitis patients with type 2 diabetes mellitus: A preliminary observation.

Journal: Journal of dental sciences

Published: October 16, 2018

Clinical spectrum of male patients with OFD1 mutations.

Clinical spectrum of male patients with OFD1 mutations.

Journal: Journal of human genetics

Published: October 01, 2018

Showing 1-12 of 22

Last Updated: 09/26/2026