Junko Ueda

Wako, Japan

Last Updated: 09/26/2026

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Found 31 publications

Genome-wide identification and characterization of QTLs for transcriptional noise in human midbrain cells.

Genome-wide identification and characterization of QTLs for transcriptional noise in human midbrain cells.

Journal: Cell reports
Published: November 28, 2024

Transcriptomic dysregulation and autistic-like behaviors in Kmt2c haploinsufficient mice rescued by an LSD1 inhibitor.

Transcriptomic dysregulation and autistic-like behaviors in Kmt2c haploinsufficient mice rescued by an LSD1 inhibitor.

Journal: Molecular psychiatry
Published: January 05, 2024

A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis.

A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis.

Journal: Psychiatry and clinical neurosciences
Published: November 29, 2023

LINE-1 hypomethylation, increased retrotransposition and tumor-specific insertion in upper gastrointestinal cancer.

LINE-1 hypomethylation, increased retrotransposition and tumor-specific insertion in upper gastrointestinal cancer.

Journal: Cancer science
Published: July 24, 2023

Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk.

Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk.

Journal: Cell genomics
Published: April 14, 2023

Identification of epigenetically active L1 promoters in the human brain and their relationship with psychiatric disorders.

Identification of epigenetically active L1 promoters in the human brain and their relationship with psychiatric disorders.

Journal: Neuroscience research
Published: February 02, 2023

Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder.

Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder.

Journal: Molecular psychiatry
Published: August 22, 2022

Cell-type-specific DNA methylation analysis of the frontal cortices of mutant Polg1 transgenic mice with neuronal accumulation of deleted mitochondrial DNA.

Cell-type-specific DNA methylation analysis of the frontal cortices of mutant Polg1 transgenic mice with neuronal accumulation of deleted mitochondrial DNA.

Journal: Molecular brain
Published: November 04, 2021

Cell type-specific DNA methylation analysis of the prefrontal cortex of patients with schizophrenia.

Cell type-specific DNA methylation analysis of the prefrontal cortex of patients with schizophrenia.

Journal: Psychiatry and clinical neurosciences
Published: April 12, 2021

Decreased DNA methylation at promoters and gene-specific neuronal hypermethylation in the prefrontal cortex of patients with bipolar disorder.

Decreased DNA methylation at promoters and gene-specific neuronal hypermethylation in the prefrontal cortex of patients with bipolar disorder.

Journal: Molecular psychiatry
Published: December 09, 2020

Identification of somatic mutations in postmortem human brains by whole genome sequencing and their implications for psychiatric disorders.

Identification of somatic mutations in postmortem human brains by whole genome sequencing and their implications for psychiatric disorders.

Journal: Psychiatry and clinical neurosciences
Published: November 08, 2017

Identification of somatic mutations in monozygotic twins discordant for psychiatric disorders.

Identification of somatic mutations in monozygotic twins discordant for psychiatric disorders.

Journal: NPJ schizophrenia
Published: October 03, 2017
Showing 1-12 of 31

Last Updated: 09/26/2026